Navigating MS, Together

Most MS information isn’t written with your 20s or 30s in mind. Our newly diagnosed guide ‘Navigating MS, Together’ is.

Newly diagnosed guide

What's inside

Our guide covers:

  • First steps to take after diagnosis
  • What MS is, common symptoms and misconceptions
  • Practical advice for helping you manage symptoms, and choose a treatment
  • Preparing for appointments, and advocating for the support you need
  • Knowing who to tell and advice for sharing your diagnosis
  • Understanding the support available to you and how you can access it
  • Inspiring experiences from people in the MS Together community
  • A handy summary of tools and resources

How to access it

Our guide is launching soon and will be available below. You can choose the format that works best for you.

Download the PDF

Keep a copy to read in your own time. This will be available soon.

Request a printed copy

If you’d prefer a physical version, you can request one for a small donation to help cover printing and postage. The booklet will be available soon.

No one is excluded based on ability to donate. If cost is a barrier, please get in touch at hello@mstogether.org

For healthcare professionals

If you support young adults aged 18–35 and would like printed copies for your clinic, we’d be happy to arrange this.

Contact us about clinic copies
Two people talking at an MS Together event

Made by people with MS, for people with MS

This guide has been created by people living with MS. That’s what makes it different.

It’s written like a friend guiding you through your diagnosis - not a textbook, not a hospital leaflet, and not a list of worst-case scenarios.

It reflects real conversations, real worries and real life in your 20s and 30s.

Because the people who shaped it have been there too.

Person with MS learning more from an MS Together leaflet

Why we created it

Before writing this guide, we hosted focus groups and surveys with our community.

Young adults told us:

Cross icon

Some weren’t given much information at diagnosis

Cross icon

Some were given too much, and it felt overwhelming

Cross icon

Some felt the resources they were directed to didn’t speak to them or reflect their life stage

What people wanted was simple ...

Tick icon

Some felt the resources they were directed to didn’t speak to them or reflect their life stage

Tick icon

In one place

Tick icon

Relevant to their real lives

So that’s what we created it ...

Acknowledgements

This resource was developed with input from people living with MS, healthcare professionals and members of our wider community.

We’re grateful to everyone who shared their experiences, insights and expertise to help shape it.

We would also like to thank Merck for providing funding to support the production of this guide. Merck had no involvement in the development, content or editorial decisions of this resource.