Having an invisible disability (ID) and/or invisible chronic illness (ICI) means that many things change. Just because you can’t see the changes doesn’t mean they aren’t real.
Most people don’t understand much about these disabilities/diseases and their effects, and of those that think they know, many are actually mis-informed. In the spirit of
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Having invisible illnesses (for me, fibromyalgia is the heavy hitter) is so hard, especially for people who are younger. When I was in my teens my teachers gave me hell for "making up" my symptoms because one day I was okay and the next I wasn't.
I've learned over the years that those who are blessed with healthy bodies sometimes forget what it's like to not have that. It's not a bad thing to forget, but when you are friends with someone who doesn't have that kind of reality, it changes things.
Something else I have used often is the Spoon Theory. Giving a visual explanation of why I can't do something helps so much. And when I tell someone else who has health issues similar to mine that I am "low on spoons" it's immediately understood.
Here's the link if you want to read it. It's rather short, but super helpful. :)http://www.
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For example, the people who have never suffered from depression, who think it's just a case of feeling a bit down, and just having to buck yourself up to get out of it.
It's one of those things that I think only people who have experienced it directly, can really get it.
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