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Katie Beckett death on May 18th

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Family Voices Extends Condolences on the Occasion of the Passing of Katie Beckett

Albuquerque, New Mexico, May 18, 2012.

Family Voices would like to extend our deepest sympathy to Julie Beckett and Mark Beckett on the occasion of their daughter Katie Beckett’s passing this morning, as well as to Katie’s family, friends, colleagues, and loved ones.  Julie Beckett is one of the founders of National Family Voices and both Julie and Katie have been dedicated advocates for children with special health care needs for decades.

 

For Information Contact:
Melanie Rubin, mrubin@familyvoices.org,
505-261-3214


To Read More About Katie:
Go to www.facebook.com/
InMemoryOfKatieBeckett

 

 

It was in support of her daughter’s in-home medical care that Julie successfully advocated for a waiver of the rules that required children with special health care needs to be in the hospital in order to receive Medicaid funding for acute care. In November of 1981, when Katie was three, President Reagan allowed Katie to go home in time for Christmas and receive her Medicaid-funded treatment at home. At a press conference, Reagan explained the child was being kept in the hospital because of Medicaid rules which forbade paying for her home care, even though the cost to the government would be one-fifth the hospital charges of $10,000 to $12,000 per month. "When we see a case of this kind," Reagan said, "it reveals that hidebound regulations can be a tremendous expense to the taxpayers and do no good for the patient."

Reagan’s intervention set a new precedent, and shortly afterwards the government allowed exceptions in other states so that parents like the Becketts, who made too much money to qualify for Medicaid, could receive at-home coverage of extreme medical costs for their children. This provision became known as the “Katie Beckett Waiver.”

In the three decades since that time, more than a half million children have received waivers to get their care at home.

Katie’s illness began at the age of six months when she contracted viral encephalitis followed by a grand mal seizure which sent her into a coma. The encephalitis attached to her central nervous system and caused nerve damage to various parts of her body, most significantly affecting her ability to breathe. She was placed on a ventilator and later a tracheotomy was performed. She subsequently required multiple medical procedures and was completely paralyzed. Although the paralysis itself eventually resolved, she could not breathe on her own at all until she was almost two years old. She continued in hospital care until the age of three, when President Reagan’s historic decision made it possible for her to go home.

 

Katie was later able to function without a ventilator for hours at a time, although she required some at-home medical assistance each day.

In the Fall of 2002 Katie wrote:

“I started my advocacy career at age ten. It was not my choice but rather a path chosen for me. It was not until I was twelve or thirteen that I realized the important work I was able to do because I was who I was, and how much this worked helped other kids. I realized that this was something I was born to do, so I was willing to take on the extra attention given to me by other students and teachers when I returned home even if it was embarrassing at times. Being singled out even for doing something so rewarding is uncomfortable and can create tension with other students. It made it difficult sometimes to fit in and just be normal.”

Katie continued her advocacy work throughout her life in support of children with special health care needs. For example, in the fall of 2010, Katie and Julie Beckett presented in Washington, D.C., for a celebration of the 75th anniversary of a provision of the original Social Security Act that set up federal programs to promote maternal and child health.

Katie, then 32, spoke to an audience of children's advocates. She was introduced by Donald Berwick, the head of Medicare and Medicaid, and spoke right after White House senior adviser Valerie Jarrett.

"Just because you reach a certain age does not mean that you are miraculously cured of all the things you have endured," she told the crowd, arguing for an expansion of home and community based care so that people with disabilities have more options to live outside of nursing homes and institutions.

Dr. Sophie Arao-Nguyen, Executive Director of National Family Voices said today:

“Katie was a great role model and quiet warrior whose work helped countless children across the United States. Julie, our prayers and thoughts are with you today as we wish peace for you and Katie, and for Mark, your family, and loved ones, in this moment of Katie’s passing.”

Memorial Service information will be communicated when it is available.

 

 

 

Sincerely,

Melanie Rubin

Director of Communications & Strategic Initiatives

National Family Voices

mrubin@familyvoices.org

505-872-4777

www.familyvoices.org

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A beautiful tribute to Katie, aired on National Public Radio, is available at the link below:

 

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SERVICES FOR KATIE BECKETT

Services for Katie Beckett will be held Thursday, May 24 at Teahan Funeral Home, 3100 F Avenue Northwest Cedar Rapids, IA 52405, from 4-8 pm with a vigil at 4. Her funeral will be Friday, May 25 at St. Matthew's Catholic Church, 2310 First Ave NE, Cedar Rapids, Iowa 52402 at 10 am.

 

SCHOLARSHIP FUND

A scholarship fund in Katie's name for a student with a disability or special health care need has been started at Mount Mercy University, 1330 Elmhurst Drive NE, Cedar Rapids, Iowa 52402.



