We’ve developed several materials as communication and educational tools to help inform medical providers, as well as provide pertinent insurance and family information. Access them now.
This booklet will provide a helpful overview of the multidisciplinary team approach, what one can expect during a typical clinic visit, as well as additional options for care and support from providers outside of the core care team.
It can be overwhelming to learn that you or a family member has ALS. Receiving the diagnosis of familial ALS can raise extra questions and concerns about the future. This booklet will help answer these questions and provide information to support you and your family.
This resource guide is the result of many years of clinical social work practice and research with families, children, and youths affected by neurological illness.
The ALS Association joined with 32 consumer and patient advocacy organizations in calling on Congress to enact legislation in response to the COVID-19 pandemic that protects and expands access to quality, affordable health insurance.