Take Action!
We achieved substantial support for respite care services in the U.S. House of Representatives. Now, MS activists turn our focus on the Senate.
The Lifespan Respite Care Act's enactment in 2006 represented a major step forward in recognizing the importance of and addressing the needs of family caregivers. While the law offers a great opportunity, since its creation, it has been severely underfunded. Contact your Senators today and urge them to support full funding for Lifespan Respite in FY 2011.
Up to one quarter of individuals living with MS require long-term care services at some point during the course of the disease and often, a family member steps into this caregiver role. Approximately 50 million family caregivers in the nation are responsible for 80% of long-term care. The value of uncompensated family care giving services keeps growing and is currently estimated at $375 billion a year. The Lifespan Respite Care Act supports much needed short-term care that helps these individual or family caregivers take a break from the daily routine and stress of providing care.
The Act authorized funding beginning in FY 2007, but did not receive an appropriation until FY 2009 and was significantly underfunded at $2.5 million in both FY 2009 and FY 2010. Write your Senators today and urge them to support full funding for Lifespan Respite in FY 2011.
To keep future MS activism messages out of your junk folder, add the following address to your contacts or safe sender list: MSActionNetwork@nmss.org
Thursday, April 1, 2010
Subscribe to:
Post Comments (Atom)
Blog Archive
-
▼
2010
(69)
-
▼
April
(10)
- National MS Society, Greater New England Chapter N...
- The National MS Society
- MSConnection Spring 2010
- MS Auto Rally
- Join Us. Act Now!
- Participate in a Health Physical Activity Survey ...
- Federal Focus-April 2010
- Affordable Access National Call-In Day
- The National MS Society and MS LEARN ONLINE presen...
- Increased Support for Respite Care Services
-
▼
April
(10)
About Me
- Steve
- North Grafton, Massachusetts, United States
- Well-educated, disabled at this point with Multiple Sclerosis. I am very glad that I was able to do the things that I have been able to do over the years. had to change the picture, this one's more realistic.
No comments:
Post a Comment