Our Members - Their Stories
MDANZ members share their personal stories of living with a Muscular Dystrophy condition.
"Don’t ever give up" - Lara Elliott
Having a rare disease hasn’t held Lara Elliott back from making the most of her life and fulfilling her dream to become a mother. She shares her story with Melanie Louden ahead of Rare Disease Day on February 28, 2021.
Rare disease teaches Louise to be kinder to herself and others
From a GP who said it was all in her head, to facing her fears, Louise Davy is determined not to let the rare disease she has limit her. She shares her story with Melanie Louden ahead of Rare Disease Day on February 28, 2021.
Rolling with the punches and dancing to her own trumpet
When Freda Evans was diagnosed with Pompe disease more than 30 years ago she decided then and there that the condition would not rule her life. Anything people said she couldn’t do, she has done – including travelling the world alone.
The sky’s the limit for Dylan
Dylan Schneider explains how the Duke of Edinburgh’s Hillary Award is opening up new, and impressive, opportunities for him.
Flynn’s wheels bring freedom and independence
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A “spectacular recumbent” bike is seeing 17-year-old Flynn Mitchell get back into the outdoors again, which is having a positive impact on his mental well-being and… is leaving the rest of his family in his dust.