I got through the worst of my illness by surrendering to it. Accepting I wasn’t a head case as my GP suggested. I got worse before I got better, but I was put in touch with MIND a charity for mental health of all sorts. Through them, I began to recognise my triggers, which were mostly stress induced. Another GP temporarily put me on anti-depressants, which helped me to reset myself mentally and physically. I came off the prescription early because I didn’t want to become addicted. I started dieting and gradually became a bit more alert, lost weight, less pain. I've piled on the weight again, particularly due to lockdowns, so I’m battling with myself again. I’m 60 next week and first noticed fibromyalgia in my early 40s. Every activity I do, I feel dread, but congratulate myself when I achieve something, like hoovering, cutting the grass, being on top of the laundry, etc. Simple things I couldn’t do, but I get through it now.
I’m glad you found some relief. As I read about the time you got it was the same for me. I was in my 40’s and thought I had arthritis because achy joints, chronic fatigue, very sensitive to moisture, and humidity was difficult but winters were the worst. I turn 60 in September and my husband and I built a home in Albuquerque and moved from Iowa. The difference in New Mexico weather is it’s very dry which has helped me immensely. I have a flare every time it’s going to rain. Mine is the day before and day of. I had to have a knee replacement almost 3 years ago in Iowa and it’s a matter of time for my left knee. I own an insurance agency and love it. It helps with feelings of youth. I’m active but I will say by Friday I’m so tired. I make myself go out with my husband on Saturday nights. We go out to dinner and I enjoy a few cocktails but don’t drink much. I just do what I can and if I need rest I rest.
Thanks for your comment - Peter is amazing and his CFS recovery (Fibromyalgia recovery) is truly inspiring. I am always uplifted whenever we have contact. :)
Peter and Dan thank you so much for offering hope, encouragement and inspiration. Peter I am thrilled for you and so happy to hear how your life is now indeed full and blossoming. Dan I listen to your talks every morning...soon to run out but like Peter will re-listen. Your generous and caring spirit for this community of people is so noble, beautiful and of huge need and great importance. Love and peace to you both and all who listen. I wish you well. Tara xx
Hi Tara - glad you enjoyed Peter's recovery story and that you are listening to all the recovery interviews. There are lot's more to come - hope to get many more published in the coming months. Hope to share your story one day soon! :)
Very happy for this guy but trying to understand this: He's been sick for 11 years, bed-bound and suicidal for 2 years, has tried literally everything and gone into thousands upon thousands of dollars worth of debt trying to get better, and when he finds this program and recovers 80% in 6 months, 110% in 12 months, he considers that "slow." If I made that kind of progress after all of that, I would call every single medical professional and tell them a miracle just occurred. That is BEYOND my greatest expectations by a factor of ten billion. Absolutely insane to call that slow.
Yes, when you put it in perspective like that, it's still a fast recovery isn't it. But I think people always look to get quick feedback to see if something is working, and when the changes come slowly, they often don't persist. Thanks for sharing your thoughts!
why would you call ''medical professionals''? they dont make money from healthy people. The pharmaceutical murdering industry is a multi TRILLION dollar/year business, do you think they want to lose that money? How old are you? 4?
@@incorectulpolitic This is one of the biggest red pills out there. Med pro are there to make MONEY. Not HELP PEOPLE. Sick people = Oh I am sick I need to be fixed let me go see med pro they studied for years surely they can help me. Sadly no. Fixed person = no more money.
I’m in Hertfordshire, UK. My husband has literary just come back from his 2nd doctor appt and exactly that was intimated . The doctor just said half heartedly ‘well what do you want from this’. Gave no real recommendation. They hated that my husband was giving his Google diagnosis.
I am mother of 3. A baby and two toddlers. I have severe fibromologia and so thankful to hear others stories. I come through abuse as a child. When I had my second baby another csection I hit rock bottom. I had severe pain every where and awful headaches. I am trying to work with diet and gentle exercise. I am doing different coping techniques because I have major triggers
My daughter started to experience almost all of this symptoms with the exception of weight loss,when she was only ten years old. She's now 15 and has been diagnosed with fibromyalgia! It's a very scary world please help!!!
OMG, I've experienced sensitivities to cigarette smoke for decades. If I breath in just a whiff, I get really ill with cold/flu symptoms. I sometimes taste the chemicals in water. Just making a sandwich triggered so much pain, that I couldn’t use my hands for a day at least. My muscles tone was that of an athlete at a time when I couldn’t get up the stairs, I was in so much pain. I was so useless, I couldn’t stay awake to listen to my children read. I literally wanted to die. I contemplated suicide, but wasn’t suicidal. I played the scenarios out in my head as I lay on the sofa alone and for hours. The house needed cleaning, the dogs needed walking, my children needed feeding, taking to school and being picked up. I sometimes had to ask a friend if she would collect them after my husband dropped them off. I felt like an utter burden too. I still do at times. I dread the suggestion of visiting places or holidays, days out. They trigger a great deal of anxiety for me. Trying to stay awake, trying to experience the moment, battling pain, organising it all. Then I don’t remember where we have been or what we did. The kids take photos, but don’t share them. They don’t understand why the photos are so important to me. They help me to remember glimpses of our time together. When I'm really tired my speech slurs and I lose what I'm saying mid sentence.
Yup sounds alot like that I have, I have chronic fatigue and fibro diagnosis too on my record. They walked out on me too. I even changed my diet to no sugar and low carb. No nausea, but memory is bad, yes on the electrical jolts, yes, horrible sleepy fatigue, ALL the time, im on depression meds high vitamin D. i am an artist and I have had hand surgery, I can not open a jar or bottle, its horrible. I have mold allergies, grass, golden rod, raw eggs, cows, but it has lessened since my cancer. No cancer now.. I cant stand those smells either and cigars are bad too to smell. Yes, my treatments morphed too, I had, its gone down now but I had bad vertigo. Yes on no circulation in hands and feet, joints, shoulders hips ankles toes fingers all bad. When I was in 6th grade I played tennis, everything wore me out. These days I can only do one activity a day. I will not swallow a camera. Like I said, I changed my diet, found out drinking cleansing drinks with lemon, apple cider vinegar, garlic, vit. B, A, E, honey, krill oil, macha tea and chaga drops, since I started that, some of the symptoms lessoned, The weather effects me huge!!
