Part 3 - Fibromyalgia: New Insights, New Hopes

[@donnaleblanc1288]

This validates me on so many levels. I''m not crazy, I'm sick. And people like him that are trying to research Fibromyalgia, give me hope to cling to. Some days my cognitive function is so bad I say nothing, because if I do, it will come out jumbled anyway. I'm just so glad that at least some dr's are listening and finally trying to "get it".

[@pattipacer7869]

Dr. Wood, finally an explanation about Fibromyalgia that makes sense. Thank you for all of the research you have done.

[@giantsfan562001]

My neck is horrible Im seeing a nero on April 8th .Im a little confused about the meds as Im sensitive to most ..Percoset 7.5 works best for me helps me get everything I need done without crying myself to what sleep I do get... but finding a Dr to prescribe it is a diff story sence its very popular on the street..Cant they find something elce to sell and abuse and leave the meds that help people alone!

[@marilynmasonis376]

I do believe, this doctor is the closest to understanding the cause, or causes of fibromyalgia, and severe chronic pain conditions in itself. I am a 21 year sufferer of constant severe pain, from a serious injury to my neck and back, after a serious car accident where I sustained a very severe cervical whiplash, and back injury on a 55 mph road where I was rear-ended severely, at a complete stop, waiting to turn left. All aspects of my life has never been the same. I lost so very much of my abilities, and so very much of my life. I finally won my disability, less than 2 years ago. I initially was diagnosed with a cervical whiplash, cervical and lumbar strain/sprain, herniated/bulging discs throughout both cervical/lumbar spine, osteoarthritis, a very high ANA, (chronic inflammation, autoimmune disease), costocondritis, asthma, copd, chronic myofascial pain, fibromyalgia, anxiety/depression. I also had a failed neck surgery in 2006, which left me in worse condition. I have been researching my severe chronic pain conditions for more than 21 years, trying to do anything and everything I can to educate myself, and help myself. I truly believe it all stems it starts in the cervical spinal column/spinal cord/discs/nerves, etc. I also do believe there may be more than 1 cause of fibromyalgia. As this very good doctor suggests. I so very much appreciate this good doctors interest, education, and passion, in trying to get to the bottom of this extremely disabling, painful, and life changing condition. Good work doctor! I am confident our future generations suffers will benefit from all your hard work and intelligence. I'm truly grateful for all your hard work and compassion. Keep listening to your patients. As a team, together we will fight, and educate each other, and eventually overcome this beast. ~I Thank You ~Much Love & Appreciation for your Support Doctor ~Marilyn 💜

[@nobsnoargue4126]

Found him...again.

[@sacredgeometry2344]

Im so sorry for your pain 😖🙏💙🙌💙 I hope you get better. There are many causes for fibromyalgia. Neck injuries Epstein-Barr Lyme's disease mycoplasma can burn your nervous system I believe these actions bring it on guess the neck injury because they attack the central nervous system. All of them involve the neck it seems. Remind flare up my neck really Hurts so I know thats the infections in it

[@marymcsherry1965]

I developed fibromyalgia after 3 years of excruciating pain from disc injury at c5 - c6. Was completely healthy before that. I hope this Dr continues with his really helpful research

[@honerdcouster8723]

Hi sweetie at least he's trying.Fact.. Doctors never look up spinal cysts. Fm. Is tarlov cyst disease period. Can be seen on imaging but doctors don't know the proper MRI technique to detect the most consequential spinal cyst in the sacrum. If this message finds you. Your gonna get much better. Jordan

[@chrissiehampton2444]

Me too. Mine was a horse riding injury. Whiplash to head/neck and shoulders as well as lower spine.

[@Luv2bfshn]

Making an appt to see my Rheumy today! My neck is also damaged. Blessings to you Doc, I'll be watching for you! Thanks for a brighter future!

[@scnordstrom420]

Thank you for this Doctor. I have Fibro and EXTREME neck pain and have for MANY years!!!!!!!!!!!!!!!!!!!!!!!!!!!! I always have pain and it feels like I cant breath, I get heartburn, headaches, and cant swallow when my neck is in pain. I have to massage it and lay down and try to straighten it... Sometimes it gets less painful.

[@charlapresley1274]

IT IS MY PRAYERS THAT SOMETHING WONDERFUL WILL COME OUT OF ALL THIS...

