During invisible illness week, we are trying to raise awareness of our diseases or disorders. One of the hardest parts about having a friend with invisible illness is knowing what to say to them or how to help them. Luckily the people at Invisible Illness Week have provided a wide variety of wonderful tips for friends and family of sufferers. Wouldn’t it be wonderful to spontaneously get flowers (assuming it’s not a trigger for you…)?
How do your friends and family help you cope with your invisible illnesses?
12 / 09
Notes
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lds-with-cfs likes this
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sheliesshattered reblogged this from girl-in-a-wheelchair
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girl-in-a-wheelchair answered:
They exist at me and talk to me.
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girl-in-a-wheelchair reblogged this from thelamedame
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healthpillow reblogged this from inspiringthoughtsintoaction
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inspiringthoughtsintoaction reblogged this from itsawonderfullife94
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inspiringthoughtsintoaction answered:
I know. some people don’t understand what I go through with headaches and migraines. It’s annoying sometimes.
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itsawonderfullife94 reblogged this from thatmword
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wearelikebutterflies likes this
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itsalllikeclockwork answered:
My best friend has taken me to the ER for some of my more serious migraine attacks. That’s really the best thing she’s been able to do for me
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dy7lan answered:
My family doesn’t acknowlege my existence. It’s my friends, well… a small handful of my friends that help by treating me normally.
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thatmword posted this
