Resources for patients and families:

The Muscular Dystrophy Association, Compassionate Care ALS, and the ALS Association work with families in New England, across the United States, and internationally. They help provide resources including equipment, educational workshops, Medicare/Medicaid assistance, guidance and awareness in living with ALS, caregiving, and end-of-life issues. Additional resources for ALS patients, including research, are also listed. Together, these groups work closely with our UMass ALS clinic to provide support and resources to all of our patients and their families and help them meet their needs. Additional resources for ALS patients, including research, are also listed.

Join our local community events to support ALS research

Our local ALS community supports ALS research to find a cure.

For upcoming events to support ALS research by The Angel Fund, visit their website for more information:

The Angel Fund for ALS Research | An Independent Non-Profit Charity