I have said from the beginning which has been thirty plus years that one of the things it feels like is that every cell in my body is sick with the flu. This makes total sense
Hi i just wanted to say this really has enlightened me and is the missing link that i have been looking for, i can put this information to good use. Thankyou
I’ve always told people my mitochondria are all screwed up!! I’ve known from an early age. Something was wrong with my body. I am in pain all the time every piece of me hurts. I’m sick and tired of it no matter how healthy I eat. I still feel shitty and I am so happy I ran across this because I am definitely going to be able to talk with my doctor about this lipid therapy you’re talking about !! Thank you !!!!!!
It is frustrating when you do not get validation for how much you suffer from this disease….I was diagnosed som 40 plus years ago by a wonderful doctor who told me this is a real disease….mine was probably caused by pesticides….
I know how you feel, I had just come out of the army which i was a nurse in (UK) felt like no one believed me the same as you, a hypochondriac.Ive just been thinking what major events happened around the world in the 70's as I had never heard of it before then......Keep on fighting honey xxx
I had been to Dr after Dr and was told it was in my head. I started seeing specialist after specialist and my last one spent 5 minutes with me and touched my elbow and forearm which was extremely painful.. He said he couldn't do anything for me and I cried. I finally found a Rheumatologist and my world changed. It's taken years of fighting for myself. I'm a retired RN now and living each day to the best of my ability.
as a mom of a daughter (35) Recently dx., how do you feel about lipid regeneration? what he is talking about here> what has helped you!? no one, not even the doctors are believing my daughter and due to past cancer,jaw surgery,and tmj, they say its a bad toothache.. and rx. more pills. like gabba!! the worst! I am so frustrated!!! ty for sharing!
First diagnosed with fibromyalgia, it turned out later that I have/had an auto-immune disease. Fibro was just a group of symptoms that many people ignored (for me) because it's been largely ignored. If it wasn't like doctors like my current GP, and doctors like you, I would have never found that out. Thank you for standing up for fibro warriors!
My mom never found a doctor to properly treat her. She got I’ll very suddenly at a time she was very vibrant. She might have been bitten by a deer tick (manufactured on Plum Island), not far from her home. She couldn’t sit comfortably. She had to sit on a tire. Her butt was all bone. No meat. Mom died way too young for her @ 81. All they did was prescribe DRUGS
Yup 47 years later also had a stroke on 4 11 2023 in my sleep and now legally blind 😴 keep on spiritually looking up. God bless you always 🙏 ❤️ 💖 ♥️ 😘 💛 🙏 Amen and Amen 🙏
Thanks yes tired of being sick tired I agree but I haven't had fibro as long as you have I have heart and lung disease, osteoarthritis a rod in my leg have broken ribs and it's on the right side and left side or fractured ribs twice on resuscitation I have 5/6 fibro's in the front from both breast bones and lower down both left and right side I have anxiety depression I work through it as I'm a fighter
I have fibromyalgia for over twenty years. Everything you said makes sense. I have chronic muscle spasms that hurt so bad it causes me to become depressed. Thank you for taking this condition serious. It really is not in our head.
Have u tried potassium rich foods? They help. So does vit B complex( natural source. Methlated) So does magnesium, but watch out for diarrhea with magnesium. None of this stuff cures our pain of course. Just better.
Yes they tried to put me on Lyrica it made me gain 25 lbs in a month as well as C one ..then the Dr 2002 diagnosed - severe chronic fatigue syndrome ( CFS) carpal tunnel both wrists surgery on my right, flare ups when it's cloudy, my Ra was normal, my ANA was positive bc of my inflammation in my body.. cortisol sky high..my thyroid symptoms, Thyroid tests normal, pre diabetic, obesity from craving sugar and carbs, connection, IBS, Chronic muscle spasms take Flexeril on flare ups, Dr, gave me 3X a day Hydrocodone and Tylenol 325 mg and ibuprofen together almost killed my liver was in failure after bedridden for 2 yrs the more I took the more with exhaustion, chronic insomnia, depression anxiety, PTSD, meds help me, prayer has helped me the most, reading or listening to niv bible daily helps me I try to do both 1 hr each a day I am believer in Christ he has proven so many miracles in my life, true Christianity " is not a religion " it is a faith based relationship with Christ..I talk to him daily..I cry out to him when I can't take it anymore I'm 63..live alone..if u ever get in trouble call out to Jesus Christ to help you even if your dying he said in his word ( the Bible) if you all on him he will save you..Shalom 🙏🪖🗡️📖🔥🪔📣⚔️📜
There is help for this your just looking in the wrong place.Find a functional medicine doctor..Ask for a thyroid panel and get a reverse t3 done.Read hypothyroidism type 2. And Mary Shomons book.Look her up . Her book was a wealth of information .Get educated and learn .You will recover
@@kkx23 - I so agree! Proper treatment of subclinical hypothyroidism is essential and usually entails taking natural thyroid (ins. won't pay for it), taking enough of it for your lab results to be at the "hyper" level, and going by how you feel, not lab results. Sleep is essential too. I've found timed release, low dose melatonin to be the best for that.
I have had fibromyalgia for almost 50 years, actually before there was actually a name for it. In the beginning, doctors called it fibrositis until they found out it was not like arthritis - not an "itis" but instead the pain was in the muscles and the fibrous tissues that surround the bones - a cousin to rheumatism. I am now 70 years old and so have suffered with it for most of my adult life. I went from doctor to doctor trying to find out what was wrong with me, many trying to tell me it was all in my head (which I knew it was not). Finally, my family physician diagnosed me because he constantly read the JAMA magazines so he stayed on top of all the new information that was coming out all the time. I have never been able to tolerate Lyrica or Neurontin which is usually prescribed for fibromyalgia so my only alternative has been to rely on pain medication, prescribed to me by a trusted pain specialist, but even with pain medication, it does not relieve all the pain but makes it a little more tolerable. I also suffer from degenerative disk disease and have had 7 herniated disks in my neck and back, also suffer from spinal stenosis - so my life has been one of nothing but pain. How can I find a doctor who knows what you are talking about regarding trying to reverse fibromyalgia?
Hi Linda, so sorry to hear you've been suffering from this debilitating condition for a lifetime! I totally feel for you! I was also diagnosed with " fibrositis" 🤔 when I was 18 years old I am 58yrs now. A few years later I had Fibromyalgia syndrome 🙄 It's a nightmare living with this invisible demon. I have been taking Lyrica for about 9 years. Hope you manage to sort some pain relief.
I too have fibromyalgia scoliosis and degenerative discs in my neck and from the tailbone with 3 discs that slide over my tailbone.. it's so hard, but I deal with it.. I was diagnosed with fibromyalgia about 10 years but it's been happening for longer than that I pray for you my fibro warrior, maybe some day... People won't have to suffer so I was an active child participated in sports in school. I did hard work in my adult life... Now I'll be 60 in a few days and miss taking long walks, running, playing sports.... I miss WORK!!! I don't know if I call it a disease or disorder... I know they call it a disease, because mentally I still feel young, I still want to participate in life and be active with other, but I can't make plans from now to an hour from now. Stay strong Blessings and prayers to you 💜✨🙏🕊️🙏✨💜
Yes. Exactly the way I get treated for innate knowledge, wisdom, discernment, today! 2023. Eat as close to real food as possible. Less processed meats. Unless you, yourself hunt for your own. Chemicals are everywhere! Sky is now chemical plasma. Electromagnetic fields. Nano particles. Nano metals. Barium. Strontium. Aluminum. Detox and fast. Drink warm lemon water to start your day. Never drink iced water. Room temperature. Consume a diet of: Breathing deeply. Lots of sunshine. Walking. Noticing beauty. Hugs. Sweet grateful words. Reading by candlelight. Prayer.
True, some people haven't got any idea what it's like they think that your exaggerating but I've also heard people say that too about Lupus and MS suffers are also misunderstood. However, saying that explaining and re educating them about simple things like it's an autoimmune disease & my body is stuck working overtime constantly it gets tired quickly too. Information is the key I find, let them know that it's inherited & in our DNA. It's also up to us to keep up with the latest research too. I personally have tried the infusion therapy & it helped me to reduce my medication from a dozen to half a dozen, got me out of bed more, less siestas + less pains. Good Luck everyone & happy healings 🥰
@@brightwhitelight9445 Everything you said is brilliant 👏 I will definitely start using what you said more in my life, especially with the people that just don't get it, and just think I'm lazy...I hate it 😮💨 educating really IS key to eventually being heard and understood better than we all are now!
Those people that say we don't have it need to shut their mouths. It real painful and not fun to live with. Do not tell people they don't have something when your not in their body. How dare they
You have to fight and fight like hell, I get injections from in my head all the way down to my feet...now I'm tired of fighting im 55 and was diagnose in 1992...best of luck to you
Except most of us have nowhere to get infusions, because we all have "fainting lady syndrome!" I go to a research hospital, Cleveland Clinic, they don't even have a Dr that wants to talk about Fibromyalgia!
@@OubreMedical please advice on finding a top treatment centre in Toronto. I was a patient at Mount Sinai WASSER pain management...but since new Director he has told me the centre can't deal with my pain and I need to go back to my MD. I was a patient for about 8 years before that🤕
I have suffered from fibromyalgia for over 30 years. I have had doctors accuse me of exaggerating my pain, and one doctor told me not to tell anyone that I have fibromyalgia because I would be labeled as "crazy"! My family scoffed at my diagnosis and said, "I just don't think you can handle pain!". I am crying as I listen to this. It is the first time anyone has given me an explanation to what is causing my pain and suffering. I need all of this information; what foods to avoid, what supplements to take, and how I can get my life back. If at all possible, could you direct me to the resources that I need to get well? Thank you so very much!
I feel your pain! I was the same way and as a nurse, I heard so many times in the ER where I worked, “Oh, they’re a nut job!” Doctors thought they were drug seekers and I witnessed these things while suffering with it myself. I told no one I had it because of the label a person received who said they had fibromyalgia. The doctors at Mayo in Rochester Minnesota helped me when I was at my worst. Thank God for them and the Dr. In the ER one night who was so kind and compassionate who told me to go there. I will never forget him and his nurse. The first people who treated me like I mattered. Yes, I still suffer today but I also believe that by the grace of God, He will heal me one day. God bless you! 🙏🏻
I suggest watching the youtube videos of Martin Rutherford. Avoid pinning all your hopes on people who are trying to sell something or promising some kind of cure in a pill.
Perhaps you can eliminate inflammatory foods like tomato potato cream dairy gluten then try them after several weeks without. If I eat whipped cream, I have all over body pain. Tomatoes give me joint pain. Dairy and gluten make my gut miserable. I hope that is a start for you.
Thank you, thank you for sharing, Sarita. I feel that also and have not heard anyone else relate that just taking a breath is tiring. In fact sometimes it seems it takes all I have. God bless you and praying for a cure or better meds that will help more than the ones out there now.
I was diagnosed by two doctors that said I had the Fibromyalgia they have seen. Years later I found I was allergic to milk lactose. The lactose gets in your muscles and make them achy. When I switched to lactose free milk, all my problems were gone. I also discovered I’m an Empath and picking up others physical and emotional state. Which was so exhausting
Wow did it really. That's great. Yep, the same as you, listen to everyone's problems but don't get much back unfortunately. I've decided that the so called friend of over 40 years and who abused me and told me there wasn't anything wrong wuth me, weren't worth me being so upset over. So, I made a choice to say goodbye. I can't be there for everyone. I'm flat put being here for myself. It's excruciating, daily pain from my head to my feet. I also need a replacement knee which will happen next January. I can't walk and to be quite honest, the thought of even 5 minutes exercise is impossible.
You're rh negative. These doctors have been selling our lab work blood behind our backs. Our blood is called "Pedigree Blood" and they get over $1,000 an ounce. All the doctors have been keeping it a secret. Some of us have copper blood. We're acidic, not alkaline, and need a different diet. Our frequencies are higher than other people, and our bones have a special resonance. Our Amyloid fibrils behave differently; they knit and weave and bind, so that we end up with a lot of Amyloid plaques. Rh negative knees, Alzheimers, urinary/bladder/kidney problems, auto immune, lupus/Lyme ... all neggie diseases. Our vision and eyes are different too. This guy knows it. Crimes Against Humanity, and Medical Experimentation. Trump signed an Executive Order that starts with my name on my clean date from 15 years of an obscene amount of prescriptions, December 27, 2017. All their assets are going to be seized and there will be Nuremberg Trials. ~Pure aQuatic COPPER Magdalenien Rh Negative Blood (MAGA was my great grandmother's nickname,) The Holy Grail Bloodline ~Oraphim, Double Diamond Sun CHRISTOS dna with the genetic code for original humans ... geneticists call us "Organics," and our Mitochondrial dna has the "god-gene" or "X-Factor." You probably have "M's" on your palms with "X's" in the middle. Our palms and feet have special "Palmistry" markings. Eye have Infinity Symbols under each ring finger. The doctors identify us at birth, and the government tracks us from cradle to grave. Our Intelligence Files call us "Targeted Individuals" and if we have abilities like Telepathy (Celts) or Telekinesis (Eastern European) then they call us "Empowered Individuals." Look up both of the above topics and you will find information on being an Empath also. ♾♎ Omegaperfectstorm! LuvQ'all! 888girl! Text Trump 88022
Glad that worked for you. I always drink lactose free milk IF I drink milk. For me, it makes zero difference. I did have a food allergy test, but was not allergic to milk as you were.
Yes. Begin with researching a bit, and try out LDN, low dose Naltrexone. No need to thank me, just do yourself the favor of giving yourself the chance to try it out. The only chemical thing I'll ever put in my body again for healing. It is POWERFUL for all autoimmune matters.
I'm there with ya Becky. Almost 30 years (since highschool) of fibromyalgia + all the other crud. Having thyroid (Hashimotos) does not help. It's always something. Prayers to you.
@@OubreMedical Dear Doctor, very interesting..I have fibro, and have suffered with it for over 30 years...what is your opinion of LDN? It has really helped me with the chronic pain, however I'm still suffering with chronic fatigue, daily. If I could just get that part straighten out I'd be GOOD.
I have had fibromyalgia for 20 years! I also have neuropathy, and I am not diabetic, nor have I had a stroke! They call it genetic, since my grandpa had it! I can spend 20 hours a day in bed! I use to work as a Nurse, and be extremely active! I would work 8 hours and come home and nap for 3 hours! When I use to be active, I would have to take a nap after any activity, even driving! I feel like I'm just waiting to die! At age 55, this isn't living! I am not depressed, I have been in the past! I long for having a whole life again! I want to live!
I know exactly how you feel!!! I’m also suffering with fibromyalgia!! I have neuropathy as well!!! All my doctors do is throw pain pills at me! I hate living like this!!!
I am so sorry. I feel your pain. I too have fibro and many associated diseases and have forced to retire after 38 years j the nursing profession. I find the one of the hardest things is to constantly defend a position I'd rather not have. I'd rather be working feeling that feeling of having improved the quality of someone's life however small, than living in this broken body with the broken brain. Prayers and best wishes.
@@OubreMedical I have heard many times over the 33 years I've had fibromyalgia that I need to heal my gut. I did have terrible yeast infections but I went off all grains, dairy, sugar etc early, and kept off them for 10 years. I got better by about 10%. If it is a microbial problem how do I fix it. I live in Australia and I can't find any doctors who seem to be able to help me actually FIX my gut. What type of doctors should I see?
