
North Wales charity helps grandmother, 80, get benefits
The not-for-profit organisation, which supports people over 60 living in private homes, has helped clients secure £1 million in unclaimed benefits.
Mrs Williams said: "I fell by the gate trying to bring the bin in.
"I fell backwards, and two ladies who were passing, one was actually a paramedic, helped me up.
"They insisted I went to A&E because I had banged my head.
"The following day the neighbour across the road advised me to phone Conwy and Denbighshire Care & Repair."
Caseworkers helped Mrs Williams secure the higher-rate Attendance Allowance of £110.40 per week.
The charity also fitted rails at the front and back doors, on the stairs, in the hall, porch, and downstairs toilet.
Mrs Williams, a former music teacher at Ysgol John Bright in Llandudno, said: "You lose confidence after a fall, so having the rails helps, it makes me feel safer.
"I can't bend then come back up without feeling breathless and dizzy, so it's important to have the rails to hold onto.
"The bathroom is just transformed now, it's fabulous.
"It has a walk-in shower and handrails to help me.
"Without all their help, I don't know how many falls I would have had.
"The workers who came here were brilliant, and every night they were cleaning up after themselves, I didn't have to do a thing."
Amanda Derbyshire, her caseworker, said: "It all helps with independence and staying at home, which is what we all want.
"It's about staying at home as long as possible, staying somewhere where you want to be."
The charity also contacted NHS falls teams, helped the couple apply for a Blue Badge, and arranged for the fire service to check and replace their smoke alarms.
Ms Derbyshire said many people do not realise they are eligible for the Attendance Allowance.
She said: "The Attendance Allowance is a non-means-tested disability benefit for people of state pension age and they can claim for it if they're having difficulties with day-to-day personal care tasks.
"A lot of people don't want to see themselves as disabled or having difficulties but I always say it's worth applying, because it can open the doors to other things such as Pension Credit."
Lynda Colwell, chief officer of Conwy and Denbighshire Care & Repair, said: "We help them access the benefits they are entitled to, which can significantly improve their quality of life and reduce feelings of isolation and loneliness."
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South Wales Argus
an hour ago
- South Wales Argus
Doctor's comment about head size led to one in a million diagnosis for baby boy
Conor O'Rourke, now three, was treated for vein of galen malformation (VOGM) with a new surgical technique by specialists at Alder Hey Children's Hospital in Liverpool in what is thought to be a world-first. The condition – which affects roughly 10 to 12 babies in the UK each year – causes the veins and arteries in the brain to connect abnormally, increasing bloodflow and leading to severe complications if undetected. Conor was one of a rare subgroup of patients, meaning the usual treatment did not work. His mother Lucy O'Rourke, 36, from Bolton, described the last couple of years as an 'out of body experience' for her and husband Sean O'Rourke, 38. She told the PA news agency that Conor was around eight or nine months old when she took him to an appointment for a potential umbilical hernia, a usually harmless condition when the intestines bulge through the opening in muscle near the belly button. She said: 'He was looking at his his belly button, and then suddenly wanted to ask me questions about his head. 'And obviously I was slightly confused at that point. I didn't really know what the issue was, I'm just looking at my beautiful baby, and didn't think that there was an issue.' Mrs O'Rourke said the consultant asked about the shape of her son's head, adding: 'He felt like he had quite a pronounced forehead; it was quite a large head. 'And he had very visible veins on his forehead, and his temples, round his eyes. And we had seen those things, but obviously we didn't in a million years think that there was something sinister going on. 'We thought he was very fair skinned, and that was why we could see his veins. 