Former England rugby captain Kevin Sinfield is set to embark upon his most gruelling challenge yet to raise vital funds for charity MNDA.
After he captured the support of the nation when he completed the mammoth task of running seven marathons in seven days back in December 2020, and raised well over £2.7 million in the process, the Oldham-born 41-year-old has announced that he will attempt to run a whopping 101 miles in 24-hours.
The challenge is called #TheExtraMile, and this time round, he hopes to raise £100,000 for those impacted by motor neurone disease.
Sinfield will attempt to run from the home ground of Leicester Tigers – the club which he has joined the coaching staff of – to Emerald Headingley Stadium in Leeds in 24 hours, and it’s all to raise funds for the MND Association and The Rob Burrow Centre for MND.
His fundraising and awareness efforts are inspired by Sinfield’s friend and former Leeds teammate Rob Burrow, who was diagnosed with MND in December 2019.
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🗺️ 101 miles ⏱️ 24 hours 💙 £100,000
Today, Kevin Sinfield announced his latest challenge in honour of @Rob7Burrow and families affected by motor neurone disease.#TheExtraMile Challenge.
Speaking to MNDA ahead of tackling the new challenge, Kevin said: “Undoubtedly, this will the toughest challenge I have ever attempted.
“But I know it will mean so much to so many people if we can reach our fundraising target.
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“In my short time at the Tigers, the people in Leicester have made me feel so welcome and it is wonderful that we have been able to come up with an event that starts in Leicester and finishes with us coming home to Emerald Headingley.”
Initially, Sinfield and his team had planned to run 100 miles, but the actual distance has worked out to be 101 miles – hence the run being named ‘The Extra Mile Challenge’.
Sinfield and his team will cover the route – which will be publicised in advance, so well wishers can come out to cheer them on – in 7km stages, each of which must be completed inside an hour with the next starting on the hour.
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The challenge will begin on Monday 22 November.
👏 On November 22/23, Kevin Sinfield will be aiming to raise £100,000 as he runs the 101 miles from @LeicesterTigers to @leedsrhinos in 24 just hours!
“The response from the public last year was breath taking and I know, from feedback we have received from the MND Association, every penny that was raised has been put to good use to help members of the MND community across England and Wales,” Kevin continued.
“The more money we can raise, the more people we can help and ultimately find a cure for this cruel disease.
“We have seen science and research do some incredible things over the last year and I know so much work is going on to find a breakthrough for MND.
“I am sure there will be tough times as we pound the streets during the day and night, in cold November temperatures, but knowing the good we can all achieve together will be a huge motivation for everyone involved.”
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Kevin appeared on BBC Breakfast yesterday to talk a little more about the challenge.
“Kevin, you give us inspiration, you give us hope that there may be a future”⁰ On #BBCBreakfast campaigner Cris Hoskin, who lost six family members to MND, has this emotional thank you for Kevin Sinfield as he announces a new charity challenge 💕 https://t.co/chPkhtmLbkpic.twitter.com/PvFVUZinwW
In addition to public donations, Sinfield is hoping to attract five key benefactors – whose logos will appear on his running vest – to donate £20,000 each.
This should then double the proceeds raised to £200,000.
Donations will be split equally between the Leeds Hospitals Charity appeal to build the Rob Burrow Centre for MND supporting people living with the disease and their families, and the MND Association, which funds multi-disciplinary care across the country, as well as research into potential treatments.
Over £11,000 has already been raised, with donations rising every minute.
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You can find out more information, and make a donation to Kevin Sinfield’s ‘The Extra Mile Challenge’ here.
Featured Image – Twitter (@MNDA)
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Government announces homebuying overhaul to fix country’s ‘broken’ housing system
Emily Sergeant
The Government has announced what it’s calling the biggest shakeup to the homebuying system in this country’s history.
In a bid to ‘rewire a chaotic system which has become a barrier to homeownership for thousands nationwide, the Government has today (Monday 6 October) unveiled proposals that it says will speed up the long-drawn out and costly process of buying a home by four weeks.
The Housing Secretary says this will not only save people money, but unnecessary stress too.
The proposed new plans would see sellers and estate agents required to provide buyers with ‘vital’ information about a property upfront – including the condition of the home, leasehold costs, and chains of people waiting to move.
