Welsh father calls for blood donors after saving son's life
Seven-year-old Jasper Hodgson-Smith, from Swansea, was diagnosed with a rare and life-threatening blood disorder called Activated PI3K Delta Syndrome (APDS).
His father, Matt, was found to be a perfect stem cell match, giving Jasper a second chance at life.
Matt donating stem cells (Image: Welsh Blood Service) The family is now sharing their story during National Blood Donor Week, which runs from June 9 to 15, to encourage more people across Wales to donate blood and stem cells through the Welsh Blood Service.
Sophie Hodgson-Smith, Jasper's mother, said: "From eight months old, Jasper exhibited numerous symptoms, including lethargy, persistent high temperatures, and a lack of appetite.
"Due to the rarity of his blood disorder, it took a long time to identify his condition, which was thought to be chest infections, meaning he was regularly prescribed antibiotics and admitted to hospital around six to eight times a year."
Matt with his son (Image: Welsh Blood Service) APDS is extremely rare, with Jasper believed to be the only child in Wales with the condition and one of just 35 patients in the UK.
APDS affects the immune system, and for young patients, a stem cell transplant is often the only curative treatment.
Jasper's care involved multiple blood and platelet transfusions, immunoglobulin replacement therapy, chemotherapy, and ultimately a stem cell transplant.
Only one in four patients in the UK will find a family member who is a suitable match.
Mr Hodgson-Smith said: "Blood disorders are as life-threatening as cancer and require just as much resilience.
"Some people think donating stem cells may be painful or invasive.
"For me, the process was simple.
"I would do it again in a heartbeat if it meant saving someone's life."
He donated his stem cells through peripheral blood stem cell transplantation, a procedure that collects stem cells from the bloodstream using a special machine.
Jasper's mother said he remained positive throughout his treatment.
She said: "Despite everything he's faced, Jasper has remained incredibly strong and full of life—always dancing, singing, and making people smile, even during the toughest days.
"Once Jasper is feeling fit and well, we are looking forward to spending more time as a family and have lots of beach walks and adventures planned with our dog, Pip."
The Hodgson-Smith family hopes their story will inspire more people across North Wales and beyond to consider donating blood or stem cells.
The need for donors is ongoing, with more than 15,000 blood donations required annually in North Wales alone to support patients at hospitals including Ysbyty Glan Clwyd, Ysbyty Gwynedd and Ysbyty Wrecsam Maelor.
Frank Murphy, who lives in Wirral but worked at HMP Berwyn near Wrexham, was recently recognised by the Welsh Blood Service for helping to potentially save more than 1,200 lives.
Not only has he donated blood more than 40 times, but he also encouraged colleagues at HMP Berwyn to donate on more than 400 occasions.
Mr Murphy said: "Giving and supporting others to give blood and to save lives has, in my eyes, always been a must and a duty, and encouraging others to donate is a great feeling."
Appointments to donate are available across the region.
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North Wales Chronicle
14 hours ago
- North Wales Chronicle
Welsh father calls for blood donors after saving son's life
Seven-year-old Jasper Hodgson-Smith, from Swansea, was diagnosed with a rare and life-threatening blood disorder called Activated PI3K Delta Syndrome (APDS). His father, Matt, was found to be a perfect stem cell match, giving Jasper a second chance at life. Matt donating stem cells (Image: Welsh Blood Service) The family is now sharing their story during National Blood Donor Week, which runs from June 9 to 15, to encourage more people across Wales to donate blood and stem cells through the Welsh Blood Service. Sophie Hodgson-Smith, Jasper's mother, said: "From eight months old, Jasper exhibited numerous symptoms, including lethargy, persistent high temperatures, and a lack of appetite. "Due to the rarity of his blood disorder, it took a long time to identify his condition, which was thought to be chest infections, meaning he was regularly prescribed antibiotics and admitted to hospital around six to eight times a year." Matt with his son (Image: Welsh Blood Service) APDS is extremely rare, with Jasper believed to be the only child in Wales with the condition and one of just 35 patients in the UK. APDS affects the immune system, and for young patients, a stem cell transplant is often the only curative treatment. Jasper's care involved multiple blood and platelet transfusions, immunoglobulin replacement therapy, chemotherapy, and ultimately a stem cell transplant. Only one in four patients in the UK will find a family member who is a suitable match. Mr Hodgson-Smith said: "Blood disorders are as life-threatening as cancer and require just as much resilience. "Some people think donating stem cells may be painful or invasive. "For me, the process was simple. "I would do it again in a heartbeat if it meant saving someone's life." He donated his stem cells through peripheral blood stem cell transplantation, a procedure that collects stem cells from the bloodstream using a special machine. Jasper's mother said he remained positive throughout his treatment. She said: "Despite everything he's faced, Jasper has remained incredibly strong and full of life—always dancing, singing, and making people smile, even during the toughest days. "Once Jasper is feeling fit and well, we are looking forward to spending more time as a family and have lots of beach walks and adventures planned with our dog, Pip." The Hodgson-Smith family hopes their story will inspire more people across North Wales and beyond to consider donating blood or stem cells. The need for donors is ongoing, with more than 15,000 blood donations required annually in North Wales alone to support patients at hospitals including Ysbyty Glan Clwyd, Ysbyty Gwynedd and Ysbyty Wrecsam Maelor. Frank Murphy, who lives in Wirral but worked at HMP Berwyn near Wrexham, was recently recognised by the Welsh Blood Service for helping to potentially save more than 1,200 lives. Not only has he donated blood more than 40 times, but he also encouraged colleagues at HMP Berwyn to donate on more than 400 occasions. Mr Murphy said: "Giving and supporting others to give blood and to save lives has, in my eyes, always been a must and a duty, and encouraging others to donate is a great feeling." Appointments to donate are available across the region.
