Updated posted by Jolene Hale 18 days ago
Before the recent news from the...
Before the recent news from the doctor, Isabella asked me to go to Disneyland, I pushed this thought to the back of my head not believing its something I could make come true now, but with the news from the doctor being that Isabella doesn't have long left with us I don't want to live with the regret of never taking her back to meet the princess, so I plea to you all for your help in making one last wish come true for a truly inspirational little princess.
on top of all this we are trying to make Christmas special for her last with all 3 of my daughters together. A very close friend is making over her church at Christmas for a winter wonderland for Isabella and her sister, close friends and family and for those that supported us, please get in touch if you can help donate lights Christmas decorations party food or small gifts for santa to give out to bring a smile to each and every child this Christmas time xx
Updated posted by Jolene Hale 29 days ago
Recent update on Isabella, Firstly Isabella...
Recent update on Isabella,
Firstly Isabella is still an amazing little girl and made it to 3 years old, to us (her family) it shows how truly amazing she is to have fought for so long. It will be two years next month.
Next Wednesday will be Isabella's last ever chemo treatment as all the treatment she has received is starting to take its toll on Isabella's body, we was hoping to do 12 months of prolonging but that isn't meant to be, Isabella suffers a lot so we have decided as a family it is in Isabella's best interest to stop after next weeks cycle. (we would have then done ten)
The doctors lead us to believe that we have Isabella until next June but by stopping the treatment this time may come before then, we hope and pray that Isabella will fight to live many more months, which ever its meant to be we will deal with it as a family and always put Isabella first.
we wont win the battle but were trying to win the fight, our fight now being to keep Isabella as pain free as we possibly can and to give her a wonderful life, with amazing memories so her sisters will be able to look back and over look the bad times with smiles and fond memories of there very much loved sister.
On a much brighter note we are now the proud owners of little lions den (a very fitting name chosen by Isabella's uncle for our little lion), as of the 1st march 2014 a new season it will be open for under 3's suffering with cancer and there siblings to run away to, if you know of anyone that would benefit from a little ''runaway'' please do get in touch to see if we can help.
Thank you to everyone who has supported us to get to this far, I hope you can find a small place in your heart to continue to support Isabella and little lions den, we will continue to fund raise to make little lions den possible as we no only to well a break is sometimes all you need to carry on the battle.
If you would like to follow Isabella's fight daily or when possible to update please like her facebook page called ''Isabella coomber and little lions den''
lots of love and wishing you all good health always xxxxxxxxx
Updated posted by Jolene Hale 4 months ago
Latest update... We have been told by...
We have been told by 2 different radiologist that specialist in brain tumours that there is NO cure for Isabella's cancerous brain tumour and to enjoy what time we have left with her. The words came as "Isabella will never grow up" all we can do us try and prolong Isabella's life and give her the best possible quality of life.
After speaking to her neurologist we believe the time Isabella has left could only be 10 months.
As a family we have decided to give Isabella everything possible in sure a short amount of time and to builds amazing memories as her siblings are so young we don't ever want them to forget her.
We are also bring the plans for a holiday home for children under 3 years old suffering with any type if cancer and there siblings forward and will continue to fund raise for this and to give Isabella the world or as much as we can and for as long as time allows, please follow Isabella's journey on Facebook for daily updates. Thank you all for your support in this nightmare battle.
Life is for living doesn't matter how long or short that may be, make the most of every moment xxx
Created by Jolene Hale on July 27, 2012
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Some of the team will be walking over the 02 on Sunday if u can please sponsor them.
posted by Jolene Hale 6 months ago
GOD BLESS, SHE IS IN MY PRAYERS..XXXX
posted by Chris Evatt 7 months ago
Hope your little girl gets the treatment she needs xxxx
posted by Denise Grice 8 months ago
Reading this has reduced me to tears..im amazed she doesnt qualify for NHS funding and you're having to raise that huge amount of money to get her the treatment she needs! Both myself & my son want to help raise money towards her treatment by running for Isabella in the 10k London run on the 14th of July....
posted by Colleen Baker 9 months ago
reading your story has just made me cry my eyes out id like to donate and will be today. i hope Isabella gets the treatment she needs and welldone to zoe and terry for everythink they did yesterday. its a shame i couldnt make the event i would liked to of been there all my love char
posted by Char Pierpoint 9 months ago
please ring me on 07789192119 would like to donate in cash live just five minuets away
posted by Vicky Stokes 11 months ago
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