Showing posts with label vagina. Show all posts
Showing posts with label vagina. Show all posts

Wednesday, January 29, 2014

Love & Pancakes: Being Intersex, a Day in the Life.

A cute story about my husband 
and my intersex condition, 
Complete Androgen Sensitivity Syndrome (CAIS). 
Seriously, it's a cute story.


As mentioned in my previous blog posts, The Secret Inside Meand The Secret Inside Me, Part 2: Feeling Shame, I didn't find out about my AIS condition until I was 35 years old. Although I had my undescended testes removed (gonadectomy/ orchidectomy) when I was 18-years old, back then, I was only told by the doctor, geneticist, and my parents that I was going to have a "radical hysterectomy" or I would die of cancer. (You can read all about that in the two above links.) 

All through high school I begged my mother to please take me to a doctor because I was convinced something was wrong because I had not started my period. She told me I was still too young, that I was a virgin, and she did not want me to be examined "down there" until I was 18 years old. I made her promise to come with me to a doctor when I turned 18. A week before high school graduation I made a doctor's appointment with a local OB/GYN, scheduling it a few days after my 18th birthday.

My mom was holding my hand in the examination room. The doctor walked in and introduced himself to us. (I had found him in the phone book.) I put my feet in the stirrups as he instructed and he lubed up his gloved fingers. The first thing he said -- in a surprised manner -- was "What?! There's no cervix! There isn't anything!" My mom and I looked at each other like, "Wha?" He then took his gloves off and said, "Please get dressed and the nurse will lead you into my office. We need to talk." When he left the room my mom began to cry and I was stunned at his words so I just hugged her and told her it would be all right. The first thing he said to us in his office was, "You need to have surgery immediately or you will die of cancer." It was all a blur after that.  He said he made an appointment for both my parents to take me to a genetic counselor and gave my mother the information. I was quiet and in shock. My mom cried silently to herself as I drove home. I really don't know how I was able to drive and did not remember driving us home. From the two blog posts mentioned above you will read that my parents were eventually told the truth about my "syndrome" but were advised by the doctors not to tell me. So they didn't. "For [my] own well-being."

After the so-called "hysterectomy" aka "mystery surgery" I suffered deep depression and I took the semester of my first year of college off and never left the house. I burrowed myself at home and turned somewhat agoraphobic and refused to leave home in my depression. I eventually went to community college because I was basically disinterested in school and had to figure out what I wanted to do with my life. I was 19-years old. My doctor had told my parents about dilators to stretch out my blind-ending vagina but at that time (after my surgery) they said I was a virgin and didn't want me dilating "down there." That is what my crotch was referred to back then, "down there." 

When I was 20-years old I entered university and it was all kind of a blur but decided to study hard and forget about all the crap about my feeling shame and feeling like something was wrong with me. I told myself to "snap out of it!" Back then I never considered counseling nor did my parents ever suggested anything like that.

Anyway, I met my amazing and loving husband at the university campus. We immediately fell in love. It happened so fast that he proposed to me two weeks after he met me. We hadn't had sex. When he asked me to marry him the first thing that I thought in my head was, "Uh-oh, if I say yes then I have to tell him I can't have kids." I did not know at the time that I was a genetic male or about AIS except that I was unable to have kids. 

Of course, I fell in love too, and wondered at how lucky I was that someone would even love me. I immediately said "yes." I did not realize that he would get so excited about marrying me and that all he could talk about was how beautiful our children would be. I was so overwhelmed and terrified. He couldn't wait to get married and have children and start a family. I got scared. He had joined the Marines immediately after high school then he added two more years in the national guard. After that, he began undergraduate school the same year I entered the university. What solidified our relationship was when his father was asking about where my family came from and it turned out my uncle and he had been best friends in the 60's and 70's and had worked together in town and it didn't hurt that they were both veterans who had served in WWII. Small world. It all seemed like "it was meant to be."

As I stated before he proposed to me two weeks after I met him. He kept talking about how great our life would be. He talked about his plans for our life. He was excited about having children and asked me how many I wanted. Yikes! I eventually broke down and cried to him that I couldn't have kids and then showed him my pencil thin surgical scar across my lower abdomen and told him he didn't have to marry me and that we can just be friends. He began tearing up. He was very sweet. We were both sad. I told him to go home and think about what he really wanted and that I couldn't lie to him so I had to tell him the truth of what I knew at the time. (When I play this conversation in my mind, in retrospect, it makes me see it as a dramatic Mexican novela on Telemundo: The tears. The hugs. The sadness. The angst. My self-deprecation. My sacrifice to give up a man I loved because I wanted to be truthful. The stuff of soap operas!) That same night he called me on the phone and told me he didn't care that I could not have children. He couldn't see a life without me and that he loved me so much. He felt in his heart that I was his soul-mate. I felt the same way.

