Navigate ALS with Neil
An Educational Blog/Vlog
Fighting ALS for over 20 years
Neil Cottrell, President of the Joe Martin ALS Foundation, draws upon his experience of being a caregiver to share tips and methods to provide the best care for people living with ALS.
These Blog/Vlog (video and text with links and info) entries will be short and straight to the point to help families navigate the many challenges of living with ALS. As the disease progresses new hurdles arise, but there are tools and techniques that can help make these a little easier to overcome.
Click here for: I have ALS. Now What??? – by Ken Menkhaus Description: This set of short essays is written by someone who was diagnosed with ALS in March 2018, and is written for others who have just learned they have been diagnosed with ALS. It tries to anticipate the most common issues faced by […]
ALS Advocacy Day/Conference provides people with ALS(PALS), their caregivers, and organizations like The Joe Martin ALS Foundation an opportunity to learn about the latest in ALS research, treatments, and to engage our Congressional representatives with legislative “asks” that are crucial for families fighting ALS. I always enjoy this event in Washington DC because I am […]
Join Neil Cottrell, President of the The Joe Martin ALS Foundation, on a journey through the airport from the perspective of a person living with ALS, and learn how to tackle some of the challenges of flying with ALS.
The Joe Martin ALS Foundation's mission is to empower families as they face the challenge of living actively with ALS by providing home care and other services at no cost.
We believe a strong support net can help people living with ALS (PALS) and their families obtain the best caregiving techniques, equipment, and bolster their will to fight this disease.