Throughout his career Rob defied the odds against him [at 5ft 4in and weighing less than 10st he was invariably the smallest man on the pitch] and hes determined to defy the odds again, Lindsey says. Robert Geoffrey Burrow MBE (born 26 September 1982) is an English former professional rugby league player. Oh yes, hes used to me talking every minute anyway, Lindsey says with a laugh when I ask if Rob can concentrate while we talk. The 38-year-old was diagnosed with Motor Neurone Disease, a degenerative nerve condition that currently has no cure, in December 2019. Looking back we had everything. "You and your family are truly an inspiration," one fan, Tracey Vickers, Tweeted. And remember, Rob, when you broke your collarbone? For now, Bowen believes he is dealing with the illness and will keep that focus, saying he does not want to look "too far into the future" and instead enjoy living in the present with his family. Ive got too many reasons to live., They were proud when Maya auditioned successfully for a part in a television show on Nickelodeon, as well as a role in Carmen. I am hard working and . Rugby League World Cup: Rob Burrow to be guest of honour, Rob Burrow: Rugby league star and fundraiser made MBE at Windsor, After Burrow was diagnosed with MND in 2019, Sinfield began a. . He stares at a screen and his eyes pick out individual letters so he can slowly type out words and sentences. I have no intention of thinking that way. Watch Katie Oscroft's report: Leeds Rhinos rugby legend Rob Burrow awarded honorary doctorate, Rob Burrow: Money raised by Kevin Sinfield seven marathons to fund MND research. But I still love every minute we have together. Sometimes, his short bark of mirth makes it sound like he is crying or struggling for breath. The second love story is between Rob and Lindsey. Rob has inspired so many people to join the fight against MND. Rob Burrow: Living With MND was aired on BBC2 on Tuesday 18 October and is available on iPlayer. More research needs to be done.. I have not thought about that part of my journey, he says. has a ravaging form of motor neurone disease, Observer's report on the 2011 Grand Final. "Sport is powerful enough to bring communities together. ", Rob said: "I was still coaching and living a pretty normal life, I've declined a lot since then because you become more centric. If you spin it on its head, the message I hope people will take from it is that life is for living and, despite what life throws at you, you can still have happy times and happy memories despite the heartache and the sadness.. My sole goal is to see my kids reach some milestones and Mayas achievement was amazing. New book details the enduring partnership of the former Leeds Rhino and his wife, Lindsey, and their refusal to give up living life to the full despite his MND. When he is ready a recorded version of his voice says the words out loud. It gives you more incentive to never give in. Please note: Orders are currently being dispatched within 24 hours via Royal . I know I am still their daddy but, when its not on your terms, it is horrible. In another testing final against St Helens, Burrow receives a pass just over the halfway line at Old Trafford. "It affects the sufferer but also the whole family, especially my wife. This is the second time Rob has generously allowed the cameras into his home to raise awareness, after sharing the first year after being diagnosed in the documentary Rob Burrow: My Year with MND, which was released in 2020. One of Great Britain's greatest rugby league players, Rob Burrow, is being helped into a swimming pool by his wife, Lindsey. There is no evidence that anything causes MND. One of the first things. In his book, which is released on August 19th, Burrow revealed that they have kept adaptations in their home to a minimum as they don't want their kids growing up in a hospital-style environment. That was really reassuring for me because I knew Rob was in a good place and, despite his struggles, he didnt have any regrets., I ask Rob if he still likes to watch rugby league? Lindsey seems to do the work of three people during every long day which starts for her at 5.30am and ends near midnight. To Rob,andhis family,thank you for bravely sharing your story, for raising awareness of MND, and for allowing the world to see how motor neurone disease affects thousands of families in the UK, every single day. Kevin Sinfield greets Rob Burrow on day five of his seven marathons in seven days fundraising challenge for the Motor Neurone Disease Association. As long as Rob can use his legs we'll keep him going. I am much younger and my body was a lot stronger when I got diagnosed. "He'll sit and watch television and I'll make him his breakfast and get him his lunch and take him to the toilet throughout the day. We use your sign-up to provide content in ways you've consented to and to improve our understanding of you. The 38-year-old, who won eight Grand Finals and 20 international caps during a long and memorable career, has a ravaging form of motor neurone