This Unknown Nutrient For Fibromyalgia, Chronic Pain & Neuropathy
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- เผยแพร่เมื่อ 30 ก.ย. 2024
- In this video we examine the evidence for small fiber neuropathy as a driver of fibromyalgia and other chronic pain disorders. We also look at a nutrient which can help to resolve the pain and restore nervous system function: Agmatine!!!
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I have fibromyalgia and osteoarthritis. My knees and fingers joints are all bone to bone . I’m almost 53. I take care of my 34 year old daughter with severe cerebral palsy. I’m in constant pain pretty much every.
No one can see my body’s problems therefore everyone thinks I’m fine. But I’m not. I grit my teeth so much I have broken many. I honestly feel alone people don’t understand and or care that I’m not ok. If I did not have my faith in Jesus I would have given up on life a long time ago. Prayers for you who are suffering in pain.
I have the same 2 diseases it's a nightmare. I'm sorry about your daughter. Prayers. We're almost Home. Stay Strong and Faithful ❤
My mother also has both of these conditions and whilst I am extremely understanding and empathetic towards her, a few of our family members are not and often dismiss her pain/suffering. It’s not fair, I wish people would understand how bad these conditions can affect people. Sending all my love, thoughts and prayers to you xxxxxxx
Have you been checked for Asperger's ADHD are you hypermobile the join can ware down earlier but that doesn't mean always mean pain check out TMS Dr schubiner
1. Eat Bone broth,
2. Drink cold lemon rind water
Drink the water and refill till rind gets soft. Do not throw it out!!
3. Bless your water
4. Take 2aspirin with 2 vit c together with
And hot strong coffee.
Do not take separately
I feel pain constantly also,,I'm praying for you.
For me one of the most most shocking things is , for years I’ve searched for answers from doctors….. instead I’ve ended up getting them from TH-cam instead and for free. Very grateful 😊
Just as a side note if one is dealing with health issues, chronic pain, fatigue and depression and anxiety look at your situation if you are being psychologically abused and manipulated it will wreak havoc on your health.
Yes, exactly.
Yes, I agree. The stress in my life made pain much more intense
Yes that's it
My ex tormented me every day for 18 years, in and out of court and he used money and intimidation as weapons. I think the stress absolutely brought on fibromyalgia.
I've lived this. Ex-husband was a narcissist who was psychologically abusive. We lived with his grandmother, who had her moments, too. I was walking on eggshells around them. Under his "tender loving care," I developed fibromyalgia. To add insult to injury, he didn't believe that I was suffering from a real medical condition! Once, he got very angry with me for daring to ask him if he could rub a sore spot on my back. So, yes, you can develop fibro from psychological abuse!
In Canada, fibromyalgia is now classed as a neurological disorder. This, in turn, probably stems from a deeper systemic problem. Researchers in Italy have found that fibromyalgia patients suffer from malfunctioning or compromised mitochondria. This of course includes the mitochondria in the brain, the spinal cord and the entire nervous system (as well as every other cell in the body).
I would also like to recommend this book by
Daniel C. Dantini MD
"The New Fibromyalgia Remedy: Stop Your Pain Now with an Anti-Viral Drug Regimen."
I had already noticed my daily headaches went away when I took acyclovir. Now I manage EBV and HCMV with supplements.
I had intense pain throughout my body. My immunologist had me get a small fiber biopsy done. It didn't find anything. Dantini also said to address food sensitivities. I gave up gluten, foods high in nickel, and milk products. Goat milk was worse than cow. I had to give up even butter :-(
After watching Elliott's video, "Thiamine: A UNIVERSAL "Stress Protectant" Across The Natural World (Detailed Version)," I believe Thiamine is another way to defeat the Epstein-Barr Virus and other related herpes viruses.
This makes sense to what you said.
It is now classified as neurological in the US as well.
@@ParallaxView111 did the drug cause any side effects any hypomobility taking b1 a month no results yet
The video recommends these for fibromyalgia:
- Agmatine 1000 - 2000mg
- Thiamine mega dose
- CoQ10
- Magnesium
- Calcium-D-Glucarate
Thank you 👍
You are appreciated
Thank you 🙏🏻
Thank you
Would be nice if it had the daily recommended dosage. Does he have it listed anywhere?
I was diagnosed with Fibromyalgia and neuropathy after a car accident. It was years of constant pain everywhere before an infectious disease doc tested my Vit D level. It was the lowest he’d ever seen in a living patient (3.1). I got a call to come do an immediate cardiac stress test because at that level your muscles are literally ripping apart. Pain improved dramatically after Vit D level got up to normal. Every fibromyalgia patient I’ve told that to whose gont their Vit D level tested has been deficient.
My husband's vit d tested at 0. The Dr said it would take him 2 years to get it up to normal taking 5000iu a day. I guess because he had the gastric bypass years ago. He was scared to take his vit d because of his calcium level getting to high and him having more kidney stones. He had many. And all but 2 had to be removed surgically.
I was deficient as well, but once my levels reached normal and stayed that way consistently for a year, it did not improve pain level or intensity.
Never take vitamin D3 without vitamin K2. K2 pulls the calcium out of the blood stream and pushes it into the bones where it belongs.
@@hollyalbertson1237 I believe that taking vitamin K2 (usually in the form of MK7) will help take care of all that calcium - making sure it goes into the bones and not the blood stream. I take 10 to 20 thousand IUs of MK7 about 5x per week. Am 81 y/o - in other words, still living! 😍
I don't have Fibromyalgia but suffer from Chronic Pain and understand how terrible life feels so i hope this helps them👍
Thank you. ❤
❤
Try carnivore
Im 70yrs old also having pain around my breast & in the diaphragm area...burning,pins & needles,tightness.Im praying thatcJesus heals me & I'll pray for you too.He's our Healer & He loves us.Praise the Lord!🙌😇
Why are you praying for Jesus to choose you for a miracle that most likely won't happen? God seems very fickle with who He chooses for a miracle. That doesn't sound like He is "good." Get help from a doctor for your pain, please!
I’ve struggled with Fibro for more than 20 years. I’ll share with readers what has helped me. Acupuncture!!! I went to a Chinese Dr in my city who had a reputation for helping many patients. Everyone’s different but, for me, they did a lot of pints up and down the liver and gallbladder channels (which are associated with conditions of the nervous system). They also did Moxa on same channels.
I also take a high quality (methyl) B-100, and B-12. I also take Magnesium Glycinate. And I use Magnesium Oil on the skin, in some areas that typically hurt.
All of these measures combined make a huge difference in the condition for me.
There is also a psycho-spiritual element to it (for me), meaning sometimes certain stressors can trigger the condition, such as handling matters of the heart.
I am very interested in acupuncture for fibromyalgia. It makes so much sense to me, especially because the tender points seem to be on the meridians. I am going to investigate this further! Thank you for sharing.
What dose b1? Did you try the agmatine.
I was diagnosed with Fibro. 1998 and was close to going on disability. I took a course on allergies reduction. Found that I am highly allergic to wheat.
After no wheat gluten for 2 years I had no symptoms.
This should be looked into as many people in the course had dramatic changes in their health for the better.
I have been tested for that and that is not what’s wrong with me.
@@josieeckwright370 keep looking
Thankyou, this is awesome to know! I have to ask my doc for a gluten allergy test
Going GF has helped me tremendously. I am not positive for celiac because I have a genetic condition called IgA deficiency. So therefore my Celiac test comes back false negative.
Yeah, unfortunately after going on a strict diet, it wasn't what was my problem.
The problem with symptoms is that they can belong to other diseases also. My son kept telling his doctor that his legs were always hurting and he felt like his bones hurt. The doctor actually told him your muscles hurt but your bones can't. Well one day he had kidney failure. In the hospital they did thorough blood tests. They came back and said they wanted to do bone biopsy. It confirmed what they suspected with the blood test. He has multiple myeloma. That was his legs hurting and bone pain. But it took a very thorough blood test and bone biopsy to diagnose.
Is he okay now?
Poor Kid , 🍀💜🍀
He has his good days as well as bad. There is really no cure for multiple myeloma.
@@alissagonzales735 What a trial! Bless him and your family!
Did they check his Vitamin D level? All the best with his health.
I had fibromyalgia for years, I was in horrible pain. The muscle of my back would become like a giant cramp for several days. This was usually trigger by an emotional upset. For a reason not related, i decided to start eating only organic food and my pain little by little disappeared. I haven't had a fit in years. I notice that when i eat food from regular supermarkets again for a short while, the fibromyalgia creeps back. I can't explain what's going on but i am convinced there is a relationship with diet and the quality of our food.
The potassium you're eating is helping with your back pain. Low potassium high sodium diet is the cause of back pain especially when the pain is idiopathic.
Food absolutely definitely affects our health
It makes a lot of sense to me why you feel the benefits of organic vs supermarket, it's an obvious but sadly ignored fact that with modern farming the intensive methods have created dead soil (hence the need for artifical fertilsers) lacking in many minerals etc you would expect to find in healthy organic soil, as a consequence even fresh produce from supermarkets will not be as nutrious as fresh organic produce
Average of 2 kilos of artificial chemicals are consumed by eating supermarket foods per year. That's like 2 bags of sugars worth !
That's interesting ? . You clearly witnessed emotional upset disturbing your nervous system, however you turned your attention to food being the problem . That sounds a little like emotional avoidance , a known protection mechanism to avoid intolerable emotions that can cause symptoms when not expressed..
I’ve had fibromyalgia since childhood but only diagnosed by a rheumatologist 8 years ago :) I am now 64 years young.
I also have had Graves’ disease in my 20’s which then became Hashimoto thyroiditis in my forties along with elevated leptin.
My experience with doctors, specialists and functional medicine practitioners has been unhelpful and that’s being polite.
I became my own health and wellness doctor from my own research which has been a slow road but I have made immense progress with improving my pain, mobility and fitness.
