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A woman is going to be a surrogate mother for the fourth time at the age of 50, even though the birth could be the ‘hardest yet’. Dawn Allen, a surrogate applications and agreement co-ordinator for Surrogacy UK, who lives in Derbyshire with her husband, Matthew Allen, 51, an archivist’s assistant, and has two of her own children, Alex, 17, and Sam, 27, offered to become a surrogate for the first time at the age of 36 after being inspired by a documentary over 20 years ago. Dawn has had three surrogate babies and three unsuccessful attempts, one of which ended in miscarriage, but all of her births have been “moments that will stick with (her) forever”. She was unsure if she was going to do it again until she met a friendly couple, Nicky Spence, 39, an operatic tenor and broadcaster, and Dylan Perez, 33, a classical pianist, through Surrogacy UK. Dawn makes sure her husband is on board with the surrogacies and bonds with the intended parents, as he is “as much a part of this as (she is)”, and has to “support” her through the pregnancy. She is not too worried about her age affecting her likelihood of becoming pregnant and has said she “wouldn’t have offered if I didn’t feel physically able” but is aware that the birth could be the hardest yet. “I know it’s going to be hard because I’m older now, but, at the end of the day, nine months out of my life is nothing when you’ve got a chance to give parents a lifetime of happiness,” Dawn said. Dawn was first drawn to becoming a surrogate more than 20 years ago, explaining: “I watched a documentary in the late 90s all about surrogacy and I thought, one day I’m going (to) do that. “I met Matthew, my husband, 23 years ago, and about a month into dating I said, ‘Oh, by the way, one day I’m going to be a surrogate’ – he looked at me like it was completely crazy.” Before Dawn became a surrogate, she had two sons of her own. She said: “About 18 months after having Alex, I brought the subject up about surrogacy, and we looked into it.” In 2008, Dawn joined Surrogacy UK, the UK’s leading not-for-profit surrogacy organisation, and soon began to use their online platform for surrogates and intended parents, as well as going to face-to-face socials, to see if she could find a couple she connected with. Dawn explained: “It’s just about meeting up with people and finding people that you connect with and have things in common with. “You then have a getting-to-know phase, where you hang out with the intended parents for about three months, and then you can make the decision if you’d like to proceed.” Dawn’s husband was very supportive of her decision, and she thinks it is important he connects with the intended parents too. She said: “Matthew is my main support – he’s as much a part of this as I am. “He’s the one that’s got to support me, as well as my children, so it’s important to me that they all get on with the people we decide to help.” A year after signing up to Surrogacy UK, in 2009, Dawn had an unsuccessful surrogacy as the embryos were of poor quality, but in 2012 she had a surrogate baby for a same-sex couple, using her own egg. An attempt to help a third couple in 2013 failed, but in 2015 she gave birth to a daughter for a same-sex couple – the same year, she began working for Surrogacy UK as a surrogate applications and agreement co-ordinator as she wanted to help other surrogates and intended parents. In 2017 Dawn miscarried a surrogate baby, but that couple has since had two children with another surrogate, and in 2021 she had a surrogate baby for another same-sex couple. Dawn explained how she has felt after giving birth: “I think, for me, it’s one of those moments that will stick with me forever. “You’re seeing people that you’ve become really good friends with, become parents, and you’re there in the moment they get to look at their child for the first time and hold them for the first time,” she said. “It was really, really emotional – there were lots of tears every time.” Dawn never felt it difficult to give the baby to the intended parents, explaining: “It was very clear in my head that baby wasn’t mine – it was the intended parents’ pregnancy, it was their baby. “I think you bond with your intended parents more than the baby.” Now, aged 50, Dawn is hoping to become a surrogate again, after meeting same-sex couple Nicky Spence and Dylan Perez on Surrogacy UK’s platform in November 2022. She explained: “I hadn’t made my mind up 100% if I was going to do it again, but I started chatting to Nicky and I asked my husband if he’d like to come along to a social online to meet them. “They were both lovely and my husband thought they were really nice too, so I made them the offer to start the official getting-to-know period the next day.” Nicky added: “We feel so lucky to have become friends with Dawn through Surrogacy UK and when she offered to help complete our family we couldn’t