Jim dreams of flying | Short film about ParkinsonsParkinsons UK2026-09-18 | Jim dreams of flying | Short film about ParkinsonsThe Parkinsons Virtual Biotech: hope for treating dyskinesia (NLX112)Parkinsons UK2024-01-09 | Dr Arthur Roach, Director of the Parkinson’s Virtual Biotech at Parkinson's UK, and Dr Adrian Newman-Tancredi, CEO and Co-founder of Neurolixis, discuss a pioneering partnership that has led to hopeful results from a clinical trial of NLX112. For more information, visit parkinsons.org.uk/virtualbiotechThank you for supporting Parkinsons UK in 2023Parkinsons UK2023-12-13 | A special thank you message from Parkinson's UK and a look back on all of the incredible highlights and achievements that our supporters made possible this year. We can't do it without you.
Thank you for supporting the Parkinson's community in 2023.New research for better treatmentsParkinsons UK2023-11-08 | The gift we all want is a cure and new treatments for Parkinson's. Pioneering research projects are getting us closer to a day without Parkinson's.
We're working with scientists across the country, finding, developing, and funding pioneering research projects.
Help get us closer to a day without Parkinson's. Make a donation today at parkinsons.org.uk/get-involved/support-research-breakthroughsThe Parkinsons Virtual Biotech and the Parkinsons Foundation: a strategic partnershipParkinsons UK2023-10-18 | ...Listening in on a conversation - hear from a leading Parkinsons scientistParkinsons UK2023-09-03 | Dr Dayne Beccano-Kelly studies communication between brain cells using research models of Parkinson’s. His team are aiming to decipher how miscommunication arises at the earliest stages of Parkinson’s, and find new ways of correcting it before significant loss of cells in the brain, and symptoms appear.
In this interview he talks about his research and why meeting with the Parkinson's community is so important.Walk for Parkinsons - 2023Parkinsons UK2023-08-11 | Walk for Parkinson’s raises money for research into new treatments and a cure. Find a walk to get active, meet people and fund life-changing research.
There’s no cure for Parkinson’s yet. Help us move closer by joining a walk near you. parkinsons.org.uk/get-involved/walk-parkinsonsJon Goodwin, Virgin Galactic Astronaut 011Parkinsons UK2023-08-10 | Best wishes from us all at Parkinson's UKStories from the WPC: Episode 3Parkinsons UK2023-07-28 | In this final episode, Kimberly, Nick, Sophie and Shafaq meet David Sangster in Barcelona to reflect on the World Parkinson Congress. David also shares some sights and sounds from the #wpc2023 including Jonny Acheson’s keynote address on science, research and the Basílica i Temple Expiatori de la Sagrada Família.Stories from the WPC: Episode 2Parkinsons UK2023-07-20 | Kimberly, Nick, Sophie and Shafaq share their experience of air travel and special assistance at the airport. They also tell us what’s in their bag, as they pack for Barcelona.Stories from the WPC: Episode 1Parkinsons UK2023-07-19 | Meet Kimberly, Nick, Sophie and Shafaq. Filmed a week before the World Parkinson Congress 2023, diagnosed with Parkinson’s at a relatively young age, they share their expectations about the Congress in Barcelona.Gardening with Parkinson’s - Roger and Jenny BatemanParkinsons UK2023-07-11 | The National Garden Scheme have been supporting Parkinson's UK since 2012. In that time they have donated £1.75 million to support people living with Parkinson's.
In this film Roger and Jenny Bateman talk about their love of gardening and how this has benefited Roger deal with many of the symptoms of Parkinson's that he now experiences following his diagnosis.What Parkinsons and Pride mean to me: Ians storyParkinsons UK2023-06-27 | Ian, who has Parkinson’s, is a member of the London Gay Men’s Chorus. As they prepare for their upcoming concert, Proud, Ian tells us what being ‘proud’ means to himYou are not alone - Davids story with ParkinsonsParkinsons UK2023-05-17 | "Every day in my life is different. Learning to manage Parkinson’s has been a challenge and I would most certainly have struggled without the support from Parkinson’s UK, my local nursing team and a Parkinson’s and dementia group."
David is 59 and from Tameside. He first noticed symptoms in 2012 but it was not until 2015 when he was finally referred to a specialist that Parkinson’s was diagnosed. This is his story.Could Parkinsons begin in the gut?Parkinsons UK2023-05-09 | Researchers believe that sticky clumps of alpha-synuclein travel from the gut to the brain using the vagus nerve, and form Lewy bodies. Can you give what you can, to keep Professor Spillantini’s research moving forward?
