Muscular Dystrophy Campaign
Experience Muscular Dystrophy
Muscular Dystrophy Campaign for Government funding. This has information about efforts to increase government spending for muscular dystrophy in the UK.Muscular Dystrophy Campaign for Government funding A simple less than a minute petition for someones life time

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Muscular Dystrophy Duchenne Campaign Every Race Minute Senda Against Campaign Than Group Message See Support Conditions And Diseases Neurological Disorders Muscle Diseases Muscular Dystrophies Muscular Dystrophy Campaign Email Petition Gvernment Funding Support Pledge
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Best entries for Muscular and Dystrophy
1 About Muscular Dystrophy
Personal page
Personal page with muscular dystrophy links and other personal content by individual with a type of muscular dystrophy called Friedreichs Ataxia.
Posted Dystrophy Trial Muscular Michigan Ataxia Personal Alternative Events Matt Oldies Downriver Downrivermall Salts Mdhome Iwanted Cure Conventional
Personal page with muscular dystrophy links and other personal content by individual with a type of muscular dystrophy called Friedreichs Ataxia.
Posted Dystrophy Trial Muscular Michigan Ataxia Personal Alternative Events Matt Oldies Downriver Downrivermall Salts Mdhome Iwanted Cure Conventional
2 Muscular Dystrophy Campaign
Muscular Dystrophy
Muscular Dystrophy Campaign for Government funding. This has information about efforts to increase government spending for muscular dystrophy in the UK.
Muscular Dystrophy Duchenne Campaign Every Race Minute Senda Against Campaign_ Than Group Message See Support
Muscular Dystrophy Campaign for Government funding. This has information about efforts to increase government spending for muscular dystrophy in the UK.
Muscular Dystrophy Duchenne Campaign Every Race Minute Senda Against Campaign_ Than Group Message See Support
3 FSH Friends Forum
Mailing list
Mailing list for people affected by and having an interest in Facioscapulohumeral Muscular Dystrophy as well as other types of Muscular Dystrophy.
Mailing list for people affected by and having an interest in Facioscapulohumeral Muscular Dystrophy as well as other types of Muscular Dystrophy.
4 FSH Muscular Dystrophy
Discussion group
Discussion group for people who have Facioscapulohumeral (FSH) Muscular Dystrophy, as well as family and friends.
Discussion group for people who have Facioscapulohumeral (FSH) Muscular Dystrophy, as well as family and friends.
5 Living with Duchenne Muscular Dystrophy
Stacy Spence
Stacy Spence, a gentleman from New Zealand, describes his life with Duchenne Muscular Dystrophy.
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Stacy Spence, a gentleman from New Zealand, describes his life with Duchenne Muscular Dystrophy.
Yahoo Geocities Help Policy Sign Copyright Maps Sorry Archives Archiveorgreach Visit Guidelines Hosting Terms
6 Limb Girdle Muscular Dystrophy
Discussion group
Discussion group open to anyone interested in making friends, sharing information and providing support for persons affected by Limb Girdle Muscular Dystrophy.
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Discussion group open to anyone interested in making friends, sharing information and providing support for persons affected by Limb Girdle Muscular Dystrophy.
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7 Muscle Disease
Discussion group
Discussion group for parents with children that have a Congenital Muscular Dystrophy, whose child was born with a muscle disease that does not fit any of the other Muscular Dystrophy Associations 40 identifed neuromuscular diseases.
Discussion group for parents with children that have a Congenital Muscular Dystrophy, whose child was born with a muscle disease that does not fit any of the other Muscular Dystrophy Associations 40 identifed neuromuscular diseases.
8 Hope for MD
Hope for
Hope for Muscular Dystrophy Community is a support group that provides emotional and educational support to family members of those with Muscular Dystrophy.
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Hope for Muscular Dystrophy Community is a support group that provides emotional and educational support to family members of those with Muscular Dystrophy.
Navigationshilfey
9 Duchenne Muscular Dystrophy Support eGroup
International Rare
International Rare Disease Support Network (IRDSN) eGroup for making friends, sharing information and providing support for persons affected by Duchenne Muscular Dystrophy.
International Rare Disease Support Network (IRDSN) eGroup for making friends, sharing information and providing support for persons affected by Duchenne Muscular Dystrophy.
10 Christians With Duchenne Muscular Dystrophy
Mailing list
Mailing list for Christians who have Duchenne Muscular Dystrophy.
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Mailing list for Christians who have Duchenne Muscular Dystrophy.
