Government Advocacy

Advocacy is an important part of our Chapter's mission. We are proud to join with our PALS to advocate for the needs of people with ALS and their families.

Update on Speech Generating Device Coverage Policy from Centers for Medicare and Medicaid Services - April 29, 2015

ALS Advocates  have made some big progress in expanding access to speech generating devices. Click here to read the most recent news from CMS as a result of your hard work.

National Advocacy

Each May, the ALS Association holds an Advocacy Day and Public Policy conference in Washington, DC.  We meet with every legislator representing our service area—22 in all—to educate them about ALS and urge their support for The ALS Association's Public Policy Priorities.


To learn about the National ALS Advocacy Days, visit

By Phone: you may also register by calling the Public Policy Department at 1-877-444-ALSA.




Legislative Priorities

Appropriate $10 million to continue the National ALS Registry 
At the Centers for Disease Control and Prevention.

The Administration and Congress have made the establishment of a national ALS patient registry a top priority through the enactment of the ALS Registry Act in 2008 (P.L. 110-373) and by appropriating funding to develop and implement the registry in each of the past seven years.  These actions have enabled the CDC/ATSDR to launch the first ever national ALS registry.  Using a variety of enrollment strategies, including online self-enrollment, the registry currently is identifying the number of cases of ALS in the U.S. and collecting data that may help us learn what causes the disease and how it can be treated, prevented and, ultimately, cured.   

However, funding is necessary in FY 2013 to continue the registry, coordinate federal efforts, help people with ALS enroll in the registry and conduct outreach activities to identify ALS cases in all 50 states, including in rural and underserved areas and minority populations.  Moreover, continued funding is needed to collect additional information about ALS cases, explore the possibility of adding a biorepository that collects blood and tissue samples and enable the registry to advance clinical trials to develop new treatments for the disease.

Appropriate $10 million to continue the ALS Research Program (ALSRP)
At the Department of Defense (DOD).

Studies supported by the DOD, Department of Veterans Affairs, National Institutes of Health, Harvard University and the Institute of Medicine among others repeatedly have found that military veterans, regardless of branch or era of service, are approximately twice as likely to die from Lou Gehrig’s Disease as those who have not served in the military.  

In order to support our nation’s military heroes in the fight against ALS, Congress and the DOD established the ALS Research Program (ALSRP) in FY 2007.  Unlike many other research programs, which focus on basic science, the ALSRP is promoting translational research and is specifically designed to find new treatments for ALS, a disease for which an effective treatment currently does not exist.  The ALSRP also is funding the best science as funding is provided on a competitive grant basis and projects are peer reviewed.  While Congress has continued to appropriate funding for the ALSRP, including $6.4 million in FY 2012, the current funding level will only be able to support approximately 4 to 5 projects, yet over 100 are submitted to the program.  As a result, under the current level more than 95% of submitted projects will not receive funding.  Opportunities to discover and deliver a treatment to veterans will be lost, leaving them – and all people living with the disease – with no effective treatment option.   By appropriating $10 million for the ALSRP in FY2013, Congress can continue this vital program and take steps to ensure that our nation continues to fight for our veterans just as they fought for us.  

Enact the MODDERN Cures Act, H.R. 3497

Regulatory barriers and limited incentives to pursue innovation have hindered the development of new treatments and diagnostic tools for ALS and other diseases with unmet medical needs. In fact, people with ALS will die in an average of just two to five years because an effective treatment does not exist and because diagnostics and biomarkers have not been identified that can speed diagnosis, improve care and lead to the discovery of new treatments.

The MODDERN Cures Act (Modernizing our Drug and Diagnostics Evaluation and Regulatory Network), introduced by Congressmen Leonard Lance (R-NJ) and Jay Inslee (D-WA), would accelerate the search for a treatment for ALS and other diseases by removing the barriers that limit medical innovation and by providing incentives to develop new treatments and diagnostic tools that can improve, prolong and, ultimately, save lives. Specifically the bill will: encourage research on treatments, which have been set aside in the lab, but hold promise for treating diseases with unmet medical needs; remove barriers and provide incentives to develop new diagnostics; and ensure timely and appropriate reimbursement for new tests and treatments so that patients have access to the latest medical technology as soon as possible.

Photos of Advocacy in Action


Senator Robert Menendez
Congressman Rush Holt

Congressman Charlie Dent
Congressman Matt Cartwright

Congressman Glenn Thompson
Congressman Thomas Marino
Congressman Mike Fitzpatrick
Congressman Chaka Fattah

Click here to learn more about national ALS Advocacy.

State Advocacy

We also conduct advocacy efforts on the state level. We are currently working with the Pennsylvania legislature to receive funding for ALS programs and services.

Click here to learn more about our advocacy efforts in Pennsylvania.

Advocacy Delivers!

Did you know that ALS Advocates helped enact the national ALS Registry Act and secured over $20 million in funding?  Check out some of the many accomplishments due to our tremendous team of advocates from Pennsylvania, New Jersey, and Delaware.

Click here to learn more.

Advocacy Stories

Click here to read stories of ALS Advocates

Honoring Veterans throughout the Greater Philadelphia region.

To learn more, click here


Get involved with ALS Advocacy!

For more information about our Chapter's advocacy efforts, contact Tony Heyl at (215) 643-5434 or

Advocacy Materials for Download

Letter urging Governor Corbett to support ALS patient care

Petition for New Jersey Tax Bill to Fund ALS Patient Care

"Become an ALS Advocate" Brochure
A document written by People with ALS on why they are involved with Advocacy

ALS Advocacy Delivers
Quick facts about the success of ALS Advocacy

ALS In the Military


The ALS Association Greater Philadelphia Chapter
321 Norristown Road - Suite 260, Ambler, PA 19002

The ALS Association is a 501(c)3 nonprofit organization and donations are tax deductible to the full extent of the law.