Busy teacher and musician, Stuart, had a shock when he was first diagnosed with MS. Determined to manage his multiple sclerosis, he joined MS organisations for support.

For many people living with MS and mobility issues, getting around can be challenging. Antoinette talks us through her recent experience travelling in and around London using her powered wheelchair.

Diagnosed with MS and later cancer, Jane channelled her energy into writing and is now a published author.

When Jen and her husband decided to start a family, she had to make a tough decision to change MS medication from Plegridy to Copaxone. Read on to find out how it went.

July is Disability Pride Month. This blog looks at how there is still much work to be done to raise the visibility of disabled people across society.

Kate received her MS diagnosis in 1987. Whilst times have been tough, her love for life has really kept her going.

Simone talks to us about caring for her husband who has MS and how she too needed to go through a grieving period following his diagnosis.

Leoni and her partner found true love a number of years ago and believe that everyone deserves a loving relationship, with or without MS.

Passionate politician Mags Lewis lives with MS and feels that society is missing out by not including disabled people.