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There
are many community-based programs and projects
occurring
throughout Michigan that involve genetics
education,
genomics,
birth defect prevention, or family support
and
advocacy.
Is your organization involved in one of
these
activities?
Please let us know by e-mailing genetics@michigan.gov.
Are
you planning a special event open to the
public? Please be sure to post it on the
MiGenetics events
calendar!
Angelman
Syndrome Awareness Day
Governor Jennifer Granholm proclaimed May 17,
2008 as Angelman
Syndrome Awareness Day at the request of
Debbie Brockie, whose young daughter Molly is
affected with the rare genetic condition. Families
will celebrate the day with a Walk-a-thon in
Detroit. Visit the Angelman
Syndrome Foundation, Inc. for details. Named
for the English pediatrician, Dr. Harry Angelman,
who first described the condition in 1965, the
syndrome causes severe, lifelong developmental
disability. Angelman
Syndrome is thought to occur in about 1/10,000
to 1/20,000 individuals which means between 6 and
12 Michigan babies are born with the syndrome each
year. Angelman Syndrome affects both males and
females of all races and ethnicities. Although
caused by a change in the genetic material on
chromosome number 15, it usually is not inherited.
The Brockies and other Michigan families want
to increase community awareness of Angelman
Syndrome. View a photo album of the 2007 Angelman
Syndrome Awareness Day Walkathon and more of Molly
Brockie’s adventures at www.myangelMolly.com.
For more information about Angelman Syndrome,
visit www.angelman.org
or call 1-800-432-6435.
Get
involved now!
"Show
the Love" for Michigan kids with sickle cell
disease!
Children's
Hospital of Michigan is in a contest
sponsored by Colgate-Palmolive and the Starlight
Starbright Children's Foundation to help children
with sickle cell disease and their families have a
better experience when they are in the hospital.
The organizations are donating "Fun
Centers" to nine hospitals across the
country, and the winning hospital in the
"Show the Love" competition will win an
additional unit. Read the Detroit Free Press article
or simply cast
your vote before February 29, 2008.
Recent
Happenings
Midwest
Community Genomics Forum comes to Flint!
On
Friday, October 12, 2007, community forums on
genomics, funded by the National Human Genome
Research Institute, were held simultaneously in
five Midwest States including
Illinois
,
Iowa
,
Michigan
,
Minnesota
, and Missouri . In
Michigan, "Genomics, Community, and Equity: A
Continuing Dialogue," was hosted by Flint
Odyssey House, Inc. Health Awareness Center.
Members of the community were invited to attend
the forum, held at
Genesee
Intermediate
School District in
Flint, which provided an opportunity to
hear national experts and participate in
discussions about issues in
genomics. More information on the forum and
continuing dialogue about genomics is available
at www.GenoCommunity.org.
Fetal
Alcohol Spectrum Disorders (FASD) Awareness Day
To acknowledge FASD Awareness Day on Sunday,
September 9, 2007, the Michigan Fetal Alcohol Syndrome
Prevention Project and Detroit Department of
Health & Wellness Promotion held a special 2-day exhibit
on September 6th & 7th open to the public. The
exhibit focused on FASD,
its cause, prevention methods, and strategies for
working with individuals affected by FASD.
Screening for women 18-44 years old interested in participating in the FASD
Prevention Program was also available. For more
information on the event, call (313)
876-0347 or (313) 876-4514. 
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