Kaleigh's Trust - Our Battle with DIPG

Twitter

Tuesday 19th April 2016, this was the day our world turned upside down and heart shattered to pieces as the consultants confirmed the diagnosis that Kaleigh had developed a condition called DIPG. At the time, we had little knowledge of what this was except we were told there is currently no known cure and this news left us devastated. Like any parent in our predicament, we

will do everything we can and cling on to even the faintest of hope. Since the launch of this page Kaleigh has already received 24 out of her 30 daily radiotherapy sessions at University College Hospital in London. The daily commute to the hospital is tiring for the whole extended family, but nothing beats home comfort for Kaleigh and being able to be with family / friends and especially her little younger brother. With this webpage we hope to bring an awareness and share our experience with others. With great support from family and friends, we will remain strong and keep on battling as we truly believe "No Cure Today, Does Not Mean No Cure Tomorrow". If you would like to contribute financially to Kaleigh's medical support, please click on the Donate button or the chuffed link within the site.