Trishna Bharadia BA(hons), MFPM(hon)

#HealthAdvocate #patientadvocate #patientengagement #multiplesclerosis #ms #chronicillness #patientleader BBC Strictly Come Dancing;DM 4 bookings;Views my own

[Jon Strum @RealTalkMS_jon]

https://t.co/rX4h9QG7PK What happens to MS during pregnancy? And what about after? We’re diving into the science + real-life planning with Dr. Riley Bove (@BoveRiley @UCSFHospitals @UCSF) on RealTalk MS.🎧
#MultipleSclerosis #WomensHealth #RealTalkMS

[MS Australia @MS_Australia]

Researchers from Griffith University are seeking participants with progressive MS for STOP-MS, a trial investigating the use of antiviral drugs to reduce progression of disability in MS.

The trial will be conducted at sites across Australia.

Learn more👉 https://t.co/Cahf6WwoeL

[MS Society Scotland @mssocietyscot]

Do you live in Ayrshire? Diagnosed with MS in the last 2 years, or waiting for answers?

Join our in-person event to pause, ask questions and connect with others who understand.

📆 Mon 1 June
🕟️ 4.30–7.30pm
➡️ https://t.co/PQFNeudpce

You don’t have to navigate MS alone 🧡

[Movers & Shakers: a podcast about Parkinson's @moversand6]

Not everyone is affected by the same #PD #symptoms, and our host Sir Nicholas Mostyn hasn't yet had to worry too much about Speech and Language #Therapy.

He tells us in the clip below his experience with his voice and advice for those keen to preserve theirs..

[MS Australia @MS_Australia]

🔬Help shape the future of MS research in Australia

The preliminary report of @MS_Australia's Research Program review is now available on the survey page, and your feedback will help shape the next phase of MS research in Australia.

Take the survey 👉 https://t.co/FH77Q0Qx8m

[Jon Strum @RealTalkMS_jon]

https://t.co/05NYZeBG7w 📊 MS doesn’t present the same way for everyone—and understanding that matters. Catch up with the latest RealTalk MS episode exploring real stories, real research, and real progress. 🎧
#MultipleSclerosis #RealTalkMS #MSResearch

[ECTRIMS @ECTRIMS]

🔎 Best of #ECTRIMS2025: Pathogenesis Highlight

A study of 10M+ US military personnel led by Prof. Alberto Ascherio shows higher Vitamin D levels strongly reduce MS risk in White individuals. In Black individuals, the effect was less pronounced, pointing to further biological mechanisms.

📌 Explore the full Pathogenesis Track in the Best of ECTRIMS 2025 Slide Deck.

Download here ➡️ https://t.co/SD3oOSE78I

#ECTRIMS2025 #MSresearch #MSPathogenesis

[MS Society UK @mssocietyuk]

Can you summarise your research in a 60-second ‘elevator pitch’?

We’re inviting PhD students and postdoctoral researchers to step in front of the camera for our first ever ECR video competition.

Submit your entry by 12pm on Tuesday 14 April.

Read more: https://t.co/ARzvQbofth

[Jon Strum @RealTalkMS_jon]

https://t.co/aX85uDWEni The 2026 ACTRIMS Forum reminded us that progress in MS comes from innovation and mentoring the next generation of MS researchers.

Catch up with RealTalk MS before the week starts. Listen wherever you get podcasts. 🎧
#MSResearch #RealTalkMS #MultipleSclerosis #ACTRIMS #ACTRIMSForum #ACTRIMS2026

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

It was great chatting to Emma Sutcliffe for an ISPEP (The International Society for Patient Engagement Professionals) PEP Talk! Available on podcast streaming channels and via the ISPEP hub.
https://t.co/DDs2hI57HV

[MS Society UK @mssocietyuk]

It’s important not to be hard on yourself if it’s hard to stick to goals.

Especially because living with MS can be unpredictable.

Meet Amy 👋 She tells us how the spoon theory has helped her be kind to herself 🥄 And to be flexible.

Read Amy’s story: https://t.co/rs9RrA6INy

[The Neurological Alliance @NeuroAlliance]

Government has extended the UK Rare Disease Framework. But with people with rare neurological conditions continuing to face delays to diagnosis, insufficient care coordination and poor access to treatment, this extension must be used widely
More at https://t.co/Qe5HozRNbo

[Jon Strum @RealTalkMS_jon]

https://t.co/IXy3fLs1Md Progression without relapses? PIRA can feel confusing—especially with a relapsing-remitting MS diagnosis. Dr. Stephen Krieger helps make sense of it on RealTalk MS. 🎧 #MultipleSclerosis #RealTalkMS @SKriegerMD

[The Evidence Base @TheEviBase]

How #AI-assisted screening can improve efficiency and accuracy in targeted literature reviews | @thermofisher https://t.co/CG1RBrdJdJ

[PxP @PxPHub]

At #PxP25, we hosted three unique sessions that weren’t recorded for our YouTube channel to create a safe space for open dialogue. Check out the anonymized illustrations from these sessions here, along with other artwork from this year’s conference:
https://t.co/HXtNIOHQR5

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

The recording for the Asian MS webinar "Exploring healthcare experiences of Black and South Asian people affected by MS" is now available to watch on YouTube! https://t.co/W2SJbPBS1r

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

@ParkinsonsUK @mssocietyuk I've heard it's the same with MS. Maybe something you could look into?

[MS Society UK @mssocietyuk]

🙌 Huge thanks to @katrinamurray71 for speaking up in Parliament this week on the need for faster diagnosis and better access to specialist MS care.

[Trishna Bharadia BA(hons), MFPM(hon) @TrishnaBharadia]

I just signed @PCR_News' petition calling for the Government to commit to a national prostate cancer screening programme for all high-risk men. Screening will save lives. Join me and add your name! #prostatecancer https://t.co/gakI190xYf

[MS Australia @MS_Australia]

The McDonald Diagnostic Criteria for MS have now been published, offering clinicians tools to support earlier diagnosis & improve health outcomes.

Adoption into clinical practice is expected to follow as awareness & access to diagnostic tools grow.
https://t.co/q9zp8DD16g