May 21, 2012
 
 
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Click Here for the Video

 Save the dates:
 
Friday, May 6, 2011 Hartig Family Fundraiser  More details to come
 
Sunday, May 22, 2011 StopHD Cool Cars for a Cure go to http://www.stophd.org/ for details
 
Saturday, June 11, 2011 Northern Indiana Walk for the Cure
                                                       Click here to register   Click here for the event flyer
 
Saturday, September 24, 2011 Nancy L.Irwin Memorial Walk for the Cure
                                                                                             go to http://www.stophd.org/  for details
 
Can you spare 2 minutes of your time to show your support for
patients and families touched by Huntington's Disease?

Please visit http://www.thepetitionsite.com/1/Indiana-HD-Parity/
and sign the online petition in support of the HD Parity Act!
 



Huntington's Disease Society of America
Senator Kirsten Gillibrand (NY) to introduce the Huntington's Disease Parity Act!

Take Action!

Act now to secure original cosponsors
 

In order to maintain our momentum in the 112th Congress, we need your Senators to commit to become “original cosponsors” of the legislation today.

Act now to maintain our momentum! Contact your Senators and urge them to sign on as original cosponsors of the “Huntington’s Disease Parity Act” today!

The Huntington's Disease Parity Act is important for all people affected by Huntington's disease (HD).  If enacted into law, your Senators can make it easier for individuals with HD to receive Social Security Disability benefits and Medicare coverage, dramatically improving the lives of all people affected by HD.


Emailing your Senators takes just a minute, but will lead to life-long improvements in the way HD is treated in this country.  We have provided you with a pre-written email message to your Senators. We also encourage you to add your personal story about HD and how it has affected your family.

Thank you in advance for your support of this effort.  Please forward this message to everyone you know who cares about HD, because we want to generate as many emails as possible.  As always, don’t hesitate to contact me with your questions, comments, or concerns. 
Sincerely,


Jane Kogan
Program Services & Advocacy Manager

Can you spare 2 minutes of your time to show your support for
patients and families touched by Huntington's Disease?

Please visit http://www.thepetitionsite.com/1/Indiana-HD-Parity/
and sign the online petition in support of the HD Parity Act!
 
 

 
 
IN Chapter HDSA --- P.O. Box 2101, Indianapolis, IN 46206 --- (317) 271-0624 ---mailto:info@hdsaindiana.org