believe it. “We feel in very safe hands as she’s the kindest and most experienced surrogate you could wish for. ” Dawn did not have any doubts about her age affecting the likelihood of her getting pregnant. “So luckily, we’re using the same clinic that I used in my last journey, so they know my medical history,” she said. “Yes, I’m a lot older now, but after all the checks and tests they’ve done, they’re happy with me from a medical viewpoint. “I wouldn’t have offered if I didn’t feel physically able.” After doing some background digging on the future fathers, Dawn discovered that Nicky is an opera singer and broadcaster and his husband, Dylan, is a classical pianist. Dawn’s last surrogate baby was Luca, who was also for someone in the public eye – Aled Haydn Jones, the head of BBC Radio 1, and his partner, Emile Doxey. She said: “I have been teased about I only do celebrities now. But I had no idea that they were quite well known – I just knew Dylan played the piano and Nicky was a singer. “Nicky has performed with Shirley Bassey and lots of other people.” From November 2022 to February 2023, Dawn, her husband and the two intended parents have been getting to know each other. Dawn said: “We hang out all the time, they come and stay at our house or we meet up for meals, we’ve even been to Berlin with them and ended up in a bierkeller.” I think the pressure comes from, we want it as much as they do Dawn Allen In January 2023 they drew up an agreement regarding the pregnancy and the birth, and everyone was happy to proceed. Now, embryos are being created, using the intended parents’ family member’s eggs, and Dawn is hoping to get pregnant in the next few months. Dawn said: “I’m feeling really positive, there’s no pressure from them at all, but I do sometimes put a bit of pressure on myself because I really want to give them a baby. “I think the pressure comes from, we want it as much as they do.” Dawn thinks it is unlikely that she will have another surrogacy, saying: “I think this has probably got to be it with my age. “I think the only way I could do it was if we got pregnant really quickly this time around, and Nicky and Dylan wanted the baby to have a sibling more or less straight away.” Read More ‘You always feel like you’ve done something wrong’: Why UK surrogacy laws need a ‘real overhaul’ Children born via surrogacy or egg or sperm donation ‘should be told when young’ Tom Daley unveils photographs of newborn son Phoenix Rose: ‘He’s just perfect’ Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

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A young woman whose health “deteriorated rapidly” after being diagnosed with long Covid and suffering a liver bleed is now in a wheelchair, feeds herself through a tube in her chest and has been unable to urinate in three years. Abigail Snowball, 29, was told she suffered from a rare condition known as Fowler’s Syndrome a few months after she was diagnosed with long Covid in July 2020 and her bladder stopped working. The social worker, from Northumberland, says she was “never sick” and enjoyed long runs before testing positive for coronavirus in early 2020 and feeling a sharp pain under her ribs which scans showed was a bleed on her liver. Abigail had not fully recovered from the virus and since the diagnosis, her health has gone from bad to worse, to the point where she has not been able to urinate in three years. She now depends on her husband Mark, 34, to carry her to the bathroom so she can empty her bladder, which can take up to four hours, and has not been able to enjoy a mouthful of food for nearly a year. “I had never really been ill before,” Abigail told PA Real Life. “As a child, I was always really lucky and never poorly. I look back at pictures from before Covid and I don’t even recognise myself.” Abigail had completed a 20-mile race, the Run Northumberland BIG 20, just a week before testing positive for Covid and having to quarantine away from Mark, who works in maintenance for Nissan. “It was very much at the start of the pandemic, back at the time when there weren’t any vaccines or much testing,” she said. “It was just tiredness like I’ve never felt before in my entire life. I remember having a cup of tea and struggling to lift the mug up.” Like many other people’s experience of catching Covid, Abigail’s health improved over the next 10 days. “I did get better, but I never fully recovered,” she said. But a couple of months later, while visiting her parents, Jane and Ray Cresswell, in Cornwall on holiday, she suddenly began feeling a sharp pain under her ribs. “It was a really strange location to have pain,” she added. She visited the GP a week later and was admitted to Northumbria Specialist Emergency Care Hospital (NSECH) in July 2020, where scans revealed Abigail had suffered a bleed on her liver. “That’s when they diagnosed me with long Covid,” she said. “There was no other explanation, because