Discussion Topic

Do you want to merge with another MP group or keep this group seperate?

Posted on 02/21/09, 10:32 am
Hi everyone,
In another post, Rich was kind enough to let us know that there is another Myofascial group on ds (Wow- I had no idea). Do you all want to keep this group here as a seperate group, or do you want to try to merge with that group? I'm open to either. I like our little group here- but there is also merit for joining the other group (which seems to have a bigger base and more posts)... Lets take a vote...
JC
Showing 5 Replies
  • Reply #1 02/21/09  12:24pm
    The other one moves quicker for more responces im happy with both though so it dont matter to me hugs charlene
  • Reply #2 02/26/09  8:19am
    I wasn't aware that there was another group. I think the key is whether we feel as though we can recieve/give more information by having a larger group. There are times I am frustrated by the lack of activity here, and I am partly to blame as I don't post as often as I should. I, too, will go with the group census.
  • Reply #3 04/07/09  4:28pm
    I just found this site while responding to a members comment.

    Count me in whatever you decide
  • Reply #4 06/15/09  6:40pm
    Sorry I have not been around lately...havent done much of anything all the way around in life...YET do not stop only when the body quits-you all know what I mean! I've missed all of you though!

    I had no idea that there was another group as well...they still list us as a "syndrome"...

    I am in what ever Blue22 decides as well-You are a great leader and we all appreciate your hard work.

    Respect-
    Nancy
  • Reply #5 07/03/09  5:50pm
    Hi Nancy,
    Thanks- that is really kind of you to say. My vote is to keep this group open. I know that it is mostly quiet- but I want it to stay open so that we can support each other whenever we need. We are a community.

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This group is for people who have Myofascial Pain Syndrome- anyone with a diagnosis of MPS is welcome to join. Our mandate is to provide support, information, and friendship to people with MPS.


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