Boy With Vagina

Boy With Vagina

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'I actually thought it was a joke. I didn’t even know this was possible. I was like ‘haha where are the cameras’? Then they showed me my uterus on the screen'.
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A teen born with male genitalia and raised as a boy has become pregnant after finding out last year that she also has working ovaries, a uterus, cervix and fallopian tubes.
Mikey Chanel, 18, was raised as a boy, but always felt ‘he’ was different from his male peers.
In fact, tests done on Mikey as a foetus in his mother’s womb revealed him to be a girl, so his family and doctors were surprised when he was born with male genitalia
For more Health & Wellbeing related news and videos check out Health & Wellbeing >>
“It was obvious to everyone that I was different right from the start,” said Mikey, who lives in Boston, Massachusetts and worked as an events coordinator before the pandemic.
“At age five I’d be playing with my aunt’s purses and putting on my mom’s lipstick.
“I never felt like a boy. I was quite effeminate and I never really went through a whole ‘boy puberty’ thing.
“I only have a tiny bit of facial hair. I’ve always had a feminine-shaped body, with hips and a butt.
“I got bullied at school, everyone told me I was a faggot, a tranny, since third grade, before I even knew what it meant really.”
Mikey came out as gay aged 13, and later wondered if he might be transgender.
The truth was only revealed by accident last year when Mikey was undergoing some routine tests at the doctors.
“I had been having a weird feeling after peeing and after sex, so they did an ultrasound of my urinary tract,” said Mikey.
“They told me that I had a cervix, ovaries, uterus and fallopian tubes and that I could get pregnant if I wanted to.
“I actually thought it was a joke. I didn’t even know this was possible. I was like ‘haha where are the cameras’? Then they showed me my uterus on the screen.”
Mikey was diagnosed with Persistent Müllerian duct syndrome (PMDS), a rare condition in which a person has male external genitals, with female reproductive organs internally.
Doctors advised Mikey to have an immediate hysterectomy.
Mikey added: “People with PDMS are susceptible to cancer and tumors and the risk is lessened if you have a hysterectomy.
“My male parts came back infertile but I was told that my ovaries were functioning.
“I was in a state of shock for a couple of weeks then I realized that I wouldn’t be able to have a child unless I carried it myself, and soon.
“I always knew I wanted to be a parent, I used to play with baby dolls when I was little and I’ve always seen kids in my future, so I decided, ‘it’s now or never I have to try and get pregnant.’”
Mikey then underwent a series of fertility procedures including ICSI and in which donor sperm is injected directly into a woman’s egg to create a fertilized embryo.
During a laparoscopic procedure called ZIFT embryos were placed in the fallopian tubes.
Because Mikey does not have a vaginal opening three fertilized embryos were implanted into her fallopian tube via an abdominal cavity.
“I was told there was only about a 20 percent chance it would work, but it worked, and I was so shocked but happy” said Mikey, who is now four months pregnant.
“I can’t wait to be a parent,” she added.
Mikey has been prescribed estrogen to help with the pregnancy and she hopes to continue to transition further after the baby is born.
“I feel more like a woman now than ever,” she said.
Mikey is speaking out about her experiences to raise awareness of PMDS and help people understand that it is a normal medical condition that could happen to anyone at birth.
She also wants to break social stigmas related to gender nonconformity.
“Nobody really speaks about this, most people have never even heard of it,” she said.
“There isn’t a lot of research about it and there aren’t a lot of tests, often it’s found accidentally, like in my case.
“I feel like there should be more research, I’m just trying to educate people about it. Once people understand it could break a really big stigma with gender and within LGBT communities.”
By Douglas Whitbread / Health & Wellbeing
By Katie Dollard / Health & Wellbeing
By Douglas Whitbread / Health & Wellbeing
By Katie Dollard / Health & Wellbeing

This is actually pretty informative.

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Goddamnit WET...I told you...give me a picture and an idea...and I'll see what I can come up with...otherwise....just take some shit outa one of my accounts av history

my farts smell like shit covered rotten eggs

I'm a magnificent specimen of hillbilly grossness

Replies not required unless you feel the urge to do so, then by all means, bottom for my comments.

No, you...you wimpy little girly man.

I could see a vagina quicker than any of you could.

what the fuck is goin on in this gay-ass place?

but hurting as far the little one eyed penor can see.

i wonder if its one of those twats that looks like an exploded raost beef

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This woman was born without a vagina

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A British woman who underwent surgery to improve her sex life ended up with none — after her vagina mutilated her partner’s penis.
Theresa Bartram, 50, of Brighton, suffered from stress incontinence after giving birth to her only child, sending her confidence in bed plummeting, The Sun newspaper reported .
After going seven years without sex, she underwent an operation to lift her prolapsed bladder with a plastic mesh sling called a transvaginal tape, which stopped her leaking.
The joy of sex resumed for a couple of years, but things went horribly wrong in 2009, when her vagina almost cut off her partner’s manhood.
“It was like it had grown teeth,” she said. “His willy was bright red and spouting blood. There was a big red stain spreading between us on the sheets. After that, he was scared of my lady garden and approached it as if it was a Venus flytrap and he was a bluebottle (fly).”
Bartram thought the mesh inside her caused the man’s gruesome injury, but her doctor kept saying it was working fine.
Six months later, the despondent couple broke up and she grew terrified of having intercourse again.
Bartram went on a diet and began exercising, but a few months later began suffering from serious health problems, including a bloated stomach, severe stomachaches, diarrhea and vomiting.
She was diagnosed with irritable bowel syndrome and given antidepressants. Eventually, she had her gallbladder removed.
Finally, in 2015, she was told the mesh had to be removed urgently because it had breached her vaginal wall and caused an abscess that turned septic.
During the surgery, it was discovered that the mesh — which had been fitted too low — had turned hard.
“It felt like razor-sharp teeth, hence why it had ripped a chunk from my boyfriend’s willy,” she said.
The removal of the mesh left her incontinent again.
“I was told this simple procedure would cure my incontinence and give me more confidence on the bedroom, but it has ruined my life,” said Bartram, whose vagina has been left numb.
“It made my vagina deadly and forced me into a life of celibacy. It could have killed me,” she said. “I’m pleased the mesh is gone but it has left my body and my vagina a total mess. I wear padding all the time and sleep on incontinence sheets.”
Bartram has joined Sling The Mesh, a group that is fighting the controversial medical procedure, which has been suspended in Scotland and is under scrutiny worldwide.
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