We are just in the beginning stages of developing a place for patients with CFS to see what our group is all about as well as for the members to stay connected. The hope is to document what has happened in meetings, perhaps develop a "great medical professionals" referral list, other resources such as books, youtube videos; we are limitless really! If you have thoughts, ideas, suggestions, constructive criticisms, feel free to send any of the above my way.
I will be managing the blog so you can email me at email@example.com
Bonkers for blogs,