Living with Parkinson's is tougher than people think. But it doesn’t define you. You are still you. You can still do amazing things in spite of Parkinson’s.
Parkinson’s is different for everyone. Different symptoms, different experiences. Diagnosis is scary and there’s currently no cure. Living with Parkinson’s can be challenging but one thing stands out. The Parkinson’s community is bright and brilliant.
Thank you to everyone who helped us shine a light on Parkinson's! 💙High Intensity Workout with Neuro Heroes | Parkinsons UK |Parkinsons UK2023-04-17 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Feeling good and up for a challenge Neuro Heroes really put you through your paces with this workout!
Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exerciseHigh intensity workout with Reach Your Peak | Parkinsons UK |Parkinsons UK2023-04-17 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Break a sweat and lift your mood with Reach Your Peak!
Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exercisePoetry by people with Parkinsons - for World Parkinsons DayParkinsons UK2023-04-11 | We’re shining a light on Parkinson’s. This is a poem by people with Parkinson’s for World Parkinson's Day.
With thanks to the Parkinson's community for the poem and all those featuring in the film, additional clips from Owen Scurfield and Brett NewCarol reads a poemParkinsons UK2023-04-11 | Carol reads a poem written by someone in the Parkinson’s community. She shares how it reminds her of her husband.
Want to tell your Parkinson’s story in a poem? Learn more and take part in World Parkinson’s Day: parkinsons.org.uk/get-involved/world-parkinsons-dayFeaturing poems across the UK: Mark’s storyParkinsons UK2023-04-11 | Mark Catterall is CEO of Smart Media Group. His company donated digital advertising space to display poems from the Parkinson’s community across the UK. He was instrumental in getting other companies to do the same. He talks about this amazing support, what it means to him and his own Parkinson’s journey.
Want to tell your Parkinson’s story in a poem? Learn more and take part in World Parkinson’s Day: parkinsons.org.uk/get-involved/world-parkinsons-dayPoems for Parkinson’s in SunderlandParkinsons UK2023-04-11 | Poems for Parkinson’s comes to Sunderland. Listen to some poetry and hear the thoughts of people in the Parkinson’s community.
Want to tell your Parkinson’s story in a poem? Learn more and take part in World Parkinson’s Day: parkinsons.org.uk/get-involved/world-parkinsons-dayModerate intensity workout with Neuro Heroes | Parkinsons UK |Parkinsons UK2023-04-10 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Let Neuro Heroes push you today with this energetic workout. Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exerciseLow Impact Workout with Reach Your Peak | Parkinsons UK |Parkinsons UK2023-04-03 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Looking for a low impact workout? Reach Your Peak have a fantastic session right here.
Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exerciseLow to Moderate intensity workout with Neuro Heroes | Parkinsons UK |Parkinsons UK2023-03-27 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Parkinson's UK worked with Neuro Heroes to create this low to moderate intensity workout.
Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exercisePeople with Parkinson’s can’t wait for better careParkinsons UK2023-03-22 | People with Parkinson’s can’t wait. Can’t wait for appointments. For mental health support. For medication.
We need your help to make sure people with Parkinson's get the care they need. We’re starting with access to the right doctors, nurses, and other healthcare professionals.
We want NHS England to have a plan that allows people with Parkinson’s to access consultants, nurses, physiotherapists, mental health professionals, speech therapists and occupational therapists. And we’re calling on new local integrated care boards (ICBs) to do that.
Join our campaign to improve Parkinson's care parkinsons.org.uk/get-involved/cant-waitChair Workout with Reach Your Peak | Parkinsons UK |Parkinsons UK2023-03-17 | Whether you have Parkinson's or live with someone who does, there is no one-size-fits-all approach. But being active can help manage Parkinson’s symptoms, and has a positive impact both physically and mentally.
Parkinson's UK worked with Reach Your Peak to create this chair based workout.
Find out more about physical activity and exercise with Parkinson's parkinsons.org.uk/information-and-support/exerciseLiving positively with Parkinsons - Tizzys StoryParkinsons UK2023-02-22 | "I've noticed a huge difference in myself physically and mentally because I do so much exercise".
Tizzy was diagnosed aged 25. Exercise, a positive attitude and being open about the condition are what keeps her going.