I've had fibro for 33 years. This is the first video I've ever seen of yours (and the 1st time I'm hearing most of this information.) Thank you for sharing! Looking forward to learning more.
The thing is, they probably do know, but to keep us all dependent on drugs for life, maintaining a healthy bank balance, between both them, the doctors and the pharmaceutical industry. We will be only informed the truth, by people like this. I have happened on this clip accidentally. Not really surprised to hear this. No one has ever been able to explain Fibromyalgia to me. This is so wrong.
As a massage therapist for 21 years, I found that what people with Fibromyalgia feel like is just "frozen muscles". It is as if the nerves are just frozen. When this happens, blood flow can now move through at a normal pace. It is lack of blood flow that usually causes muscle pain.
@@joysoyo2416 So this happens because your nervous system is in the Fight or Flight mode. Our breathing literally regulates our nervous system. IF you take deep long breaths, this will shut off the fight or flight, and turn on the Parasympathetic Nervous System. It is all about the breath, and sleep. You must get good restful sleep also.
@@treecek also putting your tongue pursed between the lips , and Breathe in ,close your eyes breathe out , open the eyes, this taps into the vagus nerve which relaxes the fight or flight
I have Fibro for over 25 years. I have experienced so many surprising symptoms. You mentioned the heart not being one of the organs effected. Well for me, I have had 4 or maybe more "heart attacks" that turned out to be my Fibro causing severe pain in my heart and sternum. So always go to the ER to get checked out, no matter what! My advice to everyone!
Same here! Nerves and muscles pain in heart area. Starts suddenly and causes strong fatigue, but heart is fine. Have to take muscles relaxant, when it happens. Cracking chest/thoracic muscles/ribs makes feel better (which is the proof, that the problemis not in the heart)... for a very little bit, but the pain quickly comes back. When it starts, it lasts for a few days, which is another proof, that it is not heart problem.
Yyes! I went to er earlier this year.. Felt lie someone was stabbbing my heart over and over again Dr did all tests said not heart attack but your pain levels are so high its sending blood pressure through the roof
Yes Joyce, I wonder how spraying millions of gallons of weed killer on two are wheat and corn has affected the human body. Our soil is contaminated and where I live we have something called pfas in our water. Extremely carcinogenic. So then we drink pallets of bottled water and there's millions of tiny pieces of plastic being consumed. The women that got this 35 years ago probably were not eating McDonald's everyday. They were probably making dinner every night and raising many children keeping busy. Why did they get fibromyalgia? Did they have leaky gut 35 years ago? Were all their mitochondrial cells broken up? Of this one thing I have no doubt, this doctor as well as many more with their good intentions and no scientific paperwork to back it up except their own statistics from what they see will become extremely rich and get very large subsidies for their studies. But most people with fibromyalgia can't work an 8-hour job. we are getting rich from having fibromyalgia. The real money is in saying that you can cure it. A few months ago a doctor discovered that a brand new medication that he had developed was blocking pain signals from the brain and allowing fibromyalgia sufferers to exercise and have a better life. Who's right here? I'm just tired and I don't like condescending doctors. Sincerely, Carly
@Elvis Edge RR Woodward while both are antibiotic theyre not the same thing and dont affect the organism the same way sodium chloride is essential for life while glyphosate is not and assault the organism via the shikimate pathway
Hi Dr. Oubre! Thanks for explaining fibromyalgia so well. I've been living with Fibro for years now but was only diagnosed a few months back. My doctor also diagnosed me with Benign Joint Hypermobility Syndrome. The cumulative effect of Fibro and BJHS plus the PCOS and IBS I've been living with for years now has made my life really difficult.
Hello, could I please ask what joint hypermobility syndrome is and the symptoms. I have had fibromyalgia for 30 years, but the past five years I have had severe chest/ribcage pain and difficulty breathing. My heart and lungs have been checked out, but no diagnosis. I am in constant pain and discomfort and find it difficult to take a deep breath as everything feels so solid and tight and stiff, it s so debilitating. Thank you for any feedback. Hope you are having a good day/ night!!!! Hugs
@@pamelasmith2625 ... Hi Pamela, I thought I'd chime in since I've been researching it for a couple years. It is listed under the 'tent' of connective-tissue disorders. You might want to search online "Connective Tissue Disorders". I was diagnosed back in 1996 with Fibromyalgia, but as the years went by, I realized it didn't cover all my symptoms, like stretchy skin, very easy bruising, spontaneous bleeds, having most of my internal organs drop out of place due to my ligaments giving out, ect. I highly suspect I have Ehlers-Danlos, which is also a connective tissue disease. There are 13 or 14 sub-types. Generally, connective tissue will cause the opposite of what you describe (your mention of everything feels so solid, tight, and stiff), however, you could have 2 problems fighting against each other, like me...I have Rheumatoid Arthritis which makes you stiff and tight, and EDS which makes you loose and floppy, esp. in the ligaments attached to bone. Have you tried "Symptom-Checker" online???
@@pamelasmith2625 you may have ribs misaligned. A chiropractor can put them back. I have fibromyalgia. My ribs go out. Think I have EDS too but most Dr are mid taught about it and ignore it. My Brighton test would have showed I had it when younger before fibromyalgia & SLE.
I have had fibromyalgia for 35 years. Believe me it is real. It took 3 doctors to diagnose me. We had a conference one day and I had never heard about it before. I have hurt so badly, I could not get up in the mornings. I was so tired all I wanted to do was sleep. The depression was horrible. But I had great doctors that understood. I live with it and prayers certainly help. My faith has always pulled me thru. I know it will never go away, But I do pray for a cure.
I have had Fibromyalgia since 1992. I saw 5 doctors until a Rheumatologist diagnosed me. I did a diary of symptoms and foods that made me feel worse. Lack if good digestion can make you feel worse. Took myself off Dairy and wheat. Difficult life with symptoms and pain throughout my body. Sometimes very severe pain.
Thank you for posting. Fibromyalgia research has come a long way since my diagnosis in late 90's. There is no doubt that my mother suffered from Fibromyalgia as does both my daughters, genetics play a role in Fibromyalgia that isn't widely discussed in the medical field I hope this changes for future generations.
Your leaky gut is caused by glyphosate. So is your Fibromyalgia. Do some more homework. Direct that to naturalists..holistic...anyone opposing govt lies.
I am a 71 year old woman who was diagnosed with fibromyalgia when I was 32. At that time no one knew what the word meant and I had to do what little research there was on it myself you are so wonderful to listen to. I am definitely going to work on my gut thank you so very much
Hmm... years of acid reflux that cause couldn’t be identified. Years of allergy testing. That we did know, it was an allergy. Testing never found the allergen, but I stopped coffee for adrenal issues and all acid reflux went away.
@@elizabethtovar3603 coffee caffeine repeatedly shocks jolts the adrenal system fight or flight response so constantly that the adrenal system degrades and then gives up, resulting in a hot flash fritzout final desperate efforts to right itself, before it fails to function at all. all due to being beaten up by coffee...coffee is a drug and a dehydrant. both my hubby and son quit coffee and now feel much better.
Hello! I am from the UK, but up until recently, it was not recognised as an illness. You are classed as lazy etc; which is not fair! I also have arthritis in all my joints, so double the pain and little relief from pain medication! I think it is over due, that the Doctors in the UK, realise this and research more as you do, to help patients instead of being closed minded! Thank you, Anna.
I was diagnosed last year with fibromyalgia, and bk and forth trips to the doctors for the last 3years I eventually got the answers I was looking for and yes your right. I live in the uk aswel, but I started seeing female GP because my old GP he said it was stress with working nights, but i knew there was something wrong, we know our own body's. Maybe if went private we could of been diagnosed earlier
I agree that many UK Drs haven't a clue about Fibro, I just wish they paid more attention to what we say. Luckily the Dr who finally diagnosed mine was an Australian locum and was on the ball. However Dr Oubre's video has been really informative. Thank you Dr.
It was a Physiotherapist that told me I had Fibromyalgia, many, many years ago. Dr's never really believed in it, so all through the years I have just had to put up with it. My daughter now has it. I also have Psoriatic Arthritis & I am on medications for that, but no one Mothers about Fibro...Sp plsed I see this video. Will discuss with GP.. I am in the UK.
So true its the most frustrating thing for a pereon to go through even eating can be so tiring have a couple of days of bursting energy and then days of dehabhilatating almost comatose type symptoms where I can put my body into a shut down mode and sleep for 24+ without u using the toilet or eating tryin to wake me is almost totally impossible and I wake with drunk type balance slurred speech eyes rolling. The pain middle and pelvic part in back is excruciating. I do have spondylitis in my full spine. But I kno the fibro is something that is a problem in my brain and spinal cord. Its not just muscles as they say its definitely alot more to fibrom. Great information. Thanks
I accidentally came across your video and Thank God I did! I have been suffering from Lupus & Fibromyalgia for the past 10 years & also have severe asthma, hypertension, PTSD & just recently got diagnosed with diastolic dysfunction. This dr. is amazing and it's so refreshing to see him explain all this information regarding Fibromyalgia and how it all this makes sense! The doctors I have seen past & present just don't get it and don't understand what Fibromyalgia really is. It's so frustrating talking to dr's about symptoms and they look at you like you're crazy and like it's all in your head. I go home a lot of times and cry because nobody gets it... Just wanna show my appreciation for taking the time to do this awesome video dr. and am definitely going to make big changes in my diet. I have been thinking about going vegan for some time now but, I love steak & chicken! I have recently lost weight over 20+ lbs. over a 6-month period without even trying or dieting. I went from 126 to 102 lbs. So, don't know what I can eat or try that is healthy and can make me gain some of that weight back.
You should try a plant based diet. Plant based protein is not as hard on your kidneys as red meat is. Chicken is not as bad as steak. You just have to cut down on the bad stuff, if you don't want to eliminate it entirely from your diet.
I've been vegan for years but it didn't stop me from getting fibromyalgia and the only thing that has helped so far has been cutting out msg, taking ldn and meditation. Some research says that fibro is an auto immune disease of the opioid receptors in the body, others say it is a problem with the endocannibinoid system, others that it's an insulin resistance problem (because fibro patients treated with a drug for type 2 diabetes (metformin) also have a huge reduction in their pain.) Then there's the medical trial (hopefully starting next year) to see if the BCG vaccine will help fibromyalgia by changing the immune system. I think there are different types of fibro with difference causes and therefore different solutions. It may be that all the theories are correct because there are different types of fibromyalgia
@@BlackbirdGirl72I got rid of my old amalgam fillings as the dentist recommended. Hadn’t had a cavity in 25yrs & after fillings were replaced in 3 yrs I had a cavity inside every tooth in my mouth! I had beautiful teeth, most thought I’d had braces but didn’t. I was diagnosed with fibromyalgia 35yrs ago, then sjogrens, then multiple back disc degeneration & osteoporosis & migraines & colon cancer in 2000. I’m so tired of fighting pain for over half my life! Now my 17yr old granddaughter was just diagnosed with fibromyalgia & having a difficult time getting around without a cane or walker! I wish I had all the answers especially for my granddaughter! I’ve been obviously very understanding with her & am sharing things that have helped me. My heart breaks for her being so young. One of the hardest things is to discuss chronic pain with anyone whose never experienced it! So I don’t bc most don’t have a clue what it feels like to have pain constantly & never will till they experience it for themselves! Health, happiness, love & movement if possible everyone!
Dr Oubre I’m going to continue looking into your videos (this is my first video to see if yours). I was diagnosed with fibromyalgia when is was 22 (I am now 41). I am insulin resistant and on metformin. I was gaining weight no matter what I did. I began researching intermittent fasting. I decided to try IF along with a low carb diet. This meant I cut out almost all gluten, processed foods and diary. It took about four months before I started seeing weight loss but only 2 months before I stared seeing a decrease in my fibromyalgia symptoms. As soon as I started eating gluten/processed foods/diary again, my fibromyalgia symptoms began to return. After watching this video, it is beginning to make a little more sense. Thank you!
Well done to you the government and food industry also big pharma are all linked putting this crap in our foods they are slowly poisoning us , stay away from all oils and sugar that's hard to do when it's in everything
I sent this to my dear sister friend who is debilitated by this disease... i pray for her continually... I’ve never heard someone speak like this! Thank You! 💜🙏🏼🛡🗡👑📖🔥
I cured my fibromyalgia by detoxing. I went from feeling 92 yrs old to feeling like a 20 year old again. I still struggle with balancing my diet to keep myself clean but agree that the Liver and gall bladder play a role - now I work on Liver cleanses for better health.
I used homeopathic nosodes to detox vaccines, heavy metals, viruses, mycoplasma, & Lyme Disease. I used homeopathic products from Clinicalnutritioncenters & Pure Formulas, & I used colloidal silver from Herbal Healer.
I don´t get why there are so many theories about fibromyaliga. For me it´s so clear: when you have Fibromyalgia and you do a sleep study, it is pretty clear that people with Fibro don´t get any deep sleep, REM sleep. That alone can explain all of the symptoms: pain, fibro fog, fatigue...
Jeanette Kniebusch Hello! I love the way your opting for an all natural alternative like I was! I have one other All Natural solution for you... A Much More Effective for sleep and is also fantastic for every human being but especially for Fibro and Mito Conditions and symptom control. Pure Safe Full Spectrum CBD Oil....However!!! As Long as it is the RIGHT Blend of Cannabinoids that are Pure Hemp Extract/Tincture, Made from the Entire Plant NOT the “Seeds of the flower”, Federally Tested and Approved for its Purity, Toxin Free and 0% Chemicals as well as bacteria like E. coli that they also keep finding in the testings of most CBD Oils out popping up all over the place. That the hemp plants Also are Grown by a Completely Tested and Federally approved Organic Farmer (and tested farming soils for passing for 100% containment’s and chemical free!), comes from a Manufacturing plant that is FDA Approved and manufactures their Own FULL Spectrum CBD and it always has to have a QR Code on the bottle for its transparency and it has to have a “COA” on each batch that is produced. Which when you scan the QR Code on the bottle, will Pop Right Up That products COAs So you can read Exactly what the Tested Levels of the Pure CBD oil are. If the company/CBD Doesn’t Have All of these above, then it will do harm to ones health rather than getting the tremendous health benefits that a Pure Full Spectrum CBD Oil provides to the entire system. Keep Shining and Living Healthy and All Natural Jeanette! 😊
I have suffered for years and finally getting a sleep study I'm excited as I've heard that I will be a new person after the study and treatment so fingers crossed
Thank you for this! I have been suffering with fibro for years, without any education about this disease or how to fight it. I thought it just is what it is. Planning on binging your videos today in the hopes of educating myself and making some changes in my life. I've always said there is nothing yet invented on this planet to help ease a flair; your education may be just the tools I need to take back my control. Again camt thank you enough
I have told numerous doctors my symptoms. I have almost every symptom you talked about. I had a doctor that put "fibromyalgia" in my chart, but never once spoke to me about it. Thank you for this info.