Ya, I did all that, I memorized my fibro folder hand outs from the doc and even did the exercises. nothing helped. Ohhhh I know the hard to get to the store thing!!! the vibrating is horrible but it dont last for mem comes and goes. I will try yoga.
Rather than trying one thing or another, see if you can build up a comprehensive set of strategies like Peter and others do. Have you seen the ANS REWIRE intro lessons? They explain why this is key!
Tai chi works best for me! Gentle, mild stretching and slow movements loosen up my tight spasming muscles without triggering more painful spasms. Feels like I had a wonderful massage plus meditation...😊
Ive never heard anyone describe the electric jolt thing before! I tried to explain to people how i often felt electric jolt exactly like touching the metal side or screws of electrical outlet box. People look at me like im crazy. Also have ibs symptoms and extreme fatigue. Thank you for the leads on what may really be the problem.
I was getting those plus,I started seeing things. So I started taking vitamin D3,Hemp seed oil and DHEA to see if any of that would help. WOW! what a difference,I hardly have any pain any more,I also have osteoarthritis and scoliosis. Not saying I never have severe pain,I do once in a while. But I sure don't hurt like I use to and I don't even take all of that every day. After first I did,but then I started slacking off and it still helps. However,I also have diabetes so they gave me gabapentin for the numbness in my legs and pain. But now i ran out and can't afford to go back to the doctor,I get Cellulitis a lot have it now with a cut on the bottom of my foot. Happy when I turn 65 in June,so I can get medicare.
I have been sick like this for 11 years but I felt this way for most of my life. We lived in a apartment where you could smell gas all the time. I have often wondered if that had caused it.
I developed night vision issues with it but im not giving up !!! Thank you so much ... this is very inspiring... know that god knows every part of your pain yall he will never leave us n you dont get heal without actions ... change your diet... slowly start walking with the help of somene if u cant on your own... laugh have fun dont put deep negative thoughts into it .. that feeds it... n stay positive
I have the low grade fever and cold hands and feet, electrical jolts that could be anywhere in my body but this does not last long. My biggest issue is the burning kind of pain in my hips and my shoulder blades and left neck and severe insomnia. Ambien CR really helps me to go to sleep. But my doctor or any doctor they could not prescribe this for so long. If I have a choice , I will rather take this until I die at least I will not be in so much pain because the pain is worst when I can't sleep even just for 3 hours.
Aloha Peter, thank you so much for sharing your story and congratulations on your one day at a time victories. My PCP unfortunately also does not understand the suffering and pain that I’ve been experiencing for years and refuses to give me something for my anxiety and all this full body pain that actually works. I can so identify with you and your courageous struggles. Your story just made me almost (and maybe will) break down in tears. I’ve been sent from doctor to doctor to doctor and nothing has really helped. I’ve tried many holistic practitioners and diets and herbs and, and, and, to no avail. You are right, ”Acceptance is the Key.” It helps keep me somewhat sane but doesn’t take away the pain. I shall continue my search and push myself to try to exercise. I’m in my 70’s and just don’t know how much more of this I can take. Your story is both touching and inspiring 🥲💪🏼💜.
Sorry I do understand and I am only 39 . I have suffered for years fibromologia. It is like torture. My children and wonderful husband is what helps me.
You sound like me. Years and years,I've gone through this.😞 I have to tell everyone not to touch me,because my skin hurt. I couldn't explain why,and still can't,,until today.
My situation sounds exactly like his. Loss forty pounds. Pain in top of my thighs. Tingling hands and feet. Tired eyes. Brain fog. Going to Mayo in April.
Great to hear this, has anyone on thse pages had my peculier symptoms, i felt like i had the menopause again in minituire, im 62, they were vague menopause syptoms that stopped happening years ago, thats when i knew the ANS had some mixed messages going on
I had virtually all them but I had like a slicing knife feeling along both sides of my back. I did the same and watched a video about getting green vegetables everyday in a juice, I thought no point in not trying it after a few days the pains started easing. I still get pains but the difference is I can live without wanting to end it all
I’m bedbound with Fybro totally alone and in agony all the time. Three years since I left my house. Now I have cataracts in both eyes and can no longer read or drive or see details on screen etc. pretty sad state of affairs. I don’t know what to do anymore. This video is interesting, it nice to see someone recovering, though it seems you need a lot of money to get there. I have no money so I guess I’m stuck. I used to be a musician too with a fantastic life, four children and seven grandchildren, I had a great life. I want my life back. I fight depression and refuse to wallow but it’s a struggle. Help.
Sir , am also suffering of fibromyalgia at same time having also osteoporosis, hypothyriodism, chronic sever insonmia for 8yrs now ( am taking RIVOTRIL 1mg at bedtime without this i never fall to sleep - am taking this medicine 8yrs ago) and high blood my illness is so complicated thats why i need ur help theres a times that i can't tolerate the pain in body especially in my joints. Pls i want to join in ur group so that i can heal in my illness , in GOD help.
Omg I'm stuffing most of the symptoms Peter is talkin bout have fibromyalgia wish I have had for a few years which for the last 2 years has got worst to the point I have a wheelchair I live in England doctors don't seam to know alot bout this how can I get tested for this please help me ur's Kim.
It would have been nice if he had talked a bit more about his day to day life when severely ill and his family life. From his story I am going to guess he did not have to shop, cook or clean and could focus almost completely on recovery? I don't see how people do these programs and gradually increase exercise when they already have to exceed their limits on a daily basis just to take care the basics like eating and washing clothes.
Some people have a lot of support during recovery and some people have very little or none. If you look at people who try to simply 'gradually increase exercise', their success rates are pretty low. Most people tend experience a flare up from the activity sooner or later, no matter how gradually they increase. Having said that, physical activity can be very helpful, but not in isolation.
