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Post Interferon Syndrome

Infectious Diseases | Last Active: Dec 8 6:35pm | Replies (538)

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@jenglereckedbin

Like you and so so many more of us post treatment. I went back to my GP several times each year since 2006 and never got anywhere. I had a brain tumour removed in 2000 and after therapy etc regained my driving licence and back to work for a few years before the treatment. So obviously over the years I pinned all my symptoms etc onto that operation pre treatment. It's only since I found this site that everything makes sense. We must all be strong and hope an investigation will begin like the infected Blood one starting April 2019

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Replies to "Like you and so so many more of us post treatment. I went back to my..."

Hello, I often sit n think how one person could feel this darn bad all of the time. the pain in my bones is overwhelming, fatigue that gives me no choice but to lie down several times a day, muscle spasms contort my body, my memory is really really bad...i don't see me being able to function at all in the next few yrs and there is no way out. my daughter is also a RN n i don't even think that she takes me seriously...no one does but uall on this site. i just started my my 37th antibiotic in just two yrs thanks to CVID with predominant B cell damage thanks to interferon/ribaviron. i am gonna start on CBD oil soon due to all of the great work that it has proven on the human body...this is scientific proof. has anyone ever hear of LDN therapy??? I have heard great things about this but doesn't seem to be available anywhere near me. God bless all of u going this hell.