disease. This may include adverts from us and 3rd parties based on our understanding. Riluzole, for example, is the "only medication that's shown a survival benefit for people with motor neurone disease". As Rob types, Lindsey says: Hes more interested in kicking a football at the moment but I think hes got Robs sporting genes. I enjoy watching the Rhinos on TV but I sometimes wonder: How the heck did I compete for so long? But I dont criticise them because everyone can see a gap on the TV but I know how hard it is to do with a split-second on the field. You can donate and see updates of his progress on his Give as you Live donation page . Rob is such a wonderful man and I am the person I am because of him. The pain and the sorrow are hidden then in the shadows beyond the summerhouse. It is like conducting two contrasting interviews simultaneously but they make it easy. It has completely changed my life, he says. Mackenzie Heaton tweeted: "Brings a tear to the eye! In the new BBC documentary, Rob Burrow: Living with MND, viewers witnessed how motor neurone disease can affect the body. For people who have been through tough times with Covid it will make them feel that, no matter how hard things become, there is always something to look forward to in life. She has to do the horrible stuff you don't ever talk about.". I think about a stereotypical doctor on TV and I struggle to remember how many women are put in front of a camera. If it was down to me, I joke, I would sack Sinfield from his position as director of rugby at Leeds Rhinos and make him prime minister. The documentary shows his wife, Lindsey, who Rob met when they were teenagers, care for him as she juggles looking after their three young children, 10-year-old Macy, seven-year-old Maya and three-year-old Jackson, as well working for the NHS as a physiotherapist. When I tell Lindsey and the kids I love them, you never know how far you are from telling them that for the last time., Robs voice fills the room again now. Every day, an average of six people are diagnosed with MND. Were out in the garden in Castleford, at the home of Robs parents, and there are times when its possible to almost forget the deadly impact of motor neurone disease. The 2011 Grand Final. Burrow, who had already won the Harry Sunderland Trophy as man of the match in the first of the Rhinos' previous Old Trafford victories over Saints in 2007, scored a brilliant individual try in the first half, then laid on the match-winner late in the second for Ryan Hall with another thrilling scamper. Thats why its vital we get more research done. Scientists want to establish centres of excellence for research. With your help, we hope to save other families from the heartache of an MND diagnosis in the future. "Rob obviously wants to start games, but he's shown humility and integrity to do things for the benefit of the team. 294354 VAT Registration no. I would not be the person I am today without the experience I got from playing rugby league, the friendships and bonds and life experiences, travelling the world.. I imagine him writing in silence, looking at the screen with his determined gaze, as he forms the words. A few days later, when Rob writes to me about Lindsey, I think of our afternoon in the summerhouse. Hed do a better job than Bo-Jo, Burrow replies, the laugh muffled inside him. Consequently, the muscles weaken, stiffen, and waste, affecting the way a person walks, talks, eats, drinks, and breathes. asks Dr Jung. How to get into rugby league - a crowd-pleasing, physically demanding game with few stoppages and plenty of pace. Rob was diagnosed with MND in December 2019. You could not put into words how grateful I am to have met Lindsey. Absolutely legends Rob Burrow and Kevin Sinfield. "First it comes for your voice. That depth of friendship, which he has with so many of his former teammates, means Rob is relieved he resisted offers to leave Leeds. Pasta and meat are difficult because he needs to chew those. Jude de Vos: 7 Stories of MND. In November 2022, former team mate and fellow Association patron Kevin Sinfield OBE will take on his third challenge raising money in Robs name. If you wish to donate to the MND Association, you can add a donation to your cart when purchasing products or by visiting the Donate page on our website. The programme follows Rob on a trip to the swimming pool with wife Lindsey, cheering on his children at school sports day and an appointment with his neurologist. There is currently no cure for the degenerative disease. If Lindsey felt down he would join her in a slump of depression. Simple things are now possible, like being able to ask the kids: Hows your day at school been? Or he says: Lindsey, can I have a coffee? Its lovely for me and the kids. See today's front and back pages, download the newspaper, order back issues and use the historic Daily Express newspaper archive. Id like my kids to do whatever sports they desire, he said with the use of eye-recognition technology. Kevin starts the challenge on Sunday 13 November. While