Intermittent fasting including longer fasts OMAD
Plants, nuts and healthy seeds
No grains gluten free
No dairy
Low toxin products in body care
Clean eating as much as possible
No processed foods if possible
Organic or throughly washed fresh produce
Exercising everyday, yoga, Pilates, walking, weightlifting, qigong
Hydrotherapy pool
Meditation
Mindfulness
Sauna, steam room and spa pool
Everyday is a new day
I take supplements and am trying higher doses of B1 along with a B complex, B12, vitamin D, Zinc, Glutamine, pea protein, also other supplements and foods that have high nutritional content.
My health has improved significantly over the past year with increased fasting and exercising. I also lost 13kg and am working on loosing another 10kg this year.
Thank you for all your content it’s appreciated that we now have so many good people like you offering sound advice.
Keep trying... keep learning.... the Dr can only prescribe something for you to try. No..... one has to try natural things for yourself. I am 64 also. I have had fibromyalgia my whole life. I know I have even as a child. So many different problems. You are doing it right.... congratulations!!!!!! Life is better only because you did it yourself. I am trying to learn all I can to feel better... for me!!!!!
I would add massage. It helped me a lot!
Congratulations! Try the Co- enzyme B with P-5-P(B6) 100mg and Benfotiamine 300mg, Alpha Lipoic Acid 600mg excellent for neuropathy used in Sweden.
Thanks for sharing. What helps my husband was some of the things you mentioned, change in diet, cut down on sugar. I'm glad he found a doctor who is knowledgable and open-minded on the use of supplements. He prescribed alpha lipoic acid, quercetin, turmeric, PEA. My husband's pain also caused him to have heart palpitation in the morning. Some days the pain was so intense, he couldn't work. So, we did a lot of things besides seeing specialist pain doctors who gave pain medication that helps a little but don't reach his pain area. We went to healing conferences to get people to pray for him, diet change, supplements (trial and error, it is different for everyone, I read a lot of medical studies and tried many things on him, some started out promising like ACV, lemon, lion mane supplements, yet these ended up causing him pain, so I learned every BODY is different. Now, I'm stuck with 20 over supplements that he can't take and we narrowed down to alpha lipoic acid, PEA, quercetin, turmeric that helps him. A new one I'm trying for him is broccoli sprout because it is an Nrf2 inducer. I also tried ASEA redox gel because my friend who had polio (when she was a child) told me it works for her because she still suffer nerve pain. It was part of an MLM product, sounded like scam at first, but hey, when you are sick, you try all kinds of snake oil. I think ASEA gel helps him too. I gave some gel to my sister when her parakeet was dying from a tumor/lump. It has stopped eating or flying, the vet said there's no cure. So we decided to risk it. She applied the gel on the bird, cover its eyes and shine infra red light on the lump for a few minutes. The bird is now flying around. So, I truly believe the ASEA gel helped. Another anecdotal, last week her backyard chicken was dying, the chicken was already 6 years old, I told her not to force feed anymore, just let it go. She decided to rub ASEA gel on the old chicken and shine infra red on it, just like the parakeet. In a week, the chicken recovered! I was shocked. I decided to become part of the MLM :), never thought I would join an MLM. I'm not trying to sell it here. Just sharing. If I sell it here, I would discredit this whole story. I hope it would help someone who suffer nerve pain. Now, my husband has healed so much, we are so thankful. I credit it to all the prayers of my church friends, supplements, ASEA. I hope this will help others too.
Washing regular fruits WON'T REMOVE THE PESTICIDES😤😤💀💀
I’m 41 and have fibromyalgia, avascular necrosis of the knees and hips, as well as degenerative disc disease. In the US, fibro is still considered a fake disease. I also have kidney issues and a history of acute kidney injuries. Last time I went to the ER, thinking I was having another, they told me everything was fine, even tho my CT scan was abnormal and I had abnormal blood work and urine. Before they did the tests, they seemed concerned but everything seemed to change when I mentioned I had fibromyalgia and took pain meds regularly.
@@heathergreenakers yup,!! With fibro you need to do your own research. I finally got a Dr. Who gave me a diagnosis. Forty
THANK you, doctor, for acknowledging and supporting the science of NUTRITIONAL DEFICIENCIES in this video!
Thank you, this is really useful. There is an autoimmune aspect, which I feel is the cause of Fibro being misclassified as a rheumatic disorder. I would suggest you that, and this does not argue your premise, that you cannot ignore the part of Fibro that is a sleep disorder. The context is there. This is not due to pain, but an organic reaction in the limbic system that does not allow for deeper level of sleep. Could you address this?
Considering the mind body connection is critically important in overcoming health issues. For those that doubt its relevance, I completely understand. I spent years dismissing it. After years of suffering I finally entertained the findings of Dr. Sarno and after doing the work (releasing repressed emotions) my pain went from an 10 (barely able to walk) to a ZERO. If it didn’t happen so profoundly I’d still be in the doubting camp. Look, I understand, believing our physical body is so deeply affected by our emotions is hard to accept. But if you can put that aside for long enough and do the steps necessary to release the repressed emotions, you’ll find out just how effective it is. Sarno was a pioneer in this field but there’s a lot of other experts to consider. Find one that resonates with you and reap the benefits.
Agree completely. I read a book about Dr Sarno and was blown away. He has an incredible success rate. I also read a fascinating study where they told people with severe knee pain that they were getting a knee replacement. They put them under anaesthetic, and made an incision, but didn't replace their knee. When the patients woke up, they all reported that the pain was completely gone, despite having the same old knee. The mind is so powerful.
Yeah, right. Still no pain? Did it last?
@@thomasprislacjr.4063 Yes still no pain. Doing the work also helped my digestion and energy levels.
Hi I have fibro. Can u pls share what book it is...
@@thomasprislacjr.4063yes, still no pain. It’s lasted for 11 years so far. I’m just one person. The same has happened to hundreds of thousands. Take some time to look into it…. without prejudice
I found out that I have a mutation in my dna called MTHFR which now tells me why I have had so much overall body pain. It is due to a lack of absorption of lots of B1, B12, B9.and other amino acids and stops the body from ridding itself from toxins ... what you are saying about a lack of B1 sounds like a pretty good theory to me. But you cannot just take thiamine or folate because the dna can't convert it. It needs Methylfoliate, etc. I can't explain it all here. But some say this is in 40 % of the population, which sounds more like some kind of a poisoning from the environment to me. DNA doesn't just mutate, something we were exposed to, my husband and I both have this and lived around loads of factories as children. I am curious to find out how this has happened.
If a person has slow COMT of even one of the slow alleles it’s important not to supplement with ANY methylated vitamins.
People are now saying to the detriment of a large potion of the population, that we need to take methyl folate and methylcobalamin. This is the worst thing a person with slow COMT can do for their many severe symptoms. Be careful what you tell people because methylated vitamins make many people suicidal.
Your body might have a hard time absorbing thiamine. That’s where benfotiamine comes in. Benfotiamine, which turns into thiamine once it’s inside your body, may build up to helpful levels more easily. I too had high levels of B12 showing up in blood tests. When a vitamin isn't absorbing it will show up at high levels so I started taking methylated B12. I also think processed foods is a big part of American's health issues. Look at the junk they put in it which is essentially poison.
Don't ford vitamin b8 b6 12 to yes this is what the problem is genetic food poison us especially if we have Asperger's ADHD hypomobility that's why they are not interested because big pharma want the profits we have seen nothing yet going to be mayhem in 10 years
MTHFR sounds like a good name for it. It's only missing the K
@@antonystringfellow5152 Right?! I'm glad I wasn't the only one who thought of that 😂
Dr. Barbara O’Neill shares a lot of information and remedies.
Like applying cayenne pepper to the soles of your feet for the treatment of neuropathy.
Blessings and healing energy to all ❤
Thank you for stressing how important it is to find the root cause of a patient's Fibromyalgia. Unfortunately, patients often stop seeking the root cause once their doctor shrugs and tells them they can't find anything wrong so it has to just be Fibromyalgia. After several years of exhaustive tests wielding negative results, I kept searching and finally came across a diagnostic blood test to confirm it. Okay, great. Then I had a 5 month battle with severe IBS that oddly led me to an Upper Cervical Care Chiropractor who showed me a cone scan of my very crooked neck. 2 days after my first adjustment the IBS disappeared - so that's when I personally started to think of the connection between the nervous system and my Fibromyalgia (instead of autoimmune). This then led me to my current spine specialist and the discovery of L2-L3 Spondylolisthesis and degenerated disc! I've started a course of physical therapy including using a lumbar traction machine which gives me great relief but only lasts for a couple of days. I'm therefore keen on trying these nutrients you discuss as well for long-term pain relief.
Hi.similar, decades of agony ,sufferring pain.tried everything including lots of the supplements. No relief.
Did you go to Top Chiropractic? I am considering going to see an Upper Cervical Chiro and interested to hear your experience
Try some natural anti-herpetic therapy (no coffee, limited total caffeine, lysine on empty stomach 1 hour before meals, no high arginine/citrulline foods, maybe lower total protein intake for some time, inosine, elderberry, vitamin c, cordyceps, etc) and see if it lessens your tension and fibro.
My teacher cures the pain no one else seems to, Dr Klinghardt. He finds reliably there is an underlying infection that even the brain may not see. By finding and treating that (retroviruses, Lyme co- infections, etc) the pain resolves quickly. Our Seattle area finest NDs, MDs send their incurable to Sophia Clinic. He has students around the world, but takes some sleuthing. Best of luck.
That's incredible to hear, truly. I have a horrible posture (especially in the neck and thoracic spine) and also burdened by a lot of digestive issues. I'm currently fixing my posture, and I hope it will alleviate some of my digestive problems.
Hi Elliot. A massive thiamine fan here and bought some Agmatine following this video but then tried something that seems to be making the biggest difference and I believe may be at the root of these problems. I have chronic pain and neuropathies and POTS and hEDS. I was at a and e this weekend pseudo seizures due to cerebral blood flow problems and dysregulated heart rate and blood pressure and dehydration despite oral rehydration of 2L. Realising a probable problem with extracellular ATP (after much research) I ended up with magnesium. I have been supplementing quite a lot in bioavailabile forms, 1200mg as taurate, glycinate and Threonate daily or so and so didn’t believe I could have a deficiency. Taking your ttfd at 100mg / day also. Reading up on it though and having gastrointestinal problems from childhood it came to light magnesium really needs to be transdermal. I was semi regularly using magnesium chloride flakes in the bath as I was aware of this but not often.