We got married six months later. I was 21 years old and he was 26. We had a beautiful and big wedding in a humble and old little Catholic church and vowed our undying love for better or for worse and all that stuff. Half my home town showed up and we literally had a 3-day wedding celebration.
Fast forward to me at 35-years old. I eventually said enough is enough. All these years of wondering about that surgery when I was 18-years old. My conversation with my sister who is also CAIS who told me all she knew was that we were born with a "syndrome." I eventually got my medical records and learned the name of the syndrome was "Feminizing Testicular Syndrome" and, in the age of the world wide web, finally learned everything about this mysterious syndrome. 

That night, at 2 a.m. I had a huge stack of information that I had read through. At the time, some of the information I did not understand in terms of karyotypes, 46XY, and all the other genetic verbage that was making my head spin. However, I kept digging and researching until I finally understood what I was learning about myself. My medical records were pretty specific since I was constantly referred to as "the affected male." 

In the wee hours afterward I cried. I had to tell my husband, who was asleep in the bedroom on his third dream. Before he had gone to bed he had asked me to make him a great breakfast in the morning and that he wanted pancakes. I promised, then kept on frantically researching on my brand new desktop computer. Anyway, I ran into the bedroom in tears with a stack of paperwork in my hands and tearfully woke him up. He jumped out of bed scared that something had happened. I blurted out the name of the syndrome and that I was "A genetic male!" And then proceeded to ask him if he was going to divorce me. My histrionics were very dramatic. Like a soap opera: the streaming tears, the pleading eyes, the hand wringing, the shaking and sobbing, etc., all on my part. 

He hugged me tight and kissed me. He then wiped the tears from my face and said I was "stuck with [him]." He said he loved me so much that NOTHING (he stressed this emphatically) was ever going to keep us apart. "Not even [my] genetics?" He said, "Fuck that! You think I care about any of that after being married this long?" By then we had been married 14 years. I was relieved and wanted to hug and kiss him all the rest of the wee hours. But then he said, "Now leave me alone to finish my dreams and, DON'T FORGET, you promised to make me pancakes in the morning!"

See, I told you this was a cute story. All the fears were inside of ME. My wonderful husband had nor has he had any issues about my genetics. All the years of feeling ashamed and sad not knowing the real truth about myself was the worst thing, even moreso than the a facts about my AIS.

To date, we have been married for 31 years and he doesn't have any plans yet to trade me for someone else. He's a keeper. I am truly blessed!






Thank you for your support and advocacy!

All rights reserved. Blog posts by Zoltana-of-the-Desert. Permission is required to copy or disburse any content of Zoltana-of-the-Desert. Thank you.

Thursday, March 10, 2011

The Secret Inside Me

A dear friend of mine wears a t-shirt that says it all: 
"1 in 2000 People are Intersex. 
Do you know any? 
Are you sure?" 
(c) 2011 Zollies-Spot. All rights Reserved.

Don't Judge Me: Learn Something From Me

We all have secrets. Secrets so deep that you may never tell a soul. Can you imagine blogging and telling the world about your deep dark secret? I'm coming out of my cave, my deep dark cavern to tell you that I am an intersex individual who was born with a difference in sexual development and many people out there in the world may think they don't know anyone like me; however, you may have a friend or relative like me, or may have met a person like me and you may not even know.

Intersexed individuals are like the lost tribe that has remained hidden in the wild jungles and people are just now learning about them. Or that rare plant or animal species that we never knew existed but has always been in existence. Oh, it hasn't been by choice that people like me aren't very public to the masses. It's just that, in the past, people like me have been stigmatized, marginalized, and made to feel as if we don't belong in the cog of the wheel of humanity:  their version of the binary "norm." But things, they are a-changin.

Here's a little information to try to enlighten those that have never heard the term, Intersex.

What is the definition of Intersex? The online explanation says:  "“Intersex” is a general term used for a variety of conditions in which a person is born with a reproductive or sexual anatomy that doesn’t seem to fit the typical definitions of female or male. For example, a person might be born appearing to be female on the outside, but having mostly male-typical anatomy on the inside..." 
For a full definition see http://www.isna.org/faq/what_is_intersex.

I'm not anyone special, except to my dear friends and family. Actually, I'm just like you. A person who lives in this world. Who loves and dreams and has hopes and aspirations just like you.  I am also not that different from you. If you are a woman reading this I want you to know that I am like you. I am feminine. I identify as a female. I was raised as a female and, like you, I have been called a "beautiful woman" at least one time in my life by a special someone. I AM LOVED.

