My daughter Jasmine Wharton age two fights for her life every single day due to Krabbe leukodystrophy.
Why is this important?
My daughter Jasmine Wharton age two fights for her life every day because she wasn't screened for this disease because it is NOT on the Newborn screening in Michigan. Even if a baby had it they would detect it early and do a cbt (cord vlood transplant or a bmt (bone marrow transplant) showing very good results to those that are dected early enough to recieve treatment. PLEASE help make it Jassy's Law By helping out and signing this petition so no other child or parents have to go through this horrible disease!