A serum magnesium test from June 2020 was mid range normal but apparently this is not an accurate representation of cellular magnesium. I also knew I had some sort of cellular hypoxia and had symptoms of CFS that thiamine helped but was still getting worse.
So I started to use a magnesium chloride oil as often as possible and in 36 hours my heart rate and blood pressure are so much better. Standing it was 130 sometimes up to 170 and now it’s down to 105. Lying down it was 85-100 now it’s 65-79. My fatigue is almost non existent and I’ve stopped peeing all the time.
Serum mineral levels I believe are inaccurate at a cellular level as the body will fight to keep those normal (even though mine wasn’t even checked at a and e). I believe I probably had a cellular potassium deficiency also. Testing red blood cells is more accurate and biolabs in the U.K. do a red blood cell magnesium test. For sick people I don’t believe oral magnesium supplementation is enough and in chronic illness I don’t believe serum levels are accurate.
I believe that lifelong thiamine deficiency may be due to life long magnesium deficiency inherited from my mother as she had had pre eclampsia when she was pregnant with me and has Had high blood pressure ever since. I developed adhd at puberty when more magnesium is required, depression and anxiety, have had joint pain since I was 8 yo. Massive issues with acetylcholine slow gastric emptying and irregular heart, blood pressure and blood glucose…. Fatigue. Serious cognitive issues - It all seems related.
I would advise that cellular magnesium be tested and tbh even if that were normal if there were symptoms I would try transdermal magnesium in the chloride form daily which seems to have changed my life in 36 hours (but i was bedbound so just being able to get around seems like a miracle!) I just wonder if this is a piece of the puzzle that we may be missing as it seems to make sense given that it is required as a cofactor for thiamine and Many other processes. Extremely high supplementation transdermally may be required to correct deficiencies at a cellular level that are under the radar? For me it seems it may be true.
Wow just start using it in my bath will see. I am taking mag taurate, Have you try it ? Did not see difference with bisglycinate and citrate give diarrhea. Next is mag taurate, orotate or threonate, which one should I try ? I also receive my TTFD today.
You should do a video explaining all this, amazing.
I have chronic fatigue, fibromyalgia, and several cervical spine issues (neurosurgeon wants to do surgery but I'm holding off). I definitely have nerve issues. Exercise intolerance. Also heat and cold intolerance. Numerous other conditions. Oh, and several deficiencies. I take elemental magnesium and will switch up the kinds I take from time to time. I've taken only the higher quality without fillers. I just haven't noticed much difference while I've been taking it for several months now. Years ago, I had tried magnesium spray topically, and didn't notice much. Maybe I should try it again along with my supplements. I've spent so much money over the years without any noticeable relief. So now I'm about to start taking the thiamine. Along with my activated B complex (methyl), bioavailable elemental magnesium, vitamin D - K2, and non-fortified nutritional yeast that I'm already taking (without any improvement lol). Oh, and now I ran across another nutrient with this video.. HUGE SIGH. I just want something to help. Being disabled, I can't afford anything else. I'm also incorporating neuroplasticity techniques that help to rewire the brain and deal with brain body connection that is often overlooked but could be the root cause for many, or at the very least, a strong contributing factor. I'm still learning as I'm having to teach myself and can't afford to hire someone. But I think this is extremely crucial for all of us who have chronic conditions. Regardless of what the particular issue is. Just leaving it here in case it helps someone. Thanks for the magnesium transdermal recommendation as maybe it'll enhance what I'm taking or amp up the effects 🤞
@@karine8738 yes, I read the citrate has a harsher structure to it and can scratch up the intestinal wall. I avoid it. I also avoid oxide which is the cheapest form, least absorbed, and causes stomach distress. It's the most common form used in laxatives. Both should be avoided imo. I took a combo before of the taurate and glycinate. I honestly didn't notice anything. But perhaps on it's own, it would be. I think taurate is often used by athletes with recovery if I remember correctly. Muscles and energy/fatigue. The threonate is known for crossing blood barrier (although I've found some doctors who believe all bioavailable forms do to one degree or another- which is contradictory I know) and improving cognitive function along with healthy sleep. The orotate is known for supporting heart health, like blood pressure and cardiac function.
Excellent observations about magnesium. Indeed, relatively high doses 800-1200 mg may have tremendous effects on neurological conditions including pain, so the question is why does it happen. Your idea about cellular affinity to magnesium may be a thing.
I was diagnosed 35 yrs. ago with fibro around age 35. I am now 70 with little quality of life. I fought various Drs. back in SC and now NM. I do have issues with heart palpitations and diagnosed 8+ yrs ago idiopathic neuropathy because Drs. couldn't said I wasn't diabetic so it had to be something else. My condition has gotten worse to point where Drs. just think I am a Dr. shopper or hunting for opioid. Yes, the pain is so overwhelming that people's attitudes today are nonchalant to suffers. I could not take normal prescriptions for neuropathy, so I have gotten worse. It is finally good for not being a mental weakling.
I don't like when the doctors think that u just want opiods....I just want the pain to go away & have quality of life!!!! but they choose to leave us in severe pain!!
opiods won't be addictive if u take them the way they are prescribed!!!
Bless your heart.
Just wanted to say, " I care."
I was diagnosed by a free thinking, compassionate doctor who didnt care what other doctors thought of him for taking FMS seriously.
Magnesium was a big help to me, but I've lived with the pain for 50 years. It is a very cruel medical problem. I too cannot take prescription pain relievers.
I have been blessed with a very caring husband for 46 years who "gets" me and FMS. I am thankful to Jesus, every, day.
God bless and heal you🙏✝️
My story is exactly the same !
Please research the carnivore diet for autoimmune. Whatever fibro is classified as, I can tell you my quality of life has vastly improved and my pain levels are nearly zero most days. It has taken 5 months to get to this point. But I saw improvements within the 1st 30 days. I caved and ate a piece of cake last weekend, and my pain came back. My energy was gone, and every joint in my body hurt like they did before. Diet has so much to do with health. Prior to carnivore, I was paleo and found some relief, but not like I have on the carnivore diet. Be open to the fact that we have not always been given the truth regarding meat, cholesterol, and heart health.
Avoid monosodium glutamate. In the US, Cambells soup refuses to label it that way because it costs them sales. It causes migraines and chronic pain. It can also go by the names "beet root extract" or "yeast extract". It used to be in Chinese food in restaurants lately I find it more often in Japanese restaurants.
I had an accident at 17 years which impacted my spine. After a major car accident I had really bad whiplash injury which caused pain for over a year. Then after marriage breakup in 1997 I was diagnosed with fibromyalgia and chronic fatigue after MS was ruled out. Then in 2016 I became paralysed from waist down and was eventually diagnosed with Transverse myelitis which involved same area of spinal cord as previous two traumas. ( myelin sheath was stripped from cord)I believe all were connected. Doctors seem to have little knowledge. Every thing I have learned to help cope with my condition of severe nerve disfunction and pain has been through research. This video is very very helpful to understand how to help me cope . Any pharmaceuticals dampen down or dumb down my brain and energy
I always thought MS was suspected with damage to the myelin s. I only just discovered also that Trigeminal neuralgia also was strongly linked to MS. I had that for 3 months 10 years ago. Not been tested for MS.
I have been diagnosed with both Fibro and ME. When referred to the weight loss clinic, on speaking to the nutritionist for diet advice for both these conditions and weight loss, she didn't know of the connection between diet and the conditions. My response was that I obviously knew more than her so she was no use to me. The problem is that the NHS aren't given funding to investigate the option of diet and some conditions. They are happy to prescribe me multiple prescriptions, but not find healthier, and free lifestyle options. I guess I just answered this myself!
Tell me about it! Grrrrrr
@ Lyn Jermey unfortunately this is a global problem nutritionists, dieticians, GP’s and also specialists alike are not trained to understand specific nutritional needs related to fibromyalgia nor any health conditions. This lack of education and knowledge is due to medical training and at best a doctor will get very little education on nutrition. Unless they have a particular interest in nutritional medicine there’s not much point in seeking advice from any of them.
I’ve spent large sums of money seeing all of the above without one giving me sound recommendations.
My research was done on listening to science based functional medicine, Andrew Huberman and mark Hyman and any others that make sound sense.
For me my diet and lifestyle changed for the better when I started IF, stopped eating meat, fish, dairy and gluten. I think if your body is suffering removing toxins and foods that cause inflammation is the way to improve your health. Fasting allows the mitochondria to recover and regenerate so this has allowed my body to heal itself.
This all sounds drastic but I did changes over five years and have found it to be sustainable and preferable to being in constant pain and constant physical stress.
The saying we are what we eat and looking at holistic and ancient cultures how they treat the mind and body as a whole rather than western medicine prescribing drugs and giving a referral to a specialist that does nothing for you that is proactive is demoralising.
The problem is that a doctor will use a blood test as a measure to say whether or not we are unwell. Since many health problems fibromyalgia being one of them do not show any reading on a blood test it’s often undiagnosed and misunderstood. However even if it is diagnosed toxic drugs are prescribed rather than a helpful holistic approach.
I hope you continue to research and be your own best advocate. It is also helpful to focus on mind, body health not just nutrition for the body the mind and body are interconnected.
:)
same issues as you, Doctors are quite thick in the UK, we have to help ourselves.
Same i NZ, they have no clue! Even admitted it. I have ME 17 years, quite mild, but 3 years ago I got ‘chronic pain’. I tried the Mind Body thing watching various trainers on TH-cam, Dan Buglio for one. But in a year no better. So I think it’s another ME symptoms.
Uneducated
I have been taking L-ARGININE and VIT-B1 for 3 weeks now after watching this video, as well as TENS stimulation of my vagus nerve nerve and my symptoms have greatly reduced. So Thank you EONUTRITION
Interesting do you have fibromyalgia?
