Article: "Five Things I Wish I'd Known Before My Chronic Illness"

Good article:
ā€œFive Things I Wish I’d Known Before My Chronic Illnessā€

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Brilliant article you found there. Certainly takes one to recognise the pitfalls as you might say. Trouble is. I wonder how many people realise MAV - and indeed classic migraine - is a ā€˜chronic’ illness. Medics never mention it or at least none ever have told me. Helen

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Buzzzz!! That’s incorrect and quite negative. A ā€˜chronic’ illness is one that lasts a long time (eg > 3 months) but may go away. What an utterly negative way to kick off an article.

There are several board members who have gone into remission.

Remain positive people!

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And some of us who’ve had MAV 20+ years and have no expectations of a cure. Acceptance is not negative.

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Of course it isn’t. Doesn’t make the article’s definition of ā€˜chronic’ any less wrong.

MAV is chronic in the definition of the article.

What does that even mean?! A single article does not change a word’s meaning!

So you want people to believe they will never get better?

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One dictionary definition I checked says, persisting for a long time, or constantly recurring. No mention of never going away so maybe that was journalistic licence/bit of sensationalism. I always think of ā€˜chronic’ more in terms of causing severe symptoms over prolonged periods of time and stemming from something which is in essence incurable rather than permanent. To use the term ā€˜into remission’in itself infers eventual return of something not currently visible but likely to recur. Helen.

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Great article! I really relate to the everyone offers you advice. I’ve had so many people say just do this or that. I wish it was that simple.

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Same here. I have a friend who said, ā€œOh, I got vertigo once and I went to the doctor and they did the Epley maneuver on me and that fixed it.ā€ Then when I told her that what I have can’t be fixed by the Epley maneuver, she just gave me a puzzled look.

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Lovely post Anna

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I definitely agree with this one too. I wish i’d known to tune out this advice, and to not listen to other people and let their opinions make me feel bad. I think it’s really important with migraine to find your own way, because it’s so individual, rather than believing that what everyone else is recommending is the way to treat yourself.

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