King Family

Hi Shanelle,

I hope this email finds you well.

I just wanted to send a quick message to introduce myself as I'm a writer for Lucky Break magazine here in NZ and I've just read about wee Oliver and Ethan. This must be an incredibly frightening time for Corinne and Mike!

I wanted to reach out in support as I'd love to share their story in our magazine in the hopes we can help raise awareness for DMD as well as some funds for them in the process.

Let me know your thoughts and feel free to pass on my details to Corinne if this is something that may be of interest.

Warm regards,

Ashley

acameron@bauer-media.com.au

Hello, where abouts is the family based , I too have an almost 8 year old that was diagnosed 5 years with dmd, and also developmental delay, we are in Auckland .

Hey, just to let you know there is a family in Ireland with 3 boys affected by same condition http://www.irishmirror.ie/female/family/archie-george-isaac-naughton-were-3226172 could be a good support for you.

You are in my thoughts - we have a different type of muscular dystrophy in our family so I understand how devastated you must feel.