[@mindfulblessings5202]

I didn't have any issues with health ( including fibromyalgia, myofascial syndrome, chronic pain syndome, etc.) until a few months after my car accident. I was hit by a drunk driver on my way home from work. I was sitting at a stop light on the highway, she said she didn't see my car or the stop light. She hit me 65 miles an hour....so I do believe that is what all the issues came from.

[@sridmn1275]

Goosebumps when he said the future is bright! I hope you find success with your research because Fibro is something which most of the Doc's here don't even know about.

[@marymastandrea2640]

Been waiting since 1992 for somebody to come up with an answer a doctor I could actually see that could help me

[@holly0297]

Find a caring rheumatologist. If he/she doesn't seem to listen or want to help you, keep looking until you find the right fit. Having FMS means having a close relationship w/your doctor. It is an ever-changing and frustrating illness, so your doctor should be patient, understanding, and helpful. Most importantly, he should believe you and that it's not your fault. I've had some bad ones, and that's just another stressor leading to even more pain and illness. Good luck!!

[@Travelwise65]

Interesting. I was diagnosed with FM in 1982, long before most doctors had heard of it. I've been on a long downward slide since. Three years ago I was told that I had hypothyroid (related to low iron intake). Last year I was in a severe car accident and had an MRI taken of my neck-which showed rather advanced spinal stenosis which is pinching my spinal cord 24/7, but most severely when I work at my desk, which I do 60+ hours a week. Time to see a new specialist!

[@dianaboughner7977]

Thank you for all of this research and validation of the "fibro monster." Now I know why I get so dizzy when I look up. I have multiple chemical sensitivities and pills are sometimes necessary for the pain but leave me feeling more ill than the daily fibro. Cannabis really helps but the cost is prohibitive (pun intended) and the synthetic version is a chemical nightmare. Exercise, diet, stress reduction, and "balance" in everything are keys to a less painful life but there is always pain to deal with and a change in barometric pressure is a guaranty to a pain flare. Hopefully, a cure will be found sooner than later as more and more people are getting this painful and complicated syndrome.

[@vihaanjaxxon218]

I know I'm kind of off topic but do anyone know of a good site to stream new series online ?

[@boonerowen8127]

@Vihaan Jaxxon flixportal :P

[@vihaanjaxxon218]

@Boone Rowen Thank you, I went there and it seems to work =) I appreciate it!

[@boonerowen8127]

@Vihaan Jaxxon Happy to help xD

[@curryindustriesltd.2311]

Thank you for the extremely informative presentations. When I see my doc next week I'll be better informed to talk to her about my FM. It's been so frustrating to be dumped by one doc and then see a new one that is just as indifferent. I have a degree in psychology with a particular interest in brain funtion, so this all makes a lot of sense to me.

[@ArmoredSt]

God love u. I have it as well and can't get the real help I need because of the same thing. I am praying for u, I am prayin for us all.

[@Defiantwonder]

I want to thank you so much for sharing this with Me, and the many I know with Fibromyalgia.. Love learning more and understanding more about what is going on for me.

[@lorrainecameron578]

Thank you so much for the work you have done, I have Fibromyalgia and Joint hypermobilty, tyroid troubles, I am also worse when hormones change to point I know when I will be floored, iron has always been low, and when the dislocated, shoulder knee, hip toes and fingers, the pain in my back, and neck, I cant move, at all and house bound. This has opened new doors for me. Thank you for asking why and doing something about it. What hope this is given when there has been none THANK YOU !!!

[@KidCity1985]

It's interesting to look back at these old theories.

[@gaynergladwin993]

thanks so much for this... as a fibro sufferer.. my neck has been horrendous ... it is definitely a huge (long term) symptom of fm for me.. as is anaemia (iron deficiency) but the docs said it wasn't 'normal' type of anaemia.. that my cells were behaving strangely.. this is chronic but became dangerously serious a few years back..

[@kimworthem3914]

OMG, Finally something and someone that makes sense. Have had many many neck problems for years. Thank you

[@leannes.9859]

My husband just thinks this is all in my head and I need to just toughen up. I live in constant pain every single day of my life. I have no family...no support...I just really feel like taking my life some days.

