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Galaxy Tribute
Funds
Bradley Sumner-Guest
 
Our son, Bradley, was born on
5th May 2005. He was a healthy baby, if a little irritable, but
fed well and developed OK, although he couldn’t sit unaided, bear any
weight, crawl or roll over. He couldn’t eat solid food as it made him gag.
When he was eight months old he started vomiting for no reason.
A few weeks later Bradley’s
breathing became shallow and laboured; he was very sleepy and hadn’t had
anything to drink for hours. The doctors were very concerned, Bradley had
to endure several blood tests, have a drip placed in his foot, he had a
lumbar puncture, a MRI scan and a heart scan. It was clear that something
was very wrong with Bradley. Over the next few days Bradley was out of
immediate danger and was feeding again when we were told the news. The
consultant had all the test results and had confirmed a diagnosis of Leigh
Disease. Leigh Disease is terminal. You can’t cure it. Our beautiful
little boy was going to die. Nobody could tell us how long he had left.
Two months later, the day
before his birthday, Bradley became seriously ill again. This time he had a
seizure and was taken into intensive care. We had him Christened there on 6th
May 2006.
Bradley passed away in his
sleep on 22nd May 2006, exactly three months since diagnosis.
We as a family were lucky
enough to be able to spend the last few weeks of Bradley’s life with him at
the Acorns Children’s Hospice. They looked after all of us twenty-four
hours a day,. We didn’t have to worry about anything except Bradley. Their
care doesn’t end when a child dies, we (Mom, Dad and Bradley’s two sisters)
were able to stay at the hospice with Bradley until the funeral and they
even helped us to make the arrangements.
We are opening this Galaxy
Tribute Fund in memory of a brave little boy, our son, Bradley.
Till we meet again
Love from
Mommy, Daddy, Becky and Emily
x x x x
Below, Nigel Eaton, Chair of
Climb presents the Star to Clare Sumner and Warren Guest at the Climb 2007
Conference in Dudley.

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