Wow - God is working!! We are so blessed to be a part of your daughter’s regenerative medicine healing journey! We would absolutely love to have you in our office to get to the root cause of your daughters symptoms, in the meantime, know that we are praying for her complete healing💛

They do know, it's in their interest not to share it with you.

The ama would not want us to know how to help ourselves using the wise ones He created. The ama... crime against Americans. Dr. Hauser, wise man, man of God, educating.

As someone who troubleshoots electrical problems, it's common sense that the main wire being pinched will screw up the whole system. The nerves are basically the body's wiring harness. When your car's computer (your brain) throws a check engine light, its rarely actually an engine problem. It's almost always an electrical problem. Step one is always to check your wires and sensors. Make sure they're getting constant voltage. Sometimes it's fine while the car is parked but put it in gear and let it start moving around... this guy would make a good mechanic.

@@misterbulger Yesss!!! Love this statement. Perfect👏🏽🙂

when I was 4 I was diagnosed with hyper-mobile Eds, and then when I was 9 I was diagnosed with Pots

@@pianoistic5548 How old are you now and how are your symptoms?

@@juicedcactuz1738 im 13 and i do dislocate my knee caps, but i do see a joint doctor every 3 months and a cardiologist every 6

@@pianoistic5548 I'm sorry you've gone through that at such a young age but I'm glad you've found a channel like this one 🙏

For me/cfs how were you diagnosed? Was it based on any imaging or lab result

Glad you were able to make a connection to your case and hope that you will be able to find a Prolotherapist who can assess you in person and make some recommendations soon.

tyvärr det är sant Pernilla

Satisfaction

I have sent people to see you.

Same here. I also live in Sweden. I started seing RGB halos around light sources back in 2021. It also came with double vision. Pulsating low pitched tinnitus and spasming of the jagular veins as well as confusion/memory loss. Rotation vertigo and nystagumus. I was sent home from the ER multiple times and written of as suffering from somatization syndrome. All symptoms didn't occur at the same time. Some developed slowly one at a time over a few weeks. The halos persisted since. Then I got a relapse back in october with the exact same progression of symptoms. And this time the halos covers half my vision if I try to drive at night time so I had to stop doing that. I also have a worsening of tinnitus, the sensation that I will go blind. Telangiectasia all over the nose. Hyperadrenerg POTS with severly elevated diastolic BP. Erectile dysfunction. Chronic hip and back pain. And my voice has changed. I was a singer now I can't open up my sinuses which is needed for singing. I can't play computer games in 3D because I've lost the sense of dept. I used to compete in Quake Champions but had to quit that as well. So no more music, no more sex, and no more video games. And a hell of a lot visual disturbances. I was diagnosed with ME/CFS back in 2016. In 2019 my thumb all of a sudden went completely numb. I got an MRI which showed bone growth between vertabrae. A spine specialist thought I had "a hidden degenerative spine illness" directly translated from swedish. But my GP doesn't understand this. I have also developed issues with mast cell activation becsuse my tachycardia get worse with histamine rich foods. I feel like I'm slowly dying.

Thank you for your very kind words, Rose. We agree that EDS patients have been underserved, and often unacknowledged altogether, for so long by most mainstream medical systems, and we're doing what we can to raise awareness of hopeful options that may be explored. Sending you much love back and wishing you all the best in health!

My give away symptoms that I had EDS. Or just Hyoermobility syndrome My soft velvety skin that bruised so easily , Needing 6 x more injections , dentist , numb me up Lack of saliva , Blood noses when a teenager Chest pain Profuse sweating My skin was the absolute and recent exposure to Black mould The huge red rashes Hot flushing Big mast cell activation for sure I swear by clinical Pilates for strength especially if pain. Is in low back or pelvis Good luck

@@merrilynstanger7241 I’ve been diagnosed :) since this comment also diagnosed with fibro and POTs

Hi Amber, Thank you for your very kind feedback. Wishing you all the best on your health journey and finding a great doctor. If you feel that you would like to come to our center in the future, you are welcome to reach out to us directly to start looking more closely at your case. Take care, Amber. Blessings!

Pain is all in the head, literally. I said this at my pain management course when the course leader was talking about how pain works. I was half joking!

Thank you, Michelle. Our team thinks you're amazing too! Have a beautiful day! :)

Thank you for sharing, Dulcimerist. We hope you will continue to have relief from your symptoms, and we wish you all the best in health!

