Post-COVID Recovery & COVID-19 Support Group

Hi. I’m desperate. I hate my life ever since I got severe Covid in 2023. I developed Guillian Barre syndrome and it comes back every...

I contracted Covid (confirmed - twice with tests) in early March. No fever or chills or lung issues. Horrible nasal congestion and headaches. Lasted about...

Hi everyone. I’ve been suffering from I’m pretty sure are the effects of Long Covid, but I’ll try to give as much details as possible,...

I have had long Covid for over a year, experiencing most of the symptoms noted by the CDC - coming, going, returning, and evolving. Today...

Good morning, my name is Chris. Over the past two months I have experienced moderate joint pain to no excessive pain in my large joints....

Oh this group is such a help and for it and to Mayo for it, thank you. From the start (April 2023 after COVID early...

Hi, all! It’s been so helpful seeing that it’s not just me still dealing with issues after Covid. I tested positive on December 31 of...

You're going through a lot. We all are. So this community is vital. Being a part of the many studies helps the research community to...

Is “long covid” actually mitochondrial disease? Has anyone gone to a Mitochondrial disease Is “long covid” actually mitochondrial disease? Has anyone gone to a Mitochondrial...

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...

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...

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...

I am desperate and I can't find anyone out there that is talking about this. It has drastically altered my quality of life. If I...

Recent reports are coming out that after initial recovery from covid, some are suddenly becoming very ill again with the virus. A recent article from...

I have read multiple people on the forum talk about a significant other not taking the reality of long Covid seriously. I have the exact...

Hello- I’m looking for others diagnosed with POTS, whether you had it before or after COVID. I’d like to know if you’re willing to share:...