Thank you for this video! You have restored my faith in modern medicine. Your explanation was clearly the most informational than any other explanation told to me. I had fibromyalgia about 20 yrs ago. I saw a several doctors and they told me the pain was all in my head. Luckily, I saw a MD as a recommendation of a friend and she told me I had fibro. She recommended antidepressants but I respond very poorly to them. A friend of mine who improved her fibromyalgia gave me a long list of vitamins, minerals and supplements along with Epsom salt baths and sauna and the symptoms, especially the pain, muscle fatigue and brain fog improved drastically. Over the years, I introduced coffee enemas, pemf and red light/NIR and I’m the healthiest I’ve ever been. I also became a multiple modality energy healer/reiki master. Vitamin infusions weren’t available then but I did b12 injections, which helped big time. I also healed my gut and don’t consume gluten and dairy. My body craves whole foods and occasional seafood. Raw grassfed meat helped especially when I healed from late stage Lyme disease a few years ago. I am going to look into lipid therapy to strengthen my mitochondria. I detox regularly to maintain because I know my body doesn’t detox as efficiently as others. It’s probably because of my mitochondria needs a little TLC. Thank you again 🙏🏻
This is the best video to explain not only fibromyalgia but how our system works. I have had crohns and colitis and now the muscle pain and mind issues with memory and brain fog. Thank you for this video!
Thank you for talking about this it makes sense what you're saying I think this will help a lot of people I really wish more doctors knew about fibromyalgia and would take it more seriously and quit thinking that people are making up symptoms and just because you can't see it doesn't mean the person is faking
I had an 8 month flare up where I was close to death and near suicidal towards the end. I don't have the time to go into too many horrible details here, but it was caused by a poor diet. I had to cut up and looked ripped for a job (stuntman/entertainer) and I noticed that my pain was less when I had more muscle. So, I went on an old multi-set training and calorie loading regimen of mine. I couldn't get enough calories in eating clean, so I started ingesting a ton of dirty calories. Very soon, my body started to shut down and fall apart. At the end I was 140 lbs (down from my normal 175), with dark circles under my eyes. I was stuttering, having panic attacks and I could barely breath, think, talk or read a book. The bottom line is: f*ck sugar. And if man made it, don't eat it. When you're shopping for healthy food, just remember: If it has a mother, it's okay to eat. If people ate it 200 years ago, it's okay to eat. Shop at the back and to one side of the grocery store - the produce department and the butcher. Drink at least a gallon of water a day and stay away from anything artificial - eat only organic, pesticide free, steroid free foods and pay attention to were your meat comes from. I'm now a father, a winning men's physique competitor and a firefighter - with fibromyalgia. It's still very difficult some times, but it's never been like that 8 months again, ever. Eat clean and stay healthy people!
i shared this with my friend because she had to stop working due to severe pain from fibromyalgia. I shared with her to clean the gut first, detox and then change the eating habits, that was a year ago. I feel bad because she was working on her doctorate, teaching and raising her son and now she is restricted to the house. I pray she watches this video and make those changes
@@angelaquintero1977 find your food triggers . Add a probiotic ( colon health or align ) it takes a few months( sometimes a year ) to heal the cut . Sugar / processed / refined carbs/ meat injected , processed lunch meat with colors 😞 avoid . Change over to fresh vegs , chicken breast , salad ( I do lettuce mushrooms a little blue cheese ) blueberries strawberries watermelon. As soon as I put bad foods in , it’s starts to attack . I’m still learning trigger foods .
Dr. OUBRE, I live in Ontario, Canada and would be grateful to know of any Doctors here know how to treat Fibromyalgia with the infusions you talked about with Lipids. We need help like this everywhere, and your program studies and education of our medical doctors needs to be done widespread asap so that we all can end or greatly improve on this suffering. Thank you Dr. For a VERY educational and helpful video.
Yeah, I try to do everything right. I'm really sick of myself. You got to keep moving & believe there will be an answer. This Dr. makes more sense than many before.
I recently saw a pain management specialist here in Citrus Co., FL. He explained to me that fibromyalgia is an overactive central nervous system. He has prescribed low does Natroxlene for my pain. You start at 1.5 mg and work up to your best dosage. He has some patients on 9 mg, but most of his patients are on 1.5 mg or 3 mg. After you are on the medication and your fibromyalgia calms down, your other pain is then unmasked so you can begin treating it. I was diagnosed with fibromyalgia in 2002. I also have chronic myofascial pain, osteoarthritis, bilateral carpal tunnel post op, cervical degenerative disc disease and low back pain. This is the most hope I have had since 2002 for pain relief from fibromyalgia. Just sharing for others with this condition.
Goddammit woman, your comment should be in bold giant capitals!!! You are so correct in that it is a brain based illness! I too have found latest findings explaining this! So many people going off to change their diets after seeing this video, what a load of tosh! Even in the video description he has said it MAY be the reason! He's not even convinced enough to claim outright that he has 100% proof! Yet the sheep blindly follow... What's happened to people lately that they are so easily manipulated??? Where's their common sense! I wish I could make everyone who's seen this video read your comment!!!!! 😘😘😘
Brenda Fuller - thank you .I met a lady who also tried this for her fibro with excellent results .It is not easily available in the UK and requires a private prescription but I shall look into it .
I was just diagnosed with fibromyalgia,diabetes,anxiety,depression I had for over 15 years and arthritis.Never in my life have I ever experienced soo much pain in my body.I just had a procedure done on my thumb because I had trigger finger.
I am so thankful that I found your channel! Living in a small city in Canada, and have been on a pain and symptoms rollercoaster for the last 6 years, however, as you mentioned, I have had some symptoms, but not as severe, from as long as I can remember. When my symptoms and pain started to get worse, and because they were so varied, and changed, sometimes weekly, or even daily, I was first sent to a psychiatrist, which was very unsettling, because I knew, I wasn't being believed. My symptoms still kept changing and getting worse, so I was then sent to a wonderful Rheumatologist, in a neighboring city,, who ran a series of tests, including bloodwork, and was diagnosed with MCTD, however, my Rheumatologist, was not certain this was an accurate diagnosis, as my symptoms, were not that, of her other patients, so she kept investigating, and by pure chance one appointment, she was touching certain parts of my body, which most all the points were painful, and she asked have I ever noticed this, and I replied, oh yes, I have had that sensitivity for years now, and she started discussing fibromyalgia with me........I have since done some research, and found varying symptoms and pain levels can occur, as you discussed, so I am still discovering all that fibromyalgia can be. I was hoping with all your knowledge, if you could answer a few questions for me. Do a lot of people with fibromyalgia, also have a positive blood test for MCTD., of is fibromyalgia, part of a MCTD symptom, as I have not seen this included with the 6 other diseases, normally associated with it. any information you could provide, would be greatly appreciated 😊
Thank you so much for this information! My poor mom has suffered for way too many years. She has been on & off of hydrocodone. This finally makes sense. I feel God led me to this video. I have ALWAYS researched & tried to find ways to help her, BUT NOW I AM DOING IT FOR ME. About 6 months ago I started having aches & pains. I was devastated because I've watched her suffer with NO ANSWERS OR RELIEF. I haven't been to a doctor yet, because I'm so sure they would want to put me on medications, just like her. Thank YOU! I will be waiting for more of your videos!❤
I’ve been suffering from wide spread pain since I was 22. Now 58. I have managed two long term careers one was psychiatric nurse for 33 years. Then I trained and did something completely different in my early Forties and did Community Liaison Officer. Sadly now I struggle to work but manage a few hours a day with a struggle. I have my thoughts on this. I feel trauma triggers either mental or physical trauma.
@@UncaTuck they have to be Organic? I heard coffee enemias make Your hair beautiful. Your right, about organic. You putting the coffee up you a-s.of course Organic. LoL
You worked as a psych nurse.. Have you read the psych books. And history of psych treatments? Maybe you caught one of the VIRUSES GIVEN TO PSYCH PATIENTS IN ORDER TO CONTROL THEM. THINK ABOUT IT. It's in the books. However IT IS ALSO TRUE THAT EXTREME TRAMA EFFECTS THE THE BODY, THE IMMUNE SYSYEM AND MANY OTHER PHYSICIAL FUNCTIONS. AS WELL AS NEUROLOGICAL. AND SO DOES STARVATION. YOUR A NURSE. RESEARCH IT. BUT FIBROMYLIA IS VERY REAL. WHATEVER THE CASE. COULD ALSO BE VACCINATIONS. I DID HEAR SOMEONE SAY POST POLIO SYNDROM. NOT SURE WHAT IT REALLY IS. BUT HES TELLING US WHAT IT IS. EXERCISE AND SUPPLEMENTATION WAS WORKING. BUT IT WOULD TAKE YEARS. AND CONSISTENCY.
Amen to your theory of trauma. My fibromyalgia didn't start until I had a severe mental trauma, my mother's started after her husband of 67 years passed out on the expressway while she was in the passenger seat. My younger sister lost her husband after he was coming home from a outdoor church meeting in the Bahamas. The man who was driving ended up flipping the Jeep and it broke her husband's neck. Finally my oldest sister almost lost a child and it was so devastating. I see a familial DNA and a trauma-based trigger for fibromyalgia. But what do I know? I just eat well and manage to sleep well and am watching my husband die of cancer. And then there's the pain. My favorite is the one where I feel like someone is jamming an ice pick into my ear. Or maybe it's that once or twice a month I can't see clearly for a week. No, it's when I feel like someone has taken a metal bar and hit me across my shoulder blades and then in the middle of my back and finally across my waist. No, this isn't living, this is surviving. Giving you a Gentle hug, Carly
Your presentation was very enlightening. I can't remember a time I wasn't in agony. My symptoms really started when I was a teenager. Finally I have some more knowledge and a better explanation for all of what I've been feeling. I look forward to watching you again. Maybe you could give some tips on how to heal the gut. That's something I can't even get from my GI doctor. Thanks for your help.
Dear Dr Philip, after about 25 years of pain etc etc, i have now stumbled upon this video. I could not believe my ears. I am in tears of relieve! Our family is wridden of cancer, BRCA positive, lupus. 😨😰😥😭 i will immediately forward your details to our various doctors from South Africa. May God bless you abundantly. 🇿🇦
Excellent information and I like his natural presentation and new dimension of hope for so many. 20 year fibro. slide. Really thought there was no real answers, or cure. Thanks Jody
@@marilynsinquimani4994 Please forgive me for this, but I tried Dr. Grundy's products for the gut, spent quite a bit of money, and they failed to meet his hype. I am very dissappointed in his products. I suggest you research any plan you're interested in. It's really a shame, because I was very pro-Grundy. After this experience, I won't buy any of his products again.
This is an absolutely amazing video! I always said o feel like something is wrong with my cells. Of course people really thinking I’m crazy. This explains so much of what I believe in and knew deep down in my heart. This is the other reasons why medication and opiates do not work for fibromyalgia. High freaking five x 2 🙌
Your understanding and explaining about fibromyalgia is very good in fact is so good I finally understand more about the illness. Thank-you for shining a light on us sufferers. I look forward to hear more of your kindness in helping to cure this but my biggest hope is a preventer discovered so no one else goes through this awful pain. A C section and appendix was very mild compared to fibromyalgia.
Wow, watching your video teared me up. I had fibromyalgia pain for almost 6 years now and I am 26 now . I have consulted many doctors, physio therapies, ayurveda medicines , western medicines everything. Doctors did not know why I was getting these pains. Eventually the doctors said it was all in my head and they even suggested me to go to a psycho therapist. After a point, i even stopped saying my parents what i am going through just because no one would understand how painful it can be. Finally you saying that its an actual pain and there is a treatment, made me cry . Finally someone understood these pains 🙏🏻 and actually finding out why this condition occurs and thank you so so much. You gave me a hope . Thank you . 🙏🏻
This makes a whole lot of sense... and confirms my personal story of how this disorder was activated within my body... thank you for putting this so simply... 5 years ago I was diagnosed with a dissociative disorder which was caused by trauma growing up... it was this diagnosis that eventually made my doctor look at my VitD levels after years of complaints... after 3 years of up and downs... I have been told that it is likely a genetic disorder that disables my ability to absorb from the sun... it also appears to be rickets resistant... thus my dietary intake is the only source of VitD... I was lucky enough to be raised on wholesome backyard food... so my VitD as a child would have been fine... it was after an incredibly low Vit D level 2 years ago that I developed the Fibromyalgia symptoms... and even though my VitD level is now climbing to normal... the Fibromyalgia symptoms are worse than ever... so what has been my main focus?... developing and changing my diet to be closer to what I ate growing up... despite the childhood trauma... a vitamin deficiency is what brought my life to a halt... Sharing for those that were told for years you are crazy... and it turned out it was not in your head... my head has a whole other crazy... dont ever ignore that 'GUT' feeling...
My naturopath recently put me on Malic Acid. I'm doing a liver cleanse for a month, and she also put me on a pre/probiotic. I am extremely vitamin D deficient and can't get in the sun often enough because of work, so I got a tanning bed (for free on Craigslist and relamped it with the best lamps) while also taking d3 with k2. Fish oil, curcumin, coqu10 are in my daily along with magnesium at night, which helps relax me and helps with restless legs and cramps. I started taking Previgen for my ridiculous, debilitating brain fog. We will see if this helps. I have had the worst flair up this past year after I lost my dad. My diet went to hell and of course the sadness really triggered my pain. My pain recently went through roof and I had to start cutting out the crap from my diet. Growing up in the 80's was not good for dieting. We were bombarded with horrible processed foods and "fat free" foods. My house was loaded with diet sodas, margarine and packaged foods. Even our vegetables were in cans. It seems mom cooked out of boxes and cans. She still eats like this but is suffering from Multiple Myeloma and I can't stop wondering if her diet didn't cause this? We won't know, but she just cant change. Does ANYONE beside me suffer from severe BONE pain? My bones are what hurts the most. I am a sever insomniac as well and haven't slept all night in over 25 years. I would say I don't sleep more than 4 hours total a night. I am rambling...I'm tired and in pain. God bless you all and I will try to update in a few months on my new regimen. Thank you Dr.
Oh if only I were there or you were here. I'm 74 years old and have suffered from fibro for many years but was not diagnosed until the early 90's. I'm in Oroville, California and am hoping that you might be able to put me in touch with a doctor near me who is knowledgeable in fibro treatment. It would be so wonderful to experience some relief. In the meantime I'll continue to watch your videos and do what I can to help myself. Thank you
Food allergies can definitely be a huge issue. Personally I have MCS with minor pain symptoms, not fibro specifically, but I believe they and chronic fatigue/ME are all in the same family of illnesses. I have huge relief from diet changes, although I do the high carb raw (fruits, greens, omega 3 seeds) plus steamed veggie route and my symptoms are drastically reduced. When I had my food allergy test I tested highly allergic to most other foods. Although doing a natural antibiotic Sibo treatment reduced my food intolerances quite a bit too! Glad you found something to help!
Thank you so much for this awesome information. My mom has fibro and I hate seeing her go through this. She is so brave, goes to work, doesn’t like to complain but I know it bothers her to the max. This information was SO helpful. I would like to know a little more about this, I believe it would help my mother greatly. If you lead me to where I can find more info and how to proceed properly to heal her that would be awesome! Thank you once again for this very accurate and important information!
Fibro took my walking from me. I went from being energetic to wheelchair user and have no independence.the pain is horrendous too... The rest of my body is really bad too...I wish people were more educated about fibro...people think your lieing or exaggerating cause you look OK... Thank you for uploading, very interesting information
THANK YOU! Your information is very helpful. I’m a retired critical care/ ER nurse who had to stop working because chronic pain became so bad. I worked until age 57, then I had to go on disability. There are days that I can barely get out of bed because the fatigue feels like you’re in the ocean tied to cement blocks. Fortunately my close friends get it. I’m now 61 and was just diagnosed with fibromyalgia. I thought I had long Covid causing this.
