Neurology of Cervical Instability:Vagus Nerve webinar - Part 3 - Ross Hauser, MD

[@cynthiastogden7000]

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 🇬🇧.

[@riteshnayak80]

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

[@CHRISTSPIRACY.comJESUSwasVegan]

thats the sad part, we are persecuted and ridiculed by docs and left to feel hopeless and isolated and even question our own sanity because they are too arrogant to bother researching!

[@tommyboy1986]

yeah thats a problem with many dr's, they have peoples health and lives at stake and yet most are not willing to do any research . It's just a factory assembly line style pill farm for easy to diagnose health issues , if you have something more rare or complicated good luck.

[@CaringmedicalProlotherapy]

Thank you for your kind feedback. Glad we can be of help in making sense of the neurology and possible underlying structural causes behind many of these related conditions. Wish you all the best in health!

[@Medietos]

@@CHRISTSPIRACY.comJESUSwasVegan I have been wondering about the process of them shutting off their conscience and ideals about helping patients and doing a good job. It probably helps the worse part of them to dominate, that their superiors(?) tell them to, want them to deceive, cheat, withhold, waste and use patients. And that Drs can claim they have to follow orders.

[@jamesnguyen7069]

what docs are u going to

[@joshuatmorton5716]

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!!

[@kyshtakyshta3248]

love this hope you are feeling better

[@CaringmedicalProlotherapy]

Thank you for sharing, Joshua. Sounds like you're doing a great job of taking steps to improve your health and stay active and in tune with your activity level and how that affects your cognitive ability. Good for you for making positive changes to both your intake of food and in social media! If you feel that you need our team in Florida in the future, we'd be happy to review your case in more detail and possibly help you here. We wish you all the best in health!

[@bethany7646]

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!!

[@nealschuurmans299]

Iookooikkkkjnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnnno

[@loveKG26]

They do they just use such symptoms to match up with the medicine industry services prescribed pills…..

[@nickwilliamssr6156]

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...❤️

[@savvyconsumer7342]

Here also. I actuality was dying. This is a terrible condition

[@roxyduncan8557]

Dr Ross is my hero! Had i not found him, totally by accident,

[@Oona707]

This is slowly dying

[@cheekytiki194]

This is exactly how I was feeling- that I was slowly dying . This is life changing! I am so thankful for Dr Hauser and his team.🙏

[@haysheryl2677]

I feel like I a slowly dying. I have had several cervical injuries.

[@alexlee8639]

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

[@c_farther5208]

In the U.S., medical care is a service and costs money, who would want to cure people with sugar free diets or vagal health, how would these corporations and doctors are incorporated, how would they make money? The tax alone on sugar ingredients in our food supply is a huge tax collector for the federal government as well. Suffering is good for the American economy.

[@BoysLikeMeee]

@@c_farther5208 🙄

[@leubanks3921]

Agreed. I’m going to try and get a telehealth with them ASAP to see if I’m a candidate for the this.

[@awareness9166]

Pple need to open up their mind to look into such treatment instead of popping western medicine s.

[@michaelh102]

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!

[@CaringmedicalProlotherapy]

Glad to help you connect the dots on your case, and hope that you will be able to use the information to get a treatment that will resolve your symptoms. We understand how long and tough the road can be with chronic pain and these autonomic nervous system symptoms. Wishing you all the best in health!

[@itumelengbaheteng8624]

B

[@freedomforever1962]

IS THIS TEST COVERED BY INSURANCE??

[@elkierose6228]

And me.

[@trinakozak4557]

Any place in California for this type of treatment?

[@sbrazwell42]

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

[@infinitum5425]

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!

[@sheilasmith1109]

You really need to look into EMF’s with all the frequencies you’re around! Check KZbin for video on air pods and cell phones. Working in the tech world is amplifying your exposure!! I’ll get the link and post it here! Take care!

