"I believe a cure is possible and we will eliminate the challenges of MPS. Join us to make this a reality for Evan Abel and all children living with MPS"

My goal is to raise $2,000
Total: $150

Evan's Story

Evan is 11 years old and has Sanfilippo syndrome. He was diagnosed in August, 2008 after 4-1/2 years of searching for answers to his mental and physical decline. Evan originally reached many milestones as a baby. Then, as a toddler, we began to notice developmental delays. Although he was a very active little boy, he babbled constantly and had many recurring visits to the Doctors for ear and respiratory infections.

Evan does not talk anymore and requires frequent rest periods throughout the day. He is still very active and needs to be closely supervised. Evan can be described as a 4’5”, 80 pound toddler. He is very loving and such a blessing. He teaches us how special life is every day. We know as Evan gets older he will continue to regress because Sanfilippo has no current treatments or a cure.

This year we will be hosting our 3rd Annual Spaghetti Dinner, A Wish for Evan. We have raised almost $20,000 in the past two years for Sanfilippo Research and Family Support programs with the National MPS Society. This year all money raised will be for Sanfilippo Research and to help researchers discover a treatment that might benefit Evan in his lifetime.

For more information about the National MPS Society please visit www.mpssociety.org. Before leaving our site, consider making a difference in Evan’s fight for life with research for Sanfilippo.

Event Date: October 20, 2012
Event Time: 5-8 pm
Cost: $8 per person (Kids under 7 eat free)

There will be a silent auction, flat screen TV and shotgun raffles as well as T-shirts for sale.

Event Flyer
More About Evan FlyerThanks for visiting my page! Please help me with my fundraising by contributing to this great cause!

Making a donation is easy and safe – simply click the “Donate” button in the upper right to donate.

Make sure to bookmark this page and come back often to check on my progress!

The mission of the National MPS Society is to fund research and provide support for families affected by MPS and related diseases.

Please help our family and support the National MPS Society. Every donation will make a difference in the lives of those affected by MPS and related diseases. Please visit www.mpssociety.org for more information.

Messages in Evan's Guestbook

Write a message

Your email address will not be published.

Our Mission

The National MPS Society exists to cure, support and advocate for MPS and ML.

Contact Us Family Support Programs