Thank you for this video, I've been diagnosed with fibromyalgia and seen many specialists and they're only solutions were prescriptions that made me even sicker, definitely going to try these detox/ lifestyle tips.
Well every thing makes sense now. I had a hysterectomy 37 years ago and I haven't been well since. I now have fibromyalgia. I have done every thing, seen every one and still ill. I saw a private Doctor who said I have mitochondria dysfunction. I'm now just about to start LDN. Low does naltrexone. Can't afford to see you, and Doctors are a waste of time. I have been ill so long now. And I have no quality of life. I'm 69 now and life seems so hopeless.
Eileen, I’m with you! I’m 68 and feel 108. Diagnosed 23 years ago. Nothing has changed but the date. When the fatigue and pain are too much, Iam in bed just wanting everything and everyone to go away. Take this pill, that pill, try this or that. I DON’T want to. I just want my life back. I’m surprised my husband is still around. He works a lot, even though he is retired. He started a business. I have beautiful, young grandchildren I want to enjoy. Their parents want me to travel with them. How can I? I will try the clean gut and get away from dairy and sugar. My bones are crumbling and I need Vitamin D and calcium. I’m just recovering from my fourth foot surgery. It has been terrible. Sorry to vent. The best to you on your fibromyalgia journey. If you find something that works, please share.
Wow!!! This is such an amazing video thank you so much! I have been dealing with this fibromyalgia mitochondria since 2004 I was 24 years old now I'm 46 and this is the first description that makes complete sense to me. I have been so very discouraged and overwhelmed for so long because I feel like no doctor understands what it is I'm going through and I've always just been fed pain pills pain pills pain pills now my body is so used to them it's discouraging! I'm excited to learn more about this! As is my body! What a wonderful video to come across this morning! I look forward to searching for more of your videos! Good now I'm off to work! Thanks again!
There is a fasting summit starting Monday. I purchased it because i wanted to start watching it in December to prepare for a water fast the beginning of January (only 4 day). They covered water fasting in part of the summit. Long story short - going into autophagy and then stem cell rejuvenation. Do you think it's possible for the body to get rid of the damaged cells (8:48) on it's own through the autophagy process? Supposedly it's 300X the autophagy process starting on day 4 of a water cleanse. Great video, thank you. I have known many people with FM and they're offered virtually no hope. I really don't understand why you don't have a million subs - seriously. You explain things so well and cover some really important topics.
Wow, thanks again for the compliment, Pam :). I'll get more subscribers over time. It just takes a while I guess. In regards to your question about getting rid of damaged cells via autophagy, you have to remember that when you destroy a cell, the other cells nearby take its components in order to build new cells. So, even though you are undergoing autophagy, you will inevitably recycle some components. With autophagy, you completely destroy the proteins inside the cell, but you cannot break down the fats of the cell membrane as well (otherwise, the autophagy process would consume the whole body). I would consider it like this. Your neighbor moves out, so you use the wood to add on an extension to your house. But, you didn't take the furniture. So, if the wood was rotten, it is now a part of your house. Same goes with damaged cell membranes (fats). Your nearby cells will absorb those damaged fats and incorporate them into their cell membrane. You need new components in order to flush the old components out. Using phosphatidylcholine (Essentiale N) is like adding water to a bucket filled with blue dye. Eventually, the blue dye will get lighter as you dilute it out. I still have a lot to learn about fasting and autophagy. The research is very promising thus far though.
@@OubreMedical geez - best explanation EVER! I had no idea. The fasting summit started today but I already watched a lot of the video's. In listening to them, this wasn't the picture I had of autophagy. Thank you for painting such a clear picture on such an exciting/important/fun topic.
I can see everything you are saying makes complete sense ,but what good is it to know, if we cannot get the treatment.I am in the UK,and as far as I know this treatment is unknown here,
I get my Phosphatidylcholine from Europe, so it's not known there. You can investigate the food sources of the nutrients that I speak of. Then eat those foods!
Hazel hello hazel I’m in uk also and there is no treatment like this dr has explained It makes so much sense though what he sd . I go to a clinic in Bedford to have oxygen therapy injection and after all these years of pain It has helped a little .. his name is Oliver . Hope today hasn’t been so bad . My days are bad always The pain is chronic ..
Hazel i'm in the UK I was diagnosed about six years ago and I go to the pain clinic and I get a lot of pain killing treatment. I've found the doctors have taken me seriously since day one and done everything they possibly can for me.
It’s real all right, I wouldn’t wish fibromyalgia on any one. Pain being the worst, along with fatigue and sleeplessness. I’m glad more information is coming out regarding fibromyalgia, I believe healing the gut is very important. Thank you for this video, I’ve really enjoyed watching this.
WOW!! Amazing day with you. I’m a fibromyalgia patient and yes! You’re right- my body’s pain it’s increasing bad specially in my back around my spine. I do watch what I eat but my stomach hurts not matter what. Thank you for your help and kindness with the seminar. Blessings to you and your team. 🙌🇺🇸💐🇨🇴💝
But only just recently.I have suffered for 21 years.I have been laughed at by professionals.I have been told to get out of bed and walk around my home when I couldn't even move a muscle.Infact how I have been treated is beyond disgusting.However,I have written all my experiences down and hope to name a d shame every so called "doctor" who dared treat me like I was lying or looking for attention.Once the science proves how real Fibromyalgia is then I shall happily expose these low life's who should not be in the medical profession.I know about this living hell than they do because I have lived it for 21 year's.I live in N.Ireland.
Have to say I agree with Jane. I have had fibromyalgia for 23 years and was told by my doctor that, that's what they call it when they don't know what it is. I am glad that diagnosis and acceptance is better these days.
@@lesleyjones8469 When I got diagnosed Lesley they didn't have a name here.The professor told me "you have a condition that won't kill you but will torture you for the rest of your life".I asked him was it Fibromyalgia and he just looked at me.He wasn't prepared to name it.I had done my own research.Then when I went to a pain management doctor.I said I had Fibromyalgia and he laughed at me.I walked out and filled a complaint.I refused to attend the pain management clinic again.Im 22 years suffering this year and still there are no answers.I believe the health service know what causes Fibromyalgia and won't say because it's possible their fault.Any research I have done I have found that people who suffer have some things in common.I wish you well in your day to day hell that is Fibromyalgia.God bless you.☘️
I cured my debilitating fibromyalgia through diet. I also stopped taking medication. Keto carnivore is life changing. Doctors will only medicate you to death unless they understand nutrition, which is rare.
@@carolweaver3269 Carol, it's not something you can buy. It's a very strict high fat diet. Nothing can clean out the carbs. You just have to stop having them. It's extreme and I did a similar diet many years ago. I felt so much better if not cured. Trouble is it is very limiting and hard to keep to. But I am thinking of getting back onto it to get relief. There is plenty of info in books and on the net.
It has to do with food allergies. When I had my food allergy test I tested highly allergic to almost everything except for fruit, vegetables, and meat- Personally I follow a high raw high carb diet and it has been immensely helpful. Also doing a natural antibiotic (bereberine, garlic, oregeno oil) to help with sibo allowed me to eat things I used to be allergic too, although I still stick with mostly raw fruit and veg. Good luck!
This is spot on . 35 years ago I was told I had fibromyalgia and now that I have SIBO I finally know what’s really going on . No the long road to recovery.
Thanks for the information packed video Dr. Oubre! There are definitely ways to help fibromyalgia. Functional medicine approaches are making great strides in fibromyalgia outcomes 🙌
My issue is that I not only have been diagnosed with Fibromyalgia but now a Neuromuscular disorder. I also have severe spine disease which produces its own set of symptoms, osteoarthritis everywhere, bowel and bladder disfunction, and I see 5 specialists. I don’t know what’s going on bc this all came on after my spine surgery & a traumatic time after that. It’s like everything just snowballed. It’s only been 4 years since my fibromyalgia diagnosis. I always had spine problems. I don’t know what to do. I just want to give up sometimes. But this gives me hope that there may be a treatment for the fibromyalgia at least. I hope one of my doctors knows about this but I kind of doubt it or already would’ve tried it. Thanks for giving me this space to vent. I’m happy for those who can get this treatment and be cured! Thanks to this physician for helping so many people get well.
This is a great video. Your explanation for treatment is very similar to what I’m told by acupuncturists. Too bad not all functional medicine doctors share the same mindset re: fibromyalgia. Thank you for sharing and informing !💜
Prior to my diagnosis, I was vegan (the healthy vegan... there are vegans who consume unconsciously). The protein I use is plant based with probiotics. I have a history of ulcers since teenage years, so keeping my gut strong was nothing new to me. I fully believe that the gut is our foundation of health. Before I used to blame and question my clean eating habits (post-diagnosis) but how I realize that sometimes unexplained things can happen so it’s best to rework the healing plan and just allow yourself to be present and optimistic during the process...✌🏿💜
![โรงเรียนดัดสันดาน นักเรียนเถื่อน..!! [โรงเรียนไดเม่]](http://i.ytimg.com/vi/vRKPeXn4Fl4/mqdefault.jpg)
I have said from the beginning which has been thirty plus years that one of the things it feels like is that every cell in my body is sick with the flu. This makes total sense
The flu times 10!😫🥲
Hi i just wanted to say this really has enlightened me
and is the missing link that i have been looking for, i can put this information to good use. Thankyou
I’ve always told people my mitochondria are all screwed up!! I’ve known from an early age. Something was wrong with my body. I am in pain all the time every piece of me hurts. I’m sick and tired of it no matter how healthy I eat. I still feel shitty and I am so happy I ran across this because I am definitely going to be able to talk with my doctor about this lipid therapy you’re talking about !! Thank you !!!!!!
It is frustrating when you do not get validation for how much you suffer from this disease….I was diagnosed som 40 plus years ago by a wonderful doctor who told me this is a real disease….mine was probably caused by pesticides….
I was exposed to pesticides….I was diagnosed with fibromyalgia 40 plus years ago…
I've had fibromyalgia for 45 years. As an RN, it made me feel guilty as no one believed me. They all thought I was an hypochondriac.
As a nurse also with FM, I thought I was crazy because absolutely nothing made sense with the changing pain/fatigue/brain fog.
I know how you feel, I had just come out of the army which i was a nurse in (UK) felt like no one believed me the same as you, a hypochondriac.Ive just been thinking what major events happened around the world in the 70's as I had never heard of it before then......Keep on fighting honey xxx
I had been to Dr after Dr and was told it was in my head. I started seeing specialist after specialist and my last one spent 5 minutes with me and touched my elbow and forearm which was extremely painful.. He said he couldn't do anything for me and I cried. I finally found a Rheumatologist and my world changed. It's taken years of fighting for myself. I'm a retired RN now and living each day to the best of my ability.
So sorry... can relate
as a mom of a daughter (35) Recently dx., how do you feel about lipid regeneration? what he is talking about here> what has helped you!? no one, not even the doctors are believing my daughter and due to past cancer,jaw surgery,and tmj, they say its a bad toothache.. and rx. more pills. like gabba!! the worst! I am so frustrated!!! ty for sharing!
First diagnosed with fibromyalgia, it turned out later that I have/had an auto-immune disease. Fibro was just a group of symptoms that many people ignored (for me) because it's been largely ignored. If it wasn't like doctors like my current GP, and doctors like you, I would have never found that out. Thank you for standing up for fibro warriors!
#Fibrowarriors
My mom never found a doctor to properly treat her. She got I’ll very suddenly at a time she was very vibrant. She might have been bitten by a deer tick (manufactured on Plum Island), not far from her home. She couldn’t sit comfortably. She had to sit on a tire. Her butt was all bone. No meat. Mom died way too young for her @ 81. All they did was prescribe DRUGS
Hello. What autoimune disease did you have? So I know what to check for me.Thank you
I have none. It was my mother who suffered with Lymes and fibromyalgia. Dr prescribed Drugs killed her.
Me too! Infuriatimg..
My go to saying is "I'm sick and tired of being sick and tired ".
Yup 47 years later also had a stroke on 4 11 2023 in my sleep and now legally blind 😴 keep on spiritually looking up. God bless you always 🙏 ❤️ 💖 ♥️ 😘 💛 🙏 Amen and Amen 🙏
I got bored off saying it.
Thanks yes tired of being sick tired I agree but I haven't had fibro as long as you have I have heart and lung disease, osteoarthritis a rod in my leg have broken ribs and it's on the right side and left side or fractured ribs twice on resuscitation I have 5/6 fibro's in the front from both breast bones and lower down both left and right side I have anxiety depression I work through it as I'm a fighter
@@Eileen-d2p I am so 😔
@@clairechampagne6996 God bless you also.
I have fibromyalgia for over twenty years. Everything you said makes sense. I have chronic muscle spasms that hurt so bad it causes me to become depressed. Thank you for taking this condition serious. It really is not in our head.
Have u tried potassium rich foods? They help. So does vit B complex( natural source. Methlated) So does magnesium, but watch out for diarrhea with magnesium. None of this stuff cures our pain of course. Just better.
Yes they tried to put me on Lyrica it made me gain 25 lbs in a month as well as C one ..then the Dr 2002 diagnosed - severe chronic fatigue syndrome ( CFS) carpal tunnel both wrists surgery on my right, flare ups when it's cloudy, my Ra was normal, my ANA was positive bc of my inflammation in my body.. cortisol sky high..my thyroid symptoms, Thyroid tests normal, pre diabetic, obesity from craving sugar and carbs, connection, IBS, Chronic muscle spasms take Flexeril on flare ups, Dr, gave me 3X a day Hydrocodone and Tylenol 325 mg and ibuprofen together almost killed my liver was in failure after bedridden for 2 yrs the more I took the more with exhaustion, chronic insomnia, depression anxiety, PTSD, meds help me, prayer has helped me the most, reading or listening to niv bible daily helps me I try to do both 1 hr each a day I am believer in Christ he has proven so many miracles in my life, true Christianity " is not a religion " it is a faith based relationship with Christ..I talk to him daily..I cry out to him when I can't take it anymore I'm 63..live alone..if u ever get in trouble call out to Jesus Christ to help you even if your dying he said in his word ( the Bible) if you all on him he will save you..Shalom 🙏🪖🗡️📖🔥🪔📣⚔️📜
Constant, unrelenting pain can be extremely depressing.
Exactly
I knew I wasn't making it up. Why would anyone want the hell I am going through???
Absolutely ! Let's not forget being called a hypochondriac by doctors, family etc.
I know the feeling because I have fibromyalgia too
I know it used to be so frustrating being told it was all in my head
There is help for this your just looking in the wrong place.Find a functional medicine doctor..Ask for a thyroid panel and get a reverse t3 done.Read hypothyroidism type 2. And Mary Shomons book.Look her up . Her book was a wealth of information .Get educated and learn .You will recover
@@kkx23 - I so agree! Proper treatment of subclinical hypothyroidism is essential and usually entails taking natural thyroid (ins. won't pay for it), taking enough of it for your lab results to be at the "hyper" level, and going by how you feel, not lab results. Sleep is essential too. I've found timed release, low dose melatonin to be the best for that.
