Webinar

Gather around, good people!  I AM ALS is hosting a Town Hall on Thursday, February 2nd at 5 pm, ET!  Brian, Sandra, and I AM ALS’s board will give a presentation on Synapticure, how I AM ALS has taken steps to create an Independent Committee for any matters related to Synapticure, and, of course, answer […]

Receiving an ALS diagnosis is devastating for many reasons, including the knowledge that with a progressive loss of function will potentially come the loss of employment and much-loved activities. This is why the Many Shades of ALS (MSOA) team here at I AM ALS wants to talk to you about a powerful antidote to the […]

One of the most common comments we hear is how hard it is to maintain friendships once someone is diagnosed with ALS. Join us to hear examples of friends who are making the best of a bad situation, examples of how to support a friend with ALS, and how people with ALS can continue to support their support squad!