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My Boy, Duchenne & Me

Not just life as a mother, but an unexpected one as a mother of a son with Duchenne Muscular Dystrophy

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Tag: William

4 years on

4 years on

January 28, 2020January 28, 2020 Jo EamesLeave a comment

4 years into this journey – a journey no one could ever imagine unless they walk the steps we do each and every day. I read back on my blog that I wrote in the days leading up to William’s diagnosis, the affects of how a simple telephone call can change the world as you… Continue reading 4 years on

Worth it – I think!

Worth it – I think!

April 18, 2018 Jo Eames2 Comments

So we are now into set 3 of William’s steroids (He’s 10 days on 10 off – thick pen on the calendar is a must) and it’s safe to say I think we made the right decision. That is me and Matt, no doctors really make a decision for you, you have to have it… Continue reading Worth it – I think!

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Defending William Against Duchenne

Keep up with all our news on the big build and William’s developments:

Facebook: www.facebook.com/DefendingWilliamagainstDuchenne/

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Account Number: 83768740

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All proceeds donated into this unincorporated charity will be used for the development, wellbeing and happiness of William Eames. 

 

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