📢 Join the Lived Experience Expert Panel (LEEP) at @MS_Australia!
We’re seeking to diversify our LEEP to bring a range of expert insights that will shape our work in advocacy, research, policy, and more.
Apply today 👉 https://t.co/0Pi6s4Gq7a
📅 Deadline: 13 Dec 2024
Thrilled to have helped coordinate the launch of the Crisis Toolkit! This valuable resource, developed by researchers supported by @MS_Australia and @RedCrossAU, helps people living with a disability or chronic health condition create effective crisis plans.
Researchers supported by @MS_Australia with @RedCrossAU have updated tailored resources to help people living with a disability or chronic health condition create a crisis plan, known as the Crisis Toolkit.
Read more 👉 https://t.co/yXEQbDb8tX
#MS#MSresearch
MS Australia’s inaugural symposium, held in partnership with @Sydney_Uni's Brain & Mind Centre will advance our collective commitment to the Pathways to Cures research strategy.
📅 29 November 2024
📍 University of Sydney
🎟️ FREE
Register👉 https://t.co/usDY8d83ro
#MSresearch
MSBase is 20 years old!! and holds >110,000 patient records. Dedicated clinicians all over the world contributes data with >110 papers, many that have changed clinical practice. We are so grateful to all the supporters of our mission to improve the lives of people with #MS.
🎙️Thet Raw Nerve podcast: @DrJMorahan, and Dr Heidi Beadnall, neurologist and MS researcher at the @Sydney_Uni, sit down with @RohanGreenland, to preview the highly anticipated #ECTRIMS2024, starting this week — the world’s largest MS research congress!
https://t.co/YIKHZSMPGw
#Breaking: Two new papers published in MS Journal highlight the impact of global collaboration on research toward finding a cure for #MS!
➡️ Updated Pathways to Cures Roadmap
➡️ Global Research Landscape Analysis
Find out more 👉 https://t.co/hILtvOG3ob
#MSresearch
🎙️In today's episode of The Raw Nerve, we commemorate #NationalPainWeek & explore chronic pain & MS.
Panel members include @ChronicPainAus chair, Nicolette Ellis, @MS_Australia Advocate Deanna Renee & Dr Alice Saul from @ResearchMenzies.
Listen now 👉 https://t.co/NKnyuNiMs6
Attending the National Summit on Neurological Conditions at Parliament House was inspiring. Experts, policymakers, and advocates united to raise awareness and support for those living with neurological conditions 🧠. @NeuroAllianceAu@MS_Australia#CountUsIn
The Count Us In campaign aims to create meaningful change by raising awareness, advocating for policy reforms, and empowering people affected by neurological conditions.
Find out more 👉 https://t.co/Peoh1cgb2B
#CountUsInNeuro
#MEDIARELEASE: National Summit to demand action for millions of Aussies living with neurological conditions.
Despite being among the nation's top disease burdens, neurological conditions remain under-recognised and underfunded.
#CountUsInNeuro
https://t.co/XasCBHYuP9
The AMSLS is a study collecting data used to improve health outcomes for people with #MS. Participating involves completing surveys in the comfort of your own home.
Contribute to making real-life change now, in the lives of people with MS.
Learn more👉 https://t.co/9XRkQUwWwQ
The time to diagnose MS has improved, but we still have a way to go according to the #AMSLS. Better investment in research for earlier diagnosis is urgently needed! Huge thanks to @ResearchMenzies and our Lived Experience Expert Panel for their invaluable insights.
#MediaRelease: A new report has revealed the prolonged time to diagnose #multiplesclerosis (MS) and highlighted the urgent need for increased investment in #MS research and enhanced awareness of the disease.
#WorldMSDay#MyMSDiagnosis
https://t.co/I8Lyr87fJD
🎉 Huge congrats to Associate Professor @MasturaMonif for winning the Leonard Cox Award at the ANZAN ASM! 🏆 Established in 2000, this award honours early-career researchers in neuroscience. Mastura’s inspiring talk on her neuroimmunology journey was incredible! 🧠 #ANZAN2024
On the Raw Nerve this week, host @RohanGreenland sits down with #TheMay50K Community Manager Sophie Drummond & @TLukerPhD to discuss the importance of The May 50K & some of the exciting MS research projects that benefit from funds raised.
👂Listen now 👉 https://t.co/UuezYKfjDS
Just over a week until The May 50K kicks off! 🥳 Excited to hit the pavement for 50km, all to fuel MS research. 🏃♀️👟 Join me in supporting this vital cause by donating here! 💪 Let's make strides together towards a world free of MS. ❤️https://t.co/Vv69zCtaAB
MS Australia-supported researchers have developed a suite of free tools for researchers that will enable them to apply standardised definitions of clinical outcome measures in #MS.
#multiplesclerosis#msresearch
https://t.co/07osOmRUEE
So proud of all the hard work, dedication, and innovation that have made this milestone possible. Here's to many more years of growth and prosperity! #proudwife
Today we celebrate 20 years of e-flo Computers! Thank you to all the staff whose hard work and dedication has made this company what it is. Here's to at least another 20 years of building lasting relationships, learning, and supporting our clients 🎉
JOIN THE MAY 50K TODAY 🏃♀️ — YOUR IMPACT COULD BE LIFE-CHANGING!🔬
Your participation in The May 50K will accelerate research into prevention, better treatments and ultimately cures for multiple sclerosis.
Register The May 50K 👉 https://t.co/Iv4ramWoNP
#TheMay50K#May50K
Big shoutout to the incredible team behind InforMS! 🎉 Your dedication and hard work are truly appreciated. Proud to be part of the team who helped develop this! 👏🏻🌟
InforMS is a new MS management app designed to help people manage their #MS.
Set to launch in mid-2024, InforMS will allow people to track their MS and their healthcare more easily, to help make shared decisions with their healthcare team.
https://t.co/WSrA21LB1y
This May, join #TheMay50K and smash your fitness goals as you help raise funds to support life-changing research into the prevention, treatment and finding a cure for #MS.
https://t.co/Iv4ramWoNP