Just because you can’t see it, doesn’t mean it’s not there!

It’s been a while since I wrote something MS related. The past couple of days something has been occupying my thoughts though. How others view you when what you have is an invisible disease. Invisible to all but you that is.

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365 (or is it 366?)

About a year ago I published my first post. I don’t remember the exact day – lately my memory, among other things, is not what it used to be – but I know it was right before my birthday. Well, that day is upon us once again.

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Finally something gone right

There is a saying that goes a bit like “when nothing goes right, go left.” Over the past nine and a half years, it seems all I had been doing was going left. In my personal life, in my professional life, and especially when it comes to health. I have been through half a dozen different treatment options, and while some were more successful than others (I was surprised to see that the alternative treatments worked better than traditional medicine), there was always a drawback, some side-effect, something making me a bit unwilling to trade a “normal” life for my new normal.

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