Earlier quoted context omitted.
You might also want to have her CSF independently tested for nematode worms. (what I mean by this is to put it under a microscope). it surely won't hurt, as some pathologists (although not published yet in the medical literature AFAIK) are finding them in all the samples they have tested for. More information: https://youtu.be/aTPU87CKQLQ?t=6m30s If this proves to be the case for your aunt, the good news is that anti…
I looked into both of those researchers. I could find nothing published by them with regards to MS. They do both seem to have published on Lyme disease. Can you provide any published research to back those youtube videos? Maybe I'm wrong here, but this feels like giving medical advice based on very little hard evidence. Considering I have a loved one with MS, I find such advice sickening. You see this with many termi…
(I know, harsh words. But I needed to get this off my chest)
Taking this out on someone with carefully worded suggestions that only advocate testing is also "being a fucking asshole." Because very frequently the people putting out such info are giving testimony from firsthand experience because they know firsthand what a fucking nightmare it is and if they got better, it only seems the decent thing to do to share info that might help some people with the same diagnosis they had. And then they will run into this kind of ugliness ten thousand times, no matter how carefully they word it.