WEBVTT NICHOLE: 5 FOR GOOD, AND UNCONDITIONAL BROTHERLY LOVE. ED: TERRY’S FOUNDATION FOR MUSCULAR DYSTROPHY IS BRINGING TOGETHER FAMILIES IMPACTED BY THE DISEASE WITH LEADING EXPERTS IN THE FIELD.

On April 17, raffle tickets for the Muscular Dystrophy Family Foundation Chopper went on sale for $20. The MDFF chopper was custom-built by Orange County Choppers and tagged with the agency’s slogan ...

ST. LOUIS — After spending a lifetime accepting checks donated to the Muscular Dystrophy Association, KSDK anchor-reporter Mike Bush got to present that organization with a check. The TEGNA Foundation ...

A New Jersey man and two others from the JAR of Hope Foundation will walk 300 miles across four states, starting Saturday from Shrewsbury with stops in Worcester and Webster, to raise money and ...

Leah Messer’s daughter Ali was diagnosed with muscular dystrophy after Leah noticed that Ali’s leg was growing differently than her sister Aleeah’s leg. It took a while before an official diagnosis ...

Jett Foundation, a non-profit organization dedicated to raising awareness and funds for Duchenne muscular dystrophy, has helped a family from Chattanooga purchase an accessible van through their ...

The program is being administered by Jett Foundation, a national nonprofit headquartered in Plymouth, Mass., which works to empower people and families impacted by Duchenne muscular dystrophy through ...

A group of New Jerseyans who are members of the Jars of Hope Foundation walked 260 miles from Washington D.C. to Old Bridge to raise money for muscular dystrophy research.

Hamburg, Germany - 21 August 2013: Evotec AG (Frankfurt Stock Exchange: EVT, TecDAX, ISIN: DE0005664809) and the Jain Foundation today announced that they have extended and expanded their research ...

NASHVILLE, Tenn. (WTVF) — The Nashville Fire Department's annual "Fill the Boot" fundraiser is underway. Firefighters will be on the streets all week to ask for donations on behalf of the Muscular ...

The US HHS has added Duchenne muscular dystrophy and metachromatic leukodystrophy to newborn screening, citing benefits of early detection and access to FDA-approved treatments.

People diagnosed with myotonic dystrophy type 1 have difficulty unclenching muscles due to a genetic defect that generates toxic material within their cells. There is currently no treatment. In a new ...