Fiona Lindop MBE

Fiona is a specialist physiotherapist in Parkinson's and Clinical Therapy Lead for Parkinson’s UK Excellence Network. Views are my own.

[The PSP Association @PSPAssociation]

#Health & social care professionals: Join us in #Aberdare, South Wales on Fri 3 July for our free PSPA Awareness Event! Learn to spot signs of PSP & CBD, understand progression, and explore support. Hear from our Helpline Care Navigator, Dionne. Book free: https://t.co/41hL5CEEmt

[Fiona Lindop MBE @FionaLindop]

@jonny_acheson @WorldPDCongress Delighted to hear this! Just the right place for it to be on sale!!

[The PSP Association @PSPAssociation]

Want to boost your team’s PSP & CBD knowledge? Our Helpline Care Navigators offer short, interactive sessions—online or in-person—for #health & social care professionals. Learn about symptoms, causes, progression & support. Contact: 0300 0110 122 or [email protected]

[The Neurological Alliance @NeuroAlliance]

TODAY with 35+ orgs we launch our call for a Modern Service Framework for neurological conditions. The government has already committed to some MSFs. Now we need the same commitment for the 1 in 6 people living with a neurological condition. Learn more https://t.co/o5Bw1aIqpT

[The PSP Association @PSPAssociation]

Corticobasal Degeneration (CBD) is even rarer than PSP. Professor Huw Morris shared the main symptoms of CBD and what to look out for when trying to diagnose the condition. You can watch the video here: https://t.co/M31tTrGBek. #CorticobasalDegeneration #CBD #Neurology

[The PSP Association @PSPAssociation]

Health & social care professionals: Join us in #Stirling for a free PSP & CBD #Awareness Event on Thurs, 18 June at 1:45pm! Learn to recognise symptoms & support those affected. Book your free ticket: https://t.co/GuE9Ij2Lag #PSP #CBD

[The PSP Association @PSPAssociation]

📣 Neuro2026 Call for Abstracts is OPEN! Share your #research on PSP, CBD, or related # tauopathies/proteinopathies. Submit studies, QI projects, or case reports by 30 June. 🔗 More info & submit: https://t.co/PoBqmSsqpC #Neuro2026 #PSP #CBD #MedicalResearch #NeuroScience

[The PSP Association @PSPAssociation]

New research part-funded by PSPA highlights the importance of spotting early PSP symptoms. Our Eye Red Flags poster helps Opticians identify changes in eye movements, eyelids and fixation. Download & share: https://t.co/AAnNYs3jAX #PSP #Optometry #EyeHealth #EyeCare

[Fiona Lindop MBE @FionaLindop]

Great new video from Moving Medicine helping to encourage physical activity for everyone - it really can help so many symptoms of lots of conditions (especially Parkinson's!)https://t.co/aGi5qf5ndO

[Chartered Society of Physiotherapy (CSP) @thecsp]

📢 Physiotherapy is on Westminster's agenda on Thursday 23 April.

Ask your MP to attend the debate on the AHP workforce.

This is a key opportunity to raise the profile of physiotherapy.

📨 Invite your MP - more info https://t.co/BknXWroulK

[Liv Strachan @LivStrachan23]

Living with Parkinson’s doesn’t mean missing out. It means finding new ways to connect, feel good, and stay empowered. Join us for a relaxed, welcoming evening designed especially for younger women, where you can share experiences, build friendships, and take time for you.

[The PSP Association @PSPAssociation]

🎟️ Tickets are now available for Neuro2026! Join us and @CurePSP for the PSP & CBD International Research Symposium, 5–6 Nov 2026 at Hilton Bankside, London. Hear from global experts and discover the latest in PSP & CBD research. Book now: https://t.co/oAiwxUS0U9 #Neuro2026

[The PSP Association @PSPAssociation]

Primary #healthcare professionals: After our #cognition masterclass, download our #guide on Cognition in PSP & CBD. It covers condition presentation, cognitive impact, and assessment tips. Share with colleagues to help raise awareness! Download: https://t.co/thsCMfvHYV

[The PSP Association @PSPAssociation]

Supporting families affected by PSP & CBD in Northern Ireland? We’re considering a new online support group and want their input! Please share this meeting and encourage them to attend on Tue 14 April, 11am–12:30pm. To attend, email [email protected]

[Fiona Lindop MBE @FionaLindop]

@jonny_acheson And you’re still an absolute inspiration!

[Parkinson's UK @ParkinsonsUK]

Over half of people living with Parkinson's may experience freezing. It can happen at any stage, but is most common in advanced Parkinson's.

But you're not alone. For more information and advice, visit: https://t.co/mTvsNkNktX

[Jonny Acheson @jonny_acheson]

‘Access to healthcare easily - that's what we need’

24 NHS professionals living with Parkinson’s share their powerful collective message: ADAPTS WELL. From diagnosis to the Equality Act, hear why hope and proactivity are non-negotiable

https://t.co/KpbOx9zii9

#Parkinsons #NHS

[Fiona Lindop MBE @FionaLindop]

@jonny_acheson Such a powerful message! And so necessary!!

[Neurology Academy @TheNeuroAcademy]

Together with the @MSAtrust we’ve launched an online course for all #healthcareprofessionals who work in #neurology or with neurological patients and would like to learn more about #multiplesystematrophy (MSA) management and care: ➡️ https://t.co/VNz9TgsaZW

#MSAawarenessmonth

[Parkinson's UK @ParkinsonsUK]

We are so sad to hear of Dame Jenni Murray’s passing. She was a devoted advocate for people living with Parkinson’s, her support helped raise awareness across the UK and shone a light on the challenges faced by families affected by the condition.