Do you go somewhere for the tens stimulation or do it yourself? I have a Pots so anything that stimulated the vagus nerve definitely sounds interesting to me
How are you getting on now?
Some more info would be greatly appreciated.
Thanks💐
Ten stimulation of vagus?
What it Ten stimulation
Great post. As a person with Fibromyalgia I can say with conviction that it is not neurological in total. Neurological reaction is a symptom which developed as a result. The causes of fibromyalgia are extremely varied. I personally was hit by an array of events before being diagnosed. I had Bilharzia, got Coxsackievirus and Epstein Barr after it while going through a divorce. So the shock to my nervous and immune system was severe. The physical effects are extensive, varied and complicated. Not many people talk about the malfunctioning adrenals either. MostFibromyalgia sufferers have a severe Magnesium and Iron shortage too. Off course there are other shortages too. There's a lot of reports about the benefits Benfotiamine now. So far Dr Jose Montoya from Stanford was on the front line of research, but unfortunately he was fired due to misconduct allegations.
I've had Fibromyalgia since my young 20's... I'm nearly 57 now. I have pain constantly sometimes it gets fired up in some areas for long periods of time. I also have Raynauds, type II Diabetes, Dercums Disease and ADHD. My hands are normally up to 5 degrees hotter than the rest of my body and my arms can be cold while my hands are hot. If my hands get cold then my whole body is freezing. Go figure. I struggle with trying to sleep as I am as I often say "The Princess and the Pea" as anything that pushes or pokes on me will irritate me ... light bothers me when I try to sleep... most of the time I'm just exhausted.
❤
I can so relate my hands and feet are boiling, light gives me terrible headache. I've been trying magnesium malate, bamboo bed sheets and intermittent fasting. It's a roller coaster ride most days, I feel hormones are a problem too but I can afford doctors for that 🙃 it's a lonely path
@@buffy2658 I've been taking a Magnesium with all 3 Citrate, Malate and Glycinate... I take 3 daily... I'm still so tired I can hardly stay awake... but part of that is due to working 3rd shift... so they tell me. I invested in a light therapy light... it doesn't help.
@@buffy2658 I wish you well with all my heart!
I don't know if you will ever read this but your problems sound a lot like mine Raynauds, Sjogrens etc etc - anyway 3 years ago started using stinging nettle tincture for pain and it has been a life changer. Also use 'electrolyte powers' for the energy problems and that works too.
Does anyone get feet and leg pain? Like top of the feet pain? Tibia and calf pain? Ankle pain?
I get pain on the top of my feet, especially in the morning. I guess I'll add that to the list for my next doctor's appointment.
Great pain in feet and legs plus arpund breastbone at times.😢
I had a chiropractor for 30 years who treated me. I walked out of his office WHOLE every time. I’ve never found another chiropractor who was as thorough as he was. I haven’t found 1 who could treat my pain but he always did. Regular doctors just wanted to prescribe nerve or pain killers. They said that all my X-rays looked normal. The chiropractor says that they only look for a break or compressed vertebra. So when a rib is out, they don’t notice that. My chiropractor passed away and I’m barely coping with the pain im in. I’m just grateful I had him to treat me and give me a quality of life for th years I did.
Look firva chiropractor with integrative training. ❤😂
I had a similarly transformative experience with a chiropractor, he clearly and comprehensively taught me why I hurt after two decades of other doctors just pushing drugs to mask it. He took the time to show me the source, I made adjustments, and healed. It was life-altering and also mind-opening.
Agreed, any Good doctor is hard to replace. I've a chiropractor who has kept me out of surgery for decades. I've both a slipped and a bulging disc. he's about ready to retire and I've not found anyone else who can restabilize my back. While I've learned how to reset some minor displacements on my own it is hard to get a vertebra in the midback into place.
@@happygardener28 Say this 3x fast: "Mares eat oats and Goats eat oats but little Lambs eat Ivy."
@@FutureSuperstars5761 Or spell Mississippi and Cincinnati three times in one breath
Elliot I appreciate you mentioning B12 deficiency. I have seen people diagnosed with Fibro having amazing results on B12 injections; repairing the symptoms of demyelination (such as neuropathy, myalgia, numbness, pins and needles, etc) caused by a lack of B12.
I have fibromyalgia and taking DIY methylcobalamin (a form of B12) powder capsules, is that okay? Or does it have to be a B12 injection to be effective?
Hi Elliot, just found all your info about B1. Thanks for sharing this with the world.
I'm interested to know where does B12 deficiency fit with all of the symptoms linked to B1 treatment. I have many of the symptoms related to B1 deficiency that you mention, however, I was previously informed that these symptoms related to B12 deficiency.
Ive been injecting B12 EOD for 13 weeks and taking 5mg folic acid most days. Whilst this seems to have helped somewhat, in the last 2-3 weeks I have gotten really bad neuropathy. It got better for a bit but now it's worse. I was told this is wake up (paradoxical) symptoms but now I'm wondering if it's B1 deficiency.
Could taking high dose B12 and B9 increase B1 deficiency/ symptoms due to creating an increased need for B1?
@@soniap2891 I used to self inject B12. It was the kind that started with a C. Don't do that. I didn't know. That's one of the worse forms. It's toxic. It's what's most commonly prescribed too. It may have gotten my levels up with my blood work, but that's the only thing I noticed. No improvement whatsoever. Including with my neuropathy. I personally would recommend at the very least, an activated B complex- methyl form, and elemental magnesium before I would do the injections. I'm also about to order B1 supplements, but haven't taken them yet. Oh, and I eat non-fortified nutritional yeast regularly. I'm hoping the B1 is going to be what shows me the most improvement. I'm sick and tired of being sick and tired. But plz avoid the B12 shots that are in the C word form. I can't remember how to spell it. But it's the most commonly used form. I've learned through my own mistakes and from those who've shared theirs, and I try to pass it on. You can raise your levels with a methyl B12 form, pretty quickly. Just don't forget to take it with a cofactor and a B complex.
@@SuperBlake89 B12 injections didn't help my neuropathy or any other issue. I have chronic fatigue, pain, fibromyalgia, and numerous moderately severe cervical spine issues- neurosurgeon wants to do surgery. You're better off taking an over the counter methyl B12 form with activated B complex. And elemental magnesium. I'm also about to order B1 supplements. I'm thinking the B1 may be the problem or a huge culprit. But you still need the other B's to keep from developing a deficiency in them. Magnesium as your cofactor and to assist the B1 at the intercellular level. Some people use and recommend more than that, but that's at least the basics for starting. Elliot has other videos on thiamine. Including one o watched yesterday for fibromyalgia. Just go to his channel and search. I figure I'll start out kinda slow cause I don't think I can handle feeling much worse, which would be my luck lol. I'd rather it take longer to achieve results than to be severely sick but in a shorter time.
@@ThisIsNotMyHome
co factor ??
Please look into the fact that everything you’ve discussed here is very common in the Lyme and Toxic Mold community aka CIRS…..Chronic Inflammatory Response Syndrome. Highly complex. Look it up here in the tube, there are some enlightening lectures.
i have videos on this
Excellent video thankyou 👏🏻 I always said no to people who suffered with Fibromyalgia, who came to me for massage. I did not agree with that treatment at all, as I believed it would orly flare-up their pain even more. It may have benefitted them while they were having the massage, but not afterwards. As I always believed their complaints about the type of pain they were suffering did not stem from joints , tendons, muscles, but rather the Nervous System. With any disease or ailments relating to the body, it must firstly be treated at the root core, and then alternative method's to follow. Although Massage is wonderful and healing to the body, I do not believe it benefits Fibromyalgia patient's the way people thinks it does. It actually flares up the the nerves even more , not soothe and calm them down. Maybe later in the journey will massages benefit, but certainly not while there is a flare-up. I believe it aggravates it even more. People may disagree with me, but it is what I have learned and seen through the year's dealing with client's. Thank-you 🕊🤲🏻🕊
Glenafoleyfoley168……… Absolutely and exactly correct about massage therapy with FM!! A light touch massage does cause less reactive reactions to massage and very light massage can help because it seems to awaken the nerves and the stagnant blood flow in us. That’s great! I still have a day of mild FM the day after, but move Thru it okay. If it’s medium light massage, it is not light enough! It also helps to straighten ones posture up somewhat from having pain and dysfunction. Once every three weeks I’d recommend this. If not super light, then don’t bother with massage therapy if it flares up your fibro! Also, the human to human light touch you get in light touch massage can be helpful to release the mental and emotional pain we accumulate from being treated poorly by folks or spouses who don’t want to understand the multiple food and chemical sensitivities and reactions we have and our need for a cleaned up lifestyle. Not fitting in with lifestyle that they tolerate and process normally. Although, eventually those bad lifestyles will bite them back…..keep the faith! 😘
@@CoccazMom well said. Light touch often is more help than traditional massage when dealing with FM flares. With the idiots putting up high damage emf towers all over now, thus trend is only going to skyrocket, unfortunately. High emf leads to b1 deficiency which is related to many domino effect problems all because of the highly damaging emf signals. It affects animals and plants as well.
@@CoccazMom Thankyou 🕊🙏🏻🕊
How can you treat nerve problems?
@@thetony8959
It depends on the cause behind it.
I found out i have the MTHFR gene mutation which prevents all vitamin Bs from being methylated and used by the body. Supplementing with methylated vitamins and Low Dose Naltrexone has been a game changer for me. Especially the LDN.
Where can I find those? I have the MYHFR and I’ve known for de cause that my body doesn’t convert the bs to energy.
How did you find this out may I ask?
This should be funded by public health system :( supplements are so expensive in new zealand
@@krystal3822 an oral cheek swab test. My doctor did it in the office. But I think there are tests now you can order online.
@@ShelleyPolarbelle ldn stands for low dose naltraxone it is a prescription medication in higher doses it helps w the effects of withdrawal from alcohol or drugs in low doses it can help w pain and insomnia like that in fibromyalgia.
