Weʼve raised £187,636 to Help Luke get the life saving treatment he needs & let him live his life xx
- Tranent, United Kingdom
- Funded on Monday, 30th April 2018
Crowdfunding is a new type of fundraising where you can raise funds for your own personal cause, even if you're not a registered nonprofit.
The page owner is responsible for the distribution of funds raised.
update: Thank you so much to everyone that is continuing to support us it means the world to us. Luke is now recieving Intra-arterial chemotherapy & immunotherapy im monterrey mexico. Luke has had 7 IA treatments & 4 immunotherapy treatments and has reaponded well so far 🙏🙏🙏 we have seen tumour shrinkage, cyst shrinkage, less cancer activity where cells are dying & much clinical improvement. We need to continue with these amazing treatments & your all helping us do this thank you xxx
UPDATE: Thank you so much for everyone's support so far, the response has been amazing. As you will see below when this campaign was started we were raising money to pay for CED treatment, the target was reached to allow us to pay for this. We have hit a stumbling block with CED as a cyst has developed which at the moment means that CED is not possible until the cyst disappears. We still very much have CED in our sights but we need to consider other options quickly also. Thank you so much x
Follow the Help Luke Facebook page: https://m.facebook.com/groups/147131445783134
This is Luke Stewart, son of Jennifer and Mark, brother of Lewis and Lochlin. Luke is 7 years old and has just been diagnosed with a very rare brain tumour, called a Diffuse Intrinsic Pontine Giloma (DIPG). The best way to treat this rare tumour is for Luke to take part in a ground breaking clinical trial. He will receive CED (Convection Enhanced Delivery). This trial will help not only Luke, but children worldwide in the future.This treatment does not come cheap, it is Circa £100,000.
We are reaching out to the British Public to help us raise the funds required for Luke to have his treatment down in London.
Luke, his brothers and friends are not aware of the situation and we would like to keep it that way for obvious reasons. We would appreciate it if you could respect the families wishes and not pass this information onto your children.
If your children do ask about Luke, please could you say that he has not been feeling too well, and that he needs to be looked after by a doctor in London.
We need to raise this money really quickly to get Luke onto this trial, to try and save his life.
If you are doing any other fundraising events and are looking for a charity to support, please do get in touch also.
Thank you so much for taking the time to read.
Please feel free to share this.
- 2 years ago
Jennifer Ure Stewart2 years ago
Thank you to everyone that has continued to donate. We feel very lucky to be here in Mexico & Luke is responding well to treatment, the wonderful doctors are very pleased. 2nd treatment scheduled for next week & we have just heard that Luke will be able to start Immunotherapy a lot quicker than we thought which is simply amazing. Please please keep sharing our story & just giving page to give our boy a fighting change to kick DIPG's butt 💙💙💙xxx Thank you to each & everyone of you xxx
Share this update to help us raise more
Jennifer Ure Stewart started crowdfunding
Leave a message of support
Apr 30, 2018
Apr 27, 2018
marie theresa quinn
Apr 3, 2018
Thinking and praying for Luke .
Mar 2, 2018
Was in at Linn-tech the other day and got an update. As a parent myself, your continuing story just resonates very deeply. How couldn't I continue to offer this smallest of gestures. Best regards.
Feb 22, 2018
Best wishes x
Feb 13, 2018
Feb 4, 2018
Great people make things happen
Do you know anyone in need or maybe want to help a local community cause?
Create you own page and donʼt let that cause go unfunded!About Crowdfunding
About the fundraiser
Jennifer Ure Stewart
Tranent, United Kingdom
We are a loving hard working family with 3 little boys Luke being the oldest @ 7 Lewis 5 & Lochlin 1. We are desperately trying to save our special boy DIPG is an awful disease that doesn't have enough awareness & funding to help us & others. please share far & wide thx u xx