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Parent Project Muscular Dystrophy
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ParentProjectMD
Joined: August 15, 2007
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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.
Country: United States
Website: http://www.parentprojectmd.org
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About Duchenne muscular dystrophy (Duchenne)  
Duchenne is the most common fatal genetic disorder diagnosed during early childhood. A progressive muscle disorder that causes loss of muscle function and independence, Duchenne affects approximately one out of every 3,500 boys and 20,000 babies born each year worldwide. The disorder manifests primarily in boys because the affected gene is found on the X-chromosome. Duchenne knows no other boundaries, touching all races and cultures.

Parent Project Muscular Dystrophy (PPMD) estimates that there are approximately 15,000 young men with Duchenne alive today in the United States. Duchenne can occur during any pregnancy regardless of family history. To date, there is no cure or treatment to stop the progression of Duchenne, and young men with Duchenne typically live only into their twenties.
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7 months ago 1,510 views ParentProjectMD
Advocacy Matters
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[TRANSLATED] Advocacy Matters
[TRANSLATED] Advocacy Matters
PPMD Founder and President, Pat Furlong and PPMD Chairman, John Killian, discuss t...
8 months ago 495 views ParentProjectMD
Coach to Cure MD
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[TRANSLATED] Coach to Cure MD
[TRANSLATED] Coach to Cure MD
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9 months ago 1,026 views ParentProjectMD
Introducing Our Pledge to End Duchenne
1:54
Parent Project Muscular Dystrophy introduces the pledge to end Duchenne.
11 months ago 1,541 views ParentProjectMD
Rocky Run 2: On the News in Philadelphia
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This was a 3 mile roundtrip course which leaves the Loews Philadelphia Hotel and m...
11 months ago 481 views ParentProjectMD
Olympic Swimmer Announces Endorsement Pledge
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Olympic Swimmer Ryan Lochte announces endorsement pledge for Parent Project Muscul...
11 months ago 1,274 views ParentProjectMD
Micah and Addison's Story
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Addison and Micah are fighting Duchenne Muscular Dystrophy. This is a story of the...
1 year ago 5,537 views ParentProjectMD
BrainPOP - Distrofia Muscular De Duchenne
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Tim y Moby, los integrantes del querido dúo animado de BrainPOP, presentan el tema...
1 year ago 6,356 views ParentProjectMD
BrainPOP animation about Duchenne Muscular Dystrophy
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BrainPOP's beloved animated duo, Tim and Moby, present the topic of Duchenne in th...
1 year ago 12,095 views ParentProjectMD
Genes
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[TRANSLATED] Genes
[TRANSLATED] Genes
World Rare Disease Day is being held Feb. 28, 2009. Join the fight to raise aware...
5 months ago 4,062 views AddiCassiFund
Hunt for Reed
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[TRANSLATED] Hunt for Reed
[TRANSLATED] Hunt for Reed
Donate at www.parentprojectmd.org. Video produced by Kerri Navarro, edited by Laur...
1 year ago 894 views todfrank
Channel Comments (3)
hdiho (3 months ago)
Bless you Pat....your love and inspiration gives us all hope.
orangefruit (1 year ago)
You guys are an inspiration. I hope you all achieve your goals
From a random occupational therapy student in AUS
Keep up the good work.
jacqui818 (1 year ago)
Thank you, Pat, for your continued inspiration and strength. This video gets all of our voices heard. We love you Nicolas!
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