Just found it linked up on Muscular Dystrophy UK's FaceBook page:
https://www.facebook.com/musculardystrophyUK/
You have to scroll down a bit, it was posted on Feb 16th at 10:58 although I don't know where that time/date stamp is generated....There are over 300 reactions and over 100 shares on the FaceBook platform alone for this post.
Researchers in the US have identified a new drug that has the potential to treat facioscapulohumeral muscular dystrophy (FSHD). The drug - called apabetalone - has the ability to switch off the DUX4 gene, which is overactive in people with FSHD.
Find out more about apabetalone >> http://bit.ly/2lVPVUi.
