Community blogs

Hannah is a Research Communications Officer. She tells us the ins and outs of research communications at the MS Society and why it’s such a rewarding job.

I’ve loved Christmas since I was a child, but somehow some of the shine and sparkle came off it when I got older.

We're here to support you through the festive season. Discover tips on how to stay safe this Christmas as the COVID-19 pandemic continues.

This year has been a challenging one. But we've achieved so much thanks to your support. From fundraising to campaigning, join us as we look back on 2021.

Avoiding burnout over Christmas is essential for tingly mum. Find out how she makes Christmas work for her.

Christmas can be a demanding time. Find out how Sarah Rees manages her time and enjoys the festivities.

From resting to asking for extra help, discover Jenny's top five tips for enjoying the festive season.

Today is the UN’s International Day of Persons with Disabilities, a day to celebrate disabled people across the world. Disability inclusion is essential for human rights, sustainable development, and peace and security.

We’ve launched a new strategy setting out our commitment to equality and how we’re planning to be a more diverse and inclusive organisation. Our Chief Executive Nick talks us through the plans.

Emily was diagnosed with MS while studying at Wimbledon College of Arts. So when COVID-19 hit, finding room for self-expression became a creative project.

Caz has been living with MS for 21 years. She sees it as the ultimate teacher in life lessons.

I have a birthday coming up, it’s a 21st birthday, so a special birthday - it’s for my MS.

Stuart was diagnosed with MS 30 years ago. As our MS Helpline celebrates its 30th birthday, he looks back over his MS journey, and how he came to be a helpline volunteer.

Whether you have MS yourself, or are a friend or family member – our MS Helpline is here for you. 4 people tell us what it’s meant to them.

Over the years, Sam's found walking sticks really handy. She tells us how she's gone from feeling self-conscious to embracing them.

After being diagnosed with MS in 2019, Ayad began the journey of re-evaluating my life and accepting what was and wasn’t possible for me anymore.

Sasha and her children are starring in our Stop MS Appeal campaign this Christmas. She shares why it’s so important to her.

After an unexpected diagnosis of MS just over one year ago, Max found acceptance in a new country, with help from our MS Helpline.

MS Society volunteer, Jessica, shares her experience of representing people living with MS at our Neurology Now parliamentary event. And on speaking to MPs about the realities of UK neurology services.

Shereena was diagnosed with MS in 2009 at the age of 17. Now she is beginning HSCT treatment on the NHS.