Have you been cured of POST COVID?
I would love to hear from folks that have been cured from Post COVID. What were your symptoms.... what things helped you improve? what things made it worse for you?
I ask because I am currently on a recovery journey - would love to understand what you've done
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
wonderful to hear good news.
continued good and better health…
i will mention infusions to my functional medicine dr.
thank you for sharing.
If your doctor agrees, I advise you to start with a low dose the first time and build up. Blessings.....
thanks
No cure for me, but I have been able to resume more physical activity. Actually walked 4miles! My leg muscles previously would have started feeling wooly afterwards when resting,
but I was ok this time.
Once in a while I get a brief taste of a food, a few seconds, then it's gone.
My brain fog gets prominent when I get stressed. No multi-tasking either.
My gift for cooking has gone.....I get confused now & have to strictly follow written recipes.
Many many other symptoms have altered my abilities, but are not life threatening.
I am not suffering pain as so many others are. My lungs&heart are well. My family supportive. I am blessed, but I am not my real regular self by any means & I am praying for us all to find a "cure".
Thanks J, I'm a Canadian in the Vancouver BC area, where most Long COVID clinics are now closed. In any event my GP advised against pursuing it as she said their recommendations tended to be very generic and unhelpful. Including 12 or more medical tests I've been following alternative medicine treatment (all on my own dime, and hence expensive) with some possible mild help (such as micro-dosing Naltrexone, and various supplements). No real improvement yet after 2+ years of Long COVID. Hanging in with you all, by God's grace :).
Wow! What a marathon! I live in Canada and not sure what your insurer covers with all this treatment, but other than traditional treatment covered by our government health care plans, we're on our own for alternative treatments (which I've been pursuing for 2+ years of LC). I'd love to try out much of what you describe, but I can't afford yet more on my own dime.
@joanma Thanks for this encouraging post.. any report of recovery, even slow, is helpful. I will look into the book you recommend. Also ...good to know about the Mayo clinic... and look forward to your reports on your progress.
Im with you! My lungs were never affected. My heart does a lot of weird things, but yet when monitored out in ER for this. They never have found anything. EKG's wore a heart monitor for two weeks, echo etc. I pressed the button on the heart monitor several times when I was having an episode and wrote the date and time so they could look back. There was just one little detection on their end. On the one they could track that was bad with chest pressure and extreme palpitations, they saw just minor disturbance. It's like this little mario brother man gets inside runs around causing chaos abs noone can catch him. That's how I visualize it! It's crazy as is the inner trembling that you cannot see on the outside. Bazaar!
Still have heart palpitations from May Covid and headache and neck pain. Sleeping better. Aby thoughts? Sometimes I feel like the headaches come from no caffeine. I didn't drink a lot of coffee. Always water to start then a cup of coffee. I drink 84 ounces of water a day. I give blood every 8 weeks except that timing in May-mid July. Wonder if I should stop or do less. 74 years old.
Interesting segment on WCBS (NYC) news tonight about long covid neurological issues. Apparently researchers at Penn have linked residual covid in the gut with interference with serotonin production that led to brain fog, memory problems, etc. This could lead to treatments (fingers crossed).