Jamie T
@JaaamieT
fighting against duchenne muscular dystrophy to save my boy 💚
💚Jamie’s Journey: An Update 💚 This is Jamie. 💚 I want to share an update on his health, the incredible support we’ve received, and what life is really like fighting Duchenne muscular dystrophy (DMD). From daily therapies to our fight for treatment, here’s what it really…
Wow.We managed to fill this today - some incredible generosity - Thankyou everyone who shared/got involved - Tonight’s bonus ball from the National Lottery 9:30pm - good luck everyone 💚
Good morning guys - I’m still pushing really hard to fill the spots of this bonus ball - Colin & his wife are still in hospital with there son with no news on when getting out. I am reducing prices from £10 to £5 to try & fill this up - everyone who has bought tickets I will give…
If anyone like a chance of winning 2 signed framed Celtic shirts please get in touch - It is going to be a massive help towards a family who are going through a incredibly tough time 💚🙏
I’m doing a bonus ball to raise money for something a little different here. A family who live not to far from us are going through a extremely difficult time - There son was born with the same condition as my son Jamie (Duchenne Muscular Dystrophy) He has also been born with…
I’m doing a bonus ball to raise money for something a little different here. A family who live not to far from us are going through a extremely difficult time - There son was born with the same condition as my son Jamie (Duchenne Muscular Dystrophy) He has also been born with…
Massive thanks to the @CeltExchange for their support 👉 Join using TOMMYS code TPQ50 for 50% off your first month and a portion every month goes to Tommys fundraiser 🍀
For every sign up using 👉 code you’ll get TPQ50 for 50% off your first month And the @CeltExchange bhoys will make a monthly donation to Tommy Quinn’s neuroblastoma fundraising campaign #teamtommyquinn
ACSOM viewers of Ardoyne - Thankyou for your support of my boy 💚 I can’t wait to update everyone soon on Wee Jamie’s treatment progress there is some really positive news ahead of us & we couldn’t get there without you all 💚💪
Thank you to the ACSOM viewers from Ardoyne who raised another £1250 to support Wee Jamie Tierney. Paddy and the lads are different class. Shares mean the world to Wee Jamie & his family: gofund.me/ec305c39
A phenomenal venue, filled with some of the best people I’ve been privileged to meet & this generosity, while almost expected given the character of those in attendance, still….absolutely floors me! Thank you, every single one of you 🙏🏻👏💚🫶
Thank you to the ACSOM viewers from Ardoyne who raised another £1250 to support Wee Jamie Tierney. Paddy and the lads are different class. Shares mean the world to Wee Jamie & his family: gofund.me/ec305c39
Amazing guys who put on an amazing night💚
Thank you to the ACSOM viewers from Ardoyne who raised another £1250 to support Wee Jamie Tierney. Paddy and the lads are different class. Shares mean the world to Wee Jamie & his family: gofund.me/ec305c39
Thank you everyone for supporting my wee Jamie boy 💚💚 this means the world to us as a family 🌎 💚
Thank you again to the generous ACSOM viewers who raised another £263 to support Wee Jamie Tierney at our Belfast event. To keep up to date with Jamie’s progress, please check out the following link: gofund.me/ec305c39 Shares mean the world to Wee Jamie & his family 🙏🏻
Jurassic Future Walk into a clinic in 2030. Get one CRISPR injection. Your diabetes is permanently cured. No more insulin shots. No more glucose monitoring. Done. Or: AI scans your DNA at birth, spots cancer, and prevents it decades before it develops. This isn't sci-fi. It's…
This is scandalous! As families living with this condition, the government should roll out the red carpet to accommodate. Not make life more difficult
We sold our family home for many reasons — it was a townhouse with too many stairs, completely unsuitable for Jamie. We needed to find a way to give him independence. Our son Jamie has Duchenne Muscular Dystrophy — a muscle-wasting disease with no cure. His needs are increasing…
How many people know what Duchenne Muscular Dystrophy is ? I never untill 3 years ago when I was handed a leaflet with the stages of DMD & told to go home & enjoy my son - This disease is one of the most catastrophic disease . No cure - Only deterioration - The drugs that are…
