My conclusion is there are probably very few true hypochondriacs only people who never get a true diagnosis of their illness. Thank you for your videos. Wish I could visit you but live in 🇬🇧.

This channel is unbelievable. U guys are covering stuff that 99.9% of the docs have no clue of!!!

It's unbelievable to me that I never heard of this angle on cognitive symptoms till this week. Have felt like I have been declining mentally since I was in grade school around middle school. 27 now and last 2 years I got into keto/carnivore around the same time as I got into rock climbing, sleeping in a hammock and deleted social media. Felt like a kid again. Alert, could read complicated texts, problem solve, felt emotions and could understand them. Then I stopped rock climbing as much and slowly the symptoms came back and I thought it had to be diet related. Now I realize that while diet is very important, it's more fundamentally a neck problem that was being alleviated by postural improvements associated with rock climbing and consistently sleeping on my back due to hammock sleeping. Thank you for putting all this out!!

Watching Stefanie's story felt like validation for my own testimony. I actually thought I was slowly dying until I just found you. Thank you for restoring my hope for life! The real road to recovery can actually begin now...❤️

I hope this revolutionizes the medical industry Dr. Hauser. This will potentially help alleviate suffering of millions, including mine.

Dr. Hauser is a genius. I wish more doctors and specialists could have the knowledge that he has. I also wish I could fly to Florida to receive life changing treatment from this wonderful man. After watching just a couple of his videos, I felt like I knew exactly what I need to do to finally get on the road to recovery but simply don’t have the money to do so. I’m sure there are thousands of people in the same situation. It’s a shame that this information this isn’t more widely known- I think we could all do with a Dr. Hauser in our lives!!

i wish i had a doctor like you. this has ruined my life. im 42 now and my family have persecuted me because results come back normal and they dont care and when i learn and help myself they call me crazy. totally ruined my life and i cant thrive to even finish a course even tho im highly intelligent. im going to waste

This is a real eye opener..who knew why we are all such a mess...just incredible. Thank you.

Every word this lovely monotone man says is about me. Another way of putting it is that this has been going on for a long time. Thank you so much!

I LIVE IN SCOTLAND. YOU'RE BRILLIANT.

Thank you for sharing all of your research findings. I'm a manual therapist and advanced craniosacral therapist with 26 years exp. One of the most difficult things to try to get my clients to understand is that while they want instant symptom results, they also need vagal tone and ANS normalization, which means consistent gentle work and a primary focus in their life on getting consistent quality sleep and being willing to deal with past emotional trauma through forgiveness, prayer, self awareness, etc. Your presentations are like a shot in the arm for me to really ramp up my encouraging patients to commit to the totality of treatment that I offer as well as commitment to sleep. Also, I wish the TMS/PPD organization (Tension Myositis Syndrome/Psychophysiologic Disorder) would acknowledge this somato-physiological nature of the disorders that they treat. I have tried to speak to them about it but they don't acknowledge it. To me it's beyond obvious: vagal tone disorder is the primary cause of TMS/PPD and virtually all health problems. Thank you so very much for your pioneering work!

I couldn't believe what i was hearing! It was everything i have symptoms for

Thank you for making these videos❤ I have hypermobile EDS and literally every symptom you have covered I am 39 and have studied medicine in school for 3 years and for 10+ independently trying to figure out what was causing all of these issues. Seeing your videos, I was literally in tears because it finally helped to put all the pieces together and explain everything I have been dealing with my entire life. Finally being able to show my family proof of what I've been saying for years is something that is priceless. It truly is an invisible illness because we suffer from so many seemingly unrelated things that seem common and are generally thought of as not serious on their own, like acid reflux or fatigue, and are often dismissed by doctors who don't understand that it's just not that simple. Discovering the cause of the problems in the 1st place was the hardest part for me and took over 30 years, managing them on my own has been the next biggest challenge. Something I never thought would happen was finding a solution that could actually fix the problem. I finally have hope that eventually I may not have to deal with these problems and can have a somewhat normal life. ❤❤ The most stressful part for me has been trying to hide all of these issues from everyone because no one understands them and I'm sure everyone who is dealing with this is more than familiar with all of the negative advice and comments, and simply the negative opinions people have in general when you try to explain any of this to them, that it is a lot easier for us and much less stressful to just hide it as best as you can from everyone you know. Unfortunately it doesn't work with your closest family, and that has caused the most stress.

