Meet Jacqui Beck a 19year old teenager without a vagina.
Jacqui, has MRKH, an rare syndrome which affects the reproductive system - meaning she has no womb, cervix or vaginal opening.
She was only diagnosed after she went to her GP about back pain - and mentioned in passing that she hadn't started her periods.
Tests
revealed her condition and that where her vagina should be, there is
simply an ident, or 'dimple' - meaning she is unable to have sex or
carry her own child.
Women
with the condition appear completely normal externally - which means it
is usually not discovered until a woman tries to have sex, or has not
had her first period.
Miss Beck, from the Isle of Wight, admits when she was first diagnosed, she felt 'like a freak'.
'I'd never considered myself different from other women and the news was so shocking, I couldn't believe what I was hearing.
‘I
was sure the doctor had got it wrong, but when she explained that was
why I wasn’t having periods, it all started to make sense.
‘She then explained that I would never be able to carry a child and might have to have surgery before I could have sex.
‘I left the doctors in tears - I would never know what it was like to give birth, be pregnant, have a period. All the things I had imagined doing suddenly got erased from my future.
'I was really angry and felt like I wasn’t a real woman any more.'
Because
she had never attempted to have a physical relationship, Miss Beck had
never noticed the problem herself. Had she tried, she would have
discovered it was impossible for her to have sex.
She
said: 'It wasn’t really a conscious decision not to have a boyfriend, I
just didn’t really fancy any of the boys in my area, which is lucky,
considering what I know now’.
MRKH
affects one in 5,000 women in the UK. Most discover they have the
condition because they haven't started their periods, but some find out
when they struggle to have intercourse.
Miss
Beck explained she has a 'dimple' where her vagina should be so from
the outside it looks normal - which explains why the condition wasn't
detected earlier.
Despite
the shocking news, she is trying to see her condition in a positive
light - and even as a way of making sure she meets the right man.
She said: 'If he has a problem with it, then he’s not the kind of guy I want to go out with.
'I’m
a hopeless in romance and I see it as a great test of someone’s
character. Instead of focusing on it putting off men, I actually think
it will help me find, “the one”.
'I
want to be upfront with any man I meet and tell him straight away
about my condition. I don’t want him to feel tricked into being with
me.
‘I
will feel more comfortable if they know the truth and besides, if they
run at the mention of MRKH then I don’t want to be intimate with them.'
She
says that as a teenager, she was blissfully unaware of her condition -
with no idea that the development she was waiting for would never
happen.
'When I was 14, my friends started
talking to me about their periods. They started carrying tampons
around, complaining about cramps and sharing notes on what it was like.
‘For a year I waited to go through the same, until at 15, everyone I knew had started their period apart from me.
‘I didn’t panic though, I’m tall and skinny and thought that might be something to do with me being a late developer.’
Instead, she focused on her future and when she was 17, applied to attend a music college in Guildford.
But after suffering from pain in her neck in summer 2012, she went to see her GP.
'While
I was there, I mentioned I hadn’t started my period yet. I still wasn’t
overly worried but I thought it was worth saying something
‘My
doctor was very surprised but didn’t seem to think it was serious. He
just suggested that he would do some scans to see what the problem was.'
When scans showed nothing, she was referred to a gynaecologist, who immediately spotted something was wrong.
Miss Beck said: ‘My other scan results had been sent to her and just from looking at them, she knew I had MRKH.
‘She
sat me down and basically explained that I didn’t have a womb, or a
vagina, that I was born without them and instead just had a small dimple
in it’s place.'
So
mortified by what she had heard, she was too embarrassed to admit to
family and friends she had the condition - let alone the prospect of
telling any future boyfriends.
She said: ‘I was too embarrassed to call my mum and talk it through with her, so instead, I sent her an email.
'She called straight back and came over to Guildford the next day from the Isle of Wight.
‘Although
mum was upset for me, she tried to focus on finding out as much about
the condition as possible, so we could understand it.
‘She
also encouraged me to focus on the bright side. We laughed as we listed
all the things I wouldn’t have to go through, period cramps,
childbirth, smear tests - to try and look on the bright side.’
Focusing
on her treatment, Miss Beck was admitted to the Queen Charlotte and
Chelsea Hospital in London, which specialises in the condition.
There,
she was given dilation treatment, which involved using different sized
dilators to try and stretch her vaginal canal - but was told if it
didn’t work, she would have to be operated on.
She said: ‘I spent two days there, getting taught how to use the dilator and learning more about MRKH.
‘The
first time the nurse showed me how to use a dilator I nearly died of
embarrassment. But now I've got used to it, I see it as any other form
of treatment.
‘At
the hospital, they referred me to a network of other women who have the
same condition. It was great to speak to other girls who felt like me.
‘I stopped feeling so lonely and it also gave me hope as I spoke to women who had gone on to have a full sex life.’
Thankfully,
her treatment has worked and if she continues she will not need surgery
and when she chooses to, will be able to have intercourse.
Further down the line there are more difficult conversations she will have to have to have when she wants to have children.
She
said: ‘I’m not at an age when I’m thinking about kids, but I think that
will hit me later on. I will use a surrogate, or adopt, but I will have
to make sure any guy I meet is ok with that too.
‘Again,
I try and take it as a blessing that, unlike woman who discover they
can’t conceive when they are already trying for a baby, I have time to
get used to the idea.’
For
Miss Beck, her one hope is that the condition becomes more well known,
so that other women realise they have it earlier than she did.
‘I had only told five of my best friends, but then I realised it’s not something I should be ashamed of.
‘If
I had cancer, or, any other medical issue, people would be supportive.
So, I recently came out to everyone on Facebook, telling them about my
condition.
‘I was surprised at how positive everyone was, they said I was brave and beautiful, now I wish I had been open about it from the beginning
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