WHAT WE'RE ABOUT

RBI focuses on using expressive writing, design-oriented work, photography, media, research, and community input to fuel fat positive, body acceptance, discussion, and outreach. Our goal is to redefine the way we view and think about body image, size, fat, discrimination, health, fitness, wellness, mental/chronic illness, stigma, and other related topics.

We are constantly redefining our own perspectives, and therefore tend to write a lot about our personal experiences. Many followers and contributors are living with anorexia, bulimia, body dysmorphic disorder, depression, and a variety of other body image disorders or mental illnesses, so please be respectful and remember that health applies differently to everyone. Any and all potentially triggering content will be prefaced with a trigger warning.

RBI supports all races, genders, classes, and sizes. We try our best to make this a safe space for everyone. If we are not doing our job or checking our privilege, we invite you to please inform us.

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We are not health professionals. Any and all advice provided on this blog is supported only by our own research, studies, and personal experiences; nothing more.

This blog is part of the Safe Space Network.

thoughty:

I’m a young, short, blond haired, browned eyed girl. I have EDS type 3, and although many people will have never heard of it, it fucking hurts. I occasionally use crutches at home for the times where I can barely stand, but I do not use them outside yet (When I’m too sick I don’t even think about stepping out my front door.) But that isn’t even the start of what comes with my illness.

When you look at me, you can bet your sweet ass that I don’t look disabled, or whatever people think a disabled person should look like. Even people in the medical profession question me, but I know I’m in pain, you just can’t see it. Now, I’m not criticizing anyone for their preconceived notions of disabled people, since before I got sick, I was small minded and really had no idea that an invisible illness may have even existed.

The message I’m trying to put across here is; try to be a bit more open minded towards people in general. Don’t give that healthy looking guy a hard time for not giving up his seat on the bus, he may be in just as much pain and discomfort as someone fifty years older than him.

30 notes

\This was posted 8 months ago
1This was reblogged from thoughty-deactivated20121219
  1. larasmash reblogged this from gettingbetterfaster
  2. misandristscum reblogged this from gettingbetterfaster
  3. ijustcantbreathewithoutyou reblogged this from gettingbetterfaster
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  5. gettingbetterfaster reblogged this from redefiningbodyimage
  6. boywithavagina reblogged this from meanderingmanatee
  7. enviableapocalypse reblogged this from katthulhu and added:
    Reblogging this to share. This is how I feel, I’m twenty years old, bright eyed, purple haired, fairly fit despite a...
  8. power-squirrel reblogged this from redefiningbodyimage and added:
    My sister has EDS among some other things including a recently discovered gluten allergy. She’s told the receptionist at...
  9. meanderingmanatee reblogged this from redefiningbodyimage and added:
    I love this so much. It applies to so many different illnesses and people. It’s completely possible for someone to have...
  10. twofish reblogged this from redefiningbodyimage
  11. thepragmaticnihilist reblogged this from redefiningbodyimage
  12. snapbackmountain reblogged this from redefiningbodyimage
  13. katthulhu reblogged this from redefiningbodyimage and added:
    One of my best friends has this :C it hurts her greatly..
  14. heartsafetypinnedtohisbackpack reblogged this from redefiningbodyimage

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