In any event, I find Dr. Hauser’s talks, interviews, & presentations to be most fascinating. Especially since I am currently in the process of studying as many sources as possible on the vagus nerve, aka: Vagal Neural network, and its anatomy, physiology, function, pathology, treatments, et al.

I used to describe the feeling like when you hold your breath and you start to panic and feel like you're about to pass out that's exactly how it feels......but the difference is that it doesn't stop when you take a breath 😢

This is absolutely mind blowing!! I have suffered ( inexplicably!) SO many of the symptoms listed here: palpitations , arrythmia, fog,wildly fluctuating BP followed by cold hands & feet , dizziness/lightheaded, imbalance , tinnitus , digestive issues, visual aura ( not mentioned here but I'm certain it's related ) & probably all because I'm an IT tech & spend hours hunched over a computer! I have suspected neck issues ( I hear cracking , & grinding when I move my neck) but this video has absoluitely hit the nail on the head! I'll be calling you up soon doc ' even tho I'm not in the USA!

Stephanie is a trooper. I feel bad for her, poor thing has been through hell. Bless Her

I AM SO DELIGHTED TO HEAR, YOU TALK ABOUT THIS. WELL DONE SIR.

THIS MAKES SENSE. I HAVE BEEN DIAGNOSED WITH MS OF THE BRAIN. EVERYTHING HERE MAKES SENSE.

This is such an eye opener. This is the kind of stuff they should teach you in elementary school.

So relatable, this story. Solidarity to Stephanie.

I'm at 29:21 & you just answered what no Dr. out of at least 14... has been able identify. I've told them all about this spasm I get @ end of breastbone, top of diaphragm. They can drop me to my knees. It feels like a ♥️ attack & ulcer attack at same time. Many of the spasms include Abdomal Aorta standing out ( you can see it) & thudding like a galloping horse. So painful. After a bit, it feels like wrong signal gets sent & enough gastric acid dumps into stomach to digest a whole turkey. I had a serious horse accident & also a big surgery on right side of neck. I have so many symptoms & also told my PCP your exact words - I told her I feel as if my body is ALWAYS in Fight or Flight mode. This video is speaking to me. Thank you!!!

Wow. Love this I spen half my day lying down,because “I don’t even have the energy to sit up”. Constant tachycardia and grossly irregular heart rate. Plus lots more .. Is there someone in Australia who does this system ... in Sydney hopefully. ?

This guy is a lifesaver!!!!! God bless him!

Praying that the Almighty God give the ultimate strength, wisdom and good health to all doctors who provide medical attention and advice to every patient suffering due to chronic stress being brought by covid 19.

I know exactly how she feels. I fell and fractured my spine and it also caused 2 herniated discs in my neck and 2 in my thoracic spine. I've lost down to 103lbs. No one would take it seriously that something had to be wrong. When it started, I used a cane for navigating stairs etc. I'm in a wheelchair now. They just fixed the two herniated discs in my neck. They were compressing my spine terribly. The surgeon had a difficult time getting it all out. My 75 yr old mother drives me around everywhere too. The doctors just act like you're a drug seeker and blow you off. They did this to the point that we're concerned about the long-term problems with my spine due to their neglect. I have almost all of these symptoms.

Cervical instability is pretty comon in EDS patients as well as Hypermobility, MCAS and Gastroparese.

Yes, I had doctors tell me I was attention seeking, psychosis and blew me off as well. So hurtful and traumatizing.

In Kaballah, the tactical sephiorth are known as netzach and hod. These are the feminine and masculine principles which rule the left and right leg respectively. Being "over tactical" in the feminine or masculine aspect will cause the leg that is opposite side of your sex to get disruption. This led me to study pingala and inga, because there is not bridge between kundalini and kaballah in regards to the vagus nerve. This channel was recommended to me after weeks of searching. You have brilliantly woven together years of information that I have been searching for.

It does get so discouraging when your pain is repeatedly dismissed by doctors. It happens even when there is obviously something physically wrong. I’ve heard so many times that I should not be in the pain I’m in.

I’m in terrible shape but in Colorado! Thank you immensely! ❤️❤️❤️

Thank you for this most excellent video! My 91 yr old mother has kyphosis and a lot of health problems, and a son has problems from a motorcycle accident. Other family members have other vagus nerve symptoms! Thank you 🙏God bless you!

I am an acupuncturist and alternatives medicine therapist i work with vagus nerve very much and helping people. With acupuncture is possible too .we can activate vagus nerve and strength the tendons . I am glad to hear your seminar it was very useful.