'Looking back now, I look at pictures, and I think, 'oh yeah, you can sort of see now', knowing what we know. But in that moment in time, I was a new mum, first-time mum, didn't really spot anything untoward, really.' Mrs O'Rourke said that at the time of the appointment, Conor had not yet sat up on his own but had met all his other milestones. She was warned to take her son to A&E if he suddenly started vomiting or was difficult to rouse after sleeping, although she was reassured it was probably nothing to worry about. However, Mrs O'Rourke said the conversation played on her mind, and she called her GP the following day. Conor with dad Sean (left) and mum Lucy (right) (Lucy O'Rourke/PA) Conor was sent for an MRI in March 2023 and the couple were not worried until they were called into a family room. At that stage, doctors did not know what was wrong with Conor but told the family he had a 'significant brain issue' that would require surgery. The results were assessed by specialists at another hospital, with more scans ordered for Conor. 'It was only after those scans that they said to us that they think that it's vein of galen malformation and then started to explain to us a little bit what that meant,' Mrs O'Rourke said. 'But in reality, they'd never seen it before in Bolton.' Mrs O'Rourke said the experience was 'terrifying' and the couple felt 'helpless'. 'Throughout the whole of this, really, it's definitely been a bit of an out of body experience,' she told PA. Conor was sent to Alder Hey and had three operations called endovascular embolisations, which involves inserting a small, flexible tube called a catheter into the arteries, usually from the groin. Medics use X-ray imaging to guide the tube through the body and into place, and then inject a glue-like substance to block off the artery. In some cases, the same procedure can be performed by inserting the catheter into the veins. However, Conor is one of a rare subgroup of patients where veins block off and doctors can no longer get to the malformation. When this happens, the jugular veins – a set of major blood vessels in the neck – also block off, causing the veins from the brain to try and drain elsewhere. According to the toddler's surgeon, Conor Mallucci, this was causing swelling and damage to the toddler's brain stem and spinal cord, leading to him to deteriorate. Mr Mallucci told PA: 'It's a fight against time, and that happened quite early in Conor, which is why we had to come up with this alternative route.' The operation involved accessing the malformation through Conor's skull to target the affected blood vessels. He recovered well and is now considered '99% cured' by Mr Mallucci. Mrs O'Rourke said the family feels lucky in some ways. She said: 'As much as I feel like this is an incredibly unlucky diagnosis, I sometimes have to pull that back and think actually we were incredibly lucky in a lot of ways. 'We were already under a consultant at Royal Manchester Children's, who mentioned something. 'And then we were also incredibly lucky, in a way, that I'm very much an over-thinker, and I was an anxious mum, to not leave it there. 'And thank goodness that we did. Because if we didn't, I don't know where we would actually be.' Conor recently graduated from nursery and will be attending pre-school with his peers in September. Mrs O'Rourke said she is 'so proud' of her 'resilient' son, adding: 'At one point they were saying, 'we may want to hold him back' and 'maybe it might be a bit too much for him'. But they've said now that they think he's doing incredibly well. 'That's brilliant. And it was just magical to see him.' Mr O'Rourke has also committed to running the Manchester Marathon next April to raise money for Alder Hey. 'Thank you just doesn't cut it,' Mrs O'Rourke said. 'They not only saved his life, they saved ours too.'


Glasgow Times
an hour ago
- Glasgow Times
Doctor's comment about head size led to one in a million diagnosis for baby boy
Conor O'Rourke, now three, was treated for vein of galen malformation (VOGM) with a new surgical technique by specialists at Alder Hey Children's Hospital in Liverpool in what is thought to be a world-first. The condition – which affects roughly 10 to 12 babies in the UK each year – causes the veins and arteries in the brain to connect abnormally, increasing bloodflow and leading to severe complications if undetected. Conor was one of a rare subgroup of patients, meaning the usual treatment did not work. His mother Lucy O'Rourke, 36, from Bolton, described the last couple of years as an 'out of body experience' for her and husband Sean O'Rourke, 38. She told the PA news agency that Conor was around eight or nine months old when she took him to an appointment for a potential umbilical hernia, a usually harmless condition when the intestines bulge through the opening in muscle near the belly button. She said: 'He was looking at his his belly button, and then suddenly wanted to ask me questions about his head. 