The only thing that sets me apart from "normal" women is that I am intersexed.  What does that mean? Well, my genetic/DNA makeup is XY/male but even though I have male chromosomes my external genital development continued among the female lines at birth because the embryonic testes that developed inside of me, although they produced male hormones, were not able to continue along the lines of the male genital development. This syndrome is called Androgen Insensitivity Syndrome (AIS) which means that my fetal body tissue was insensitive to the male androgens I was producing.  Therefore, I developed physically as a female, by default. My exterior is ALL woman but because my body was confused I didn't develop reproductive organs. I cannot have children. The older literature regarding this syndrome used the stigmatizing term, "Testicular Feminizing Syndrome."

The medical community at the time never told me what was wrong with me, yet I was already 18 years old. Doctors told my parents not to say anything to me because I would become suicidal or go crazy. The doctors and geneticists were like gods to people of my parent's generation. So, like good parents and doctors of their time, I was instead told that I may die of cancer and that they had to remove my "ovaries" as soon as possible.  The problem with this is that what they were removing were not ovaries but undescended testes. I also did not have cancer.  I was a shy girl and I was stunned and never asked any questions.  I was just scared. Very scared. I did not find out the truth of my "syndrome" until the advent of the Internet in the 1990s. The world wide web provided me its font of information at a touch of a button.

My journalistic background also dove me into heavy research and I read everything I could read about this syndrome.  Then, I read my medical records. The enlightenment was cathartic in the sense that I was relieved to know the facts about me. The mystery and the guesswork was taken out of the equation. Of course, my freakish feelings were still a part of me because I was made to feel that way by lies and innuendo. My records termed me as a "male-pseudo hermaphrodite" and throughout my records I was referred to as the "affected male." Shocking? Yes. But I was also relieved that it was all laid out in front of me in black and white, in print. My research answered all of my questions. A doctor was not around to lie to me. A doctor was not around to stammer at me and not look me in the eye. Have you ever been at "rock-bottom" in your life? I have. But from that "rock-bottom" ignorance I emerged like the legendary Phoenix and like all of us, when we are thrown into the bowels of something unknown, I just dealt with it and became empowered by what I learned about myself.

The journey I have traveled has been filled with obstacles like anger, shame, and very very sad and inner feelings of not really belonging or even being able to identify with others' "womanhood." For example, the rites of passage every young pubescent girl experiences. I did not experience the explosion of changes of a young girl: the dreaded "period", the hair growth in places you weren't expecting, the acne, etc. 

I usually describe my genitals like this: I have a beautiful "blind-ending" vagina with labia and a nice little clitoris. What does a "blind-ending" vagina mean? Think of a pool table with pool pockets. My vagina is like a small pool pocket that does not lead anywhere. I was born with no reproductive organs like a cervix, uterus, fallopian tubes, etc. It's funny how I will go to a doctor's office and will be asked when I had my last period. I just honestly say, "I've never had a period." Then the questions begin, "What do you mean?" "Every woman has had a period!" That is when I can educate nurses or doctors if they are honest with me and admit they do not know what it means to be an intersex individual or about my AIS.

I can always tell when either they don't care or if they don't understand even when they do not admit they don't understand. Because the conversation usually goes like this:


Nurse: Are you on your period or when was your last period?
Me: I am an intersex individual. I have no reproductive organs.
Nurse: Ok, but when was your last period?
Me: I have no reproductive organs.
Nurse: Do you have children or have you ever been pregnant?
Me: I have no reproductive organs.

When this happens I begin to wonder and get worried. I will then explain very carefully my situation. I usually carry printouts of information and flyers explaining intersex conditions with information about support groups so that medical staff can have the information handy to offer parents or patients if they encounter any other intersex patients. I always authorize them to feel free to give people my contact information if any parents or intersex individuals would like to talk with me so that they don't feel so alone.

The journey to my discovery has been long. Very long. And this journey with its twists and varying crossroads has made me feel empowered enough to come out of my shell and inform and educate others. I am an advocate for people like me that haven't come out of their own cavern. I am their voice. There are others like me and we are banding together to be heard and to let others know that we are here living among you and that we DO belong to the human spectrum.

Note: Think of the term Differences of Sexual Development as the umbrella that covers many types of conditions like my AIS.  You can learn more about AIS or about other conditions like Swyers Syndrome, Congenital Adrenal Hyperplasia (CAH) and other differences via the world wide web or by following the links below. When you do learn more, I urge you to tell a friend what you learned so that they can tell their friends. After all, you may one day meet a person like me if you think you haven't already and you will be able to listen to their story with compassion and with respect and understanding.

