Cade Lindsey just received a devastating diagnosis. Genetic tests revealed that Cade has spinal muscular atrophy type 1, a genetic disease that leads to muscle weakness and atrophy. This precious, beautiful little boy has a tough road ahead with medical treatments to try to improve his motor function and his quality of life. One shot of nusinersen, a ground-breaking, disease-modifying treatment, costs an outrageous $125000! He needs a series of 4 shots (one every 2 weeks) to start as soon as possible.
Thank you for support and donations for this loving family who are always so giving to others!
Follow Cade’s story and brave battle against this disease on his FB page - Cade Maverick - SMA Warrior\
All proceeds to these products will go directly to Cade.