How long have you had post-covid?
I´m hopin that my son and I recover soon. Of course. We´ve had it for six months now.
How long have you had it?
Would love to hear from those who are still as ill, as well as those that have started recovering and those who have recovered.
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
i think it's here to stay too, just like we have to deal with some sort of flu every year but i think this covid thing will be all year instead of seasonal..hoping i'm wrong, it's just what i think...i call it the Demon Virus...
Congrats on getting disability. I was told I need to work another two years before I can apply again. I am a teacher/tutor, right handed with a right hand and right leg tremor. Writing is not fun.
I HAVE HAD POST COVID FOR. 7 MONTHS. NO RELIEF
Had Covid last week in October 2022. Took me about 3 1/2 months to feel normal again. Was very tired and needed to stop whatever I was doing.
I walked whenever I could and increased my distance. I believe that this helped in my recovery. My PCP was ok with what I was doing.
Good luck to you both.
So sorry to hear that! Did you have an attorney help you? After I got denied the first time, I got one, and it helped a lot. By law, they can only charge a flat fee, which would come out of any back pay. I believe it’s like $3-4k. Best of luck to you! ❤️🩹
Had covid in Dec 2019 and have been in long covid since Jan 2020...internal tremors have been 24/7 since summer of 2021 and though the fog has lifted somewhat the lack of sleep makes daily living a challenge.
Going on 2 years. Like a roller coaster- start to get better and then regress. Warm weather has helped me. To anyone experiencing the LC roller coaster- keep fighting- we are all warriors and it takes alot of time, patience and self love/care. Its ok to feel like a defeated warrior sometimes- but every time you fall and get back up- you continue to be a strong, brave person- who is not defined by LC. This will pass. Sending hope out.
Since November 2020 slowly getting better
Same here...Got Covid late Feb-early March 2020. Then had to have my gangrenous gall bladder removed April 1st. So, between recovery from that and covid LC symptoms, I'm not sure when LC set in but, here it is close to 3 years later and am still dealing with LC "normals" ...extreme fatigue, brain fog, complete exhaustion following a simple 20 minute walk...But the internal tremors are truly disturbing...frightening actually, as my wildly creative imagination visualizes the tremors as the covid virus nibbling at my central nervous system.
I share so many of your symptoms! Scary to read that the lc vibration is damaging your organs...and the tremor is so constant is worrying...and my lc is messing with my thyroid, up and down with the dosage, but many have it worse, so hang in there and get some sleep!