Hi James. I know how you feel. As a father and husband, I need every day to put a smile on my face, take care of my job, few hours a week. Deal with all the guilt, shame of being a half man. Dealing with fatigue, dizziness and brain fog. It is so hard dealing with, and the same time see life passing by you, and not really being able to participate in it
Oh, I understand about the taste of water being chemically. Yuck. I can even taste that chemical in lettuces, presumably because it is washed in the same water. I gave up eating lettuces unless I could soak it in my home filtered water.
Did you ever get worried it was ALS? My mom just passed of that and I have a lot of your symptoms plus tons of stiffness and pain in hands and feet. It’s horrible 😢 Thank you for your helpful video!
Just lost my.mum.to severe ms and that's what's been worrying me though clear MRI last time and just havi g another are you hypermobile we both have had heds and àspergers but my father had CFS now ok
Why express gratitude every day to people, praying 🙏 & giving Thanksgiving to God, read your Bible every day & get to know Him as a friend. He is the only person that can help you. I have had Lyme Disease since age 5, started being sexually abused at age 3, tested positive for Epstein Barr virus, Fibro, IBS, COLITIS, ETC. My symptoms are too many to list. I'm 77 now & am amazed that God has helped me through. Pain is off the scale & taking MS.
I'm going to be have a test to see how bad it's progressed..pain wise.. So I go for an MRI I hope the results will shows something so I can at least get. The Right meds.. Thank you for story.thankyoù...AnotaMaree from South Carolina
It's not a treatment Paulo - it's and education and training program. Current prices are on the website, but make sure you watch the 4 intro lessons before committing to the program! - ansrewire.com/enrol/ You can request the intro lessons in the 'learn more' tab!
so I have only been diagnosed as chronic pain irretractable pain and triangle something for my face my symptoms, let's start off I have a genetic disorder which I found by this whole nightmare so I was always happy never been depressed or had any problems great life very happy couldn't want for anything so happy 3 beautiful kids my husband sucks but I didn't know because he was just another child I took care of wasn't til I became broken that I realized how he was useless and such a problem to me but I never lingered on things ever a problem arise I solve it move on and keep going on January 23 2017 I was hit head on by a 85 yr old who took his son in laws car and was speeding he dropped his phone and went down to get it and hit me head on in my lane hit so hard my head hit the dash the seatbelt retracted ripping through my shoulder I went backwards so hard it broke the back of my chair I went through to the back seat the lap band of the seatbelt pulled on my hip hard my head went into my chest slamming my entire body weight of just under 200 which was all muscle my size was 12/14 lose and a tight 10 in some situations I could carry 100pounds of animal feed in one arm on my shoulder be able to use the other arm to open containers doors to then to rip open bag and fill containers I had strength I could carry all three kids we used to do late night fire drills use a fog machine red lights with sheets set up and close off differnt ways so they would know what to do I liked to be prepared and I could just pick up a heavy goat no biggie milked them 2 times a day I would pick them up carry put them on the milking table I was fit but this weight 16 times my weight first hitting the dash with face then head into chest slamming my neck into the back seat back hard knocked me out while I knew I had been in a car accident I woke up to a man standing over me he had my phone in his hand and when I opened my eyes I could see my credit cards up on my dash my windshield I had my money stuff in my center consel area they were thrown around and this man was over me with phone I Don't know why I was so confused I thought I was being robbed then this sweet older man maybe about 55 to 60 he came out his house to see my car there in his yard I was hit so hard the front was crushed and spun around and landed into the yard of a house on a cross street my car was flung basicly with the front end smashed in the airbags didn't go off and I'm still mad the insurance company my lawyer didn't go after the faulty airbag but I don't see what it could have done maybe stopping me from hitting so hard my head forward but I belive had it gone off I might have been stuck and died because I was left of the steering wheel when I hit and then of the side airbags I mean could be worse I have days I'm very glad I'm alive but it's hard when suffering so much but this caused so much pain as soon as I figured out I was alive not being robbed this man wanted to call my husband but I didn't know what the phone was I knew it was my phone but I didn't know what it was how to use it what the man was asking me I was just I don't know it was weird I knew it was my phone but I didn't know what a phone was if that makes sense so this man got my phone open and called my husband who didn't answer then called 911 and gave me the person and I was in so much pain it was like I couldn't find words the man gave her the address of where we were gave me my phone and he went to see the other car I belive I couldn't see him I just started shaking and I didn't know what was happening I was crying I kept saying my son my son she asked where he was I said I don't know she got ahold of my husband and he said he was at school and he was going to get him the messed up part is I asked him to before I left the house 1st time in 23 years did I ever ask him I was signing a contract took me 3 months to get done that was 3million had things worked out but I got nothing because I couldn't function I was broken next I know there is a crew pulling me out the back of the car on a board which was so horrible I was screaming in pain I was sure I broke my neck I was panicked that I wasn't going to walk again it was so bad my body just shivered I didn't know why and it was causing pain and they kept telling me it was normal I kept saying I need to throw up and they kept telling me I was ok I wasn't like they were arguing with me and forcing me not to the cop came over and wanted my keys and for some reason I didn't want to give them to him I was like no ur going to Robb me it's my car I didn't want to give them to him and he was like why can't u give me ur keys and I was arguing with him its my car not urs I have no idea what my brain was thinking it had its own thing going on and it wasn't with me at the time because I clearly know I was in the accident but at the same time I had no idea what was happening but I remember it all like it was yesterday so clear but making new memories is almost impossible it's so weird alot of stuff I have no idea like I know I get to hospital I don't know how we got there I remember being put in the vehical and being in the bed at the hospital but nothing in between at all I remember some lady coming up taking video of me and saying I can't belive u hit my dad and I said the empty black car hit me I was going to get my son then I started crying weres my son omg where is he then the cop said something to me and then got upset and then the ambulance guy was dressed like a women and she said it's OK we know what happened there were people