Help cover costs for Mable's SMA treatment

My name is Nichola and I'm fundraising for my dear friend and her sweet baby.

It's been a difficult year for the Allen family. After an incredibly difficult hyperemesis gravidarum pregnancy, bedrest, and more IVs than Mom can count little Mable joined their family. Within days a routine newborn screening uncovered a life changing problem. Sweet little Mable was diagnosed with SMA. Spinal Muscular Atrophy is a rare degenerative disease that up until 4 years ago was largely untreatable. Gratefully new gene therapy has made incredible strides with this disease giving Mable and her family hope for her future.

Although insurance should cover the astronomical cost of her treatment, the Allen's face extra costs of traveling 3 hours for her treatment. Gas, food, lodging, and anything else they might need for her specialized care add up quickly, especially when Dad has been out of a job since April.

Please consider helping this family and sweet little Mable get her life saving treatment.