medical trial

The last couple of blogs I’ve written have been quite serious in nature, not to mention a little infrequent. For that I’m sorry, but to me this feels the most sobering one yet. Monday (tomorrow!) marks five years since my diagnosis and it’s not without...

I know I’ve mentioned this before but MS has really altered my perspective on a lot of things. Even on my worst days, I keep trying to find the positives. I don’t think I’ve ever been the complete optimist but I recognise that I’ve needed to try to stay...

The real push to finally write this down started after I took place in a clinical trial last year. Going through all the blood tests etc. was ok but every time they did the ECG there was a concern and my blood pressure was a little high. My BP was easy...

Firstly, apologies to Shakespeare for messing with his words but giggling about these things is truly my best coping mechanism. Secondly, apologies that I’ve taken so long to write this but will probably be blogging like a mad woman in the coming weeks....

After a truly demoralising two years, I'm sat here in a little discomfort but with a soppy smile on my face... Until very recently, I believed I had PPMS (Primary Progressive Multiple Sclerosis) which is pretty depressing and turned my life upside down....