478 total results
Comments (447)
I was diagnosed with POTS after my 1st time with COVID.
https://connect.mayoclinic.org/comment/1158604/
For me, the fatigue does get worse when I experience hunger, but shouldn’t really be hungry....
https://connect.mayoclinic.org/comment/1121800/
Please check out information on ME/CFS and POTS. I have both after Covid and both my...
https://connect.mayoclinic.org/comment/978654/
My husband has LC, and experiences extreme increases in heart rate when he stands. He was...
https://connect.mayoclinic.org/comment/1211660/
I had POTS before COVID, but it got worse after COVID. And you’re right, there is...
https://connect.mayoclinic.org/comment/1121358/
No, I’ve seen my cardiologist for pots and oncologist for chronic leukemia. I’ll try your suggestion...
https://connect.mayoclinic.org/comment/1267978/
That definitely sounds like POTS. I was diagnosed with POTS after having covid. It’s been 9...
https://connect.mayoclinic.org/comment/749876/
What is POTS and LDN? Help the uninformed by using complete words. Thanks.
https://connect.mayoclinic.org/comment/836706/
POTS because it causes my showers to create more fatigue than exercise, fatigue, lack of refreshing...
https://connect.mayoclinic.org/comment/1304670/
I just started on 1.75mg. I have PoTs too, so super sensitive.
https://connect.mayoclinic.org/comment/1124302/
My child had that after developing POTS following a viral illness (not COVID). The doctor said...
https://connect.mayoclinic.org/comment/802301/
Every evening I run a low grade fever for 30 minutes. I thought it too weird...
https://connect.mayoclinic.org/comment/1169879/
I agree. I had POTS, fibromyalgia and central sensitization syndrome prior to Long COVID, and if...
https://connect.mayoclinic.org/comment/1075934/
This is NOT in her head. My Electrophysiologist seems to be the only one taken ng...
https://connect.mayoclinic.org/comment/754480/
I had Covid Jan 2020. (East Coast) Developed into Ling Covid, then Essential Thrombocytosis and POTS.
https://connect.mayoclinic.org/comment/1241951/
Compression. Calf or leg sleeve. I have this sensation with POTS unless I'm wearing leg compression.
https://connect.mayoclinic.org/comment/874612/
I have gone through the U of M Post Covid Recovery Group Clinic. I loved it...
https://connect.mayoclinic.org/comment/801864/
My daughter developed POTS after a viral illness and had many similar symptoms - exhaustion, physical...
https://connect.mayoclinic.org/comment/795190/
I have had the same symptoms on and off. It's very disturbing and I feel unsure...
https://connect.mayoclinic.org/comment/738396/
I'd suggest periodically searching in PubMed (open to the public) on this topic to keep abreast...
https://connect.mayoclinic.org/comment/805794/
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