Love Transmission Charity Organization

Love Transmission Charity Organization Transmitting Love, Igniting Hope: Love Transmission Charity Organization

Together for Short Lives is providing financial support this winter for the families most in need. These grants will mak...
29/03/2023

Together for Short Lives is providing financial support this winter for the families most in need. These grants will make it possible for the most vulnerable families to continue to care for their child at home.

When a child is diagnosed with a life-limiting condition, parents suddenly need to navigate a complex world of medical and social services, and many will need to give up their job to care for their child full-time. Added to the pressure of paying rising energy bills to keep their child alive, some parents are feeling overwhelmed and stressed about how they will make ends meet – when all they want to do is to spend time with the child they love so dearly.

By donating to our you can help families make the most of their time together this festive season.

“George is one of the most medically complex children there is. We have so many pieces of medical equipment to keep him ...
27/03/2023

“George is one of the most medically complex children there is. We have so many pieces of medical equipment to keep him alive. . . I already pay almost £400 a month for energy, and this is expected to double.”

Today we have launched a new emergency Cost of Living Support Fund to help as many families as possible across the UK with spiralling energy costs for equipment keeping their seriously ill child alive. Money raised through this fund will go directly to families in need, to ease soaring bills so they can focus on making lasting memories and enjoy a Christmas that may be their last. Help us help them by supporting this emergency fund by spreading the word.

In honor of National Rare Disease Day, we want to recognize Genentech for making wishes come true for children with rare...
27/03/2023

In honor of National Rare Disease Day, we want to recognize Genentech for making wishes come true for children with rare diseases. Thanks to Genentech and their continued generous support to Make-A-Wish America, wish kids like Ellie, who wished for a pink golf cart 💗 will receive renewed hope for the future. 🌟 Thank you, Genentech, for joining us in honoring kids like Ellie on this special day. 💙

Our mission is to provide the very best care and support possible, at home, for children and young people with life-limi...
27/03/2023

Our mission is to provide the very best care and support possible, at home, for children and young people with life-limiting and life-threatening conditions and their whole families – for the whole journey in life, at the end of life, and in bereavement.

🧮 The count is in!After a jam-packed year of fundraising, where we...🎽 Completed the Great Bristol 10k Run 👕 Had twelve ...
27/03/2023

🧮 The count is in!
After a jam-packed year of fundraising, where we...
🎽 Completed the Great Bristol 10k Run
👕 Had twelve Dress-Down Friday's
🏉 Held three sweep stakes
🎭 Hosted a Barcan+Kirby Quiz
🍰 Held four Bake Sales
🎫 Hosted two raffles
👟 Signed up for the 2023 London Marathon

💜 💛 Our nurses Bryony and Gemma recently took this gorgeous photo on a recent visit to give some respite care. His smile...
27/03/2023

💜 💛 Our nurses Bryony and Gemma recently took this gorgeous photo on a recent visit to give some respite care. His smile says it all.💜 💛

Jude was born with a condition called restrictive cardiomyopathy, a disease that causes a stiffening of the heart muscle...
27/03/2023

Jude was born with a condition called restrictive cardiomyopathy, a disease that causes a stiffening of the heart muscles. After Jude received a heart transplant, his wish was the opportunity he needed to reclaim a piece of his childhood – and share a unique bond with his mom, who battled the same condition as a child and was also granted a wish. 💙 Celebrate the this by visiting wish.org/heart and learn more about Jude's Walt Disney World wish experience, along with other incredible wish kids fighting against heart conditions.

We are thrilled to announce Red Robin Gourmet Burgers as a new national partner with Make-A-Wish! 🌟 Beginning Feb. 20, R...
27/03/2023

We are thrilled to announce Red Robin Gourmet Burgers as a new national partner with Make-A-Wish! 🌟 Beginning Feb. 20, Red Robin will donate 10 cents from every kids’ meal purchased. Share a memorable meal with your family, either dine-in or to-go, and help transform lives, one wish at a time. 💫 Visit wish.org/redrobin for more information. Thank you, Red Robin, for helping to create life-changing wishes for children with critical illnesses!

(3/3) When Chairalis finally had the chance to see her new smile for the first time, her face lit up with amazement, her...
27/03/2023

(3/3) When Chairalis finally had the chance to see her new smile for the first time, her face lit up with amazement, her eyes filling with tears of joy. She could hardly believe that the bright, dazzling smile in the mirror was her own. “Her wish has helped her a lot,” said Carlos, Chairalis’ dad. “She’s more secure and able to smile and express herself. Plus, her inner beauty now shines through her new, beautiful smile ... It’s motivation to keep fighting alongside her day by day.” 😁 Keep following our social pages for even more “Stories of Strength” 🌟

(2/3) After her rare genetic disorder caused her dental health to deteriorate, Chairalis knew that her heartfelt wish wa...
27/03/2023

(2/3) After her rare genetic disorder caused her dental health to deteriorate, Chairalis knew that her heartfelt wish was to recapture her confidence by restoring her beautiful smile. “When I found out that my wish was going to be granted, I felt super happy because I’ve wished for this for a very long time,” Chairalis said. “When my teeth are perfect, I’m going to spend all day laughing.” 😀 There’s more coming! Follow along with “Stories of Strength” to see the impact of Chairalis’ wish

“My first Mother’s Day was in the Neonatal Intensive Care Unit in Bristol when Izzy was a week old. I woke up to find a ...
27/03/2023

“My first Mother’s Day was in the Neonatal Intensive Care Unit in Bristol when Izzy was a week old. I woke up to find a card with a photograph inside and the nurses had taken prints of her hands and feet. It meant the absolute world to me, especially when we didn’t know how long we might have with her at that point.”
Emma is Mum to seven-year old Izzy who was born with kidney failure, and four-year-old Seb. We've been sharing stories with Morrisons to show that Mother's Day is very different for each and every Mum out there.
In her young life, Izzy has already had 20 operations and in 2019 was able to have a kidney transplant. Izzy is tube-fed and still requires care and support from their local children’s hospice, Jessie May Children’s Hospice at Home. Our partnership with Morrisons is helping to raise vital funds for the 54 children's hospices across the UK, including Jessie May.

Here is a beautiful picture of Hope enjoying 'We're Going on a Bear Hunt' read by Mary, one of our Jessie May nurses. 🐻 ...
27/03/2023

Here is a beautiful picture of Hope enjoying 'We're Going on a Bear Hunt' read by Mary, one of our Jessie May nurses. 🐻 🐻
Hope, we are loving your smile and your guinea pig top this morning!

Address

Broadwick Street
London
W1F0DL

Website

Alerts

Be the first to know and let us send you an email when Love Transmission Charity Organization posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Shortcuts

Featured

Share

Category