Supporting New Zealanders
to Live Well with MS

Trusted information, support, and a connected community for everyone impacted by multiple sclerosis.

4800
New Zealanders living with MS
0
The average age of diagnosis
0
New diagnoses each year
0
times more women are diagnosed
4800
New Zealanders living with MS
0
The average age of diagnosis
0
New diagnoses each year
0%
Women living with MS

Help us create a better future for people with MS in New Zealand - every action helps strengthen our community. Join us and make a difference today. You can donate. fundraise. join our events.

My Story. My Strength. My MS.

By sharing your journey, you can bring hope, understanding, and practical support to others facing similar challenges. Personal stories help build awareness, reduce stigma, and remind us all that no one faces MS alone.

Your voice can inspire change and strengthen our community.
If you would like to share your experience, we would love to hear from you.

My Story. My Strength. My MS.

By sharing your journey, you can bring hope, understanding, and practical support to others facing similar challenges. Personal stories help build awareness, reduce stigma, and remind us all that no one faces MS alone.

Your voice can inspire change and strengthen our community.
If you would like to share your experience, we would love to hear from you.

Living with MS on the West Coast: Vanessa’s Story
I was 22 years old when my body first sent me a signal that something wasn’t right. I was experiencing...
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Adventure, Grit, and Heart: Meet Team Murray Sisters
Hi, I’m Sarah Murray; adventure racer, shearing contractor, mum of three boys, happily married and proud...
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From Diagnosis to Distance: My MS Journey and the Power of Setting Goals
In early 2020, I started noticing strange things happening to my body. I couldn’t walk in a straight...
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From Dizzying Speeds to Vertigo - Jackson's Journey to Diagnosis
Hi my name is Jackson Ruakere, I’m 30 years old, a plumber and gasfitter by trade and like to consider...
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MS Care Can’t Wait - And Neither Can We
MS Care Can’t Wait – And Neither Can We I join the MS Society of NZ in calling for urgent investment...
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Pushing Past Limits: My Life-Changing Outward Bound Experience
When I first signed up for Outward Bound, I didn’t know exactly why I was doing it. But somewhere deep...
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Living with MS on the West Coast: Vanessa’s Story
I was 22 years old when my body first sent me a signal that something wasn’t right. I was experiencing...
Read More
Image description
Adventure, Grit, and Heart: Meet Team Murray Sisters
Hi, I’m Sarah Murray; adventure racer, shearing contractor, mum of three boys, happily married and proud...
Read More
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From Diagnosis to Distance: My MS Journey and the Power of Setting Goals
In early 2020, I started noticing strange things happening to my body. I couldn’t walk in a straight...
Read More
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Need Support?

You’re not alone.
Connect with your local MS Society for personalised advice, peer support, and practical help.

Latest News & Stories

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Advocacy
MY MS My Story
Funding
Life with MS
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What’s changing in April for people who use flexible funding
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Living with MS on the West Coast: Vanessa’s Story
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Neurology Research Review - Issue 93
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New Zealand’s Neurologist Workforce: A 2024 Analysis of Demand, Supply and Projections
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P1000018088
Swimming the Cook Strait to Support People with Multiple Sclerosis
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Want to shape the future of MS Care in New Zealand?
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