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Cholesterol-lowering tablets may slow brain shrinkage 

Willeke moved to Ireland from her native Belgium in 2002. Diagnosed in 2005, she was intent on being a voluntary advocate for people with MS after her retirement 4 years later. Willeke has been described as inquisitive, tenacious and very independent. She hopes to keep on writing when her eyes permit her to, and to help others see sense in what is often MS-nonsense.

Free event for people with neurological conditions and their families

Free events for people with neurological conditions and their families in Galway, Limerick and Kilkenny

Diagnosed with MS in 1988, I was told that there was no cause, no treatment and no cure and to add to my emotional turmoil there was no definitive diagnosis either. That didn’t leave a lot of hope for the future but my mother’s brother, who also had MS, helped me through the earlier days, weeks and months. 

Mary O Rourke and Conor Devine guest speakers this year!

While in Barcelona the topic of MS and Young Adults was discussed. It was interesting to me, as I am the youngest person I know with multiple sclerosis. I know some very inspirational people with MS who happen to be older than me, but I sometimes feel as if my concerns as a 26 year old are irrelevant to many of the people I know with MS. Maybe, because they already have established careers, are married, have bought their own house and achieved many of the things that I find I am holding myself back from. I'm sure there are people who are older who experience the same concerns as I do. This blog is for anyone who reads it and anyone who relates to it!

Recently I was lucky enough to attend a media briefing in sunny Barcelona hosted by Novartis (makers of Gilenya) ahead of a conference - Advancing Research in MS and the Brain.

Senators voice concern at the state of neurological services

Results launched during Brain Awareness Week