who saw it all and he she yelled at the lady to stop harrassing me finally the she got the keys from me then I remembered being in the hospital and this dr grabbed my hand I was crying begging his to make the pain stop and he said I'm so sorry u have lung cancer and it's really bad an I just kept begging please I can't take the pain I'm going to throw up and then a nurse said something then my husband showed up with my crying son who had just came from the scene and my son was hugging me saying he loves me and the pain was so bad I started screaming just yelling screaming like a horror movie and my husband asked what was wrong and I said the pain I can't take the pain then he found out they didn't give me anything this whole time my son said the car was so bad he thought I was dead that blood was everywhere I don't know what was going on then the next thing I remember was like a years later going into surgerys like I was outside my body while inside it was weird really weird I couldn't speak for awhile I've seen videos but I have no memory of it at all but I wasn't able to speak communicate and I had like no movement abilities I wasn't able to walk use my left arm at all I've seen the videos of me just screaming in pain they tried alot of medication trying to find something to work but I had so many allergies to everything they gave me
so my symptoms are now I have these electric shocks that my face goes all blank on the one side like it dropped and this horrible pain of being electrocuted with this burning horrible sharp stabbing tingling pain, I have put on 100 pounds, I have food allergies wheat milk sugar from cane sugar shellfish all fish seafood some beef causes hives swelling of mouth tounge face entire body on fire hives that look like small pox all over my body redness like a sunburn sometimes vomiting hiccups the fish part causes anyphlactic shock only a epi pen can stop and hospital visit my Brian kind of shuts down I get confused alot no idea what's going on I feel exhausted but can't sleep I go 3 to 7 days without sleep all the time the most sleep I get is 20mins but then I can't move I'm so exhausted just can't move at all have problems opening my eyes feels like my left eye is being pushed out of my skull feels like I can't lift my head my muscles all gone I can't lift 5 pounds, pain in so many areas of my body I have gastritis so the hospital tells me I'm hungry but I can't eat then throw up when I do try to eat some sweating shaking vomiting is a constant everyday migraines that litterly cause my face to deform hurts from the not able to move my face it's horrible and happens daily I need help to walk I need help to talk i need help to get dressed I can't brush my hair I can't lift my left arm my body will swell for no reason won't be able to open my hand or hold things my entire left side is broken like I am allergic to so much latex foam glues pesticides on foods the tape from bandaids or the tape they use some plastics all kinds of things from swelling turning red hives extreme itch like on fire itch from hell that never stops no matter what I'm tired all the time but in so much pain I can't sleep lose vision all the time get stressed over not knowing what's going on when I get confused which is often and 2 times since started writing I can't tolerate the phone texts sounds light just so many things I just wish I would get better have a way to know what's going on so I could be come fixed I just wantto go around and find help to fix me or just lower the pain some the biggest problem is my husband uses it to his advantage I have no clue whats going on and I can't leave or get up without his help or get dressed and he has full control of my house he has trashed my house destroyed my kids my life no one comes to see me or asks how I am I think they just all forgot about me I have major tummy issues all the time I just want sleep so badly 😢 more then most things but
Pls Peter,u don't mention if u have gained your weight back now,have u? Because I also have experienced tremendous weight loss,i would like to know if u gained your lost pounds back?
CFS Unravelled thanks a lot for replying,it means so much to me. I asked because I am also a naturally slim person but I have become skin and bones,thank u.
Oh man!! I’m sorry. I have a 2 yr old baby and my biggest fear she has all the genetic markers for this hell disease. Do you know what triggered yours and hers? I hope it gets better for you both.
I have no idea if you will get this reply since it has been 2 yrs. I just have to say, you KNOWING it's cause is ALWAYS and ONLY PSYCHOLOGICAL STRESS. I DONT HAVE ENERGY TO DANCE AROUND THE ISSUE. YOU ARE TOTALLY IGNORANT. AND YOU ARE HURTING PEOPLE WHO ARE LEGITIMATELY ILL.
Why this disturbing, disgusting and distracting music . Fibromyalgia sufferers need remedy but not the dirty music. Please delit dirty music viewers want to hear the remedies in calm atmosphere.
First step may be to watch the 4 free intro lessons and then check out the FAQ's. If you still have questions, you can post under the relevant lesson or contact me via the ANS REWIRE website.
I got through the worst of my illness by surrendering to it. Accepting I wasn’t a head case as my GP suggested. I got worse before I got better, but I was put in touch with MIND a charity for mental health of all sorts. Through them, I began to recognise my triggers, which were mostly stress induced. Another GP temporarily put me on anti-depressants, which helped me to reset myself mentally and physically. I came off the prescription early because I didn’t want to become addicted. I started dieting and gradually became a bit more alert, lost weight, less pain. I've piled on the weight again, particularly due to lockdowns, so I’m battling with myself again. I’m 60 next week and first noticed fibromyalgia in my early 40s. Every activity I do, I feel dread, but congratulate myself when I achieve something, like hoovering, cutting the grass, being on top of the laundry, etc. Simple things I couldn’t do, but I get through it now.
I’m glad you found some relief. As I read about the time you got it was the same for me. I was in my 40’s and thought I had arthritis because achy joints, chronic fatigue, very sensitive to moisture, and humidity was difficult but winters were the worst. I turn 60 in September and my husband and I built a home in Albuquerque and moved from Iowa. The difference in New Mexico weather is it’s very dry which has helped me immensely. I have a flare every time it’s going to rain. Mine is the day before and day of. I had to have a knee replacement almost 3 years ago in Iowa and it’s a matter of time for my left knee. I own an insurance agency and love it. It helps with feelings of youth. I’m active but I will say by Friday I’m so tired. I make myself go out with my husband on Saturday nights. We go out to dinner and I enjoy a few cocktails but don’t drink much. I just do what I can and if I need rest I rest.
Literally you are describing my symptoms
I can smell and irritated by a cigarette that is 100 m away of me.
It feels so great to listen to peoples stories that i can relate to. It helps with the loneliness and legitimacy of it all. 😊 Thanks for sharing.
Well Done Peter and may your life get better and better!!
Peter you are an inspiration. I am sorry for the childhood trauma you had to endure.
Thank you so much, Peter, for sharing your story and thank you, Dan, for putting up these success stories. Most inspiring.
