Some of you may have wondered where on earth I’ve been for the past year and a half! Well, apart from getting a new diagnosis and learning ways to manage the condition (a future blog post), I’ve been heavily involved in a group called the MS Hampshire Collaborative Working Group and a survey of MS […]
What is the Hampshire MS Services survey? Read More »
In my last blog post, I introduced you to the MS Hampshire Collaborative Working Group and our survey. We wanted to know what level of care people with MS are getting from their local MS healthcare team. Does it depend on where you live? and what happens if you don’t have good access, or any
The Hampshire MS survey results Read More »
Wowee. There was such a buzz of energy, support, understanding and positivity at the first ever conference for young people with Multiple Sclerosis! I am on a natural high, completely overwhelmed by our community. MS Sessions 2017, thank you! There’s so much content I need to share with you dear reader, but to kick things
MS Sessions 2017 Day 1 – a Young Person’s Conference Read More »
Would you be interested in being involved in a trial for treatment of spasticity? The trial uses a new drug called VSN16 and is recruiting right now, with recruitment running for the next few months until all spaces are filled. In order to be a potential candidate for the trial, you must: have spasticity – if you are unsure,
Spasticity Trial Now Recruiting 2016 – new drug VSN16 Read More »
You might have heard about this in the news (again!): Scientists close to a cure for MS. To be honest, I heard this on the radio this morning whilst waiting for a blood test in my GP surgery but disregarded it. I zoned out, not just because waiting for a blood test is far from my favourite pastime