I've had fibromyalgia for many years. I'd tried so many things to stop the pain but it just wouldn't let up. Then I read in the comments of another post on this subject that a tablespoon of Nutritional Yeast a day stops the pain. I tried it and I've had very little pain since. I'm still exhausted a lot of the time but the pain is gone. Please try it.
B1 and limit candida overgrowth with limited sugar intake...These two things brought me back to life.
I am convinced that fibromyalgia is a neurological disorder. I have fibromyalgia and what the doctor calls a smallfiber neurophaty. I know how it feels and how it behaves. I am sure that those two diagnoses are strongly connected. I wish i knew how to make it go away. Ann
Finally a REAL PERSON SPEAKING!! Thank you for that. ✌🏻
3:28 Hint. 3 out of 4 inhibitors are hormones. On a rheumatology slide. FM people really need a solid endocrinology work up. (as well as rheum) Approx 25% are GH insufficient. Treatable. Cortisol/high/low adrenal problems can also cause FM symptoms. I'm glad you ended by saying it's good to get to the root cause. (No one gets their substance P tested--via spinal tap--which makes a lot of FM chatter hogwash.)
Problem still is many of us tested have results that show we should be in excellant healh. Its good news and bad.
Benfotiamine - Benfotiamine is a lipid-soluble derivative of thiamine. The increased lipid solubility of benfotiamine allows it to penetrate nerve cells more easily. After oral intake, benfotiamine shows increased bioavailability compared with an equivalent dose of water-soluble thiamine.
Its important to research the side effects of agamatine. It gives me brain fog, decreases working memory. Simultaneously though it suppresses impulsive and racing thoughts such as in ptsd.
Please search for the function of Magnesium L- threonate, it might help with your case
Fibromyagia = Idiopathic intercranial hypertension = chronic fatigue syndrome = multiple chemical sensitivity - they are all manifestations of exactly the same thing! Central nervous system disfunction often caused by Toxins / virusrs etc trapped in the brain / central nervous system. Better functioning glymphatics can help these conditions tremendously. Great video. 😊👍❤️
Look up fluoroquinolone toxicity also.
They are all linked, mine started with CFS but ended up becoming MCS that I still have to this day
What helps the most with the glymphatic drainage besides sleep ?
Your comment made more sense than 5 doctors I’ve seen! Any resources u can share?
@Shan I have that. The first month's were hell of Earth.
I was diagnosed with fibromyalgia when I was 26. It bloody ruins my life.
Have you tried a keto/carnivore diet?
only if you all eat the same crap food, drink alcohol or sugar beverages, ...
@@Lamz.. I did for 1 month but I'm starting it again tomorrow and I'm gonna do it for all of next year
@@deooptimomaximo9843 Good on you. Real food is the basis for optimal health, my friend. It's vegetable oils and carbs/sugars that make us sick. Your results will be spectacular, no doubt about it.
I'm in remission. High protein diet. Vitamin d, probitics l glutamine and weight lifting. Gluten makes my bladder feel like I'm on fire
I had NEVER heard of agmatine! Thank u!!
Me either, but I take L-Arginine every night because I read somewhere it helps with sleep...and it does seem to help my sleep. Although, I have to wonder if there's some issue with my mitochondria turning it to the Agmatine.
@@creatuitiveguru is that what Agmatine is? ....L-Arginine?
@@Mortthemoose What is arginine? Arginine, also called L-arginine, is an amino acid used by the body as a protein building block. It's also an intermediate metabolite in the urea cycle and the nitric oxide cycle.
Even my skin hurts,Im losing the feeling in my feet yet they hurt at the same time.
I know the feeling. Have been on youtube the whole day scouting for infos what would help. I tried already so much without any improvement. So take the next step, maybe i get lucky.
My skin used to hurt. Plus a multitude of other things. I was B12 deficient VitD and VitC deficient.
Just because a B12 test doesn't show a deficiency it doesn't mean you're not. In still healing after nearly 2 years of daily injections. B1 is also helping to address things B12 hasn't. B1 has helped my painful feet and legs.
@@binathere2574 Those are the supplements I am taking but I get extra B1 from "Braggs" nutritional yeast.I have only had one B-12 injection this year, I need to just buy some and give it to myself.Be well! 🙋🏻♀️🕊️
Trauma is also a huge cause. Everyone I know who has it (just like you describe and like I have), were sexually abused as children.
My son and I have both
I am currently exploring Fibromyalgia and Chronic Fatigue Syndrome as a diagnosis (as a means of finding solutions) and it made sense how they connected to past trauma, which I had not been aware of before. Sexually abused here too. It takes a massive toll. Big hugs x
Emotional abuse here. Abuse comes in many forms.
I have fibromyalgia and definitely was not abused in any way as a child!
I believe fibro that starts as a child is indeed connected to trauma. That being said, I believe fibro can show up in a person at any given age and for reasons, I hope they will one day discover. I won't give up hope that research and funding will continue for people like us! Whether you are a top athlete or a mom like me, we are all in this.
🔴🔴🔴PLEASE DOES ANYONE HAVE THE DOSAGES FOR THE THIAMINE AND ARGENINE I JUST DO NOT HAVE THE MONEY TO PURCHASE THE PROTOCOLS LET ALONE THE TREATMENT AND I’M AT THE END OF MY TETHER AS I CANNOT MOVE OFF THE COUCH ITS HIDEOUS.
Start with sulbutiamine 200mg 2x daily and increase if your symptoms do not improve...Agmitine start with 500mg 2x daily....TAKE BOTH ON EMPTY STOMACH...Watch all EO NUTRITION VIDEOS !
I started getting symptoms of fibromyalgia last year. It was like a blanket of pain on my entire back that would come and go, along with many other symptoms. I found that sugar was the biggest trigger for me. I went carnivore, then slowly added just a few foods back, and I felt so much better. I’m hoping this solves mine.
I went to my drs to plead for some sort of diagnosis which my symptoms are classic for fibro. I asked could it be …. She replied I’d have to look up fibro but if you have the symptoms then you must have it ! What am I to diagnose myself now ?
I’ve been suffering for quite a few years but my symptoms fall on deaf ears. Who and I how do I get to see an expert in this ?
This man looking better and better every video,quite reasonable cause to at least to listen to him.
He looks like Alain Delon.
Aaaaand my rheumatologist said he can’t diagnose fibromyalgia because I have small fiber neuropathy. Neurologist shrugs, agrees and does nothing. Sooooo, here we sit….Can’t argue with drs who don’t keep up on current studies.
You can change Drs or seek 2nd opinions.
Very interesting theory. My journey has been one with MS. I was accused of all of these kind of pain syndromes to autoimmune disease. Maybe there is more than one thing going on. It took google to the doctor for nearly 30 years before they found all the lesions. Had they listened to me….I might have gotten help a lot sooner. I’m convinced that we’re still in the dark. I’m bitter. Lost my life, spent at least a million, and became disabled at 33.
I have events in the spine where I’m feeling awful in general, my back thoracic and down ramps up in pain and broken glass is the only description.
Prayers for you PreWar.. 🙏🙏💗🙏🙏
You sound alot like me.
I feel for you 💔
@@PenelopePitstop888 thanks Penelope. That’s a lovely name and what strange, strange world where we haven’t thought or invented our way through it. These left turns in life are so confusingly difficult to navigate. Very interesting theory….
Have you tried the carnivore diet yet?
If you have root canals read the book Root Canal Coverup by George Menig
My mother had poliomyelitis as a child and most of us also took our polio "sugar" cube as a child. Her nerve centers died in her lower body as a small child and she was paralyzed waist down however within a week began coming back (however science says the nerve centers are inferior)...and she was diagnosed w fibro as an elderly adult a few years after I was post mono/ebv. She also has celiac. She cannot maintain iron in her blood but had anemia in childhood too. My gut says this is all connected. Glad you persist in your study and care for your clients and the field at large. Gratitude.
Not sure about the situation - but I urge you to read up on MORLEY ROBBINS (utubes etc). He knows *all* about the Iron and Copper story.
Astounding, unknown information …
Do not miss …
🤗
Very odd...my mom, too. She was 2 or 3 years old and couldn't walk until after a lot of physical therapy. Her lower spine sort of "fused" itself or something, she could never sit cross-legged. She got rheumatoid arthritis and lupus later in life. I got trigeminal neuralgia when I was about 27, I think. It came after a long period of being ridiculously tired after my 2nd baby, but no Dr could ever find anything wrong. At perimenopause I began developing fibromyalgia, that is now disabling. Just got my TTFD today to start. Fingers crossed.
@@creatuitiveguru how are you doing after taking TTFD
I am 44 years old and have been fighting fibro since in my 20’s. The change happened after I was required to take 2 doses of the Hep B vaccine in nursing school. I struggled through a 20 year career as an RN, but just couldn’t manage any longer. I am absolutely convinced that my fibro was auto-immune related. I am also convinced that all the antidepressants and gabapentin that got prescribed in those 20 years have worsened my symptoms, not helped. Once I was off all those meds, my fibro got better. I still have exacerbations after physical activity or stressful events, but at least it’s not continuous wide-open pain.
(PSA- do not stop antidepressants or gabapentin cold turkey! The withdrawal symptoms can be extremely harmful!)
In the years since my unofficial retirement, and especially after witnessing the political takeover of healthcare and the silencing of so many in the industry in 2020, I am ashamed that political activists and the mainstream media has ruined any chance of REAL healthcare in this country. If there’s to be any healing of my body, I’m gonna have to do it myself!
@@americanrn125 when I first developed FM i wasn't on any medication, could have been caused or triggered by DV, but I'm not positive about it.
Very interesting. In the immediate, Another thing that reduces symptoms is an anti-histamine called Claritin. Don’t know why this particular antihistamine works but it does.
it could help for sure if one has a Histamine Issue and or MCAS.
Hi Doc, I wonder how much B1 hcl would you recommend to see noticeable change and what co factor needs to keep in check while taking B1. Thanks
I take the Benfotiamine of the B1..
