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So far Boris M Struk has created 132 blog entries.

Australia Post – we deliver. Sometimes…

Australia Post – we deliver. Sometimes... I read a few months ago that there were more than 1.1 million complaints to Australia Post in 2016-2017 and that figure was actually down by 30% over the last previous two years.  Apparently the drop did not indicate an improvement in customer service. This implies that people probably [...]

By |2018-10-16T11:00:39+00:00October 16th, 2018|Boris M Struk, Media, news|0 Comments

Live Q&A Brings Renewed Hope

Live Q&A Brings Renewed Hope Last night the Australian Regenerative Medicine Institute (ARMI), Monash University and Muscular Dystrophy Australia held a Facebook Live Q&A “You Ask We Answer” event where the MD community had the opportunity to have their questions answered in real time by a panel of experts in MD. The panel included: Boris [...]

Putting Lycra before Wheelchairs

Putting Lycra before Wheelchairs Yesterday, I learned that in the Greens world there are no disabled people. No small feat considering that 1 in 4 Australians has a form of disability. I am outraged at the lack of inclusion and total selfishness that the Greens Councillors are displaying. Our community needs more help getting around, [...]

By |2018-09-17T15:35:05+00:00September 14th, 2018|Boris M Struk, Media, news, policies|0 Comments

FSHD Research Projects

Advertising and promoting Facioscapulohumeral dystrophy (FSHD) Research Projects Researchers at The Royal Children’s Hospital are looking for children and adolescents aged 6-18 years who have been diagnosed with FSHD, to participate in one or both of these studies: The effect of the nutritional supplement (creatine monohydrate) on strength and muscle mass in children with FSHD [...]

By |2018-09-14T09:40:25+00:00September 14th, 2018|disorders, research, trials|0 Comments

Lord Mayor of Melbourne and Superhero – Sally Capp

“I’ve donned my cape for Superhero week to show my support for all the young superheroes living with muscular dystrophy. Let’s get behind this great cause!” Lord Mayor Sally Capp. MDA Facebook Page

By |2018-09-03T13:21:47+00:00September 3rd, 2018|ambassador, Event, fundraising, news|0 Comments

DMD Lifetime Mobility Scale Research Study

DMD Lifetime Mobility Scale Research Study Muscular Dystrophy Australia is assisting the UC Davis Neuromuscular Research Center in USA to seek participants for an online survey about movement and daily living abilities for people with Duchenne muscular dystrophy. The Duchenne Muscular Dystrophy Life-Time Mobility Scale (DMD-LMS) is a set of questions that ask about how [...]

By |2018-08-16T18:28:09+00:00August 16th, 2018|disorders, research, trials|0 Comments