Guest guest Posted May 10, 2004 Report Share Posted May 10, 2004 > Just reading about the MS societies, I wonder if they have the interests > of MS patients as their foremost priority. Various attempts by MS'ers to > discuss LDN with them have not made any headway. The only voice they > support is of the drug companies. I have not thought much of the society for a long time. Ever since finding out they cut off the local MS support group because they held a small fund raiser to help pay to cater a holiday party for themselves. The rules of the MS society are that ALL money raised must be sent to them ONLY, not even used by the groups themselves for their own members. Anyone around here newly diagnosed and asking about support groups gets told there are none by the society because of this. It is an unspeakable cruelty to these people, many of which are very scared about what's happening to them and having just being told they have an incurable disease. The group continues on, but with no official acknowledgement, so they are only known about if you get lucky and word-of-mouth info finds it's way to you. It's been this way for years. Doug Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.