I figured that I might as well start
from the beginning, easiest place to I suppose, and tell my story in four
parts: how I came to have kidney failure; my time during my transplantation; my
decline; where I am now.
"Yeah, I ate s**t."
Always a definite ice breaker!
And, yes, it is true. I ate s**t. That is how
my kidney failure started.
I always try to make my story humorous. Maybe it makes it
easier to deal with but the truth is I did, genuinely, eat cow excrement and contracted E-coli
0157 less than a week before my third birthday.
(I must warn you now that I will probably be
quite explicit in describing medical things so if you're squeamish, look away
now).
I should also point out that I did not
intentionally eat said faeces. I grew up on a farm and our family dog rolled in
manure. I hugged the dog and consequently got the manure on my hands. Me, only being
three, put my hands in my mouth... and that's how it happened!
Within a matter of hours of eating the excreta, I started to have all of the usual E-coli symptoms, low fever, nausea, vomiting, bloody diarrhoea. My Mum, who clearly
knew something was wrong, took me straight to the doctors. She took me there
three times over the course of a couple of days but was told over and over by
the doctor that she was "a neurotic mother and your child only has a tummy
bug. She will be fine in a few days!" - this may be why I have doctor
trust issues!
Anyway, on the third day my
Mum, bless her, rushed me to A&E where the doctors immediately spotted what
was wrong. I have never really heard what happened after that. All I know is
that a little boy, the same age as me, in the bed next to me, with the
same disease, died. I cannot begin to bring myself to think of the
pain that my parents felt and I can imagine the trauma has probably never left
them. Without my mum's determination, I would not be here, writing as I am.
For almost four months I was
in intensive care, with my Mum constantly by my side. I was read to, soothed by
her kind voice and loving intent. I know that she always cared for me and she
would have never left me, loving me the way she always has done, every day.
I was finally allowed home
after five months of being in hospital but I would never return to a normal
life. I was on peritoneal dialysis for 12 hours. Every day. I was unable to do a lot of
activities children of that age are suppose to do like go swimming, go to
sleepovers with my friends, do any physical sports or eat chocolate, crisps,
chips, any sort of junk food (which, in hindsight, is not a bad thing).
I was unable to do a lot of
things but there was one thing I was always extremely wealthy of,
Love.
There was not one day where
I did not feel cherished by those around me. Whether it was my parents, the
nurses who looked after me or my amazing relatives. Coming from such a strong family
has moulded me into who I am. We have laughed together, cried together and most
importantly supported and loved each other through hard times.
No matter where you get love
from, may it be your family, friends, work colleagues, fourth cousin twice
removed, it is so important to have that network of people you can rely on
in times of need.
For four years I was
on PD dialysis until January 2000 when my Mum donated one of her kidneys to me.
Though I will never be able to express my gratitude, I hope she knows how
grateful I am for what she did for me.
So, even though I ate s**t,
those four years of my life, until my transplant, shaped me into who I am and -
not being immodest - I think I rock! Actually starting to sound like my
Auntie right about now...
Until next time,
Kate x
I think every kid has been there at some level.
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It is not easy to manage babies with such serious sickness.
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