'And obviously I was slightly confused at that point. I didn't really know what the issue was, I'm just looking at my beautiful baby, and didn't think that there was an issue.' Mrs O'Rourke said the consultant asked about the shape of her son's head, adding: 'He felt like he had quite a pronounced forehead; it was quite a large head. 'And he had very visible veins on his forehead, and his temples, round his eyes. And we had seen those things, but obviously we didn't in a million years think that there was something sinister going on. 'We thought he was very fair skinned, and that was why we could see his veins. 'Looking back now, I look at pictures, and I think, 'oh yeah, you can sort of see now', knowing what we know. But in that moment in time, I was a new mum, first-time mum, didn't really spot anything untoward, really.' Mrs O'Rourke said that at the time of the appointment, Conor had not yet sat up on his own but had met all his other milestones. She was warned to take her son to A&E if he suddenly started vomiting or was difficult to rouse after sleeping, although she was reassured it was probably nothing to worry about. However, Mrs O'Rourke said the conversation played on her mind, and she called her GP the following day. Conor with dad Sean (left) and mum Lucy (right) (Lucy O'Rourke/PA) Conor was sent for an MRI in March 2023 and the couple were not worried until they were called into a family room. At that stage, doctors did not know what was wrong with Conor but told the family he had a 'significant brain issue' that would require surgery. The results were assessed by specialists at another hospital, with more scans ordered for Conor. 'It was only after those scans that they said to us that they think that it's vein of galen malformation and then started to explain to us a little bit what that meant,' Mrs O'Rourke said. 'But in reality, they'd never seen it before in Bolton.' Mrs O'Rourke said the experience was 'terrifying' and the couple felt 'helpless'. 'Throughout the whole of this, really, it's definitely been a bit of an out of body experience,' she told PA. Conor was sent to Alder Hey and had three operations called endovascular embolisations, which involves inserting a small, flexible tube called a catheter into the arteries, usually from the groin. Medics use X-ray imaging to guide the tube through the body and into place, and then inject a glue-like substance to block off the artery. In some cases, the same procedure can be performed by inserting the catheter into the veins. However, Conor is one of a rare subgroup of patients where veins block off and doctors can no longer get to the malformation. When this happens, the jugular veins – a set of major blood vessels in the neck – also block off, causing the veins from the brain to try and drain elsewhere. According to the toddler's surgeon, Conor Mallucci, this was causing swelling and damage to the toddler's brain stem and spinal cord, leading to him to deteriorate. Mr Mallucci told PA: 'It's a fight against time, and that happened quite early in Conor, which is why we had to come up with this alternative route.' The operation involved accessing the malformation through Conor's skull to target the affected blood vessels. He recovered well and is now considered '99% cured' by Mr Mallucci. Mrs O'Rourke said the family feels lucky in some ways. She said: 'As much as I feel like this is an incredibly unlucky diagnosis, I sometimes have to pull that back and think actually we were incredibly lucky in a lot of ways. 'We were already under a consultant at Royal Manchester Children's, who mentioned something. 'And then we were also incredibly lucky, in a way, that I'm very much an over-thinker, and I was an anxious mum, to not leave it there. 'And thank goodness that we did. Because if we didn't, I don't know where we would actually be.' Conor recently graduated from nursery and will be attending pre-school with his peers in September. Mrs O'Rourke said she is 'so proud' of her 'resilient' son, adding: 'At one point they were saying, 'we may want to hold him back' and 'maybe it might be a bit too much for him'. But they've said now that they think he's doing incredibly well. 'That's brilliant. And it was just magical to see him.' Mr O'Rourke has also committed to running the Manchester Marathon next April to raise money for Alder Hey. 'Thank you just doesn't cut it,' Mrs O'Rourke said. 'They not only saved his life, they saved ours too.'