Magnesium Malate 1200 mg b4 sleep with 5mg amitryptline and i can actually get put of bed:)
Loving all this information
Thank you for a most informative video. Thank you for caring & sharing. God bless you. ✝️ 🙏
Left out implants, bioengineered foods, and anything synthetic!
More on the root causes, especially rare one and how to tests for it for small fiber neuropathy. It is devastating condition.
I've had fibro for over 50 years, there is not much I haven't tried but I do find fasting the most effective tool, on day 3 all my symptoms melt away. I will try high doses of B1 as that is a new idea to me. Thank you for all your work. UPDATE: I took 800mg of B1 five hours ago, I usually take 100mg daily. My back spasms have gone😲UPDATE I can' believe it's been 2 months! I have now tried all 4 forms of B1, hardest to tolerate was TTFD, daily migraines for 7 days, very tearful, low mood. I found exactly as Elliot says - the need for Potassium and Magnesium rocketed, without those my symptoms actually increased. I am stabilising now. Mornings I take 300 mg B1, 150 mg TTFD and a B.complex with Magnesium with 1/2 tspn Potassium Citrate in my coffee (makes it slip down like oiled silk!) Early/mid afternoon another 200 mg B1 and 200 mg Benfotiamine. I use Electrolyte powders 4 times daily too. I consume a desert spoonful of Nutritional Yeast most days and have ordered B12 tablets to add. The dreaded back spasms have not returned, nor the tinging/stabbing oral sensations. I have more energy, not huge amounts but I'm better able to function than with full CFS. I am also using a good quality probiotic powder as I have high antibiotic use history from treating Lyme. This definitely works, YIPPEE, AT LONG, LONG LAST!! My GP said I was the worst case of Fibro she'd ever seen, told me there was no hope, only pills & coping skills, to which I said NO! That was 8 years ago, I made up my mind then to fight it....To anybody who is bed bound, please do try this, go slowly, I did too much too soon! ELLIOT....THANK YOU.
Please give an update when you can. 💐
I've had Fibro for 37 years and have taken 600-1,200 mgs. daily of Benfotiamine (lipidized B1) for many years. It has not helped my pain, but I will try raising it to1,800 and see what happens.
I don't know if I have fibro, but fasting works miracles.
I feel so much better!
Now I wonder if I also have some sort of fibro...
@@meagiesmuse2334 How did that go? Have you tried longvida tumeric? And omega 3 and vitamin D with K2/MK7 and NAC?
@@theancientsancients1769 - It has not made any difference so far, but it's only been one week, and this sort of thing needs a 2 month trial. I get nothing from tumeric, and have tried 5 different brands over the past couple of years. I take omega 3, D3, the MK7 type of K2 and many more every day for years. I've taken NAC twice daily for over a decade, and take many more supplements. Imo, if the sleep disorder (the alpha-delta sleep intrusion) in FM is not resolved, nothing improves much. My sleep has gotten worse due to the health problems FM causes long term, so I wake up every 2 hrs.
My pain feels like lactic acid build up. The exact pain you would get after working out with weights.. Next day pain.
I had the same thing and read that lactic acid buildup that doesn't resolve naturally is due to mitochondrial dysfunction. Don't know if it's true, but I don't make mitochondria and, thus, negligible amounts of ATP.
Feeling a pain like after workout but without an actual workout is a dangerous symptom. It signifies that lactic acid is building up in your body causing a systemic lactic acidosis. This is a hallmark sign of a tissue hypoxia / mitochondrial dysfunction during which the aerobic glycolysis rate is degraded and your body switches to anaerobic fermentation producing tons of lactic acid along the way and very little ATP.
Possible common causes: anemia, toxins, metformin, nutritional deficiencies, especially thiamine deficiency; Lyme disease, post-covid.
You should pay a full attention to this symptom because it is often a sign of the upcoming onset (or significant worsening) of various neurological conditions including neuropathy, fibromyalgia, shortness of breath, cognitive decline. You may also feel lethargic, asthenic, and increasingly fatigued.
@@kdrum90 I thought that's what I just said. Guess I need to brush up my communication skills. Thankfully, I no longer have the problem.
Magniesum malate 400 mg at morning
Any recommendations to heal spider veins?
Im active, generally eat healthy, never been overweight.
I had severe fibromyalgia in my 40’s, and was diagnosed with severe hypothyroidism and Crohn’s in my late 50’s. Both almost killed me besides statin drugs and extremely elevated levels of Triglycerides and Cholesterol and blood loss. I was sleep walking too. It took 8 years before my blood work came back to normal. I’m now 66, my blood work is near perfect and I’m on 9 life maintenance meds in the lowest doses possible along with dietary supplements. It sounds like a lot of drugs but none are controlled substances. The only pain I have comes from degenerative spine and disc disease from hard work with having Ehler Danlos Sydrome.
Epstein Barr was the start of all my health issues back in 86. Fibromyalgia, neuropathy, chronic fatigue, candida, amyloidosis, etc. Reminds me of what is now called long covid which I understand can reactivate Epstein Barr. I found this interesting: There are multiple theories for how EBV could trigger CFS/ME. Maria Ariza at the Ohio State University Wexner Medical Center, US, and her team have proposed that EBV produces a pathogenic protein called deoxyuridine triphosphate nucleotidohydrolase (dUTPase) that causes neuroinflammation and triggers CFS/ME. This dUTPase protein altered the gene expression of proteins that influence fatigue, pain synapse structure, and function, as well as tryptophan, dopamine, and serotonin metabolism.
Same with me. Epstein Barr is no joke. Never the same again after that virus 22 years ago
90% of humans carry virus.
DO YOU HAVE ANY FURTHER THOUGHTS ON THIS POSSIBILITY?
I am very interested in any known correlation or links and information about how the Mitochondria might be involved here.
I have pretty bad Fibro, which I have dealt with for many years, starting with CHRONIC FATIGUE.
I have always suspected issues with mitochondria disfunction or desease.
I noticed how you mentioned that in our bodies, the mitochondria are what converts to the Agmatine.
VERY INTERSTING!
Yeah, ditto!
My ears pricked up at that too.
It is also where the spike protein does dammage. I'm living hell since covid (and especially the vax)
Yes have taken large doses of NADH and Cq10 and Korean panax ginseng for 20 years many university studies do concur helps the fatigue. The pain on other hand...Diagnosed in 1988 cfs and fibro have my own study published in Journal of Musculoskeletal Pain in 2000.
Look for the 'Wahl's' diet...as in Dr. Terry Wahls. She is a neurologist and created a diet to heal her M.S. she did research and now it is also a book she wrote. Watch her 'TED' talk on this.!!!!! I have been following her diet now for 4 weeks and am amazingly getting better from fibromyalgia, lots of pain, M.S. type symptoms and Hashimoto's thyroiditis. Take care!
Carnitine and CoQ10 affect the functioning of the mitochondria. I couldn't remember the name in an earlier comment and said chromium by mistake.
I'm a 53yr female, and my GP don't recognise fibro at all. I just keep getting told I'm stressed. thank you.
Yr doctor is not educating himself. Get a new one.
@@patjonker6576 I hate Dr's who tell a patient stress...was told that until drove myself to hospital with 2 blocked arteries.
the more i look into the whole b vitamin complex and foods it seems impossible to get the rda and even higher without supplementation.. also because alot of the vitamins seems to be very sensitive to heat and stuff which we all use to cook our food, what are your opinions on b vitamin complex in liquid form ?? im def going to try the supplement route
Apparently I had fibromyalgia for several years. I started my keto eating regime so I had a reason to start taking VitD3 and K2 along with supporting amounts of Magnesium, potassium, selenium, zinc and a few others. I'm not sure which one it was or if a combo of along with the diet itself, but the pain all went away. Gone for good along with migraines, joint aches, calcium in the blood which caused high BP, and other similar conditions. Doesn't need medication from the doctor that will kill you in the end. Just cut out the carbs and the sugar, take some vitamins and a few minerals, get over it and get on with living life!
Can you please tell me the dosages of everything you take?
Clissa T good for you keep up the work
@@jules3975 Dosages are written on all packs. And in anycase you should visit your alternative health care person to be sure they are suitable for you. Some things are specific to individuals.
@@jules3975Idk why people gatekeep vitamins. Lol. Anyway, try taking Source of Life Liquid Gold Multivitamin as a start. NAC is a good supplement. Liquid Vitamin D by Carlson. Add it into your liquid multivitamin. Then take a multi mineral. Preferably one with Fulvic Acid. Potassium should be the Life Enhancement brand. Calcium Magnesium from Country Life. Then top off all your Amino Acids. 😊
Yes to all of these things!
Hi Elliot im just wondering if you would consider OXALATES as an inflammatory antagonist towards these neuro malfunctions. I have published a book "Are Our Superfoods Silently Killing Us?" about OXALATES. i have finally excluded most of these foods from my diet after listening to you and Sally Norton. Oxalates are probably the "sprouting" form of calcium that is not been detected. Maybe go back to basics and then review this information from the OXALATE point of view.
Agmatine is banned in the US. Probably because it works and it will hurt the pharmaceutical companies pockets or otherwise known as the FDA.
I studied Agmatine in Longevity and Nootropics research. 8:34 and on to the summary 1000 to 2000 mg of Agmatine paired with Thiamine mega dose, CoQ10, Magnesium, and Calcium-D-Glucarate. etc. 7:34 Things it can help treat
The Divided Mind book by Dr. Sarno offers an interesting point of view on psychosomatic disorders, suggesting fibromyalgia is one of them.
BS
Please can you do a video on tinnitus and natural cures.
Also emphysema, particularly the impact of diet on this.
Hi, I’ve found tinnitus is from too much salt in the diet so low salt diet should show good results
Search for liam solution to Tinnitus
I've been sick for most of my life, over 40 years. It's just gotten worse and worse. I've been trying for several years, since I found out about small fiber neuropathy and its link to fibromyalgia, to get tested for it. This is proving impossible so far, but I haven't given up because my life story as it pertains to my health was spot on being revealed by the leader in the link between small fiber polyneuropathy and (often undiagnosed, as was in my case) juvenile fibromyalgia. I'm convinced this is where my health issues stem from.
