518 total results
Comments (487)
Yes , it is difficult to unpick symptoms from existing diseases from new ones, that are...
https://connect.mayoclinic.org/comment/1156706/
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/
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/
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/
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/
I just started on 1.75mg. I have PoTs too, so super sensitive.
https://connect.mayoclinic.org/comment/1124302/
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/
My child had that after developing POTS following a viral illness (not COVID). The doctor said...
https://connect.mayoclinic.org/comment/802301/
This is NOT in her head. My Electrophysiologist seems to be the only one taken ng...
https://connect.mayoclinic.org/comment/754480/
No, I’ve seen my cardiologist for pots and oncologist for chronic leukemia. I’ll try your suggestion...
https://connect.mayoclinic.org/comment/1267978/
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 see a physical therapist who specializes in Long Covid, and one of the things she...
https://connect.mayoclinic.org/comment/1366270/
POTS because it causes my showers to create more fatigue than exercise, fatigue, lack of refreshing...
https://connect.mayoclinic.org/comment/1304670/
YouTube has the CHOP PROTOCOL EXERCISES for pots. Long Covid meds? Which meds were recommended to...
https://connect.mayoclinic.org/comment/1366356/
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