I am starting research for a documentary film on ME/CFS. I'm looking for a few PWC's and/or their families to participate. I have CFS, and have been documenting my experience with video for many months. I would like to incorporate the stories of several other PWCs. If you think you have a story to share, and are interested in telling it, PM me for more details. And if you happen to know anyone who works professionally in film (in any capacity), and may have a passion for ME/CFS or health in general, drop me a line!