[@infinitum5425]

@@sheilasmith1109 hey thanks very much Sheila , really appreciate it. I'll try somehow to mitigate those EMF's. 😉

[@Mayankpaul6]

Delhi me hospital hai kya

[@theideasman6018]

DR Alex Tubio. KZbin him. Stay strong

[@mahesmuniandy5004]

U have breathing issue?

[@PropheticCoachTheresa]

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!

[@y.beckett1811]

I need this evaluation. How do

[@y.beckett1811]

I want to try this

[@francesg.1587]

How do I get your evaluation please?

[@rasheedahkriel7184]

Hey there, Well said! 💯.. God bless you an Everyone reading this😊

[@bradstein8776]

I would love to chat with you on the phone, if possible. Very well said

[@wmgodfrey1770]

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.

[@CaringmedicalProlotherapy]

Hi Wm Godfrey- Thank you for taking the time to leave your feedback. We wish you all the best in your research and in health!

[@osirissbeautifulworldoftin6982]

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.

[@CaringmedicalProlotherapy]

Hi Claire, Yes, we completely understand where you are coming from. Sadly, it is common for people to essentially give up trying to "convince" other people that their hypermobility condition is real. It is so awful what people go through, especially with those closest to them who just do not understand. It takes the toll from being primarily physical to then include a lot of emotional and spiritual damage that people suffer, and it is not uncommon for new patients to arrive in our office feeling pretty defeated by years of feeling this way. While they can feel their body becoming more unstable or "like it's falling apart" no one believes them and they are dismissed or labeled as "attention-seeking." We hear so many heart-breaking stories from our new EDS patients while we're going through their very long medical histories of their attempts to get to the bottom of their condition all while feeling quite alone in the quest. The good news is our team is very passionate about helping these people, and we do! We're on the same team and see incredible transformations in people. We're really sorry that you have been experiencing the physical and emotional stress of hEDS for so long, and we'd love to help you if you want to reach out to us directly to review your case to see if we can help turn it around. Wish you all the best in health and healing! Take care for now.

[@gloriakummer5357]

I have EDS too and about ready to give up.

[@justin.w9771]

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

[@drunkmanonlaptop1035]

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

[@ellinmarch1122]

I have hope for answers now! Thank you!

[@drunkmanonlaptop1035]

I LIVE IN SCOTLAND. YOU'RE BRILLIANT.

[@roxyduncan8557]

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

[@mdee860]

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!!!

[@CaringmedicalProlotherapy]

Thank you for sharing M Dee. Glad that you are connecting the dots on your case and finding some possible avenues to explore going forward. We wish you all the best in health! Appreciate you taking a moment to share your story.

[@mdee860]

@@CaringmedicalProlotherapy - eeks, left out the main stuff, 15 yrs after horse accident & being told I had GERD, finally found my way to UPENN Musculoskeletal Center. They DX, after many MRIs: missing disks c4-c7 - bone on bone, foraminal & central stenosis, Anterolisthesis, Ridiculopathy, bulging c1-c3, bone spurs, uncovertable facet stuff (last stage) etc. I am finally connecting the pressure on my head, VHR - variable heart rate & the spasms, nausea, random inhalation issues, heat & cold fluctuations & my Reynauds with CCI. Eye Drs. DX after 3+ hour tests, a TBI - Visual. Do you think you can help me? I am so tired of living like this. I am in NJ & can come to Ft. Myers. My PCP has been circling around Autodysnomia, ME/CFS. I have also been looking at much research & have included searches on Vagus & Phrenic Nerve damage. I refuse to have multilevel fusion until someone can give me a DX that encompasses all of this, not just my arms & shoulders w/only a 60% chance of "some improvement." PS: practically begged Spine Surgeon @ UPENN for an upright MRI. He wasn't interested in my opinion, so, nope.

