It's been a while since I have written- just taking a little break- As my RSD gets worse I just find it so hard to cope and sometimes hearing how bad everyone is doing just makes me feel sadder. But on the other hand I love this forum and the nice people I have met here
Im am so frustrated with the lack of research in this area! I am sick of hearing it as a "Mystery Disease" -Its not such a mystery with so many people affected!
We need for the public to be more aware and I dont know how we can do that? RSD should be as familar as MS or ALS-!

Sorry to be venting but I am just so frustrated! My friend who also has RSD really bad in her mouth now said her mouth felt like it was being stuck with 1000pins!
Just inhumane.....
I am reading the "secret" but I am finding it hard to use with the pain issue!

Thanks as usual for listening

Debbie