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11 Myotonic Dystrophy 2
Discussion group
Discussion group for those who have genetically confirmed cases of Myotonic Muscular Dystrophy type 2 or who have received a preliminary diagnosis for it.
Discussion group for those who have genetically confirmed cases of Myotonic Muscular Dystrophy type 2 or who have received a preliminary diagnosis for it.
12 Walk Of Life
Biography of
Biography of Chris Barratt, a teenager with Duchenne Muscular Dystrophy
Sign Now People Account Places Lifestream Policy Everything Advertise Login Inc Social Networks Networks Read Trademarks
Biography of Chris Barratt, a teenager with Duchenne Muscular Dystrophy
Sign Now People Account Places Lifestream Policy Everything Advertise Login Inc Social Networks Networks Read Trademarks
13 DMD Information
Duchenne muscular
Duchenne muscular dystrophy, an introduction, the causes, biology reviews, and treatment options.
Therapy Treatment Dmd Gene Genes Biology Mda Contagious Cause Research Proteins Chromosomes Cell Introduction Myoblast Duchenne Rock
Duchenne muscular dystrophy, an introduction, the causes, biology reviews, and treatment options.
Therapy Treatment Dmd Gene Genes Biology Mda Contagious Cause Research Proteins Chromosomes Cell Introduction Myoblast Duchenne Rock
14 Alaska To Argentina By Motorbike
AMCHALLENGE is
AMCHALLENGE is a fundraising venture for Muscular Dystrophy. Photos and text.
Fundraising Crewe Amchallenge Progress Alaska Route Muscular Objectives Quentin Argentina Dystrophy Motorbike Nat Sponsors Page Xrv Campaign
AMCHALLENGE is a fundraising venture for Muscular Dystrophy. Photos and text.
Fundraising Crewe Amchallenge Progress Alaska Route Muscular Objectives Quentin Argentina Dystrophy Motorbike Nat Sponsors Page Xrv Campaign
15 The Muscular Dystrophy Forum
An online
An online support group for people affected by any neuromuscular condition.
An online support group for people affected by any neuromuscular condition.
16 JeffSpace: The Webpage
About Jeff
About Jeff McAllister, who has Duchenne Muscular Dystrophy. All about his friends, family, interests, disability and life.
Yahoo Geocities Policy Copyright Help Sign Visit Finance Popular Sports News Movies Privacy Archiveorg Games
About Jeff McAllister, who has Duchenne Muscular Dystrophy. All about his friends, family, interests, disability and life.
Yahoo Geocities Policy Copyright Help Sign Visit Finance Popular Sports News Movies Privacy Archiveorg Games
17 Jeff Grey
Jeffs experiences
Jeffs experiences with Duchenne Muscular Dystrophy, especially medical and equipment issues including non-invasive ventilators.
Equipment Infovr Md Main Equip Mail Although According Anyway Mainqt Duchennestory I Aided Approximately
Jeffs experiences with Duchenne Muscular Dystrophy, especially medical and equipment issues including non-invasive ventilators.
Equipment Infovr Md Main Equip Mail Although According Anyway Mainqt Duchennestory I Aided Approximately
18 Fight for a Future
Group for
Group for friends and family of those with Duchenne and Becker Muscular Dystrophy, seeking a treatment for slowing down or stopping those diseases.
Group for friends and family of those with Duchenne and Becker Muscular Dystrophy, seeking a treatment for slowing down or stopping those diseases.
19 Living with Muscular Dystrophy.
Information about
Information about MD, Thoms personal experience with Congenital Myopathy, chat room, message board and links.
Yahoo Geocities Copyright Help Policy Sign User Visit Movies Terms Sorryarchives Sports Sites
Information about MD, Thoms personal experience with Congenital Myopathy, chat room, message board and links.
Yahoo Geocities Copyright Help Policy Sign User Visit Movies Terms Sorryarchives Sports Sites
20 MD-List
Mailing list
Mailing list to provide support for people affected by all different forms of Muscular Dystrophy.
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Mailing list to provide support for people affected by all different forms of Muscular Dystrophy.
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21 Suzannes DMD/Autism Page
Coping with
Coping with Duchenne Muscular Dystrophy and Autism, from diagnosis at birth through third grade.
Family Suzannes Random Duchenne Dmdautism Sites Genealogy Personal List Hope Ring Dmd Page Farticlehtml Kids Disability
Coping with Duchenne Muscular Dystrophy and Autism, from diagnosis at birth through third grade.
