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The Woodlands Marathon

Saturday, February 28th, 2026 The Woodlands, TX 77380 US Directions
Fundraiser

Will "WILLPower" Byers
Running for a Cure for Sanfilippo Syndrome!

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$373

Raised of $25,000

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$25,000

My name is Will "WILLPower" Byers and I'm Captain of the WILLPower team! I am fighting for my life and racing against time to STOP Sanfilippo Syndrome!

My name is Will "WILLPower" Byers and I'm Captain of the WILLPower team! I am fighting for my life and racing against time to STOP Sanfilippo Syndrome!
 
We are Fueled by WILL Power and are running The Woodlands Marathon to raise funding and awareness for Sanfilippo Syndrome research!

Our team is running in honor of Will Byers, a brave 15-year-old boy from Spring, TX who loves to run and who was diagnosed with Sanfilippo Syndrome, Type B in April 2015. Sanfilippo Syndrome is a rare, terminal genetic disorder in which the body lacks a specific enzyme to break down cellular waste, leading to a terminal buildup in cellular tissue and organs leading to premature death. 1 in 70,000 children are afflicted with this terrible disorder.

WILL'S STORY
Will was diagnosed with Sanfilippo Syndrome, Type B (MPS III-B) in March 2015. To find out that your beautiful son has a rare, incurable, degenerative disease is unimaginable. In an instant, every dream we had for our child, from playing little league to college graduation, became uncertain. Sanfilippo Syndrome is a progressive disorder that starts to shut down the brain and central nervous system. Enzymes needed for cells to process cellular waste are missing or are poorly functioning. Over time, waste build up leads to severe disability, robbing a child of the ability to walk, talk, and do everyday activities independently, eventually leading to early death. The heart-breaking truth is that without funding there is no treatment. Without treatment, most Sanfilippo children do not reach adulthood. But, even now, we find HOPE. Please help us raise awareness and find a cure!

CHANGE WILL'S OUTCOME
We were devastated upon hearing Will's initial diagnosis, but we continue to find HOPE. We are living in a time of medical miracles and history is in the making. There are several curative and quality of life clinical trials for Sanfilippo in the pipeline, but we still need YOUR HELP. These amazing studies and trials are happening in part because other Sanfilippo families have made their voices heard and raised awareness and funding to make treatments no longer a far-off dream, but a potential reality. And now we join their voices, and we ask you to join with us. Become fueled with WILL Power and donate today!

All donations go directly to Cure Sanfilippo Foundation (Tax ID: 46-4322131), a non-profit 501c3 organization and will be used to fund research and upcoming clinical trials for the treatment of Sanfilippo Syndrome. All donations are tax deductible. For more information on the Cure Sanfilippo Foundation, please visit www.CureSFF.org.

Contact information: 
Email: willpowermps@gmail.com 
Facebook: www.facebook.com/willpowermps 
Twitter: @willpowermps
Instagram: @willpowermps

Recognitions

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Top Donors

$373 Raised By 8 Donors

$200 on behalf of Eve Kneller
$103 from Facebook Donation
$25 on behalf of Nanda Havemann
$10 on behalf of Gisela Vega
$10 from Anonymous
$10 from Anonymous
$10 from Anonymous
$5 on behalf of Annie Behr

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