Isabella Dunn Benevolence Fund
Isabella is a sweet and hard-working 8 year old girl who was diagnosed with Spinal Muscular Atrophy when she was 2 years old.
SMA is a debilitating, progressive, motor neuron disease (much like ALS) that affects body functions including breathing, swallowing, walking, and sitting. It is the leading genetic killer of children under two. There is no cure and no treatment available for Isabella in the USA.
The only treatment available for Isabella is stem cell treatment from umbilical cord that she needs every 6 months. With Isabella’s determination, stem cell treatments and therapies, she continues to be stable against the progression of this devastating disease.
Thank you for your life changing support!