I have followed MDSG and admired the work with families affected by myotonic dystrophy for many years.  I am motivated to be a Trustee as the challenges and effects of DM are close to my heart after my father and extended family were diagnosed with the condition.  In 2014, I was diagnosed with DM1.  I am learning, understanding and coming to terms with the challenges both mentally and physically, on a day to day basis.

I realised how much more awareness was needed and I am eager to put my time towards helping those where I can.  I would therefore like to use my skills towards MDSG and help to steer it to greater success.

I served as secretary and head of business for a charity, namely Blackburn Youth Zone.  I was responsible for the membership base, developing the income through fundraising and managing the governance department and dealing with Charity Commission.

Not only am I and members of my family affected by myotonic dystrophy, but I have significant experience of a charitable organisation.

 

 

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Get involved

We welcome new members and new ideas

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What is DM?

Myotonic Dystrophy is a condition affecting 1 in 8000 adults

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MDSG can help

Offering friendship and support to all those affected

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Research

Keep up to date with research in this field

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