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ME/CFS South Australia Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.
Disclaimer
ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.
Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.
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Solve ME/CFS Initiative: Your Advocacy In Action – ME/CFS Senate Resolution Passed!
Saturday 25 May 2019
From the Solve ME/CFS Initiative:
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Your Advocacy in Action: ME/CFS Senate Resolution Passed!
Your ME/CFS Advocacy Week efforts made a difference! The Senate Resolution in support of International Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Awareness Day is now the official stance of the U.S. Senate and the U.S. House introduced a matching resolution (H. Res 399) this week.
For ME/CFS Advocacy week (April 1 – April 7,2019), Solve M.E., led a nationwide effort to raise awareness, advocate for increased federal funding, and tell the stories of people with ME/CFS. Our 3rd Annual ME/CFS Advocacy Day in Washington DC, in partnership with #MEAction, drew over 240 registered ME/CFS advocates to attend 185 meetings (23 of them member-level!) with members of Congress and their staff.
Thanks to the combined efforts of our community, the US Senate has taken a stand for ME/CFS! This action was a joint partnership between Solve M.E., #MEAction, and the Massachusetts ME/CFS&FM Association.
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Registered Charity 3104
Email:
sacfs@sacfs.asn.au
Mailing address:
PO Box 322,
Modbury North,
South Australia 5092
Phone:
1300 128 339
Office Hours:
Monday - Friday,
10am - 4pm
(phone)