[@batemanhornecenter]

L.S We stand beside you. The isolation these illnesses, Fibromyalgia and ME/CFS typically come with are debilitating and often insult to injury. We are working on mainstreaming these illnesses within the medical community and that often is paired with advocacy. You will be happy to hear that most physicians we speak with these days are no longer in denial that these diseases are real. They know that they are. This was a critical step, because now the real work of research discovery can begin. Bateman Horne Center would like to help you anyway we can. This coming weekend there is an ME Action Support Group for Caregivers call. He may not be quite ready for that, but if you are interested, I'd like to work with you to help your family understand and validate your need for help. If you have the ability, please reach out to me at [e-mail].

[@MM1902KB]

Hi Lea, I am so very sorry to hear the way your husband thinks. That is so sad and wrong. The pain is bad enough, (and believe me I understand, because I too have fibro). Having the person that is suppose to be closes to you treat you this way, is just all kinds of wrong. You wrote your post a year ago, so I truly hope things have improved for you by now. I know this next sentence may sound harsh, but maybe a good start in your healing process would be looking for a new partner. Your husbands lack of caring and sympathy is shameful and should be unacceptable.

[@Ethericrose]

​@Miss Myrtle's Haven I agree, yet it is difficult to just up root, especially if there are children involved. No one believed me at first, even now I believe they (family) think I'm exaggerating my pain. My son will say, mom? If you were in that amount of pain you would be rushing to the hospital. I've learned not to talk about it, people get fed up of hearing I'm in chronic pain all the time. I also take each day as it comes and no longer feel guilty for simply taking care of my needs. I try to be gently proactive one day and rest the next, and this seems to be helping somewhat. Sending healing energies to those in this feed, please know we are no alone. Especially when we have Doctors like Dr Bateman to fight our corner. 🤗💐

[@annawasterbyjara9527]

This is very, very great work ❤

[@fionavanwaveren-wilshire4779]

Great in sight.

[@heatherhart7319]

You make the most sense out of every doctor I have seen. I would like to thank you for your dedication and the message of hope you have given many, especially me, who struggle everyday just to make it through ~ Thank you, thank you, thank you, from the bottom of my heart.

[@carolanneconnolly-brown6781]

Wow that is very interesting. I hope this knowledge gets out there soon a c we can all get treated.

[@tiannaclouse9295]

I learned a lot and had a lot of "I have been saying that " for years. It makes a lot of sense and has touched on many points of what we live through. I have FMS and 80% of my S symptoms I have had since early childhood but have also lived through child abuse from a small toddler. It was very fascinating to hear the idea of different FMS it makes complete sense I love these lectures! Thank you will be looking for more!

[@kimverber6114]

❤️MG‼️ I just wanna Thank You so much for your compassion you've shown by the extensive study's & time you put in to getting to the core of this horrible condition so many of us live & deal with daily. You've shined a light of hope at the end of a tunnel for me that I thought was nothing more than a dark abyss of my existence. This 3 part video has valuable information & very much appreciated and I'm gonna Share the Hell out of it because it much too important not to⚕️. God 🙏Bless & ✌️ ❤️ & 🎼

[@feonajen5858]

So how man of u us have gluten allergy/intolerance with fibro.... considering how it opens the door to so many autoimmune disorders and other diseases. .

[@sacredgeometry2344]

The gluten intolerance is from the mold content and the body cant process gluten. fibromyalgia also goes with Lyme disease most tests maker out positive igenex is the most reliable one

[@suem8591]

Thank you for this!

[@holly0297]

This is phenomenal! My concern is - that was 2010. It's 2013. Where's treatment? Where are the newly trained (and *schooled!*) doctors? This happy news, considered in context w/the timeline, just makes me sad. Does anyone know of any more progress toward a treatment?

[@ladyangi100]

THANK YOU I LOVE WHAT YOU FOUND OUT

[@charlotteortiz1233]

Thank you ❤️

[@anncrow2709]

when you have suffered with fibromyalgia for years, this video was comforting to know someone understand the syndrome, I have thyroid problems had a hysterectomy at 26 due to polycystic ovaries and have been disbelieved by many doctors over the years, so good to know that I am not nuts, it is real, bizarre but real

[@customcakery1975]

This video series has really made sense to me! I have been diagnosed since 2004, and since then have gotten a whole lot worse. I have 2-3 "good" days a week. What type of specialist should I see?