Amazing information thank you Doctors

Literally everything Stephanie is dealing with is exactly what I have been dealing with since childhood ... I am watching with so much hope because if this can help her, then I know it will help me ❤

I’ve been hypersensitive for as long as I can remember… anxiety, depression, panic attacks. I found out this week that I had a compression fracture in C6 estimated 20 years ago. I believe the injury happened when I was about age 5, I dove into a jacuzzi, saw stars and chipped my tooth. And then I’ve also had concussions and whip lash from soccer in my 20’s and early 30’s. Im hoping after 36 sessions with the chiropractor that he will fix this issue. I sobbed for five minutes yesterday because I feel like omg I have an answer and a way to fix it!

This is 1000% me! I have had all these symptoms for over 15 years.

Over 8 years ago I had two strokes from a high stressful situation. And for over 5 years I have been suffering from Menniores. I a now hoping that this knowledge will be beneficial for me when I learn and apply it.

WAHL. ABSOLUTELY BRILLIANT. YOU'RE BRILLIANT . YOU'RE MAKING SENSE.

That was very interesting thanks for the information and making your self available to people.

Thanks for this scientific seminar

GREAT WORK,,, keep up the pressure,, we need PROPER CARE,,,,,,,,,,, cheers to you,,,,,,,,,,,,,,

When I first started getting ill , my stress was extremely high, my cortisol was 3x higher than normal, I have IIH and fibromyalgia and uterine and digestive problems , my back and limbs in constant pain n joints !

This is tremendous information. I appreciate it. I think I found the answer to what is happening to me. Will be in touch. Thank you doctor.

Dr. Hauser im astonish to hear what exactly describes my health issues 🤦🏻‍♀️ For so many years, dealing with various doctors of different specialties and finding nothing specifically to provide a diagnosis is very upsetting! Praying for a miracle, always asking God for a doctor that help me in this battle 🙏and i think I found you as the answer to my prayers. I’ll do anything in my power to have an appointment with you but first I have to make a plan and do some research about where to stay in Fort Meyers for a month to get evaluated by you and discuss the treatment. Thanks God I found you 🙏 Thanks for helping us in the middle of this turbulent time, God bless you forever🙏🤗🤗 I’m in NY

I read all these symptoms and they are very familiar. CCI, too, says the out-of-state neurosurgeon. You have the most comprehensive grasp I have seen. Having a high level of negative reactions though, to many substances, I fear the injections could be bad for my brain.

Docs get paid to push drugs so fda despises natural health care. I am naturalist and I went off everything they were giving me for all my diseases and I have been healing myself with natural remedies so I finally started getting better it's still taken years for me to get this far back to healthier. Still have laundry list of conditions and diseases. But I prayed so hard for god to show me if my spinal surgery next month is his will and trying to research to show my fam why this cervical disc bulge and reverse curve and syringomyelia is the problems root to all of my disease and fibromyalgia and literally every single thing on your slides are me circling all the conditions I have and symptoms that are linked to my neck. You literally just put the puzzles pieces of my life long health together this is incredible and I can't wait to have surgery. Who says I can't wait to have cervical spinal surgery hahaha sound crazy. The risks outweigh the benefits that's why theyr so ready to do it. I migraine every single day I am not living I am not existing anymore. I have withered away

ABSOLUTELY CORRECT. I WAKE UP AT NIGHT. MY LEFT ANKLE KEEPS FAILING.

Thank you! Dr. Hauser !

Gave up sugar-fructose-corn syrup, and no more stiffness, no more digestion problems, no more bowel diarrhea problems, no more headaches; I look younger, everything seems healthy. Everything we buy has sugar in it. It has been a month without it and I feel so cured. Wonder what this smart man thinks of sugar and the vagal nerve.

Great info! Had a crippling cervical injury which resulted in a rotation, now I know how to treat it! Many thanks from Canada

ABSOLUTELY BRILLIANT.

That's it Doc you are my new friend. From gallbladder irritable bowel system you have explained and gave us a neurological answer with a physical therapy kick in the butt..!

ABSOLUTELY CORRECT.

I always find it beneficial watching your videos with not so complex but great health tips because they work and help to improve one's health. Thank you so much, Dr A Mandell!

