Mrs
Nichols has not eaten food for seven years and gave birth to children
William, three, and Felicity, 11 months despite not being able to eat
during her pregnancy
The first time Nicola Nichols felt ill was in 2008, she
could eat or drink and vomited up to 50 times every day. After
undergoing several tests the young woman was diagnosed with
gastroparesis – a condition in which the stomach muscles are
paralysed, resulting in food remaining in the stomach for an abnormally
long time. It is usually caused by diabetes, Parkinson’s or as a
complication of surgery, but sometimes there is no clear cause and
sufferers report they after coming down with flu, a virus, food
poisoning or after taking antibiotics.
Nicola Nichols, 25, has to be fed through a tube directly into her bloodstream
Mrs
Nichols is kept alive by a food and glucose bags that feeds directly
into her blood stream, and a glucose bag that provides her with
energy. She has a food bag two days a week and a glucose bag five days a
week, which both have to be stored between two and eight
degrees. Despite the chronic illness, she has managed to give birth to
son William, three, and 11-month-old daughter Felicity.
The two children were both born healthy despite their mother being unable to eat for two.
Mrs
Nichols has been told she will never eat again, but she says despite
this, she feels lucky and her and her husband Ben, 27, call their
children their ‘two miracles’
Speaking about her unusual condition the woman says,
“We
always say that you take eating and drinking for granted until you
can’t do it. I still cook the kid’s teas and it smells and looks great
but if I even had a bite then I’d be in crippling pain. It has a real
impact on your life because you can’t make any last-minute decisions –
everything has to be planned months in advance. You have to have the bag
delivered there, the bag has to be stored in a fridge between two and
eight degrees, everything has to be deep cleaned – sometimes it just
really isn’t worth it.
Mrs Nichols was struck down with mild flu in 2008, and after this vomited up to 50 times a day
It’s
funny
because it really restricts your life but, obviously, I wouldn’t be
here without it so it gives me life too. A side effect of the TPN is
that your hair can get very thin and fall out. My hair came out in
clumps and I lost the majority of it and poor William (her son) said it
scared him, which broke my heart, so Ben (her husband) chopped off all
my long hair. It’s awful for a woman to have to go through that – but
after he did mine, he shaved his hair off too in support.
A side effect of being fed through a tube is that Mrs Nichols’ hair became thin and fell out, something she finds difficult
We
always say that someone else is always worse off. I’m lucky that I have
two beautiful children despite my problem. William was fed off my old
tube and Felicity was fed by TPN. William knows it’s different and will
always say as soon as we meet anyway “my mummy is fed by a tube”, which
really breaks the ice. Felicity is just coming up to the age where she
keeps grabbing the tube and that’s not too helpful. On days I feel like I
can’t take it anymore, seeing my children faces lit up is all I need to
keep going.”
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