
Uncertainty over blood test service in North Devon
She said: "I have not slept properly since 17 February when I found out about this and all my symptoms are being exacerbated by the stress I am under."The difference is going to my local surgery which is less than a mile away or going to the Royal Devon and Exeter (RD&E) which is a 78 mile (126km) round trip for a 30 second blood test."
Michelle VonAhn, 68, from Holsworthy has neuroendocrine cancer, and requires a monthly blood test before receiving ongoing treatment at North Devon District Hospital in Barnstaple.She said this decision could result in her having to make a 60 mile (96km) round trip to get a blood test."I think it's unreasonable to expect people living in a rural environment like this to travel so far for something which is such a basic diagnostic technique. "There needs to be a local solution."
A spokesperson for NHS Devon said: "NHS Devon continues to work closely with the Royal Devon who have this week described to us the plans they are putting in place to ensure they can provide secondary care requested blood tests (that are currently provided by Ruby Country Medical Group) from April 1, 2025."We will continue to support them to ensure this is achieved and Royal Devon will provide further updates and information to Ruby Country Medical Group and patients regarding access and location of services as soon as it becomes available."
Dr Rachel Ali, chair of the Devon Local Medical Committee, said about a quarter of GP practices in Devon have decided to stop offering blood tests requested by hospitals.She said: "We've been offered a little bit of money towards the costs of running this service but it doesn't cover the costs. "It means practices are having to pay out of their baseline in order to do blood tests for the hospital that the hospitals are already paid to do."Because they are having to do that, they are going to have to stop doing other things and practices do not want to stop offering their patients important general practice services."She said hubs have been set up in areas including Plymouth, South Devon and Torbay to carry out this service.

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Metro
6 days ago
- Metro
My GP laughed when I reported feeling like a ghost touched me
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A family member once suggested that the obvious answer was that it was 'all in my head'. Funnily enough, in a way, they were right. In 2020 I had a relapse – where new symptoms arrive or old ones get worse – that was so catastrophic it left me with a numb left side, limping, falling asleep in unexpected places and feeling constantly queasy until eventually I landed in casualty. Another MRI scan (I'd lost count of the number I'd had by then) was ordered, only this time, it showed that my brain was peppered with scarring where MS had damaged my brain and spine. In all likelihood, I'd had MS this whole time but the scarring before this major attack had always been minor and therefore didn't show up on tests. Now though, the damage was pronounced and dramatic making it impossible to miss. Finally I had the diagnosis I'd been searching for, for 19 years. You'd think, after all that time I'd be ready for it. 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Where I used to go to the theatre twice a week or spend hours walking my dog around London, I now spend much more time at home. Luckily, I've found pleasure in reading and watching films. On the days when my symptoms are less, I embrace them wholeheartedly, making the most of that time to do things I otherwise can't now. As a result, we are planning on swapping the hectic whirl of the capital for a slower pace of life on the South Coast. Mainly, I wish there hadn't been 19 years of the merry go round of 'does he/doesn't he' have MS. Having a diagnosis wouldn't have changed what medical treatment I had because the MS wasn't bad enough then to need medication, but it would have helped me feel validated. Chris Bridge's latest book Sick To Death came out on 27 March. Order your copy here. Maybe then I wouldn't have spent almost two decades feeling like I was being dismissed and labelled as being hysterical or making it all up. Perhaps I wouldn't have been left to cope alone each time the MRI scans were clear. Whether the scans were or weren't showing MS, I was struggling and deserved support and understanding. I know my story is not the only one like this: Many people frequently have neurological symptoms without a diagnosis and are often dismissed. But people with functional symptoms (symptoms with no obvious physical cause) need and deserve as much help as anyone else – we just don't always get it. I'd like to see that change. More Trending In the meantime, I've channelled my anger and frustration into writing. I've always written and am a crime fiction fan so decided to write about a woman with neurological issues and the chaos that ensues when she's drawn into a murder plot. This lead character is discredited, disrespected and coping alone. Sound familiar? Mainly, the catharsis from expressing my feeling of alienation, fear and rage on the page has been intense, but finally my 'special little syndrome' has found a home on paper and I feel seen. View More » This article was originally published March 25, 2025 Do you have a story you'd like to share? Get in touch by emailing Share your views in the comments below. MORE: I had sex with a man I loathed – and it was incredible MORE: I was punished for not telling my boss about my disability MORE: 'I was 17 when I had my first day of school' Your free newsletter guide to the best London has on offer, from drinks deals to restaurant reviews.