they tested for blood disorders and carried out a scan. “They asked me if I had a fall or accident, but there was literally nothing.” Abigail was recovering from her liver bleed in hospital late one evening when a nurse asked when the last time she urinated was. “I actually thought, ‘god, it wasn’t since this morning’,” she said. “From that point, my bladder never regained any function. That was really the start of my health declining quickly.” Doctors hoped her bladder block was simply a result of the liver “trauma” and that she would be on the mend soon. But, sadly, this was not the case. A few months later, Abigail was diagnosed with a rare condition called Fowler’s Syndrome, which causes women to have problems passing urine. Abigail’s condition has deteriorated over the past few weeks and she is now losing weight rapidly. “I am now sleeping on the sofa downstairs and my husband Mark is having to carry me to the toilet and back again,” she said. “We can spend up to four hours at a time trying to drain my bladder, and the pain is just unbearable. “I went from running 20 miles to using a wheelchair. You don’t realise how inaccessible the world is until you are in that position.” Since the diagnosis, Abigail has spent more than 350 days in hospital and undergone 12 surgeries, including one in October 2021 to try and reconstruct her bladder. To make matters worse, she developed intestinal failure last year, which means she can no longer eat food. “I haven’t eaten anything in a year now,” she said. Instead, she is fed through TPN (total parenteral nutrition), a tube in her chest which delivers nutrients directly into the blood stream. Abigail and Mark, who married earlier this year in May, both received close to six months of training on how to perform the feeding procedure given there is a high risk of infection. “We had never even heard of that – being fed through a line into your heart,” she said. Abigail has been told by doctors that her liver bleed was “extremely likely” to have been caused by Covid. While Covid is known to harm the lungs, it has also been found to affect other organs, including the heart, liver and kidneys, but wider research is needed to better understand its long-term effects. Liver problems are common among patients with Covid-19, according to a study carried out by researchers at Oxford University and published in the peer-reviewed journal Hepatology Communications. Abigail, whose condition is considered “severe”, is hoping to receive specialist treatment in London, known as bladder Botox, which involves injecting Botox into the bladder every three to nine months, but there is no guarantee this will work. “Because of how severe and complex my case is, we’ve exhausted all our options here and the doctors are saying that I need to see the specialists in London,” she said. “Removing my bladder completely remains on the cards, but it’s incredibly high risk because of my intestinal problems. “There is no cure for Fowler’s, so it’s about managing it in the best way possible.” The combination of health conditions has left Abigail unable to perform everyday tasks. “It’s funny because the things I want to be able to do are so normal,” she said. “Just being able to wake up, take the dog for a walk and go to work. “Things that in the past, I completely took for granted.” To help cover the costs, Abigail’s friend Emma Holt has set up a GoFundMe which has received thousands of pounds in donations. “We never imagined in our wildest dreams that we would raise the amount of money that we have already,” she said. “It’s the one thing that really keeps us going, when things are really difficult. “Knowing that we have so many people behind us and supporting us is amazing.” Fowler’s Syndrome is most often caused by infection or following surgery or trauma, but a link to long Covid has yet to be established and more research is needed. Dani Coombe, CEO, Fowler’s Syndrome UK said: “It’s too early to say if long Covid is a trigger for Fowler’s syndrome; we haven’t seen an increase in Fowler’s and retention post-Covid yet, and there is no indicator that urinary retention gets worse. “Our research into what patients believe triggered their urinary retention shows that infection is the most common trigger at 57 per cent, followed by surgery in 32 per cent of patients and trauma at 19 per cent. “It would be noteworthy to see in coming years if there is an increase in women with Fowler’s because of the trauma of Covid-19.” Read More Fake meat is dying, but that shouldn’t mean the end of veganism What I gained (and lost) from walking 10,000 steps a day for five months Woman behind ‘not real’ plane tirade identified as marketing executive with $2m home Charity boss speaks out over ‘traumatic’ encounter with royal aide Ukraine war’s heaviest fight rages in east - follow live

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NEW YORK--(BUSINESS WIRE)--Jun 20, 2023--