Bubble Foundation UK, Newcastle upon Tyne Videos

Videos by Bubble Foundation UK in Newcastle upon Tyne. Saving lives of babies born without an immune system. We’re changing Paediatric Immunology.

Follow the bubble on Instagram

Did you know you can follow the Bubble on Instagram? Stay up to date over there as alot more people share their stories there and we reshare all the time!
https://www.instagram.com/thebubbleuk

Other Bubble Foundation UK videos

Follow the bubble on Instagram
Did you know you can follow the Bubble on Instagram? Stay up to date over there as alot more people share their stories there and we reshare all the time! https://www.instagram.com/thebubbleuk

Evie and Katie singing
We just found re-found this Gem of a video! Evie Needs a Hero singing with nurse Katie! To follow Evies story you can subscribe to her page on youtube! https://bit.ly/3aiPFKM #immunedeficiency #immunedisorder #severecombinedimmunodeficiency #primaryimmunedeficiency #primaryimmunodeficiency #scid

WRAPPED - 23 Ward 3 staff walk 10k steps a day
Wow. WHAT A MONTH! Over twenty Ward 3 staff have successfully completed their 10k a day step challenge. Here's the step challenge wrapped video you've all been waiting for! Guess how far they've walked in the comments before the big reveal!! We want to say a huge huge thank you to the team, patients and families who made this possible alongside the local companies who sent gifts to the staff as prizes. If you'd like to congratulate the team comment below or head over to JustGiving and say thanks! x https://www.justgiving.com/campaign/stepchallenge #stepchallenge #newcastleupontyne #primaryimmunodeficiencydisease #SCID Brian McFaddenThe Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle Chronicle

A message from our lovely nurse Laura 🥰 To show your support you can donate below to help reach our target so we can give patients and families a warmer welcome in what can be a terrifying world that they’re stepping into. We know that not everybody can donate but tapping one or all of the share buttons helps too! Thank you everyone🙏 https://www.justgiving.com/campaign/stepchallenge #scid #severecombinedimmunodeficiency #primaryimmunodeficiency #primaryimmunodeficiencydisease #primaryimmunedeficiency #chronicgranulomatousdisease Brian McFadden

Happy Friday everyone. What a week, in and out of the ward. They've been stepping in hail and shine! So here's the latest WARD 3 JUNE step challenge leaderboard. WE HAVE A NEW LEADER! The Ward 3 crown has been officially transferred. What will tomorrow bring? Becky had the crown briefly on Wednesday as she snook up fast and overtook Molly. We'd all love to know what they've been doing to get their steps in... Neil visited Gill this week and turned down a seat and a coffee as he 'wasn't staying long and needed to get his steps in'😂We've heard videos from the staff are in the works showing what they get up to 😌 Thank you all very much for your support so far! Trustee Dan x P.S if you know anyone who would like to donate prizes for the Ward 3 staff for the end of the step challenge, please mention them and we'll DM privately. We have a few already! --- Why are we doing this? --- The children on Ward 3 in the Great North Children’s Hospital are isolated in their air-locked cubicles, but for months at a time. No sun, no wind, no rain and no immune system. Most would die before their first birthday without treatment. This fundraising campaign ran by our ward 3 colleagues will help give our patients a better childhood under these conditions offering toys, entertainment and pain distraction units as well as funding the research that actually helps fix their compromised immune systems. That’s why the Ward 3 staff are walking 10k steps a day this june, for the patients and for their families too.@

Ward 3 Step challenge results Sunday 2nd
We have a new overall solo leader for our Ward 3 June 10k-a-day step challenge 😄Molly isn't too happy... Thank you so much for all your support so far. You’re helping save the lives of children born without an immune system and allowing us to give families a warm welcome to the ward when they travel far and wide to stay with us during the transplant. Thank you, as ever, to our Ward 3 staff who work tirelessly to help these families. If you haven’t already, you still have time to sponsor all 25 staff doing this month’s 10k a day step challenge. We're only 2 days in! You are also able to create a fundraiser yourself! Message us if you want to know how! x Dan, Trustee

