Abortion

PA House Bill 1500: One Small Step Towards Victory

On June 9, the Pennsylvania House of Representatives passed a bill that would ban abortions solely because of a prenatal diagnosis of Down syndrome. This pro-life victory served as a small but significant step to promote the dignity of all human life.

The bill, known as House Bill 1500, was introduced by Rep. Kate Klunk, R-York, in December 2020.

“Most of us know of a family touched by a Down syndrome child, and know these children grow to lead joyful and fulfilling lives,” Klunk said when introducing the bill.

In current Pennsylvania law, it is legal for a woman toreceive an abortion prior to 24 weeks gestation for any reason deemed necessaryby a physician, with the exception of selecting the sex of the child. This billwill broaden that restriction through the same means in the case of a positiveDown syndrome diagnosis.

“People with Down syndrome are living longer than ever and they’re happier than most of us,” said Rep. Kathy Rapp. “So why are many of them being aborted, why? It’s a curious and heart-wrenching question, because there never has been a better time in all of history for people with Down syndrome.”

“We need to stand up for those who do not have a voice herein Pennsylvania,” added Klunk. “And that’s what this bill does. We have theresponsibility to stand up for those children who receive that Down Syndromediagnosis in the womb, and we shouldn’t allow them to be discriminated against becausethey have one extra chromosome.”

Rep. Paul Schemel acknowledged unborn babies with Down Syndrome as falling under the Americans with Disabilities Act of 1990, which protects the disabled from discrimination in all areas of public life, including jobs, schools, transportation, and public/private affairs. “The principle underlying the legally protected classes is that we don’t treat certain people differently because of their condition, be it race, sex, disability, etc. We don’t treat the disabled differently just because they are disabled. That would be wrong.”

The bill came through the House with a passing vote of 120-83,a major victory for the pro-life movement.  But why is it so significant?

The reason is not only because unborn babies with Down syndrome are receiving justice and protection, but the bill itself is one of the first steps to shift the focus of the abortion movement from the woman alone to the unborn child in her womb. Once we can shine a small light on the humanity and life of the unborn, we can open a door to complete, undeniable justice for them all.

May we continue to pray for our state senators, as they prepare to vote on the Down syndrome bill in the weeks to come. May we pray that Governor Wolf may also begin to see this bill in a different light. And may we continue, one small step at a time, to proclaim the humanity in all unborn life.

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Abortion

Viable: A Life-Changing Story of Post-Abortive Redemption

Playwright John Hoover remembers a moment long ago, when a spark was ignited inside him. Little did he know that years later, that spark would blossom into the life-altering reality known as Viable the play.

In 1984, when attending a pro-life symposium in California, Hoover listened to a woman speak out about her experiences as a former abortionist. This woman was from the Middle East and had been performing abortions for years before her eyes were opened to the painstaking reality of abortion.

“God took the scales off her eyes,” said Hoover. “She realized what she was doing and quickly became a pro-life advocate”.

The woman described that in early days, abortion failures were common, which resulted in physically impaired and developmentally-challenged children being born alive. To prevent potential lawsuits, procedures were developed to ensure that the baby in the womb would be undoubtedly dead.

After listening, Hoover couldn’t help but wonder: “what would the world be like if women weretold the truth of abortion?”

He remembered reading a survey which first informed women about the procedures done to abort an unborn child. Afterwards, they asked if the women would still obtain an abortion. 90 percent of women responded “no.”

This alarming response gave Hoover an idea, one that he carried with him for 25 years. In 2019, he finally put it on paper.

According to the play’s website, “The Viable storyline captures an unforgettable confrontation as an aborted child visits her mother nearly 30 years later. The mother has carried guilt and grief for all that time, trying all the while to protect her emotional stability by professing the mantras that abortion providers originally used to comfort her”.

With nothing but three actors and two chairs, Viable invites viewers on a journey ofcontinued healing as Judy, the mother, searches for a ray of hope after walkingfor decades in post-abortive shame and regret.

When asked about the primary audience, Hoover said that whenwriting the play, he assumed that it would be targeted at women who had lostchildren to abortion. However, everything changed on the very first night ofthe production, during a scene when Judy rushes through the audience in adramatic exit.

