New England MS Branch

New England MS Branch The New England MS Branch is both a support group and fundraising branch (under the auspices of MS Plus).

We raise funds to directly support people in our region, making life a little easier while dealing with the challenges of multiple sclerosis.

Whilst this is an American based site, there is a lot in this article that is relevant and helpful to those with MS here...
17/12/2025

Whilst this is an American based site, there is a lot in this article that is relevant and helpful to those with MS here in Australia.

From disease-modifying therapies to symptom management strategies, thereโ€™s more than one path forward. https://bit.ly/45oE6x4

It is sad to see the number of Australians with MS is increasing. If you know anyone in the New England with MS, especia...
10/12/2025

It is sad to see the number of Australians with MS is increasing. If you know anyone in the New England with MS, especially newly diagnosed, please let them know we are here to support them.

A new report from our MS Research Flagship's health economics group has found that multiple sclerosis (MS) is costing Australians more than $3 billion a year, and the number of people with MS is up 77% since 2010.

๐˜”๐˜ถ๐˜ญ๐˜ต๐˜ช๐˜ฑ๐˜ญ๐˜ฆ ๐˜š๐˜ค๐˜ญ๐˜ฆ๐˜ณ๐˜ฐ๐˜ด๐˜ช๐˜ด ๐˜—๐˜ณ๐˜ฆ๐˜ท๐˜ข๐˜ญ๐˜ฆ๐˜ฏ๐˜ค๐˜ฆ ๐˜ข๐˜ฏ๐˜ฅ ๐˜๐˜ฆ๐˜ข๐˜ญ๐˜ต๐˜ฉ ๐˜Œ๐˜ค๐˜ฐ๐˜ฏ๐˜ฐ๐˜ฎ๐˜ช๐˜ค ๐˜๐˜ฎ๐˜ฑ๐˜ข๐˜ค๐˜ต ๐˜ช๐˜ฏ ๐˜ˆ๐˜ถ๐˜ด๐˜ต๐˜ณ๐˜ข๐˜ญ๐˜ช๐˜ข 2025, commissioned by MS Australia, found that almost 38,000 Australians are now living with MS. Tasmania continues to have the highest prevalence in the country, with 190 cases per 100,000 people, nearly double the rate in Queensland and Western Australia.

MS is the most common acquired chronic neurological disease affecting young adults, often diagnosed between ages 20โ€“40. It can lead to job loss, financial strain and reduced quality of life. The report highlights the urgent need for investment in support services, early intervention and prevention.

Tasmaniaโ€™s high MS prevalence is a stark reminder of why our research in this space is critical.

โ€œOur vision is to improve health and wellbeing of Tasmanians through world-class research. We strive to reduce the burden of diseases such as MS to our community, and these findings reinforce that commitment,โ€ said Professor Tracey Dickson, Director of Menzies.

Photo caption: ๐˜™๐˜ฆ๐˜ฑ๐˜ฐ๐˜ณ๐˜ต ๐˜ข๐˜ถ๐˜ต๐˜ฉ๐˜ฐ๐˜ณ๐˜ด (๐˜“-๐˜™) ๐˜—๐˜ณ๐˜ฐ๐˜ง๐˜ฆ๐˜ด๐˜ด๐˜ฐ๐˜ณ ๐˜‰๐˜ณ๐˜ถ๐˜ค๐˜ฆ ๐˜›๐˜ข๐˜บ๐˜ญ๐˜ฐ๐˜ณ, ๐˜‹๐˜ณ ๐˜‘๐˜ถ๐˜ญ๐˜ช๐˜ฆ ๐˜Š๐˜ข๐˜ฎ๐˜ฑ๐˜ฃ๐˜ฆ๐˜ญ๐˜ญ (๐˜ญ๐˜ฆ๐˜ข๐˜ฅ ๐˜ณ๐˜ฆ๐˜ฑ๐˜ฐ๐˜ณ๐˜ต ๐˜ข๐˜ถ๐˜ต๐˜ฉ๐˜ฐ๐˜ณ), ๐˜—๐˜ณ๐˜ฐ๐˜ง๐˜ฆ๐˜ด๐˜ด๐˜ฐ๐˜ณ ๐˜๐˜ฏ๐˜จ๐˜ณ๐˜ช๐˜ฅ ๐˜ท๐˜ข๐˜ฏ ๐˜ฅ๐˜ฆ๐˜ณ ๐˜”๐˜ฆ๐˜ช ๐˜ข๐˜ฏ๐˜ฅ ๐˜‹๐˜ณ ๐˜Ž๐˜ญ๐˜ฆ๐˜ฏ ๐˜๐˜ฆ๐˜ฏ๐˜ด๐˜ฐ๐˜ฏ ๐˜ข๐˜ต ๐˜ต๐˜ฉ๐˜ฆ ๐˜”๐˜ฆ๐˜ฏ๐˜ป๐˜ช๐˜ฆ๐˜ด ๐˜๐˜ฏ๐˜ด๐˜ต๐˜ช๐˜ต๐˜ถ๐˜ต๐˜ฆ ๐˜ง๐˜ฐ๐˜ณ ๐˜”๐˜ฆ๐˜ฅ๐˜ช๐˜ค๐˜ข๐˜ญ ๐˜™๐˜ฆ๐˜ด๐˜ฆ๐˜ข๐˜ณ๐˜ค๐˜ฉ

