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DF<br />
<strong>Magazine</strong><br />
05 <strong>MDF</strong> notice board<br />
06 National news<br />
07 MD information<br />
26 Health news<br />
MD INFORMATION<br />
07 Congenital muscular dystrophy<br />
10 Emergency alert cards<br />
Events<br />
14 Make Today Count Tandem Skydiving <strong>2017</strong><br />
15 Muscular dystrophy awareness run<br />
15 “Oomies se road trip”<br />
People<br />
16 Just live! So says Anne-Marie<br />
18 Iman Casoojee<br />
20 Tribute feature: Patrick John Artman<br />
21 Ride London: Barbara’s story<br />
22 Exondys 51: the Roe family’s story<br />
23 Ella and her ‘cheeky feet’<br />
Regular Features<br />
28 The View from Down Here<br />
29 Doctor’s corner<br />
30 Sandra’s thoughts on …<br />
Research<br />
24 Dystrophin mutation in Duchenne mouse model<br />
25 Myotubular myopathy gene therapy trial<br />
25 Bone health in people with FSHD<br />
C O N T E N T S<br />
Published by:<br />
Muscular Dystrophy Foundation of SA<br />
Tel: 011 472-9703<br />
Fax: 086 646 9117<br />
E-mail: national@mdsa.org.za<br />
Website: www.mdsa.org.za<br />
Publishing Team:<br />
Managing Editor: Pieter Joubert<br />
Copy Editor: Keith Richmond<br />
Publishing Manager: Gerda Brown<br />
Design and Layout: Divan Joubert<br />
Printer: Qualimark Printing<br />
Cover photo of Ludick Fouche courtesy<br />
of Angelos Frantzeskos.<br />
Future <strong>Issue</strong>s:<br />
April 2018<br />
(Deadline: 2 March 2018)<br />
The Muscular Dystrophy Foundation<br />
of South Africa<br />
We are a non-profi t organisation that supports<br />
people affected by muscular dystrophy and<br />
neuromuscular disorders and that endeavours to<br />
improve the quality of life of its members.
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