The Lame Dame

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Posts tagged with "invisible disability"

Submission to TheLameDame from snouted

Me and my best friend the first time I needed to use a scooter to enjoy the zoo (pain/fatigue).  I don’t always think of myself as Having A Disability and then I remember, that’s called ‘stigma’ and having my best friend with me helps me with THAT too :)

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Good friends often make navigating the world easier for me, it’s nice to have someone to create a bubble of fun and happiness with, not to mention someone to help be sassy with strangers when they’re jerks (or maybe that’s just me). You both are adorable and that hat is GREAT, Thanks for the submission! 

Take Care - Kendall

thisisableism:

Disabled not differently abled.

What is an Invisible Disability?

i-need-that-seat:

I don’t agree with everything in this article (e.g. “just because a person has a disability, does not mean they are disabled”) but a LOT of the info here is informative and easily digestible. (e.g. “Often people think the term, disability, only refers to people using a wheelchair or walker. On the contrary […] 74% of Americans who live with a severe disability do not use such devices.”)


Also I’ve started reading the articles on the Invisible Disabilities Association website and zomg I’m probably gonna start posting them on this blog pretty much nonstop. :)

Haven’t submitted in ages….life’s been kicking my ass.
So my once local pain is now radiating through my whole body.  It sucks.  With the pain I’ve got in my wrists, elbows, and shoulders now, it’s almost impossible to get a bra on at all, and it is always extremely painful.
So, I’ve decided to give bralessness a try!  I’m trying to break out of the internalized misogyny that tells me I need to wear a bra all the time, especially since I’m busty.  I’m layering tanks under my shirts so there are no nip-throughs, but I know there’s this gross idea that it’s “unfeminine” or “brazen” or just not “classy” to go without a bra.  But I don’t give a shit about those things, I give a shit about lessening my pain.
Anybody else had to do this?  Or just do it because of preference?  Bra-removal always was a great part of my day, so I’m feeling pretty satisfied with the decision, at least for now.  Dunno if I’ll be comfortable keeping it up during our 100F-degree summers though….
I only wear a bra when I absolutely have to. I’m usually in layered outfits or wearing a scarf to sortof mask the wobble, and it hasn’t been a problem for me 
Rest Out with your Chest Out ;)

Haven’t submitted in ages….life’s been kicking my ass.

So my once local pain is now radiating through my whole body.  It sucks.  With the pain I’ve got in my wrists, elbows, and shoulders now, it’s almost impossible to get a bra on at all, and it is always extremely painful.

So, I’ve decided to give bralessness a try!  I’m trying to break out of the internalized misogyny that tells me I need to wear a bra all the time, especially since I’m busty.  I’m layering tanks under my shirts so there are no nip-throughs, but I know there’s this gross idea that it’s “unfeminine” or “brazen” or just not “classy” to go without a bra.  But I don’t give a shit about those things, I give a shit about lessening my pain.

Anybody else had to do this?  Or just do it because of preference?  Bra-removal always was a great part of my day, so I’m feeling pretty satisfied with the decision, at least for now.  Dunno if I’ll be comfortable keeping it up during our 100F-degree summers though….

I only wear a bra when I absolutely have to. I’m usually in layered outfits or wearing a scarf to sortof mask the wobble, and it hasn’t been a problem for me 

Rest Out with your Chest Out ;)

inspiration porn - am I doing it right?

inspiration porn - am I doing it right?

i-need-that-seat:

wheeliewifee:

chronicallykatie:

AMEN!

Fantastic!
Same goes for so many other illnesses, and even other forms of cancer…

Raise awareness! Ask questions, look it up, and don’t let any kind of “stigma” keep you from learning and teaching.

i-need-that-seat:

wheeliewifee:

chronicallykatie:

AMEN!

Fantastic!

Same goes for so many other illnesses, and even other forms of cancer…

Raise awareness! Ask questions, look it up, and don’t let any kind of “stigma” keep you from learning and teaching.

(Source: isometimesironmyshirts)

Nov 6

Hidden Disability and Voting Options

i-need-that-seat:

Marissa, who runs AbledIs, wrote this article about voting with an invisible disability. She talks about the awkward experience she had at a polling place in 2008 and hopes that Americans with invisible disabilities will not stay home today. Definitely a good read, and super relevant today!