Head to the link in the comments to read more about our report ๐Ÿ‘‡

This free online course is very good for those newly diagnosed with MS as well as for family and friends who are also tr...
07/12/2025

This free online course is very good for those newly diagnosed with MS as well as for family and friends who are also trying to understand what us happening to their loved ones. It is well presented, easy to follow, and can be watched at a time frame that suits the viewers. Enrolment for 2026 are open now.

Since our free online course launched in 2019 we've had more than 55,000 people enrol and learn with us.

If you know someone who has missed out, share this post and let them know that enrolments for 2026 are now open!

Sign up today or learn more ๐Ÿ‘‡
https://ms.mooc.utas.edu.au/i/msums

A good explanation of managing Relapsing Remitting MS. I hope it's helpful.
07/12/2025

A good explanation of managing Relapsing Remitting MS. I hope it's helpful.

Manage relapsing-remitting MS with confidence: https://bit.ly/4mPjSDX

05/12/2025
05/12/2025

People with relapsing remitting MS can now access injectable Ocrevusยฎ (ocrelizumab) through the Pharmaceutical Benefits Scheme.

Important and good news for those on Ocrevas.
05/12/2025

Important and good news for those on Ocrevas.

It is now officially summer. Hope you can all stay as cool as possible.  Here is some information to help you do that.
05/12/2025

It is now officially summer. Hope you can all stay as cool as possible. Here is some information to help you do that.

When the temperature climbs, your symptoms might too, but you donโ€™t have to let the heat dictate your day. โ˜€๏ธ

If youโ€™re living with MS, you might recognise the frustrating pattern of fatigue, blurred vision, muscle weakness or brain-fog triggered by warmer days. That happens for a clear reason: heat-sensitive nerves slow down when you get too warm, making it harder for your body to keep up.

Here are some practical ways to help you stay cool and comfortable:
โžก๏ธ Drink plenty of cool water and avoid too much caffeine.
โžก๏ธ Wear lightweight, loose-fitting clothes and a wide-brimmed hat when outdoors.
โžก๏ธ Stay shaded or air-conditioned: use fans, close curtains, avoid direct sun.
โžก๏ธ Carry a misting spray or cooling towel for your face & wrists when youโ€™re out.
๏ธโžก๏ธ Plan your day around the cooler parts; mornings or evenings are often better.
โžก๏ธ And remember: symptoms triggered by heat are usually temporary and will ease once you cool down.

Want to learn more or find tailored support? Visit our website and reach out to our MS Nurse, because you deserve to feel comfortable, confident and in control all year round.

02/12/2025

With the year quickly coming to an end it is time for the final get together of the New England MS Branch for 2025. Our final Branch/Support meeting will be held on Wednesday 10th December at the Armidale Bowling Club at 11am. As in the past our meeting should be short and sweet as we will follow it with our Christmas lunch. As always, members plus family, carers , etc are all welcome to finish our year off in a fun social way.

01/12/2025

There have been many significant milestones in Stephanieโ€™s journey since her MS diagnosis but returning to the workforce is right near the top. โค๏ธ

After a long period of being unable to work due to her disability, Stephanie has found her confidence, purpose and routine again in a part-time admin role she truly enjoys.

โ€œMy team is very accommodating, understanding and empatheticโ€ฆ Before that, I felt like I had no purpose and I actually missed work. Iโ€™m really happy there.โ€

For many people diagnosed at the peak of their careers, the thought of leaving a job they love can feel overwhelming. Thatโ€™s why our Employment Support Consultants and Occupational Therapists are dedicated to helping people stay employed, feel supported, and find roles that match their passions and potential.

Because meaningful work isnโ€™t just about income; itโ€™s about identity, connection and hope.

CoAct

15/11/2025

Can existing medications hold the key to new treatments?

Join the International Progressive MS Allianceโ€™s webcast featuring leading researchers who are exploring innovative trials that repurpose drugs for progressive MS.

๐Ÿ“† Thursday, 20 November
โฐ 3:00am AEDT

Registration will ensure access to the webcast post-event if you are unable to join live.

Register: https://bit.ly/44awCOm

11/11/2025

BREAKING NEWS: Roche have announced that their BTK inhibitor, fenebrutinib, has achieved successful trial results in both relapsing-remitting and primary progressive multiple sclerosis. While we have to wait until the full data is presented at upcoming conferences to know the entire story, this is positive news for the treatment of MS.

Read more: https://www.roche.com/investors/updates/inv-update-2025-11-10

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PO Box 4013
Armidale, NSW
2350

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