People with MS different experiences of MS drugs and treatments, from DMDs to alternative therapies.
Laura's story: my Covid-19 vaccine experience
Laura, a Community Staff Nurse who was diagnosed with MS 11 years ago, shares her experience of receiving the Covid-19 vaccine.
Hellie's clinical trial adventures the epilogue
In a this blog, a person with MS chronicles her journey taking part in a clinical trial for the drug bexarotene. This is the final part where the results of the trial are in...
Choosing a disease modifying drug: Maria’s story
Maria was diagnosed with relapsing remitting MS last June. Here she shares her experience of choosing a disease modifying drug. "It’s scary being asked to make such a massive decision, so if you do feel afraid, that’s normal," Maria tells us.
Choosing a disease modifying drug: Laurens's story
What do you do when the disease modifying drug (DMD) you've chosen isn't working? In this guest blog, Lauren shares her thoughts around choosing an MS treatment and what it is like having to change to a new one.
Kate in clinical trial land
Kate guest blogs about her experiences taking part in a clinical trial for the drug bexarotene.
Choosing a disease modifying drug: Toni's Story
Choosing a disease modifying drug (DMD) is an individual decision and it can be important to weigh up your options and think about what might work best for you. In this guest blog, Toni shares her experiences of choosing an MS treatment and explains what it was like to start on Plegridy.