For Caregivers: Online Resources​

Navigating the role and responsibilities of caregiving for someone with ALS can be challenging. It can be just as tough on you as it is on them. We’ve gathered some resources to help you on your caregiving journey.


I AM ALS is revolutionizing how we cure ALS by empowering and mobilizing patients, engaging with policy-makers and offering vital resources for people impacted by ALS.

Northeast ALS Consortium (NEALS)

Our mission is to translate scientific advances into new treatments for people with Amyotrophic Lateral Sclerosis (ALS) and Motor Neuron Disease (MND) as rapidly as possible.

ALS Association: Navigating ALS

The mission of The ALS Association is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.

ALS Finding a Cure

ALS Finding a Cure is pleased to launch an eight part video series on living with ALS.

The Lanier Law Firm

ALS Finding a Cure and its We Care program strives to provide caregivers with as much information as possible.  Being a caregiver is a unique challenge regardless of the condition. The Lanier Law Firm, dedicated to assisting those who are suffering with Mesothelioma, provided a resource for their clients’ caregivers.  We thought it was well developed and wanted to share with those who are on their caregiving journey.