[@CaringmedicalProlotherapy]

@@mdee860 We have definitely seen and spoken with many people with similar circumstances who are having a really tough time getting testing or any doctor to try and listen to what they're saying about the neck symptoms. Sorry that you are going through all of this. Again, glad you are listening to your gut and trying to do your research on what could be going on. We would be happy to do an in-depth look at your case and see if it sounds like a good fit for our center. Here is a link to our case intake form which you can complete and upload with your scans: www.caringmedical.com/hauser-neck-center/ Look forward to talking with you and seeing if it sounds like we can help. Take care for now.

[@divine1052]

Hope you've been improving, since your post. Where you able to get any help from the Medical Caring Center? 🙏❤️

[@simonbastin5346]

I've just seen this and I have exactly the same problem....I've been told it's acid reflux but I KNOW it isn't....what you describe has been happening to me for years....I've learnt to live with it but it has so many knock on effects it's frightening and so debilitating......I'm in UK and trying to find help locally.....no luck yet

[@osirissbeautifulworldoftin6982]

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 😢

[@womensglobe4182]

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.

[@CaringmedicalProlotherapy]

Thanks for sharing! Glad you found it useful and we wish you and your patients all the very best in health!

[@drunkmanonlaptop1035]

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

[@leontemonica7645]

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

[@osirissbeautifulworldoftin6982]

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 ❤

[@c_farther5208]

Just try this, just try it. Go 6 weeks without sugar, fructose, corn syrups, chemicals of all kinds, just whole foods and see how you feel; I will guarantee you, you will heal yourself.

[@sneakypress]

Dear C_Farther, We have been doing exactly this for 25 years, and yes, it is a fantastic treatment program from the point of view of limiting symptoms and preventing further deterioration. However, everything Doctor Hauser is discussing in these videos appears to be spot on and only time will tell if the treatments he proposes is are relevant to the collection of signs and symptoms we are all enduring. It seems to us that in many cases, injury to the back - and most importantly the vertebrae - is what underlies the development of the condition. ?!?

[@SmoothOperator319]

@@c_farther5208 tried that for 6 years… where is the guarantee?

[@kbellmurray]

So relatable, this story. Solidarity to Stephanie.

[@jeffgarrison7056]

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

[@luzlombardi6747]

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

[@lauriegmurray]

Did you get to see Dr Hauser? Would love to talk. I am in NYS too (near Ithaca).

[@mariaboyd7380]

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.

[@pattiissa9035]

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.

[@marykennedysherin3330]

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!

[@K-Blao]

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.

[@424io]

The gypsies are the missing tribe of Israel, this the reason they're are nomadic always on the move, travelers.

[@snowyowl6892]

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. ?

[@lindawaxman570]

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.🙏

[@CynthiaHunterNightwillow]

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.

[@CaringmedicalProlotherapy]

Hi Cynthia, Thank you for sharing. So sorry to hear about your fractured spine and the subsequent events that have cause so many awful symptoms! Glad that you connected with Stefanie's story and we hope that you will be able to get some relief as you heal from your surgery. If you feel that you need our team here in Florida in the future, you are welcome to reach out. We wish you all the best in healing! Take care, Cynthia.

[@CynthiaHunterNightwillow]

@@CaringmedicalProlotherapy tyvm i appreciate that

[@bartowflorida]

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

[@G.G.8GG]

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.

[@CaringmedicalProlotherapy]

Thanks for sharing. We hope that you find the ideal treatment for your situation. Take care, Esther.

[@nalignmentwlifehealinglife]

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

[@CuddleClaw.]

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!

[@emonhosen535]

I hope you get well soon.. Btw, what are you symptoms?

[@ronnipassmore8717]

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

[@altamau8678]

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.

[@argentinarodriguez4170]

Please, did you really find the answer? I hope you did! I just listened to the doctor and I also believe I found the answer to my problem, too!!😇😇😇😇

[@msyhan9576]

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!

[@inspiremearts]

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

[@k.c.whatyoudidthere]

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

[@darlenericotta7550]

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

[@AllenBarclayAllen]

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..!

[@jacqulineloncke8696]

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

[@drunkmanonlaptop1035]

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

[@c_farther5208]

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.