Burrow can no longer talk without the assistance of a machine, and he can't walk on his own two feet, he hopes the programme will be a "beacon of hope" for other families in the same situation. I imagine their darkened house and both of them trying to find sleep at the end of another draining day. Of course, in later years, his speed, intelligence and bravery made such doubts redundant. When Sinfield ran seven marathons in seven days last December, on behalf of the Burrow family and the fight against MND, Rob said: We all need a friend like Kevin.. The ex-Leeds Rhinos scrum-half scooped the Helen Rollason Award for his incredible work in raising awareness for the debilitating disease MND. Rob Burrow scores the opening try during the Engage Super League Grand Final match between St Helens and Leeds Rhinos at Old Trafford in 8 October 2011. Brave and humbling to let us in . We can, we will.. Antony Bray Head of Quality. Jesus, Im still in bits hours later. Broadcast in 2022, the BBC documentary Rob Burrow: Living with MND took an intimate look at Robs life with MND more than two years on from his diagnosis. It is a degenerative condition for which there is no cure. It feels almost magical as his familiar Yorkshire voice fills the room even though Burrow is smiling gently rather than moving his lips. I will accept the award on his behalf. An England and Great Britain representative, he spent his entire 16-year professional career with Leeds Rhinos in the Super League, making over 400 appearances between 2001 and 2017. It has felt strangely natural to reflect on the inevitability of death not long after Rob has grinned at the revelation that when one of his old teammates, Barrie McDermott, the imposing former prop, visits him he ends up laughing so much that he cannot stop farting at the same time. Written by Ben Dirs, the accomplished ghostwriter, the manuscript is currently being read by Rob. There are times when I think about death, the 38-year-old told me in May, but Im not afraid of dying. Rob and Lindsey have been together since they were 15 and he said: Theres something beautiful about being cared for by the only girl youve ever loved.. Set up your fundraising page for our MND Centre Appeal. In late 2019, Rob Borrow and his family learned that he had an incurable disease that would require 24-hour care. The Leeds Rhinos stalwart and his wife Lindsey look back at his storied career and share their heartfelt journey since he was diagnosed with motor neurone disease, Rob Burrow can no longer talk and yet, on a rainy bank holiday evening at home in Pontefract, he answers another of my questions about life and death. Rob Burrow has no regrets about playing rugby league and would not discourage his children from following in his footsteps. This leads to dependency and a reduced life span.". "I'm a prisoner in my own body. But was he scared on the field? Dr Jung says Rob is a favourite patient because of his positivity and spirit, and also because he has done so much to raise awareness of MND. Its quiet and peaceful in the summerhouse where Rob and Lindsey Burrow sit together. In Robs book, Dr Jung explains that her MND patients want to find peace in their heads. His wife Lindsey agrees as she revealed the illness has taken hold faster than they had anticipated. Rob has three children under the age of eight and is battling hard to raise awareness and support fundraising to aid research into MND. Robs moving memoir, about his rugby career and his extraordinary resolve as he fights against MND, is published this week. Essentially a private person, Lindsey opens up about the difficulties the family experience and, movingly, contemplates a future without her childhood sweetheart. The former Leeds and Great Britain scrum-half is now confined to a. Pale Yorkshire sunshine streams in through the windows. "I'm not holding back and let you in to my life for the day. ", Gary Marks wrote: "The Rob Burrow / Kevin Sinfield bit (and they both got awards) had me in floods of tears. Rob Burrow believes lockdown has "accelerated his demise" with MND spreading to other parts of his body. Rob was diagnosed with motor neurone disease in December 2019. When he is ready Rob turns to us with a smile. He was a tower of strength and I thought: If Rob can be positive about this, well make the best of it. I also remembered my line manager at work telling me she had lost a family member through a heart attack and they hadnt had time to say everything they wanted to say or to make more memories together. In this heart-breaking 30-minute BBC Two film, viewers get unparalleled access to his life. I did not think she signed up to look after me so soon," he jokes. Rob is such a wonderful man and I am the person I am because of him. Days after the diagnosis, a distraught Lindsey started crying at a cash machine when she couldnt remember her pin number. I loved it, Rob tells me. ", Wife Lindsey says: "I can't imagine a world without Rob.". After Burrow was diagnosed with MND in 2019, Sinfield began a series of fundraising