Caregivers of Myasthenia Gravis

A myasthenia gravis diagnosis of a loved one impacts more people than just that one individual. It can also take a toll on the family, friends, and supporters around them. Below are resources specific to those in the caregiver role.

Caregiver Action Network (CAN) is the nation’s leading family caregiver organization. It works to improve the quality of life for tens of millions of family caregivers. 

Caregiving.com is committed to engaging and empowering family caregivers worldwide via a multi-faceted support model delivered through our leading-edge platform.  

MedlinePlus is a service of the National Library of Medicine (NLM), the world's largest medical library, which is part of the National Institutes of Health (NIH). They present high-quality, relevant health and wellness information that is trusted, easy to understand, and free of advertising, in both English and Spanish.

If someone you love has been diagnosed with MG, you want to be as helpful and supportive as possible. Research has shown us that family and friends play a very important role in helping a loved one deal with a chronic illness. 

National Alliance for Caregivers envision a future where family caregivers thrive because caregiving is sustainable, equitable, and dignified. 

Well Spouse Association is a nonprofit membership organization, that advocates for and addresses the needs of individuals caring for a chronically ill or disabled partner.