The results are in for the first day of the Ward 3 Step Challenge! See who takes the lead. Thank you so much for all your support so far. You're helping save the lives of children born without an immune system and allowing us to give families a warm welcome to the ward when they travel far and wide to stay with us during their transplant. Everybody now knows what it's like to be isolated after COVID; these children are isolated in one room for months at a time-no sun, no wind, no pets-and these donations help give them a better childhood under these conditions, as well as fund the research that actually makes them better. Thank you, as ever, to our Ward 3 staff who work tirelessly to help these families. If you haven't already, you still have time to sponsor all 25 staff doing this month's 10k a day step challenge. Xx

Great news! Latvia has officially launched Newborn Screening for SCID! This remarkable advancement means that newborns in Latvia will receive timely identification, giving them a crucial chance at survival. Newborn screening for Severe Combined Immunodeficiency (SCID) is a critical public health program aimed at detecting SCID early in infants. SCID is a group of rare, life-threatening genetic disorders characterized by a severely impaired immune system, making infants highly susceptible to infections. Early identification through screening allows for timely medical intervention, significantly improving survival rates and health outcomes.#worldpiweek2024 #scid #pid #primaryimmunodeficiency #primaryimmunedeficiency #severecombinedimmunodeficiency #severecombinedimmunedeficiency #chronicgranulomatousdisease #immune #immunesystem #immunedefense #immunedisorders #immunedisorder #immunedeficiency #latvia🇱🇻 #latvia

Fantastic!! After having his own transplant in November last year, David has just raised over £1000 as he wanted our bubble children to have nice Christmas presents . A huge well done to David and Eva and to all 40 of you who donated - David is over the moon and has a huge smile on his face! Our play team Laura, Gemma and Kayleigh are on it and know exactly what to do! If you know anyone who donated, please share our thanks!! Charlotte, Uncle Warren, Kay White, Nathan Howarth, Julie Loch, Auntie Angela, Kev, Kevin Booth, Zakariah, Mrs Laura Farley, Donna Clarke, Janice & Kris, Owen, Ian Hartley, Stuart and Helen Hartley, Sue Oates, Helen Hartley, Liz, Emma, Andy & Flo Bamforth, Nikki Reeves, Roanne Newman, Joshua Moore, Frances Veal, Caroline Howarth, Oliv Sanderson, Rachel Agus ( Olivs mum ), Samantha Louise, all at 69, Eva Cooper, and all of the Anonymous folks

Fantastic!! After having his own transplant in November last year, David has just raised over £1000 as he wanted our bubble children to have nice Christmas presents🥹. A huge well done to David and Eva and to all 40 of you who donated - David is over the moon and has a huge smile on his face! Our team are on it and know exactly what to do! 👏 If you know anyone who donated, please share our thanks!! Charlotte, Uncle Warren, Kay White, Nathan Howarth, Julie Loch, Auntie Angela, Kev, Kevin Booth, Zakariah, Mrs Laura Farley, Donna Clarke, Janice & Kris, Owen, Ian Hartley, Stuart and Helen Hartley, Sue Oates, Helen Hartley, Liz, Emma, Andy & Flo Bamforth, Nikki Reeves, Roanne Newman, Joshua Moore, Frances Veal, Caroline Howarth, Oliv Sanderson, Rachel Agus ( Olivs mum ), Samantha Louise, all at 69, Eva Cooper, and all of the Anonymous folks "Well done champ, you smashed it, it’s a great idea raising money to give presents to the children who are in the position you’ve been in" "Well done David, you & your Mum are amazing. Cheering you on with your fundraising to help bring smiles to all those brave children this Christmas"

Brian McFadden wins £7,250 for charity
Our President Brian McFadden has done us proud! Winning £7,250 for The Bubble Foundation on the EULegendsTour! How good is that?! x

We sent a message of good luck to Brian during his tournament
Ahead of his final round... We had a little inspirational message for our president Brian McFadden 🙏🙊 Thank you for EULegendsTour team! #WCSGF "Make that ball fly without wings!" Lyrics: We got a little BUBBLE of our own You need to get the ball in that hole Taking the shots that no one else knows We couldn't do it without you Sung by: Kayleigh Douglas play team and Nurses Fay Hetherington and Chloe Lord

We had a visit from the teachers of the Bridges School today bringing some Christmas cheer!🎄

Thanks to all of our families and friends for coming along to make our 30th birthday so special. Here's a clip from ITV Tyne Tees See any familiar faces??

repeat offender drawn by Alfie

Oscar M's repeat offender