Advocacy Webinar Today

Headline: May HD Awareness: Educate the Media about the Huntington's Disease Parity Act


Title: Educate the Media about S. 648 & H.R. 718

 

There are now 59 cosponsors of The Huntington's Disease Parity Act (H.R. 718)! Additionally, Senator Charles Schumer (D, NY) has been added as a cosponsor of the Senate companion, S. 648! HDSA Advocates are making great strides, and we need to continue our momentum by maintaining the pressure on Congress. Will you send a letter to the editor of your local newspaper about the Huntington's Disease Parity Act?

 

Letters to the editors are a great way of showing Congress that the Huntington's Disease Parity Act matters to you. Sending a letter to the editor is easy, and can make a huge difference. Click here for a letter you can personalize and send automatically through the HDSA E-Advocacy Center. Just enter your zip code to get started.

 

There's More! Today, Tuesday May 17, at 12:00pm EST, join HDSA Advocacy Manager Jane Kogan and Advocates Lauren Holder, Denise Wilders, and Lindsey Zan for a very special advocacy webinar. Click here to register.

 

The HDSA National Call in Day, May 31, is only two weeks away! Ask your friends and family to join you in calling Congress for the Huntington's Disease Parity Act by signing up to be HDSA E-Advocates at www.!hdsa.org/join

 

If you have any questions about The Huntington's Disease Parity Act, please contact Jane Kogan at jkogan@hdsa.org or 800-345-4372 ext. 226.