Western Telegraph
2 hours ago
- Western Telegraph
Doctor's comment about head size led to one in a million diagnosis for baby boy
Conor O'Rourke, now three, was treated for vein of galen malformation (VOGM) with a new surgical technique by specialists at Alder Hey Children's Hospital in Liverpool in what is thought to be a world-first. The condition – which affects roughly 10 to 12 babies in the UK each year – causes the veins and arteries in the brain to connect abnormally, increasing bloodflow and leading to severe complications if undetected. Conor was one of a rare subgroup of patients, meaning the usual treatment did not work. His mother Lucy O'Rourke, 36, from Bolton, described the last couple of years as an 'out of body experience' for her and husband Sean O'Rourke, 38. She told the PA news agency that Conor was around eight or nine months old when she took him to an appointment for a potential umbilical hernia, a usually harmless condition when the intestines bulge through the opening in muscle near the belly button. She said: 'He was looking at his his belly button, and then suddenly wanted to ask me questions about his head. 'And obviously I was slightly confused at that point. I didn't really know what the issue was, I'm just looking at my beautiful baby, and didn't think that there was an issue.' Mrs O'Rourke said the consultant asked about the shape of her son's head, adding: 'He felt like he had quite a pronounced forehead; it was quite a large head. 'And he had very visible veins on his forehead, and his temples, round his eyes. And we had seen those things, but obviously we didn't in a million years think that there was something sinister going on. 'We thought he was very fair skinned, and that was why we could see his veins. 'Looking back now, I look at pictures, and I think, 'oh yeah, you can sort of see now', knowing what we know. But in that moment in time, I was a new mum, first-time mum, didn't really spot anything untoward, really.' Mrs O'Rourke said that at the time of the appointment, Conor had not yet sat up on his own but had met all his other milestones. She was warned to take her son to A&E if he suddenly started vomiting or was difficult to rouse after sleeping, although she was reassured it was probably nothing to worry about. However, Mrs O'Rourke said the conversation played on her mind, and she called her GP the following day. Conor with dad Sean (left) and mum Lucy (right) (Lucy O'Rourke/PA) Conor was sent for an MRI in March 2023 and the couple were not worried until they were called into a family room. At that stage, doctors did not know what was wrong with Conor but told the family he had a 'significant brain issue' that would require surgery. The results were assessed by specialists at another hospital, with more scans ordered for Conor. 'It was only after those scans that they said to us that they think that it's vein of galen malformation and then started to explain to us a little bit what that meant,' Mrs O'Rourke said. 'But in reality, they'd never seen it before in Bolton.' Mrs O'Rourke said the experience was 'terrifying' and the couple felt 'helpless'. 'Throughout the whole of this, really, it's definitely been a bit of an out of body experience,' she told PA. Conor was sent to Alder Hey and had three operations called endovascular embolisations, which involves inserting a small, flexible tube called a catheter into the arteries, usually from the groin. Medics use X-ray imaging to guide the tube through the body and into place, and then inject a glue-like substance to block off the artery. In some cases, the same procedure can be performed by inserting the catheter into the veins. However, Conor is one of a rare subgroup of patients where veins block off and doctors can no longer get to the malformation. When this happens, the jugular veins – a set of major blood vessels in the neck – also block off, causing the veins from the brain to try and drain elsewhere. According to the toddler's surgeon, Conor Mallucci, this was causing swelling and damage to the toddler's brain stem and spinal cord, leading to him to deteriorate. Mr Mallucci told PA: 'It's a fight against time, and that happened quite early in Conor, which is why we had to come up with this alternative route.' The operation involved accessing the malformation through Conor's skull to target the affected blood vessels. He recovered well and is now considered '99% cured' by Mr Mallucci. Mrs O'Rourke said the family feels lucky in some ways. She said: 'As much as I feel like this is an incredibly unlucky diagnosis, I sometimes have to pull that back and think actually we were incredibly lucky in a lot of ways. 'We were already under a consultant at Royal Manchester Children's, who mentioned something. 'And then we were also incredibly lucky, in a way, that I'm very much an over-thinker, and I was an anxious mum, to not leave it there. 'And thank goodness that we did. Because if we didn't, I don't know where we would actually be.' Conor recently graduated from nursery and will be attending pre-school with his peers in September. Mrs O'Rourke said she is 'so proud' of her 'resilient' son, adding: 'At one point they were saying, 'we may want to hold him back' and 'maybe it might be a bit too much for him'. But they've said now that they think he's doing incredibly well. 'That's brilliant. And it was just magical to see him.' Mr O'Rourke has also committed to running the Manchester Marathon next April to raise money for Alder Hey. 'Thank you just doesn't cut it,' Mrs O'Rourke said. 'They not only saved his life, they saved ours too.'