The Power of Giving Back
GivingTuesday – the global day of giving Join us for the 7th annual GivingTuesday on December 3, 2019! GivingTuesday is a global day of giving that happens each year after Black Friday and [...]
A DMD gene therapy has been placed on clinical hold
Following the occurrence of a safety incident, the FDA has placed on hold the clinical trial for SGT-001, the Solid’s gene therapy candidate for Duchenne muscular dystrophy (DMD). This [...]
Teaming up to take down Duchenne
Research and collaboration are bringing Canadians closer to a cure than ever before. However, many parents fear that access to treatment may come too late for their child. by Denise Deveau, Sep [...]
Living with DMD, Carl’s resilience
Notes from the “Living with DMD” web-doc Tecima Productions team. Carl’s resilience. Our small production team travelled across Canada, meeting with families whose children have Duchenne [...]
A Race Against Time to Access New Treatments
Duchenne muscular dystrophy seen through the eyes of the families There are over 7,000 rare diseases in Canada. Duchenne muscular dystrophy (DMD) is one of them. DMD afflicts children, especially [...]