I have had fibromyalgia for almost 50 years, actually before there was actually a name for it. In the beginning, doctors called it fibrositis until they found out it was not like arthritis - not an "itis" but instead the pain was in the muscles and the fibrous tissues that surround the bones - a cousin to rheumatism. I am now 70 years old and so have suffered with it for most of my adult life. I went from doctor to doctor trying to find out what was wrong with me, many trying to tell me it was all in my head (which I knew it was not). Finally, my family physician diagnosed me because he constantly read the JAMA magazines so he stayed on top of all the new information that was coming out all the time. I have never been able to tolerate Lyrica or Neurontin which is usually prescribed for fibromyalgia so my only alternative has been to rely on pain medication, prescribed to me by a trusted pain specialist, but even with pain medication, it does not relieve all the pain but makes it a little more tolerable. I also suffer from degenerative disk disease and have had 7 herniated disks in my neck and back, also suffer from spinal stenosis - so my life has been one of nothing but pain. How can I find a doctor who knows what you are talking about regarding trying to reverse fibromyalgia?
😪 I hope you find something that eases things 🙏
Look up a functional medicine physician on ifm.org
It's never too late to start healing!
Hi Linda, so sorry to hear you've been suffering from this debilitating condition for a lifetime! I totally feel for you! I was also diagnosed with " fibrositis" 🤔 when I was 18 years old I am 58yrs now. A few years later I had Fibromyalgia syndrome 🙄 It's a nightmare living with this invisible demon. I have been taking Lyrica for about 9 years. Hope you manage to sort some pain relief.
@@OubreMedical where are you located?
I too have fibromyalgia scoliosis and degenerative discs in my neck and from the tailbone with 3 discs that slide over my tailbone.. it's so hard, but I deal with it.. I was diagnosed with fibromyalgia about 10 years but it's been happening for longer than that
I pray for you my fibro warrior, maybe some day... People won't have to suffer so
I was an active child participated in sports in school. I did hard work in my adult life... Now I'll be 60 in a few days and miss taking long walks, running, playing sports.... I miss WORK!!!
I don't know if I call it a disease or disorder... I know they call it a disease, because mentally I still feel young, I still want to participate in life and be active with other, but I can't make plans from now to an hour from now.
Stay strong
Blessings and prayers to you
💜✨🙏🕊️🙏✨💜
Thank you so much for this! Most people treat people like us with fibromyalgia, like we are crazy!
Yes. I agree we get treated like we stupid,crazy and hypochondriacs because there are so many symptoms
Yes. Exactly the way I get treated for innate knowledge, wisdom, discernment, today! 2023.
Eat as close to real food as possible. Less processed meats.
Unless you, yourself hunt for your own. Chemicals are everywhere!
Sky is now chemical plasma.
Electromagnetic fields.
Nano particles.
Nano metals.
Barium. Strontium. Aluminum.
Detox and fast.
Drink warm lemon water to start your day. Never drink iced water.
Room temperature. Consume a diet of: Breathing deeply. Lots of sunshine. Walking.
Noticing beauty. Hugs. Sweet grateful words. Reading by candlelight. Prayer.
@@jessiea4779 yes!!
True, some people haven't got any idea what it's like they think that your exaggerating but I've also heard people say that too about Lupus and MS suffers are also misunderstood. However, saying that explaining and re educating them about simple things like it's an autoimmune disease & my body is stuck working overtime constantly it gets tired quickly too. Information is the key I find, let them know that it's inherited & in our DNA.
It's also up to us to keep up with the latest research too.
I personally have tried the infusion therapy & it helped me to reduce my medication from a dozen to half a dozen, got me out of bed more, less siestas + less pains. Good Luck everyone & happy healings 🥰
@@brightwhitelight9445 Everything you said is brilliant 👏 I will definitely start using what you said more in my life, especially with the people that just don't get it, and just think I'm lazy...I hate it 😮💨 educating really IS key to eventually being heard and understood better than we all are now!
This explains it all in under 12 mins. Yet it’s taken decades for a lot of medical professionals to do the work and research. Thank you 🙏🏽
🙏🏼
Those people that say we don't have it need to shut their mouths. It real painful and not fun to live with. Do not tell people they don't have something when your not in their body. How dare they
If those non believers had fibro for a week, they’d soon know what fibromyalgia is all about.
A Never ending vicious cycle. It takes over your life.
I'm so sorry you feel this way. I say this as I am laying in bed right now dealing with hip and back pain. You are not alone 😞
Yes my Loves
It happened to me at 26 yrs old after the dr gave me 2 flu shots at the same time
Wow, that's insane! I use to get flu shots too. I didn't know they were not healthy.
You have to fight and fight like hell, I get injections from in my head all the way down to my feet...now I'm tired of fighting im 55 and was diagnose in 1992...best of luck to you
Wow, this is like having a free of cost visit to the best fibro doctors office.
Haha, glad I could be of service :)
Yes indeed, I totally agree!
Except most of us have nowhere to get infusions, because we all have "fainting lady syndrome!" I go to a research hospital, Cleveland Clinic, they don't even have a Dr that wants to talk about Fibromyalgia!
@@OubreMedical please advice on finding a top treatment centre in Toronto. I was a patient at Mount Sinai WASSER pain management...but since new Director he has told me the centre can't deal with my pain and I need to go back to my MD. I was a patient for about 8 years before that🤕
@@Thebohemiangirl1 I know know anyone in Toronto :(
I have suffered from fibromyalgia for over 30 years. I have had doctors accuse me of exaggerating my pain, and one doctor told me not to tell anyone that I have fibromyalgia because I would be labeled as "crazy"! My family scoffed at my diagnosis and said, "I just don't think you can handle pain!". I am crying as I listen to this. It is the first time anyone has given me an explanation to what is causing my pain and suffering. I need all of this information; what foods to avoid, what supplements to take, and how I can get my life back. If at all possible, could you direct me to the resources that I need to get well? Thank you so very much!
I feel your pain! I was the same way and as a nurse, I heard so many times in the ER where I worked, “Oh, they’re a nut job!” Doctors thought they were drug seekers and I witnessed these things while suffering with it myself. I told no one I had it because of the label a person received who said they had fibromyalgia. The doctors at Mayo in Rochester Minnesota helped me when I was at my worst. Thank God for them and the Dr. In the ER one night who was so kind and compassionate who told me to go there. I will never forget him and his nurse. The first people who treated me like I mattered. Yes, I still suffer today but I also believe that by the grace of God, He will heal me one day. God bless you! 🙏🏻
I suggest watching the youtube videos of Martin Rutherford. Avoid pinning all your hopes on people who are trying to sell something or promising some kind of cure in a pill.
Perhaps you can eliminate inflammatory foods like tomato potato cream dairy gluten then try them after several weeks without. If I eat whipped cream, I have all over body pain. Tomatoes give me joint pain. Dairy and gluten make my gut miserable. I hope that is a start for you.
its a B1 thiamine deficiency
@@mpg.1 mast cell diet, anti inflation foods. Good call.
Wheat is often a problem for people.
Worth a try
Vitamins need balance as all work together
I'm tired of being tired and I even get exhausted just to take a breath.
Me too.
Thank you, thank you for sharing, Sarita. I feel that also and have not heard anyone else relate that just taking a breath is tiring. In fact sometimes it seems it takes all I have. God bless you and praying for a cure or better meds that will help more than the ones out there now.
Nice dog
Who are you seeing and are you on any meds?
Me too. Trying talk on phone or people can g breathe out of breath. It's hot worse
I was diagnosed by two doctors that said I had the Fibromyalgia they have seen. Years later I found I was allergic to milk lactose. The lactose gets in your muscles and make them achy. When I switched to lactose free milk, all my problems were gone. I also discovered I’m an Empath and picking up others physical and emotional state. Which was so exhausting
Wow did it really. That's great. Yep, the same as you, listen to everyone's problems but don't get much back unfortunately. I've decided that the so called friend of over 40 years and who abused me and told me there wasn't anything wrong wuth me, weren't worth me being so upset over. So, I made a choice to say goodbye. I can't be there for everyone. I'm flat put being here for myself. It's excruciating, daily pain from my head to my feet. I also need a replacement knee which will happen next January. I can't walk and to be quite honest, the thought of even 5 minutes exercise is impossible.
Try raw milk. Store milk is garbage.
You're rh negative. These doctors have been selling our lab work blood behind our backs. Our blood is called "Pedigree Blood" and they get over $1,000 an ounce. All the doctors have been keeping it a secret. Some of us have copper blood. We're acidic, not alkaline, and need a different diet. Our frequencies are higher than other people, and our bones have a special resonance. Our Amyloid fibrils behave differently; they knit and weave and bind, so that we end up with a lot of Amyloid plaques. Rh negative knees, Alzheimers, urinary/bladder/kidney problems, auto immune, lupus/Lyme ... all neggie diseases. Our vision and eyes are different too. This guy knows it. Crimes Against Humanity, and Medical Experimentation. Trump signed an Executive Order that starts with my name on my clean date from 15 years of an obscene amount of prescriptions, December 27, 2017. All their assets are going to be seized and there will be Nuremberg Trials.
~Pure aQuatic COPPER Magdalenien Rh Negative Blood (MAGA was my great grandmother's nickname,) The Holy Grail Bloodline
~Oraphim, Double Diamond Sun CHRISTOS dna with the genetic code for original humans ... geneticists call us "Organics," and our Mitochondrial dna has the "god-gene" or "X-Factor."
You probably have "M's" on your palms with "X's" in the middle. Our palms and feet have special "Palmistry" markings. Eye have Infinity Symbols under each ring finger. The doctors identify us at birth, and the government tracks us from cradle to grave. Our Intelligence Files call us "Targeted Individuals" and if we have abilities like Telepathy (Celts) or Telekinesis (Eastern European) then they call us "Empowered Individuals." Look up both of the above topics and you will find information on being an Empath also.
♾♎ Omegaperfectstorm! LuvQ'all! 888girl!
Text Trump 88022
Glad that worked for you. I always drink lactose free milk IF I drink milk. For me, it makes zero difference. I did have a food allergy test, but was not allergic to milk as you were.
@@LemonThyme1933 The other night I ate a bowl of cereal and used half and half, so good, but boy did I pay for that. I woke up to a big poopy mess 😂
We need more educated doctors that understand Fibro and not brush us off as just another Fibro symptom. I wish you were here in Idaho.
Were is this Dr
Yes. Begin with researching a bit, and try out LDN, low dose Naltrexone. No need to thank me, just do yourself the favor of giving yourself the chance to try it out. The only chemical thing I'll ever put in my body again for healing. It is POWERFUL for all autoimmune matters.
I agree ! I wish he was in the UK
He practices in Texas I'm moving to Texas LOL
Lisa Kostelecky
Dr bill Mugg in So Hadley, Massachusetts
I want to get rid of fibromyalgia. I'm so sick of being sick I took cancer before fibromyalgia. . I don't have a life. Thank you, love your video.
Glad I could help!
I'm there with ya Becky. Almost 30 years (since highschool) of fibromyalgia + all the other crud. Having thyroid (Hashimotos) does not help. It's always something. Prayers to you.
Have you tried LDN? It's changed my life...
@@OubreMedical Dear Doctor, very interesting..I have fibro, and have suffered with it for over 30 years...what is your opinion of LDN? It has really helped me with the chronic pain, however I'm still suffering with chronic fatigue, daily. If I could just get that part straighten out I'd be GOOD.
@@OubreMedical Where are you located? I would love to be treated by you. Very interesting..
I have had fibromyalgia for 20 years! I also have neuropathy, and I am not diabetic, nor have I had a stroke! They call it genetic, since my grandpa had it! I can spend 20 hours a day in bed! I use to work as a Nurse, and be extremely active! I would work 8 hours and come home and nap for 3 hours! When I use to be active, I would have to take a nap after any activity, even driving! I feel like I'm just waiting to die! At age 55, this isn't living! I am not depressed, I have been in the past! I long for having a whole life again! I want to live!
Sounds like you need a functional medicine doctor. And someone needs to evaluate you for heavy metals.
Dr. Philip Oubre, MD guys like you are hard to come by. I’m near Huntsville, AL. Have any colleagues this way??
I know exactly how you feel!!! I’m also suffering with fibromyalgia!! I have neuropathy as well!!! All my doctors do is throw pain pills at me! I hate living like this!!!
I am so sorry. I feel your pain. I too have fibro and many associated diseases and have forced to retire after 38 years j the nursing profession. I find the one of the hardest things is to constantly defend a position I'd rather not have. I'd rather be working feeling that feeling of having improved the quality of someone's life however small, than living in this broken body with the broken brain. Prayers and best wishes.
@@OubreMedical I have heard many times over the 33 years I've had fibromyalgia that I need to heal my gut. I did have terrible yeast infections but I went off all grains, dairy, sugar etc early, and kept off them for 10 years. I got better by about 10%. If it is a microbial problem how do I fix it. I live in Australia and I can't find any doctors who seem to be able to help me actually FIX my gut. What type of doctors should I see?
I've had fibro for 33 years. This is the first video I've ever seen of yours (and the 1st time I'm hearing most of this information.) Thank you for sharing! Looking forward to learning more.
Me, too !!
@@wordgirl6267 me too. Over 30 years now. I'm tough. This has been awful.
thiamine b1 deficiency. avoid coffee
So very sorry, but think I can say that I have had fibromyalgia for some 75 years! After a polio vaccine given as a schoolgirl,
This makes so much sense! Why don't most doctors know this. Especially rheumatologist!
It's not profitable
The thing is, they probably do know, but to keep us all dependent on drugs for life, maintaining a healthy bank balance, between both them, the doctors and the pharmaceutical industry.
We will be only informed the truth, by people like this.
I have happened on this clip accidentally. Not really surprised to hear this. No one has ever been able to explain Fibromyalgia to me.
This is so wrong.
not in "main stream" medicine so till peer reviewed paper published in the journals
it wouldn't be taught to doctors.
As a massage therapist for 21 years, I found that what people with Fibromyalgia feel like is just "frozen muscles". It is as if the nerves are just frozen. When this happens, blood flow can now move through at a normal pace. It is lack of blood flow that usually causes muscle pain.
Omg you are so RIGHT it feels like the muscles are RIGID, and I get palpable lumps of pain! They stay for MONTHS may be years!
@@joysoyo2416 So this happens because your nervous system is in the Fight or Flight mode. Our breathing literally regulates our nervous system. IF you take deep long breaths, this will shut off the fight or flight, and turn on the Parasympathetic Nervous System. It is all about the breath, and sleep. You must get good restful sleep also.
@@treecek also putting your tongue pursed between the lips , and Breathe in ,close your eyes breathe out , open the eyes, this taps into the vagus nerve which relaxes the fight or flight
Thank you! GTK!
@@treecek so it's fair to say this happens to people who have suffered or been abused?
I have Fibro for over 25 years. I have experienced so many surprising symptoms. You mentioned the heart not being one of the organs effected. Well for me, I have had 4 or maybe more "heart attacks" that turned out to be my Fibro causing severe pain in my heart and sternum. So always go to the ER to get checked out, no matter what! My advice to everyone!
Same here! Nerves and muscles pain in heart area. Starts suddenly and causes strong fatigue, but heart is fine. Have to take muscles relaxant, when it happens. Cracking chest/thoracic muscles/ribs makes feel better (which is the proof, that the problemis not in the heart)... for a very little bit, but the pain quickly comes back. When it starts, it lasts for a few days, which is another proof, that it is not heart problem.
b1 thiamine deficiency. avoid coffee
This is what I’m going thru.
