6 things everyone should know about MS

Multiple sclerosis (MS) affects over 2.8 million people globally and around 74% of those diagnosed are women.¹ Yet despite these numbers, many people still don’t fully understand what life with MS really looks like.

From hidden symptoms to evolving treatments, the reality of MS is far more complex than most realise. This World MS Day, we’re shining a light on the condition – because awareness isn’t just helpful, it’s powerful.

Here are six things everyone should know about MS.

1. The early signs of MS are often invisible, but very real

MS doesn’t always make a loud entrance. In fact, early symptoms are often subtle and easily dismissed. Vision problems, numbness, fatigue, clumsiness, dizziness – these can all be early warning signs.²

Because they can mimic stress or everyday exhaustion, many people don’t realise what’s going on until much later.

If something doesn’t feel right, don’t brush it off. A check-up with your GP could lead to early support and a much better outlook.

2. MS affects women more and often in the prime of life

Most people with MS are diagnosed between the ages of 20 and 50.² These are often the years when people are focusing on careers, relationships and starting families.

A diagnosis can feel overwhelming, but it doesn’t mean your goals are out of reach. With the right support, life with MS can still be full, vibrant and meaningful.

3. There’s no one-size-fits-all approach to living with MS

Living well with MS is all about listening to your body and finding what works for you. For some, that’s gentle movement like yoga. For others, it’s focusing on rest, nutrition or mental health.³

“I am still running my business, hanging with my family and having tons of fun with my tribe. Every May 25th on my ‘diagnosiversary’, I raise a glass and toast to my good health,” says Vickie, an Overcoming MS member.

Access to information and choices can make all the difference.

4. MS treatments are advancing and they matter

While there’s currently no cure for MS, there are more treatment options than ever before. Disease-modifying therapies (DMTs) can help reduce flare-ups, slow the disease and improve overall quality of life.⁴

It’s important to work closely with your medical team to find a treatment plan that fits your goals. Shared decision-making leads to better, more personal outcomes.⁴

5. MS and pregnancy? Yes, it’s possible

Many women with MS go on to have healthy pregnancies and children. The key? Support – from doctors, midwives, and loved ones.²

Every pregnancy journey is unique, and with the right care, motherhood is absolutely within reach.

6. No one should face MS alone

MS can feel isolating, but you’re not on your own. Online communities like MyMSTeam offer connection, advice and real-life stories from people who get it.

“What I wish I had heard when I was first diagnosed was that life is going to be different now, but not as different as you think it is. There’s going to be a new normal, but it’s going to be OK. It really is,” says Jenny, MyMSTeam member.

Let’s change the story – together

Whether you’re living with MS or know someone who is, understanding the condition and sharing real experiences can shift perspectives and open up possibilities.

Learn more, share your voice, and explore empowering options on the Roche MS page.

References:

1. https://www.nationalmssociety.org/

2. https://www.mymsteam.com/

3. https://overcomingms.org/latest/i-am-living-well-multiplesclerosis? gad_source=1&gad_campaignid=22564896677&gbraid=0AAAAAC10A0qqCg250T_F1PkQTu

O3NE8Hn&gclid=Cj0KCQjwotDBBhCQARIsAG5pinMA6HPoqOdqAifEhFopoIkswQSGXcta8-

1IfEvD5plMeUBYLsqsVGkaAuJhEALw_wcB

4. https://www.ajmc.com/view/ongoing-review-of-dmts-necessary-among-patients-with-multiplesclerosis

5. https://www.roche.ch/en/solutions/focus-areas/multiple-sclerosis

M-ZA-00002513/May2027