Our President Michael Crawford CBE presents this month’s BBC Lifeline Appeal on behalf of The Sick Children’s Trust
News • Jan 12, 2018 15:06 GMT
Find out all about our BBC Lifeline Appeal. Michael Crawford CBE visits our 'Homes from Home' to help raise awareness of The Sick Children's Trust.
News • Jan 08, 2018 14:27 GMT
The parents of Alfie Knight, who was born weighing just 545 grams, were given a room at Eckersley House for over ten weeks whilst he received life-saving treatment in Leeds General Infirmary
News • Jan 03, 2018 09:00 GMT
Laura and Chris Penfold are on a fundraising mission to raise money for The Sick Children's Trust after we supported them when baby Willow was born 13 weeks early and needed lifesaving treatment at The Rosie Hospital.
News • Jan 02, 2018 16:46 GMT
We supported Ivy's parents when she was flown from Malta to Great Ormond Street Hospital for heart surgery.
The world of prematurity is one that you never think you are going to be a part of until it happens. You have a lifetime membership to a club you didn’t want to join.
News • Dec 24, 2017 15:06 GMT
Baby Willow was born on 28 December 2016 at just 27 weeks old. Now the Penfold family are getting ready to celebrate her first Christmas after a tumultuous start to the year.
News • Dec 24, 2017 12:49 GMT
Freddie is a baby boy who was born with tracheo-oesophageal fistula (TOF) and oesophageal atresia (OA), which meant the lower part of his food pipe was connected to his wind pipe. As a result he underwent his first corrective operation at only 24 hours old. The Sick Children’s Trust supported his family at Magnolia House whilst Freddie was being treated in Sheffield Children’s Hospital.
News • Dec 23, 2017 09:00 GMT
Henry, was diagnosed with leukaemia back in September. Having been transferred to Leeds General Infirmary (LGI) for lifesaving treatment, his family were supported by The Sick Children’s Trust. Fortunately Henry has made it home in time for Christmas, and although he is still undergoing treatment as an outpatient, is excitedly getting ready to celebrate with his family.
We were told Tessa was one in 500 million and only 37 cases like hers have ever been recorded in medical history
News • Dec 22, 2017 12:04 GMT
Tessa Evans was born with an incredibly rare facial anomaly called arhinia, which means she has no nose. It is an extremely rare condition, with 47 reported cases in the history of modern medicine to this day. When she was born her parents were told she was one in 500 million, although since then the odds have gone down to one in 20 million.
Through all the tears and heartache we have been through we all stick together and continue to smile, for our amazing daughter and little heart warrior
News • Dec 21, 2017 10:16 GMT
Ellie, was just six weeks old when doctors diagnosed her with a rare congenital heart condition. Just two days later, Ellie took a turn for the worse, and was rushed into theatre at Freeman Hospital. Whilst she recovered from the operation her parents stayed at Scott House, along with Ellie’s older sister, Izzy.
Family support The Sick Children's Trust's Christmas appeal as thanks for giving them a ‘Home from Home’
News • Dec 19, 2017 12:50 GMT
Alexander Morris' family have donated £210 to our Christmas appeal, bringing us closer to our target of £13,140, enough to keep our ten 'Homes from Home' running over the festive period!
Treetop and Magnolia Houses have been our lifeline during our darkest times, without them we don’t know how we could have coped
News • Dec 18, 2017 14:42 GMT
Zac Keith was born with hydrocephalus and cerebral palsy in January 2013 at just 29 weeks. His parents were supported by The Sick Children’s Trust after he was transferred to Sheffield Children's Hospital. 2017 has been a tough year for Zac, who has been in and out of hospital and once again his family have been supported by the charity on three separate occasions.
"Friday 13th is an unlucky day for some, but for Tom and I, it was the amazing day we got to meet our son for the first time."
News • Dec 14, 2017 13:02 GMT
Albie’s parents knew he would need lifesaving surgery soon after birth and had heard about the work of The Sick Children’s Trust. Their baby spent over three weeks recovering in hospital and during this time the charity supported his family at Eckersley House. And as thank you, Albie and his family have joined in The Sick Children’s Trust first ever Christmas appeal!
News • Dec 13, 2017 13:20 GMT
Edward's parents are supporting The Sick Children's Trust's Christmas appeal as thanks for giving them a 'Home from Home' at Stevenson House.
News • Dec 12, 2017 15:27 GMT
The Sick Children's Trust is delighted to announce Irish Classical Soprano Margaret Keys as an official charity ambassador.
Family support charity’s Christmas appeal as thanks for giving them a ‘Home from Home’ when their baby was seriously ill in hospital
News • Dec 12, 2017 11:59 GMT
At a week old, Chace underwent major surgery to remove 40cm of his bowel as a result of necrotising enterocolitis. We supported his family at Magnolia House on two occasions and now his family are encouraging others to donate £30 to our Christmas appeal, to give another family a 'Home from Home'.
News • Dec 11, 2017 12:19 GMT
At just seven weeks old Kobi became seriously ill and was diagnosed with multiple heart conditions, which led to him spending his first Christmas in Leeds General Infirmary. The Sick Children’s Trust has supported Kobi’s family at Eckersley House since his first admission. As a thank you, Kobi's family have joined in The Sick Children’s Trust’s first ever Christmas appeal!
News • Dec 07, 2017 17:00 GMT
Martyn Large is dreaming up at least a hundred challenges to raise money for The Sick Children's Trust, who have given his daughter a 'Home from Home' at Scott House whilst little Ellie has been receiving treatment in hospital.