[@magicalpatterns]

Doctors take my body and do whatever you need to do for research. I'm dying slowly and something is burning me with a lighter all over me all day. The pain is unbearable and I have gone to Mayo Clinic and I'm literally dying and it doesn't show. HELP meee, I need you. I'm a mother of a 3 year old son and I can't do anything is like a cancer but I won't die from this is only the turture for the rest of my life? Thanks

[@honerdcouster8723]

Not at all will you suffer forever. You are speaking of cerebral spinal fluid leaks caused by a sacral spinal cyst Tarlov.cyst disease. Have a nuerologist do an ent have him explain whats going on in the sacrum. Get a dorsal root ganglion nerve block injection. You won't have pain every day.

[@MM1902KB]

Hi Magic Patterns, How are you doing these days. Some of us really care.

[@NovemberRain-1975]

Constant crunching and cracking in my neck all the time burning sensation in the muscles ect AND dizziness

[@courtneyritter1285]

I had a rheumatologist work up. They said my vitamin c and d levels were very low. The diagnosis: “ the good news is you don’t have lupus or rheumatoid arthritis. But you do have scurvy and ricketts . I think you have fibromyalgia, follow up with your family doctor.” I also had an increased dhea level. Was never tested for epstien Barr. Still very symptomatic and working full time, which kicks my butt and I have nothing left for myself, friends or family 👎

[@ronyalemerrill]

Thank you so much for these videos and your research!!!! God bless you!

[@Ethericrose]

I've had chronic pain since a small child ( I had a lot of trauma in my childhood). As an adult, I was diagnosed with PMDD. To reduce Premenstrual Dysphoric Disorder, I had my ovaries removed. Since I had them removed, pain has increased tenfold, and I struggle to walk these days. I am prescribed 3 types of high-end pain meds that hardly touch my pain. I'm sitting writing this, and my body is screaming. I also have a diagnosis of Hypomobile Elor Danlos Syndrome, my joint hurt due to constantly subluxation or dislocation. The Rheumatoid Specialist told me, "It's all in your head, and there's no cure, so you'll just have to live with it as best you can!" I intend to forward your presentation to my GP. Oh! I also have chronic neck pain, so I will be booking an appointment for a massage to see if it helps ease pain levels. Thank you for all your hard work. Thank goodness there are people like you in the medical world that care about their patients. It's incredibly rare these days.

[@ashleyandlara4247]

"the future is bright" once we find out the true reasoning of this horrible condition and cure.

[@johnjohn-wc8fz]

this guy should have the nobel prize just for linking the dopamine aspect as makes proper sence that pain pills dont work ...thank you

[@giantsfan562001]

Also because of a medical reason my iron was 6 for quite some time until they fixed the problem ..I cant go out into the sun I get horrible rashes and scar.My vit D is 10 they put me on 50k a week I took 1 and now have constant ringing in my ear...I cant live much longer with this pain!And I cant find a Dr who will treat me for it ...

[@peace4848]

my nick hurts lots .. if I'm sad that makes my nick hearts even more

[@niabailey3933]

Wow eye opener. I suffered from. Chrinic fatigue snd back nerve pain as u have a tarlov cyst and hip impingement. I had facis injections ehich where agonising it was horrific because of my pain levels. Because of severe dental priblems the doctors put me on morfine which didnt work and this video explains why . She then put me on lyrica which has changed me the difference is amazing im not quite there and changing doses but read its for fibro and reasearched that and foud this video . Xx

[@holly0297]

Me too! Severe neck problems and chronic anemia. What do you have? Surgery did not make my fibro better but it lessened some of the paresthesia and radiculopathy in my arms, plus healed some of the horrendous headache from the disc that had burst into my spinal cord canal. My neurosurgeon practically laughed about my fibromyalgia, saying my pain was ALL from my neck. Idiots! lol

[@dReZbEeZ]

i constantly have to rest because of my fibromyalgia. amitriptyline helps me a lot with sleep and mood stabilization. i have had constant trauma throughout my life of 40 years and my body and brain can’t take anymore. or so my doctor says. therefore i have this fibromyalgia, but my compression is in my lumbar not my neck , my sciatica gets the brunt quite easily if not that my hips feel like gravel and water sloshing around in constant pain. when i do over push myself ( which happens easily) i do get a lot of pain in my neck. i see blue dots, my arms go numb and i have nerve pain that radiates from my neck to my jaw line along the mandible to the mental foremen, so ya , it totally sucks. i have the most comfort when i’m lying down. my bipolar doesn’t help any or the DDD in my lumbar plus pinched nerve in thoracic spinal column. so now when ppl ask me what wrong i have to ask do you want the short or the long version? too much conflict with friend or family flare the whole body up. so i try to live easy breezy. still isn’t enough tho.

