Support groups are great if we can find one in your area.
Here are two sites where you could search, if you haven't seen these already.
The second best is Here (o: }
Actually, that should be the other way around. "Here" is Here, 24/7 and support groups members unfortunately do sleep now and then ... ha. And usually take naps, ta-boot.
It took me two years of being alone before I found folks in my area.
I don't go to the meetings normally, because I can't ... but stay in touch with the ladies from two Groups.
That helps, but being here has been really great.
I don't have to stay on the CFS subject. I can cruise around to others and realize, it could always be worse. Always.
Anyhow, I just feel bad though that most of you all are so young and having this. I just pray you can see a total remission. I have a two friends who are 20 to 40 years older than you and both are in remission. NEAT !
Don't give up hope and do what you can, when you can. I'm on the puter mostly, and that can make a day fly by and be very rewarding after a while.
I'm on this Forum and one other. The other is not for us sick folks ... but that's good because I can get my mind off of me and "it" and get into talks about
Anything you may be interested in, probably has a Forum. That can be fun.
I wish I could take all of your CFS from you because I'm older and I'm stuck home anyways. ha.
My heart really does go out to you all, and I'll be rootin' for ya's that life will look brighter, with new high-points and interesting distractions, with Spring around the corner.
God Bless y'all.
LateNeuroLyme + CFIDS = Lord knows what.
Romans 8:28 ~ And we know that ALL things work together for the Good, Y
for them that Love God, for them who are the called according to His purpose.