Family Suzannes Random Duchenne Dmdautism Sites Genealogy Personal List Hope Ring Dmd Page Farticlehtml Kids Disability
22 Kellys Summer Camp Adventures
Created by
Created by a former camper at a Muscular Dystrophy camp. Provides information and a pictorial look into the activities for children at these camps.
Summer Kellys Camp Web Visit Close Spangled Blast Link Star Adventures Sitessponsored Look
Created by a former camper at a Muscular Dystrophy camp. Provides information and a pictorial look into the activities for children at these camps.
Summer Kellys Camp Web Visit Close Spangled Blast Link Star Adventures Sitessponsored Look
23 Angels Among Us
Inspirational and
Inspirational and informational site by a woman with FSH Muscular Dystrophy. Family page with pictures of her children, and MD page of what it was like to grow up different. Guestbook. Florida.
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Inspirational and informational site by a woman with FSH Muscular Dystrophy. Family page with pictures of her children, and MD page of what it was like to grow up different. Guestbook. Florida.
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24 Kevin M. Rudolphs Exciting Site
Kevin, who
Kevin, who has Duchenne Muscular Dystrophy, attends the University of Louisville and has a web business as well. Interests, hobbies and accomplishments plus lots of MD links. Kentucky.
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Kevin, who has Duchenne Muscular Dystrophy, attends the University of Louisville and has a web business as well. Interests, hobbies and accomplishments plus lots of MD links. Kentucky.
Navigationshilfe Ty
25 Society for Muscular Dystrophy Information International
Features organization
Features organization background, disease information, newsletters, membership information, resources, and contact details.
Navigationshilfe Ty
Features organization background, disease information, newsletters, membership information, resources, and contact details.
Navigationshilfe Ty
26 Society for Muscular Dystrophy Information International
Features organization
Features organization background, disease information, newsletter, membership information, and related resources. Contact details are also given.
Navigationshilfe Ty
Features organization background, disease information, newsletter, membership information, and related resources. Contact details are also given.
Navigationshilfe Ty
27 DMD Transitions
Support and
Support and information helpful to the daily care of those with Duchenne Muscular Dystrophy, focusing on the transition from walking to adulthood (approx. ages 10-18) and adaptations parents find helpful. Those affected by DMD and BMD are welcome.
Support and information helpful to the daily care of those with Duchenne Muscular Dystrophy, focusing on the transition from walking to adulthood (approx. ages 10-18) and adaptations parents find helpful. Those affected by DMD and BMD are welcome.
28 The Jones Family DMD Site
Learn how
Learn how a family copes with Duchenne Muscular Dystrophy in son, Bradley. Bradley is about 7 years old.
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Learn how a family copes with Duchenne Muscular Dystrophy in son, Bradley. Bradley is about 7 years old.
Create Tripod Tripodcomhosting Couldnt Page Please Signup Website Lycoscom Shopping Requestedlycos
29 DMD Support List
Mailing list
Mailing list to provide support for people affected by Duchenne Muscular Dystrophy.
Mailing list to provide support for people affected by Duchenne Muscular Dystrophy.
30 Haynes Family DMD Info
The Haynes
The Haynes family talks about their sons Duchenne Muscular Dystrophy and provides information and links on resources, current research and help. South Carolina.
Yahoo Business Email Plans Marketing Small Ecommerce App Hosting Local Gallery Help Advisor Has Geocities Shut
The Haynes family talks about their sons Duchenne Muscular Dystrophy and provides information and links on resources, current research and help. South Carolina.
Yahoo Business Email Plans Marketing Small Ecommerce App Hosting Local Gallery Help Advisor Has Geocities Shut
31 Dysferlin
Discussion group
Discussion group intended to give patients, families, researchers, and others the opportunity to share information, experiences, and advice about Dysferlin deficiency, which causes Miyoshi Distal Myopathy and Limb-Girdle Muscular Dystrophy type 2B.
Discussion group intended to give patients, families, researchers, and others the opportunity to share information, experiences, and advice about Dysferlin deficiency, which causes Miyoshi Distal Myopathy and Limb-Girdle Muscular Dystrophy type 2B.
32 Cell Therapy Research Foundation
Not-for-profit medical
Not-for-profit medical research foundation working to find a treatment for muscular dystrophy and other genetic diseases through cell/gene therapy. Site describes treatments and clinical trials.
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Not-for-profit medical research foundation working to find a treatment for muscular dystrophy and other genetic diseases through cell/gene therapy. Site describes treatments and clinical trials.
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