[@CaringmedicalProlotherapy]

Hi C_Farther - That is excellent to hear about your noticeable improvement by giving up sugar! Way to go! We wish more people would do that! We've written extensively on this topic in our books and within handout materials for our patients. One of the top things people can do to improve their health is eliminate processed foods and sugars. For some people, even their typical daily fruit intake is too much sugar. For others, some fruit and natural sugars are ok or an occasional treat is not going to cause them extreme symptoms. But we find that diet is very important in reducing unnecessary stress on our immune system. Wish you all the best in continued good health!

[@augustaporter3735]

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.

[@spierre7879]

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 :/

[@Ray-cc3vh]

Let me know if you find anyone. I'm also in Perth western Australia

[@dutyofcall7659]

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

[@lorriecunnington4109]

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.

[@kbellmurray]

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.

[@CaringmedicalProlotherapy]

Yes, Stella, it is heartbreaking when doctors only rely on MRI findings or something like that and do not see anything wrong so they just dismiss the patient's symptoms. Sorry you have been experiencing all of this throughout your long journey with these symptoms.

[@CHRISTSPIRACY.comJESUSwasVegan]

hug. im 43 and came across the vagus nerve idea in a house episode years and years ago and have spent my life ridiculed and imagining my funeral and because docs acted like theres nothing wrong, my kids dad told them i was making it up for attention and alienated me and they felt betrayal and mistrust and one wont even talk to me. id say most people who find themselves here on this page can relate

[@CHRISTSPIRACY.comJESUSwasVegan]

and they dismiss anything you find "on the internet" its very traumatic

[@terriepage5386]

​@@CHRISTSPIRACY.comJESUSwasVegan I have to agree I have been going to docs for 10 yrs trying to find my problems .I found a functional doc who had diagnosed me with Hashimoto's, I found out yesterday I also have celiac. I have the fast and slow heart rate ,bloating ,never know if I'm going to wake up energized or tired .I have neck pain at times that goes from the left and right shoulder I have had several whiplashes . I have been looking up stuff on the vegus nerve but if I say anything to docs they avoid it. Are there any docs like you here in Idaho I am desperate.

[@rickspalding3047]

Most people don't care, had a friend that said somethings wrong, took 10 yrs to find out he had lymes

[@jomacTinyadventures]

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 !

[@leubanks3921]

Can correcting Cervical instability correct IIH?

[@dana102083]

@@leubanks3921 that's a good questions for a doctor! :) but if you correct alignment, blood flow and CSF flow can be better, so can cautious and meaningful posture and movement, stabilizing and strengthening muscles, and holistic care (emotions effect posture, sleep posture, shoe-hip- alignment all the way up) there's other things too to align and promote being "straight". I have EDS and ligament laxicity, no one will check me for instability in Canada as we only have one doc to fix it and we don't have scans to look for it (upright flexible MRI). I eat a ketogenic diet to control my sleep, hormones, pain, minimize subluxations, ketones benefit the brain, decrease my brain fog.. much more.. list is long. If you want more info I'd suggest popping by my facebook group, keto for chronic disease management. There's some decent connective tissue/collagen/vitc and general cell function info to benefit us zebras in the midst-- are you a zebra too? I'm an open book willing to chat. I'm sure many EDS folks are here, whether they know it or not!! :) Take care xx

[@leubanks3921]

@@dana102083 My neck is so stiff and hurts all the time, head pressure is horrible. I have cervical instability per mri of upper cervical. Drs in Memphis just tell me I have autonomic dysfunction which is causing my hr and bp increase when I stand. I feel like I have IIH because of head pressure symptoms being so bad with headaches. When I lay down things setting and head feels better. I’ve also just found out I have chronic Lyme. I’m worried Inhave a csf leak because in may 2018 I was bending over a copier at work and the is clear with a brown tint liquid poured out of my nose. Did it that day and another day a few days apart. I went to school nurse and she said probably just sinus so I never thought much more about it. Fast forward all my autonomic issues started March 2020. So something is causing this head pressure. Is the Dysautonomia, Lyme, possible CSF leak causing all this crazy. Finding a dr that understands this appears to be impossible.