Thank you for all your videos. I'm working on my wellness. It went haywire after covid GI infection as did my church group. They got well I didn't, I've had weird symptoms since. Your information is clearing up the mystery. Jesus is my source of life so I'm good there.🙏

Just wow! I can’t believe it’s taken me this long to hear this and find this video. All on the back of more digestive issues and needing to book into my doctor to try and get some help. Thank you!! I do need someone in Perth Western Australia however to help me - always the way trying to find someone in Australia who does this sort of treatment :/

I have gastroperesis, gastric pain x 6 weeks. Can’t give me a reason why, my heart rate drops to the 40s and it’s get irregular and sometimes,It goes too fast. So other things you have talked about that I have. Everything is a autoimmune disease. My liver is bad not,from drinking . Anxiety, pancreatitis, had dysphasia. I found you and I have been told nothing wrong. But I’m in constant pain . I was told in November I might need a pacemaker. I’m still waiting for to see that doctor and we are in June. Wow you just keep naming things that I have. Also my extremities go numb when I lay down. Had cervical,surgery on one day two days later was going back for another cervical surgery and I came out with lacerations and possible whiplash. Then dysphasia, heart rhythm problems. Gut problems. Sleep apnea high cortisol levels,hypo thyroid. Too many things to even mentioned. I’m treated like I’m crazy 😜 I know what I feel. And I feel like my Health has been going down hill. I’m told this is how it’s going to be then I found you. I have to see if I, covered under my insurance.

I have most of the symptoms that you're talking about here. Tomorrow will be the 25-year anniversary of a car accident I was in when I was 8 months pregnant. I had bad whiplash and a pretty bad concussion to where I lost my equalibrium. I have been in PAIN every since. Over the years, I feel like I've tried everything to understand why. After having Covid, it's been the worst. I'm a long hauler. I at one point had an MRI, and they said that I had 2 herniated disks, but it wasn't affecting my nerves. I believe he said it was C4 and C5. I'm not positive. I was also just told that they think I have EDS. Do you think that it could still be my upper cervical spine, or does it matter about where the herniated disks are? I desperately need help. This is the most hope I've ever had. I'm so thankful that I happened upon you.

I am an upper cervical chiropractor: you understand the spine better than most of us...

Thank you for helping all of us telling the world long things that you do not understand this is so wonderful I can't stop listening oh my

We have to make Dr Hauser with Caring Medical Comprehensive H3 Prolotherapy go viral

Oh you need to do one on Myalgic Encephalomyelitis/Chronic Fatigue Syndrome ✊ many sufferers have been getting surgery for CCI/AAI and Tethered Cord syndrome which corrects their symptoms or improves them dramatically. People might want to avoid the cervical surgery if possible. 🤔

Doctor Hauser. Whish I had your help years ago. It took me since 2010, to comvence neroligest here in Tampa to use TMS transcranial magnetic stimulation that Israel have been using at least twenty years..! USF HAD a clinic in their syc-ward right across the street from the VA hospital and it was virtually unused for PTSD military people it was made for by Brainsway of Israel..!

Movement is definite. Each time it creates pains all over. The fact it's not seen after several mri done is scary.

Love Dr Hauser addressing the vagus nerve is so crucial to our health! . But I don’t buy the prolotherapy will do the miracle job. It may help but the the main point is getting healthy from the basics and life style. I’ve been through the hell from the instability of C1 and C2. I have achieved having no pain and all the symptoms are almost gone just going through the basics.

I wish you were my doctor , I am in Johannesburg South Africa , I am suffering cervical spine disc injury instability and lost of balance for 12 years now 2023 . Thank you so much for making those videos I have got no doctor having ability to help me and now it's my problem alone every one is getting tired of helping me

i also have autism and i feel this is very related and caused by vaccines and scoliosis

Thank you soon much .I read alot,and was wondering by I am having a few things ,this is exactly it.

i get the circulation issues when im laying down especially on my back. im vegan most of my life with a healthy diet but need digestive enzymes with every meal etc.. i have had periods of feeling the neck area swollen and i get really out of it and when i dry my hair i have the urge to use the heat on that part of my neck, it gets itchy and theres a pleasure pain thing. i have all those symptoms and i get whole body neuropathy

I know that I have upper cervical weakness, I've had facial paralysis on the left side for almost 6 months and am going in for my second MRI on the 22nd of this month. Today is the 15th of June 2022. I had no idea that I was claustrophobic until now, but I do, and, this is causing me a great deal of stress as I almost decided to not keep the appointment. They can't put me to sleep. Everything I'm hearing from everybody here sounds exactly like what I'm going through. I've been praying to God as this is and has been one of my worst nightmares. They are going to have me take a pill for my anxiety but I hate to take drugs also, I'm at a loss as to what to think anymore. I wish I was whole. Lastly, I've lost more than 25 pounds also. It's as difficult to chew as difficult as it is to swallow.