[@alwayslove6290]

I wish all Dr's had this Dr's understanding. Also are the Dr's would take our knowledge Seriously and not put us down because we don't have a Dr's Degree.

[@finxenvy1975]

The neck theory is valid if you look at my case For 10 years the work I did involved a lot of what you mention with tilting the head . But a year and a half ago I saw a chiropractor and the x-ray showed two of my cervical discs are "fused" The neck isn't even the worst of my pain. Where the pain began was in my lumbosacral area. I don't believe they're related unless my neck problems also caused a shift in my pelvis. But in the pelvic area, when thinking back to childhood, there was always a problem The femoral head on my right never had full mobility. I also KNOW one leg was significantly shorter than the other. Thinking back I remember when I would walk with someone I always ended up slowly pushing them over as we walked. I couldn't walk straight. Was always at an angle I also have a flat foot on the left not the right. I'm uncertain whether or not I've always had Because about 2 years ago I landed on my foot funny and felt that tendon at the bottom of your foot pop. It was excruciating and felt good all at the same time Of course, it's my longer leg that has the flat foot. The left leg. Add to that, I realized 2 years ago that I'm autistic. Not diagnosed yet. But I have the gait that has been researched as common in autistic people Where the one leg is stiff as a board and holds the majority of your standing weight while the other leg is bent slightly at the knee It's hard to say whether or not the femoral ball was the way it was at birth or if it developed as a result of the longer left leg tilting my body and put all the weight on the right leg My pain began mid-January 2020 and I haven't had a pain-free day since. Up to this point, doctors have really been no help . Along the way, after a bad referral by my family doctor to a movement disorder clinic, he ordered an MRI for my brain just to rule out multiple sclerosis There was an abnormality on my left prefrontal cortex. Specifically in the white matter. But they are not 100% certain it's demyelination Whether it's related or not I do not know. However, my right side has always been considerably weaker than the left. When the pain started, It really became noticeable to me. Now, I have less sensation on my right side than I do on my left I thought perhaps the brain lesion was congenital. Affecting the muscle and nerve development on the right side of my body and left side of my face. When I saw the neurologist, he didn't have much to say about it and quickly moved on to the pain issue. Just over 2 and 1/2 years of doctor's appointments and physical therapy that did nothing, I get a fibromyalgia diagnosis. All I could think to myself was, that's what doctors diagnose you with that when they don't know what's wrong. To this day, 3 years and 8 months later, I've received no help. I'm on a waiting list for the pain clinic. I have received no outside financial assistance since September 2020. That's when my employer's Insurance company cut me off. Oh, and to compound the problem, unresolved grief and chronic stress with periodic occurrences of severe acute stress. As well, because My autism went unnoticed, I spent my life looking to the outside world to learn how to "behave" I developed social anxiety In junior high and "depression" at 19. Both of which only got worse even after 10 years of off and on psychotherapy. My anxiety is now a full-blown phobia. Perhaps even anthrophobia. It's worse when it's somebody in a position of authority. Where getting what I need is dependent on them. I'm currently living in my barn where I ran my business on my dad's farm I'm more than certain that I have been stuck in fight or flight since April of 2022. After an acute stress occurrence, I developed panic attacks and prolonged anxiety attacks. I've had malaise everyday since then as well. Then in August, after another acute stress episode, the malaise became full blown nausea. Plus headaches everyday that made me dizzy and fuzzy. By the end of a day I had to squint my eyes If I wanted to move otherwise the nausea and dizziness would be overwhelming. This is also around the time I developed high blood pressure. Brain fog or executive dysfunction from the constant fight or flight started to affect my life October of 2022. That's also when I believe burnout occurred. By January of 2023, burnout became exhaustion. Or maybe it's the other way around Fatigue hit me around April. It's gotten worse since. To the point that even when I'm sitting up I'll nod off. Here's the point where I don't remember what I just told you. I would go over it but I'm already exhausted from the effort and thinking about it causes me anxiety And if I don't send it now as is, I'll end up getting distracted, frustrated or think "what's the point"?

[@jarjarbinx71]

Your awesome buddy thankyou hears to your faith! 🤞❤x I'm not convinced I,m going to be treated now after 21 year headaches fog etc 7 years both shoulders damaged restricted for too long suffering but will try and put ignorence in there face! Cheers👍 kind regards

[@Gena777-r95]

Does the spinal cord compression show up in a normal MRI? I have severe neck problems right now there's a lot of inflammation

[@moname7017]

I have all of those underlying stressors.