My own summarized research on healing pain: The body primarily needs good fat and cholesterol (grass fed butter, avocado, coconut, oily fish, pasture eggs) to feed the cell membrane, keep it supple, and to feed the brain. Also, water and fat soluble antioxidants, vitamin c rich foods (eat them with fat) to nourish the mitochondria and cell watery environment. Tip: Alpha lipoic acid and aloe vera juice carry vitamins into the cells. Additionally, the nervous system is an essential pillar whose sheath requires methyl b vitamins + additional b1 in the form of benfotiamine. Tip: Combine with quercetin for anti inflammatory boost. STOP drinking cow milk and yogurt, nobody needs those, they destroy your joints and your skin, switch your cheese to goat and sheep. STOP buying gmo soy, canola and cottonseed ladden processed foods, start cooking. Eat fruit, fat, proteins and greens rich in minerals. Clean up your bread, quit the pasta. Cleanse the pathways with turmeric, the liver with dandelion or milk thistle. Sorry for the admonishing sounding tone 😅 but I've been helping others heal for 20 years and I've seen what poisons the body and what doesn't. It pains me to see the pain in the comments 😱❤. People have the ability to claim their healing process back and get off the sick train if they choose to do so, even though the journey might be felt differently by each and take a different amount of time for each. We have to unlearn what hasn't worked so far though, and adopt a new learning process that listens to the body. STOP and ask yourself: are you truly doing your best or are you participating in your own abuse? We all get a chance at a clean slate /plate. Love and Light 😊💜💫
Yes we know all that, but where to get all that goodies? Unless you live in country side and grow or are rich to buy it all from around farmers.
Can't even trust organic products in supermarkets, they are organic!!
But living in a block of flats or a house on the city's....
@@aldastroud9671 what do you eat over 7 days and what country do you live in?
When taking Alpha Lipoic Acid (ALA) be sure it is the R-type. Most ALA's are the S-type which is synthetic and has less bioavailability. The R-type cost a bit more but since the body utilizes more of the dosage it ends up being cheaper. The comments on fats is real. Fat has been villified by the Medical Mafia (FDA, AMA and Big Pharma) but good fats are essential. The brain needs fat. Take benfotiamine with fats. Good advice all around. Thank you
My daughter is allergic to goats milk. 🐐 it's not for everyone.
@@marleneholloway7775 Correct, it's not for everyone and because it's not essential to consume animal sourced milk, you could even consider that a blessing in disguise or at least a saving on your budget. There is no need to replace it with cow milk. That said, if you see this rather as a curse, be aware that allergies come from a gut imbalance causing absorption issues so you may want to look into foods that deliver prebiotics and enzymes. Wishing your daughter good health 🤗💜💫. Be well.
Edit: to clarify: allergies come from a gut imbalance when they are not generated by the food itself being loaded with allergens and toxic components.
Hi there
Thank you for providing such informative info on such painful conditions
I have had Fibro for 29 yrs now, along with IBS, overall Guttate Psoriasis since age 4, through Zoladex I was prescribed came Osteopenia them Osteoporosis. I have also had a Hiatus Hernia for approx 29 yrs as well, which I was told the medication can contribute towards Osteoporosis as well, of which I am not on anything for
My Consultant recently told me how concerned he was after he looked at a DEXA Scan and how low my markers were
I was also diagnosed about 2 yrs ago with Osteoarthritis in my feet and hitch I was told would sadly spread
My sleep pattern is horrendous, my stomach is constantly bloated and I am exhausted and in diabolical pain on a daily basis. I am now fifty eight and sadly this does control my life
I have no one to help me ( I am in the UK) and life is a struggle
I feel ashamed of how much is wrong with me as I don’t drink or smoke etc or go out to do any hobbies as even my hands are painful
I did want to ask how would I be able to tell the difference between SFN and Fibro
I have considered Stem Cell Treatment from a reputable company and strongly considered moving abroad as living like this plus becoming older- well the thought is unbearable
Thank you
I have neuropathy...I wonder what the connection is to histamine intolerance, sulfur intolerance and endometriosis....I have all of these issues. Im working with someone on these conditions but it definitely takes a while to heal. The reason i ask is because I have also read endometriosis areas in the body grow new nerves as well and so people with my condition are more sensitive to pain...or we feel pain in new places with each new lesion. Just a thought.
Poor u! I'm so sorry🙏🏿🙏🏿💖💖
Would not surprise me to learn they are all linked. The question is how...
@A.M. Z.
May I ask which brand of b1 (TTFD) are you taking n what dosage? Thanks!
@A.M. Z. This was a great read-thanks so much for sharing. I start my Thiamine experiment today!
@A.M. Z. yep ive been reading hormonesmatter avidly. Starting today on 50mg TTFD, B complex, mag glycinate and electrolytes. Will let you know how i get on x
I started b1 and niacine, this is verry interresting. The flush works magic. The heat goes too all the tenderpoints. I will continue, the heat and itching is a bit scarry at first. I feel better after the flush and my nek schoulders feel much better!
Also take nac with clycine ❤
Take the niacin with a meal - you don't get the itching, redness and flushing
Yeah, the flush may be a necessary function to help your condition, maybe add Lions Mane mushroom to that to help nerves to repair themselves.
Thank you. It seems to make sense though I’m not sure I understood it all.
I seem to experience pain in peculiar ways. If I get a true physical problem in one area it seems the rest of my body comes out in sympathy and I get widespread pain issues.
I find magnesium helps with muscular pain when I’ve over exerted. A whole food plant based diet has also helped with general pain and tiredness.
I think it was constant use of antibiotics which started off my fibromyalgia.
Ready made plant based foods at the grocery stores etc are super harmful and full of bad and harmful ingredients. Super healthy!
If trying plant based, then for goodness sakes make your own foods and buy organic. No use making matters worse for yourself down the road!
Years ago I had both Fibromyalgia and ebv together. There was no remedy...I knew it was emotional, so I cried and cried and cried...6 months later both had disappeared!
I’m so happy for you. There’s definitely an emotional component.
Interesting
I’ve been crying for 47 years and it hasn’t helped yet 🤷♀️
@@CheapsKate77 Think of the crying as cleansing. Literally removing toxins and emotions from the body each time! Also, use the alchemy of the shower to was away negative emptions like sadness, loneliness, anger and replace them with joy, love, acceptance and excitement as you gently wash with soap. Let us know how you feel.
Can fibromyalgia be psychological, like a trauma for example? Because people with complex trauma could experience these symptoms?
Thoughts and believes spread over to the body, causing it to become ill?
I have chronic fibromyalgia. I am not deficient in any vitamins but the pain is constant and sometimes unbearable. I just deal with it. I am sometimes in bed all day sometimes I am out and about.
I eat no grains, no sugar or processed foods. I follow Terry Wahl's diet, she is a neurologist, has a TED talk and book, plus research of how she aided the healing of her M.S. It is amazing. I have been on it for 4 weeks, so thankful that the pain is gone now! I had so many M.S. and fibromyalgia symptoms. I also have hashimoto's thyroid disease. So, it helps me to follow the diet and live my life more joyfully now!
@JESUS IS LORD Thank you
I haven't had a really good day in years - only when i take a quite big dose of Tramadol - and that is something i don't want to do often, because of the addictive potential. The bed has been my best friend even when it doesn't help laying around, nothing gets better. And i was all my teenager years super active, barley sitting, when walking better go fast, do a lot of things at the same time and Hyperfast..... and now NOTHNIG :( But i have new hope now, that one of these supplements B1, B12, high Mg, Agmatine - let's hope for the best for all of us and pray.
Hi there! This is quite an interesting study and informative video! Just to share here some info which might be helpful to those who read this...spinal cord injury and suffered Fibromyalgia many years in the past, but never took any medicine for it, instead I did massive doses of Vitamin B complex and of course Thiamine and doing wonderful now. I even used Agmatine before but I quit that and kept on taking B complex along with a few other natural supplements, it works for me. I can confirm that you are right on the spot with your studies and that your videos are quite helpful.
Thank you!
May I ask why you stop taking Agmatine and what brand of B complex are you taking? Appreciate your help 🙏
@@moniryousefian8782 That's a good question and deserves an answer, I'll be glad to answer to your question hoping it helps.
Agmatine Sulfate was good for just a short period of time for me, it helped a bit when it did, but I soon began to notice a fragility in my vessels and veins and even my heart was feeling fatigued from taking it. Agmatine S. makes the blood more fluid and some of us may needed more than others and some don't, we are not all made the same, hence it is a good rule to either consult a good naturopathic doctor or monitor ourselves mindfully, it's not easy to detect the changes that our body makes when not fully connected within, I cannot stress it enough, when we want to do things by ourselves the inner connection comes first.
As far as the B-Complex goes, I take different B-Complex and other supplements, as long as they come in a natural form and not in a synthetic form, this is another important factor to take in consideration at any given time. Most labels won't mention anything about the product form or original derivation from, labels can be very deceiving at times. It took me a few years and many naturopathic books to learn just about this topic. Some supplements claim to be natural and some of them may very well be but then when you check the inactive ingredients you might find out that the inactive ingredients interact with the active ones, so you really need to pay close attention to every details. I personally found Standard Process to be a good reliable source and yet, that is not the only source; in fact, I use other vitamins and supplements, I supplement more of the Thiamin, Pantothenic Acid as well as others. My Fibromyalgia comes more from the nervous system being hypersensitive and the damaged spinal cord.
Not all Fibromyalgia come from the Nervous System, so it is important to be able to explore the nature of the dis-comfort and what generates it.
I don't know how far I can extend my knowledge and experience in here and even then I came to realize that sometimes what works well for one may not work for another. For instance, just to give you a better idea of what I am saying here, for my life companion I had to put together another protocol, indeed we share only some of the supplements in common but for some others what works for me it doesn't work for him and vice versa. I spent many years studying herbology, naturopathy, Ayurveda, TMC etc. My best suggestion for a good blood flow and good energy is that there's nothing better than Qi-Gong practice, yet as far as the vitamins and supplements goes, I personally stick with natural only. Elliot's studies and advice are always a great addition to someone's own knowledge, but they need to be taken for what they are, "knowledge" to apply them properly it requires wisdom. I hope this helps you and whoever happens to read this.
