I received an email about 10 days ago and just kept forgetting to look at it with much detail. I took a look at it today and while it's not Down Syndrome Awareness Month still, thought it would be good to share nonetheless.
Celebrate the UPside of Down™ during National Down Syndrome
Awareness Month: Dispelling Myths and
Smashing Stereotypes
Dr. Julia Kinder is celebrating National Down Syndrome
Awareness Month with a Sweepstakes,
Photo Contest, and a Petition to Medical School Faculty
across the United States.
Cape
Girardeau, MO – October 18, 2012 – Dr. Julia Kinder, practicing
physician, national speaker, and an advocate for children with special needs,
is celebrating National Down Syndrome Awareness Month with an online Photo
Contest, Sweepstakes, and a very important Petition. These can be found on her
website, www.JuliaKinder.com. The photo
contest gives families of children with Down syndrome an avenue for showcasing
their child’s abilities. The sweepstakes offers fun awareness products created
by Dr. Kinder while drawing attention to dispelling the myths and stereotypes
surrounding Down syndrome. The newly
launched petition calls upon medical schools to provide more training on Down
syndrome.
“No parent should
feel like their baby's life starts out with a death; the death of their dreams
for the future, the end of their hope for a happy, healthy child,” said Dr.
Kinder, owner of JuliaKinder.com. “But it happens every day, because physicians
who deliver the diagnosis of Down syndrome often give inaccurate, incomplete,
and negative information that intensifies the unfounded fear of this
diagnosis.”
Currently physicians
do not receive training on giving the diagnosis of Down syndrome in a
productive way, according to Dr. Kinder. Nor do they learn of needed resources
for parents and baby. Medical education focuses on the possible health and
learning issues, which not every child will encounter. Physicians do not
understand what a child with Down syndrome is like outside of the medical
aspects. What is crucial to every baby with Down syndrome is that they begin
receiving early intervention and therapy immediately. Medical education does
not cover this topic, therefore, physicians are missing a crucial piece of
information to pass along to new parents.
Dr. Kinder has
been a practicing physician for the past decade. However, eight years ago when her daughter was born with Down
syndrome, she discovered her medical training did nothing to prepare her for
raising a child with Down syndrome.
“Ella is
completely healthy and smart, which contradicts everything I learned about Down
syndrome,” said Dr. Kinder. “Medical school taught me about a laundry list of
health problems and mental retardation, none of which applied to my child. I
had no practical information on how to take care of her. I didn’t know she
needed to start therapy immediately. When she was born, the doctors and
hospital gave me no information or resources. I left the hospital without so
much as a pamphlet.”
According to Dr.
Kinder, the information on Down syndrome that doctors give to new parents tends
to focus on the potential medical and learning problems. Doctors have not been
trained to explain to these new parents that a child with Down syndrome is more
like other children than they are different, and that many of the medical
issues never materialize. Parents leave the hospital with the impression that
their child’s prospects for a happy, healthy, and fulfilled life are grim.
Unfortunately, many parents admit they struggled to connect emotionally with
their baby during those first few months, as if unconsciously attempting to
prepare for some awful manifestation of the diagnosis.
“I have decided to
tackle this issue head-on,” states Dr. Kinder. “It is unacceptable for the
medical community to contribute to a new parent’s fear of their own baby. This
negative emotional state can prevent parents from providing the appropriate
care their newborn needs. Babies with Down syndrome must start early intervention
and therapy immediately - it should not be delayed because doctors fail to give
parents complete and accurate information, along with resources for support.”
Dr. Kinder has
spent eight years speaking to the medical community, future teachers and
therapists, and to the general public regarding Down syndrome, as
well as counseled hundreds of new parents. In 2009 Dr. Kinder began blogging on
the topic, giving new parents hope and direction. She has devised fun ways to dispel the myths and darkness by promoting
positive phrases such as “My kid has more Chromosomes than yours” as well as
the “UPside of Down” concept. She encourages others to proudly display the
UPside of Down with car decals, shirts, bracelets, and other awareness products
that she has developed. Dr. Kinder has
created
a tribe of families who support each other and spread awareness. Their motto
is, “Go beyond just surviving [with Down syndrome] to Thriving - become a
Thrivalist!”
“I want to show
the world the UPside of Down syndrome and I want to improve the education
medical students receive on helping new parents,” said Dr. Kinder. “My ultimate
goal is for the birth of every baby with Down syndrome to be celebrated, and
for every baby to receive the care required to maximize their developmental
potential.”
About Dr. Julia Kinder
Dr.
Julia A. Pewitt Kinder is an accomplished national speaker, early childhood
education advocate, author and practicing physician. She and husband Mitch
reside in Cape Girardeau, Mo., with their three children, Ella and twin boys
Paxton and Dexter. Dr. Kinder is
licensed to practice in both Missouri and Texas and is in private practice with
her brother in Jackson, Missouri. She also serves as a hospice physician for
Tri-County Hospice. In addition, Dr. Kinder is a certified fitness instructor
and promotes easy ways to incorporate exercise into daily routines. More
information about Dr. Kinder can be found on her website at www.JuliaKinder.com.
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