challenges. It feels almost magical as his familiar Yorkshire voice fills the room even though Burrow is smiling gently rather than moving his lips. His latest challenge, Ultra 7in7 will see Kevin running from Murrayfield Stadium in Edinburgh to Old Trafford in Manchester in just 7 days the equivalent of around 40 miles a day. Rob Burrow has been raising awareness of the disease since his diagnosis in 2019 A 77,777 donation has been presented to Rob Burrow to help him live with motor neurone disease (MND). I think like you, but my mind doesn't work right. As soon as I start talking about Rob and the children and the future, thats where it pulls at your heart strings. Former rugby players are 15 times more likely to suffer from MND than the average person according to a new study, but Burrow, who was diagnosed with the disease in December 2019, is not entirely convinced by the findings. What does your dad always say, Rob? Lindsey and Rob Burrow have been together since they were 15. In an Interview with ITV Calendar at Headingley Stadium, he told Duncan Wood: "I believe lockdown has accelerated my demise because it got me out of my routine. I have read it and Dirs has captured Robs old voice, and good cheer, while documenting the two love stories framing his life. It makes me want to see more triumphs., But there is sadness too. Id much rather that than feeling sorry for myself. I can't move my body.". Klicken Sie auf Alle ablehnen, wenn Sie nicht mchten, dass wir und unsere Partner Cookies und personenbezogene Daten fr diese zustzlichen Zwecke verwenden. Antony's public profile badge Include this LinkedIn profile on other websites. Rob said to me [last year]: I dont know if this is going to be my last Christmas. That really hit home. Rob burrow receiving his MBE today for his services to rugby league and the MND Community in London, with his wife Lindsay. As a member of Deloitte's Global Employer Services group, I specialize in expatriate taxation, serving international clients in the areas of the management of international mobility policies,. He had a wonderful career and he loved playing rugby. Watch the full documentary tonight on BBC Two and iPlayer tonight at 7pm pic.twitter.com/UkuHirUtYR, BBC Breakfast (@BBCBreakfast) October 18, 2022, A film about love, support and determination , @BBCBreakfast documentary Rob Burrow: Living with MND airs tonight on @BBCTwo and @BBCiPlayer at 19:00 BST. Ive had a great life so I dont need anything else. The 38-year-old, who won eight Grand Finals and 20 international caps during a long and memorable career, has a ravaging form of motor neurone disease. The MND Association focuses on improving access to care, funding research, and campaigning for people living with, or affected by, MND. Geoff is so positive and thats where Rob gets it from, Lindsey says. Ill support the children whatever they do but it wouldnt bother me if Jackson was a ballet dancer.. ", "Kev is like a brother," says Burrow. The 'first noticeable' sign that your cholesterol is high, Acholic stools are 'the most common' sign of pancreatic cancer, Harry Potter star Robbie Coltrane was 'fighting pain 24 hours a day', Three fruits that could 'naturally dissolve' potentially deadly blood, 'Melena' stools could hinting at a fatty build-up in the liver, Eating nuts could lower the risk of a deadly tumour, Crisps drive atherosclerosis that can lead to dangerous blood clots - Smoking gun, 'Omicron outbreak' surges in the UK - new 'top 5' Covid symptoms, 'All the blood was rushing from my ear,' Jackie Chan on his injury, Mike Tindall on the 'hardest thing' about his father's illness, Music mogul Jamal Edwards died from a cardiac arrhythmia. But his eyes confirm he is laughing. It is the only way that the former England, Great Britain and Leeds. "The smile on Rob Burrows face says it all. The children just love life and waking up on a morning and seeing the three children happy and smiling, it keeps you going.. But his mum and his dad have been great and its given Geoff such focus. I cant believe what I did.. But the kids keep us busy and theres never a dull moment, is there, Rob? Last updated on 18 October 202218 October 2022.From the section Rugby League. Following the huge success of the launch of the Leeds Rhinos 2021 Legend shirt, OXEN have now introduced four more items which are exclusively available by CLICKING HERE. If you are an overseas customer who wishes to place an order, then please contact our sales team on 01604 611777. There are incredibly emotional scenes when she talks about the prospect of life after Rob. You and your family are truly an inspiration . He told Lindsey that, while he accepted the hard truth of the diagnosis, he would fight the prognosis and try to live for longer than the doctors predicted. Just seeing him on the floor, almost looking lifeless, was hard. You know, one of the first things Rob said on the day he was diagnosed was: Thank goodness its not you or the kids. Then, in the car on the way home, he was a bit worried. He and his wife, Lindsey, who