CONTACT INFORMATION FOR JULIE BECKETT

Correspondence for Julie Beckett can be mailed to her home address:

2222 First Ave. NE Apt 502
Cedar Rapids, Iowa 52402

or emailed to: waivermom@earthlink.net

 

NATIONAL PUBLIC RADIO REPORT

A beautiful tribute to Katie, aired on National Public Radio Saturday, May 19, is available at the link below:

http://www.npr.org/2012/05/19/153076971/katie-beckett-leaves-legacy-for-kids-with-disabilities

 

STATEMENT BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES

FOR IMMEDIATE RELEASE
May 20, 2012
Contact: HHS Press Office
(202) 690-6343

From Secretary Kathleen Sebelius on the passing of Katie Beckett

Katie Beckett was a quiet hero and an inadvertent pioneer in the civil rights movement for people with disabilities. When she was only three years old, her family and her doctors wanted her to live at home despite her extraordinary medical support needs. At that time, Medicaid would not cover the cost of her medical services in the community -- only in the hospital. Thanks to her mother Julie's tireless advocacy, in 1982 Medicaid policy fundamentally shifted to allow people with significant healthcare needs and disabilities to receive care at home.

Over the past thirty years, the "Katie Beckett Waiver," a Medicaid program, has provided over a half million children with disabilities the chance to live at home with their families and participate in their comm unities instead of living in hospitals and institutions.

As a result of this change, Katie was able to grow up as a typical young woman living with a disability -- going to college, working as a writer and public speaker, and living an independent life -- and in the course of her journey, Katie inspired a whole generation of young people with disabilities and their families.

Katie will be missed by many across the country, but her determined advocacy, and that of her family, has changed countless lives for the better. Our thoughts and prayers go out to her parents, Julie and Mark, and all in the disability community who mourn her passing.

 

OBITUARY

Mary Katherine "Katie" Beckett passed away at St. Luke's hospital on Friday, May 18, 2012. Known as Katie to many, her life and legacy will long be remembered.

Born March 9, 1978 to Mark and Julie Beckett at St. Luke's, she will be remembered by many who passed through those doors; Dr.'s, nurses, therapists, food service workers and cleaning staff who all loved and cared for Katie and her special needs. Her parents are most grateful for them in their instrumental role in her young life.

Katie is survived by her father, Mark William Beckett and stepmom, Linda and stepsister, Chelsea Lee; her mother, Julie Beckett; grandpa, Larry Beckett, & step-grandma, Maxine Houser; "Irish" family aunt, Mary Barbara Lenz of Dubuque, Iowa and cousins, Laura (Gustavo), Lisa & great niece, Frances, and Dr. Joe & Hannah; uncle, John Joseph O'Connell III (Mary Jo) and cousins, Shannon (Nick) Lampe, John IV (Angie) O'Connell & great niece, Abby, Ashleigh and Casey O'Connell; aunt, Maureen (Chris) O'Connell Barry and cousins, Shaun (Ashley) & great niece Sophie, Kelly (Adam) Fabor & great niece, Raven, and great nephew Duncan and Bailey (Matt Keister); uncle, William Ryan (Mary) O'Connell and cousins, Ryan and Colton; uncle, Michael (Brenda) O'Connell and cousins, Michael Jr. and Zachary John O'Connell, and Amanda DeDecker; uncle, Patrick (Sheryl) O'Connell and cousins, Candace (Ryan) Murphy and Brandon O'Connell & great niece Kaylyn; uncle, Jamie (Dawn) O'Connell and cousins, Megan and Shamus O'Connell. They will all live to support her memory.

Katie lived at St. Luke's Hospital for 3 and ½ years in the Pediatric Intensive Care Unit and came home on December 19, 1981 but only after Congressman, Tom Tauke and Senators. Chuck Grassley and Tom Harkin, and President Ronald Reagan and Vice-President George W. Bush pushed to have an exception to Medicaid policy changed. Today, this monumental legislation is still referred to as the "Katie Beckett law" and now over a million individuals who would be living in hospitals or care centers are cared for at home and in their communities. She was always an advocate for people with disabilities and special health care needs, testifying many times before Congress, and speaking across the country telling her story and making sure people paid attention to "including" people with disabilities in everyday life.

Katie was a writer, dying before she could complete her novel. She had a quick wit and a joyful presence. Always tiny in stature, but with an intellect that warned you to tread lightly. She will be greatly missed by her close friends Beth, Julie, Erin, Shaun, Cassie and Jessica as well as her family and the many people who benefited from the work she did. She leaves behind her "children", the many stuffed animals who were her greatest confidants. She will miss Red Lobster, Barnes & Noble, Starbuck's, Joe Raposo from Dream Street, WWE wrestling, and her unending love for Shaun Veers.

Waiting to greet her at the golden gates are her grandparents, Peggy Beckett and John and Barbara O'Connell, her beloved Dr. Darrel Dennis and her other "parents", Polly Egan Arango and David Woll.

Services will be held Thursday, May 24 at Teahan Funeral Home from 4-8 pm with a vigil at 4. Her funeral will be Friday, May 25 at St. Matthew's Catholic Church at 10 am.

According to her wishes her body will be donated to the University of Iowa to help healthcare workers learn from her experience. Even in death, she wanted to give back.

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