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relapsing ms

When I was initially diagnosed with MS, I read a lot of stories online that suggested my life would now virtually be over. My neurologist had told me “whatever you do, don’t go home and sift through Google results about MS”. Although I understood that this was certainly great advice...

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Recently, my co-blogger Amber acknowledged her six year anniversary of her diagnosis-date. My own one year D-Day anniversary took place earlier this month, and while I too need no excuse to eat cake, I have chosen a different way to...

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Thanks to everyone who's taken the time to read my first blog, and especially to those who took the time to comment. I love that I'm not alone in the MS closet, it's nice and cosy!
The topic for my second blog post was a simple choice for me. I feel I need to address the 'elephant in the...

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My diagnosis didn’t come quickly! It took just over twelve months, three relapses, three MRI’s, one lumbar puncture, two neurologists, one urologist, one physiotherapist and a speech therapist, before it was confirmed. In amongst that was the most stressful traumatic year in my life. I lived in...

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An Epic Journey

In my introductory post, I alluded to the series of challenges I faced over the many months it took to reach a definite diagnosis of MS. I am following that up in this post by providing an overview of my perceptions of...

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The Unaffected One

I have been living with rrMS since 2002.  As someone who is mainly affected by the “invisible” symptoms of MS, such as fatigue, vision problems, intermittent vertigo, a subtle tremor and balance issues, I can generally choose who is aware of my diagnosis and who is not. I work...

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Living with MS: Five moments I knew I am sick

Living with MS is not pleasant. But one gets used to it. It becomes a little mundane, and quite frankly, I’m bored with it.

But a few moments have cut through the boredom and stunned me. Some I found funny, others not so much. Surprisingly, all have occurred when I have been relatively...

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