Tim Coetzee

Chief Advocacy, Services & Science Officer at the National MS Society | Views and opinions are my own

[Rachel Horne @RachelHorne19]

Just ONE WEEK to go before applications close for the Rachel Horne Prize for Women's Research in MS.
Submit by Tuesday June 11 at 11:59PM Eastern Standard Time (Canada & US).
For more info:
https://t.co/MjkVfi4n3D
The winner receives $40,000.... and a tasteful trophy.

[ACTRIMS® @ACTRIMS]

REMINDER - Less than 1 week left to submit your applications for the 2024 Rachel Horne Prize for Women's Research in MS! DEADLINE: June 11, 2024. For more information or to apply visit: https://t.co/Hh8swtVzJB

[ECTRIMS @ECTRIMS]

📣 Live Tomorrow: Experts discuss navigating the complexities of ageing with MS. Join this free webinar with @tim_coetzee of the @mssociety, @XMontalban of @cemcat_em, @GravesNeuro of @UCSDHealth, and Dr. Eva Strijbis of @AmsterdamUMC.

Register Here 👉 https://t.co/mboXgTXr0X

[Lisa Doggett @lisadoggettmd]

It’s GO TIME!!! We’re off in a few minutes to bike the Texas #MS150 - 160 miles over two days. We are raising awareness and funds to support people living with MS. Wish us luck. #MS #multiplesclerosis @mssociety

[ECTRIMS @ECTRIMS]

🧠 Experts are meeting in Philadelphia to discuss #ageing and #MS at a workshop by the International Advisory Committe on Clinical Trials in MS, ECTRIMS & @mssociety. Learn more about this topic - join our webinar 🗓️ 30 April at 16:00 CEST. Register now! ➡️https://t.co/ZZvI9LtWQT

[National MS Society @mssociety]

#MSNews: UCLA neurologist Dr. Rhonda Voskuhl wins 2024 John Dystel Prize for MS research. She is being recognized for her innovative research to understand mechanisms underlying sex differences in MS and advancing women’s health.

Read more: https://t.co/WfJF6HQnxA

[MS Activist @MSactivist]

Thank you @HouseCommerce for highlighting the need to expand and protect access to telehealth services. Join fellow MS Activists by contacting your Members of Congress and urge them to support #telehealth today: https://t.co/umbX8ktKG5 #MSActivist

[MS Activist @MSactivist]

Click here ➡️ https://t.co/8EXLNTIHrU to watch live!

[MS Activist @MSactivist]

HAPPENING NOW: Virginia #MSActivist Jeanette (@MSWinners2008) is testifying in front of the @HouseCommerce committee on the importance of #Telehealth. Watch live: https://t.co/8EXLNTIHrU

[Tim Coetzee @tim_coetzee]

Thank you to @bbctanyabeckett and @BBCTheInquiry for the opportunity to talk about the great strides we are making in #MS. It was great to join Professors @TZiemssen, @jeffreyhuang, and @ClaireShannonLowe in this conversation.

https://t.co/76GbHpKoAj

[Tim Coetzee @tim_coetzee]

Congratulations to Dr. Rhonda Voskuhl on being selected as the recipient of the 2024 John Dystel Prize for MS research.

https://t.co/vMtlE8SoaY

[ECTRIMS @ECTRIMS]

🎙️ In our new podcast, we look at discussions underway to revise the #MS diagnostic criteria with guest, Xavier Montalban, Chair of the International Advisory Committee on Clinical Trials in Multiple Sclerosis. 🎧 Listen now ➡️ https://t.co/nRetKc8lGK

[ECTRIMS @ECTRIMS]

🏆 Congrats to Sergio Baranzini of @UCSF for winning @Mssociety's Barancik Prize for Innovation in MS Research. 🎧 Don't miss our recent podcast with Sergio and @AdilHarroud of @mcgillu on their discovery of the first #genetic marker for #MS severity. ▶️ https://t.co/co3p7hnrKB

[National MS Society @mssociety]

This month, we are honoring Black History Month by sharing stories to shine a spotlight on the unique challenges and experiences of being Black with MS. #BlackHistoryMonth #BlackMSExperience

Learn more about MS in the Black Community: https://t.co/WwpPRY6JyF

[ACTRIMS® @ACTRIMS]

Congratulations to Sergio Baranzini on being named the winner of the NMSS Barancik Prize for Innovation in MS Research. Dr. Baranzini serves on the ACTRIMS Program Committee and will receive the award and give the Prize Lecture at the #ACTRIMSForum 2024. https://t.co/7h4qEHMCz8

[Tim Coetzee @tim_coetzee]

Congratulations to Sergio Baranzini on being selected as the next winner of the Barancik Prize for Innovation in MS research. Looking forward to seeing his talk at @ACTRIMS 2024!

https://t.co/3jmbLXMw2l

[Tim Coetzee @tim_coetzee]

Thank you @ECTRIMS for the opportunity to share perspectives on the patient community day at #MSMilan2023. The patient community day is a great example of leadership in action. Patients, researchers, patient organizations, and professional societies coming together to solve MS!

[ECTRIMS @ECTRIMS]

Patient Community Day "gives you a window into the life experience of people affected by #MS," says Tim Coetzee of @mssociety. In our new ECTRIMS Podcast, Tim and Bonnie Higgins discuss the importance of the event and their experiences. 🎧 Listen now ➡️ https://t.co/8DL1fuJIxH

[Tim Coetzee @tim_coetzee]

There were some remarkable #MS moments in 2023. Here are a few moments that inspired me in 2023 - along with my pick for the top moment. Looking forward to what 2024 brings. Together we are stronger!

[National MS Society @mssociety]

2023 was an incredible year: from event participation, to donors, to MS activist successes, funding research, and more! Thanks to everyone who made this possible 🧡

[Tim Coetzee @tim_coetzee]

Today I was pleased to join colleagues from the @nmssocietyuae and @MSIntFederation for an educational session for leaders of MS organizations during the MENACTRIMS Congress. Inspired by the passion and commitment of our movement. Together we are stronger!