For a continuation of this story, click this link for 
Part Two: Feeling Shame

"The bottomless pit of shame is a stifling tourniquet around any motivation or drive or creativity.
Shame is only good for writing sad poetry like a cutter slowly ticking away at your own flesh to feel something: even if it is only emptiness." The Secret Inside Me, Part 2: Feeling Shame


Resources and Websites:
  1. Definition of Intersex via ISNA: http://www.isna.org/faq/what_is_intersex
  2. AIS-DSD Support Group: http://www.aisdsd.org/
  3. The Kinsey Institute: http://www.kinseyinstitute.org/
  4. I recommend reading Alice Dreger's work. She has written "Intersex in the Age of Ethics" and "Handbook for Parents of Children with Disorders of Sex Development (DSD Consortium, 2006)" at http://alicedreger.com/books.html
  5. Definition of Differences of Sex Development: http://en.wikipedia.org/wiki/Disorder_of_sexual_development
  6. Article regarding differences of sexual development/intersex in Stanford medical magazine: http://stanmed.stanford.edu/2011spring/article4.html

All rights reserved. Photograph and blog post by Zollies-Spot. Permission is required to copy or disburse any content of Zollies-Spot.
Orchids are all around you!

www.aisdsd.org

The Secret Inside Me

A dear friend of mine wears a t-shirt that says it all: 
"1 in 2000 People are Intersex. 
Do you know any? 
Are you sure?" 
(c) 2011 Zollies-Spot. All rights Reserved.

Don't Judge Me: Learn Something From Me

We all have secrets. Secrets so deep that you may never tell a soul. Can you imagine blogging and telling the world about your deep dark secret? I'm coming out of my cave, my deep dark cavern to tell you that I am an intersex individual who was born with a difference in sexual development and many people out there in the world may think they don't know anyone like me; however, you may have a friend or relative like me, or may have met a person like me and you may not even know.

Intersexed individuals are like the lost tribe that has remained hidden in the wild jungles and people are just now learning about them. Or that rare plant or animal species that we never knew existed but has always been in existence. Oh, it hasn't been by choice that people like me aren't very public to the masses. It's just that, in the past, people like me have been stigmatized, marginalized, and made to feel as if we don't belong in the cog of the wheel of humanity:  their version of the binary "norm." But things, they are a-changin.

Here's a little information to try to enlighten those that have never heard the term, Intersex.

What is the definition of Intersex? The online explanation says:  "“Intersex” is a general term used for a variety of conditions in which a person is born with a reproductive or sexual anatomy that doesn’t seem to fit the typical definitions of female or male. For example, a person might be born appearing to be female on the outside, but having mostly male-typical anatomy on the inside..." 
For a full definition see http://www.isna.org/faq/what_is_intersex.

I'm not anyone special, except to my dear friends and family. Actually, I'm just like you. A person who lives in this world. Who loves and dreams and has hopes and aspirations just like you.  I am also not that different from you. If you are a woman reading this I want you to know that I am like you. I am feminine. I identify as a female. I was raised as a female and, like you, I have been called a "beautiful woman" at least one time in my life by a special someone. I AM LOVED.

The only thing that sets me apart from "normal" women is that I am intersexed.  What does that mean? Well, my genetic/DNA makeup is XY/male but even though I have male chromosomes my external genital development continued among the female lines at birth because the embryonic testes that developed inside of me, although they produced male hormones, were not able to continue along the lines of the male genital development. This syndrome is called Androgen Insensitivity Syndrome (AIS) which means that my fetal body tissue was insensitive to the male androgens I was producing.  Therefore, I developed physically as a female, by default. My exterior is ALL woman but because my body was confused I didn't develop reproductive organs. I cannot have children. The older literature regarding this syndrome used the stigmatizing term, "Testicular Feminizing Syndrome."

The medical community at the time never told me what was wrong with me, yet I was already 18 years old. Doctors told my parents not to say anything to me because I would become suicidal or go crazy. The doctors and geneticists were like gods to people of my parent's generation. So, like good parents and doctors of their time, I was instead told that I may die of cancer and that they had to remove my "ovaries" as soon as possible.  The problem with this is that what they were removing were not ovaries but undescended testes. I also did not have cancer.  I was a shy girl and I was stunned and never asked any questions.  I was just scared. Very scared. I did not find out the truth of my "syndrome" until the advent of the Internet in the 1990s. The world wide web provided me its font of information at a touch of a button.