[@CaringmedicalProlotherapy]

Hi Loretta, Yes it can, in our experience. We discuss this in other videos and will have more specifically on IIH in the coming months. Here is a recent one you may find interesting: kzbin.info/www/bejne/gIXJoGNsjsqHha8 Hope it helps in any way. Take care, Loretta.

[@dana102083]

@@leubanks3921 lyme mimicks eds symptoms as its attacking the connective tissued :( sometimes stiffness comes after being mobile, too.. Thats unfortunate the nurse lead you astray, id definitely get a transferin? test and collect the flyid cleanly if it happens again. Have you seen a neurologist? A functional doctor i think would be the best from what i know but rheumatologists may help treat it. Im in a good leak group if you need to ask people questions about steps but theres specific cranial groups. Let me know 🙏

[@davidedeblasio1783]

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

[@CaringmedicalProlotherapy]

Thank you for your kind words, Davide. Cheers!

[@yourcoachbladimirsantos5136]

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

[@privateaccountfor1252]

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🙏

[@womensglobe4182]

Thanks for this scientific seminar

[@meiliu1020]

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.

[@JacksonStar4757]

How did you heal then if you didn't get prolotherapy? Cervical instability is a structural problem that needs fixed and lax ligaments don't just heal on their own

[@TeslaWorkshop]

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

[@CaringmedicalProlotherapy]

We are glad that you were able to get some answers to help advocate for yourself!

[@drunkmanonlaptop1035]

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

[@snowyowl6892]

Mine too - v painful - and my left knee fails me occasionally ... I wonder ...

[@immaculavilson-paul8181]

Amazing information thank you Doctors

[@drunkmanonlaptop1035]

ABSOLUTELY BRILLIANT.

[@joelee5875]

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.

[@Afitz4420]

Thank you! Dr. Hauser !

[@ryanneilcarr]

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. 🤔

[@CaringmedicalProlotherapy]

Thanks Ryan- we will work on it. All the best to you. Take care.

[@osirissbeautifulworldoftin6982]

Yes ME/CFS / Fibromyalgia and MCAS all have huge communities online and to my knowledge very few are aware of the connection to the vagus nerve. This would really help A LOT of people.

[@jmcmondego]

This might be the case of Jeniffer Brea...the lady that filmed Unrest. She had ME/CFS and after correcting craniocervical instability and tethered Cord Syndrome her symptoms went away

[@mdee860]

Ryan C - Yes, Yes, Yes!!! Did you read the article in Hope Rising: 'Could CCI/AII be causing my ME/CFS' !?? Amazingly enlightening.

[@mdee860]

@@CaringmedicalProlotherapy - PLEASE read that article from Hope Rising - "Could CCI/AII Be Causing my ME/CFS. Game changer.

[@jaymevogl4338]

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 💜

[@RS-hj7ow]

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.

[@CaringmedicalProlotherapy]

Hi Shane, Thank you for sharing and very sorry to hear about how bad these issues have become for the past 15+ years. Glad you are looking into possible options to explore. If you are thinking about seeing us in Florida, here is a link to contact us at the neck center: www.caringmedical.com/hauser-neck-center/ Wish you all the best in getting to the bottom of your symptoms and restoring your vagus nerve function and spinal stability! Take care, Shane.

[@AllenBarclayAllen]

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..!

[@margaretneanover3385]

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

[@beutel6116]

Consider having an upright CT.

[@duchessmartinez2035]

Watching on KZbin, 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!

[@drunkmanonlaptop1035]

ABSOLUTELY CORRECT.

[@VusiHlophe-jt8hh]

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

[@jilliansunrise7006]

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.

[@bonnierandklev1463]

Please share

[@jilliansunrise7006]

@@bonnierandklev1463 Hi, lavender essential oil rubbed on the vagus nerve in my neck 3 times a day and before bed. I also drink lavender tea.

