We’ve had a few Birthdays over the last week,

The Bradley Lowery Lowery Foundation would like to wish Jack and Maddi a huge HAPPY BIRTHDAY to

Jack Hall who was 14 on Saturday Birthday on Saturday and Maddi Thurgood's who is 17 Today.

Let wish our smilers a huge Happy Birthday !!! ...

You can donate to Maddi by texting GENE96 £amount to 70070

Or Visit her Facebook page here:

You can donate to Jack by texting STEM94 amount to 70070

Or Visit his Facebook Page here:
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Please keep supporting Bradley’s legacy by following the progress of his charity

Your Newsfeed recently shows only posts from the same few people, about 25, repeatedly the same, because Facebook has a new algorithm. 🙅🏻‍♀️
Their system chooses the people who will read your post. However, I would like to choose for myself, Therefore, I ask you all a favor - If you are reading this message leave me a quick comment, a "hello", a sticker, whatever you want, so you will appear in my news feed‼️
Otherwise Facebook chooses who to show me and I don't need facebook to choose my friends! 🤬
Do not hesitate to copy and paste on your wall so you can have more interaction with all your contacts and bypass the system. That's why we don't see all posts from our friends.😮
Thanks for the heads up from those who already copied and pasted the above.

Anyways here is a beautiful smile to cheer up your day.

Remember guys smile and the whole world smiles with you.
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Watch out for these stickers coming through your door, The Bradley Lowery Foundation are now working closely with Clothes Aid.
Do you have any unused clothes you would like to donate. These Stickers/Bags will be coming through your door soon.
The Bradley Lowery Foundation will get 100% of the profits.
This is great news for the foundation.
We would like to say a huge thank you to Ear For Alex, for the lovely smiles he gave us for these photo's. xxx
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Lazy Sundays normally means one thing. I sit and watch videos and look at photos of my boy. Iv come across this one and I think it’s very fitting. This message off Bradley is for everyone that has supported and are still supporting the #bradleyloweryfoundation
Yesterday we held a DKMS registration day at the Cleveland centre in Middlesbrough. We had a great day but still need to find a match for many children like Chloe.

We are looking to hold more registration days so if you have any ideas for venues please comment and let us know! Maybe we would hold one in your work place

You can also register online here:
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Here it is, big news for josh.


He’s enjoying his first night in his cosy bed!

This really will change his life, thanks to everyone that has supported josh and helped him get this far.

We are still aiming to do the rest of Joshua’s bedroom with interactive floor, ball pit etc so watch this space!

Thank you all again.
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Alfie is coming up 16 next month, he has been fighting Neuroblastoma for over a decade. He has a message for everyone fighting this great fight xxx
We would like you all to meet Huey.
Huey was born 14 weeks early. He fought for his life in an incubator, battled through 2 brain surgeries, and had many blood transfusions to name just a fraction of the struggles he has faced in his tiny life. Huey has cerebral palsy, dystonia, chronic Lung disease and severe reflux. Working with Huey’s family we are trying to raise £4000 for a piece of equipment that could get little Huey walking.

To learn how to donate and read more about Huey’s journey please visit his Facebook page here:
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#throwbackthursday to finish the day off with ❤️💙 #bradleyscheekysmile #gorgeous #bradleylowery #bradleyloweryfoundation
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Kaleigh was diagnosed on the 19th April 2016 with a very aggressive brain tumour called DIPG.
When Kaleigh was first diagnosed she had 30 radiation treatments however on the 28 Dec Kaleigh progressed and has to have a further 10 session of radiation.
After extensive research Kaleigh was going to be the first child in the uk to have a treatment called CED at the Harley street clinic in london, unfortunately due to further progression and growing cysts on Kaleigh’s brain, this treatment could no longer be done.
Through the research the parents carried out, they discovered a treatment on Mexico, and took Kaleigh over to start their treatment, although, the Drs in the uk advised us not to go, they have continued to support the family and Kaleigh.
Drs in the uk give children only 9 month after diagnosis, however after receiving treatment in Mexico Kaleigh has reached her 2 year milestone, this is fantastic news for Kaleigh and her family.
Please post a heart in the comments to show your support xxx
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We think it is probably time we explain what DIPG is for all of you that may not know.

DIPG is a rare brain cancer, found mostly in children. The tumour is found in the middle of the brain making it very difficult to treat. Currently the treatment options in the UK are very limited this is why children like Kaleigh and Edie are travelling to Mexico for Intraarterial treatment. At present there is no cure for this harsh cancer but the treatment offered in Mexico has been proven to reduce or stabilise the tumour.

To read more about Kaleigh’s story please visit her Facebook page here:
To read more about Edie’s journey please visit her Facebook Page here:
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You all remember Benji, his family where fundraising to get cochlear implants. Well Benji has had the implants, he is out of surgery and doing well. Post a heart to let him know we are thinking of him ❤️❤️❤️x x x
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SPIDER-EDE number 41

You can’t actually bet on this horse in the Grand National but you can back her by texting the money you would of put on.

TEXT edie03 £?? To 70070
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This time last year on the Grand National day, we were on driving down to Liverpool not knowing what to expect. Bradley was super excited and he had that big most amazing smile on his face.
From the start to finish the experience was amazing and Bradley had a fantastic time, memories I will never forget. If I could turn back time and have these special moments back, in fact if I could just have him back and be locked in a small room with nothing to do I would in a heart beat as my boy could lighten up the dullest days, my heart aches to have him in my arms.

In reality I know I can’t have him back so what I do instead is try my hardest not only to keep his legacy going but the most important thing is to help other families, Bradley is a guardian angel looking over the children we help. I like to call them Brad’s little smilers.

Today at the Grand National is all about one of Bradley’s little smilers. The beautiful Edie has been giving the honorary 41st runner. This will not only hopefully raise some much needed funds for Edie but raise awareness for DIPG brain tumours.

To donate to Edie you can text edie03 £? To 70070
Bradley last year at the Grand National and Edie with her beautiful smile.
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Had such a brilliant day today, met such inspirational people! Unbelievable the legacy Bradley has left. #grandnational
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Wow how handsome does Bradley look on this photo? he was super excited to try his suit on ready for the Grand National it was so cute to see. I’m sure he is looking over us and watching everyone having a good time. Thank you so much to the organisers of the Grand National at Aintree Racecourse for putting this big smile on Bradley’s face and giving us memories to treasure.

This year it is The Spider-Ede Appeal - DIPG Awareness turn, please get behind her guys.
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Or wow this video that has been created from the Organisers of Randox Health Grand National for Edie is amazing. It has had me in tears, have a watch and let me know your thoughts.
I have been so excited to let everyone know that this years organisers of the Randox Grand National and the Jockey Club have once again went above and beyond.

This year not only are they supporting the Bradley Lowery Foundation they have got one of our beautiful children as the honorary 41st runner. The Spider-Ede Appeal - DIPG Awareness the beautiful Edie will have her own race card just like Bradley.

I have so many mixed emotions about this, I am totally and utterly heart broken as I don’t have Brad here with me. However on the other hand I am filled with pride and remember how much this meant to me last year. The fact that another parent gets to feel the happiness and the overwhelming feeling about their child having this honour makes everything I do to support my BLF families worth it.

This is incredible because it’s not just about raising funds to save Edie’s life it is about raising awareness. Take a look at the link to read more about this fantastic story.
We would like to announce our partnership with Clothes Aid. Look out for our special Bradley Lowery Bags dropping through your door soon 💙
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Happy #nationalsiblingsday everyone 💙💙
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