Glad you uploaded the full interview as it was very inspiring. So happy for Peter
Thanks for your comment - Peter is amazing and his CFS recovery (Fibromyalgia recovery) is truly inspiring. I am always uplifted whenever we have contact. :)
Peter and Dan thank you so much for offering hope, encouragement and inspiration. Peter I am thrilled for you and so happy to hear how your life is now indeed full and blossoming. Dan I listen to your talks every morning...soon to run out but like Peter will re-listen. Your generous and caring spirit for this community of people is so noble, beautiful and of huge need and great importance. Love and peace to you both and all who listen. I wish you well. Tara xx
Hi Tara - glad you enjoyed Peter's recovery story and that you are listening to all the recovery interviews. There are lot's more to come - hope to get many more published in the coming months. Hope to share your story one day soon! :)
Very happy for this guy but trying to understand this: He's been sick for 11 years, bed-bound and suicidal for 2 years, has tried literally everything and gone into thousands upon thousands of dollars worth of debt trying to get better, and when he finds this program and recovers 80% in 6 months, 110% in 12 months, he considers that "slow." If I made that kind of progress after all of that, I would call every single medical professional and tell them a miracle just occurred. That is BEYOND my greatest expectations by a factor of ten billion. Absolutely insane to call that slow.
Yes, when you put it in perspective like that, it's still a fast recovery isn't it. But I think people always look to get quick feedback to see if something is working, and when the changes come slowly, they often don't persist. Thanks for sharing your thoughts!
why would you call ''medical professionals''? they dont make money from healthy people. The pharmaceutical murdering industry is a multi TRILLION dollar/year business, do you think they want to lose that money? How old are you? 4?
@@incorectulpolitic This is one of the biggest red pills out there.
Med pro are there to make MONEY. Not HELP PEOPLE.
Sick people = Oh I am sick I need to be fixed let me go see med pro they studied for years surely they can help me.
Sadly no. Fixed person = no more money.
So happy for you and Ty _ I’m recommitting to rewiring as I’m seeing the first embers of real progress
I couldn’t get an appointment with my doctor in the UK, when I did, he told me it was all in my head!
I’m in Hertfordshire, UK. My husband has literary just come back from his 2nd doctor appt and exactly that was intimated . The doctor just said half heartedly ‘well what do you want from this’. Gave no real recommendation. They hated that my husband was giving his Google diagnosis.
It gives so sosooooo much hope!!!
Most wonderful to hear this inspiring healing journey! Thank you
Glad it inspired you!
Glad it inspired you!
I too get the electrical buzzing and vibrating that comes and goes. Thank you Peter. Meditation helps me a lot too.
Hello I just listing to your recovery story
I thank God for you you so much to be thankful for amen
This was really inspiring! 1 hour well spent. Really happy for you 😊
Truly a monumental triumph. Thank you both for your inspirational stories
I am mother of 3. A baby and two toddlers. I have severe fibromologia and so thankful to hear others stories. I come through abuse as a child. When I had my second baby another csection I hit rock bottom. I had severe pain every where and awful headaches. I am trying to work with diet and gentle exercise. I am doing different coping techniques because I have major triggers
My daughter started to experience almost all of this symptoms with the exception of weight loss,when she was only ten years old. She's now 15 and has been diagnosed with fibromyalgia! It's a very scary world please help!!!
same
Tms Dr sarno
Prayers for your daughter
@@Truerealism747 def Dr Sarno
OMG, I've experienced sensitivities to cigarette smoke for decades. If I breath in just a whiff, I get really ill with cold/flu symptoms. I sometimes taste the chemicals in water. Just making a sandwich triggered so much pain, that I couldn’t use my hands for a day at least. My muscles tone was that of an athlete at a time when I couldn’t get up the stairs, I was in so much pain. I was so useless, I couldn’t stay awake to listen to my children read. I literally wanted to die. I contemplated suicide, but wasn’t suicidal. I played the scenarios out in my head as I lay on the sofa alone and for hours. The house needed cleaning, the dogs needed walking, my children needed feeding, taking to school and being picked up. I sometimes had to ask a friend if she would collect them after my husband dropped them off. I felt like an utter burden too. I still do at times. I dread the suggestion of visiting places or holidays, days out. They trigger a great deal of anxiety for me. Trying to stay awake, trying to experience the moment, battling pain, organising it all. Then I don’t remember where we have been or what we did. The kids take photos, but don’t share them. They don’t understand why the photos are so important to me. They help me to remember glimpses of our time together. When I'm really tired my speech slurs and I lose what I'm saying mid sentence.
Yup sounds alot like that I have,
I have chronic fatigue and fibro diagnosis too on my record. They walked out on me too.
I even changed my diet to no sugar and low carb.
No nausea, but memory is bad, yes on the electrical jolts, yes, horrible sleepy fatigue, ALL the time, im on depression meds high vitamin D. i am an artist and I have had hand surgery, I can not open a jar or bottle, its horrible. I have mold allergies, grass, golden rod, raw eggs, cows, but it has lessened since my cancer. No cancer now.. I cant stand those smells either and cigars are bad too to smell.
Yes, my treatments morphed too, I had, its gone down now but I had bad vertigo. Yes on no circulation in hands and feet, joints, shoulders hips ankles toes fingers all bad. When I was in 6th grade I played tennis, everything wore me out. These days I can only do one activity a day.
I will not swallow a camera. Like I said, I changed my diet, found out drinking cleansing drinks with lemon, apple cider vinegar, garlic, vit. B, A, E, honey, krill oil, macha tea and chaga drops, since I started that, some of the symptoms lessoned, The weather effects me huge!!
Ya, I did all that, I memorized my fibro folder hand outs from the doc and even did the exercises. nothing helped. Ohhhh I know the hard to get to the store thing!!! the vibrating is horrible but it dont last for mem comes and goes. I will try yoga.
Rather than trying one thing or another, see if you can build up a comprehensive set of strategies like Peter and others do. Have you seen the ANS REWIRE intro lessons? They explain why this is key!
@@CFSUnravelled1 thanks I will!!
