so idk if anyone else in the disabled community have seen this term being thrown around, but ive seen the words “able-passing” multiple times in the last few months, both on tumblr, irl, and in articles.
and tbh, i see people who use the term try to explain it as “when you dont look disabled, it is assumed that you are abled and you dont face the same discrimination that a visibly disabled person would, it is like youre not even disabled”, ive had it explained in different ways, with different words but that same result.
because apparently having your disability erased cause you dont look disabled isnt real, or being told that its like youre “not even disabled” is apparently not ableism.
and my guy my dude, this is my opinion but its time to be real.
“youre abled-passing” is no different than “But you dont look sick”
Okay if someone is heat intolerant and they’re really upset and miserable because they’re outside or without air conditioning when it’s really hot they’re not “having a fit” or being a baby. The heat is making them violently ill and putting them in danger. It’s a dangerous health concern and you’re a huge dick if you’re minimizing that and laughing at them.
Please help me find someone else with my rare conditon
My name is Valerie, I’m a teenager, and I’m chronically ill.
I’ve been sick for a decade now, and unfortunately, I tend to get all the rare and ~special~ disorders. Because of this, I currently have doctors in nine cities spanning across five states. I battle six chronic conditions, and balancing them is a daily struggle, but I’ve managed.
But my newest condition has turned my life upside down. It’s called Recurrent Subacute Thyroiditis (RSAT) and most doctors will never see a case of this in their lifetime. I luckily have found a doctor who has least seen a few cases of this before, but I am the youngest person she has ever seen with this condition.
RSAT is an inflammation of the thyroid that causes overactivity, leading to high heart rates, trouble breathing, low blood pressure, dizziness, chest pains, insomnia, fatigue, hair loss, and muscle weakness. The overactivity lasts for about 2-3 months, and then the thyroid flips to inactivity, leading to lethargy, extreme fatigue, depression, low body temperature, and slow heart rates. The inactivity lasts for 2-3 months, making this a 4-6 month condition. I’m currently in the middle of my second episode, and my first episode was just two years ago.
I am terrified. This condition has caused me to be rushed to the ER twice. This condition has rendered me so dizzy and dropped my blood pressure so low that walking is a hazard and I am in a wheelchair. This condition has prevented me from attending school since the end of October. This condition can occur again, and there is no telling when or how often.
I’ve scoured the web, posted in countless Facebook groups, analyzed research, and even scheduled a conference call with doctors in another country to try to get some answers. Not only is there no information on it, but I can’t find anyone else with it (and due to HIPPA laws, my doctor is not allowed to connect me with the other cases she has seen). I have support from my friends and family, but they cannot even begin to understand what this is like.
I am alone in this right now, but I know the internet is a powerful place. I’ve seen other kids with rare conditions find support and/or answers, and I thought I might as well give it a shot. Please, please - even if you don’t have this condition, even if you don’t know me, please reblog this and spread this around. I just need to know that I’m not alone in this. Even finding one person who has this would make the world of a difference.
Thank you in advance. Those who know me best know I absolutely hate asking for help, but I can’t do this alone anymore.
me, with no hesitation:
Soul Eater ended over 3 years ago and I'm still coming to terms with the fact that Maka Albarn and Soul Evans will never be canon although they had such a good and completing relationship