BBC News
25-06-2025
- BBC News
Inspectors find 'widespread failings' in Torbay SEND service
Significant concerns have been raised by inspectors over special educational needs and disabilities (SEND) services in part of Devon.A report published on Wednesday by regulator Ofsted and the Care Quality Commission into the Torbay SEND local area partnership highlighted "widespread and/or systemic failings".Issues raised by the report included too many children and young people with SEND issues having to wait an "unacceptable time" to have their needs Council and NHS Devon, which are responsible for running services, said they were committed to addressing the issues raised by the report. 'Long-standing issues' The inspection, which was carried out in March, said those responsible for governance did not have an "accurate understanding" of the partnership's strategic SEND priorities."The resulting lack of strategic working and effective joint commissioning has resulted in poor communication and collaboration between the local area partnership and families," the report added leaders had not urgently of effectively addressed systemic and significant weaknesses highlighted in a previous inspection in report said: "Many long-standing issues, particularly the waiting times for assessment and diagnosis, parental dissatisfaction and the high proportion of children and young people with SEND being excluded and becoming NEET [not in education, employment or training], have remained unresolved issues."A monitoring inspection was set to be carried out within the next 18 months before a full reinspection in three years, the report partnership has been asked to prepare a priority action plan to address issues identified in the report, inspectors added. In a joint statement, Torbay Council and Nancy Meehan, director of children's services, and Su Smart, director of women and children's improvement at NHS Devon, said improvement work was already under said a number of areas were highlighted in the report as "doing well", including the work of the Mental Health in Schools Team, the strength of a neurodiversity support programme and early years statement added the partnership was committed to addressing the issues and called for "systemic reform at the national level" to help with meaningful and lasting statement said: "We are committed to ongoing improvement across all SEND provision and will continue to work with parents, carers and practitioners to develop and strengthen it."Our priority remains the wellbeing and success of our children and young people."The BBC has contacted the Department for Health and Social Care for comment.


Scottish Sun
25-06-2025
- Scottish Sun
I went to bed feeling fine but woke up paralysed – doctors blamed it on constipation but the truth was horrifying
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From that moment on, life just got better. Regardless that I've got MS, at least I know what I'm dealing with. Girl paralysed after giant critter feasted on her scalp 'I felt a big relief because I was thinking it was something that was going to kill me.' Adam began to research the condition and decided to learn as much as he could. Advertisement In denial MS is an often disabling disease that affects the central nervous system (brain and spinal cord). He admits for the first two to three years he was in denial and believed that his life didn't need to change. For the first few years he had Relapsing Remitting MS (RRMS) and he had several disease-modifying drugs to help slow down the progression of the illness. 'Some worked and some didn't,' he said. Advertisement 'Many of the treatments have side effects that make you feel even worse on top of already being ill. 'Now I have Secondary Progressive MS (SPMS), which means I have moved onto the next stage, unfortunately. But I take medication and hopefully this will slow down the progression.' If I have to go to the kitchen, it might take me five minutes – but I'm OK with that Adam Dawer Adam had to give up his job as a graphic designer and accept a slower pace of life. "If I have to go to the kitchen, it might take me five minutes – but I'm OK with that,' he said. Advertisement 'The main thing is: I'm still alive, I'm still breathing, so all is good. 'My wife is now my full time carer and I'm extremely lucky that she helps me get out and about. 'I still drive on occasion, it's the only thing that makes me feel normal like everyone else but mostly Sharon does it now.' Sharon helps Adam with all the practicalities of MS, such as preparing his scooter, wheelchair or rollator and sorting routes, finding out where is accessible or where might have dodgy pavements. Advertisement 'She deals with all of that so I don't need to because I can't anymore,' Adam added. 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It's not a one-size-fits-all thing.' 5 Adam had to give up his job as a graphic designer and accept a slower pace of life Credit: Cover Images 5 His wife Sharon is now his full time carer Credit: Cover Images 5 Despite his diagnosis Adam is happy about life and makes sure he's still present for his five children Credit: Cover Images Advertisement He is positive about his life and happy he's been able to be an active and present dad for his five children. 'When MS announced itself into my life, the youngest was five,' he said. 'I'm glad that my kids were of an age that my declining health wasn't going to impact them so much. They weren't going to grow up seeing dad be heavily disabled. 'I got to be a proper parent. I really didn't want MS to rob me of being a parent or to rob my kids of having a dad who was there. 'By the grace of God, it worked out and they're all doing their own things now. The youngest will be 20 this year. The oldest is in another country. Advertisement 'I honestly haven't been happier and mentally clearer in my life. I just had this mental clarity one day: everything's going to be OK. 'It was like a massive weight came off me. I really can't explain it. It kind of is a spiritual experience - I think having MS has been like a superpower – for my mind, the way I think. 'Everyone's got problems. But when a problem comes up for me, I think, 'Is anybody going to die? No? Then there's no problem. We can fix it.''