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Raising MS Awareness

Mar 11, 2015
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Raising MS Awareness

The Flaw in Many MS Awareness Campaigns

So, anything that raises more awareness of MS has to be a good thing then right? Awareness will allow people to realize it’s not a death sentence and sufferers can lead full and satisfying lives. The problem with lots of awareness campaigns, though, is the people they chose to represent the MS community.

It seems to me that the “face” of MS is either the over-achiever who runs marathons to raise money or climbs Everest solo! The other side is images of tragic people who can’t do a thing for themselves and live miserable existences, needing full time carers and being a burden to their loved-ones. Why do these two extremes seem to be the only way to represent MS?

The problem for me as an MSer is I don’t relate to either of these representations of MS. I can’t walk well enough to contemplate running, the results would be carnage. And I can’t lift my legs high enough to climb the stairs, let alone a mountain — but I’m not living a miserable life either! I work, I’m a mother, a wife and a good friend and I make the most of what I can do rather than focus on what I can’t.

The difficulty is that no two people with MS are the same — it’s hard to raise awareness of such a random, unpredictable condition in a way that all of us can relate to. I talk to other MSers all the time and sometimes I don’t recognize the condition they’re describing. Those who can walk normally but are crippled with fatigue or cognitive problems, for example. We have the same condition but totally different experiences of it.

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This is what campaigns need to address — the fact that MS can strike in so many different ways and no two people are the same. There are millions of people out there just getting on with life in an unremarkable way, except they live with MS too. Everything is harder for us, from work to shopping to going on holiday to looking after children, but we do it because we have to. We are not heroes or “brave,” we just get on with the cards we’ve been dealt.

Reaching Ordinary People

Awareness campaigns are vital to attract the attention of ordinary people who don’t have a clue about what we’re all living with. Research needs to be funded somehow, so anything that raises awareness has to be a good thing. If this means some of the representations in the media are extreme, then so be it! If that is what gets the attention of the public and makes people more aware, then we have to get behind campaigns and support them.

One day, with enough awareness and support they will find a way to cure, reverse or prevent the effects of MS, and I hope I’m around to benefit from it. So spread the word and raise awareness.

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Abigail Budd
Abi is a writer and blogger who also works part-time in the criminal justice system in the UK. She lives in Brighton with her family and plays an active role in the global MS community. Abi was diagnosed with RRMS in 2008 and now has SPMS, but tries to see the funny side wherever possible! Follow her blog or find her on twitter @AbiBuddcomms See all of Abigail's articles
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