As part of the media campaign we are creating a patient representative network around the world. Media may want to interview someone in a particular region to give their story a local angle. Or some stories may have particular emphasis, such as ME/CFS in children or families.
If you are willing to be interviewed, please give us your contact info and where you live (city, state, region).
Also we'd like a short bio so we know a little about you and your ME/CFS.
Thank you, thank you!
Here are some examples of what to include in the bio:
where you reside
years having ME
Career before getting ill or what you did in life
When I found out what I had, it was my first loss. I saw I would never go hiking or canoeing again, my two favorite activities. Most of my days are now spent typing on my laptop while in bed as part-time writer. I consider myself lucky that I can still do some work. I fear when my husband retires and I will not have health insurance since I have not paid into Social Security for years and am not able to hold down a corporate job. I've given up on treatments having spent thousands of dollars on supplements and travel to another state in hopes of finding a doctor who knows something about this illness. Now I just live - or don't live - within the limitations of this illness.