@medee I don't think people come back here once they are 100% better. I feel it's like that saying, "out of sight, out of mind.'
@centralx I think plenty have recovered 100%, but they don't come back here because their symptoms are gone and this site is probably the last thing on their mind. Out of sight, out of mind.
@centralx I am longing to hear happy stories of recovery but I'm not hearing them either.
I've been suffering since last spring.
I so want to see all of is get well soon.
We are so compromised, all for doing what we thought was the right thing. 😠
@thamollusk that's good way of looking at it!!
I'm determined to follow up when this nightmare is over to give others hope!
@thamollusk You are right. I don’t post much on here but I’ve been reading posts on this forum since August last year and I think there are people that have recovered or at least 90-95% recovered but don’t come back as this site is the last thing on their mind as you say.
@callie I've recovered about 80% I think. I have great weeks, but I also have relapses like everyone else. I usually only jump on here when I'm having symptoms in hopes of finding info that may help my situation. I'm definitely much better in general compared to last May.
@thamollusk That’s great news! Really glad to hear that. It gives me and lot of people hope when they read that people are recovering! Yes this forum is a good place to help find info and advice when you are struggling with symptoms.
@centralx I was recently diagnosed with a high Ana level , Rheumatologist didn’t say which one just out me on anti inflammatory medicine which I’ve only taken 4 . When the pain is so bad. Please let me know what your results are and what’s the doctor said. Thanks . Hope we all recover soon.
@centralx I am longing to hear happy stories of recovery but I'm not hesringvthrm either.
I've been suffering since last spring.
I so want to see all of is get well soon.
We are so compromised, all for doing what we thought was the right thing. 😠
@cheridoerhotmail-com my Ana was the same as yours and my anti/ nuclear is positive and my titer is high. What did doctor do for you? Are what are you doing. They ruled out lupus for me and sojourns ( however you spell that) . Other things were negative. CRAZY
@medee Almost all 3 or 4 of my flare ups have been after I had a cold or covid. I think when the immune system gets rocked, you end up with a flare up.
How long have you been into this?
I hope we're not gonna end up like this for the rest of our lives!
@centralx I think plenty have recovered 100%, but they don't come back here because their symptoms are gone and this site is probably the last thing on their mind. Out of sight, out of mind.
Hi, I'm not so sure about that. I used to be a regular here but visit less frequent now because I still have symptoms and feel conscious of the fact that people are looking for good recovery news and hope and I don't want to harp on about my miserable ongoing symptoms. I have tried many remedies all tried by people here, the only real relief I had was when I took ivermectin for a week and I had no symptoms then but when I tried it the second time it wasn't as effective. I am currently trying eastern white pine needle tea (second day) and apart from an aching stomach, my giddiness is less. I am waiting for the day when I can give good news and hope to all. 🙏
Hello,
Have you had H.pylori after the second dose?
I just got a call from my doctor that they found H.pylori in my stomach and have to start immediately on 3 antibiotics treatment.
So I have been wondering if anyone else experienced the same problem. I had my second Physer dose on November, 2021 and since than, I have been with a pain above my stomach and under my chest. The pain was very strong the first couple of days and get lighter with the time. So I am wondering if anyone eles has had the same issue?
Thanks,
Zlatka
