Receiving a diagnosis of ALS is devastating and overwhelming. There is so much to know, a great deal to consider and, typically, a long list of questions.

While no two people living with ALS are alike or will experience the disease the same way, there’s a great deal of collective knowledge and wisdom to be shared by health care providers, people living with ALS, family members and caregivers.

We want to support you throughout your ALS journey. Browse the links in this section to find support, information, answers and resources.