Joanna
Giannouli, 27, has a condition which means she has no womb, cervix and
upper vagina. Here, she explains the challenges of a syndrome that
affects around one in 5,000 women.
When we first saw the doctor, my
father put on a brave face. My mother, on the other hand, didn’t take
it so well. She blamed herself for the past 10 years. It was really
heartbreaking to see her like that.
We didn’t talk about it much for
the first five years. I wasn’t able to talk about it. I felt destroyed
and incredibly weak. My mother believes she may have done something
wrong in her pregnancy. I’ve explained to her that she didn’t do
anything wrong, it was just genes.
It’s a condition that is stigmatised. The most hurtful thing was when I was abandoned after my former partner found out.
I was engaged when I was 21,
living in Athens. When I told my fiance about the condition, he broke
off the engagement. That all belongs in the past and I am OK now. For
the past five years, fortunately, I have had a stable and loving
relationship. He knew from the beginning that I have this condition and
he chose to stay with me. He knows that maybe the future will be without
children. He’s OK with it. I’m also OK with that. I am one of the
luckiest.
My mother took me to our family
doctor when I was 14 because I still wasn’t menstruating. He didn’t
examine me because he wouldn’t touch my private parts and when I became
16 he sent me to a hospital to be checked out. They realised that I
didn’t have a vaginal tunnel and I had Rokitansky syndrome. Because I
was born without a functional vagina, the doctors had to make one in
order for me to have sex.
It went well, really well. I
stayed in a hospital for about two weeks, in order to recover. Then I
had to be about three months laying on a bed – I couldn’t get up. I did
vaginal exercises in order to expand my new vaginal tunnel. The first
sign of it is you have primal amenorrhea – you don’t have any
menstruation at all. Apart from that, you cannot have sexual
intercourse. That’s why I had major surgery aged 17. The doctors made me
a new one. It was a revolutionary procedure in Athens.
The new vagina the doctors made
was narrow and small, and it caused me a lot of pain while having sex,
and I had to expand the perineum by doing vaginal exercises. It’s a
small area underneath the vagina. It’s skin, it’s tissue, and they had
to cut it more in order to expand the entrance, as I call it.
After that I was OK physically,
but I was not OK emotionally. It’s a burden, like something that you
cannot get rid of it. I had partners who emotionally abused me about
this condition. I couldn’t have a stable relationship for many years
because of that. It is a haunting and unbearable situation. It steals
your happiness, your mentality, your chances of having a good and stable
relationship. It leaves you with a huge void that cannot be filled, it
fills you with anger, guilt, and shame.
Source: BBC
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