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.

Hayley who lives with MS, talks candidly about the importance of being seen in her wheelchair in order to spark a change in accessibility.

Helena talks frankly about her MS bladder and bowel problems and well-being, and why she finally sought help.

Andy Reynard blogs about his footballing days and how foot exercises and an electric bike keep him moving in the face of MS.