Blair family medical expenses

Ashley and Brandon Blair are wonderful people. The are ALWAYS helping others, and unfortunately now they are in desperate need of some help themselves. Earlier last month Brandon was diagnosed with myotonic muscular dystrophy. It is a degenerative disease unfortunately with no cure.  Brandon will likely have to stop working altogether which would cause their family to loose their health insurance.  Brandon may also eventually loose his ability to walk. He's only 29 years old. As if this diagnosis wasn't difficult enough to handle just a few short weeks later Ashley's 16 year old son August was diagnosed with an extremely rare disease called Marfan syndrome. There is no cure, and it effects many body symptoms, the most serious being life threatening heart complications. Its seems unimaginable, but this is what they are dealing with. They have mounting medical bills that are just going to keep piling up despite having insurance with these extremely rare and serious life long diagnoses. I want to help offset their stress by raising as much money as possible to help with these costs. They need to be able to focus on what's important, Brandon and Augusts health and wellbeing.  PLEASE donate if your able every dollar helps, and if your unable to donate PLEASE share!! Thank you!