Tai chi works best for me! Gentle, mild stretching and slow movements loosen up my tight spasming muscles without triggering more painful spasms. Feels like I had a wonderful massage plus meditation...😊
Ive never heard anyone describe the electric jolt thing before! I tried to explain to people how i often felt electric jolt exactly like touching the metal side or screws of electrical outlet box. People look at me like im crazy. Also have ibs symptoms and extreme fatigue. Thank you for the leads on what may really be the problem.
I always get electric jolt while closing my car's door.
I was getting those plus,I started seeing things. So I started taking vitamin D3,Hemp seed oil and DHEA to see if any of that would help. WOW! what a difference,I hardly have any pain any more,I also have osteoarthritis and scoliosis. Not saying I never have severe pain,I do once in a while. But I sure don't hurt like I use to and I don't even take all of that every day. After first I did,but then I started slacking off and it still helps. However,I also have diabetes so they gave me gabapentin for the numbness in my legs and pain. But now i ran out and can't afford to go back to the doctor,I get Cellulitis a lot have it now with a cut on the bottom of my foot. Happy when I turn 65 in June,so I can get medicare.
That is s anxiety symptom it's on the anxiety pages
I’ve never heard anyone say it either. I’ve been telling my doctors I feel like an electric current running through my body non stop.
It's like you're being charge up
I had like restless leg syndrome feeling throughout my whole body.
You are NOT alone. I truly get the agony. I have full body Severe RLS. TORTURE.
Sending courage.
Happens with me also ....
I have been sick like this for 11 years but I felt this way for most of my life. We lived in a apartment where you could smell gas all the time. I have often wondered if that had caused it.
Are you hypermobile
I developed night vision issues with it but im not giving up !!! Thank you so much ... this is very inspiring... know that god knows every part of your pain yall he will never leave us n you dont get heal without actions ... change your diet... slowly start walking with the help of somene if u cant on your own... laugh have fun dont put deep negative thoughts into it .. that feeds it... n stay positive
❤️thank you!
I have the low grade fever and cold hands and feet, electrical jolts that could be anywhere in my body but this does not last long. My biggest issue is the burning kind of pain in my hips and my shoulder blades and left neck and severe insomnia. Ambien CR really helps me to go to sleep. But my doctor or any doctor they could not prescribe this for so long. If I have a choice , I will rather take this until I die at least I will not be in so much pain because the pain is worst when I can't sleep even just for 3 hours.
Aloha Peter, thank you so much for sharing your story and congratulations on your one day at a time victories. My PCP unfortunately also does not understand the suffering and pain that I’ve been experiencing for years and refuses to give me something for my anxiety and all this full body pain that actually works. I can so identify with you and your courageous struggles. Your story just made me almost (and maybe will) break down in tears. I’ve been sent from doctor to doctor to doctor and nothing has really helped. I’ve tried many holistic practitioners and diets and herbs and, and, and, to no avail. You are right, ”Acceptance is the Key.” It helps keep me somewhat sane but doesn’t take away the pain. I shall continue my search and push myself to try to exercise. I’m in my 70’s and just don’t know how much more of this I can take. Your story is both touching and inspiring 🥲💪🏼💜.
Sorry I do understand and I am only 39 . I have suffered for years fibromologia. It is like torture. My children and wonderful husband is what helps me.
You sound like me. Years and years,I've gone through this.😞 I have to tell everyone not to touch me,because my skin hurt. I couldn't explain why,and still can't,,until today.
My situation sounds exactly like his. Loss forty pounds. Pain in top of my thighs. Tingling hands and feet. Tired eyes. Brain fog. Going to Mayo in April.
Well done Peter ❤
Getting rid of my mercury fillings helped my gums not to bleed as much.
I get the weird taste thing as well,and the sensitivity to smells.
Great to hear this, has anyone on thse pages had my peculier symptoms, i felt like i had the menopause again in minituire, im 62, they were vague menopause syptoms that stopped happening years ago, thats when i knew the ANS had some mixed messages going on
thank you for this
I had virtually all them but I had like a slicing knife feeling along both sides of my back. I did the same and watched a video about getting green vegetables everyday in a juice, I thought no point in not trying it after a few days the pains started easing. I still get pains but the difference is I can live without wanting to end it all
I’m bedbound with Fybro totally alone and in agony all the time. Three years since I left my house. Now I have cataracts in both eyes and can no longer read or drive or see details on screen etc. pretty sad state of affairs. I don’t know what to do anymore. This video is interesting, it nice to see someone recovering, though it seems you need a lot of money to get there. I have no money so I guess I’m stuck. I used to be a musician too with a fantastic life, four children and seven grandchildren, I had a great life. I want my life back. I fight depression and refuse to wallow but it’s a struggle. Help.
I'm so sorry and feel the same.
How are you now take a look at Dr lenz ling term suffer here
Sir , am also suffering of fibromyalgia at same time having also osteoporosis, hypothyriodism, chronic sever insonmia for 8yrs now ( am taking RIVOTRIL 1mg at bedtime without this i never fall to sleep - am taking this medicine 8yrs ago)
and high blood my illness is so complicated thats why i need ur help theres a times that i can't tolerate the pain in body especially in my joints. Pls i want to join in ur group so that i can heal in my illness , in GOD help.
Thankyou Peter. For the hope. Can I contact you please. 🥰that you recovered. Been mostly bed bound. Too xx
Omg I'm stuffing most of the symptoms Peter is talkin bout have fibromyalgia wish I have had for a few years which for the last 2 years has got worst to the point I have a wheelchair I live in England doctors don't seam to know alot bout this how can I get tested for this please help me ur's Kim.
It would have been nice if he had talked a bit more about his day to day life when severely ill and his family life. From his story I am going to guess he did not have to shop, cook or clean and could focus almost completely on recovery? I don't see how people do these programs and gradually increase exercise when they already have to exceed their limits on a daily basis just to take care the basics like eating and washing clothes.
Some people have a lot of support during recovery and some people have very little or none. If you look at people who try to simply 'gradually increase exercise', their success rates are pretty low. Most people tend experience a flare up from the activity sooner or later, no matter how gradually they increase. Having said that, physical activity can be very helpful, but not in isolation.