has been with. 316 4340 28, Benefits advice service for motor neurone disease, Needs assessment, home care and home adaptations, Benefits, financial support and cost of living, Getting the right treatment or care with MND, Information for people with or affected by MND, Information in other languages and formats, All-Party Parliamentary Group (APPG) on MND, Using animals and stem cells in our research, Cognitive change and frontotemporal dementia. Im tougher than I look.. After picking up a special BBC award, Kevin addressed the emotional audience. In December 2019, Rob Burrow was diagnosed with motor neurone disease (MND) at the age of just 37. Among hundreds of messages of praise, Burrow, who was diagnosed with MND in 2019, said: "Hope you had a great day Alfie. One day, before I know it, I wont be able to enjoy these timeless moments. Not so long ago I asked Rob: If you could go back and we were told that rugby had a part to play in you getting MND, would you change anything? He said absolutely not. BBC Breakfast presenter Dan. Burrow and Kevin Sinfield, the Leeds captain who lifted the Super League trophy for the fifth time since 2004, had both said "It's not how you start, it's how you finish" before they even left the pitch. Your mind is working normally, your body isnt., Lindsey is a marvel of good cheer and selfless commitment to her family but she admits Birthdays are hard and Christmas. If you need help or advice on donating, were only a phone call or email away. So I worried about Rob getting some form of dementia or Alzheimers which is irrelevant now., Rob has finished typing. "How do I have the conversation around death?" Jude's son Jody died of MND in 2017, when he was aged 38. Rob won eight Grand Finals with Leeds Rhinos as they dominated rugby league from 2004 to 2017 and he played 20 times for Great Britain and England in a celebrated career. While Rob methodically types his answers, Lindsey chats to me. The reality of day-to-day life with MND for rugby legend Rob Burrow MBE has been put under the spotlight on prime time television. Since, Jude de Vos has climbed Ben Nevis to raise funds for the Rob Burrow Centre for MND appeal. All the Zoom conversations, emails and texts cannot match being with them as they tell me about their summer holiday, their children and the state of Robs health. Rob also introduced a no-tears policy as an affirmation of everything good that remained in their changed lives. We will still make them happy days.. Yet, the family are determined to make the most of the time they have left with Burrow. The teams were locked at 2-2 after an attritional opening half-hour in the steady Mancunian rain when Burrow broke the deadlock with one of the most spectacular tries in the Grand Final's 14-year history. Seeing him knocked out in a World Cup game shook me. London, England, United Kingdom Founder VPS GB Jun 2018 - Present4 years 9 months London, United Kingdom ITC Secure 1 year 3 months L1 NSOC Engineer Apr 2019 - Sep 20196 months London, United. ", Thank you for sharing your wonderful family with us. Ive watched it back and there were plenty of tears, she said. Rob and Lindsey Burrow with their children (from left) Maya, Jackson and Macy. At the end the interview, Rob just had a bit of time to play the Yes/No game, showing he's clearly still got his strong sense of humour: Researchers in Sheffield working on treatments for motor neurone disease say they're making good progress, but need more funding. Rob Burrow celebrates his eighth Grand Final victory in his last game for Leeds in 2017. he played 20 times for Great Britain and England in a celebrated career, It is a challenge interviewing a man who cannot speak. Leeds Rhinos Commercial Director Rob Oates added: It is fantastic to see our partners at Oxen working so closely with the MND Association, a cause that is close to the heart of all Rhinos fans. Visit www.mndassociation.org for more information. No-one can ever take Rob's place.". Rob laughs because he knows his dad. He collected a pass just inside the Saints half, ran deliberately at two of their biggest forwards and ducked his small frame beneath a couple of bulging biceps. Since then he has used his profile to shine a light on the devastating disease, teaming up with other sportsmen including Doddie Weir and Stephen Darby to raise awareness and call for more research into the disease. He felt isolated in his stricken body. Burrow, who . Not only can it cause speech and swallowing difficulties, life expectancy can be as short as six months from the onset of symptoms. I was afraid of failing, he says, but never scared of playing., We become nostalgic when I ask Rob which game he would watch again if he could relive only one last match. He remained a one-club man right until the end for he was an academy coach when the disease changed his life. I have to ask the school to give her time off, Lindsey says. Im in more of a carers role now. I am so glad I did not move. He and Rob are so determined., Lindsey is a physiotherapist who has worked