Climbing out of a (deep) hole

Over the past month and a half, with the exception of last Monday, I had not posted anything. Nada. And while I have a tonne of explanations to offer for why that happened, I know that for most people those would just sound like an excuse to being lazy.

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Being a (MS) Jedi

It’s been a couple of weeks since my last post, and despite having promised that I would post a third post as part of my #WorldMSDay tirade I found myself being overwhelmed by the MS. So, this being the first day in a while that the “fog” has cleared up (not gone, but at least it’s not as bad), here goes.

Today we’ll discuss treatment options, and which might be best.

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Written in anger (sorry Spock)

 

I know that this breaks my unofficial “post every fortnight” rule, but I came across a story today that I just had to comment on.

During my afternoon browsing of news apps on my phone, specifically going through my feed on the BBC app, I came across this story, a blog post shared by BBC Trending. Long story short, the story outlines how pro-Kremlin Komsomolskaya Pravda supports or describes the disapproval of and ostracism of disabled people.

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Living a full life

MS takes a toll on you. Physically and emotionally. The physical part there is not much one can do about. Someone diagnosed with a chronic disease will have to accept (notice I am not saying surrender to – but more on this later) the fact that their condition will deteriorate as time passes. Deteriorate in various degrees and forms.

I started this blog with the intention of showing people that MS will not stop me in my tracks, and is not a “death sentence.” However, I thought that simply showing how strong someone with MS can be would give the wrong impression, and people also need to see the difficulties in living with MS.

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