**Submission to The Lame Dame from transgalacticwanderer**
It was hard for me to decide to submit this because I felt as if I’m inserting my privilege of being invisibly physically disabled into a space for those who are visibly disabled, but I hope that y’all will welcome me into this space.I’m Elissa, 20, visibly neurodiverse, invisibly physically disable, pansexual, grey-asexual trans* chick. One of the hardest things I’ve had face is people constantly assuming that I’m not physically disabled  but that I can’t do things because I’m fat or lazy. I’ve had a medically messy past (if y’all want to read about it more in depth check the “My History” tab on my blog), the short version is that thanks to a premature birth, hydrocephalus and a minor palsy, I have an malformed hip socket, limited range of motion/functionality in my left leg, the leg is shorter and the limp was only exacerbated by me breaking my right leg in kindergarten. This life has left me with a multitude of scars, both literal and metaphoric, and it’s taken me most of the past 20 years to begin to accept that I have the right to be proud of who I am. So much of my journey and struggles in life are tied in with my transition, it has been through my acceptance of my gender that I’ve come to embrace my scars, my flab, my limitations, my pain and my whole being.
I’m glad a space like this exists, it’s been thanks to tumblr that I’ve learned to accept my body and my experiences, and I hope that many others find the support I have.
**Note From Mod: Hello, Elissa! This is a space where folks living with disabilities or disabling conditions of all kinds can share their experiences, photos, stories, and gripes. You are most welcome here. -Kendall**

**Submission to The Lame Dame from transgalacticwanderer**

It was hard for me to decide to submit this because I felt as if I’m inserting my privilege of being invisibly physically disabled into a space for those who are visibly disabled, but I hope that y’all will welcome me into this space.

I’m Elissa, 20, visibly neurodiverse, invisibly physically disable, pansexual, grey-asexual trans* chick. One of the hardest things I’ve had face is people constantly assuming that I’m not physically disabled  but that I can’t do things because I’m fat or lazy. I’ve had a medically messy past (if y’all want to read about it more in depth check the “My History” tab on my blog), the short version is that thanks to a premature birth, hydrocephalus and a minor palsy, I have an malformed hip socket, limited range of motion/functionality in my left leg, the leg is shorter and the limp was only exacerbated by me breaking my right leg in kindergarten. This life has left me with a multitude of scars, both literal and metaphoric, and it’s taken me most of the past 20 years to begin to accept that I have the right to be proud of who I am. So much of my journey and struggles in life are tied in with my transition, it has been through my acceptance of my gender that I’ve come to embrace my scars, my flab, my limitations, my pain and my whole being.

I’m glad a space like this exists, it’s been thanks to tumblr that I’ve learned to accept my body and my experiences, and I hope that many others find the support I have.

**Note From Mod: Hello, Elissa! This is a space where folks living with disabilities or disabling conditions of all kinds can share their experiences, photos, stories, and gripes. You are most welcome here. -Kendall**

My girlfriend (Tumblr user meteloides) showing that cane users can still be sexy and smart. That’s her pharmacy tech recertification, should she feel strong enough and find a place accomodating enough in the next two years to hire her.

She has severe fibromyalgia, which was developed after pneumonia put her in the hospital for a week in February 2011.

My girlfriend (Tumblr user meteloides) showing that cane users can still be sexy and smart. That’s her pharmacy tech recertification, should she feel strong enough and find a place accomodating enough in the next two years to hire her.

She has severe fibromyalgia, which was developed after pneumonia put her in the hospital for a week in February 2011.

And from the OP of “Disbelief”

i-need-that-seat:

Oh my. I never meant for this post to spark such debates, especially ones that cost anyone precious spoons. (I’ve been fantastically low this week so I get it.)

I didn’t mean to insinuate that those with visible disabilities have any sort of privilege over those of us with invisible ones. The point of my post was that people - not even strangers, but coworkers and colleagues - assume I’m joking when they see me use a tag and say that I have a disability. The post was a commentary on the fact that it takes several minutes of “serious face” for them to understand that I’m not being facetious (who would joke about something like that??)

I read all the responses to this post and it seems it’s gotten very off the main point - which is fine, I’m all for discussion - but to bring it back, the point is that ableism sucks in ANY form, towards ANYONE with ANY sort of disability, visible or otherwise.

Take care of yourselves, everyone.

I-need-that-seat, 

I’m sorry we’ve strayed so far off the original topic, I know how distressing it can be to log in with a disagreement in the notes of your post. I’d just like to say I was partially responsible for the discussion morphing far beyond your point, and my bad.

It’s always painful to be assumed or insinuated to be faking, and one of the nastiest forms of casual ableism. It’s hurtful and unfair and sadly, not going to change for a long time unless we make it. 

I personally have two methods, first I smile and wave and yell something like “Long time no see!” or “I missed you, you bastard! Get over here!” and pretend they’re staring at me because we know each other. Or since I have gotten pretty good with my mean face (a chronic bitch face seems to help)I give them a death glare and a finger. If you look like you could breath fire, they tend to leave you alone…