Hi James. I know how you feel. As a father and husband, I need every day to put a smile on my face, take care of my job, few hours a week. Deal with all the guilt, shame of being a half man. Dealing with fatigue, dizziness and brain fog. It is so hard dealing with, and the same time see life passing by you, and not really being able to participate in it
Oh, I understand about the taste of water being chemically. Yuck. I can even taste that chemical in lettuces, presumably because it is washed in the same water. I gave up eating lettuces unless I could soak it in my home filtered water.
Did you ever get worried it was ALS? My mom just passed of that and I have a lot of your symptoms plus tons of stiffness and pain in hands and feet. It’s horrible 😢
Thank you for your helpful video!
Just lost my.mum.to severe ms and that's what's been worrying me though clear MRI last time and just havi g another are you hypermobile we both have had heds and àspergers but my father had CFS now ok
Why express gratitude every day to people, praying 🙏 & giving Thanksgiving to God, read your Bible every day & get to know Him as a friend. He is the only person that can help you. I have had Lyme Disease since age 5, started being sexually abused at age 3, tested positive for Epstein Barr virus, Fibro, IBS, COLITIS, ETC. My symptoms are too many to list. I'm 77 now & am amazed that God has helped me through. Pain is off the scale & taking MS.
Is the Lyme still active or has it gone how does one no.are you hypermobile?
Inspiring
I'm going to be have a test to see how bad it's progressed..pain wise.. So I go for an MRI
I hope the results will shows something so I can at least get. The Right meds.. Thank you for story.thankyoù...AnotaMaree from South Carolina
Anything in mri
Had fibro for a year, will it take 11 years to progress before I get better or because I’m aware of it will I be able to start recovering now
What's mcs
pls help me how can i contact u
You can access more resources at cfsunravelled.com and ansrewire.com
Can small nerve fiber peripheral neuropathy be over come, I also have fibro and cfs
How are you now?
I suffer fybro good luck my love 💐
My skin itches always and looks as if I have spots.O I have some good days mostly bad...
how much is this treatment?
It's not a treatment Paulo - it's and education and training program. Current prices are on the website, but make sure you watch the 4 intro lessons before committing to the program! - ansrewire.com/enrol/ You can request the intro lessons in the 'learn more' tab!
@@CFSUnravelled1 Page currently not loading..
Thanks for letting me know. Sorry about that - it looks like it's working now.
That could be me crazy!!
Time sick for me,is 30 plus years.
Antibiotics overuse? Maybe ciproflixacim?
so I have only been diagnosed as chronic pain irretractable pain and triangle something for my face my symptoms, let's start off I have a genetic disorder which I found by this whole nightmare so I was always happy never been depressed or had any problems great life very happy couldn't want for anything so happy 3 beautiful kids my husband sucks but I didn't know because he was just another child I took care of wasn't til I became broken that I realized how he was useless and such a problem to me but I never lingered on things ever a problem arise I solve it move on and keep going on January 23 2017 I was hit head on by a 85 yr old who took his son in laws car and was speeding he dropped his phone and went down to get it and hit me head on in my lane hit so hard my head hit the dash the seatbelt retracted ripping through my shoulder I went backwards so hard it broke the back of my chair I went through to the back seat the lap band of the seatbelt pulled on my hip hard my head went into my chest slamming my entire body weight of just under 200 which was all muscle my size was 12/14 lose and a tight 10 in some situations I could carry 100pounds of animal feed in one arm on my shoulder be able to use the other arm to open containers doors to then to rip open bag and fill containers I had strength I could carry all three kids we used to do late night fire drills use a fog machine red lights with sheets set up and close off differnt ways so they would know what to do I liked to be prepared and I could just pick up a heavy goat no biggie milked them 2 times a day I would pick them up carry put them on the milking table I was fit but this weight 16 times my weight first hitting the dash with face then head into chest slamming my neck into the back seat back hard knocked me out while I knew I had been in a car accident I woke up to a man standing over me he had my phone in his hand and when I opened my eyes I could see my credit cards up on my dash my windshield I had my money stuff in my center consel area they were thrown around and this man was over me with phone I Don't know why I was so confused I thought I was being robbed then this sweet older man maybe about 55 to 60 he came out his house to see my car there in his yard I was hit so hard the front was crushed and spun around and landed into the yard of a house on a cross street my car was flung basicly with the front end smashed in the airbags didn't go off and I'm still mad the insurance company my lawyer didn't go after the faulty airbag but I don't see what it could have done maybe stopping me from hitting so hard my head forward but I belive had it gone off I might have been stuck and died because I was left of the steering wheel when I hit and then of the side airbags I mean could be worse I have days I'm very glad I'm alive but it's hard when suffering so much but this caused so much pain as soon as I figured out I was alive not being robbed this man wanted to call my husband but I didn't know what the phone was I knew it was my phone but I didn't know what it was how to use it what the man was asking me I was just I don't know it was weird I knew it was my phone but I didn't know what a phone was if that makes sense so this man got my phone open and called my husband who didn't answer then called 911 and gave me the person and I was in so much pain it was like I couldn't find words the man gave her the address of where we were gave me my phone and he went to see the other car I belive I couldn't see him I just started shaking and I didn't know what was happening I was crying I kept saying my son my son she asked where he was I said I don't know she got ahold of my husband and he said he was at school and he was going to get him the messed up part is I asked him to before I left the house 1st time in 23 years did I ever ask him I was signing a contract took me 3 months to get done that was 3million had things worked out but I got nothing because I couldn't function I was broken next I know there is a crew pulling me out the back of the car on a board which was so horrible I was screaming in pain I was sure I broke my neck I was panicked that I wasn't going to walk again it was so bad my body just shivered I didn't know why and it was causing pain and they kept telling me it was normal I kept saying I need to throw up and they kept telling me I was ok I wasn't like they were arguing with me and forcing me not to the cop came over and wanted my keys and for some reason I didn't want to give them to him