Advocacy Effort Who supports CFS/ME in Gov.?

[Ladyliegh]

I just read that Sen. Markey (MA)has voiced his support to become an advocate for CFS/ME.
Just how many in Gov. Offices are claiming to support us in our struggle for research & cure?
Really curious about this...

 

[GG]

Support how? Having the gov't spend more? Or just getting the gov't to change its stupid name? Or?

I am not holding my breath on the Gov't being a significant factor in helping us to get more of our quality of life back! I think the Big discoveries will come from the privately funded stuff

GG

 

[Ladyliegh]

I am using my cellphone & still can't copy & paste a link...sorry
The article is on ME Action.net
(Senator Markey)

Yes, I agree too much time has been spent on the name...Feellikeshit, works for me...

 

[GG]

The ME Action video:

THANK SENATOR MARKEY FOR PROMISING TO HELP ME PATIENTS

http://www.meaction.net/2017/02/26/thank-senator-markey-for-promising-to-help-me-patients/

 

[Ladyliegh]

Thanks GG.

 

[Cort]

That's good news. There's also Anna Eschoo and I can't remember the other Congressperson in the Bay. A Kennedy is a strong supporter I believe as well and there are others.

So important to get core supporters behind us!