Lashley
Why does he wear the mask!?
Would you say that about transgender people as well?
No.
Are you a fucking moron? How can you compare the two?
Would you say that about transgender people as well?
You're probably right. I'll tell you one thing though, you can take both my arms and both my legs before you can take my daughter.The ability to reproduce is not as important as the ability to walk, hear, see.
That's right. I said that.
Come at me, bros.
No.
Are you a fucking moron? How can you compare the two?
I'd imagine people who still wanted biological children could freeze and preserve their sperm or eggs for the future. Adoption is always an option, as well.It's interesting that so many people are saying nothing is lost or impeded when transitioning from male to female (unlike able-bodied to disabled). Seems male privilege ain't worth what it used to be.
You're probably right. I'll tell you one thing though, you can take both my arms and both my legs before you can take my daughter.
That is practically word for word exact same argument people used for deriding transgender people some decades ago. If there's actual scientific research that says these people are not mentally ill, but instead have the neural mapping gone wrong in some places, I'm not going to ignore that.
as someone who identifies as otherkin i agree with this post, i do not need mental help nor am i strange for wanting to identify as a lone fox howling near the river
You're probably right. I'll tell you one thing though, you can take both my arms and both my legs before you can take my daughter.
Oh sure, it's a totally different thing with totally different ramifications. I was just idly musing that although I agree losing reproductive capacity isn't as 'disabling' as losing a limb, I'd much rather lose all my limbs than I would lose the result of my ability to procreate. I'm not really making any point, just rambling.I'd imagine people who still wanted biological children could freeze and preserve their sperm or eggs for the future. Adoption is always an option, as well.
Maybe I quite like the kid, and have an 'on and off' relationship with my limbs?This could be taken two ways; either it shows how much you love your daughter or you want to have your legs and arms removed.
One way or another, i'm wondering how certain positions will look in 10 years.
But yeah, whether this is a form of mental illness, or something else, there's no reason to ridicule these people.
Maybe I quite like the kid, and have an 'on and off' relationship with my limbs?
Endocrine Society Clinical Practice Guideline said:- Are of the legal age of majority in their nation.
- Have used cross-sex hormones continuously and responsibly during 12 months (if they have no medical contraindication).
- Had a successful continuous full-time real life experience (RLE) during 12 months.
- Have (if required by the mental health professional [MHP]) regularly participated in psychotherapy throughout the RLE at a frequency determined jointly by the patient and the MHP.
- Have shown demonstrable knowledge of all practical aspects of surgery (eg, cost, required lengths of hospitalizations, likely complications, postsurgical rehabilitation, etc).
Source
There already was discussion about how much of an advantage Oscar Pistorious might have with his artificial legs. Though I agree that when it's about actually replacing a limb, meaning that you actually having feeling in it etc., that's very far off, if ever.
Obviously depends on the reasons for doing so. If it stems from "those legs are not my own" likely yes. If it comes from "those legs are better than organic ones" maybe not.
No.
Are you a fucking moron? How can you compare the two?
these people feel equivalent to walking around in black-face, claiming they felt black inside, and should be treated as the race they FEEL they should have been born, despite it not being genetic truth.
/
Do you have any source?No need for insults, I only asked because transgender and transable are very similar.
Do you have any source?
I know you're getting at the point there's not enough medical study done yet, but the conditions appear analogous on their face. So I guess I should have said they appear very similar and there's no medical evidence suggesting they're not at this point.
Would you say that about transgender people as well?
I think that's another fallacy, braves. It's called argument from ignorance ("lack of evidence to the contrary").
But I digress.
I don't think it's purely argument from ignorance because there is some evidence in the form of reported symptoms and alleviation of symptoms via modification. Obviously the sufficiency of that evidence can and should be called into question. There needs to be further study no doubt, but it's not as baseless as me claiming there's a giant cat at the center of the universe for example.
Sure there is...
As a person born with a physical, and severe disability which has impacted my life in every way, every day... these people feel equivalent to walking around in black-face, claiming they felt black inside, and should be treated as the race they FEEL they should have been born, despite it not being genetic truth.
Edit: Incidentally, as I didn't state it very eloquently let me add...
I am sincerely repulsed by this, because it feels like people co-opting my culture, pain, and struggles. I STILL have to fight for things like benefits, or accessibility on a regular basis. I have had to halt promising career moves because a suddenly non-working power-wheelchair leaves me homebound, while looking for ways to fund a repair. There are real challenges the disabled (born, or created through tragedy) face that we as a society have yet to find good answers to.