Thank you so much doctor I am from the Dragon cafe we do so much always so to help ourselves it is a mental health charity my doctor sent me dear so many things are you have been talking about people with long-term disability yes the nerve that you're talking about it really helps so thank you so much

I left a comment here in the last hour or so. I can't find it now but would be grateful if it was deleted, which is probably in my best interest. I will keep checking back. Irregardless, this is phenomenal, ground breaking info that I am very grateful to learn. Many thanks🙏

Beautiful video I love how long it is it is so in depth and I feel like I’m learning so much now I can finally educate people on my condition

So every time I watch one of your videos, I’m convinced that I have these conditions you treat. I’ve had multiple whiplashes I have a reverse curve I’ve been a massage therapist for 31 years looking down on clients I have lax ligaments in my neck I have vertigo, low BP episodes including fainting, overheating, nausea, nystagmus in eyes I’ve been adjusted multiple times aggressively, especially atlas. I have strange cranial sensations, numbness, migraines, headaches, facial pain I have referral into both of my hands. I need to schedule a Skype 💜

I was a footling breach baby and my mom had a septum in her uterus...I had my cord wrapped around my neck 7 times and got pulled out via c section after seeing a foot come out the v way...I was blue and having a seizure. I've had stomach and intestine issues my whole life and my neck used to spasm so bad, I couldn't go to school for weeks. I was a ballet dancer and was told to quit at 12 and I'd regret it in my 40s... I do. I also wish my mom would have checked out why I was always so miserable 😞 I'm 49 next month and want my life back

This explains so much. Ive only one disk left in my neck and its herniated. I thought EDS was ground zero for all my maladies. Bilateral NTOS VTOS, DDD, Occipital neuralgia, MCAS, fibromyalgia. Bla bla bla.. I get "neck headaches" up ton4 x per day. My vision changes daily, sometimes minute by minute. First rib resection and anterior/middle scaleonectomy. So may surguries.. I can't take meds.

Soo great to listen and learn from you.

Dr. Ross my name is shane. And i have been suffering with 85% of these issues for over 15 years now. I truly dont know where to start to explain the pain, the brain fog, the gastroparises, the degrading of my body, my brain function is so bad. I cant digest food hardly. Its all started many years ago with a pain in my neck, throat and right lung, fainting, it has progressed threw out my body now. My lover doesnt work, my entire digestive system does not work. My immune system is turned off. The anxiety, obsessive compulsive issues. The light sensitivity. And on and on. My body and mind is dissolving. And im not getting any help. I hope someone how you see this. So how i can get in contact with you. Im deeply into the hopeless state at this point. Ive already lost so many years of my young. Im praying some how this messages reaches you.

I'm freaking out watching how dirty this is! No sterilize room, no sterile prep , waving need all over then sticks it in the spine! She probably also has an infection now!!

Thanks for this information. I definitely have this Problem, I will call for an appointment.

Thank you doctor for telling me all this information when doctors do not tell you what is wrong Parkinson's Disease a lot of different I'm listening to you with the listening to you all different nerves I am understanding things now thank you for sharing this got to learn a lot about yourself I hope everyone take up this thank you so much

@ 1.47hrs Rock Climbing is a great looking up activity. Clip n climb walls are made for 3 yrs - 90yrs.

This is so interesting thank you everything you talked about I have and had it for several years. I sure hope someday that I could come and visit your office and have you take a look at me . I've had so many doctors exams blood work all normal CT scan normal but I have very bad dizziness anxiety and tinnitus military vet navy engineer

