Matthew has been living with SMA, an incurable and progressive disease, for 6 years now. He is spunky, smart, a typical boy, full of life, and stronger than anyone I know. Over the past 2 years, we have been fighting to receive the miracle medicine Spinraza. It is supposed to stop the natural disease progression and improve his quality of life and strength. We are excited to see where this next year takes us, and hoping that hospitals in Georgia will begin to treat all patients living with SMA.
Approximately every 7 hours someone is born with Spinal Muscular Atrophy.
It is the #1 genetic killer of infants.
1 in 4 people are carriers of the gene mutation that causes this disease.
Please consider making Matthew’s dream a reality, to be power fast, by making a donation so he can start the 2[phone redacted] soccer season equipped with his very own Strike Force. Your kind and generous commitment to, and consideration for Matthew and family is so greatly appreciated.
With love and gratitude,
All of Matthew’s Family and Friends.
Thank you so very much.
To see more about Power Soccer please visit https://www.powersoccerusa.org/
To see more about the Strike Force chair please visit http://powersoccershop.com/index.aspx/ImageGallery/Index?productId=313
Thank you for all your support and God bless!
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