The problem is docs are so uninformed and not willing to go the extra mile. My neurologist told me she was not interested in me sharing research with her to help me. I work in the medical profession and was blown away. I was injured by th he covid vaccine and it has been almost 3 years of gaslighting or being told there is nothing they can do. I have had to research myself and tell them what I need. Good doctors are rare nowadays.
The way I test for my own EBV has been- EBV DNA whole blood lab, as well as EBV IgM and I check EBV VCA IgA too(all high for years, and an NIH dr told me they see my EBVDNA levels in HIV patients. Yet I don't have HIV. My CMV fluctuates. My CRP has been high for fewyears, and now im making kappa chains. It would be great to get solid answers, and TREATMENT to get better!
Has monolaurin been tried for long covid? Ive heard it can help with EBV(I am trying it for reactivated EBZv ive gad since 2018). Reactivated EBV is exhausting, but doctors dont do anything with it unless it is a severe infection. They dont understand that low level chronic infection is debilitating and you feel the same for years, easily exhausted. It would be nice if EBV and CFS were being taken as seriously as long covid(in all of the medical world).
I have an infection disease doctor I barely see.. even though they found a little bit of lime..cmv ans env. Should I call him back and let them know that I might be having a EBV flare up... Rash on my neck extra fatigue than normal...
Plus I am on Medicaid. Chrinic migraine. And spine pinchnnerve s . The message is a homeopathic get your immune system up... Hopefully an antiviral will help
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The problem is docs are so uninformed and not willing to go the extra mile. My neurologist told me she was not interested in me sharing research with her to help me. I work in the medical profession and was blown away. I was injured by th he covid vaccine and it has been almost 3 years of gaslighting or being told there is nothing they can do. I have had to research myself and tell them what I need. Good doctors are rare nowadays.
Thank you so very much!!!
Thank you!!
The way I test for my own EBV has been- EBV DNA whole blood lab, as well as EBV IgM and I check EBV VCA IgA too(all high for years, and an NIH dr told me they see my EBVDNA levels in HIV patients. Yet I don't have HIV. My CMV fluctuates. My CRP has been high for fewyears, and now im making kappa chains. It would be great to get solid answers, and TREATMENT to get better!
Has monolaurin been tried for long covid? Ive heard it can help with EBV(I am trying it for reactivated EBZv ive gad since 2018). Reactivated EBV is exhausting, but doctors dont do anything with it unless it is a severe infection. They dont understand that low level chronic infection is debilitating and you feel the same for years, easily exhausted. It would be nice if EBV and CFS were being taken as seriously as long covid(in all of the medical world).
I have an infection disease doctor I barely see.. even though they found a little bit of lime..cmv ans env. Should I call him back and let them know that I might be having a EBV flare up... Rash on my neck extra fatigue than normal...
If y'all not in Tennessee there is no one help with reactivate ebv, cmv mine flares I feel it ..extra fatigue. Light rash.
Plus I am on Medicaid. Chrinic migraine. And spine pinchnnerve s . The message is a homeopathic get your immune system up... Hopefully an antiviral will help
How could EBV DNA be high but with normal PCR?
It can be in saliva. In Russia they do test blood and saliva