Yyes! I went to er earlier this year.. Felt lie someone was stabbbing my heart over and over again Dr did all tests said not heart attack but your pain levels are so high its sending blood pressure through the roof
@@liveinms9949 i wd use potassium; B1 thiamine and magnesium to start with, if u have not been poked, of course.
Also The foods that cause inflammation is also filled with weed killer (glyphosate)and pesticides.
I grow and preserve as much as possible non GMOs.
Yes Joyce, I wonder how spraying millions of gallons of weed killer on two are wheat and corn has affected the human body. Our soil is contaminated and where I live we have something called pfas in our water. Extremely carcinogenic. So then we drink pallets of bottled water and there's millions of tiny pieces of plastic being consumed. The women that got this 35 years ago probably were not eating McDonald's everyday. They were probably making dinner every night and raising many children keeping busy. Why did they get fibromyalgia? Did they have leaky gut 35 years ago? Were all their mitochondrial cells broken up? Of this one thing I have no doubt, this doctor as well as many more with their good intentions and no scientific paperwork to back it up except their own statistics from what they see will become extremely rich and get very large subsidies for their studies. But most people with fibromyalgia can't work an 8-hour job. we are getting rich from having fibromyalgia. The real money is in saying that you can cure it. A few months ago a doctor discovered that a brand new medication that he had developed was blocking pain signals from the brain and allowing fibromyalgia sufferers to exercise and have a better life. Who's right here? I'm just tired and I don't like condescending doctors. Sincerely, Carly
Description
Glyphosate would affect the mitochondria as it Mitochondria and chloroplasts have striking similarities to bacteria cells.
@Elvis Edge RR Woodward while both are antibiotic theyre not the same thing and dont affect the organism the same way sodium chloride is essential for life while glyphosate is not and assault the organism via the shikimate pathway
Hi Dr. Oubre! Thanks for explaining fibromyalgia so well. I've been living with Fibro for years now but was only diagnosed a few months back. My doctor also diagnosed me with Benign Joint Hypermobility Syndrome. The cumulative effect of Fibro and BJHS plus the PCOS and IBS I've been living with for years now has made my life really difficult.
Hello, could I please ask what joint hypermobility syndrome is and the symptoms. I have had fibromyalgia for 30 years, but the past five years I have had severe chest/ribcage pain and difficulty breathing. My heart and lungs have been checked out, but no diagnosis. I am in constant pain and discomfort and find it difficult to take a deep breath as everything feels so solid and tight and stiff, it s so debilitating. Thank you for any feedback. Hope you are having a good day/ night!!!! Hugs
@@pamelasmith2625 ... Hi Pamela, I thought I'd chime in since I've been researching it for a couple years. It is listed under the 'tent' of connective-tissue disorders. You might want to search online "Connective Tissue Disorders". I was diagnosed back in 1996 with Fibromyalgia, but as the years went by, I realized it didn't cover all my symptoms, like stretchy skin, very easy bruising, spontaneous bleeds, having most of my internal organs drop out of place due to my ligaments giving out, ect. I highly suspect I have Ehlers-Danlos, which is also a connective tissue disease. There are 13 or 14 sub-types. Generally, connective tissue will cause the opposite of what you describe (your mention of everything feels so solid, tight, and stiff), however, you could have 2 problems fighting against each other, like me...I have Rheumatoid Arthritis which makes you stiff and tight, and EDS which makes you loose and floppy, esp. in the ligaments attached to bone. Have you tried "Symptom-Checker" online???
@@pamelasmith2625 ... here's a video that may help ~ th-cam.com/video/mTAWeL0FQkQ/w-d-xo.html
its a b1 thiamine deficiency
@@pamelasmith2625 you may have ribs misaligned. A chiropractor can put them back. I have fibromyalgia. My ribs go out. Think I have EDS too but most Dr are mid taught about it and ignore it. My Brighton test would have showed I had it when younger before fibromyalgia & SLE.
I have had fibromyalgia for 35 years. Believe me it is real. It took 3 doctors to diagnose me. We had a conference one day and I had never heard about it before. I have hurt so badly, I could not get up in the mornings. I was so tired all I wanted to do was sleep. The depression was horrible. But I had great doctors that understood. I live with it and prayers certainly help. My faith has always pulled me thru. I know it will never go away, But I do pray for a cure.
its a b1 thiamine deficiency. avoid coffee
I have had Fibromyalgia since 1992. I saw 5 doctors until a Rheumatologist diagnosed me. I did a diary of symptoms and foods that made me feel worse. Lack if good digestion can make you feel worse. Took myself off Dairy and wheat. Difficult life with symptoms and pain throughout my body. Sometimes very severe pain.
I pray too for a cure
@@susantisdell1725 b1 thiamine deficiency; avoid coffee
@@tanjatroonbeeckx9418 B1 thiamine deficiency; avoid coffee
finally someone that knows what he is talking about xx thank you .
Thanks for the compliment
Dr. Philip Oubre, MD my pleasure ☺️
Right!!? Finally someone who has not only heard his parents but he actually listens! And WANTS to help them!? ...it makes me want to cry...
Omg.. this makes so much sense! Thank you Dr. Oubre.
I agree totally 👍
Thank you for posting. Fibromyalgia research has come a long way since my diagnosis in late 90's. There is no doubt that my mother suffered from Fibromyalgia as does both my daughters, genetics play a role in Fibromyalgia that isn't widely discussed in the medical field I hope this changes for future generations.
b1 thiamine deficiency. avoid coffee
I agree. It has a genetic component. No docs will address this.
@@Lauren-vd4qe- Also, a build up of lactic acid - which, caffeine produces more of.
I was diagnosed with leaky gut years ago and have had fibromyalgia ten years so now I understand the connection, thank you!
Your leaky gut is caused by glyphosate. So is your Fibromyalgia. Do some more homework. Direct that to naturalists..holistic...anyone opposing govt lies.
Dementia in
@@kimberleypudifin6043 ?
I am a 71 year old woman who was diagnosed with fibromyalgia when I was 32. At that time no one knew what the word meant and I had to do what little research there was on it myself you are so wonderful to listen to. I am definitely going to work on my gut thank you so very much
Did they call it ME?
b1 thiamine deficiency. avoid coffee
Hmm... years of acid reflux that cause couldn’t be identified. Years of allergy testing. That we did know, it was an allergy.
Testing never found the allergen, but I stopped coffee for adrenal issues and all acid reflux went away.
@@elizabethtovar3603 coffee caffeine repeatedly shocks jolts the adrenal system fight or flight response so constantly that the adrenal system degrades and then gives up, resulting in a hot flash fritzout final desperate efforts to right itself, before it fails to function at all. all due to being beaten up by coffee...coffee is a drug and a dehydrant. both my hubby and son quit coffee and now feel much better.
Hello! I am from the UK, but up until recently, it was not recognised as an illness. You are classed as lazy etc; which is not fair! I also have arthritis in all my joints, so double the pain and little relief from pain medication! I think it is over due, that the Doctors in the UK, realise this and research more as you do, to help patients instead of being closed minded! Thank you, Anna.
I was diagnosed last year with fibromyalgia, and bk and forth trips to the doctors for the last 3years I eventually got the answers I was looking for and yes your right. I live in the uk aswel, but I started seeing female GP because my old GP he said it was stress with working nights, but i knew there was something wrong, we know our own body's. Maybe if went private we could of been diagnosed earlier
I agree that many UK Drs haven't a clue about Fibro, I just wish they paid more attention to what we say. Luckily the Dr who finally diagnosed mine was an Australian locum and was on the ball. However Dr Oubre's video has been really informative. Thank you Dr.
It was a Physiotherapist that told me I had Fibromyalgia, many, many years ago. Dr's never really believed in it, so all through the years I have just had to put up with it. My daughter now has it. I also have Psoriatic Arthritis & I am on medications for that, but no one Mothers about Fibro...Sp plsed I see this video. Will discuss with GP.. I am in the UK.
No money for research that doesn’t include Big Pharma.
So true its the most frustrating thing for a pereon to go through even eating can be so tiring have a couple of days of bursting energy and then days of dehabhilatating almost comatose type symptoms where I can put my body into a shut down mode and sleep for 24+ without u
using the toilet or eating tryin to wake me is almost totally impossible and I wake with drunk type balance slurred speech eyes rolling. The pain middle and pelvic part in back is excruciating. I do have spondylitis in my full spine. But I kno the fibro is something that is a problem in my brain and spinal cord. Its not just muscles as they say its definitely alot more to fibrom. Great information. Thanks
I accidentally came across your video and Thank God I did! I have been suffering from Lupus & Fibromyalgia for the past 10 years & also have severe asthma, hypertension, PTSD & just recently got diagnosed with diastolic dysfunction. This dr. is amazing and it's so refreshing to see him explain all this information regarding Fibromyalgia and how it all this makes sense! The doctors I have seen past & present just don't get it and don't understand what Fibromyalgia really is. It's so frustrating talking to dr's about symptoms and they look at you like you're crazy and like it's all in your head. I go home a lot of times and cry because nobody gets it...
Just wanna show my appreciation for taking the time to do this awesome video dr. and am definitely going to make big changes in my diet.
I have been thinking about going vegan for some time now but, I love steak & chicken! I have recently lost weight over 20+ lbs. over a 6-month period without even trying or dieting. I went from 126 to 102 lbs.
So, don't know what I can eat or try that is healthy and can make me gain some of that weight back.
You should try a plant based diet. Plant based protein is not as hard on your kidneys as red meat is. Chicken is not as bad as steak. You just have to cut down on the bad stuff, if you don't want to eliminate it entirely from your diet.
I've been vegan for years but it didn't stop me from getting fibromyalgia and the only thing that has helped so far has been cutting out msg, taking ldn and meditation. Some research says that fibro is an auto immune disease of the opioid receptors in the body, others say it is a problem with the endocannibinoid system, others that it's an insulin resistance problem (because fibro patients treated with a drug for type 2 diabetes (metformin) also have a huge reduction in their pain.) Then there's the medical trial (hopefully starting next year) to see if the BCG vaccine will help fibromyalgia by changing the immune system. I think there are different types of fibro with difference causes and therefore different solutions. It may be that all the theories are correct because there are different types of fibromyalgia
oh yea and I did get rid of my mercury fillings and went through the detox. IT DID NOT HELP ONE BIT and it cost me £15,000.
I truly believe that lupus and fibromyalgia are related I have both 😢
@@BlackbirdGirl72I got rid of my old amalgam fillings as the dentist recommended. Hadn’t had a cavity in 25yrs & after fillings were replaced in 3 yrs I had a cavity inside every tooth in my mouth! I had beautiful teeth, most thought I’d had braces but didn’t. I was diagnosed with fibromyalgia 35yrs ago, then sjogrens, then multiple back disc degeneration & osteoporosis & migraines & colon cancer in 2000. I’m so tired of fighting pain for over half my life! Now my 17yr old granddaughter was just diagnosed with fibromyalgia & having a difficult time getting around without a cane or walker! I wish I had all the answers especially for my granddaughter! I’ve been obviously very understanding with her & am sharing things that have helped me. My heart breaks for her being so young. One of the hardest things is to discuss chronic pain with anyone whose never experienced it! So I don’t bc most don’t have a clue what it feels like to have pain constantly & never will till they experience it for themselves! Health, happiness, love & movement if possible everyone!
Dr Oubre I’m going to continue looking into your videos (this is my first video to see if yours). I was diagnosed with fibromyalgia when is was 22 (I am now 41). I am insulin resistant and on metformin. I was gaining weight no matter what I did. I began researching intermittent fasting. I decided to try IF along with a low carb diet. This meant I cut out almost all gluten, processed foods and diary. It took about four months before I started seeing weight loss but only 2 months before I stared seeing a decrease in my fibromyalgia symptoms. As soon as I started eating gluten/processed foods/diary again, my fibromyalgia symptoms began to return. After watching this video, it is beginning to make a little more sense. Thank you!
Look into b12 deficiency with taking metformen!!! Please look it up! Supplement or see about getting b12 shots.
Well done to you the government and food industry also big pharma are all linked putting this crap in our foods they are slowly poisoning us , stay away from all oils and sugar that's hard to do when it's in everything
b1 thiamine deficiency. avoid coffee
Metformin stuffs up B12. Try Berberine instead.
SENDING LOVE AND HEALING ENERGY TO ALL!!!💛💛💛
I always have muscle pain In between the shoulder blades
Mee toooo
I have had pain there for years, to the point where I can’t lay on my back, everything hurts, I hate this
I can’t wear a Bra skin hurts
Yes that pain goes hand and hand with lack of energy.
Heating pad is my best friend for that shoulder blade pain.
I sent this to my dear sister friend who is debilitated by this disease...
i pray for her continually... I’ve never heard someone speak like this!
Thank You! 💜🙏🏼🛡🗡👑📖🔥
Good luck to her!
I cured my fibromyalgia by detoxing. I went from feeling 92 yrs old to feeling like a 20 year old again. I still struggle with balancing my diet to keep myself clean but agree that the Liver and gall bladder play a role - now I work on Liver cleanses for better health.
Can you say exactly how you detoxed. Thanks
What was your system
Hi, can you answer what's the best way to cleanse a fatty liver?
@@akitajapan1651 look up Dr. Berg and Dr. Allen Mandel, both here on yt. Good Luck🙏
I used homeopathic nosodes to detox vaccines, heavy metals, viruses, mycoplasma, & Lyme Disease. I used homeopathic products from Clinicalnutritioncenters & Pure Formulas, & I used colloidal silver from Herbal Healer.
That is the best explanation that I have ever heard and I've been suffering with it for 30 years.
Finally, someone knows what they are talking about❤
I'm blessed to live where there is a fibro clinic- it's a stay in clinic for 3 weeks. The education, treatments and acceptance is amazing.
Where is the location of treatment facility where you go?
Undiagnosed Lymes disease can cause mitochondrial dysfunction.
Agreed.
I don´t get why there are so many theories about fibromyaliga. For me it´s so clear: when you have Fibromyalgia and you do a sleep study, it is pretty clear that people with Fibro don´t get any deep sleep, REM sleep. That alone can explain all of the symptoms: pain, fibro fog, fatigue...
Take VALERIAN ROOT 2 OR 4 YOU WILL SLEEP W OUT GROGGY NEXT DAY. Its been used for hundreds oh for years in Europe.
Jeanette Kniebusch Hello! I love the way your opting for an all natural alternative like I was! I have one other All Natural solution for you... A Much More Effective for sleep and is also fantastic for every human being but especially for Fibro and Mito Conditions and symptom control. Pure Safe Full Spectrum CBD Oil....However!!!
As Long as it is the RIGHT Blend of Cannabinoids that are Pure Hemp Extract/Tincture, Made from the Entire Plant NOT the “Seeds of the flower”, Federally Tested and Approved for its Purity, Toxin Free and 0% Chemicals as well as bacteria like E. coli that they also keep finding in the testings of most CBD Oils out popping up all over the place. That the hemp plants Also are Grown by a Completely Tested and Federally approved Organic Farmer (and tested farming soils for passing for 100% containment’s and chemical free!), comes from a Manufacturing plant that is FDA Approved and manufactures their Own FULL Spectrum CBD and it always has to have a QR Code on the bottle for its transparency and it has to have a “COA” on each batch that is produced. Which when you scan the QR Code on the bottle, will Pop Right Up That products COAs So you can read Exactly what the Tested Levels of the Pure CBD oil are. If the company/CBD Doesn’t Have All of these above, then it will do harm to ones health rather than getting the tremendous health benefits that a Pure Full Spectrum CBD Oil provides to the entire system.