Gisele Gathings, who plays Judy in the production, remembersseeing a man walking out of the audience in tears. By the time she rushed outof the theater, the man was standing in the lobby, sobbing.

“I wanted to comfort him!” Gathings recalled. “But I had toget to my next scene.”

Gathings has observed that an abortion does not just affect women. Rather, all family members—fathers, grandparents, children, husbands, are part of the story, too.

“Delving into the emotions, the negative emotions of howabortion doesn’t just affect the woman that is post abortive, but also thefamily members that are involved. The cycle that passes down when abortion isin a family, not just one person having more than one abortion, but also familymembers following in the footsteps.”

To Gathings, the theme of Viable is not abortion, but redemption through Christ.

“It is bigger than abortion. This (abortion) can lead to various different issues and pain where people need healing. Jesus is about life more abundantly, but also about us choosing him and the choices we have to make. For me, Viable touches on dealing with and bringing up the pain that needs to be healed and addressed.”

Both Gathings and Hoover hope that this play may be what inspires families to begin conversations about their own abortion experiences, so that feelings of hatred, betrayal and regret might be replaced with forgiveness, grace and love.

Hoover is also excited to announce that the Viable tour is back in action. After months of show dates being cancelled due to the COVID-19 pandemic, Viable plans to resume its tour across the United States, with new dates and locations being added every day. The play will also be performed at this year’s National Right to Life Convention in Washington, D.C., on Thursday, June 24th. For more information, visit http://www.viableplay.org/.

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Abortion

The Ultimate Discrimination: Down Syndrome Abortions

Today I offer you some alarming food-for-thought: we are living in a society in which people have the authority to determine that one human being is more worthy of life than another.

Pennsylvania Representative Kate A. Klunk introduced legislation that would amend the Abortion Control Act to prohibit the abortion of a child solely because the child has been diagnosed with Down syndrome. Last session, the bill passed the House with a bipartisan vote of 117-76. Though it passed in the Senate as well, it was ultimately rejected after being vetoed by Governor Tom Wolf. However, Klunk is not going to let down that easily—she just reintroduced a similar bill known as House Bill 1500.

For those who may not know, Down syndrome is the most common chromosomal disorder in the United States. According to the CDC, the condition affects about 1 in every 700 births. Children with Down syndrome experience a variety of social and intellectual disabilities, as well as a range of medical complications. They are generally identified by physical characteristics such as eyelids that slant upwards, decreased muscle mass, and a trademark crease through the palms of the hands.

Aside from physical identifiers, those with Down syndrome experience cognitive and social impairments that can vary in degree.

Over a hundred years ago, Down syndrome was a dismal diagnosis for new parents. In 1910, children with Down syndrome typically did not live past the age of nine. That life expectancy soon increased to 20 years with the discovery of antibiotics, and now, the majority of Down syndrome adults live to be older than 60.

Today, people with Down syndrome are diving into theircommunities in ways never thought possible. They work in schools, health carefacilities, and all throughout the work force, and they engage in a variety ofrecreational activities like music and sports. They are universitygraduates, professional musicians, fashion designers, business owners andprofessional athletes. In addition to these, however, those with Down syndromehave always been friends, family members, neighbors and members of ourcommunities.

As writer Ziad Abdelnour wrote, “Success is not found in whatyou have achieved, but rather in who you have become”.

In a research survey of over 3,000 family members and people with the disability, nearly 90 percent of siblings indicated that they feel like they are better people because of a sibling with Down syndrome.

If you’re like me, you might know of several people with Down syndrome in your community. You are familiar with the way they can light up a room the moment they walk in. You might remember a sense of humor, a unique personality, or a refreshingly optimistic outlook on life. Just like many others, those with Down syndrome can radiate a sense of joy that can impact anyone they cross paths with, perhaps for the rest of their lives.

If the value of life in our society was measured not by achievement, but by who we are as individuals, friends and community members, would Down syndrome protection legislation still have been rejected? Would 67percent of American mothers, 77 percent of mothers in France, or 100 percent of mothers in Iceland have still chosen to abort their child after receiving a positive test for Down syndrome?

Currently in Pennsylvania, the only limitation to abortion per the Abortion Control Act is for sex-selective abortions. This seems self-explanatory—no person has the right to deny the pursuit of life to another person based solely on the discrimination of gender. The question left standing is: what makes Down syndrome any different?

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