Latest news

Chris shares his experience of being diagnosed with MS at the same time as starting hormone treatment and a surgical gender transition. 

For the last few weeks our Enquiry Service at the MS Trust has been busy with questions about the vaccination. In his latest blog piece for the MS Trust, CEO David Martin asks the question, 'Should we all be saying yes to the Covid 19 vaccine?'

...but this time they've gone casual! We are very excited to have partnered once again with Monkey Sox to bring you an exclusive MS Trust design.

While the crisis has been challenging, it has also brought innovation and an appetite to permanently change the way MS services work.

Starting a conversation about sexual problems with a health professional can often feel daunting. Lesley Catterall and Denise Middleton, two MS specialists answer your questions.

It can help to share your end of life wishes and preferences with your close family. Here we provide some suggestions to help you begin the conversation around end of life planning with your loved ones.

Julie describes the shock of both herself and her husband, Martin, receiving an MS diagnosis.

The MS Trust is delighted that ozanimod (Zeposia) has been approved in Scotland for people with active relapsing remitting multiple sclerosis.

Dearbhla Crosse discusses her surprise feelings of empowerment when it comes to dating with MS during a global pandemic.

Kaz discusses the impact being diagnosed has had on his friendships and why his MS friends are so important to him. 

Talking to your kids about MS can be daunting. In this blog Chris Wallace and his family tell how they have dealt with this together.

Pete Davis tells us how he felt falling for someone with MS and that despite everything that MS throws at them, they still make things work.