https://www.youtube.com/watch?v=rqRbXK_QVyc

Hi All, this is Admin/OP. I’ve been silent for awhile due to dealing with a lot of the challenges of this illness, but I plan to recover and to do a lot more work a lot better and quicker once I am recovered. And I plan to develop this website far beyond what it is now, and to put lots of pressure on the Open Medicine Foundation to make them research toxic mold/environmental toxins in general, and their role in ME/CFS. For now, just updating the site by posting some of these older videos should be enough to make me feel like I’m doing something.

We all know that the NIH counts on ME/CFS patients to be too weakened by their illness to fight back much, but as controversial as it may be to say I think that that this may be true of the Open Medicine Foundation too. They may be happy to not have to deal with more angry protestors–only one real thorn in their side–the thoroughly recovered, and basically fully healthy, but angry Erik Johnson. Imagine if there were many more patients like him! They would have to crumble to their demands. I’m trying to make the virtual version of that real, but an IRL version would be nice too, so if any of you are well enough to protest at Stanford, please consider it.

By the way, i’ll be adding some external links to, to sites that I think deserve the attention, if I remember to do it in between disturbing hypersomnia episodes (where I’m sleeping over 20 hours at a time).

(for SEO, some tags, lets see if this works: Open Medicine Foundation, Ron Davis, Open Medicine Foundation, OMF, CCI, Craniocervical Instability, Mold Illness, Toxic Mold, nanoparticles, MCAS)