I Never Met My Boyfriend In Person. When He Suddenly Died, I Had No Idea What To Do.
"I never got the chance to meet him or say goodbye properly. I am not really sure where to go and what to do. We planned to ...
Rare disease ruined his life
A TEEN has spent the last 10 years in a wheelchair after he was diagnosed with a rare genetic muscular disease known as ...
Capricor Therapeutics Options Trading: A Deep Dive into Market Sentiment
Deep-pocketed investors have adopted a bearish approach towards Capricor Therapeutics CAPR, and it's something market players ...
precisionmedicineonline7h
Roche Sees Strong Demand for Elevidys Gene Therapy Amid Steady Q3 Pharmaceutical Revenue Growth
About 500 children worldwide have received the gene therapy, including some families traveling abroad to gain access to it.
19th Annual Sam's Night Event Raises Nearly $1.5 Million for Duchenne Muscular Dystrophy Research
The Killian family, of Rockwall, are celebrating a record-breaking fundraising milestone with their annual Sam's Night event, ...
FiercePharma11h
Roche's Vabysmo will rise above Eylea biosim threat, exec says, as DMD gene therapy Elevidys delivers sales surprise
By squeezing Regeneron’s Eylea, eye disease drug Vabysmo has become one of the biggest growth drivers for Roche. | Despite ...
Muscular Dystrophy News12h
A new beginning of shared purpose at Shalom Medcare
Columnist Shalom Lim celebrates a new beginning in a new job, where his mission to serve fellow patients with muscular ...