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Watch A VIRTUAL Congressional Briefing Live on July 16th

  • Writer: Ilene Miller
    Ilene Miller
  • Jul 1
  • 2 min read
Watch a LIVE Congressional Briefing without leaving your home!

Learn how the National Plan for Epilepsy Act, introduced by Sens. Schmitt and Klobuchar, and Reps. Murphy and Costa will save lives and honor actor Cameron Boyce, and the many others who have died from epilepsy.

People with epilepsy have a three times higher risk of death than the general population due to preventable causes including Sudden Unexpected Death in Epilepsy (SUDEP), so it’s critical to address this issue systemically. Our expert panel includes:
 
  • Libby Boyce, Founder, The Cameron Boyce Foundation
  • Dr. Dan Atherton, MD, Associate Professor, The University of Alabama at Birmingham
  • Gardiner Lapham, MPH, RN, Co-Chair, Partners Against Mortality in Epilepsy (PAME)
  • Tom Stanton, President, The Danny Did Foundation
 

Three NEW Legislators Signed On to the National Plan for Epilepsy!


WHY? Because organizations and individuals just like YOU asked, and asked again and again.

Delighted to have Reps. Steve Cohen (D-TN-9), Rep. Henry Cuellar (D-TX-28) and long time epilepsy champion Rep. Steny Hoyer (D-MD-5) as part of the signors! We still have a ways to go! Read below for how to help!

Everything YOU Need to Get YOUR Legislators to Sign On!


The ask is simple:  Ask YOUR Legislators (House & Senate) to Sign On to the National Plan for Epilepsy NOW. After you submit your ask (via email, letter, call, in person or or via zoom meeting) - post to your social media and ask your friends, family, neighbors, and colleagues to do the same. NUMBERS, VOLUME, QUANTITY MATTER!

You can track sign ons here for  SENATE S 494 (5) and HOUSE HR 1189 (16)  We need 100's.
Visit our one stop voter voice email system (look up your legislators; personalize your message, send directly) or follow our template for creating your own message.

 

Caught In the ACT!

Thank you Ilene Penn Miller (EAN, REN) for urging support for the National Plan for Epilepsy during the "Celebrating 75 years of Scientific Discovery and Innovation: NINDS 75th Anniversary Congressional Briefing & Reception" on June 24th hosted by American Bran Coalition and many others. Recording coming soon.

Thanks also from left to right: Richard Huganir (Johns Hopkins), Dr. Edward Kaye (Stoke Therapeutics), Dr. Walter Koroshetz (Director, NINDS), Dr. Erika Augsine (Kennedy Krieger), Ilene Penn Miller (EAN, REN) and Mark Rasenick (American Brain Coalition) for sharing the extraordinary scientific advancements made possible by NINDS and life changing therapies on the horizon. Now is the time to align across ALL brain disorders, activate, and urge the preservation of funding and expansion of research.

Need additional help?

Sign up to join mtgs in your district/state; we will reach out as needed

Reach out to Katie Collins (kcollins@g2gconsulting.com) and Ilene Miller (ilenepennmiller@gmail.com)



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©2024 by Epilepsies Action Network (EAN)

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