after recently finding your channel, i haven’t ever seen better explanations of the links between FND/POTS/OI/&co - here in the UK, the NHS hardly provides any research or help (or testing!) for these problems!😅 really wish your clinic was here!🙏🏻
Very interesting. Could you provide a list, or make a video listing the abnormalities you're testing for in a new patient? Like the pupil dilation and other things you mention here. Or if it's personalized, what would you do to assemble such a personalized list of tests?
I wish I was able to access your clinic. I live in the UK and was diagnosed with pots/dysautonomia. Do you have any suggestions for how a person might improve without access to your clinic, but access to other services such as vestibular rehabilitation. 🙏
Great video to the insight of working with a patient in your clinic. How long was this patient with you was it ldid she do an intensive? What was the origin of her POTS, viral, concussion , EDS?
Thank you for your support! The origin of her POTS is a little difficult since I have no baseline of her from before she had POTS to compare, but she does not have EDS and didn’t indicate any significant past head injuries. She was with us for about a month and that was where we saw that huge turnaround in activity tolerance along. We also did a couple months of at home regiments to keep her going in the right direction! Hope this answered your question!
I’ve been dealing with post-covid disautonomia for more than 2 years, 40 years old. Tilt test is scheduled but I’ve been doing everything I can… it’s difficult to not be discouraged. When you mention CO2 levels, does that suggest that administration of supplemental oxygen might help? Also, understanding that there are many symptoms that can present, is there any common things a person can do that might help? I’ve been supplementing with Magnesium Glycinate and it has helped a bit… have had weight gain due to inactivity based on dizziness and it’s frustrating when physicians state “loose weight” as a recommendation- I was an army soldier and triathlete prior to this occurring. Is it safe to use Stim on the neck? I’m on RUclips now, probably like many of your viewers here, just seeking answers. Thank you for posting this!
I’m not sure how to ask this, but can you indicate an approximate success rate for this kind of problem? I am watching for ideas for a couple people dealing with post-covid POTS (or other post-viral POTS). I can really only make the occasional suggestion since they are overwhelmed to begin with.
I don’t have an exact percentage off the top of my head unfortunately, but I would say it’s very successful. From day one of a week long series of appointments we keep digging until we find the actual mechanism that is the underlying cause of their symptoms through many diagnostic tests. This video only outlines a few but we’ll be showcasing more in upcoming case study videos in case you were looking for more info! Hope this answers your question! If they are wanting a more one on one conversation feel free to have them contact my office! We would be happy to answer any questions!
Dr. Keiser, what is your range of cost for a complete POTS treatment plan for someone who has been dealing with symptoms for 2 yrs (not bedridden but suffering)? Would really appreciate the possible help.
Wow that's incredible! I've been labelled with M.E for 23 years . Most of that time sofa or bedridden. Definite Ortho intolerance. Also hEDS and bilateral transverse sinus stenosis and IH but not showing high pressure in lumbar puncture so not able to get stents here. Feelings of air hunger. Cold hands and feet. No medical help here .
Hi there, if you would like someone to help answer some questions or give you some advice regarding some of your symptoms feel free to contact our office!
Amazing! Could you recommend someone in Europe, preferably Germany from your network? I‘m a Long Covid sufferer and have neck instability, I‘m desperately looking for help…
I’ve been watching you videos quite often for about a year. I am interested in finding out if you can help with TOS. My daughter has multiple diagnosis EDS, FND,TOS, POTS, ASD and Tourette’s. We are from Canada but have travelled to the USA to see specialist. She’s been to the Cleveland clinic and also Chicago ( neurological wellness institute) other than getting diagnosed there seems to be nothing that has helped in improving her quality of life.
Thank you for your support! I think it would be very beneficial to get into contact with my office. You can call or text 7347075105 or email info@dr.keiser.com Looking forward to hearing from you!
Ironic you were talking about CO2. I was going to ask about it on this video in the comments. I discovered I have a below average BOLT score, (from watching a YT video about longevity I learned of this and checked it,) and wonder how this might affect dysautonomia symptoms. I have never checked this before, but I can tell you it feels like this is something that has gotten worse for me. And I certainly am more of aware of how often I sigh throughout the day and my spouse tells me. So I have been trying to catch myself doing this and stop doing this for starters. I am certain this has been messed up for since cv and forced to wear masks at work and just dealing with basic bs in general r/t this causing me to sigh too much 😂. Do you have this lady (case) working on improving CO2 tolerance?
![Seungmin "그렇게, 천천히, 우리(As we are)" | [Stray Kids : SKZ-PLAYER]](http://i.ytimg.com/vi/kAzmhLHePqU/mqdefault.jpg)
after recently finding your channel, i haven’t ever seen better explanations of the links between FND/POTS/OI/&co - here in the UK, the NHS hardly provides any research or help (or testing!) for these problems!😅
really wish your clinic was here!🙏🏻
Thank you so much, informative & helpful.