[@nonnalovepriceless]

You can have me as a guinea pig if you like . I have so much pain fybromyalgia pain for so many years I would love to finally some one to help me and that I could help others . 🙏🏼✅

[@CARMENPEREZ-nv2ge]

What new medicines are there?

[@54Stefanie]

all the Dr.'s and Specialist haven't listented to me. My neck pain is unbearable and no hope her because I have no Dr.'s here in Oklahoma and no money for gas to go to a real Dr. as you.

[@marilynmasonis376]

I'm so sorry hun. I do hope by now your insurance situation is better at least. If you are not receiving disability, please don't stop fighting for it. I understand all too well hard very hard it can be.. ~Much Love ~Marilyn 💜

[@madamequeen115]

The Neck thing is the worse of all...for me

[@yvonnesullivan4388]

Side effect amtriptline hallucinations

[@hardeepmann4322]

M in soooo much pain and my concentration is getting so poor. M FEELING LIKE I WILL GO TO DEPRESSION DUE TO THIS PAIN. M DIAGNOSED WITH FIBROMYALGIA. I really want help

[@54Stefanie]

Please use me for research...."tears"

[@chrish8871]

So do I understand correctly that if I add iron to the body ( assuming my FM diagnosis is correct and that means low iron) then my dopamine will flow and fix my FM, provided my neck will allow it? Do I have that right? Edit to add... my shoulder blade and upper left chest goes tight and stiff like cramp right up to my ear. If I put my chin on my chest, the cramps release.

[@stellamarina.]

12 years later, the future is still no bright! 😩

[@lizz486]

Wow, I just came across this - parts 1,2 and 3 - and can say I have never heard more promising explanations for causes of fibromyalgia. Yet it is 11 years since this final video came out and I am still treated like a psychiatric patient. Why hasn't the medical field used any of this valid information to develop valid treatments? It has to be money!! No money to big pharma if a person's fibromyalgia cause is diagnosed and treated properly. Big pharma would lose millions of customers (not "patients" but "customers") being treated with those "30%" medications that he mentioned. I sure wish I lived in the vicinity where Dr. Patrick W. Woods practices. No doctor that I have ever seen has this kind of knowledge about all the possible underlying causes of fibromyalgia. Certainly no one is willing to do brain MRIs while testing all the variables he reviewed in the videos. It's better for the medical field and pharmaceutical companies to keep people sick, so they keep returning for more dr. visits where they are repeatedly dismissed, ignored and/or gaslighted. But the doctor collects from the insurance & from the patient, and continues scheduling repeated follow ups while nothing changes for the patient, I except possibly the newest medications, which provide additional "kick-backs" to the medical practice. Fibromyalgia is not known to be life threatening, so it is not lucrative to actually heal these patients. There is no money to be made in actually working to reveal the true underlying cause and treat it properly. The medical practice and big pharma would lose their income-generating customers.

[@abutterfly7975]

They have claimed for decades that trauma/severe stress, and car accidents, can be causes of fibro so this is not really new news. In the 90’s I was going thru a terrible divorce and custody battle and had at least 2 car accidents with whiplashes, then I developed fibro, surprise surprise. 😳

[@yvonnesullivan4388]

I also had Epstein barr

[@ginagardiner2880]

Well at least I know why I woke up one morning and looked like a fat blob..funk en amitrypteline! You're fired!

[@honerdcouster8723]

Cerebral spinal fluid leaks caused by sacral spinal cyst Tarlov.cyst disease someday maybe doctors will look up spinal cysts. Who knows perhaps learn how to turn on the MRI with the proper technique to.detect entrapped spinal fluid or use digital subtraction mylography to find cerebral spinal fluid leaks. Fibromyalgia willbe treated right not wrong as is the current state of medical iantragenic butchery.

[@leonietrezise9198]

🤔 They suddenly realise they can money out of this condition. Damn them. 🇦🇺

[@suzannehalesuzzz4895]

Nope neck surgery. C2 -T2 . Fibro worse than ever. With each medical surgery fibromyalgia worsens and lasts longer.

[@abutterfly7975]

Or you’ve had too many whiplashes........

[@miraclebaby3028]

How about scoliosis? Having a chemical imbalance between the brain & central nervous system? Lol fat zombie OMG