Posted by Michael Wonder on 03 Feb 2016
Calgary boy needs $400K drug to treat rare form of muscular dystrophy
1 February 2016 - New drug Translarna not approved in Canada but given to a few with Duchenne muscular dystrophy.
For more details, go to: http://www.cbc.ca/news/canada/calgary/calgary-parents-raise-money-for-son-with-rare-disease-1.3426677
