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My Weak Muscles

The journey of a little girl living with Nemaline Myopathy

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Rosie’s condition “de novo”

February 13, 2017

Our genetic reports came back earlier this week and we finally have results as to why Rosie was born with Nemaline Myopathy.

In November 2016 both Iain and I went to the hospital in Bristol to give blood. These were to be tested to identify whether we carried any variants of … More Rosie’s condition “de novo”

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My Weak Muscles

You’ve found the journey of an inspirational little lady called Rosie who struggles with ordinary everyday activities like sitting, eating, walking and smiling due to a severe muscle weakness disease and mitochondrial disorder. What she lacks in physical strength she sure makes up for in mind and spirit. She is a real warrior facing every day challenges with grace and humour.

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