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Fragile Lives at The Herald (Sorry - The Herald is
having trouble with its archives, and this page will not
display properly at its Web site. Dori does have an
actual clip of this story)
Sunday
November 14, 1999
1,872 words
The Herald, Everett
Fragile
Lives
Foster parent Bonnie Swinney handles with loving care
children whose illnesses would overwhelm others
By DORI STUBBS
Special to The Herald
SNOHOMISH -- At age 60,
when most people are thinking about retiring, Bonnie
Swinney of Snohomish looks at her three adopted and
three foster children and wonders how many times she
will have to drive to the hospital this month.
Five of Swinney's kids
need more than the average mothering; they require
constant medical attention because of kidney
transplants, facial deformities or muscle deterioration.
She meets that challenge by rigging up her home with
lifesaving equipment and leaving her car in drive.
"My car just goes there
automatically," Swinney said of her frequent emergency
room trips and scheduled visits to Children's Hospital
in Seattle.
Concern for kids runs in
Swinney's family.
She grew up with parents
who took care of foster children, and her energetic
87-year-old mother, Lois Prater, now manages an
orphanage and school in the Philippines.
Fifteen years ago Swinney,
then married with six children of her own and a nurse by
trade, decided to follow in her mother's footsteps.
She applied for a foster
parenting license.
The state Department of
Social and Health Services granted her request but
neglected to send her children for several months.
"I later found out they
were waiting to give me handicapped kids," Swinney
explained.
When DSHS found out she
had a nursing background, she was offered children who
could use her help the most.
Her Chevrolet Venture
extended van faithfully makes the runs to Children's
with young lives challenged by pain, high fevers and
infections.
Like the day 15-year-old
Katia doubled over with stomach pains and 4-year-old
Anthony awoke with a high fever and 9-year-old DeAnna
was already scheduled for an EKG. Swinney needed
13-year-old Natasha's help, so that meant baby Staycee
squeezed in for the ride.
It's a usual day in the
household of an unusual woman who cares for fragile
kids.
"What she does for these
children on a daily basis is beyond the imagination of
most parents," said Bob McClintock, Everett area
administrator for Child Protective Services. "She
becomes the expert. She really knows how to take care of
medically fragile children."
The more problems or
disabilities, the quicker she invited these kids into
her wide-spread arms and four-bedroom, two-bath mobile
home resting on five wooded acres.
"It was something I wanted
to do," Swinney said. "I like the challenge of the
medical problems -- seeing what can be done and how much
I can help. Especially kids who have been neglected in
their own homes."
Her first foster baby,
Katia, survived a collapsed lung and kidney failure
before reaching Swinney's eager hands. Katia's mother,
Nadene Robinson, was a 16-year-old American Indian of
the Tulalip Tribes struggling with drugs and alcohol and
unable to care for the baby.
Katia landed in Swinney's
lap at age 10 months, her health as frail as a baby bird
who has been tossed from the nest. She was in kidney
failure. Doctors expected her to die.
Two months under Swinney's
wing and Katia perked up.
Robinson, who speaks
openly of her troubled past and her efforts to turn her
life around, credits Swinney with saving her daughter's
life.
"If it weren't for Bonnie,
I don't think 'Tia would have made it," said Robinson,
who maintains a relationship with Swinney, Katia and
Staycee, another child of Robinson's in Swinney's care.
Though Katia's kidneys
were not cured, 11 years passed before she needed
dialysis, a procedure that removes impurities from the
blood during kidney failure.
She spent two years on
that lifesaving equipment before a kidney became
available for a transplant. She suffered a series of
serious setbacks, including the failure of the first
anti-rejection drugs, before her condition finally
stabilized.
"Since July of '98, she's
only been to the hospital eight times," Swinney
announced. "Which seems like only a little to us."
Katia turns 16 this month.
She hopes to again enjoy the wind whipping her ink-black
hair behind her as she traverses the jumps, bumps and
dips of motorbike trail riding, now forbidden her
because of the jarring to her kidneys.
Swinney wants to make
Katia a permanent, legal family member, but the Tulalip
Tribal Board will only permit legal guardianship. Under
the Indian Child Welfare Act, tribes have authority over
adoption decisions.
"She has begged the
tribe," Swinney said of Katia. "The mother has begged
the tribe. But culture is everything with the tribe."
On her 18th birthday,
Katia can choose her own fate. She will make her last
name Swinney, she said.
Swinney has adopted three
of her foster kids, Natasha, DeAnna and Anthony.
"After awhile, you can't
remember if you gave birth to a child or got them
another way," said the grandmother of nine and
great-grandmother of two, who walks with a cane and
needs hip-replacement surgery. "Sometimes, you fall so
in love with a child, it's hard to let go."
Staycee, Katia's
8-month-old brother, recently joined the four youths
already living in the residence surrounded by mellow
maples that coordinate with Swinney's early American
decor. He was born addicted to cocaine.
Another family addition, a
healthy 13-year-old girl who said she has found
stability with Swinney, rounds out the foster mother's
clan.