I would love to know who your doctor is so I can get help for this issue too. Thank you.

@@gardenia7098 My prescribing doctor is in the remote town where I live, but her decision to prescribe Mestinon was based on research articles by doctors who prescribe it from large medical facilities and wrote research studies about it. Dr. Adil E. Bharucha at Mayo Clinic in Rochester, MN wrote articles about it with digestive issues. Dr. Satish Raj at Vanderbilt Dysautonomia Center in Nashville, TN and Dr. Sanjay Gupta at York Cardiology in York, England wrote articles about Mestinon in treating POTS and dysautonomia.

@@Dulcimerist Recently came across this Rx for possibly my needs, so grateful that you gave some research info. Best to you in your healing journey. 🙏❤️🌈🪶

Thanks for watching! We are so glad that it is helpful :)

May Yah strengthen you in every way needed for the endurance and much love to you on your journey.

Hi Eamon, Thank you for your very kind words. Glad the video was helpful in any way. Sounds like a tough situation. We know there are not many specialists for EDS. We wish you and your partner all the best in health and finding the best doctor possible.

@@CaringmedicalProlotherapy Thank you my friend 💛

Hi Tommy, Thanks for your kind words. Glad you have found some possible ideas of what could be happening. Wish you all the best in health and navigating your options.

Hi Joseph, Thank you for your feedback. We look forward to helping you. Wish you all the best.

Glad you enjoyed it! Appreciate the feedback.

Thank you for the comment - we are so glad that you were able to learn from this video!

Wow, Barbara - we are praying for your complete healing! Keep pushing!

Same here

Yes I was diagnosed at age 30, after 18 years of pain, failed back and neck surgeries and disabled at 28. I'm 40 now and pray I can come across the provision to get this treatment.

Thank you for your kind words, Stephanie. We wish you all the best in health! Hope to talk with you more soon.

Hi Datahound, Happy to help in any way. Thanks for your kind feedback. Take care.

Thank you, wasimganchi, and God bless you too.

Hi emily, So sorry to hear about your long-term battle with being misdiagnosed and now having to resort to the ER for care. It sounds like you've endured a lot! Glad that you have found some of the content in our webinars helpful and hope-filled for new avenues to explore in your case. We do treat patients from California, and from all around the world. We take on a lot of severe cases, however, we cannot accept every case and we also understand that it is not feasible for everyone to travel/live here for care. In the most severe cases we take, patients have to live in Florida to be nearby the center for 2-3 months during the initial treatment phase. If you would like our team to review your case in more detail and see if you sound like a good candidate and what the next steps would be, we are always happy to talk with you about your case. Feel free to reach out anytime: www.caringmedical.com/conditions/prolotherapy-neck-pain-cervical-instability/#get-help-now We wish you all the best in health and finding a provider who can work with you to get to the root causes of why you are in a rapid decline. Hang in there, emily.

Have you heard of dr. John Bergmann from Huntington beach California?

Thank you, AdamRising, for your kind words. In our experience, a chiropractor can be a wonderful practitioner for cervical instability as far as analyzing the curve and helping patients restore a proper curve along with a Prolotherapist who is working on strengthening the ligaments in order to restore and maintain that stability. We would also look for the cause of the porphyria or other nerve damage to see if there is a structural reason in the neck that is causing it, like cervical instability or dysstructure. Wish you all the best in health!

Caring Medical just one more question, if you have vagus nerve problems, digestive issues, neurological due to cervical instability or tendon laxity...can restoring the curve with chiro/stretches and strengthening these tendons be done without prolotherapy or are you saying prolotherapy is the ONLY way?! Can anything else tighten up these loose/lax tendons...for people who can’t afford the treatments or are concerned about side effects or reactions from the prolotherapy. I’m talking about neck instability/tendon laxity only...not for people with EDS. Can simply stopping cracking your own neck stop this if the curve is restored and tendons restored? Thanks!

We are praying for your healing Grace - keep fighting!

@@CaringmedicalProlotherapy thanku so much for your prayers. Wishing u and ur team all a very merry Christmas from New Zealand :)

I’m also going to fly from sacramento to Florida to see you

Hi Faith F, Not anymore. We are in Fort Myers, Florida with 2 great Prolotherapists and Chiropractor. Thank you so much for your kind words. Wish you all the best in health!

