With the help of Bradley Lowery Foundation, Yang (Mum to Kaleigh) and her wing women / men will be running the Vitality London 10k in memory of Princess Kaleigh and to raise vital funds for DIPG research.

Runners in alphabetical order: (1) Alex Dias, (2) Anna Midlane, (3) Grant Jay, (4) Hong Tang (5) Jason Skinner, (6) Jeannie Chew, (7) Louise Chappell, (8) Neil Midlane, (9) Neil Tobias, (10) Pixie Tan (11) Sabia Tobias and (12) Yang Lau

Back in April 2016, beautiful 6 year old Kaleigh was unfortunately diagnosed with the worst illness a parent could ever imagine, an illness that we had never heard of called #DIPG (Diffuse Intrinsic Pontine Glioma) a Childhood Brain Cancer which currently has No Cure, Less than 1% survival rate and typically only gives the children a median of 9 months to live from diagnosis.

Remember this illness does not discriminate among nationality, colour, gender or genetics but it does target the helpless young children typically between the ages of 4 & 10.

Kaleigh's parents Yang & Scott with the help of Team Kaleigh searched the world for treatments including Intra-arterial Chemotherapy Infusion Treatments and immunotherapy in Mexico, radiotherapy (the only recognised prolongation of life), complimentary Traditional Chinese Medicine, Bio-Energy Healing, Physiokey, change of diet, drinking Alkaline Water and daily foot massages to maintain her health. Unfortunately after 26 months Kaleigh passed away on 12th June 2018 and will be forever 8. 

if you could help raise awareness and share this link it would be much appreciated.

Kaleigh's story:

copy and paste link into the web to read

https://www.mirror.co.uk/news/uk-news/how-brave-eight-year-old-12929092