[@bonnierandklev1463]

Thank you

[@estheracosta6510]

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

[@jacqulineloncke8696]

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

[@mishaanton5436]

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.

[@Oona707]

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

[@jennifergalberth1240]

Drs fault NOT moms.

[@jennifergalberth1240]

Osteopath

[@cartb3474]

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

[@Leah_Worth]

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.

[@elizabethjones3736]

Soo great to listen and learn from you.

[@joechiro]

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

[@CaringmedicalProlotherapy]

Hi Dr. Lerano, Thanks for your kind words. Wish you all the best in health!

[@mdee860]

Dr. Leanne- for the sake of your cervical patients, please switch to Pro-Adjust type - electrical alignment, no physical manipulations. TG I never let my Chiro do a physical manipulation. Found out later, that could have killed or paralyzed me.

[@mammothunter9084]

My craniocervical instability was caused by a chiropractor. Comments like this just highlight the fact I should have never trusted my neck to one

[@joechiro]

@@mammothunter9084 your experience is as valid as mine... i advise people daily about this phenomenon... lets say, most cci is actually caused by a car accident, who do you blame then

[@joechiro]

@@mammothunter9084 the influenza vaccine causes GBS syndrome; so does influenza... this is a complex world and your comment is valid

[@JM-zq9em]

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...

[@CaringmedicalProlotherapy]

Hi J M, Thank you for sharing. In our experience, that is not odd at all. In fact, it is very common in cases of cervical instability- both pinched nerves and a feeling of panic or sudden anxiety. Sorry that you are experiencing this and hope that you are able to get to the bottom of it soon. Glad you're exploring some options. Wish you all the best in healing!

[@JM-zq9em]

@@CaringmedicalProlotherapy yeah thanks for posting your video because it finally helped me realize I wasn't going crazy

[@yosie1975]

I’m the same way !!

[@colleenbentley9985]

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!

[@CaringmedicalProlotherapy]

Hi Colleen, So sorry to hear about your husband's condition since the surgery! Glad you are doing research to see what may be happening and what you could do to help. We would be happy to review his case in more detail and see if he sounds like a good candidate for our clinic. Feel free to reach out to us directly through our website where we have a more detailed case intake form and ability to upload a recent report, if applicable. www.caringmedical.com/head-neck-specialist-visit/ Wish you all the best in health and getting to the bottom of what is happening with your husband. If you would like our help, we're here.

[@mpen5014]

@Colleen Bentley -how is your husband doing now? 🙏🙏

[@ollymounara605]

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.

[@Pslm91v14n15]

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.

[@ellinmarch1122]

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

[@jacqulineloncke8696]

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

[@sicoholic]

The Vegas nevre is also responsible for the release of the hormone oxytocin which could be considered the love and brave hormone responsible for social bonding and childbirth. This is a really big deal when we try to make sense of general anxiety and anxiety disorders. What I'm really tiring to focus the all this research on is with people who have a Hiatal Hernia that seem to have poor vagus nerve activity and crippling anxiety. Have You or your team help people with these conditions? Would be grate to get a better insight to all this.

[@CaringmedicalProlotherapy]

Hi Sai Mitch, Thanks for sharing. Our approach is to dig deeper than just the hernia diagnosis and look at the person's whole medical history and constellation of symptoms to see if there may be a reason to suspect a structural cause in the neck. With anxiety, we have even seen that this can have a structural cause: kzbin.info/www/bejne/iYHMk6ZvgNV4maM Hope it helps in any way. If you feel that you would like to potentially see our team in Florida for help directly, you are welcome to reach out to us: www.caringmedical.com/hauser-neck-center/strenuous-dynamic-vagus-nerve-testing-caring-medical-florida/ We wish you all the best in health!

[@GypsyinAus]

WoW!! do you have anyone in Australia that does this procedure?