Rhyl Journal
15 hours ago
- Rhyl Journal
Welsh father calls for blood donors after saving son's life
Seven-year-old Jasper Hodgson-Smith, from Swansea, was diagnosed with a rare and life-threatening blood disorder called Activated PI3K Delta Syndrome (APDS). His father, Matt, was found to be a perfect stem cell match, giving Jasper a second chance at life. Matt donating stem cells (Image: Welsh Blood Service) The family is now sharing their story during National Blood Donor Week, which runs from June 9 to 15, to encourage more people across Wales to donate blood and stem cells through the Welsh Blood Service. Sophie Hodgson-Smith, Jasper's mother, said: "From eight months old, Jasper exhibited numerous symptoms, including lethargy, persistent high temperatures, and a lack of appetite. "Due to the rarity of his blood disorder, it took a long time to identify his condition, which was thought to be chest infections, meaning he was regularly prescribed antibiotics and admitted to hospital around six to eight times a year." Matt with his son (Image: Welsh Blood Service) APDS is extremely rare, with Jasper believed to be the only child in Wales with the condition and one of just 35 patients in the UK. APDS affects the immune system, and for young patients, a stem cell transplant is often the only curative treatment. Jasper's care involved multiple blood and platelet transfusions, immunoglobulin replacement therapy, chemotherapy, and ultimately a stem cell transplant. Only one in four patients in the UK will find a family member who is a suitable match. Mr Hodgson-Smith said: "Blood disorders are as life-threatening as cancer and require just as much resilience. "Some people think donating stem cells may be painful or invasive. "For me, the process was simple. "I would do it again in a heartbeat if it meant saving someone's life." He donated his stem cells through peripheral blood stem cell transplantation, a procedure that collects stem cells from the bloodstream using a special machine. Jasper's mother said he remained positive throughout his treatment. She said: "Despite everything he's faced, Jasper has remained incredibly strong and full of life—always dancing, singing, and making people smile, even during the toughest days. "Once Jasper is feeling fit and well, we are looking forward to spending more time as a family and have lots of beach walks and adventures planned with our dog, Pip." The Hodgson-Smith family hopes their story will inspire more people across North Wales and beyond to consider donating blood or stem cells. The need for donors is ongoing, with more than 15,000 blood donations required annually in North Wales alone to support patients at hospitals including Ysbyty Glan Clwyd, Ysbyty Gwynedd and Ysbyty Wrecsam Maelor. Frank Murphy, who lives in Wirral but worked at HMP Berwyn near Wrexham, was recently recognised by the Welsh Blood Service for helping to potentially save more than 1,200 lives. Not only has he donated blood more than 40 times, but he also encouraged colleagues at HMP Berwyn to donate on more than 400 occasions. Mr Murphy said: "Giving and supporting others to give blood and to save lives has, in my eyes, always been a must and a duty, and encouraging others to donate is a great feeling." Appointments to donate are available across the region.