From the outside, casual
observers would note the bicycles and Big Wheels that
adorn Swinney's circular driveway. They would see the
five older children laugh, play and squabble the same as
any siblings. But if there's a crisis, the teen-age
girls scatter into an organized scramble, one taking
over dinner and another calming down excited youngsters.
"I'd never make it without
Natasha," Swinney praised her daughter. "She's my mommy.
She can pitch in and baby-sit."
With her jeans rolled up
and T-shirt pulled down to her knees, the 13-year-old
recited her accomplishments with pride.
"I cook for the little
kids, put them to bed, give them medicine and get them
up in the morning," she said.
"She has to," Swinney
added, "because sometimes we're at the ER for 10 hours
or more."
Natasha can only view her
mother through her left eye. A facial tumor causes the
right half of her face to swell, forcing that eye nearly
shut. She said she would like physicians to remove some
tumor tissue so she can see better.
"The doctors are skeptical
of removing the tumor from her face because it can cause
paralysis, and it just regrows," Swinney said.
Natasha takes comfort in
helping her mother. One of her chores is bathing DeAnna.
Born with congenital
myotonic dystrophy, a form of muscular dystrophy, DeAnna
was never expected to walk or talk.
"Babies like her have not
been kept alive long enough to know what they'll do,"
Swinney noted.
At 9, DeAnna is mentally
delayed but not physically slow. She attends school and
chats like a 3-year-old unwilling to give up her toy.
But her condition is
fatal.
She has just started
showing signs of heading downhill, Swinney said. In five
years, she will need a wheelchair and will develop
cardiac problems as her heart muscle fails. Swinney
hopes DeAnna hangs on until her 20th birthday.
DeAnna just hopes Anthony
will stop bugging her.
Active and tiny at age 4,
Anthony sports an unexplainable large belly. He weighed
just 4 pounds 8 ounces at his full-term birth and
inherited his birth mother's kidney problems. He needed
to be fed by a tube attached to his stomach until age 3.
When Anthony's kidneys
failed him at 14 months, Swinney moved him and Katia
into her own bedroom, which she arrayed with their two
home portable dialysis kits. By 8 each night, the two
were hooked up until the next morning, Katia for 10
hours and Anthony for 12.
Unlike Katia, Anthony did
not have to wait for a kidney. He had one waiting for
him.
Though the rambunctious
toddler saw nothing of his biological father, the man
did consent to donate a kidney to his 3-year-old son in
1998.
"It was the greatest gift
he could've given him," Swinney said.
Anthony now bounds up
steps and beseeches his mother with endless questions.
She happily sends her son off to preschool every day.
Her exceptional parenting
of special-needs children does not go unnoticed.
"Bonnie is amazing," said
Dr. Ruth McDonald, medical director of solid organ
transplants at Children's Hospital. "She not only does a
good job of taking care of their medical needs, but
their emotional needs. She loves them. She treats them
as if they were her natural-born children. They are a
part of her family."
Life eased for Swinney
after the successful transplants, and she decided to
concentrate on her four children and retire from foster
parenting. Until Staycee.
The drug-addicted infant
gasped once when he was born, then stopped breathing for
six minutes. "When they said he's liable to have CP
(cerebral palsy) and wasn't breathing, well, of course.
I'm a sucker," Swinney explained of her change of heart.
To keep his limbs from
stiffening, she must stretch his arms and legs several
times a day and keep him curled in a ball at other
times. Mild cerebral palsy will cause him to have
tremors later in life.
"Otherwise, he's growing
well," she said. "He's already 20 pounds. Unlike other
drug babies, he doesn't like things quiet and dark. He's
very social and makes good eye contact."
Despite the buzz generated
by the constant motion of busy kids, the tranquility in
the home resembles the peace of the goldfish that swim
around in Swinney's front-yard pond.
"I never think about life
being difficult," Swinney said of her coping strategy.
"Once in a while, I wonder what it would be like just to
be a grandmother. But I'd probably be bored to tears.
I'd probably be a school or hospital volunteer."
Nine years ago she
divorced her husband of 31 years and kept her children.
She now single-handedly manages her responsibilities. To
maintain sanity for them all, she extracts the positive
from the extraordinary.
Swinney makes time each
week to meet friends for lunch and attend Sunday church
services with all her children.
She gives thanks for
little conveniences.
For one, the school picks
up and drops off her children at the front door.
For another, the older
children help with the mountain of household tasks.
"I try to treat the kids
as normal, healthy kids. So I don't think they go around
thinking of themselves as sick. They don't normally
spend time depressed. It's all just a way of life," she
said.
But the trials are far
from ending.
Natasha requires routine
medical care to keep her deformity under control.
DeAnna's health deteriorates progressively. Anthony and
Katia suffer side effects from the transplant medication
and will need new kidneys again in several years.
"I take it one day at a
time," Swinney said of the distress and disappointments
that come with single-parenting fragile children. "I
sometimes get depressed if I look too far ahead and
worry about my children's health."
Her days as a foster
parent are numbered, she reported cautiously. A love of
nursing and children keep her going, and she delights in
her kids' successes.
But she admitted to
feeling a little tired and overwhelmed at times. She
doubts her family will expand.
"But you
never know," she added, "there's a great need for caring
for medically fragile children."
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