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Post by socrates on Sept 8, 2022 16:05:27 GMT
Awful news , i loved watching Stewy when he broke in to the first team back at Twerton he was fantastic and had a great career. Coincidentally Lead Belly who sang Goodnight Irene also had MND.
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Post by clockendgas on Sept 8, 2022 16:25:17 GMT
Very sad to hear this news,like other mention his goals during the twerton period gave me great memories, hundred percent the gas family will support a gas legend.
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Post by bidefordgas on Sept 8, 2022 16:41:51 GMT
Very sad news. All the best to Marcus and his family.
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Post by Gas-Ed on Sept 8, 2022 16:47:53 GMT
One of my all time faves. I grew up as a kid on the terrace at Twerton and Stewart was my idol.
Best wishes Marcus and family.
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Post by Gashead73 on Sept 8, 2022 17:03:15 GMT
I lost a girlfriend to this disease. It gets you gradually bit by bit and day by day. She was diagnosed about 10 years ago. It was heartbreaking watching her decline. She died last September R. I. P Donna
My sincerest and heartfelt wishes to the Stewart Family. I don't know what else to say.... I'm in tears
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Post by Colyton Gas on Sept 8, 2022 17:08:35 GMT
When he came out for an early kickabout before we played at Gresty Road once,I was there early and reminded Marcus,'Hey Marcus,you didn't score here last Season'.He was very modest,pleasant and approachable and scored in that game to put it right!!!! Assistant of course to DC and always conducted himself with great dignity.
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Post by allgasandgaiters on Sept 8, 2022 18:46:29 GMT
Terrible news. I’ve had two good friends die from MND in their 50s. It’s a b*gger of a disease. All thoughts to Stewie and his family. One of our greats. UTG.
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Post by fintanstack on Sept 8, 2022 19:01:25 GMT
Sad news.
Wish him and his family good luck.
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Post by SleepyGas on Sept 12, 2022 17:39:14 GMT
Nice gesture
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Post by Squiffy on Sept 21, 2022 22:33:50 GMT
I just read this article on the Beeb news app. I know that it is only effective for a very small number of patients but it does show that research into MND is making some progress. Fingers crossed 🤞 'Truly remarkable' drug helps motor neurone disease www.bbc.co.uk/news/health-62851186
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Post by daniel300380 on Sept 22, 2022 8:44:40 GMT
I just read this article on the Beeb news app. I know that it is only effective for a very small number of patients but it does show that research into MND is making some progress. Fingers crossed 🤞 'Truly remarkable' drug helps motor neurone disease www.bbc.co.uk/news/health-62851186Hopefully they keep making breakthroughs. It's hard as they don't even know what some of the faulty genes are for a lot of the cases, so not everyone can be tested, to see if they will get the disease. My wife and her sister have a 50/50 chance of getting it. Then if they get it, thier children have a 50/50 chance of getting it! Just have to hope they don't.
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Post by Kingswood Polak on Sept 22, 2022 9:49:59 GMT
Absolutely broken up upon hearing this. I lost a close friend to this so my only additional comment is that he has sensible medical people treating him and that they show some heart and i say this because my friend did not. I will not go into the detail as it’s still too painful for me and probably not a place to write such things. Make no mistake, this is the stuff of your worst nightmares. I can only hope that medicine has come on since my friend died and that maybe some miraculous breakthrough happens. When i first read this i actually was physically sick. I cannot sympathise or empathise enough. God bless you Marcus
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Post by Kingswood Polak on Sept 22, 2022 9:54:35 GMT
I just read this article on the Beeb news app. I know that it is only effective for a very small number of patients but it does show that research into MND is making some progress. Fingers crossed 🤞 'Truly remarkable' drug helps motor neurone disease www.bbc.co.uk/news/health-62851186Hopefully they keep making breakthroughs. It's hard as they don't even know what some of the faulty genes are for a lot of the cases, so not everyone can be tested, to see if they will get the disease. My wife and her sister have a 50/50 chance of getting it. Then if they get it, thier children have a 50/50 chance of getting it! Just have to hope they don't. Spot on. This is another side to this in that his family will be offered genetic testing, i see no point in that personally because it could leave you in a perpetual cycle of fear. Fecking heartbreaking stuff.
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Post by gulfofaden on Sept 28, 2022 2:37:29 GMT
Just reflecting on this.
2 years ago my best lifelong friend ended his life. I was very close to him at the end. He was my hero in many ways. He lived the life I wanted to lead. He encouraged me to be the same. For a man who was literally at the top of his game to be dead 9 months later was horrifying. He had it all - beautiful woman, high paid job, respect, great looking, ability to travel. It was horrifying. (Just so you know - do not mess with benzodiazepines)
Now my other main hero in my younger life, Marky Marcus Stewart, my idol as a kid, is stricken down with a horrible illness.
All it shows is while we think we drive the bus, we do not drive the bus. Fate is random and makes no sense.
The next time you’re salty the neighbour has a better car, or someone else gets a promotion, remember it’s all on loan. One day they have to give it back.
Also it’s a call to make the most of every second. Look after those around you. You are always 60 seconds away from losing it and there’s no rhyme or reason to any of it.
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Post by kylegas on Sept 28, 2022 3:35:34 GMT
First player I ever got an autograph from, bless him he had to ask my dad how to spell Kyle haha I was a very young boy back then but still remember how nice he was to me in that moment, top man. Wish him and his family all the best
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Post by gashead1981 on Sept 28, 2022 6:34:34 GMT
I worked with a chap that developed it. Rob Kerslake was his name. A lovely lovely man who has a wonderful wife and 2 beautiful kids. Well respected by everyone who was a colleague of his, good at his job, kind and compassionate by nature.
Watching him waste away before your eyes was very sad and he was 44 when he passed in 2007. I
hope one day there is a cure for this awful disease.
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Post by Deleted on Sept 28, 2022 13:14:43 GMT
I worked with a chap that developed it. Rob Kerslake was his name. A lovely lovely man who has a wonderful wife and 2 beautiful kids. Well respected by everyone who was a colleague of his, good at his job, kind and compassionate by nature. Watching him waste away before your eyes was very sad and he was 44 when he passed in 2007. I hope one day there is a cure for this awful disease. Progress is being made. Recent news
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Post by gashead1981 on Sept 28, 2022 13:18:19 GMT
I worked with a chap that developed it. Rob Kerslake was his name. A lovely lovely man who has a wonderful wife and 2 beautiful kids. Well respected by everyone who was a colleague of his, good at his job, kind and compassionate by nature. Watching him waste away before your eyes was very sad and he was 44 when he passed in 2007. I hope one day there is a cure for this awful disease. Progress is being made. Recent newsI did see that. Along with Parkinsons and Frontal Lobe Demensia progress is being made all the time.
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Post by Deleted on Sept 28, 2022 13:26:36 GMT
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Post by Tilly's Thighs on Sept 28, 2022 13:31:35 GMT
Exeter City players supporting Marcus's fundraising at FGR last week. View AttachmentBrilliant to see this.
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