Lymphedema Treatment Act Walk 2018
Donation protected
Lymphedema Advocacy Group Board Members will walk over 700 MILES from Feb 1st to the 14th in support of the Lymphedema Treatment Act!
Why Are We Fundraising?
Because passage of the Lymphedema Treatment Act is critical to help millions suffering from this treatable disease gain access to the MOST BASIC level of care!
Read more at our website: Lymphedema Treatment Act
The Lymphedema Treatment Act currently boasts over 300 critical cosponsors (a supramajority) in the House and just over 50 (a majority) in the Senate! The bill's support is broad based and bipartisan but we need your help to propel us onward to passage!
A big part of crossing that finish line involves approximately one hundred volunteers from across the country traveling to Washington, D.C. in March for an event known as "Lymphedema Lobby Days" . Typically, our bill gains dozens of new cosponsors following Lobby Days, but hosting this event comes with a hefty price tag!
Support a walker or someone you know with lymphedema by clicking the "DONATE NOW" button to make a secure online donation!
-OR-
Join us! Share this fundraiser on your social media and tell others how far YOU will walk (at home) for the Lymphedema Treatment Act between Feb 1 and 14th, 2018!
Print a flyer you can share here !
To Donate by Check: If you’d feel more comfortable donating by check, you can make checks payable to The Lymphedema Advocacy Group and mail them to: The Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.
Note: Contributions or gifts to the Lymphedema Advocacy Group are not tax deductible. As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group engages in lobbying activity, in keeping with its mission, for passage of the Lymphedema Treatment Act.
Why Are We Fundraising?
Because passage of the Lymphedema Treatment Act is critical to help millions suffering from this treatable disease gain access to the MOST BASIC level of care!
Read more at our website: Lymphedema Treatment Act
The Lymphedema Treatment Act currently boasts over 300 critical cosponsors (a supramajority) in the House and just over 50 (a majority) in the Senate! The bill's support is broad based and bipartisan but we need your help to propel us onward to passage!
A big part of crossing that finish line involves approximately one hundred volunteers from across the country traveling to Washington, D.C. in March for an event known as "Lymphedema Lobby Days" . Typically, our bill gains dozens of new cosponsors following Lobby Days, but hosting this event comes with a hefty price tag!
Support a walker or someone you know with lymphedema by clicking the "DONATE NOW" button to make a secure online donation!
-OR-
Join us! Share this fundraiser on your social media and tell others how far YOU will walk (at home) for the Lymphedema Treatment Act between Feb 1 and 14th, 2018!
Print a flyer you can share here !
To Donate by Check: If you’d feel more comfortable donating by check, you can make checks payable to The Lymphedema Advocacy Group and mail them to: The Lymphedema Advocacy Group, PO Box 1682, Carrboro, NC 27510.
Note: Contributions or gifts to the Lymphedema Advocacy Group are not tax deductible. As a 501(c)(4) nonprofit organization, the Lymphedema Advocacy Group engages in lobbying activity, in keeping with its mission, for passage of the Lymphedema Treatment Act.
Organizer
LYMPHEDEMA ADVOCACY GROUP BOARD MEMBERS
Organizer
Urbandale, IA