Scottish Sun
a day ago
- Scottish Sun
Our brave Jasper is slowly losing the ability to walk – a drug could change that but the NHS cruelly won't fund it
Find out everything you need to know about Jasper's condition below LIVING NIGHTMARE Our brave Jasper is slowly losing the ability to walk – a drug could change that but the NHS cruelly won't fund it Click to share on X/Twitter (Opens in new window) Click to share on Facebook (Opens in new window) THE family of a 10-year-old boy who's losing the ability to walk have described the 'nightmare' battle they face with the NHS to access a free drug for help. Rosie and Pete Day from Horsham, West Sussex have been fighting for the drug givinostat for their son Jasper who has Duchenne muscular dystrophy (DMD). Sign up for Scottish Sun newsletter Sign up 4 Jasper and his twin sister both have Duchenne muscular dystrophy - but Arabella is a carrier while Jasper is most affected Credit: PA 4 The Day family are fighting for Jasper to get givinostat, which can slow progression of the condition Credit: PA Duchenne is a genetic muscle wasting condition that causes progressive muscle weakness. In the UK, an estimated 2,500 people are living with the condition The Day family have twins Jasper and Arabella, and two older daughters. Both Jasper and his twin sister Arabella have Duchenne, with Arabella a carrier and Jasper the most affected - as the condition mostly affects boys. Read more on muscle conditions BEHIND BARS Woman left battling fatal 'muscle death' triggered by first ever spin class Givinostat, developed by ITF Pharma UK, can slow progress of Duchenne - keeping children on their feet for longer - and is being offered for free by a drug firm while it goes through the process of NHS approval. Only some NHS trusts across the UK, and few in England, are giving out the drug despite it being part of an early access programme since November. Families are now facing a "cruel" postcode lottery over who gets the medicine and are in a race against time, according to the charity Duchenne UK. Some NHS trusts are refusing to supply the drug while others delay it by drawing up lists of who they think should get it first. NHS trusts say they need to pay for monitoring the drug - around £1,900 per year per patient - out of their own budget. Rosie said: "We try and live in the moment and, in this moment, there's an opportunity to make a massive change to Jasper. Toddler, 3, left fighting for life after 'going off his food' - as killer cocktail of common viruses attacked his heart "We're not going to cure it, but this drug gives him the best chance of having the early life that he wants to have and what every parent wants to give their child. "It's so close - and yet we're stuck. "We're stuck in this process where there's something in reaching distance that could make a huge difference to keep him walking, keep him active, keep him with his siblings in the garden, keep him walking up the stairs, all of those things, and it just feels that we can't quite get there. "We're on the finishing line to get something that will make a difference and we can't quite get there because of the system we're in. "The drug is not going to cure it, but it will give him the childhood you would wish to give your child - to keep them playing football, coming on dog walks, being able to walk up the stairs, playing the French horn, all of those things that you dream your child is going to get to do.' She added: "It feels like a nightmare, because you know that the doctors want to give it, but when it comes to getting the drug in his mouth and seeing what it would do, we're stuck. "It's a lottery, basically, depending on where you are in the country ... and within NHS trusts themselves." 'When will I get the drug, mummy?' Jasper is under the care of the Evelina London Children's Hospital, which is only now starting to contact patients and is drawing up a priority list for who gets the drug first. "Every day that passes by is a day that we can see Jasper decline and see him struggling with his muscles," Mrs Day said. "Two weeks ago, he asked me, 'When will I get the drug, mummy?' "We're stuck in a situation over who's going to make those decisions regarding who gets the drug - of whether Jasper gets it or another boy. "For every boy it's heartbreaking, because someone ultimately is not going to get the drug at that moment based on the current criteria." She continued: "If Jasper stops walking, we're not going to get that back. We're stuck in a situation over who's going to make those decisions regarding who gets the drug - of whether Jasper gets it or another boy Rosie Day "Every day matters. Six months ago, Jasper could walk up and down the stairs easily. He can't do that now and Pete has to push him up the stairs every night. "Yet we can't give him something that is as simple as two spoons full of medicine and a blood test, and a little bit of maybe resource looking at the blood test results - that is what is standing in our way." Rosie said it was unclear how the Evelina is "going to make a fair choice" because knowing who will lose mobility is not an exact science. And she said the process is "hugely subjective" because there is no linear decline in the condition and the decisions made by NHS trusts could end up being "completely wrong". According to Duchene UK, boys whose condition is getting worse risk falling off the list entirely while waiting for the drug. Around 500 boys in the UK are eligible for givinostat, which can be taken at home like Calpol, with hospitals then doing follow-up blood tests of around eight in the first year, followed by twice a year thereafter. 4 Jasper is under the care of the Evelina London Children's Hospital, but it's unclear whether they'll give him the drug Credit: PA 4 The family say the NHS needs to urgently make the drug available to both ambulant (walking) and non-ambulant boys Credit: PA Children may also need an ECG, though these are already part of routine Duchenne monitoring. Emily Reuben and Alex Johnson, founders of Duchenne UK, said: "As time ticks by, more boys are losing out on their chance to access givinostat. "This is a simple treatment, which can be easily managed at home, and requires uncomplicated blood tests to monitor. It's free to the NHS and could offer real hope for patients and their families. "The delays are cruel and the postcode lottery is unjustifiable. We are calling on the NHS to urgently make this available to both ambulant (walking) and non-ambulant boys." To date, all health boards in Scotland are rolling out the drug, alongside those in Swansea and Cardiff. Leicester Royal Infirmary was the first trust in England to give the drug, but the Evelina has not yet, and neither have trusts in Manchester, Liverpool and Newcastle. Great Ormond Street Hospital is working to supply the drug. A spokesman for the Evelina said: "We have begun contacting families of all existing Evelina London patients who may be eligible for givinostat and are working to set up appointments in the next few months. "Our clinical team are working through our patient lists and are currently prioritising children who need the treatment most urgently, or are at a higher risk of losing movement (ambulation) soon." An NHS spokesman said: "The first National Institute for Health and Care Excellence (Nice) committee meeting to consider this treatment is scheduled to be held in July 2025, and if manufacturer ITF Pharma can offer a cost-effective price to enable Nice to recommend its use, the NHS will be ready to work with the company to explore fast-tracking access for patients. "NHS England has published guidance on manufacturer-led early access schemes, which require trusts to cover substantial costs and find additional clinical resources to administer new treatments, and we understand a number of trusts across the country are preparing to offer givinostat via such a scheme." Parents have met with Health Secretary Wes Streeting to try and speed up access.
