On May 31st, 2012 the Maxwell family boarded a plane and moved to Swaziland to live at Project Canaan. I hope to update my blog on Saturday mornings and share, as honestly as I can, the highs and lows of our life in Africa. We are living on a farm in a remote part of this tiny Kingdom and are serving the community as well as the orphans and vulnerable children of the nation. The 365 day count down started on June 1st, 2011, but the real journey begins now. Thanks for joining us.
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Saturday, August 8, 2015
This week: emergency brain surgery on one of our children. (This is not getting any easier)
Grace when she first arrived.
When you have 98 children under the age of 5 there are very
few weeks without hospital, clinic or visit to the nurse.This week was a tough one though when
we discovered that our little girl Grace had undiagnosed hydrocephalus and then
had a brain bleed when she accidently bumped her head, which quickly lead to
emergency surgery to put a shunt in her head to drain the fluid that had built
up over a year.
Who is Grace?
Grace came to us when she was 18-months old.She was a sick baby and her mother
couldn't handle a sick baby so she left Grace on the side of the road with a
note attached saying,“ My baby is
sick. I am going to see my boyfriend”.And she left.
Someone found Grace on the road, recognized her and took her
to her Grandfather’s house. He in turn sent her to the hospital with an Aunt
and by the time they arrived Grace was in a coma.This poor little girl had meningitis, Tuberculosis and
pneumonia.A week later, she came
out of her coma and was blind.
We have a policy about not accepting disabled children, but
we were not told that she was blind or severely disabled when she was placed
with us by the Social Welfare department, mainly because they didn’t know
either.That has happened a couple
of times and I can only see it as Gods’ way of making sure that the children HE
is placing at Project Canaan are accepted, rules or no rules.It’s as if HE sneaks them past us.My friend Sandra Stanley was with us
when Grace was placed in our care and it was Sandra who gave the child the
English name “Grace” because this baby had been so sick and through so much,
Sandra said that it was His Grace that would see her through.
Back to Grace.
She is a sweet baby who really struggled in the first year
she was with us.She was carried
everywhere because she couldn’t walk, crawl or even sit and while we believed
that she was starting to see something, she is almost completely blind.She was taken to Physical Therapy
religiously every week and was doing her exercises daily to try to build core
strength. Clearly her Cerebral Palsy has affected her whole body.
We wondered if she might also suffer with hydrocephalus, but
a CT scan two years ago showed that our concerns were unwarranted.
A wonderful friend and Heart for Africa supporter offered to
get Grace a specially made walker (as in a $2,000 US custom-made walker!) and
it has been life-changing for Grace. She was first strapped in to it as her
core-strength was very poor, but within weeks she was running up and down the
toddler home halls in her “car” as they call it.She was standing at the same height as her brothers and
sisters and they could now play and interact with her as they had not been able
to do before. It was beautiful to see.
In no time Grace was walking with her walker, but not
strapped in. She can walk/run only holding the handles and her strength is
Last week she had a random bump on the head. She needed 3
stitches at our clinic, but all in all it was a typical childhood injury.After a few days it was reported that
she was vomiting and her right hand was shaking.Our volunteer Nurse Practioner from the US (Brooke) immediately
took her to town to see our Pediatrician. The Pediatrician immediately sent her
to a hospital with a Neurosurgeon.The Neurosurgeon did a CT scan, which revealed Cerebrospinal fluid (CSF) that had been building for
possibly one year.The bump on the
head caused internal bleeding on an otherwise already compromised situation and
within hours of seeing the surgeon, our beautiful little Grace was having
emergency brain surgery to have a shunt put in.
I can’t begin to put words to how we all
felt and feel about this.I can’t
imagine this happening to my own biological children and how I would feel – I know
I would be frantic.But there is
something quite different when this happens to a child that you have been given
a God-given and government-given responsibility to care for.I was sick to my stomach, but reached out to our prayer
circle to join with us praying for favor and healing.
On Tuesday Brooke went to see Grace and took
in clothes for her to wear (we did not travel the day before expecting her to
be admitted in to the hospital). The hospital had her in an adult diaper and
nothing else.As soon as they
started to put her soft clothes on she starting talking fast in siSwati saying,
“Oh, they are clothing me!” (SO CUTE!)Only 5-days later she came back home to us with a draining shunt in
place and a joyous welcome by her brothers and sisters (and Aunts and Uncles!).
Thank you Treasure - you are a gift to us all.
Ian and I are problem-solvers so we will
work diligently with the team to improve our systems and training, but at the
end of the day, the Lord stepped in and saved this little girl’s life,
again.I wonder what He has in
store for our beautiful Grace.
Live from Swaziland … things aren’t always
easy here, but El Roi sees it all.