I was like no ur going to Robb me it's my car I didn't want to give them to him and he was like why can't u give me ur keys and I was arguing with him its my car not urs I have no idea what my brain was thinking it had its own thing going on and it wasn't with me at the time because I clearly know I was in the accident but at the same time I had no idea what was happening but I remember it all like it was yesterday so clear but making new memories is almost impossible it's so weird alot of stuff I have no idea like I know I get to hospital I don't know how we got there I remember being put in the vehical and being in the bed at the hospital but nothing in between at all I remember some lady coming up taking video of me and saying I can't belive u hit my dad and I said the empty black car hit me I was going to get my son then I started crying weres my son omg where is he then the cop said something to me and then got upset and then the ambulance guy was dressed like a women and she said it's OK we know what happened there were people who saw it all and he she yelled at the lady to stop harrassing me finally the she got the keys from me then I remembered being in the hospital and this dr grabbed my hand I was crying begging his to make the pain stop and he said I'm so sorry u have lung cancer and it's really bad an I just kept begging please I can't take the pain I'm going to throw up and then a nurse said something then my husband showed up with my crying son who had just came from the scene and my son was hugging me saying he loves me and the pain was so bad I started screaming just yelling screaming like a horror movie and my husband asked what was wrong and I said the pain I can't take the pain then he found out they didn't give me anything this whole time my son said the car was so bad he thought I was dead that blood was everywhere I don't know what was going on then the next thing I remember was like a years later going into surgerys like I was outside my body while inside it was weird really weird I couldn't speak for awhile I've seen videos but I have no memory of it at all but I wasn't able to speak communicate and I had like no movement abilities I wasn't able to walk use my left arm at all I've seen the videos of me just screaming in pain they tried alot of medication trying to find something to work but I had so many allergies to everything they gave me
so my symptoms are now I have these electric shocks that my face goes all blank on the one side like it dropped and this horrible pain of being electrocuted with this burning horrible sharp stabbing tingling pain, I have put on 100 pounds, I have food allergies wheat milk sugar from cane sugar shellfish all fish seafood some beef causes hives swelling of mouth tounge face entire body on fire hives that look like small pox all over my body redness like a sunburn sometimes vomiting hiccups the fish part causes anyphlactic shock only a epi pen can stop and hospital visit my Brian kind of shuts down I get confused alot no idea what's going on I feel exhausted but can't sleep I go 3 to 7 days without sleep all the time the most sleep I get is 20mins but then I can't move I'm so exhausted just can't move at all have problems opening my eyes feels like my left eye is being pushed out of my skull feels like I can't lift my head my muscles all gone I can't lift 5 pounds, pain in so many areas of my body I have gastritis so the hospital tells me I'm hungry but I can't eat then throw up when I do try to eat some sweating shaking vomiting is a constant everyday migraines that litterly cause my face to deform hurts from the not able to move my face it's horrible and happens daily I need help to walk I need help to talk i need help to get dressed I can't brush my hair I can't lift my left arm my body will swell for no reason won't be able to open my hand or hold things my entire left side is broken like I am allergic to so much latex foam glues pesticides on foods the tape from bandaids or the tape they use some plastics all kinds of things from swelling turning red hives extreme itch like on fire itch from hell that never stops no matter what I'm tired all the time but in so much pain I can't sleep lose vision all the time get stressed over not knowing what's going on when I get confused which is often and 2 times since started writing I can't tolerate the phone texts sounds light just so many things I just wish I would get better have a way to know what's going on so I could be come fixed I just wantto go around and find help to fix me or just lower the pain some the biggest problem is my husband uses it to his advantage I have no clue whats going on and I can't leave or get up without his help or get dressed and he has full control of my house he has trashed my house destroyed my kids my life no one comes to see me or asks how I am I think they just all forgot about me I have major tummy issues all the time I just want sleep so badly 😢 more then most things but
Pls Peter,u don't mention if u have gained your weight back now,have u? Because I also have experienced tremendous weight loss,i would like to know if u gained your lost pounds back?
Yes, Peter did regain weight, but as you can see from the video, he is a naturally slim person.
CFS Unravelled thanks a lot for replying,it means so much to me. I asked because I am also a naturally slim person but I have become skin and bones,thank u.
Well my comment didn't post 😢
That's frustrating! Not sure what happened - can you search for it?
I also want a chance 😔
Go for it. Seek progress not perfection - make your recovery efforts feel good.
I’ve been mostly bedridden for 5 years and now my daughter has this crap
Oh man!! I’m sorry. I have a 2 yr old baby and my biggest fear she has all the genetic markers for this hell disease. Do you know what triggered yours and hers? I hope it gets better for you both.
Your symptoms also sound like MS
Which symptoms just lost my.mum to severe ms I have CFS fybromyalgia heds
The cause is always and only psychological stress
Anxiety subconscious.
I have no idea if you will get this reply since it has been 2 yrs. I just have to say, you KNOWING it's cause is ALWAYS and ONLY PSYCHOLOGICAL STRESS.
I DONT HAVE ENERGY TO DANCE AROUND THE ISSUE.
YOU ARE TOTALLY IGNORANT. AND YOU ARE HURTING PEOPLE WHO ARE LEGITIMATELY ILL.
Nonsense
@@a13xdunlop no it’s not nonsense Karen
Stress has nothing to do with this
Why so much music in the beginning of the video .what is the use such dirty music for viewers..can stop or delete such disturbing music.
Quit your petty complaining.
Stop whining the music is fine.
You need help mentally. Seek a therapist.
Why this disturbing, disgusting and distracting music . Fibromyalgia sufferers need remedy but not the dirty music. Please delit dirty music viewers want to hear the remedies in calm atmosphere.
Wow you had to complain with 2 comments about DIRTY music. What the hell is Dirty music??
You need help mentally. Seek a therapist.
Hi Dan,
is it possible to contact you personally to ask you some questions?
E.g. via Facebook Messenger....
First step may be to watch the 4 free intro lessons and then check out the FAQ's. If you still have questions, you can post under the relevant lesson or contact me via the ANS REWIRE website.