[@sneakypress]

Hi Doctor Hauser and Caring Medical, As with many of these people, I also believe your descriptions and explanations fit my collection of signs and symptoms. Here in AUSTRALIA, there does not yet appear to be any help for people with this/these types of conditions. It appears to me that the underlying cause of (reason for) the development of the disease is damage to the vertebrae, i.e. a physical accident (in many cases), like falling on to the back, or could it be head trauma (falling and hitting the head, particularly the back of the head); or can it be a combination of both these types of events. And are there other possible reasons for the development of the condition? Thank you for all your time and energy, and great efforts to explain clearly, what is actually happening, and how it causes the physiological and pathological effects. Everyone greatly appreciates, these videos.

[@freeradical3592]

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.

[@kelliegirl011]

I be curious to see how conditions like Neurofibromatosis NF1 and tumor growth affects the vagus nerve. So need to-learn more of this.

[@sharonspencer2312]

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

[@americafirst9699]

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

[@lovingthisagain]

Where are the videos/parts where he speaks about how ppl can regenerate their vagus?

[@disdathit]

Agreed. That information is lacking. Most people will not be able to visit his practice.

[@donnavogel7131]

Does anyone know where to purchase a Parasym tVNS device in the USA. Thanks

[@knightsvoncross]

I need to transcribe this with Dr. Hauser's permission to share with my family and friends and Doctors here in VA. That are not as familiar with this research and the Prolotherapy treatment! My name is Cecily Nichols. I was a LPN and I am having these health issues since COVID. I have most of these signs and symptoms now. (July2022)

[@rickspalding3047]

What if your neck is tight? My collarbone has been pushed forward on the left, ,got a lipoma from it, and had blood clots on the other side, then a few years later diagnosed with ulcerative colitis. It's hard enough to find a dr to get an xray, who is going to do a mobile x ray on my neck. And yes, I'll adjust my collarbone and some times drop to the ground from being so tight in the neck

[@waheguruwaheguru9176]

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

[@joshs2444]

Hi Dr. Hauser. I have POTS/Dysautonomia along with many vagus nerve dysfunction symptoms. Ive long suspected of having cervical Instability and just had a Digital Motion X-ray done today. Just briefly looking over the video it showed that I have severe C1 instability along with instability at C3, C5, C6, I believe. I'm going to be getting the full written report on monday along with a couple copies of the video. I was wondering if it would be possible to send one of the copies to your clinic to get your opinion on it. As far as I'm aware there is no prolotherapy near me or even in my state. I believe prolotherapy would really help my ligament damage and want to avoid surgery as much as possible. Please let me know if this would be possible thanks.

[@CaringmedicalProlotherapy]

Hi Josh, Sorry to hear that you have been dealing with POTS and other cervical instability symptoms for so long! Glad that you were able to validate your suspicion with the DMX. Yes, we would be happy to review your DMX and more details on your case. On our website, under the Neck Pain section, you will see the Get Help Now tab and there is a detailed case intake form as well as a place to upload reports. You can also email them directly to [e-mail] as well. We look forward to helping you, Josh! Take care for now.

[@mdee860]

Josh - read the online article from Hope Rising - "Can CCI/AII (Aii) be Causing my ME/CFS & POTS?

[@ccsnaturalroute5446]

Hello josh, did you happen to find a solution? My condition is close to yours please lmk thank you

[@Nizzwell]

I have this you've described all my issues, just brain and neck scan, I have head pressure horrendously where I gave to sit down quickly.. and light sensitivity and I can feel fluid gushing behind my head where it joins the neck, I get digestive issues and I'm all over the place balance wise, electric shocks across my head up the sides and across the forehead. Constant pain up the left side of my neck. What a nightmare

[@CaringmedicalProlotherapy]

If you wanted our team to help you, we are accepting new patients, although we understand that is not always feasible for patients to travel here. Glad you are doing your own research on your symptoms and potential options to get answers on how to resolve your symptoms. Thanks for sharing your story. Sorry to hear it has been such a long and painful road. Hope to meet you in person in the future!