Awesome 👍 explaination 👌 & info - coz of Digestive Maladies 🥑 TKS 🙏

Well...looking forward to entire series. I have disk problems in neck. Don't remember the date if last MRI there. There was a CT last near 3 yrs ago. But i have been saying to myself my spine is unstable (i can feel it). Also mentioned by you lessening of blood flow to brain in a comment. I have wondered if it was CSF partially blocked. When neck off yes painful, but that isn't at a 10. However the instability causes nausea and if i don't stop what i am doing soon after the nausea hits moderate, it gets worse from moving like bending for a while or god fobid needing to lift any weight... well i vomit. Oh, joy... But interesting about the Vagus. No surgeries or previous treatments on C spine. I can't do PT bcs of this. Had a PT hurt me. I am getting weaker. In would do water therapy if i wasnt weak and run down. I was hopeful to get better. It isn't happening. I am very concerned. I am tough or was, but have always been determined. So I am guessing a novel treatment wouldn't be covered by Medicare. I am disabled due to spinal issues. Bulging disks were (6 yrs ago) T4&5. Then Lumbar moderate Deg disks and Severe at S1. Maybe 2 there like that. Don't remember right now. It is, as a surgeon 1st statement said upon seeing xrays or MRI 8 yrs ago "you've worked hard". Yes and played just as hard. Explain, he ask. More horse wrangling. Includes moving weight as bales if hay. And well as much as I think you finess a horse you may wrangle them. More knowledge now about that, but can't do it. Felling trees in forest. Various things. But i have gotten push back since that from Neurologists and PCP, MD. Surgeon said not bad enough back then for surgery. Thank God. Didnt and don't want it. I live now in Sec 8 housing and see too many post surgical failures. Also see docs ignoring for new MRI and serious failures. Some almost immediately. A kind of Chinese finger game ceiss cross failed to the point of reversal then downhill slide 2 mos later. Begging 4 MRI...not granted. A yr later finally an MRI showed collapse. And other med or longer post surgical fails. One case of a plate of titanium just split. Not from pressure. Just failed. Eee...but a few stories. I dont see surgury as an option for me. Also a surgeon whi did backs and many ppl at Hospital PT praised him. He quit doing spinal surgeries. Too daen busy in this town and he became hard to see. Then quit backs and he was at least 53. 27 yrs surgury experience ortho of course. Quit spines in @2015.

What a doctor

It might be interesting to see a conversation with Elliot Overton. He says vitamin B1 is very important for the vagus nerve. He is all about curing a lot of issues with high dose vitamin B1. Benfothiamine and allithiamin as more absorbable forms. I saw someone comment het was cured of Parkinson's by long term high dose thiamin.

my husband has been vomiting every 5-9 days for 24 hour intervals since Dec 1, 2019. He has Acalasia surgery May, 1019 and has not been well since. He has lost 40 lbs and everything he eats tastes horrible. After much research, I believe he has Vagus Nerve issues and don't know what to do!

I wonder if this could play any part in my MS. diagnosis. Most of my symptoms match this

Gee, I didn't realize that I could get better! Thanks

When it comes to the ear, we hear about 'pain' or 'hearing', but I suffer from what is likely myoclonus - persistent thumping in the ear. The only thing that can impact it positively or negatively is manual therapy to the neck. Not getting to permanent solutions, only temporary relief. I wish there was more learning out there for what I think is this rare form of cervical tinnitus.

Fantastically informative.

I recently pinched a nerve in my neck. To the point wear I'm getting tingling and numbness in my arms. But what is odd is I'm getting crazy panic attacks when the numbness comes...

Great information.

Watching on KZfaq, of course from my phone..... as I recover from chemo infusion. MCAS, Gastroperesis, GERD, trigeminal neuralgia, migraines, CNS degeneration, cervical and thorasic degeneration, as well. All so relatable. Thinking of my boss with all of her hardware in her neck and my son who "needs" his knee replaced. Learning so much!

I can pretty much guarantee you’d recommend something for me, I just don’t know if we could afford traveling clean across the country when I have two very young people who heavily rely on me being with them. Let alone the costs of treatment on top of that. I’m literally about as far away as possible without being in Alaska or canada. I also need a lot more information before I make any choices. I do appreciate all this additional information because I was only seeking c1 and c2 instability yet you very accurately described how I’ve often found restoration of symptoms by laying down and a nap. A lot gets chalked up to being a mom of young kids but I’ve actually had this effect in my late teens how I would only be able to do so much before I had to lay down and get back to it after laying down. This makes me seem very lazy to some people.. I do have my c1 and c2 shift in opposite directions about once a year or so.

This information is simply Miraculous! I came across something that helped me after a year of suffering that doctors wanted me to go on all kinds of pills. I'm willing to share with everyone.

Try having reverse lordosis and Hashimoto's I like how he includes auto Immune. I used to have Migraine with aura until something snapped in my head. When its bright I wear hat sunglasses even in the house. It took 5 years to be somewhat normal. I ditched a fusion c4/c6 in 2020 because I knew I had Atlano-Axial instability from side impact whiplash. T.bone. 25 years ago a nurse said "This is always going to bother you."

My daughter has considered Hospice. We are just now looking into this condition. She has hEDS, dysautonomia, MCAS and IIH, She has suffered immensely and is only 24 years old.