| Families with
disabled children meet at event, find valued
support in each other Heather Lalley - Staff writer
Kathy
Dalberg's 16-year-old son has cerebral palsy and
a seizure disorder and speaks only a few words.
So,
when she senses he's not feeling well -- through
his body language or whining -- she takes him to
the doctor. Sometimes that means up to six visits
a month.
"I
used to feel real guilty; now I just go,"
Dalberg told a room of families with disabled
children Saturday.
"Now
I don't feel so bad," one mother in the
audience exclaimed.
Such
revelations were the goal of Saturday's Early
Childhood Family Enrichment Day at the Coeur
d'Alene Inn.
About
25 families attended the event, sponsored by
Parents Reaching Out to Parents and Families
Together. The two groups provide support for
hundreds of North Idaho families with disabled
children.
Parents
started the day with their kids, singing and
playing with balloons. Then the children were
taken to other rooms to play, and parents got to
spend time together.
They
listened to a speaker talk about how a disabled
child affects a marriage. During a panel
presentation, they asked each other questions
about group homes, potty training disabled kids,
and the importance of neurologists.
"It
gives the parents time to get to know each
other," said Pinehurst resident Cathy
Harris, whose 6-year-old son, Elijah, is severely
disabled. "It's nice to know we're not
alone."
Elijah
was born with hydrocephaly, or water on the
brain. Now blind, he suffers from daily seizures
and has brain damage.
Harris
and her husband, James, spoon-fed their son
cereal before he went off with the other
children. Cathy Harris held Elijah's small,
tensed fists and talked softly to him while he
had a brief seizure.
"He's
like a big infant," Cathy Harris said.
"It can be stressful, but watching him
progress can be real joyful, too."
Beth
and John Bender are familiar with that kind of
stress.
The
couple did not know their son, Austin, had
developmental disabilities when they adopted him.
Austin, who's now 2 years old, suffered from
frequent seizures until last year, has poor
muscle tone and doesn't speak.
But Beth Bender, who quit
her job to care for Austin, said her son is
making improvements in therapy.
He's been able to toddle
around with the help of a walker and is now able
to sit and crawl -- things the Rathdrum family
never thought possible a year ago.
"Right now he's just
soaring," Beth Bender said. "We work
real hard."
Michele Roush of Post
Falls, whose 4-year-old son, Ben, has
hydrocephaly, said parents need to be aggressive
when caring for their disabled children.
"Just keep asking
questions," Roush said. "Question
everything. If I wasn't so pushy, my son wouldn't
be where he is today."
Memo: Heather Lalley can
be reached at (208) 765-7132 or by e-mail at
heatherl@spokesman.com.
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