Keep Shining and Living Healthy and All Natural Jeanette! 😊
I have suffered for years and finally getting a sleep study I'm excited as I've heard that I will be a new person after the study and treatment so fingers crossed
It's so WAY MORE than sleep. It's constant pain 24/7.
@@leahgeraghty1279 Lucky
Thank you for this! I have been suffering with fibro for years, without any education about this disease or how to fight it. I thought it just is what it is. Planning on binging your videos today in the hopes of educating myself and making some changes in my life. I've always said there is nothing yet invented on this planet to help ease a flair; your education may be just the tools I need to take back my control. Again camt thank you enough
b1 thiamine deficiency. avoid coffee
I’ve had it for over 5 decades. Pain 24/7 and fatigue forever. Thanks for the explanation that makes scientific sense.
I have told numerous doctors my symptoms. I have almost every symptom you talked about. I had a doctor that put "fibromyalgia" in my chart, but never once spoke to me about it. Thank you for this info.
Thank you for this video! You have restored my faith in modern medicine. Your explanation was clearly the most informational than any other explanation told to me. I had fibromyalgia about 20 yrs ago. I saw a several doctors and they told me the pain was all in my head. Luckily, I saw a MD as a recommendation of a friend and she told me I had fibro. She recommended antidepressants but I respond very poorly to them. A friend of mine who improved her fibromyalgia gave me a long list of vitamins, minerals and supplements along with Epsom salt baths and sauna and the symptoms, especially the pain, muscle fatigue and brain fog improved drastically. Over the years, I introduced coffee enemas, pemf and red light/NIR and I’m the healthiest I’ve ever been. I also became a multiple modality energy healer/reiki master. Vitamin infusions weren’t available then but I did b12 injections, which helped big time. I also healed my gut and don’t consume gluten and dairy. My body craves whole foods and occasional seafood. Raw grassfed meat helped especially when I healed from late stage Lyme disease a few years ago. I am going to look into lipid therapy to strengthen my mitochondria. I detox regularly to maintain because I know my body doesn’t detox as efficiently as others. It’s probably because of my mitochondria needs a little TLC. Thank you again 🙏🏻
This is the best video to explain not only fibromyalgia but how our system works. I have had crohns and colitis and now the muscle pain and mind issues with memory and brain fog. Thank you for this video!
Connie Wilson LDN is for you too. Look into it, several fb groups
@Dana Horton LDN works really well for IBD patients, so I agree with Dana.
Fog brain is terrible I thought I was losing my mind
Thank you for talking about this it makes sense what you're saying I think this will help a lot of people I really wish more doctors knew about fibromyalgia and would take it more seriously and quit thinking that people are making up symptoms and just because you can't see it doesn't mean the person is faking
I had an 8 month flare up where I was close to death and near suicidal towards the end. I don't have the time to go into too many horrible details here, but it was caused by a poor diet. I had to cut up and looked ripped for a job (stuntman/entertainer) and I noticed that my pain was less when I had more muscle. So, I went on an old multi-set training and calorie loading regimen of mine. I couldn't get enough calories in eating clean, so I started ingesting a ton of dirty calories. Very soon, my body started to shut down and fall apart. At the end I was 140 lbs (down from my normal 175), with dark circles under my eyes. I was stuttering, having panic attacks and I could barely breath, think, talk or read a book. The bottom line is: f*ck sugar. And if man made it, don't eat it. When you're shopping for healthy food, just remember: If it has a mother, it's okay to eat. If people ate it 200 years ago, it's okay to eat. Shop at the back and to one side of the grocery store - the produce department and the butcher. Drink at least a gallon of water a day and stay away from anything artificial - eat only organic, pesticide free, steroid free foods and pay attention to were your meat comes from. I'm now a father, a winning men's physique competitor and a firefighter - with fibromyalgia. It's still very difficult some times, but it's never been like that 8 months again, ever. Eat clean and stay healthy people!
My same experience, stopped eating sugar and started focusing on giving my body what it needs at the cellular level.
SUGAR! YES! Clean out your gut.
i have pain all over my body and the worst of it all is the pain at the back of my neck 😢....
Me too
Try picking up some.
Dragon 🐉 deep tissue salve.
Thc,cbd,cbn.
I am too tired to take this in!
A true Catch 22 :(
sharon x same here plus my legs are both restless and hurting. Argh
I know the feeling well sweetie
sharon x quit plants
sharon x i totally understand I am the same my fatigued body and brain is exhausted and it’s hard to focus on things.
Clean food is essential!!
Get the processed out of your diet!!
Detox!!!!
i shared this with my friend because she had to stop working due to severe pain from fibromyalgia. I shared with her to clean the gut first, detox and then change the eating habits, that was a year ago. I feel bad because she was working on her doctorate, teaching and raising her son and now she is restricted to the house. I pray she watches this video and make those changes
And reduce stress
Didn't help me, there has to be more than just clean eating because fibromyalgia has been around for hundreds of years
@@angelaquintero1977 find your food triggers . Add a probiotic ( colon health or align ) it takes a few months( sometimes a year ) to heal the cut . Sugar / processed / refined carbs/ meat injected , processed lunch meat with colors 😞 avoid . Change over to fresh vegs , chicken breast , salad ( I do lettuce mushrooms a little blue cheese ) blueberries strawberries watermelon. As soon as I put bad foods in , it’s starts to attack . I’m still learning trigger foods .
Dr. OUBRE, I live in Ontario, Canada and would be grateful to know of any Doctors here know how to treat Fibromyalgia with the infusions you talked about with Lipids. We need help like this everywhere, and your program studies and education of our medical doctors needs to be done widespread asap so that we all can end or greatly improve on this suffering. Thank you Dr. For a VERY educational and helpful video.
I live in British Columbia, Canada and would also like to find a doctor.
I was diagnosed at 15 I'm now 46. This explanation however is new to me and THANK THANK YOU for it.
Yeah, I try to do everything right. I'm really sick of myself. You got to keep moving & believe there will be an answer. This Dr. makes more sense than many before.
I recently saw a pain management specialist here in Citrus Co., FL. He explained to me that fibromyalgia is an overactive central nervous system. He has prescribed low does Natroxlene for my pain. You start at 1.5 mg and work up to your best dosage. He has some patients on 9 mg, but most of his patients are on 1.5 mg or 3 mg. After you are on the medication and your fibromyalgia calms down, your other pain is then unmasked so you can begin treating it. I was diagnosed with fibromyalgia in 2002. I also have chronic myofascial pain, osteoarthritis, bilateral carpal tunnel post op, cervical degenerative disc disease and low back pain. This is the most hope I have had since 2002 for pain relief from fibromyalgia. Just sharing for others with this condition.
Brenda Fuller - LDN has helped me as well.
Goddammit woman, your comment should be in bold giant capitals!!! You are so correct in that it is a brain based illness! I too have found latest findings explaining this! So many people going off to change their diets after seeing this video, what a load of tosh! Even in the video description he has said it MAY be the reason! He's not even convinced enough to claim outright that he has 100% proof! Yet the sheep blindly follow... What's happened to people lately that they are so easily manipulated??? Where's their common sense! I wish I could make everyone who's seen this video read your comment!!!!! 😘😘😘
Brenda Fuller - thank you .I met a lady who also tried this for her fibro with excellent results .It is not easily available in the UK and requires a private prescription but I shall look into it .
Hi..Are you still on LDN ..How is your fibro now
I was just diagnosed with fibromyalgia,diabetes,anxiety,depression I had for over 15 years and arthritis.Never in my life have I ever experienced soo much pain in my body.I just had a procedure done on my thumb because I had trigger finger.
Sorry to hear of your pain
Hi trigger finger means. Iam also have ulnar neuropathy
I've also heard it called a hypersensitivity disorder. That's what I tell people any more when they ask.
Also, Hypersensitivity to the Central Nervous System.
Yeap! That's what it also feels like to me, I'm very sensitive to almost everything!!!, I'm so delicate, poor me 😓
I am so thankful that I found your channel! Living in a small city in Canada, and have been on a pain and symptoms rollercoaster for the last 6 years, however, as you mentioned, I have had some symptoms, but not as severe, from as long as I can remember. When my symptoms and pain started to get worse, and because they were so varied, and changed, sometimes weekly, or even daily, I was first sent to a psychiatrist, which was very unsettling, because I knew, I wasn't being believed. My symptoms still kept changing and getting worse, so I was then sent to a wonderful Rheumatologist, in a neighboring city,, who ran a series of tests, including bloodwork, and was diagnosed with MCTD, however, my Rheumatologist, was not certain this was an accurate diagnosis, as my symptoms, were not that, of her other patients, so she kept investigating, and by pure chance one appointment, she was touching certain parts of my body, which most all the points were painful, and she asked have I ever noticed this, and I replied, oh yes, I have had that sensitivity for years now, and she started discussing fibromyalgia with me........I have since done some research, and found varying symptoms and pain levels can occur, as you discussed, so I am still discovering all that fibromyalgia can be. I was hoping with all your knowledge, if you could answer a few questions for me. Do a lot of people with fibromyalgia, also have a positive blood test for MCTD., of is fibromyalgia, part of a MCTD symptom, as I have not seen this included with the 6 other diseases, normally associated with it. any information you could provide, would be greatly appreciated 😊
Thank you so much for this information! My poor mom has suffered for way too many years. She has been on & off of hydrocodone. This finally makes sense. I feel God led me to this video. I have ALWAYS researched & tried to find ways to help her, BUT NOW I AM DOING IT FOR ME. About 6 months ago I started having aches & pains. I was devastated because I've watched her suffer with NO ANSWERS OR RELIEF. I haven't been to a doctor yet, because I'm so sure they would want to put me on medications, just like her. Thank YOU! I will be waiting for more of your videos!❤
b1 thiamine deficiency. avoid coffee
I’ve been suffering from wide spread pain since I was 22. Now 58. I have managed two long term careers one was psychiatric nurse for 33 years. Then I trained and did something completely different in my early Forties and did Community Liaison Officer. Sadly now I struggle to work but manage a few hours a day with a struggle. I have my thoughts on this. I feel trauma triggers either mental or physical trauma.
Organic coffee enemas will cure you.
@@UncaTuck they have to be Organic?
I heard coffee enemias make
Your hair beautiful.
Your right, about organic. You putting the coffee up you a-s.of course Organic.
LoL
I agree
You worked as a psych nurse.. Have you read the psych books. And history of psych treatments?
Maybe you caught one of the VIRUSES GIVEN TO PSYCH PATIENTS IN ORDER TO CONTROL THEM. THINK ABOUT IT. It's in the books.
However
IT IS ALSO TRUE THAT EXTREME TRAMA EFFECTS THE THE BODY, THE IMMUNE SYSYEM AND MANY OTHER PHYSICIAL FUNCTIONS. AS WELL AS NEUROLOGICAL.
AND SO DOES STARVATION. YOUR A NURSE. RESEARCH IT. BUT FIBROMYLIA IS VERY REAL.
WHATEVER THE CASE. COULD ALSO BE VACCINATIONS.
I DID HEAR SOMEONE SAY POST POLIO SYNDROM. NOT SURE WHAT IT REALLY IS. BUT HES TELLING US WHAT IT IS.
EXERCISE AND SUPPLEMENTATION WAS WORKING. BUT IT WOULD TAKE YEARS. AND CONSISTENCY.
Amen to your theory of trauma. My fibromyalgia didn't start until I had a severe mental trauma, my mother's started after her husband of 67 years passed out on the expressway while she was in the passenger seat. My younger sister lost her husband after he was coming home from a outdoor church meeting in the Bahamas. The man who was driving ended up flipping the Jeep and it broke her husband's neck. Finally my oldest sister almost lost a child and it was so devastating. I see a familial DNA and a trauma-based trigger for fibromyalgia. But what do I know? I just eat well and manage to sleep well and am watching my husband die of cancer. And then there's the pain. My favorite is the one where I feel like someone is jamming an ice pick into my ear. Or maybe it's that once or twice a month I can't see clearly for a week. No, it's when I feel like someone has taken a metal bar and hit me across my shoulder blades and then in the middle of my back and finally across my waist. No, this isn't living, this is surviving. Giving you a Gentle hug, Carly
Thank you so very much for saying that fibromyalgia is very real! You have no idea how much it means to hear this!
Your presentation was very enlightening.
I can't remember a time I wasn't in agony.
My symptoms really started when I was a teenager.
Finally I have some more knowledge and a better explanation for all of what I've been feeling.
I look forward to watching you again. Maybe you could give some tips on how to heal the gut. That's something I can't even get from my GI doctor.
Thanks for your help.
Thank you so much,suffering for 35 years,God bless you,dear man
Dear Dr Philip, after about 25 years of pain etc etc, i have now stumbled upon this video. I could not believe my ears. I am in tears of relieve! Our family is wridden of cancer, BRCA positive, lupus. 😨😰😥😭 i will immediately forward your details to our various doctors from South Africa. May God bless you abundantly. 🇿🇦
Excellent information and I like his natural presentation and new dimension of hope for so many. 20 year fibro. slide. Really thought there was no real answers, or cure. Thanks Jody
Sounds good but what diet heals the gut? Left us hanging on details. 512 number is no where near me.
@@kathihertz510 follow dr Gundry advises on how to cure the gut...you can find him I. Your tube Stephen Gundry...
@@marilynsinquimani4994 Please forgive me for this, but I tried Dr. Grundy's products for the gut, spent quite a bit of money, and they failed to meet his hype. I am very dissappointed in his products. I suggest you research any plan you're interested in. It's really a shame, because I was very pro-Grundy. After this experience, I won't buy any of his products again.
This is an absolutely amazing video! I always said o feel like something is wrong with my cells. Of course people really thinking I’m crazy. This explains so much of what I believe in and knew deep down in my heart. This is the other reasons why medication and opiates do not work for fibromyalgia. High freaking five x 2 🙌
Your understanding and explaining about fibromyalgia is very good in fact is so good I finally understand more about the illness. Thank-you for shining a light on us sufferers. I look forward to hear more of your kindness in helping to cure this but my biggest hope is a preventer discovered so no one else goes through this awful pain. A C section and appendix was very mild compared to fibromyalgia.
Wow, watching your video teared me up. I had fibromyalgia pain for almost 6 years now and I am 26 now . I have consulted many doctors, physio therapies, ayurveda medicines , western medicines everything. Doctors did not know why I was getting these pains. Eventually the doctors said it was all in my head and they even suggested me to go to a psycho therapist. After a point, i even stopped saying my parents what i am going through just because no one would understand how painful it can be. Finally you saying that its an actual pain and there is a treatment, made me cry . Finally someone understood these pains 🙏🏻 and actually finding out why this condition occurs and thank you so so much. You gave me a hope . Thank you . 🙏🏻
Oh my gosh the pain! 😕 My entire body feels bruised all the time.
I was diagnosed after three years and have been dealing with the pain for over 15 years. It’s so debilitating.
