Writing about MS has been both challenging and rewarding.
Some of my articles have focused on living with MS - its impact on relationships, life choices and sense of self. Others point out how even though women are disproportionately diagnosed by the disease, MS research and clinical practice has traditionally paid scant attention to our specific health needs.
Here's a selection.
SCIENTIFIC JOURNALS & POSTERS
The effect of patient involvement on MS Research learning from 10 years of the Barts MS Advisory Group
Please feel free to connect with me via X (Twitter) or LinkedIn