If you or someone you know needs any support or advice we're here for you. Visit parkinsons.org.uk/information-and-support to find out more.My friends and family support me with Parkinsons - Darshas storyParkinsons UK2023-01-31 | "They've been incredible supportive, they've been with me through thick and thin. We all lean on each other." Darsha feels lucky to have such a fantastic network of friends and family around her, but there are so many ways you can access support from within the Parkinson's community.
If you or someone you know needs any support or advice we're here for you. Visit parkinsons.org.uk/information-and-support to find out more.Living my life with Parkinsons - Simons storyParkinsons UK2023-01-24 | Simon is 41 and was diagnosed with Parkinson's 6 years ago. The news was life-changing, but Simon's adapting and learning that life hasn't got to stop. "You have to take each day as it comes and don't let it get you down," he says.
If you or someone you know needs any support or advice we're here for you. Visit parkinsons.org.uk/information-and-support to find out more.Parkinsons, DBS and Me - Episode 12: New BeginningsParkinsons UK2022-12-19 | In the final episode of DBS and Me, Jo reflects on life after deep brain stimulation. Just 10 weeks after her surgery, she can go out for dinner, put eyeliner on, and even forget she has Parkinson’s for a moment. Jo has her life back.
Thank you to the Newcastle Upon Tyne Hospitals NHS Foundation Trust and South Tees Hospitals NHS Foundation Trust for supporting our DBS and Me series. Also thanks to David Sangster for original music and the volunteers who helped with the series.
You can continue to follow Jo’s Parkinson’s journey on Instagram at @ladyduffgordon
And share Jo’s story using the hashtag #DBSandMeParkinsons, DBS and Me - Episode 11: The Follow UpParkinsons UK2022-12-12 | A month after her surgery, Jo visits her surgeon and a specialist nurse to have her DBS device programmed for the first time. She knows it won’t be an immediate fix for her symptoms, but believes it will be worth it in the end. __________
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
It’s been a long and complex journey, full of ups and downs, but the day of Jo’s deep brain stimulation surgery is finally here. __________
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit parkinsons.org.uk/information-and-support/dbs-and-meParkinsons, DBS and Me - Episode 9: Meet the SurgeonParkinsons UK2022-11-28 | After a bit of a break, our DBS series is back. In episode 9, Jo meets the surgeon that might perform her deep brain stimulation (DBS) surgery. She’s anxious and full of questions, but hopeful that she can have the treatment. __________
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit parkinsons.org.uk/information-and-support/dbs-and-me.How my Mum having Parkinsons has influenced my artParkinsons UK2022-11-24 | A group of world-class artists have come together to contribute to Me, My Brain and I, a collection of sculptures portraying what their brain means to them.
One of the 14 artists involved is D*Face, who chatted with us about why this project and charity are important to him, and what inspired his sculpture 'Brain Freeze'.
This is why we are working with scientists across the country, finding, developing and, crucially, funding Parkinson’s research.
If everyone gave £25, it would help to keep more projects like these on track. Your donation will help us get new ideas off the ground. Find out more parkinsons.org.uk/get-involved/support-research-breakthroughsParkinsons awareness raising in Central London - Me, My Brain and IParkinsons UK2022-10-31 | A group of world-class artists have come together to contribute to Me, My Brain and I, a collection of sculptures portraying what their brain means to them. Above the exhibition of the artworks, we took over the giant screen at Piccadilly Circus, in the heart of central London, to raise awareness of the condition.
The exhibition includes the likes of Tracey Emin, David Bailey, D*Face, Alex Echo and LUAP and will be on display at the inspiring Koppel X space in Piccadilly Circus. The pieces will then go under the hammer at the renowned Christie's auction house.
Find out more events.parkinsons.org.uk/event/me-my-brain-and-i/homeIm a Black Parkinsons scientist - why diversity in research mattersParkinsons UK2022-10-26 | Dr Dayne Beccano-Kelly is a Group Leader at the UK Dementia Research Institute at Cardiff University, and a UKRI Future Leader Fellow. In this film for Black History Month, he talks about the importance of diversity within Parkinson's research, his own experience of being a Black scientist and why he's passionate about helping people from under represented groups become research scientists.Parkinsons and bone healthParkinsons UK2022-10-14 | Keeping bones healthy is important for everyone and especially important for people with Parkinson’s. We share some top tips for keeping your bones in tip top condition.
Shafaq was diagnosed at 40. Weekly exercise and successive crochet projects keep her busy and help manage her symptoms. In this film, she shares her mindset and how she moved forward after diagnosis.
