OK they do for many, but not for me it seems. No this isn’t a woes me, but after 3 different treatments in it just becomes much like that Hillary Clinton meme if you’ve seen it, where you just walk (or shuffle), chuckle to yourself and you throw your hands in the air. Come on... Continue Reading →
We’ve all been there at some point, go about our daily life in whatever it consists of (work, parenting, volunteering, caring for someone/yourself, leisure activities, socialising…), but if you’re not careful too much of one, or many things, can eventually get on top of you and then BAM out of nowhere the burnout happens. Your... Continue Reading →
Hannah has wheels. Hannah has a horn. Hannah has front and rear suspension, and she is coming for you at 4 mph. I wouldn’t say that the purchase of my mobility scooter has been 7 years in the making, far from it, but definitely the last 2 or so. The absolute reluctance of owning... Continue Reading →
Almost 7 years diagnosed and numerous ‘minor’ relapses (I say minor in that I can still function with my life for the best part with a few adjustments and taking a step back for a week or so to recover (to a extent)), Rebif injections, Tysabri infusions, 2 rounds of Lemtrada, more steroid orals and... Continue Reading →
Wednesday February 13th 2013 . The day before my 25th birthday. 'You have Multiple Sclerosis'. Happy Birthday. The relapse which led to my diagnosis started mid November 2012, I used to start work at 6am, so by the time I got home at 2.30 a nap was needed, makes perfect sense doesn't it?! Now, I... Continue Reading →
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