If you follow SimpliHere on social media, you may have seen our weekly posts with tips for making life with ALS as easy as possible. We call them SimpliTips, and we’ve been sharing them every Tuesday for several months. As much as we love SimpliTips, we’re going to hit pause on them for a minute […]
First Lady of the Yankees, ALS Caregiver, and Advocacy Icon.
Amid setbacks and letdowns, the ALS community is leaning on its resilience and finding hope.
An Interview with Steven Prevost. SimpliHere has teamed up with Joe’s Brother Coffee owner and founder Steven Prevost to bring you the following interview, where we talk Steven’s connection to ALS, why he started roasting coffee, and organizations doing the important work for ALS advocacy and research. MM (00:06): Good afternoon. Just to introduce myself […]
This year’s ALS Advocacy Conference, put on by the ALS Association, looked a bit different in 2020 over computer screens and Zoom links, as did everything else this year. But as the resounding rally cry of the conference went, “ALS does not stop, and neither can we.” Many things have been postponed or cancelled this […]
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.
“Lou Gherig was diagnosed 80 years ago,” Christa Thompson reminds us, “and his doctors essentially had the same story to tell him that my husband’s doctor told us.”
“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.”
Jeremy Van Tress’ ALS story.
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.