Scott Beighton

Truly exciting times. The first ever England Women's Parkinson's #WalkingFootball trials & we need your help to spread the word! 📢 If you are a woman with #parkinsons and inspired to support our community, get in touch #WomenInSport #Lionesses #EnglandTrials #Benniman

@LivStrachan23 @ParkinsonsUK Amazing, sorry i couldn't get there.

WHAT A DAY! 🚶‍♀️ 🐶 🚶🏼 We walked… and walked… and walked… 8ish miles around Carsington water! Everyone made it round!! Amazing work! Still time to donate via the link below! Let’s get £1000!!!! justgiving.com/page/walkforpa… Thank you for everyone support @ParkinsonsUK

Ozzy speaks to all his fans. I'm not crying 🥹🥹. Rest in peace legend.

RIP Ozzy Osbourne (1948 – 2025). As a global rock icon, Ozzy inspired millions with his music, but even more profoundly, he moved the Parkinson’s community by bravely sharing his diagnosis and becoming a pioneer in the conversation around advanced therapies, including stem cell treatments. His transparency gave hope to countless individuals and families navigating this challenging journey. I am grateful for his courage, candor and commitment to progress in Parkinson’s research. We honored his story and explained the type of Parkinson's he had (PARKIN gene) in the publication The Conversation which can be read at: theconversation.com/ozzy-osbourne-…. Thank you Ozzy, you made a huge difference in the lives of many people. @FixelInstitute @ParkinsonDotOrg @OzzyOsbourne

@FionaLindop @ParkinsonsEN @UHDBTrust Great to see you still fighting our corner. Thankyou.

Fantastic to be highlighting the work of @ParkinsonsEN in Parliament today and to see the @UHDBTrust Parkinson’s PRAIS (rapid response therapy) team who were pump primed by @ParkinsonsEN featuring !

Stuart Langworthy from @thewfauk explains the need to be active with #Parkinsons & why events such as our upcoming Sport Parkinson's Try-Athlon are not just about the sport being played, it's about being together in a safe and supportive comunity. @ParkinsonsUK @CureParkinsonsT

We couldn't say it better ourselves!Our Sport Parkinson's Try-Athlon 2025 is not only about the 'trying' of new sports & activities,it's about being amongst others who feel the same. sportparkinsons.com/events/try-ath… @ParkinsonsUK @CureParkinsonsT @SpotlightYOPD #Parkinsons #community

@LivStrachan23 @DCCTOfficial @dcfcofficial @ParkinsonsUK @SportParkinsons @thewfauk Amazing job everyone.

Great session yesterday! Seeing lots of improvements in everyone’s abilities and confidence! Next Session Saturday 28th June 3-5pm Moor Farm Training Ground, Oakwood @DCCTOfficial @dcfcofficial @ParkinsonsUK @SportParkinsons @thewfauk #parkinsons #walkingfootball

@ApeTrooper_USA @krassenstein Yes I do know the meaning . And I just love it when people start getting perso al, I imagine you were one of the ones who thought drinking bleach for covid was a good idea!

@ScottBeighton @krassenstein That doesn't even make sense. This information is public and easily verifiable, genius. I don't think you know what the term "insider trading" means.

A resignation?!?

@ApeTrooper_USA @krassenstein Amazing for those insider trading.

Will you ever give Trump credit for anything? 🔴The stock market just went on a nine-day winning streak, the longest since 2004 and only the 27th time in 100 years. 🔴The S&P500, NASDAQ, DOW JONES are up 6% or higher from one year ago today. 🔴Inflation is at a four year low. 🔴The U.K. signed a trade deal that is great for America, it will benefit American farmers and the agricultural sectors immensely. 🔴The Trump administration helped to orchestrate a ceasefire between two nuclear nations. Why can't you be honest and give Trump credit for any of this?

@FionaLindop @ParkinsonsEN You will be missed Fiona.

I'm retiring from the NHS at the end of June (but will still be teaching nationally and involved in research) and also retiring from my role as Clinical Lead for Therapy for @ParkinsonsEN- Recruitment now open for CLT post: parkinsons.org.uk/professionals/…

@jonny_acheson With me it's part of my ASD diagnosis. I learnt to look at people so either just behind the person or at the ears/nose. I can't stand looking straight at someones eyes.

Has anyone ever noticed that when you talk to people with #Parkinsons they don’t always make eye contact. I am aware that I do this but have no idea why? Perhaps it helps me to concentrate on what I am saying or about to say. Would welcome your thoughts and experiences.

Nice one Joe well deserved!

@JoeGregory100 @DCCTOfficial @LivStrachan23 @SportParkinsons @CureParkinsonsT @dcfcofficial @ParkinsonsUK Thankyou Joe.

@ScottBeighton @DCCTOfficial @LivStrachan23 @SportParkinsons @CureParkinsonsT Well done Scott, and to Liv, Wilko and all at @DCCTOfficial @dcfcofficial 🐏🤍🖤⚽ Really pleased for you all in how far you've come so soon... ⚽🥅 @SportParkinsons @ParkinsonsUK @CureParkinsonsT #Parkinsons #WalkingFootball

St George's park Parkinsons walking football competition. Amazing day with the @DCCTOfficial Derby team. Huge thanks to @LivStrachan23 @SportParkinsons @CureParkinsonsT and so many others for your support and help.

@LivStrachan23 @DCCTOfficial @dcfcofficial Great day. Thanks to everyone involved.

@DCCTOfficial @dcfcofficial Squad of 10 today - first time here today! What an inspirational day! 1 more game to go! 🏆

Annie and Caroline of Parkinson’s Pioneers Women’s Walking Football Community tell us why movement is important and also how their club was founded ⚽️ #parkinsonssupport #MovementIsMedicine #communitysupport #communitysupport #womensupportingwomen #WomenInFootball

@JoeGregory100 @CureParkinsonsT @ParkinsonsUK @ParkinsonsEN @ParkinsonsENEx @PDwarriorBristl @SportParkinsons Awesome, if you ever fo another one country me in!

#ParkinsonsAwareness week 2 years ago... #ToughMudder with people living with #Parkinsons Another great adventure, with many, many more still to come... 🚶🏻🚶🏾‍♀️👨🏽‍🦯🏃🏽‍♂️👨🏽‍🦽🚶🏼‍♂️🏃🚶🏿‍♀️🤸🏿‍♀️ @CureParkinsonsT @ParkinsonsUK @ParkinsonsEN @ParkinsonsENEx @PDwarriorBristl @SportParkinsons

A significant number of people with Parkinson's, potentially 1 in 3, feel the need to hide their symptoms or diagnosis, often due to stigma and fear of social repercussions. What is your experience with this? 👇🏽