If you or someone you know needs any support or advice we're here for you. Visit parkinsons.org.uk/information-and-support to find out more.Parkinsons, DBS and Me - Episode 8: Decision DayParkinsons UK2022-09-20 | In episode 8, Jo awaits the decision from the multi-disciplinary team meeting, where health care professionals discuss individual patient cases. After a long period of uncertainty, Jo hopes she will finally know if she’s suitable for deep brain stimulation surgery.
We’re taking a short break in our DBS and Me series while we put together the next few episodes. Find out more about the series parkinsons.org.uk/information-and-support/dbs-and-meYou can help fund the Parkinsons UK Brain BankParkinsons UK2022-09-01 | Find out more about the Parkinson's UK Brain Bank and the groundbreaking research it has undertaken since 1984.
You can help fund it parkinsons.org.uk/get-involved/support-research-breakthroughsGardening and Parkinsons - Celebrating 10 years of support from the National Garden SchemeParkinsons UK2022-08-17 | The National Garden Scheme has been supporting Parkinson's UK since 2012. They have donated £1.5 million in that time to help drive better care, treatments and quality of live for people with Parkinson's.
In this stunning film, Brian tells his story of living with Parkinson's and how gardening has benefited him.
Find out more parkinsons.org.uk/get-involved/national-garden-scheme-partnershipParkinsons, DBS and Me - Episode 7: A Mothers StoryParkinsons UK2022-08-15 | In episode 7, Jo’s mum talks about what it’s like when your daughter has Parkinson’s. At first, deep brain stimulation sounded scary. But now, she desperately hopes that Jo can have the surgery.
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit parkinsons.org.uk/information-and-support/dbs-and-me.Parkinsons, DBS and Me - Episode 6: Psychological TestParkinsons UK2022-08-01 | In episode 6, Jo reflects on her experience of the psychological test - the final assessment needed to make sure she’s suitable for deep brain stimulation surgery. She’s tired, but relieved that her work is done. The final decision is in someone else’s hands.
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit parkinsons.org.uk/information-and-support/dbs-and-me.Parkinsons, DBS and Me - Episode 5: Levodopa TestParkinsons UK2022-07-18 | In episode 5, Jo goes for the first of her assessments to see if she’s suitable for deep brain stimulation surgery. She’s anxious and off her medication, but full of hope.
Some people may find parts of this episode upsetting. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.
To find out more about DBS and Me, visit parkinsons.org.uk/information-and-support/dbs-and-me.Parkinsons, DBS and Me - Episode 4: TiredParkinsons UK2022-07-04 | In episode 4, Jo talks about the challenges of living with a chronic condition. Parkinson’s means she won’t get better, but DBS has given Jo hope that, to some extent, she will feel better.
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.Parkinsons, DBS and Me - Episode 3: Dr ArchieParkinsons UK2022-06-20 | In episode 3 of our video series, Jo visits her Parkinson’s specialist to find out more about how deep brain stimulation works. Having initially being concerned about the surgery, Jo increasingly feels this treatment is the closest she’ll get to a cure. __________
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.Together we CAN find a cure.Parkinsons UK2022-06-08 | Parkinson’s is the fastest growing neurological condition in the world. It can lead to a lot of can’ts.
As Europe’s largest charitable funder of Parkinson’s research, we can change that. We can discover new treatments. Can find new therapies. Can improve understanding of the condition. Can improve lives.
Our pioneering movement is powered by you. You can fund research breakthroughs. Make a real difference for people with Parkinson’s. Now.
We can find a cure. But we can’t do it without you.
Visit our website now: prksn.uk/3wAB9HWParkinsons, DBS and Me - Episode 2: The BeachParkinsons UK2022-06-06 | In episode 2, Jo talks about her experience with Parkinson’s, how her life has changed, and why deep brain stimulation (DBS) could be the light at the end of the tunnel for her and her family. __________
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.Parkinsons, DBS and Me - Episode 1: The PierParkinsons UK2022-05-23 | In the first episode of our DBS and Me series, Jo shares the shock of her Parkinson’s diagnosis and the impact of her symptoms. Deep brain stimulation could change her life. It’s not a cure, but Jo feels like it’s all she’s got. #DBSandMe
This is Jo’s story. We know Parkinson's affects everyone differently. If you have questions or need support, get in touch with us on 0808 800 0303 or hello@parkinsons.org.uk.