Case: Functional Neurological Disorder (FND) and POTS.

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About Dr Nathan Keiser:
Dr. Nathan Keiser DC, DACNB, FABBIR is a board certified chiropractic neurologist specializing in non-surgical, non-pharmaceutical treatment of dysautonomia, traumatic brain injury (concussion), and movement disorders.
Dr. Keiser was certified as a diplomate in chiropractic neurology by the American Board of Chiropractic Neurology (ACNB) in 2010
and has since served patients from across North America and around the globe in private practice.
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The information provided in this video is not medical advice, nor should it be taken or applied as a replacement for medical advice. Dr. Nathan Keiser, its employees, guests and affiliates assume no liability for the application of the information discussed.

[@millymay0025]

This is the BEST case study I have seen regards FND and POTS. I only wish all clinicians were created equally, thank you so much for sharing as this gives me real Hope for the future of FND combined POTS. Not one person with FND thinks of symptoms in terms of faking, because they are all to aware of their crippling reality. It is simply the medical community who have and continue (in some cases) to hold this incorrect view, ignorant or unwilling to understand the latest research and the ever proved possibly modern medicine still doesn’t know everything. The whole field of Medical Neurology owe patients of FND an apology for their treatment (or lack of) of them, and ironically it’s the Doctors who most need to apologise that will have the greatest issue with it. Thank you for bringing the combination of POTS and FND together in this fantastic presentation, it’s because of open minded, investigative and proactive people like yourself that some patients are receiving the support they need! I only wish that more patients with this particular combination could receive your care.

[@ChrisGascoigne1]

Had an appointment with a neurologist the other day Nate, and they said to me that FND was something that comes about in people because their brains are constantly concentrating on individual organs in the body, hence why these organs become and remain dysfunctional. Not sure whether she was trying to imply that I had control over these things, but it didn't really make sense to me. She got me to stand upright for about 2 minutes and after that she took heart rate and blood pressure, I think it came back about 145/90 and 108 bpm; during the test I could see my feet turning more and more purple, but she didn't really make anything of it. It's funny when you've got these array of symptoms that you never had before that restrict you hugely, but nobody can explain them to you, and no-one seems to think they're at all abnormal! Thank you for this video and for everything you do for this community 🤝

[@DiegoCauliflower]

Your channel is great and the experience you have is phenomenal. One piece of advice would be to increase the microphone level of your audio. Due to you having a soft and warm voice, it is very quiet and even with my speakers volume all the way up. Keep at it!

[@jessicabellone913]

Lol I feel the same. I really want to listen to this video but I can barely hear what is being said. Volume is maxed out.

[@theslopchop]

I dont think any nhs drs in the uk will give this much care and attention to any of their patients, or even have this knowledge?!

[@cherylstransky6311]

Incredible!! So happy for her! The work you do is so special and life changing, forever grateful for the time we had under your care🙏

[@Reffinej84]

Gosh, I wish there was access to this kind of medical support here. I'm waiting for cardiology to investigate likely POTS. Also have FND. In the lead up to first ED presentation I was getting regular episodes of what I now think was Tachycardia etc and needing to go and lie down for ages. It's almost as if the dysautonomia actually led TO the FND (maybe with other triggers, too, but they feel very intertwined).

[@strengthaxlesystem]

i had tachycardia from low vitamin d

[@theslopchop]

Love all these, please keep them coming 🙏

[@clarissericardo2313]

I do you do remote consultations ? For general advice, I know you can’t treat from distance! Thank you

[@natea2006]

How did the eye movement tests and treatment relate to posture and regaining the ability to walk?

[@jedaconnor1909]

Hello, I have had a concussion since being in a car accident in december. My condition worsened substantially 10 days ago, after starting on an SSRI medication (after about 10 days of being on it). I started presenting with severe POTS symptoms. One of the main issues prior to starting the medication was severe adrenaline surges at night, sleep apnea and feeling lightheaded / feeling like I was losing consciousness when lying down. I'm wondering if you can point me in the direction of a chiropractic neurologist in Calgary, AB Canada that might be able to help me? Thank you so much.

[@k91985]

I've been trying to get a bit of sun lately but it feels like I am half way to having a seizure since spending time in the sun.

[@strengthaxlesystem]

had tachycardia and palpitations from low vitamin d, many docs ignore this, wonder if pots/fnd patients are tested for vitamin d

[@gretawaag6812]

How did you get symptoms to improve in a few DAYS?!?! I've been in PT for 11 months and I still can't walk. Does that mean it's not FND?

[@dockeiser]

When you say PT I image you mean “graded exercise”, which in some cases people can see improvement, but if you’re already in good shape then it rarely provides results. You can check out some of our other videos about what we do as far as treatment fine our more recent videos! If you would like to have a one on one conversation to get more direct answers feel free to contact our office at (734)-707-5105

[@engjelllulaj3497]

Hello since december 21 i wake up in the middle of the night my body was feeling a little shake and then i get pannic wake up my chest was numb i couldnt breathe my musscles contract barely couldnt walk couldnt breath than i was sitting in the couch i had bed filling inside my body than my neck got numb and tham my head than i had like a shoc in my upper head and feelt like electricity released through my head i have done brain mri after 6 month that this episode happend my brain was normal. i fell tightnes in muscle every day i have fear and a lot of other things like when i walk i feel like my head is blocked feeling dizzy all the time a lot of blood test and cardiological visits and they say from cardiological side there is not a problem i have heavy chest all the time of the day and the problem that i hate most is my vision i see things strange idk how to explain like with light differnce and other things that i could not describe feeling fatigue all the time having no strength no energy. today i went to a different cardiolog and he told me i had pots please can you help me ??

[@dockeiser]

Hello, is there a way you can reach out to us at the office so we can learn more about your case? Call 734.707.5105 Thanks 🙏

[@sherrybutts5947]

Wow u have been in hell a long time!! Bless ur heart!!! I believe this guy is right on the money