Adding individuals who for whatever reason want to distract from real debate does nothing but diminish us as a society.
THAT ALL SAID, I would be a hypocrite if I didn't say they have every right to see themselves however they wish, or act in this fool-hardy way. I can be repulsed, and hate that we are even having this discussion, but I would never deny them their right to do this. I am simply using my own right to say that I will not embrace or support this cause in any way, and will not go out of my way to share the limited resources the disabled already get, with such individuals.
And I do stand by my assessment that, born out of mental disorder or not, this is akin to a white-person donning black-face, and claiming it is who they are inside. I feel like if that happened outrage would be more universal, but the vast majority of supporters of this here, likewise, likely, don't know what it is to be disabled either, and it makes it easier to misunderstand the relationship a disabled person has with their identity.
Honestly, I find it hard to be angry or outraged at someone who feels they need to remove their limbs regardless of your feelings that these people are co-opting your culture. It's such an extreme course of action to try and destroy a limb to feel "right" that I have a hard time not feeling sympathy for this person. The brain is a complex thing where certain damage or abnormalities can cause some crazy serious issues.Sure there is...
As a person born with a physical, and severe disability which has impacted my life in every way, every day... these people feel equivalent to walking around in black-face, claiming they felt black inside, and should be treated as the race they FEEL they should have been born, despite it not being genetic truth.
Edit: Incidentally, as I didn't state it very eloquently let me add...
I am sincerely repulsed by this, because it feels like people co-opting my culture, pain, and struggles. I STILL have to fight for things like benefits, or accessibility on a regular basis. I have had to halt promising career moves because a suddenly non-working power-wheelchair leaves me homebound, while looking for ways to fund a repair. There are real challenges the disabled (born, or created through tragedy) face that we as a society have yet to find good answers to.
Adding individuals who for whatever reason want to distract from real debate does nothing but diminish us as a society.
THAT ALL SAID, I would be a hypocrite if I didn't say they have every right to see themselves however they wish, or act in this fool-hardy way. I can be repulsed, and hate that we are even having this discussion, but I would never deny them their right to do this. I am simply using my own right to say that I will not embrace or support this cause in any way, and will not go out of my way to share the limited resources the disabled already get, with such individuals.
And I do stand by my assessment that, born out of mental disorder or not, this is akin to a white-person donning black-face, and claiming it is who they are inside. I feel like if that happened outrage would be more universal, but the vast majority of supporters of this here, likewise, likely, don't know what it is to be disabled either, and it makes it easier to misunderstand the relationship a disabled person has with their identity.
She told Barcroft TV that her fascination with blindness started when she was a child.
“By the time I was six I remember that thinking about being blind made me feel comfortable,” she said.
Shuping says that when she was a teenager, she started wearing thick black sunglasses, and even got her first cane when she was 18.
By the age of 20, Shuping says she was fluent in braille.
“I was ‘blind-simming’, which is pretending to be blind, but the idea kept coming up in my head and by the time I was 21 it was a non-stop alarm that was going off,” she told Barcroft TV.
Her need to lose her sight increased as she got older, and by 2006, she claims she found a psychologist who was willing to help her.
Shuping says the psychologist put numbing eye drops into her eyes, and then a couple of drops of drain cleaner.
“It hurt, let me tell you. My eyes were screaming and I had some drain cleaner going down my cheek burning my skin,” she said. “But all I could think was ‘I am going blind, it is going to be okay.”
The woman says it took about half a year for the damage to take full effect.
“When I woke up the following day I was joyful, until I turned on to my back and opened my eyes – I was so enraged when I saw the TV screen,” she told Barcroft TV.
One of her eyes eventually had to be removed, her other eye had glaucoma and cataracts, Barcroft TV reports.
Shuping says she originally told her family it was an accident, but they later found out the truth.
She says her mother and sister have since cut contact.
She told Barcroft TV that she has no regrets and that she hopes to help other blind people live an independent life.
“I really feel this is the way I was supposed to be born, that I should have been blind from birth,” she said. “When there’s nobody around you who feels the same way, you start to think that you’re crazy. But I don’t think I’m crazy, I just have a disorder.”
According to Barcroft TV, Shuping is hoping her story will help raise public awareness of BIID and encourage people with the condition to seek professional help.