My journalistic background also dove me into heavy research and I read everything I could read about this syndrome.  Then, I read my medical records. The enlightenment was cathartic in the sense that I was relieved to know the facts about me. The mystery and the guesswork was taken out of the equation. Of course, my freakish feelings were still a part of me because I was made to feel that way by lies and innuendo. My records termed me as a "male-pseudo hermaphrodite" and throughout my records I was referred to as the "affected male." Shocking? Yes. But I was also relieved that it was all laid out in front of me in black and white, in print. My research answered all of my questions. A doctor was not around to lie to me. A doctor was not around to stammer at me and not look me in the eye. Have you ever been at "rock-bottom" in your life? I have. But from that "rock-bottom" ignorance I emerged like the legendary Phoenix and like all of us, when we are thrown into the bowels of something unknown, I just dealt with it and became empowered by what I learned about myself.

The journey I have traveled has been filled with obstacles like anger, shame, and very very sad and inner feelings of not really belonging or even being able to identify with others' "womanhood." For example, the rites of passage every young pubescent girl experiences. I did not experience the explosion of changes of a young girl: the dreaded "period", the hair growth in places you weren't expecting, the acne, etc. 

I usually describe my genitals like this: I have a beautiful "blind-ending" vagina with labia and a nice little clitoris. What does a "blind-ending" vagina mean? Think of a pool table with pool pockets. My vagina is like a small pool pocket that does not lead anywhere. I was born with no reproductive organs like a cervix, uterus, fallopian tubes, etc. It's funny how I will go to a doctor's office and will be asked when I had my last period. I just honestly say, "I've never had a period." Then the questions begin, "What do you mean?" "Every woman has had a period!" That is when I can educate nurses or doctors if they are honest with me and admit they do not know what it means to be an intersex individual or about my AIS.

I can always tell when either they don't care or if they don't understand even when they do not admit they don't understand. Because the conversation usually goes like this:


Nurse: Are you on your period or when was your last period?
Me: I am an intersex individual. I have no reproductive organs.
Nurse: Ok, but when was your last period?
Me: I have no reproductive organs.
Nurse: Do you have children or have you ever been pregnant?
Me: I have no reproductive organs.

When this happens I begin to wonder and get worried. I will then explain very carefully my situation. I usually carry printouts of information and flyers explaining intersex conditions with information about support groups so that medical staff can have the information handy to offer parents or patients if they encounter any other intersex patients. I always authorize them to feel free to give people my contact information if any parents or intersex individuals would like to talk with me so that they don't feel so alone.

The journey to my discovery has been long. Very long. And this journey with its twists and varying crossroads has made me feel empowered enough to come out of my shell and inform and educate others. I am an advocate for people like me that haven't come out of their own cavern. I am their voice. There are others like me and we are banding together to be heard and to let others know that we are here living among you and that we DO belong to the human spectrum.

Note: Think of the term Differences of Sexual Development as the umbrella that covers many types of conditions like my AIS.  You can learn more about AIS or about other conditions like Swyers Syndrome, Congenital Adrenal Hyperplasia (CAH) and other differences via the world wide web or by following the links below. When you do learn more, I urge you to tell a friend what you learned so that they can tell their friends. After all, you may one day meet a person like me if you think you haven't already and you will be able to listen to their story with compassion and with respect and understanding.

For a continuation of this story, click this link for 
Part Two: Feeling Shame

"The bottomless pit of shame is a stifling tourniquet around any motivation or drive or creativity.
Shame is only good for writing sad poetry like a cutter slowly ticking away at your own flesh to feel something: even if it is only emptiness." The Secret Inside Me, Part 2: Feeling Shame


Resources and Websites:
  1. Definition of Intersex via ISNA: http://www.isna.org/faq/what_is_intersex
  2. AIS-DSD Support Group: http://www.aisdsd.org/
  3. The Kinsey Institute: http://www.kinseyinstitute.org/
  4. I recommend reading Alice Dreger's work. She has written "Intersex in the Age of Ethics" and "Handbook for Parents of Children with Disorders of Sex Development (DSD Consortium, 2006)" at http://alicedreger.com/books.html
  5. Definition of Differences of Sex Development: http://en.wikipedia.org/wiki/Disorder_of_sexual_development
  6. Article regarding differences of sexual development/intersex in Stanford medical magazine: http://stanmed.stanford.edu/2011spring/article4.html

All rights reserved. Photograph and blog post by Zollies-Spot. Permission is required to copy or disburse any content of Zollies-Spot.
Orchids are all atound you!

www.aisdsd.org