Members of MS Society's Croydon Group chatting on a sofa

MS diaries

MS is different for everyone and no two people will have exactly the same experience.  Find out from our amazing bloggers about what it's like to live with MS.
Newly diagnosed with MS?

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Share your story

Do you have a story to tell about MS? We'd love to hear from you.

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Read about living with MS

Photo of Beccy Huxtable in MS research lab wearing a white coat and latex gloves

5 things I want you to know about MS

Living with MS is never dull. As well as all the symptoms, which can change on a daily basis, it feels like I constantly have to explain myself.

Find out what 5 things Beccy wishes everyone knew about MS
MS Society blogger Danielle with her dog Frank

My MS Story - My MS-iversary

Last month, it was my anniversary. It’s been 16 years since I was diagnosed with MS. It’s hardly an occasion to celebrate, but at this time of the year, I do find myself reflecting on how things have changed since then.

Read more about Danielle's MS story
Noor smiling

MS during Ramadan

Ramadan. The month of mercy as it is known amongst Muslims. It is a time for reflection, a time to reconnect with yourself, a time to be with friends and family and to give in charity.

Read Noor's blog about having MS during Ramadan
Masta Ace looks to the camera with Marco Polo in the background

Masta Ace - hip hop and MS

Masta Ace is a rapper and record producer from Brooklyn. He was diagnosed with MS in 2000.

Watch our interview with Masta Ace
Amy Thompson standing outside a door

"But you don't look ill" - the invisible symptoms of MS

Many people were shocked the first time they saw me after my MS diagnosis last year. They expected me to look different or be less able-bodied due to my diagnosis.

Read Amy's blog
Image shows Trevis Gleeson speaking at a conference

What would you tell your newly diagnosed self?

In short, what do you wish you had known then?

Read Trevis's thoughts on life with MS

Online community

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Our MS Forum

Our forum is a welcoming community of over 30,000 people who know life with MS. Whether you're newly diagnosed, have had MS for a while or care for someone who does, there's something for you.

Join the conversation on our forum
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Community blogs

Our wonderful community bloggers share their thoughts on every aspect of life with MS. Whatever you're going through, they're here to reassure you that you're not alone and offer their tips on coping.

Catch up with our MS bloggers
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Virtual Wellbeing sessions

Do you have MS, or care about someone who does? Want to meet other people who just get it? Join our Virtual Wellbeing sessions to chat, share experiences and explore different ways to live well with MS.

Find a session that suits you
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Find support near you

From support groups to information events, there's lots of ways to connect with people who understand what life's like with MS.

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