Incredible story thank you for sharing Dr. Keiser! 🙌
Very interesting. Could you provide a list, or make a video listing the abnormalities you're testing for in a new patient? Like the pupil dilation and other things you mention here. Or if it's personalized, what would you do to assemble such a personalized list of tests?
Tests don’t get someone well
I wish you were in FL
I wish I was able to access your clinic. I live in the UK and was diagnosed with pots/dysautonomia. Do you have any suggestions for how a person might improve without access to your clinic, but access to other services such as vestibular rehabilitation. 🙏
I’m bedbound with pots. I wish I had help.
Please look up the medical medium you will find real answers and how to heal
How are you now?
me too! 😢
Great video to the insight of working with a patient in your clinic. How long was this patient with you was it ldid she do an intensive? What was the origin of her POTS, viral, concussion , EDS?
Thank you for your support! The origin of her POTS is a little difficult since I have no baseline of her from before she had POTS to compare, but she does not have EDS and didn’t indicate any significant past head injuries. She was with us for about a month and that was where we saw that huge turnaround in activity tolerance along. We also did a couple months of at home regiments to keep her going in the right direction! Hope this answered your question!
I’ve been dealing with post-covid disautonomia for more than 2 years, 40 years old. Tilt test is scheduled but I’ve been doing everything I can… it’s difficult to not be discouraged. When you mention CO2 levels, does that suggest that administration of supplemental oxygen might help? Also, understanding that there are many symptoms that can present, is there any common things a person can do that might help? I’ve been supplementing with Magnesium Glycinate and it has helped a bit… have had weight gain due to inactivity based on dizziness and it’s frustrating when physicians state “loose weight” as a recommendation- I was an army soldier and triathlete prior to this occurring. Is it safe to use Stim on the neck? I’m on RUclips now, probably like many of your viewers here, just seeking answers. Thank you for posting this!
I’m not sure how to ask this, but can you indicate an approximate success rate for this kind of problem? I am watching for ideas for a couple people dealing with post-covid POTS (or other post-viral POTS). I can really only make the occasional suggestion since they are overwhelmed to begin with.
I don’t have an exact percentage off the top of my head unfortunately, but I would say it’s very successful. From day one of a week long series of appointments we keep digging until we find the actual mechanism that is the underlying cause of their symptoms through many diagnostic tests. This video only outlines a few but we’ll be showcasing more in upcoming case study videos in case you were looking for more info! Hope this answers your question! If they are wanting a more one on one conversation feel free to have them contact my office! We would be happy to answer any questions!
Mostly bed bound. I force myself to get up and do stuff. I have about 3 minutes to get back down or a faint.😢 3 yrs now after Covid.
Dr. Keiser, what is your range of cost for a complete POTS treatment plan for someone who has been dealing with symptoms for 2 yrs (not bedridden but suffering)?
Would really appreciate the possible help.
Wow that's incredible!
I've been labelled with M.E for 23 years . Most of that time sofa or bedridden. Definite Ortho intolerance. Also hEDS and bilateral transverse sinus stenosis and IH but not showing high pressure in lumbar puncture so not able to get stents here. Feelings of air hunger. Cold hands and feet. No medical help here .
Hi there, if you would like someone to help answer some questions or give you some advice regarding some of your symptoms feel free to contact our office!
Please look up the medical medium books you will find all the answers and you can fully heal.
Where is this clinic?
We’re located in Chelsea Michigan, USA
Amazing! Could you recommend someone in Europe, preferably Germany from your network? I‘m a Long Covid sufferer and have neck instability, I‘m desperately looking for help…
I’ve been watching you videos quite often for about a year. I am interested in finding out if you can help with TOS. My daughter has multiple diagnosis EDS, FND,TOS, POTS, ASD and Tourette’s. We are from Canada but have travelled to the USA to see specialist. She’s been to the Cleveland clinic and also Chicago ( neurological wellness institute) other than getting diagnosed there seems to be nothing that has helped in improving her quality of life.
Thank you for your support! I think it would be very beneficial to get into contact with my office. You can call or text 7347075105 or email info@dr.keiser.com Looking forward to hearing from you!
Please look up the medical medium books. Your daughter can heal.
Ironic you were talking about CO2. I was going to ask about it on this video in the comments. I discovered I have a below average BOLT score, (from watching a YT video about longevity I learned of this and checked it,) and wonder how this might affect dysautonomia symptoms. I have never checked this before, but I can tell you it feels like this is something that has gotten worse for me. And I certainly am more of aware of how often I sigh throughout the day and my spouse tells me. So I have been trying to catch myself doing this and stop doing this for starters. I am certain this has been messed up for since cv and forced to wear masks at work and just dealing with basic bs in general r/t this causing me to sigh too much 😂. Do you have this lady (case) working on improving CO2 tolerance?