544 total results
Comments (508)
YouTube has the CHOP PROTOCOL EXERCISES for pots. Long Covid meds? Which meds were recommended to...
https://connect.mayoclinic.org/comment/1366356/
I have gone through the U of M Post Covid Recovery Group Clinic. I loved it...
https://connect.mayoclinic.org/comment/801864/
I have had the same symptoms on and off. It's very disturbing and I feel unsure...
https://connect.mayoclinic.org/comment/738396/
If dysautonomia (POTS or other types of orthostatic issues) are present, you could try to get...
https://connect.mayoclinic.org/comment/1333234/
For anyone with POTS after Covid, there is a clinical trial of a medication called efgartigimod...
https://connect.mayoclinic.org/comment/838567/
I had very early Covid and never felt well after that. Covid affects your immune system...
https://connect.mayoclinic.org/comment/1229756/
With my ET I had what docs thought was Long Covid. I then saw a cardiologist...
https://connect.mayoclinic.org/comment/1164458/
Hi- Just wanted to say that I had an appointment with Dr. Tae Chung in the...
https://connect.mayoclinic.org/comment/1075041/
I’ve had pots for a very long time. Fludrocortisone helps push my pressure quickly but I...
https://connect.mayoclinic.org/comment/1139980/
Did anyone else’s POTs or CFS/ME meds stop working for them after Covid, or become far...
https://connect.mayoclinic.org/comment/978721/
I take, as needed, Meclizine. This was given to me for vertigo, or motion sickness. It...
https://connect.mayoclinic.org/comment/1165148/
I can’t tell if my leg problems are from LC or my POTS. I had early...
https://connect.mayoclinic.org/comment/1332403/
I have POTS. I tend to eat regular salt as much as I can. My PCP...
https://connect.mayoclinic.org/comment/1153531/
I had long Covid which caused ET, essential Thrombocytosis, and then POTS. I have different meds...
https://connect.mayoclinic.org/comment/1139751/
My son has had a bad case of POTS. I´m a doctor and one of my...
https://connect.mayoclinic.org/comment/828317/
@jrg200911 Thank you. Yes, to the whole laundry list of symptoms..I hear you. Main concern was...
https://connect.mayoclinic.org/comment/1499584/
Unfortunately yes…I’ve got dystautonomia with Long Covid…there are a number of different ones, perhaps the best...
https://connect.mayoclinic.org/comment/1408727/
I hope someone responds. I’m interested in this info too, though I don’t have POTS. I...
https://connect.mayoclinic.org/comment/1152734/
@tiredoflc I could not agree more. I have had similar experiences to yours. My internist has...
https://connect.mayoclinic.org/comment/1579919/
Hey, I also have worsened pots after covid and LC. I live in Raleigh and am...
https://connect.mayoclinic.org/comment/1122181/
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