"Okay Clay Eagle And Whitmer Panther Fans!!!!"
It is Friday, Septemeber 28th. If you are interested in volunteering to help us out this year, please contact me. This is a great event that we were involved in last year for Parent Project Muscular Dystrophy. They are one of the leading forces out there to help find a cure for Duchenne. More details to come soon... For now, we are looking for donations for our raffles and help in getting the word out to the communities to make this year a HUGE success and one more step forward to finding a cure for our boys.
Watch this video attached below to learn more on Coach to Cure MD.
ONE DAY, TWO TEAMS,
PLEASE SUPPORT THE CLAY EAGLES IN
“COACH TO CURE MD”
GAME DAY: FRIDAY, SEPTEMBER 28th
GAME TIME: 7:00PM
T-shirts, Arm Band Sales,
Coach To Cure MD is a partnership between the American Football Coaches Association (AFCA), a professional organization for over 10,000 college football coaches and staff, and Parent Project Muscular Dystrophy (PPMD), the largest national charity devoted exclusively to Duchenne muscular dystrophy.
In 2008 the AFCA adopted PPMD’s Coach To Cure MD program as one of their charity efforts. One reason the AFCA was drawn to Coach To Cure MD was because of the unique parallels between Duchenne, a disorder which robs young men of precious muscle strength and college football, a game where young men are at the peak of their muscle strength.
GOALS OF COACH FOR THE CURE ARE SIMPLE:
1. Raise national awareness of the disorder
2. Raise money to fund research for a cure
Learn more about Coach to Cure MD at http://coachtocuremd.org/
ABOUT PARENT PROJECT MUSCULAR DYSTROPHY
Parent Project Muscular Dystrophy (PPMD) is the largest nonprofit organization in the United States focused entirely on Duchenne muscular dystrophy.
Since 1994, PPMD has improved the treatment, quality of life, and long-term outlook for all individuals affected by Duchenne through research, advocacy, education, and compassion. Because of our efforts, families affected by Duchenne have better access to state-of-the-art care information, research is moving forward at an accelerated pace, and legislation now exists funding Duchenne research and outreach programs.
We take a comprehensive approach in the fight against Duchenne—funding research, raising awareness, promoting advocacy, connecting the community, and broadening treatment options. Only this comprehensive approach will lead to the day that 100% of those diagnosed can turn to a treatment that will lead to the end of Duchenne muscular dystrophy.
Learn more at ParentProjectMD.org.