Four-year-old boy has died from a genetic disorder so rare fewer than 130 cases have been identified worldwide, Alnwick, Northumberland, England, UK;...
Aidan Jackowiak Smith suffered from Cloves Syndrome which affects one
in 50 million people and has no known cure. He was born with growths
covering large areas of his body and suffered from brain damage and
epileptic fits. The little boy suffered from a severe form of the
disease but his parents Karl Smith, 41 and Vikki Jackowiak, 37, were
told there was no reason why he should have a low life expectancy.
As a baby, he had to undergo major surgery to remove a mass of fatty
tissue in his face and neck which made it hard for him to breathe and
swallow. Aidan was due to start a a pioneering drugs trial in July that
it was hoped could make further surgery unnecessary. His family together
with developed had their home specially adapted for the boy.
But unfortunately he picked up a chest infection, which developed
into the flu and then chronic lung problems. Aidan was admitted to
hospital where he was put on a ventilator. The youngster, who could
could not talk or walk but who had started school, sadly died at
hospital on Sunday.
His dad Karl said: “We are all in a state of shock at losing
Aidan at such a young age. He was a fighter to the end but in the end,
the fight was just too much for him. We will never forget him nor will
we ever forget the love and support we enjoy from the people of Alnwick,
the wider community in Northumberland and across the country during
Aidan’s all too short life,” he said.
Dad Karl left a touching tribute to his young son on Facebook last night. He wrote: “To
all our friends and family, we are very sad to say after four of the
hardest, longest weeks that our little boy Aidan lost his fight. He
tried with all his might to hang on, but it was one fight too many so
see you soon our super hero love you always and forever mammy, daddy and
brother xxx.”
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