There are many ways that you can join us and support our mission. We are adjusting to our new normal, and learning a lot about ALS. While we have several things in the works, below are a few opportunities that we are excited about.
Consider making a recurring donation directly to the #AttackLifeSloan Foundation. A 501c3 nonprofit created to assist Nick, and others with ALS, with medical needs as well as quality of life adjustments as the disease progresses.
Join us March 27th, for our first Sloan Warrior Workout. This is our first of what we hope will become an annual fun workout for all fitness levels in support of our great friend, Nick Sloan, and his family on their journey fighting ALS. For those who cannot attend, or wish to attend but not workout, please purchase an honorary ticket for $35 (plus fees), which will include a t-shirt to show your support.
Please click the link below. If your congressman or congresswoman is not a co-sponsor on this bill, please call his or her office or write a letter and help families like ours get access to ground breaking ALS research and medication.
We are so honored and excited that the #AttackLifeSloan Foundation is listed along side the many wonderful ALS organization across the US. Please help us spread the news through social media or around the water cooler.
Consider making a recurring donation to the ALS Association or the ALS chapter or your choice. The ALS Association supports those with ALS by focusing on the entire ecosystem: local care for patients; advocacy, to ensure public policy serves the needs of ALS patients;, and research to one day find a cure.