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HI. I am very severe and progressive too. Would you be open to talk about your friend? If so, please PM me.

I think it is more likely less than 5%, almost definitely less if you include the brain, if you would count all the various bodily interactions it is probably less than 1% of what can be known. This is without symbiotic liveforms we live with.

I am very severe, my CRP and ESR are non existent.

who?

There is simply no real ME unless there is a biomarker, we will not find one, if there is no subtyping. You should be happy that cci people get out of the equation. What kind of symptoms are real ME? All the best to you.

You do not know what is ME. Your ME could be totally different from any other persons ME with the same symptoms, at this point your ME is not more ME than anyones else ME, because nobody knows what is your ME or anyones ME. You definitely have reason to doubt your ME, no matter your onset...

There is no good way to diagnose mitochondrial disease with absolute certainty in people with (somewhat more certain but not definite) or without (= secondary) genetic mitochondrial disease yet. Hence, IMO, there is only a very low chance that there is not a significant group of people with...

Sounds like like classic ME symptoms to me? At least this is my experience of my ME.

Great, ty! 1.) Would he advise to try transcutane vagus nerve stimulation? If so, which product would he try and with which protocol? If he would be interrested, I‘d maybe finance a small placebo controlled study for this. If he would be interested but has no time maybe he could redirect...

Any news on this? ty!

I wish you were correct, but if so, why were Prof. Scheibenbogens Immunadsorption studies not successful?

„normal“ being higher risk for Alzheimers than „unnormal“ (being negative then)?

all norma that is all normal, will try again.

do you get this? I do, without any UTI. So what is that?

Have you tried to communicate your findings to OMF? I did so for Vermox, they said they would look into it, your experience would strengthen the need for looking into it.

so it is either „pushing“ you like an amphetamine or it has some inhibiting mechanism on a virus or it does... ?

also interesting: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077236/#!po=0.714286

ty! what dosages are you taking and do you see any issues with that? liver problems or kidney? neuropathies?

how severe are you? for how long do you take it? what was your onset like? ty!

I had short term remissions from severe pots (pots was gone) for 12 hours after Vermox intake, it is an anti parasite, I can say with a very high certainty that it was no placebo.