Did you miss the 2020 Virtual ALS Advocacy Conference? Here’s a breakdown of the conference sessions to help you catch up, stay informed, and advocate on your time!
SimpliHere founder Joanna has lived the challenges ALS patients and caregivers experience on a daily basis. So she created a tool to help.
“The hereditary chart of our family would boggle your mind. It’s filled with heartache and pain and sorrow. But there’s also support. And there’s good parts of the story, too.”
One ALS Patient Finds Hope In Family And Research Data
Anyone who thinks being diagnosed with a terminal illness means their life is over needs to meet Sunny Erasmus.
Gone are the days of relying on hand gestures and a white board.