Kutztown Football to Support AFCA’s Coach to Cure MD Program on Saturday

Kutztown Football to Support AFCA’s Coach to Cure MD Program on Saturday
8/31/2018 | Football
KUTZTOWN – Just as in years past, head coach Jim Clements and the Kutztown University football staff is wearing American Football Coaches Association patches on their shirts to promote the association and bring awareness to its programs. The season-opener was Saturday, Sept. 1.

Coach To Cure MD began in 2008 with more than 200 schools and 2,675 coaches involved. 10 years later, that effort has expanded to 620 different schools and more than 11,350 coaches wearing the logo patch on the sidelines and participating in Coach To Cure MD events – a growth of more than 325 percent.

Duchenne muscular dystrophy is the most common fatal genetic disorder diagnosed during childhood, primarily affecting boys of all races and cultures. People with Duchenne develop progressive muscle weakness that eventually causes loss of mobility, wheelchair dependency, and a decline in respiratory and cardiac function. Currently, there is no cure for Duchenne. But thanks to Coach To Cure MD and the work of Parent Project Muscular Dystrophy, there is hope.

The AFCA will coordinate a multi-platform social media campaign throughout opening weekend using the hashtag #AFCAPatch. For more information on the AFCA and its promotional patch weekend, visit www.afca.com or follow AFCA on social media. You may also call the AFCA office at 254-754-9900.

About the AFCA 
The American Football Coaches Association was founded in 1922 and is considered the primary professional association for football coaches at all levels of competition. The 11,000-member organization includes more than 90 percent of head coaches at the 700-plus schools that sponsor football at the college level. Members include coaches from Europe, Canada, Australia, Japan and Mexico.

About PPMD 
Parent Project Muscular Dystrophy (PPMD) is the largest, most comprehensive nonprofit organization in the United States focused on finding a cure for Duchenne muscular dystrophy – our mission is to end Duchenne.

We invest deeply in treatments for this generation of people affected by Duchenne and in research that will benefit future generations. We advocate in Washington, D.C., and have secured hundreds of millions of dollars in funding. We demand optimal care, and we strengthen, unite and educate the global Duchenne community.

Everything we do – and everything we have done since our founding in 1994 – helps people with Duchenne live longer, stronger lives. We will not rest until every person has a treatment to end Duchenne. Go to www.ParentProjectMD.org for more information or to learn how you can support our efforts and help families affected by Duchenne.

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