with MND patients for years. The NHS continues: "In medical research, riluzole extended survival by two to three months on average.". Lindsey will soon settle Rob into his special hospital bed, which can be raised, as it is hard for him to lie on his back. Get latest scores and headlines sent straight to your phone, sign-up to our newsletter and learn where to find us on online. Rob Burrow believes lockdown has "accelerated his demise" with MND spreading to other parts of his body. There is a gurgle of a laugh from Rob before Lindsey continues. Jenn Dodd, Regional Fundraiser for Yorkshire, Humberside and the North East said: These concept shirts combining the iconic MND Association design with Robs signature seven celebrate the incredible support from Rob Burrow over the last 18 months. I know all the great benefits of sport so I wouldnt want to put anybody off playing. The reason for doing this is to raise awareness about how brutal and cruel and devastating MND is and that it doesnt just affect the person, it affects the whole family. It just puts me in a different role. It was never intended to be in the documentary, but some of the things she said really fitted in well. His vocal cords are in the grip of MND so it is no ordinary laugh. Does her gut tell her there is a connection? England football legend Gazza will look back at his life and career at an event in Pontefract this summer with all money raised going to the Rob Burrow MND charity. The 29-year-old has endured a testing year even by the standards of his Leeds team-mates, having lost his place as the starting scrum-half and been forced to adapt to a new role as an impact player off the interchange bench. You walked off the pitch but it was difficult. Rob was diagnosed with MND in December 2019 and has documented his battle against the disease as well as his huge efforts in raising money for charity. Having listened to Dr Jung explain how much it meant to her, Rob says, I completely empathise. ", BBC Sports Personality of the Year is available to stream on BBC iPlayer now. I would have been disappointed with myself because look at the way the club helped me through the disease., Even when I remember the shimmering blue streak of Burrow in that 2011 Grand Final, and contrast it silently with the motionless man in the damaged shell of his body, Rob and Lindsey offer a fresh perspective. But, as she explains, It keeps your mind off things. Rob puts it down to bad luck. His consultant, Dr Agam Jung, calls MND "an extremely cruel condition," explaining: "You may not be able to speak, you may not be able to swallow, you may not be able to breathe independently, you have weakness in your arms and legs. Also featured on the documentary, the second focusing on Robs fight with MND, are interviews with his family, and fellow MND Association patron Kevin Sinfield. Robs doctors have stressed that more scientific research needs to be done to establish whether there are proven links between rugby-induced concussion and MND. In another scene, his mum, Irene, spoon-feeds him. When we first spoke to you in April I felt Rob looked very drawn. I would never have known I could be this positive when getting the news.. He left Wellens floundering with a classic sidestep and held off a couple more desperate cover defenders to slide over next to the posts. You need that mentality when youre up against players twice your size. The former Leeds Rhinos Rugby League player described Lockdown as 'a prison sentence' in . Rob Borrow: Living with MND aired on Tuesday, October 18 on BBC Two at 7pm. Now an MND Association Patron, Rob is one of an estimated 5,000 adults in the UK currently living with MND. In a BBC Look North interview, the ex-Leeds. Powerful, powerful men, heartwarming & moving. He said: "Rob is probably the most inspirational bloke in the UK. She gives 110% in her role as a physiotherapist, always wanting to help others and putting everyone before herself., Then, in a closing paragraph, Rob adds two last sentences. That's an example of the culture of the club.". Its really tough doing those interviews, but I dont want people to be sad. It was such small sample so I cannot really comment, Burrow said. ", Glittering drama based on the audacious Brinks-Mat security depot heist, A corrupt copper and a Leeds gangster are bound together by decades of dishonesty. "I love my wife and kids more than everything, and that will make me more determined to be alive," he said, defiantly. She almost narrated the story through it. There are times when I think about death, Rob admits, but Im not afraid of dying. People come to her clinic and say they think they have Rob Burrows Disease. Yes it is a sad story, but there is a lot of hope in there as well, seeing the kids and just how much they love life. You can unsubscribe at any time. Burrow, who won eight Super League titles during his glittering career with the Rhinos, insists he would not change anything from his past and would be happy for children Macy (10), Maya (7) and Jackson (3) to take up rugby.