@Sasha, Is Ryan Prior an ME patient, a film-maker or both? I know there was another thread on this but I can't find it now! Also, is Twitter the only way to show support? I am not on Twitter or Facebook (and very behind the times with all of this stuff) but would love to show my support!
I agree with what he said about Silicon Valley and when I was up there for my two appts at OMI, we were near Stanford and passed the bldg for 23andMe and I felt like very important work was being done for ME/CFS and maybe Silicon Valley will be where they eventually discover the biomarker and cure. I felt very strongly that I needed to support it in any way possible but didn't know what else I could do?!!
Hi Gingergrrl - Ryan is both. He was very ill but is now functioning well enough to manage to do the documentary, though I believe he has to be careful and can crash. Here's his website:
http://mecfsdocumentary.com/
He's very well worth our supporting - he's an amazing guy and he's built a great team around himself so that he's achieving great things for us.
I'm afraid I'm not very clued up on this event - AFAIK Twitter is the thing but if not, I hope social media buffs will step in and correct me!