Hi Sheena, Thanks for sharing your story and glad that you were able to find some help from your physical therapist and understanding of what may be happening in your case to cause the spasms. We wish you all the best as you work together on relieving your symptoms. Hope the webinar was able to provide some additional insight. Take care.

Wow I have all those..

It feels like impending doom

You are welcome and glad that there was some new information here that may be helpful for your case. Our hearts go out to you. We understand how absolutely horrible the pain from EDS can be. Hang in there.

Oh and I've had idiopathic intracranial hypertension, multiple sports injuries, and bendy party tricks galore.

Same with me…

Get treatment with Hauser at Caring Medical Florida, I'm doing it

Thank you, Dr. Greg william Rice, for your very kind feedback. Wishing you and your patients all the best in health!

And they think the multiple sclerosis diagnosis is just another unlucky thing I have acquired. They don’t want to see it as related to the neck issues. But it is.

Hi Lorraine, Good question. No, in fact, some patients do not know that they may have EDS prior to coming here because their other doctors had not thought to evaluate them for it, usually because they just are not familiar with EDS. But more often, patients who come to our clinic have already received the diagnosis and are looking into options for the musculoskeletal pain/subluxation aspect of their case. Either way, we are happy to evaluate someone's case to help determine if this might be a good fit for their case.

Hi Becca, Thanks for asking. We do not know of anyone with a similar clinic or doing upper cervical Prolotherapy there. We have patients who travel here from Australia, but understand it is not possible for everyone, nor can we accept all cases. If you would like us to review your case and see if it sounds like a good fit for our center, you are always welcome to reach out. Wish you all the best as you navigate your options.

Hi Shannon, Thank you for sharing. That does seem like the opposite affect, as Prolotherapy is used to help tighten the ligaments so the muscles can actually relax more and not need to keep activating due to the ligament-muscular reflex. Without knowing anything specific about your case or the exact treatment method/solution used, we couldn't shed too much light on anything. We hope that you and your doctor are able to find something to ease your chronic neck pain and tightness. If you felt that you wanted our team to review your case more thoroughly in the future, and possibly see you in our office for a Digital Motion X-ray and/or second opinion on Prolotherapy, you can reach out to us directly. We wish you all the best in healing!

Check out DNRS. It may help you with a lot of these sensitivities

Did you find anyone?

he's the one

Hi Sirri Niba Fon-Akkum, Thanks for the question. Yes, it can. We discuss this in our vagus nerve webinar series in more detail as well as some future videos we'll have coming out.

My question also. -I am in Sydney. Suspect a lot of very sophisticated equipment wd b necessary.

Any updates????

Hi Sam, we hear you and are sorry that you are experiencing this. There are things that can be done at home like diet, light exercise to strengthen, working on your HRV, however if there is degeneration, the only thing that can help heal it is regeneration which is why we do Prolotherapy. Instability is a degenerative disease that happens over time and if left untreated it only gets worse.

@CaringmedicalProlotherapy So I'm screwed without health coverage. This country is so sick and twisted.

Glad you lived till 66 you gave me hope! Just think of your misery as someone else's Victory!

😅

Hi jbirdhere11, So sorry to hear how long you've been suffering with pain. Patients do not need a referral to be seen here, but there is a case approval process. We have a very detailed case intake form to start, so you can tell us the details of your case in your own words and what your goals are, as well us upload any pertinent imaging reports or other medical records. If you seem like a good fit for our clinic, we would love to help you! Feel free to reach out to our team for a case review anytime you're ready. www.caringmedical.com/conditions/prolotherapy-neck-pain-cervical-instability/#get-help-now We wish you all the best in health!

No

Hi Chris, They may not be a good fit for our center, if their phobias are preventing them from obtaining certain testing/treatment. We cannot accept all cases, and we do a detailed clinical case review before having a patient travel here for testing or possible treatment. Thanks for the question. Take care.

We have had patients who are diagnosed later in life due to their doctors not understanding their symptoms!

I am starting through the process of diagnosis at age 66. I am doing it for my four children, 3 daughters and 1 son. I want to pass them proper information so their lives improve. I am doing it also for my remaining years; I want to enjoy my grandson, gardening, and being able to walk in our woods. It's never too late to try.

About $1660-$2000 out of pocket.