It’s hoped this will help end any last-minute chain collapses and ultimately give greater confidence to first-time buyers when they’re making one of life’s most important decisions.
The Government has announced plans to fix the country’s ‘broken’ housing system / Credit: Benjamin Elliott (via Unsplash)
Binding contracts could also be introduced to stop people walking away from agreements after buyers painstakingly spend months in negotiations to hopefully halve the number of failed transactions.
The new reforms are also proposing that prospective buyers are provided with side-by-side information on estate agents and conveyancers, including their track record and expertise, alongside new mandatory qualifications and Code of Practice to drive up standards and work to rebuild trust in the industry.
Prime Minister Keir Starmer took to Twitter this morning to address the proposed new homebuying overhaul, commenting: “I promised that my Government would fix the broken housing system.
“Buying or selling a home will be faster, unlocking the dream of homeownership and allowing hardworking people to focus on the next chapter of their lives. That’s national renewal.”
I promised that my government would fix the broken housing system.
Buying or selling a home will be faster, unlocking the dream of homeownership and allowing hardworking people to focus on the next chapter of their lives.
“Through our Plan for Change, we are putting more money back into working people’s pockets and making a simple dream a simple reality.”
Featured Image – James Feaver (via Unsplash)
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English rugby legend Lewis Moody reveals MND diagnosis
Danny Jones
Much-loved English rugby legend Lewis Moody has revealed his heartbreaking MND (motor neuron disease) diagnosis.
The Leicester Tigers and Bath icon, who was captain of the Rugby World Cup-winning England squad back in 2003, unfortunately announced to the world that he is now suffering from MND, also known as ALS (Amyotrophic Lateral Sclerosis).
Moody, 47, is just the latest well-known rugby player to have developed the progressive neurological disorder, with both former players and others being forced to retire due to the condition.
The Ascot-born rugby union veteran has admitted that the news has come as a ‘sudden shock’ to him and his family, but has been left moved by the overwhelming wave of positivity he has received since making the health update public.
We are deeply saddened to hear the news of Lewis Moody's MND diagnosis and join the entire rugby community in getting behind Lewis and his family at this extremely difficult time ❤️ pic.twitter.com/46doNRQFvq
Sharing a lengthy message online, Moody wrote: “I’m writing to share some tough news. I have recently been diagnosed with ALS, also known as Motor Neurone Disease (MND). This has been incredibly hard to process and a huge shock to me and my family.
“I feel fit and well in myself, and I’m focused on staying positive, living life and dealing with the changes / will experience as they come.
“I am being well supported by my family, friends and medical professionals, and I’m truly grateful to those who, in their time, helped progress research to support others, like me, living with this disease.”
Notable ex-pros who have sadly passed away from the disease in recent years include Doddie Weir and, of course, Rob Burrow MBE.
There is currently no known cure for MND at present, but as Burrow’s best mate and inspirational teammate, Kevin Sinfield has famously, the belief is that this is because it remains “underfunded” and a breakthrough could still be found.
Speaking to BBC Sport with his long-term partner on Monday, 6 October, ‘Mad Dog Moody’ gave a very open and honest interview about the last few weeks, going from noticing some weakness in his shoulder at the gym to having now been given the tragic diagnosis.
Lewis’ statement continues: “Since retiring from the sport I love, and alongside my wife Annie, I’ve been able to dedicate much of the past 12 years to fundraising for The Lewis Moody Foundation in support of those affected by brain tumours.
“My plan is to continue with this, but to also create an opportunity to support a charity closer to my current situation. I would be so grateful for your help with this and look forward to sharing more, once l am clear on what this looks like.
“For now, please know I feel your love and support; all l ask is that I am given some space to navigate this with my wife and sons, and those closest to us – but without doubt, I will continue to embrace life and grasp opportunities in the same way I always have.
Sharing a post of their own on social media this morning, the Red Roses wrote: “Everyone at England Rugby is saddened to learn that former captain Lewis Moody has been diagnosed with Motor Neurone Disease (MND).
“All of our thoughts are with Lewis, his family and friends as they come to terms with this diagnosis. We will be offering both practical and emotional support, and know the entire rugby community will stand with them at this incredibly difficult time.
“We encourage people to show their support through the fundraising initiatives now being set up and available through GoFundMe.”
Sending our strength and support to Lewis Moody, as well as his family, friends and fans; you can donate to his fundraiser down below.