This makes a whole lot of sense... and confirms my personal story of how this disorder was activated within my body... thank you for putting this so simply...
5 years ago I was diagnosed with a dissociative disorder which was caused by trauma growing up... it was this diagnosis that eventually made my doctor look at my VitD levels after years of complaints... after 3 years of up and downs... I have been told that it is likely a genetic disorder that disables my ability to absorb from the sun... it also appears to be rickets resistant... thus my dietary intake is the only source of VitD... I was lucky enough to be raised on wholesome backyard food... so my VitD as a child would have been fine... it was after an incredibly low Vit D level 2 years ago that I developed the Fibromyalgia symptoms... and even though my VitD level is now climbing to normal... the Fibromyalgia symptoms are worse than ever... so what has been my main focus?... developing and changing my diet to be closer to what I ate growing up... despite the childhood trauma... a vitamin deficiency is what brought my life to a halt...
Sharing for those that were told for years you are crazy... and it turned out it was not in your head... my head has a whole other crazy... dont ever ignore that 'GUT' feeling...
lol, "my head has a whole other crazy"
best quote of the day!
Best of luck in your healing journey!
b1 thiamine deficiency. avoid coffee
My naturopath recently put me on Malic Acid. I'm doing a liver cleanse for a month, and she also put me on a pre/probiotic. I am extremely vitamin D deficient and can't get in the sun often enough because of work, so I got a tanning bed (for free on Craigslist and relamped it with the best lamps) while also taking d3 with k2. Fish oil, curcumin, coqu10 are in my daily along with magnesium at night, which helps relax me and helps with restless legs and cramps. I started taking Previgen for my ridiculous, debilitating brain fog.
We will see if this helps. I have had the worst flair up this past year after I lost my dad. My diet went to hell and of course the sadness really triggered my pain. My pain recently went through roof and I had to start cutting out the crap from my diet.
Growing up in the 80's was not good for dieting. We were bombarded with horrible processed foods and "fat free" foods. My house was loaded with diet sodas, margarine and packaged foods. Even our vegetables were in cans. It seems mom cooked out of boxes and cans. She still eats like this but is suffering from Multiple Myeloma and I can't stop wondering if her diet didn't cause this? We won't know, but she just cant change.
Does ANYONE beside me suffer from severe BONE pain? My bones are what hurts the most.
I am a sever insomniac as well and haven't slept all night in over 25 years. I would say I don't sleep more than 4 hours total a night.
I am rambling...I'm tired and in pain. God bless you all and I will try to update in a few months on my new regimen.
Thank you Dr.
Amy, how are you feeling now? I’m 57 and have had issues since I was 32. I take Elavil Rx. It helps me sleep.
More sleep = less pain
Oh if only I were there or you were here. I'm 74 years old and have suffered from fibro for many years but was not diagnosed until the early 90's. I'm in Oroville, California and am hoping that you might be able to put me in touch with a doctor near me who is knowledgeable in fibro treatment. It would be so wonderful to experience some relief. In the meantime I'll continue to watch your videos and do what I can to help myself. Thank you
Now that's The real deal. Truth in medicine. Breathtaking.
I have fibro and throigh nutrtion and years of doctors and hormone s. I can now function on my best level for years. 40 yrs of chronic pain.
Keto diet with intermittent fasting- fibromyalgia gone in 3 months.
Food allergies can definitely be a huge issue. Personally I have MCS with minor pain symptoms, not fibro specifically, but I believe they and chronic fatigue/ME are all in the same family of illnesses. I have huge relief from diet changes, although I do the high carb raw (fruits, greens, omega 3 seeds) plus steamed veggie route and my symptoms are drastically reduced. When I had my food allergy test I tested highly allergic to most other foods. Although doing a natural antibiotic Sibo treatment reduced my food intolerances quite a bit too! Glad you found something to help!
I am doing this for FM (Keto) still learning.
Yeah but cheese and eggs is in the keto diet should you not eat that stuff cuz it causes inflammation
D only if your gut is messed up in which case go Carnivore or make meat stock to fix gut- so powerful.
@@brightonketochihuahuas1059 everybody's got is messed up trust me everyone needs a detox
Thank you so much for this awesome information. My mom has fibro and I hate seeing her go through this. She is so brave, goes to work, doesn’t like to complain but I know it bothers her to the max. This information was SO helpful. I would like to know a little more about this, I believe it would help my mother greatly. If you lead me to where I can find more info and how to proceed properly to heal her that would be awesome!
Thank you once again for this very accurate and important information!
Fibro took my walking from me. I went from being energetic to wheelchair user and have no independence.the pain is horrendous too... The rest of my body is really bad too...I wish people were more educated about fibro...people think your lieing or exaggerating cause you look OK... Thank you for uploading, very interesting information
THANK YOU! Your information is very helpful. I’m a retired critical care/ ER nurse who had to stop working because chronic pain became so bad. I worked until age 57, then I had to go on disability. There are days that I can barely get out of bed because the fatigue feels like you’re in the ocean tied to cement blocks. Fortunately my close friends get it. I’m now 61 and was just diagnosed with fibromyalgia. I thought I had long Covid causing this.
Thank you for this video, I've been diagnosed with fibromyalgia and seen many specialists and they're only solutions were prescriptions that made me even sicker, definitely going to try these detox/ lifestyle tips.
Well every thing makes sense now. I had a hysterectomy 37 years ago and I haven't been well since. I now have fibromyalgia. I have done every thing, seen every one and still ill. I saw a private Doctor who said I have mitochondria dysfunction. I'm now just about to start LDN. Low does naltrexone. Can't afford to see you, and Doctors are a waste of time. I have been ill so long now. And I have no quality of life. I'm 69 now and life seems so hopeless.
Hang in there please, I understand. All the way from South Africa
@@mela8940. Thank you for that. But you don't say any thing about what is wrong with you, or how or if you got well. And what you might have tried.
Eileen,
I’m with you! I’m 68 and feel 108. Diagnosed 23 years ago. Nothing has changed but the date. When the fatigue and pain are too much, Iam in bed just wanting everything and everyone to go away. Take this pill, that pill, try this or that. I DON’T want to. I just want my life back. I’m surprised my husband is still around. He works a lot, even though he is retired. He started a business. I have beautiful, young grandchildren I want to enjoy. Their parents want me to travel with them. How can I? I will try the clean gut and get away from dairy and sugar. My bones are crumbling and I need Vitamin D and calcium. I’m just recovering from my fourth foot surgery. It has been terrible. Sorry to vent. The best to you on your fibromyalgia journey. If you find something that works, please share.
Thank you sometimes I don't feel like a have a life because I'm in so much pain..
Wow!!! This is such an amazing video thank you so much! I have been dealing with this fibromyalgia mitochondria since 2004 I was 24 years old now I'm 46 and this is the first description that makes complete sense to me. I have been so very discouraged and overwhelmed for so long because I feel like no doctor understands what it is I'm going through and I've always just been fed pain pills pain pills pain pills now my body is so used to them it's discouraging! I'm excited to learn more about this! As is my body! What a wonderful video to come across this morning! I look forward to searching for more of your videos! Good now I'm off to work! Thanks again!
A friend has suffered with Fibromyalgia for years....I have sent this TH-cam link to him. Thank you!
There is a fasting summit starting Monday. I purchased it because i wanted to start watching it in December to prepare for a water fast the beginning of January (only 4 day). They covered water fasting in part of the summit.
Long story short - going into autophagy and then stem cell rejuvenation. Do you think it's possible for the body to get rid of the damaged cells (8:48) on it's own through the autophagy process? Supposedly it's 300X the autophagy process starting on day 4 of a water cleanse.
Great video, thank you. I have known many people with FM and they're offered virtually no hope.
I really don't understand why you don't have a million subs - seriously. You explain things so well and cover some really important topics.
Wow, thanks again for the compliment, Pam :). I'll get more subscribers over time. It just takes a while I guess.
In regards to your question about getting rid of damaged cells via autophagy, you have to remember that when you destroy a cell, the other cells nearby take its components in order to build new cells. So, even though you are undergoing autophagy, you will inevitably recycle some components. With autophagy, you completely destroy the proteins inside the cell, but you cannot break down the fats of the cell membrane as well (otherwise, the autophagy process would consume the whole body).
I would consider it like this. Your neighbor moves out, so you use the wood to add on an extension to your house. But, you didn't take the furniture. So, if the wood was rotten, it is now a part of your house. Same goes with damaged cell membranes (fats). Your nearby cells will absorb those damaged fats and incorporate them into their cell membrane.
You need new components in order to flush the old components out. Using phosphatidylcholine (Essentiale N) is like adding water to a bucket filled with blue dye. Eventually, the blue dye will get lighter as you dilute it out.
I still have a lot to learn about fasting and autophagy. The research is very promising thus far though.
@@OubreMedical geez - best explanation EVER! I had no idea. The fasting summit started today but I already watched a lot of the video's. In listening to them, this wasn't the picture I had of autophagy. Thank you for painting such a clear picture on such an exciting/important/fun topic.
I can see everything you are saying makes complete sense ,but what good is it to know, if we cannot get the treatment.I am in the UK,and as far as I know this treatment is unknown here,
I get my Phosphatidylcholine from Europe, so it's not known there. You can investigate the food sources of the nutrients that I speak of. Then eat those foods!
Hazel hello hazel I’m in uk also and there is no treatment like this dr has explained
It makes so much sense though what he sd .
I go to a clinic in Bedford to have oxygen therapy injection and after all these years of pain
It has helped a little ..
his name is Oliver .
Hope today hasn’t been so bad .
My days are bad always
The pain is chronic ..
Hazel i'm in the UK I was diagnosed about six years ago and I go to the pain clinic and I get a lot of pain killing treatment. I've found the doctors have taken me seriously since day one and done everything they possibly can for me.
Thank you! Suffer so much from this, have all the symptoms, feels like perpetual flu symptoms in every part of my body, just awful!🇬🇧
b1 deficiency. avoid coffee
It’s real all right, I wouldn’t wish fibromyalgia on any one. Pain being the worst, along with fatigue and sleeplessness. I’m glad more information is coming out regarding fibromyalgia, I believe healing the gut is very important. Thank you for this video, I’ve really enjoyed watching this.
WOW!! Amazing day with you. I’m a fibromyalgia patient and yes! You’re right- my body’s pain it’s increasing bad specially in my back around my spine. I do watch what I eat but my stomach hurts not matter what. Thank you for your help and kindness with the seminar. Blessings to you and your team. 🙌🇺🇸💐🇨🇴💝
thankfully in the uk its not seen as a unreal illness.
Well that's good news!
But only just recently.I have suffered for 21 years.I have been laughed at by professionals.I have been told to get out of bed and walk around my home when I couldn't even move a muscle.Infact how I have been treated is beyond disgusting.However,I have written all my experiences down and hope to name a d shame every so called "doctor" who dared treat me like I was lying or looking for attention.Once the science proves how real Fibromyalgia is then I shall happily expose these low life's who should not be in the medical profession.I know about this living hell than they do because I have lived it for 21 year's.I live in N.Ireland.
Then I need to get out of the US
Have to say I agree with Jane. I have had fibromyalgia for 23 years and was told by my doctor that, that's what they call it when they don't know what it is. I am glad that diagnosis and acceptance is better these days.
@@lesleyjones8469 When I got diagnosed Lesley they didn't have a name here.The professor told me "you have a condition that won't kill you but will torture you for the rest of your life".I asked him was it Fibromyalgia and he just looked at me.He wasn't prepared to name it.I had done my own research.Then when I went to a pain management doctor.I said I had Fibromyalgia and he laughed at me.I walked out and filled a complaint.I refused to attend the pain management clinic again.Im 22 years suffering this year and still there are no answers.I believe the health service know what causes Fibromyalgia and won't say because it's possible their fault.Any research I have done I have found that people who suffer have some things in common.I wish you well in your day to day hell that is Fibromyalgia.God bless you.☘️
I cured my debilitating fibromyalgia through diet. I also stopped taking medication. Keto carnivore is life changing.
Doctors will only medicate you to death unless they understand nutrition, which is rare.
I have read about this someplace? Guess you can buy it in a health food store? It must clean out carbs?
@@carolweaver3269 Carol, it's not something you can buy. It's a very strict high fat diet. Nothing can clean out the carbs. You just have to stop having them. It's extreme and I did a similar diet many years ago. I felt so much better if not cured. Trouble is it is very limiting and hard to keep to. But I am thinking of getting back onto it to get relief. There is plenty of info in books and on the net.
Glad it worked for you, I’ve done keto made my mood better but did nothing for my body pain.
It’s true carnivore diet cures it but I can’t seem to keep it up long term.
It has to do with food allergies. When I had my food allergy test I tested highly allergic to almost everything except for fruit, vegetables, and meat- Personally I follow a high raw high carb diet and it has been immensely helpful. Also doing a natural antibiotic (bereberine, garlic, oregeno oil) to help with sibo allowed me to eat things I used to be allergic too, although I still stick with mostly raw fruit and veg. Good luck!
I found a vitamin patch and have ordered it from PatchMD. It bypasses the digestive system. I haven’t received it yet but the reviews look good.
This is spot on . 35 years ago I was told I had fibromyalgia and now that I have SIBO I finally know what’s really going on . No the long road to recovery.
thank you j1959 .i do find myself starting conversations in the grocery stores ect. it makes my day sometimes. god bless.
Thanks for the information packed video Dr. Oubre! There are definitely ways to help fibromyalgia. Functional medicine approaches are making great strides in fibromyalgia outcomes 🙌
Statins damaged mine 5 yearsl of them
This video makes perfect sense
Hi thank,s for that talk ,just wondering if u have a book out on this please
Very interesting. Have had FMS for over 20 years. Many problems with my “gut” - like what you say.
Thank God someone understands my pain.
Research "organic coffee enemas", the cure for ALL auto-immune disease.
My issue is that I not only have been diagnosed with Fibromyalgia but now a Neuromuscular disorder. I also have severe spine disease which produces its own set of symptoms, osteoarthritis everywhere, bowel and bladder disfunction, and I see 5 specialists. I don’t know what’s going on bc this all came on after my spine surgery & a traumatic time after that. It’s like everything just snowballed. It’s only been 4 years since my fibromyalgia diagnosis. I always had spine problems. I don’t know what to do. I just want to give up sometimes. But this gives me hope that there may be a treatment for the fibromyalgia at least. I hope one of my doctors knows about this but I kind of doubt it or already would’ve tried it. Thanks for giving me this space to vent. I’m happy for those who can get this treatment and be cured! Thanks to this physician for helping so many people get well.
Thank you, as someone suffering for many years I am very hopeful since most prevailing treatments don't seem to be doing much for anyone.
This is a great video. Your explanation for treatment is very similar to what I’m told by acupuncturists. Too bad not all functional medicine doctors share the same mindset re: fibromyalgia. Thank you for sharing and informing !💜
Prior to my diagnosis, I was vegan (the healthy vegan... there are vegans who consume unconsciously). The protein I use is plant based with probiotics. I have a history of ulcers since teenage years, so keeping my gut strong was nothing new to me. I fully believe that the gut is our foundation of health. Before I used to blame and question my clean eating habits (post-diagnosis) but how I realize that sometimes unexplained things can happen so it’s best to rework the healing plan and just allow yourself to be present and optimistic during the process...✌🏿💜