Posted in Uncategorized, tagged #MENotSEID, brooke shaden, budget, chronic, enchanted sleep, fatigue, federal, fibro, fibromyalgia, fine art, funding, government, IOM, ME, ME/CFS, money, myalgic encephalomyelitis, pain, photographer, photography, research, SEID, Senate, series, syndrome, zero on August 10, 2015|
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This is going to be a quick, short and sweet update. But it’s vitally important to get the word out about this!
It was announced a few days ago that the Senate has completely SLASHED TO ZERO the meager funding allotted to ME/CFS research in next year’s budget. ME/CFS is the ONLY disease to have its entire budget taken away. But, it is
possible to change this if enough outrage is heard.
We only have a few days to turn this around. So, I beseech you all to send the attached graphic to the following email addresses asking them to stop this. Every ME/CFS sufferer in the world will thank you, as will I.
Laura_friedel@appro.senate.gov; Chol_pak@appro.senate.gov; Alex_Keenan@appro.senate.gov; Lisa_bernhardt@appro.senate.gov

Please save this graphic and send it to the email addresses above!
You can read a little more about the issue here: http://www.cfstreatmentguide.com/blog/federal-government-slashes-mecfs-funding-to-zero You are also more than free to spread/post this around wherever you’d like to get the word out more!
Thank you deeply from the bottom of my heart.
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