The Matthew Degori Lowe's Syndrome Foundation
Fundraising EventsResearch
DonationsAbout Us
What Is Lowe Syndrome?Contact Us
The Lowe Syndrome Foundation

Matthew, Age 6

Pancake Breakfast 2010

The Lowe Syndrome Foundation (also known as The Matthew DeGori Lowe Syndrome Foundation) was founded in 2006 by the parents of a child diagnosed with Lowe Syndrome. The Foundation is a non- profit 501(c)3 recognized as a public charity by the Internal Revenue Service. The mission of the Foundation is to raise much needed funds to support medical research associated with Lowe Syndrome (LS).

Lowe Syndrome is a genetic disease which affects the kidneys, eyes, brain, bones, and muscles. Multiple physical and mental handicaps are associated with this disease. Lowe Syndrome is a terminal illness in which there is no known cure and treatment is symptomatic.

Back to homepage

2007, 2009 Matthew DeGori Lowe Syndrome Foundation. All rights reserved. Site design by David Wendt, Jr.

Click here to contact us.