From the latest updates on ALS research and advocacy to information about caring for people living with ALS and inspiring stories from around the country, The ALS Association’s blog covered it all in 2022. Here is a quick look at the top ten posts our readers enjoyed most.
Maggie Broeren and Michael Coffey hosted a virtual discussion for the Wisconsin Chapter this past April where they introduced some ideas around death and dying that prompted a deeper discussion. This article touches on some of the key points of those conversations and some take aways from the experience.
Heidi Tarr Henson, diagnosed with ALS last spring, shares thoughts about her personal journey living with the disease, how she’s managing her personal changes in mobility and how she strives to just live in the moment.
Dr. Heidi Tarr Henson, a Massachusetts woman recently diagnosed with ALS, shares her reflection on how to handle life with ALS and end of life discussions.
Dr. Heidi Tarr Henson, a Massachusetts woman recently diagnosed with ALS, reflects on on in-the-moment advocacy, teachable moments and the power of setting boundaries with ourselves and others.
After Terry Peterson was diagnosed with ALS in 2019, his family decided to preserve the memories of their time together by documenting their journey in a video.
Shannon Sullivan, Care Services Manager at The ALS Association Massachusetts Chapter, pens an update for the ALS community within the Commonwealth concerning current offerings and upcoming resources.