Rare Disease Week is right around the corner, with the first meeting taking place on Monday, February 24th on Capitol Hill. In attendence will be our Illinois Chapter President, Wayne Galasek.
In anticipation of Rare Diseaes Week, we are asking all HDSA Community Members to send a letter to their Senators and Representative demanding No Cuts to Medicaid! Thousands of people in the Huntington’s disease community rely on Medicaid for healthcare. What would you or your loved ones do if your medical services, prescriptions, or home/community supports were reduced or taken away? The time to act is NOW.
The HDSA has made it easy for you to contact your U.S. Representative and Senators and tell them NO CUTS TO MEDICAID!
Using the link below, you can make your voice heard.
Family Members take Action - Huntington's Disease Society of America
For more information on Rare Disease Week, click here.
In anticipation of Rare Diseaes Week, we are asking all HDSA Community Members to send a letter to their Senators and Representative demanding No Cuts to Medicaid! Thousands of people in the Huntington’s disease community rely on Medicaid for healthcare. What would you or your loved ones do if your medical services, prescriptions, or home/community supports were reduced or taken away? The time to act is NOW.
The HDSA has made it easy for you to contact your U.S. Representative and Senators and tell them NO CUTS TO MEDICAID!
Using the link below, you can make your voice heard.
Family Members take Action - Huntington's Disease Society of America
For more information on Rare Disease Week, click here.