Andrew Kerry – Transition

I still feel like a child. I’m not ready to accept that in 4 months I will have to leave university,
find an adult job, get an adult house and do boring adult things like pay bills and watch
period dramas on Channel 4. I recently turned the grand old age of 21 which means I can
legally adopt a child and own a pilot’s licence for a plane, neither of which are top of my
priority list. However, one thing that turning 21 does mean is that I now have no excuse not
to be an adult. Between the ages of 18 and 21 I was still trying desperately to cling on to
being young by justifying a night in with a Disney movie and a onesie was a productive
and efficient form of fun. Although my views on this kind of night in are still strong, I do now
have to accept that I am growing up and this brings its own unique challenges and joys.
I was born with a rare congenital heart defect called Hypoplastic Left Heart Syndrome,
which basically means that the left side of my heart didn’t develop properly and so only the
right side of my heart functions. Because of this, growing up was different for me
compared to my peers. I always struggled to keep up with those around me, and from a
young age, had to accept that my dreams of scoring at Wembley Stadium for England
were probably not the most realistic. But even though I would never be Wayne Rooney, I
grew to realise that I had bigger dreams of my own that to me were way more exciting than
kicking a ball around and having a hair transplant.
While the rest of my class were chasing after footballs in the mud in freezing temperatures
wearing just shorts and a T-shirt, I was sat in a cupboard in the music department writing
music. Admittedly all of the music I made was terrible, but to me it was the most fun I had
ever had and I was finally focused on something I could do without sounding like a
wheezing distressed cat and being blue in the face by the end of it.
Over the years, I’ve gradually learnt what my body can and can’t handle, and although this
is hard to accept at times, I’ve learnt to live within my limitations and not be discouraged.
Instead, it’s important to focus on what you can do and work as hard as you can to make
the most of what you have! For me personally, although my “sick beats” that I made when I
was 13 were awful, I loved every second and have continued to work hard at what I do
and I’m about to come out of university with a degree in music production! In today’s age,
there are so many opportunities for those of us with limited mobility and a huge array of
jobs and courses available from music to computers, from business to film production, we
needn’t limit what we can achieve because we have a heart condition, but instead focus
on the things that we’re passionate about and make them work for us!
University has been the best experience of my life. I didn’t know how I would cope at first.
When I first came to university, I had recently struggled with an irregular heart rhythm and
had to have several ablation procedures. I had also struggled with anxiety and just 6
months before I came to university struggled with panic attacks even when I was on my
own for half an hour. Coming to university really boosted my confidence and the support
that the disability team at Hertfordshire Uni offered was really great! I was able to live in a
downstairs flat on campus and they supplied me with my own equipment so I didn’t need
to walk to the uni facilities if I was having a rough day. Nearly 3 years later, I now live in a
house off campus with some great friends and regularly walk to uni. In my second year I
was the president of the Christian Union society and had so much fun working on that!
University has given me so many amazing opportunities to grow in confidence adn in
myself as a person and I’m so thankful for the experience!
Now all I have to do is find a job… This thought is stressing me out even as I write this, so
here’s a picture of a goat to distract from the subject in question.
The whole purpose of this small corner of the internet is to talk about my experiences
transitioning from the children’s services to the adult services, so I guess I should move on
from goats and talk about the “horrors of transitioning!” I’m joking, calm your
pacemakers…it was so simple and not horrible at all!
Since about the age of 5, I have been seen at the Evelina Children’s Hospital in London.
It’s an amazing place with incredible doctors and nurses who have seen me through many
visits! For that same time, I have been under the same cardiologist who is so amazing and
I’m so thankful for, even when he tells me to man up and get over stuff that I should really
stop worrying about at times!… When I was 16 I went to a transition day at the hospital
where they went through the process of transitioning and talking about the similarities and
differences between the children’s and the adult services. They talked about getting
contact details for your new liaison nurses and reassuring us that the process would be
smooth and they were totally right.
For me the transition process was a little different and arguably easier, as my cardiologist
also worked in the adult team and so I would still be seeing the same consultant whom I
had seen for most of my life. The only difference was the liaison nurses and also the fact
that I would now be seen in St Thomas’ Hospital. Another difference that I experienced for
the first time in the summer when I went to have my pacemaker replaced was the lack of
screaming babies and joyful chorus’ of ‘if you’re happy and you know it clap your hands’.
Unfortunately this was replaced with old men snoring and needing the toilet every 10
minutes. I’m still not sure which I prefer.
My parents were really great in the transition process and in my last couple of
appointments in the children’s department, left me to have the appointment on my own so
that I could get used to asking and answering questions for myself and start taking control
of my medical condition and the decisions that go alongside it. I really believe that as soon
as you’re ready, it’s important to learn about your heart condition and start taking control of
it to give you independence for the future!
Transition really wasn’t bad! It’s allowed me to take control of my heart condition and start
making decisions for myself. This has given me so much independence and allowed me to
go to university comfortably without having my parents around but knowing they were
nearby and would help at any time. The only downside is the considerable lack of turkey
dinosaurs and smiley faces on offer at dinner time in the adult ward!

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    Nominations are open for our next Brave Hearts Awards 🏅

    We know that a lot of our young people miss out on awards and trips at school and we feel that they, like every young person should be rewarded for what they learn and how they develop 🙌

    If you know of a young person with a single ventricle heart aged between 8-17 that has achieved and grown, take a look at our list of awards on www.lhm.org.uk/youth-zone/lhm-brave-heart-awards/ 👈

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    👋 Meet Archie, he is 7 years old and was born with Tricuspid Atresia (TA) a rare congenital heart condition. Archie had his Fontan procedure in September at the University Hospital Southampton, Ocean Ward. The aim of the Fontan procedure is to give a child as much energy as having only half a pumping heart will allow. If surgery has gone to plan the children will gradually recover from the operation and go on to gain far more energy than they had before. He had a longer stay than anticipated, due to a number of complications, but was discharged in October.

    ❤️ “The staff, nurses, doctors, consultants and surgeon were utterly wonderful and we can’t thank them enough. However, it was a consultant anaesthetist, Dr Andy Curry, who stood out in Archie’s mind. His bedside manner, and the relationship of trust that he managed to build up with our very anxious little boy, was astounding to watch. So, on ‘Dress as your Hero Day’ at school, Archie wanted to dress as his hero…”I want to dress as Dr Andy because he helped save my life and he’s my friend”…gulp” – Archie’s mum Charlene.

    😻 We have been blown away by this story. A month after coming home from hospital and Archie is raising a smile, dressing up as his hero and on his way to school. This is one strong boy, as are all of the children in the LHM family.

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