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Fighting Motor Neurone Disease with the Sheffield Scanner 

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We are working to raise £2 million to establish a ground-breaking MRI-PET facility. MRI-PET is the most advanced imaging technology to date, and will transform our understanding of serious conditions like Motor Neurone Disease (MND), cancer, dementia, heart and lung diseases, Parkinson's and stroke.
We spoke to Gemma Middleton, who is living with MND, and Professor Chris McDermott, about what the Sheffield Scanner will mean for the fight against MND.
Read the feature - www.youruniversity.group.shef....
www.sheffield.ac.uk/sheffield...
youruniversity.group.shef.ac.uk/
www.sheffield.ac.uk/alumni

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13 июл 2017

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Комментарии : 25   
@andymcgovern6615
@andymcgovern6615 3 года назад
Motor Neuron Disease. We hate the sight of you.! A Voice in the Wilderness. By Andy McGovern. MND survivor. The year 2020 will go down in history. The year when the whole world slowed down. A time when people took a step back, relaxed and stayed at home, spent more time with family. People gave thanks and appreciated all that they had. Please God if I'm spared, this will be my 87th Christmas on this earth. Those old eyes have seen it all, the good and the bad. I’m thankful that life has bestowed upon me a calm perspective. For 43 years I faced each day with Motor Neuron Disease. Many days I struggled desperately searching for my inner hero. Thankfully many more days were met with humour and laughter as I deeply appreciated the gift of another day on this earth. Not a day goes by that my thoughts don't turn to my fellow warriors as united we strive to raise awareness of our plight. Any opportunity presented will always find me campaigning for our cause. Over the past months I listened with interest as the COVID-19 crisis unfolded. I watched learned scientists chase the elusive 'cure'. I heard about the billions of dollars which were being channelled to find a treatment for this virus. A bottomless budget was available. I prayed that none of the 400 MND patients in Ireland would be inflicted by COVID-19. God knows we have enough to deal with. My thoughts turn to the late Fr Tony Coote, the desperate measure he had to take to secure the services of an extra nurse for our Association. Walking from Donegal to Cork. Surely something is not right here? MND is not a virus, it's a terminal disease. Should our association not warrant more than a mere 20% government funding which it receives? Do our people not deserve more? We lose three people each week to this disease. Many people here in County Leitrim have died in silence, victims of this horrible illness. Their families watch in horror, helpless as their loved one wastes away. Good men must never remain silent. As the Blessed season of Christmas arrives, I pray it's a safe, happy and peaceful one for you all. My greatest prayer is that our turn will come. One day soon the wise men will not forget us. Please God they will come from the East bringing with them gifts of treatment and a cure for this terminal illness. Motor Neuron Disease is not an incurable disease. It’s an underfunded disease. God bless you and a happy Christmas to all. Andy McGovern. MND survivor.
@taraalan1131
@taraalan1131 Год назад
Was it PLS you were diagnosed with? It’s a less savage form of MND. I was told I had MND . - PLS - because it was slower, but they discovered 3 yrs later that treatment for a childhood Neuroblastoma had caused a severe spinal injury , spastic Quadroparesis. It’s degenerative but thankfully slow.
@eoin4768
@eoin4768 10 месяцев назад
My Uncle Roy had MND and passed away a few months ago. And he told us about handless Andy .
@ghirlB
@ghirlB 2 года назад
God bless you Gemma
@TPGMarksman
@TPGMarksman Год назад
Such a beautiful brave lady. MND is a cruel disease and she’s so young to be going through such a life changing disease. I wish her all the best for the future
@rebeccaduboise285
@rebeccaduboise285 Год назад
I’m so sorry Gemma!😢
@sandrainacio1460
@sandrainacio1460 6 лет назад
its devastating :(
@harley9831
@harley9831 6 лет назад
I’m raising money to find a cure because my nannan died a few years ago with it so I want to find a cure so people and there family don’t have to go through what we went through
@WheelchairWarrior18
@WheelchairWarrior18 6 лет назад
BitMoreOfHarlz 😟😟
@worrynot8790
@worrynot8790 2 года назад
Bro your work is tremondous because if you help people for this disease they will give you wishes
@SonuKumar-gd9vm
@SonuKumar-gd9vm Год назад
@@worrynot8790 th7do by by sending for ash PE UDZs
@SonuKumar-gd9vm
@SonuKumar-gd9vm Год назад
@@worrynot8790 for h hi igydif
@candacemurry637
@candacemurry637 6 лет назад
My mom was diagnosed in November. This diagnosis is literally killing me. Over a years time she has almost completely lost her ability to speak. My entire family including my mom are devastated.
@debbie1060
@debbie1060 3 года назад
Lots of love 💞 my dad passed away last November from MND. I understand u completely. 😥
@candacemurry637
@candacemurry637 3 года назад
@@debbie1060 thanks for responding..it was really hard. Sorry for your loss. My mom died this July 2020. We are heartbroken 💔. Take care
@suessosimplesogoodrecipes5410
@suessosimplesogoodrecipes5410 3 года назад
@@debbie1060 so sorry for your loss Debbie. My niece was just diagnosed. Big hug to you. Take care.
@suessosimplesogoodrecipes5410
@suessosimplesogoodrecipes5410 3 года назад
@@candacemurry637 sorry for your loss Candace. My niece was just diagnosed a few months ago. I'm trying to learn all I can in hopes of relieving just a bit of her discomfort. I hope you're healing and able to smile finally when you think of your sweet mom. Blessings to you. =)
@stewartboyd3128
@stewartboyd3128 2 года назад
I hear you. I lost my dad the same way.
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