Hey all, I'm wondering if someone can give me an idea of what really is out there for research/advocacy for CFS. Is any group aggressively pushing this forward? The deeper I get into research. Which is quite substantial at this point after eight years. I'm really starting to realize that we need more powerful minds in our corner. I have come across a couple people who research in the past month and the levels they have taken me to I didn't think would ever be reached.