Researchers from the University of Texas Southwestern Medical Center in Dallas have corrected Duchenne muscular dystrophy (DMD) mutations in human cells and experimental animal models using a new genome editing method called CRISPR-Cpf1. These new findings offer hope in permanently eliminating genetic mutations and rescue abnormalities linked to DMD. The study, “…
Having a chronic illness presents many challenges for patients, not only in terms of managing the symptoms they suffer but also having to deal with people’s preconceived ideas about invisible illnesses. MORE: Watch an animated explanation of muscular dystrophy here. Dr. Amy Stenehjem spent much of her career looking after patients…
New York-based Bristol-Myers Squibb announced two separate agreements with Biogen of Cambridge, Mass., and Switzerland’s Roche to license compounds that aim to treat progressive supranuclear palsy (PSP) and Duchenne muscular dystrophy (DMD). Tau protein contributes to the stability of basic cellular structures known as microtubules to transport molecules. Abnormal addition of…
Three grassroots foundations started by the families of boys with Duchenne muscular dystrophy (DMD) have come together to award a $100,000 research grant to the Kennedy Krieger Institute’s Center for Genetic Muscle Disorders to study potential therapies. The Kennedy Krieger Institute in Baltimore provides services for children…
Many people who suffer from chronic illnesses also suffer from depression. Depression isn’t something that should be overlooked; it should be brought to your doctor’s attention so that it can be treated. But how do you spot depression?  With help from prevention.com, we’ve put together a list of some of the most common physical signs…
The Boston Red Sox teamed up with the Make-a-Wish-Foundation to surprise eight-year-old Thomas Hastings with a replica baseball field in his backyard. MORE:Â Firefighters “Fill the Boot” for muscular dystrophy. According to a report on bleacherreport.com, Thomas, who was diagnosed with muscular dystrophy as an infant, wanted a…
A small protein called Myomixer plays a crucial role in the development of skeletal muscle, the type of muscles the body uses to move, according to a study that has implications for muscular dystrophy (MD). The research at the University of Texas Southwestern Medical Center could lead to treatments for the…
CureDuchenne has announced its enthusiastic support and sponsorship of California Senate bill SB 643, which adds Duchenne muscular dystrophy to California’s Genetically Handicapped Persons Program (GHPP) list of eligible medical conditions. The bill, introduced Feb. 17 by Richard Pan (D) — a pediatrician and state senator representing the…
Parent Project Muscular Dystrophy (PPMD), a nonprofit group dedicated to ending Duchenne muscular dystrophy (DMD), has named the Neuromuscular Research Center at the University of California Davis Department of Pysical Medicine and Rehabilitation a certified Duchenne care center. PPMD’s Certified Duchenne Care Center Program,…
The International Association of Firefighters (IFFA) has a long-standing relationship with the Muscular Dystrophy Association (MDA) and has been raising funds for the non-profit organization for more than 60 years. MORE: Boy with Duchenne muscular dystrophy is made an honorary police officer. Across the U.S., firefighters hold…
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