Petition Jen Brea Launches Petition to get 250 million year for ME/CFS

[Cort]

Jen just launched her advocacy site. Her first project is a petition to get ME/CFS the funding it needs

For people in the US:

http://my.meaction.net/efforts/tell-congress-to-support-funding-equality-for-me-cfs/near/new

For people outside the US:

http://my.meaction.net/petitions/us...-around-the-world-care-about-funding-equality

 

[Hello!]

It's so easy!

Just click on the link, fill in the name, zip code, and email fields, then click sign and you're done.

 

[Hello!]

Have you done this yet? It really is very easy and, hey, it might help. If we do nothing, nothing will change.

 

[Folk]

I don't think much people read this section of the forum. What about posting just this one in the section with most visitors???


Plus ask people to sign! I just got 5 or 6 more signatures by asking in some groups. (I know most of us don't like to share the disease with friends and family etc. so try the ME/CFS patients!)

 

[Folk]

I'm getting a lot of attention in 2 CFS/ME groups, loots of signatures!


I think I've choosen the words right hehe