@@shaktiveda7041 Absolutely agree. Learn for self and others how to do applied kinesiology, muscle testing. Muscle fibers react and tell all.
So the high dose vitamin B stopped fibromyalgia pain for you? And are you still taking it?
@@youknowulikeit9589 In all honesty, yes, it worked, but I also had to re-caliber it at some point. You see, our bodies are not all the same, we are all different and unique.
What might works for one might not work for another and vice versa.
Also, when it comes to healing holistically there are a lot of factors to take in consideration; also, it is important to remember that too much of something can cause an even bigger imbalance somewhere at some point or stage in life. It's not only about vitamin B, but what type of B, what's the nature or source of that vitamin, dosage needs adjustments eventually, the body also requires a balance between vitamins/minerals/amino acids, proper nutrition, exercise, etc. Of course, it is not one thing only. You probably by now have too realized that our bodies are more complex than just double on a certain type of vitamin and you'll be okay. In the same breath, I would encourage everyone to learn, embrace, and experience for themselves holistic, naturopathic medicine over the allopathic med. The body always wants to heal, unless its own time is expired. When we trust mother nature and its innate intelligence the healing can happen and it leaves no side effects, while allopathic med. on the other hand, is what I would define as a "patch work." With allopathic med. there is only the illusion of a temporary relief, but in actuality there is an energetic block happening somewhere else and it will eventually show back up at later time, sometimes with revenge hence, that is what is commonly referred to as "side effect."
Last but not least, it is crucial to understand that true healing might not happen in just three days, it depends what type of issue we're dealing with, the will power and the patience that the person has in regard of his/her own issue, the nutrition and so many other factors, however, it is the best route to take when there is true commitment to heal and to become whole again.
No surprise to me. I awake every day to awful pain which has got worse over the years (since the menopause when it first came on) and yet I have seemingly nothing wrong with me and no arthritic joints. I remember telling a doctor I felt sometimes like someone was digging pins in me, especially my limbs and he looked blankly at me. I've never found anything that helps with this.
I hope you take some Mg glycinate, bednfotiamine, methylcobalamin, and some MK7 along with your daily dose of sunshine :)
Agmatine sulfate + thiamine mega dose + Co Q10 +Magnesium + Calcium-D-Gluconate etc
After going on the Jordan Peterson/Mikhaila Petersen diet (beef, salt, water) for 1 month, I started adding 1 food back at a time. I found out I was sensitive to all grains, dairy and eggs. Getting those foods out of my diet got rid of my aches and pains. A ketogenic diet took me to the next level in terms of energy.
Yup only Ted talk to be hidden basically.
Do you have a link to where you got this info please?
@@tanyawieczorek6603 Mikhaila Peter: th-cam.com/video/7fncJdVjy5U/w-d-xo.htmlsi=YZmLyh4RKAFzB1dL
Jordan Peterson: th-cam.com/video/HLF29w6YqXs/w-d-xo.htmlsi=69_NZg-TTAhh-iZj
@@tanyawieczorek6603 Here’s another with Chris Palmer who is a Harvard psychiatrist. He says a ketogenic diet works better for major psychiatric disorders better than any medications: th-cam.com/video/AuOn_0WTKYs/w-d-xo.htmlsi=wsA9AFIlcke7aYyq
@@tanyawieczorek6603search TH-cam: carnivore diet. Avoid the videos debunking it.
I am in constant pain, since my last flu vaccine in 2018, it turned something on. Back pain, feet pain, joint pain at fingers
You might need to detox from heavy metals.
And kill the retroviruses
Go see a chiropractor, for 3 sessions. Also try a dry sauna ...do it repeatedly to revitalize your immune system and body
Also stop eating bread products and cereal products. Increasing healthy FAT intake. May I suggest Virgin olive oil, wheat germ oil, avocado oil, walnut oil, coconut oil etc....and take one serrapeptase capsule once every morning. I believe you will see excellent results in 3 or 4 days! Seriously! May God bless your journey 🙏🙏🙏
@@homeopathywellness1719 yes true, I have been drinking cistus tea. I don't know it's source though as it was in a local polish supermarket I just bought it anyway. But the right quality can take care of retroviruses. Dr. Klinghardt and Judy Mikovic talked about this.
They also say that it needs to be sweetened with Stevia as that also has antiviral/antibacterial properties.
I was one of the first people diagnosed with fibromyalgia in BC. That was almost 30 years ago. I have had so much nerve pain and acute/chronic pain.
It turns out I have Ehlers Danlos Syndrome. There's 13 types but type 3 is the most common, Hypermobile EDS. My large joints are "double-jointed". Still considered to be a rare disease although 1/5000 peolle have it.
Common symptoms include chronic pain, fatigue, brain fog, stomach issues. I also have Mast Cell allergy and POTS.
Treatment for the allergy and my life-long nutritional deficiencies have helped me almost go into remission. If not for some injuries that are difficult to heal, I would hardly have much pain. Not being diagnosed for over 25 years destroyed my body. It is taking a lonv time to get well, and I won't ever be the same as I was in my 20s.
Allergic to gluten, dairy, caffiene, alcohol, the sun and all chemicals especially perfume. Gluten affects my stomach. Caffiene makes me nauseous. Alcohol gives me bad hangovers. Dairy was the biggest surprise. It increases my pain by SO much and gives me snaphylactic migraines, szme with perfum.
I believe a lot of "fibromyalgia/,cfs is a combo of an allergy to something or things plus s nutritional deficiencies deficiency, as stated in the video. I'm living proof. Since beginning treatment 2 years ago I am in remission from Addison's Disease, Hypothyroidism, Type 2 pre-diabetes and severe osteoarthritisin my of my joints especially my knees. I am deficient in B12, iron ,vitamin A, D, magnesium and zinc tor sure. I take all the essential vitamins and minerals daily and see a Naturopath occasionally for vitamin IVs and other supplements and antioxidants like Quercitan and NAC. I also beat most symptoms of long covid, twice.
If yiu have fibro, its a good idea to rule out Ehlers Danlos and Mast cell activation syndrome or other allergies.
I have hypermobile eds n fibro as well I call it my daily battle I am always in pain n no one gets it so exhausting I've gone broke trying everything under the sun
I had a skin biopsy that was positive positive and then another that was negative. But all the symptoms that you describe is what I’m suffering with. Somebody finally put me a gabapentin after 30 years of being in pain. What a relief.
Do gabapentin make you free symptoms?
@@shamtibbi8250 it puts the pain in the background, but I have to tell you the muscle spasms overall improved. I tried several muscle relaxers, no improvement. The other thing I found medicine marijuana to be helpful for the spasms. I’ve never smoked it nor I used it in the past, but I had to resort to doing so because it was affecting my life so much. It’s legal in the state that I live in. I use the edibles
Americans need access to more types of treatment through their health insurance. Or, maybe, just make healthcare universal like in the rest of the enlightened world.
Natural Beef liver supplements gives me vit B which is lacking in my blood. Eating greens high in Vit B help as well
Could someone please link a good quality UK source for agmatine. Thanks
OMG. I have SUFFERED with idiopathic small fiber neuropathy for over 15 years. I’ve tried to keep up on research, but I have never ever heard of Agmatine! I’m truly stunned I haven’t come across this before now. Thank you thank you thank you for at least the possibility of some relief.
I’ve just now read that agmatine “agmatine inhibits opioid dependence and relapse in several animal species”. So that may also help me since I’ve been on Nucynta for many years. My neurologist seems very uninterested in small fiber neuropathy so she’s no help. She’s just a cookie cutter Dr. But my GP is more interested so I know she’ll read what I send her and give guidance re all the many other supplements I take to make sure I’m not taking things that are fighting each other before I start trying Agmatine.
OK… I got a little chatty. Just wanted to give you a thumbs up and say thank you!
This is a fascinating idea and it gives me some hope. If the pain associated with fibro and (non diabetic) neuropathy could possibly be linked to spinal cord issues, would it follow that a serious injury to the spinal cord could lead to fibro/neuropathy of lower legs, etc? In early 2000, I had a fall in which my L4 vertebrae was completely crushed. I've had never ending back pain since then, but in later years I've had all over pain (my doctor had diagnosed fibromyalgia) and in more recent years, neuropathy in lower legs/calves, as well as episodes of numbness and pain in my feet, and periodically in my hands. I will read your information and I appreciate this so much.
Hello 🤗 Beautiful Lady 🌹, How are you and the weather condition like?
Naturopathic health practitioner here...
et al
Fact - Fibromyalgia is under the Herpes Umbrella
along with Epstein Barr; Lupus; MS; Parkinson's and more
and are stress triggered ...
and according to stressors will come and go
I just keep moving but it's pain everywhere all the time.
You've got a gift for teaching and such a God sent caring soul!! Ages of wisdom beyond the average practitioner🙏🙏
My 3 go-to are R-lipoic acid, omega 3 fatty acids, and chelated magnesium.
Thanks Elliot. Great video. I have a chronic pain syndrome and have suspected that my problem stems from some sort of neurological re/cross-wiring of my nervous system, perhaps in the spinal column.
A lot of what is mentioned in this video makes sense.
Looking to get Intrathecal stem cell treatment in the next few months but will be exploring some of what you mention here to see if it helps in the meantime.
Will check out your other videos too.
In one reading of fibromyalgia it was said, in the spinal cord there is a substance named Substance P, and it is too high in FM persons. It's called substance P..
I would recommend everyone listen to Dr. David Brownstien on the benefits of iodine. Taking 8 liquid drops of iodine daily worked wonders for my fibromyalgia.
How do we know where to get these vitamins? Many OTC vitamins are basically crap.
Is there a way we can find GOOD supplicants?
Pure Encapsulations.....only the vitamins no extra stuff.
@@Sakuragaokaeibikoen Pure Encapsulations is the name of the company?
Are you a sales person for them?