Join Team Ugamuga for the MDA Muscle Walk.
Date: Saturday, April 27th
Place: Houston Galleria
Make a Muscle. Make a Difference.®
On April 27, 2013, the Heeg family and friends will participate in their second Muscular Dystrophy Association (MDA) Muscle Walk. Our participation is personal. In November 2011, our father, husband and friend, Mark Heeg, was diagnosed with Amyotrophic lateral sclerosis (ALS), commonly known as Lou Gehrig's disease.
During the 2012 Muscle Walk, Mark was able to walk with his family and friends. This year, he will be rolling. Mark can no longer stand or walk. He can no longer get into bed, cross his legs, breathe, or eat without assistance. Despite the physical losses, however, we have not lost our love for each other as a family, the support from our friends, or the hope that one day there will be a cure for this terrible disease.
Our hope for a cure and support has been provided by the wonderful people at the MDA. While the MDA is focused on finding a cure for ALS, the MDA also helps families cope and adjust to life with ALS. Through our quarterly MDA Appel Clinic visits, we have had access to the best specialists - neurologists, pulmonologists, physical therapists, social workers, occupational therapists and others. We have also had access to the best equipment and tools to make our lives easier - the Trilogy breathing machine, M300 power chair (we have affectionately named "Sparky"), a Hoyer lift, and an eye gaze computer.
Please join us in the Muscle Walk. We will have a great time supporting a great cause. You can also make a donation today and support the families who depend on MDA. Together, we grow stronger.
Mark, Peggy, Taylor, and Madison Heeg
Alex and Allison Sandlin
(Boots, Digger, Google, and Siri too)
|Team Ugamuga - Join Team||Raised|
|Denotes a Team Captain|