Post-COVID Recovery & COVID-19 Support Group

I’m now 6+ years into Long Covid with disabilitating symptoms never improving: high BP at rest but with ‘postural hypotension, not Pots’ , diagnosed with...

Long COVID has upended our lives, that I know. For those who've had it since 2020, I do not know how you have survived if...

I first contracted Covid in 2022. Then contracted again in 2023 & 2024 ( I had 4 vaccines). Then, after getting over the covid virus...

Im new to this forum and look forward to speaking with everyone. I hope this can be a help to all.I was diaginosed with a...

good evening, i guess we just say whats on our mind? Help. to tell the truth ive never been more scared in my life. my...

First - I thank the Lord I found this forum. I knew there had to be others having strange, unexplained issues. November of 2021, I...

I have posted before and read all of your posts, at least as many as I can. This month is 2 years I have been...

A long post in hopes of learning of others who have had symptoms that were not initially experienced but came on in waves. After reading...

So I had Covid in May this year and I had become extremely congested to the point I could barely hear and I also developed...

I was diagnosed with POTS about 8 months ago when at my PCPs, I was dizzy and my face went numb. 180/120. A quick dose...