I only listed the ones I can definitely relate too!
wunderslondon:
30 Things About My Invisible Illness You May Not Know
2. I was diagnosed in the year: 2011!
3. But I had symptoms since: as long as I can remember. Since I was 12 years old.
4. The biggest adjustment I’ve had to make is: YEAH BED AT 9:30 WHAT’S UP WITH THE COOL KID OVER HERE WUT WUT
5. Most people assume: that their fucking mother or their fucking sister is going through the same thing I am with THEIR fibro! And everyone’s fibro is different, people without fibro don’t get that, I think.
6. The hardest part about mornings are: Convincing myself my legs will hurt less when I stand up.
9. The hardest part about nights are: “Man my legs hurt man my legs hurt man my legs hurt man my—” “SHUT UP BRAIN I’M TRYING TO SLEEP” “LOLNEVRARR”.
10. Each day I take __ pills & vitamins: Four or five, I’d say.
11. Regarding alternative treatments I have tried: MASSAGESSSS EVERYONE DO EM IF U GOTZ TEH FIBRO GET MASSAGES ALLA TIME DO IT QUICK NOW FAST
12. If I had to choose between an invisible illness or visible I would choose: “visible! People dont treat you like a liar then.” AMEN, PERSON I TOOK THIS FROM
13. Regarding working and career: Why does fibro have to limit my career?…
14. People would be surprised to know: Even though I’m cheerful and happy, I’m in pain aaallllll ttthhheeee ttttiiimmmeeee and I’m tired allll ttthhheee ttttiiiimmmeee even though I fake my way out of it.
21. If I could have one day of feeling normal again I would: Go jogging, or exercize in some way, and I’d stay up as late as I could and go out until like 5 AM!!
22. My illness has taught me: People are wussies, pain is all about mind over matter, especially with fibro, and DRY COLD WEATHER IS A CHODE.
24. But I love it when people: TREAT ME LIKE A NORMAL PERSON WHEN I SAY “HEY NOT THE HIPS PLZ” which my friends are very good at!
26. When someone is diagnosed I’d like to tell them: “Dude, listen, you still feel as shitty as you did before, but now it has a name and you get drugs to make it better. So cheer the fuck up.”
27. Something that has surprised me about living with an illness is: People give you so much pity n shit when really, at least for me, I’m the only one that can really help myself.
29. I’m involved with Invisible Illness Week because: I have fibromyalgia, no one in the medical community gives a fuck, and I feel the same pain someone with like fuckin’ lupus has every day. I should be given a fair chance in the medical community.
Wunderslondon tumblr!!! >>>>> http://wunderslondon.tumblr.com/
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