Living with ALS

First I want to thank you for reading this. As most of my friends and family know I was recently diagnosed with ALS (amyotrophic lateral sclerosis) ALS is a nervous system disease that weakens muscles and impacts physical function.
In this disease, nerve cells break down, which reduces functionality in the muscles they supply. The cause is unknown. There is no cure. Safe to say this has been an extremely difficult time for me and my family. There’s a few reasons I’m making this go fund me, most importantly so that I can plan for the future. If/when I can no longer work I want to make sure my kids are able to be financially taken care of and not put that stress on my family. The money will also go towards medical equipment I may need in the future as well as making sure the time I have left is spent creating beautiful memories with my family. I understand during this pandemic money is not something everybody has to just give away so I truly appreciate every donation no matter how big or small. Thank you & I love you all