Any other recomended CFS/ME forums with more traffic?

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astroman
Veteran Member


Date Joined Mar 2014
Total Posts : 4952
   Posted 3/28/2017 1:03 PM (GMT -6)   
The Lyme forum here is one of the best, a great source of info, and highly used. CFS, on the other hand, seems minimally represented, sorry, just my observation. Life is short, I need to learn some info, so I'd like to find a forum that is more widely used if there is one.......know any?

thanks in advance

straydog
Forum Moderator


Date Joined Feb 2003
Total Posts : 16383
   Posted 3/28/2017 4:01 PM (GMT -6)   
astroman, you are right, this is a very slow forum. They have not had a mod over here in a long time I don't think. When there is not a mod to keep things going they tend to not have much activity.

You may look on FaceBook to see if there is a forum there. I don't do FB but I know they have a ton of groups. Good luck.
Susie
Moderator in Chronic Pain & Psoriasis Forums

ladybugdreams
Veteran Member


Date Joined Jun 2008
Total Posts : 730
   Posted 3/29/2017 2:42 AM (GMT -6)   
Yes, this is a very slow forum. I stuck it out here for quite a while but it never picked up. I go to Pheonix Rising which is a very active forum for ME/CFS, also I have used Daily Strength, another good forum. I hope this helps you. I tried to email you but for some reason it said there was a problem. Hugs, Denise
Fibromyalgia-dx'd: 2006, ME/CFS-dx'd: 2006, Holt-Oram Syndrome dx'd 1975, reduced lung capacity dx'd 2009, nasal allergies, food allergies, depression (lifetime problem) IBS, neuropathy in hips

I have 4 children & 7 grandchildren.

As apples of gold in silver carvings is a word spoken at the right time for it. Prov. 25:11

Lily Silver
New Member


Date Joined Apr 2017
Total Posts : 18
   Posted 4/14/2017 3:15 PM (GMT -6)   
I find that healthrising is an excellent forum for cfs/me. I will find the link one moment....

Lily Silver
New Member


Date Joined Apr 2017
Total Posts : 18
   Posted 4/14/2017 3:17 PM (GMT -6)   
https://www.healthrising.org/forums/

there are also a lot of good resources there and the people are friendly.

there are a lot of great facebook groups. One really good one is called Chronic fatigue syndrome wellness and a support.

Lily Silver
New Member


Date Joined Apr 2017
Total Posts : 18
   Posted 4/14/2017 3:18 PM (GMT -6)   
I wonder why links do not appear. I am going to try once more:

https://www.healthrising.org/forums/

there are also a lot of good resources there and the people are friendly.

there are a lot of great facebook groups. One really good one is called Chronic fatigue syndrome wellness and a support.

Samwildre
New Member


Date Joined Apr 2017
Total Posts : 1
   Posted 4/14/2017 3:59 PM (GMT -6)   
Am I in the right place CF
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