Has anyone else had their chronic pain disappear while on Paxlovid?
So, I've got (diagnosed) Polymyalgia Rheumatica, in remission, and a whole host of other things. Like, CFS, right hip avascular necrosis, prominent epidural fat in multiple locations in my spine, just to name a few. But what's happened today takes the cake. Over 90% of my pain, which is chronic, has disappeared while I am on Paxlovid for having Covid. I've had to take the Paxlovid now for 3 days, I got on it early because my new "cold" moved quickly down into my lungs and I got seriously nauseous. That, doesn't happen for me, with colds, do we tested me (at home) for Covid, two times and both were positive. I currently have a good medical team, they called in the Paxlovid, and no other changes. I have good care at home, but 3 day in, almost all my pain is gone. Not that I'm complaining but I'd like to know what this might be. A pain management doc did do epidural steroid into L5 some weeks ago and it's true I've been slowing losing weight already, so that seems to be the first line of defense regarding dealing with epidural fat. I only learned about that a few days ago, and that sure gives me motive to lose more weight, but it's not like I have in just the last few days. Ideas? Meanwhile, I was taken off of all NSAIDs for CKD Stage 3 a month ago, so the pain went up, not down. What is the Paxlovid doing that makes my pain go away?
Interested in more discussions like this? Go to the Chronic Pain Support Group.
We’re you able to walk prior to taking the Paxlovid?
Yes. Had a lot of pain in shoulders and hips and back.
Disappeared about 12 hours after the first dose and stayed gone till about 12 hours after the last dose.
Interesting. Doesn’t seem like taking Paxlovid for the rest of your life is a viable option?
With the pain I’m in(8 most days), it would be tempting.
I have read of some studies of giving Paxlovid up to 15 days for long COVID. Many of my pain symptoms and fatigue came after a bout of Epstein-Barr virus about 20 years ago.