I wrote this blog a long time ago and at the time choosing not to post it mainly because it was pretty raw and I suppose part of me wanted to protect people ...

Well the last 6 months has been rather manic in our family and as I begin to embark on the second half of my 10th season shearing in NZ after celebrating Ell...

Today marks the start of something Daddy has done for you. You loved the Shearing, you loved the shows. Daddy decided before you fell ill that he was going t...

23rd April 2018, 13:02 “I’m really sorry she has gone now” Nothing and I mean NOTHING can or will prepare you for holding your first born in your arms while ...

The last week was a busy one for Team Grace, we had lots going on for Fundraising in various locations across the south of the UK. Thursday night saw Grace’s...

This day last year as we were about to embark on Lambing season Grace was walking round checking our sheep with mummy, granny and the dogs, having a great ti...

Grace was incredible at expressing her feelings, interacting, getting along and making friends with other children and adults something that her school notic...

I won’t lie it was mixed emotions this week, I was so Excited to start making memories with the little dude (Grace’s brother) share and show him what we did w...

Amazing people do amazing things and that is exactly what Grace's Godfather Karl Fletcher and his cousin John Dyer are doing... In April they are breaking ou...

7 Months have passed.... How has Grace been gone for 7 months? That’s 214 days, 5136 hours or 30 weeks and 4 days either way it’s too long! I haven’t had a c...

Graces Daddy is off to New Zealand again soon to shear sheep for a few months, this year Elliot and me are going as well for a few weeks. It’s bitter sweet a...

A few weeks ago nearly 7 months after Graces passing I was plagued with guilt... yes guilt! I was raised to be courteous and polite as a child this is someth...

Team Grace took on The Winter Wolf Run It was Cold, Smelly, Muddy and tough but that’s nothing compared to what people living with Mitochondrial Disease fa...