Visit Abbie's website at www.abbiesarmy.co.uk

Abbies Army achieved its own Charity Registration number 1149400 at the beginning of November 2012. We are now listed as our own entity on JustGiving and can be nominated as a beneficiary charity on fundraising pages. Due to this, this page is now CLOSED should you wish to DONATE please head to our charity account www.justgiving.com/abbies-army  THANK YOU for all your wonderful support and messages here. xx

 

Our story begins on April 13th, 2011 the day our whole existance was turned upside down. Abbie our darling 6 year old daughter had been unwell in that she was a little lacking in energy and seemed to have trouble controlling her eyes...our feeling was that perhaps she was diabetic and needed an opticians appointment, how wrong could we have been?...

 

A visit to the doctor lead to an urgent appointment with a consultant paediatrician at our local hospital, who revealed that they suspected and were investigating the presence of a brain tumour. A later MRI scan showed a mass in her brainstem and their suspicions were confirmed.

 

Abbie was diagnosed with a rare, incurable and inoperable Diffuse Intrinsic Pontine Glioma, the only standard treatment for which is palliative radiotherapy. Over the course of the next two months Abbie endured and battled through her treatment at The Royal Marsden Hospital in Sutton,Surrey, the care received was exceptional.

 

Abbie recovered enough to enjoy one last holiday, we took a cottage in Dorset which I had taken with her religiously (almost!!) every summer for the last 3 years...we loved it there so much only this time grandparents and aunties and uncles came to. She was a little tired and for us it had a totally different relevance to those previous visits but Abbie had fun, the weather was great and there was plenty of wave jumping and swimming going on!

 

To be delivered the death sentence that is DIPG for your child is surely the cruellest and most harrowing experience that any parent should have to face. At times the emotional strain is completely overwhelming and yet we paint on a smile as if all is normal for our amazing children. Abbie only ever believed that she would be well again and all she would speak of the whole time would be getting back to school with her friends where she belonged.

 

DIPG affects upto 40 children per year in the UK with an age range of between 5-10 years . It is extremely agressive with a median survival rate of between 9-12 months. We had exactly 5 months to the day from when Abbie was diagnosed, we managed to get her home from the hospital for one last night of cuddles in familiar surroundings with her family around her, and sadly she slipped away in our arms the following morning on Sept 13th 2011.

 

We are supporting Nottingham University's Childrens Brain Tumour Research Centre as we made contact with Professor David Walker initially... and although we could be offered no hope for our gorgeous girl their vital research will hopefully bring forth much needed advancements in the treatment of this universally fatal  tumour and other paediatric brain cancers. She was our whole world. No parent ever wants to hear that there is no cure and no hope and they should never have to.....

 

Abbie's Mummy & Daddy.  Forever 6 in our hearts.

 

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