Being a mum is a whirlwind on its own, but navigating motherhood while living with MS brings a unique set of challenges that not everyone "gets." If you’re looking for a space to relax, share stories, and meet others who truly understand your journey, we have some exciting news!

This edition is packed full of lots of interesting articles, updates, news and events. We hope you enjoy this latest newsletter. from The Bruightwell Team

Every year on the last day of February, the world turns its gaze toward a community that is often invisible, yet 300 million strong. February 28, 2026, marks the 19th annual Rare Disease Day.

We’re delighted to announce that we have retained our 5-star Food Hygiene rating! The Brightwell Café has become a wonderful addition for everyone who visits the Centre,

As we look ahead, Audrey will be bidding farewell to us at the end of February 2026 as she prepares for an exciting new chapter in London, where she will continue developing both her physiotherapy career and her dance journey.

Over the years, The Brightwell has run a series of articles about some of our members' journeys with their specific condition. This article focuses on the amazing Roger Forbes!

The Brightwell would not be able to run without fundraising. There are many ways in which groups or individuals can support us to provide therapies and care for our community of members. One of which is our incredible Corporate Supporters Network, The Brightwell 100.

Please help us deliver the strongest campaign by completing our survey

Trish Smith, a Volunteer and Veteran of Oceans of Hope UK, has kindly written this article for us, which we hope you will find interesting...

Come and join us for our next Quiz Night on Wednesday 26 February!