Links to Muscular Dystrophy sites from the UK, Canada, Malaysia, Ireland, Australia and the USA. At the My Becker's Story Muscular Dystrophy Connect page you will find even more stories about people living with Becker's as well as other forms of Muscular Dystrophy!
Becker's Muscular Dystrophy webpages
BeckerMD.org is a great site which includes a forum about BMD http://beckermd.org/
Becker Muscular Dystrophy Network Canada
(click here)
(click here)
Becker's United is a UK based BMD Support group
www.beckerunited.com/
Becker Muscular Dystrophy Facebook Discussion Group
(Click Here)
My Becker's Story
Becker Muscular Dystrophy Facebook Discussion Group
(Click Here)
My personal blog about living with Becker's Muscular Dystrophy.
If you are a parent, friend or someone who has recently been diagnosed or are living with Becker's Muscular Dystrophy please visit:
www.my-beckers-story.blogspot.com
If you are a parent, friend or someone who has recently been diagnosed or are living with Becker's Muscular Dystrophy please visit:
www.my-beckers-story.blogspot.com
Muscular Dystrophy webpages
-Muscular Dystrophy Canada's mission is to enhance the lives of those affected with neuromuscular disorders by continually working to provide ongoing support and resources while relentlessly searching for a cure through well funded research.
-MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research. This US based Association also provides comprehensive health care and support services, advocacy and education.
-Parent Project Muscular Dystrophy’s mission is to end Duchenne. We accelerate research, raise our voices in Washington, demand optimal care for all young men, and educate the global community.
-The Muscular Dystrophy Campaign leads the fight against muscle disease in the UK.
-The Muscular Dystrophy Association of Queensland Inc. today is building on the hard work of these early volunteers. The Association is incorporated and is recognised as a credible and accountable provider of services to clients with MD and their families.
-Muscular Dystrophy Ireland (MDI) is a support organisation for individuals with muscular dystrophy and their families. It was founded in 1972 by a group of parents from the west of Ireland whose children had the condition muscular dystrophy.
CureDuchenne is a grassroots effort to bring back focus. There not here to create a profit-making organization. CureDuchenne was started by parents whose only child has DMD. If one son can be saved, there is hope for all.
Life with Muscular Dystrophy Webpages
Stephen's Piece of Life
-Stephen created his blog to tell his story about his life and living with Duchenne Muscular Dystrophy.
Fazz Fadhilah vs Muscular Dystrophy
-Fazz from Malaysia set up this page to create awareness about Muscular Dystrophy (MD) as well as to lobby for a better policy dealing with MD sufferers.
If you would like to have your site added please contact me.
