You don't know how strong you are, until being strong is the only choice you have

The emotional impact of an MS diagnosis can be hard to deal with for the whole family. The Bunby’s (Natasha, Marc, Deon and London) tell us about the ups and downs of living with MS, how they support each other and their advice for other families.

Being diagnosed with MS can sometimes affect your sex life, but we know that people can often feel too embarrassed or awkward to seek out support. This Sexual Health Week (14-20 September 2020), we want to normalise the conversation around sex and MS and break down some of those taboos. Here, MS nurse Shamayne Evetts, who works in the Dorset area, writes about what her service is doing to offer support and shares some advice for people with MS who may be experiencing problems with sex and intimacy.

Letisha Charles-Thomas received her diagnosis of MS (multiple sclerosis) in May 2019 after numerous appointments and tests.

Nigel Bartram, diagnosed with primary progressive MS (PPMS) in 2009, tells us how humour has helped him during times of adversity – and inspired him to create a new book to raise funds for the MS Trust. But he needs your help.

Two years after her mum was diagnosed with MS, Sian Spence received the same diagnosis. Here, Sian shares her journey and what's she learnt along the way.

In his latest blog Martin Baum discusses how raising awareness of the invisible symptoms of MS can only be a good thing.

Julie Stevens - AKA Jumping Jules - turned to poetry to help her make sense of MS and, over 100 poems later, she says it has brought her incredible happiness. Here she tells us about her MS journey and her dream to publish her own book of poems.

After attending her first yoga class, Ali Morton felt like she was "seeing light through a grey cloud of depression". She was inspired to quit her busy job as a primary school teacher and become a yoga instructor. Here, Ali tells us about her MS journey, the benefits of yoga for people with MS, and shares some yoga exercises for fellow MS'ers.