‘I lost friends over my rare, incurable condition – they didn't believe me'

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‘I lost friends over my rare, incurable condition – they didn't believe me'
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  • 📰 MetroUK
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Even doctors and nurses ask Megan what her condition is.

Megan Jinks has lived with aches and pains that ‘feel like she’s been in the gym for hours’ since she was 12.that causes chronic inflammation of the muscles and skin.

Megan first noticed something was wrong as a pre-teen, when she experienced weakness and joint pain, but doctors dismissed her symptoms as ‘growing pains’. However, it was her mum who insisted she be seen by aMegan Jinks with her partner Jason Poole Following a biopsy, Megan was diagnosed with dermatomyositis in 2014 and prescribed steroids to try and manage the condition, which came with side effects – such as weight gain causing a ‘moon face’.

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