Karen Walker

[MDS @movedisorder]

Thank you to the outgoing founding Co-Editors-in-Chief of Movement Disorders Clinical Practice, @kailashbhatia and @mmerello, whose contributions in establishing and growing the publication have built a legacy for MDS. @MDCP_Journal @WileyNeuro https://t.co/R9j8v7WhJx

[ConceiçãoBettencourt @saobettencourt]

I am delighted to have presented our #dementia #epigenetics work at the 11th Westerberger Herbsttagung on the Perspectives of Molecular Neurobiology, Osnabruck. I look forward to new collaborations #Alzheimers #FTLD #research. @ARUKscientist
Bonus - London views on my return 👇

[The Neurological Alliance @NeuroAlliance]

The right care at the right time means people can stay healthy and live well for longer, whether this is completing day-to-day tasks, being able to socialize, or staying in education & work.

Ask your next MP to become a #NeuroChampion now: https://t.co/4UTUlBrDSn #GE2024🗳️

[Cat Hobbs @CatHobbs]

Here are YOUR PUBLIC SERVICES that 5 Prime Ministers have stolen in the past 14 years

Don't let them get away with it #bbcqt

[MSA Trust @MSAtrust]

We want to extend a massive THANK YOU to our incredible supporters who helped raise funds for the MSA community this May. We deeply appreciate your dedication to supporting the Trust. Without your enthusiasm we couldn't continue to provide our free support services.

[The Neurological Alliance @NeuroAlliance]

Please sign the Right to Rehab petition now and help make it mandatory that there is a rehabilitation lead and strategy in every hospital and health board. Thank you. #RightToRehab #RehabLegend

https://t.co/3Habc7JIBC

[Dr Viorica Chelban @VioricaChelban]

How cool is that! @clambert112358 Researchers transform Parkinson’s tremors into music | UCL News - UCL – University College London https://t.co/m3Gmjal1nV

[MSA Trust @MSAtrust]

Many families find solace in creating an online MSA Tribute Page. This can be a meaningful way to remember loved ones, while supporting a charity close to your heart - https://t.co/G6MWQaYZWQ

[The Neurological Alliance @NeuroAlliance]

We work together to support people with neurological conditions. We inform policy, raise awareness and support the improvement of services, coming together to campaign on shared issues. Find out more https://t.co/Lo0mmVnFfp #OneNeuroVoice

[MSA Trust @MSAtrust]

It is #MSAAwarenessWeek. Help us to spread awareness of this progressive neurological condition that affects around 3,300 people in the UK and Ireland.

Keep your eyes on our social media over the coming week for ways to get involved and please share our posts.

[Carol Bewick @BewickCarol]

What a massive impact this is having for research charities and research careers in the UK! From everyone @amrc and who will benefit- thank you

[The PSP Association @PSPAssociation]

Next week is #BrainAwarenessWeek. We are joining the UK Neurological Alliances to share
#OneNeuroVoice and raise awareness of organisations across the country that support people living with neurological conditions. Keep an eye out for our posts and get involved!

[Dr Viorica Chelban @VioricaChelban]

You can now catch-up with all the talks from our amazing presenters #MSAResearchSymposium at https://t.co/0aftwICPkw

[UCL Brain Sciences @UCLBrainScience]

Prof Henry Houlden leads the @IonSynapse lab at @UCLIoN and plays a key role on the @GenomicsEngland board for rare diseases as part of the 100,000 Genomes Project.

He explains what attracted him to research rare diseases ➡️ https://t.co/fgPFg48UPQ

#RareDiseaseDay

[MSA Trust @MSAtrust]

MSA is one of 6,000 recognised rare diseases in the world and today is #RareDiseaseDay.

This year's theme is Share Your Colours - Help us spread the word about MSA and the impact that it has on people diagnosed and their families by sharing this post or contributing yourself.

[The Neurological Alliance @NeuroAlliance]

💡Did you know that almost half of rare conditions are neurological?

On #RareDiseaseDay (29 Feb) we're proud to join @GeneticAll_UK to raise awareness and celebrate our incredible members who do so much to support people affected by rare neurological conditions!

[NCL_RareDisease @NCL_RareDisease]

... (part 2) - collaboration locally, with @NHIPartners @NewcastleHosps @NIHRNewcBRC , nationally @GeneticAll_UK @rarediseaseuk @ and internationally through @eurordis @irdirc @EJPRareDiseases @rarediseasesint and many more 💜#rarediseaseday

[IPPOSI @IPPOSI]

Today is #RareDiseaseDay2024. We'll be joining @RareDiseasesIE and @NI_RDP at Farmleigh in Dublin. "Looking to the Future for Rare Diseases" @roinnslainte. Join online at: https://t.co/RhhLPSmi93 #shareyourrare

[European Academy of Neurology @EANeurology]

With 300 million people worldwide living with rare diseases, #RareDiseaseDay calls us to unite for equity—ensuring accessible diagnosis, treatment, health, social care, and opportunities for every unique journey.

#EANeurology

[Karen Walker @KarenMSATrust]

#MSATRUST delighted to be at #Ratediseaseday in Dublin, listening to updates on Genome screening, plans for rare disease policy and meeting with European policy makers,