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Around the country, some parents who know about the government's
baby DNA collection, are avoiding the
newborn genetic testing program
altogether to keep government from taking and claiming ownership to
their child's DNA. They weigh the risk and the rarity and decide not to
participate in the testing program. Others
opt for private newborn testing (see Part 10). Sylvia Au at the Hawaii
Department of
Health said at the December 2009 newborn screening forum:
"...because there is a lot of media around newborn
screening, we’ve had more refusals lately, although you can only refuse
for religious reasons in our state, but we’ve been told that they
specifically point to Minnesota as a case of why they don’t want
newborn screening because they don’t want their data going to get
stored somewhere and they don’t want it used for intelligence and other
things."
Why haven't parents been informed about the storage, use and sharing
of their newborn's blood samples by State health departments? At the
December 7, 2009 forum,
Sharon Terry, President and CEO of Genetic Alliance, explained,
"The fear is that more people will choose to not have
newborn screening if they were more aware....People basically said
you
will destroy the newborn screening
system by calling to people’s attention that in fact there is one, and
that they are using these samples at least for quality control QC/QA
stuff."
At the September 2009 forum on the use of residual newborn dried
blood spots, professor Dr. Sharon Kardia reported that one-third of
the women surveyed would consider opting out of newborn screening
if
asked about the future storage of their baby's blood spot. Dr.
Aaron
Goldenberg from Case Western Reserve University said at the December
2009 forum, "if people are not aware of what's happening to their
sample they may be more wary of newborn screening generally. And we can
all probably agree that that would not be a
good thing." He added,
"If we deny people some
control, even an opt-out, kind of provoke that mistrust, or that
refusal, there may be a backlash against newborn screening in
general."
Dr. Kardia, who conducted focus groups on the issue, explains several
other points of concern for parents:
"In Michigan where the long list of public surveillance databases
can be
relatively scary. To imagine that your child’s bloodspot is going
to be then hooked up to everything from immunization records to
hearing
records to vital statistics, you know, you name it, and we’re going to
try to link bloodspots to databases, is a very scary prospect.
Protection from requisition by criminal justice system or Homeland
Security is necessary. This came up over and over again. "
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