ME/CFS Worldwide Patient Alliance

Discussion in 'Fibromyalgia Main Forum' started by UsedtobePerkyTina, Aug 21, 2010.

  1. UsedtobePerkyTina

    UsedtobePerkyTina New Member

    We have a name, chosen by patients.

    We are still moving fast. We are working on logos now. We are asking for input for what the main message or wanted action should be. We are still receiving donations. Research is being conducted in building facts, a group is looking into opportunities for free PSAs. By the end of this weekend, we hope to have a separate website.

    Please check us out now at Go to the bottom right to see "Discussion Board" and feel free to give your comments.

    Also, if you would like to donate and you are not on Facebook, then go to P.A.N.D.O.R.A.'s home page at - Please note that because Google has given P.A.N.D.O.R.A. a grant, any associated processing fees through Google are absorbed by Google. If you donate $10 through Google, it will save P.A.N.D.O.R.A. the cost of fund-raising fees. Be sure and note that the donation is for the Our Voice, Our Message, Our Lives campaign.

    Also, on the PANDORA website, you can use PayPal. You can donate through the home page of P.A.N.D.O.R.A. Be sure to write in the cause name intended as P.A.N.D.O.R.A. currently has 7 causes on Facebook.


  2. UsedtobePerkyTina

    UsedtobePerkyTina New Member

    We have a press release. Go here to see it:

    If you would like to send it, just follow the instructions and put your own name for local contact person at the bottom.

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