An ALS/MND diagnosis brings an immediate need for information, care, and support. This page points to key resources for finding services, connecting with others, and staying informed — whether you are newly diagnosed, a caregiver, or further along in the journey.
Find a member association
The Alliance’s member associations are the primary source of local support for people living with ALS/MND and their families. They provide information, services, and connections to care in their regions. Many also offer support groups, advocacy resources, and programs specific to their communities.
Find a member association in your region
Find a clinic
Multidisciplinary ALS/MND clinics bring together specialists from neurology, physiotherapy, occupational therapy, speech therapy, respiratory medicine, nutrition, and other fields. Access to a multidisciplinary clinic is an important part of care for people living with ALS/MND.
Search the Global Clinic Locator
Find a clinical trial
Clinical trials test new treatments and interventions for ALS/MND. Participation in a trial may be an option at various stages of the disease. Your care team can help determine whether a trial may be appropriate for your situation.
View drugs and treatments in development
Find a support group
Connecting with others who understand the experience of ALS/MND can be an important source of support. Many member associations offer or can refer you to local support groups for people living with ALS/MND and their caregivers.
Find a member association to locate support groups in your region
Events and programs
The Alliance and its member associations offer a range of events and programs throughout the year, including webinars, community gatherings, and research-focused meetings. The Alliance calendar lists upcoming events open to the broader ALS/MND community.