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Births of babies with Down syndrome in Europe fall sharply amid increased prenatal testing

January 5, 2021 CNA Daily News 0

CNA Staff, Jan 5, 2021 / 03:31 pm (CNA).- The number of babies with Down syndrome who were born in Europe fell by half between 2011 and 2015— confirming the fears of pro-life campaigners in the UK, who have long argued that increased prenatal testing for Down syndrome has led many women to abort their children.

A study published during December 2020 in the European Journal of Human Genetics examined the years 2011-2015 to determine the number of babies born with Down syndrome across all countries in Europe, and compared those numbers to estimates of how many babies would have been born with Down syndrome had they not been aborted.

The study found that 54% fewer babies with Down syndrome were born during that period in the United Kingdom than estimates would have expected— a figure roughly in line with the European average.

Notably, in the UK, non-invasive prenatal testing for Down syndrome has been available since 2012 to any woman willing to pay the £500 bill, the BBC reports.

In Spain and Italy, the percentage of reduction was 83% and 71%, respectively.

Abortion is legal in the United Kingdom until the 24th week of pregnancy, except when continuing the pregnancy is dangerous to the physical or mental health of the mother, as well as in cases where the baby will “suffer from such physical or mental abnormalities as to be seriously handicapped.”

For these disabilities, which can include Down syndrome, cleft lip, and club foot, abortion is legal up to birth. Most of the country’s 200,000 or so annual abortions take place before 13 weeks.

Right to Life UK, a pro-life group active in the country, has documented several instances of women being pressured to abort their children as a result of the prenatal test, with one mother reporting that she had been “offered about 15 terminations,” including when she was 38 weeks pregnant. By some estimates, nine out of ten women in the UK who receive a diagnosis of Down syndrome abort their child.

Increased use of NIPT have prompted several medical professional organizations in the UK, including The Royal College of Obstetricians and Gynaecologists, to issue guidelines urging doctors not apply pressure for abortion based on the results of the tests.

An investigation last summer found that the number of births of Down syndrome babies has fallen by 30% in National Health Service hospitals that offer NIPT.

The “Don’t Screen Us Out” campaign in the United Kingdom has, for the past four years, been drawing awareness to and seeking to change the UK’s abortion laws, seeking to amend the Abortion Act 1967 so that abortions for non-fatal disabilities are outlawed in the third trimester, which starts around 28 weeks of pregnancy.

Lynn Murray, a spokesperson for the group, told CNA in an interview last year that the campaign began in response to the government’s proposal of a relatively new screening method for Down syndrome— known as “cell-free DNA” tests— that, according to the government, would find an additional 102 cases of Down syndrome a year.

Given the high rate of termination for babies in the UK found to have Down syndrome, the campaign formed in order to try to get the government to assess the impact that the non-invasive prenatal testing technique— which is already being offered at NHS hospitals— would have on the Down syndrome community. The campaign attracted attention among Britons with similar concerns, she said.

Early last year, a 25-year-old British woman with Down syndrome, Heidi Crowter, launched a lawsuit against the UK government seeking to change the laws.

Crowter is joined in the lawsuit by Cheryl Bilsborrow, the mother of a two-year-old with Down syndrome, who has said that she was strongly encouraged to have an abortion after doctors performed the screening test on her unborn child. Máire Lea-Wilson, mother of nearly two-year-old son Aiden, who has Down syndrome, also has joined the lawsuit.

In October, the High Court of England and Wales agreed to hear the legal challenge.

The UN Committee on the Rights of Persons with Disabilities has consistently criticized countries which provide for abortion on the basis of disability. In some countries, such as Iceland, the abortion rate for babies believed to have Down syndrome is close to 100%.

Servant of God Jerome Lejeune discovered the genetic cause for Down syndrome— an extra copy of chromosome 21— in 1958. He spent the rest of his life researching treatments and cures for the condition, advocating against the use of prenatal testing and the abortion of unborn children who were found to have Down syndrome.

Berthe Lejeune, Dr. Lejeune’s widow, has said her husband was heartbroken that many doctors and governments have since used his discovery to “screen out” babies with Down syndrome, targeting them for abortion.

“He thought that all doctors would be happy to find research to cure them,” Lejeune told EWTN Pro-Life Weekly in 2017.

“But sadly, all government[s], not only in France, said: oh, it’s a wonderful discovery. You can detect these little sick children before they are born, and so take them away with an abortion.”


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News Briefs

Colorado medical practice to offer specialized care to adults with Down syndrome

December 21, 2020 CNA Daily News 0

Denver, Colo., Dec 21, 2020 / 07:15 am (CNA).- In a first-of-its-kind initiative, a Catholic-run healthcare practice in Colorado will partner with a major foundation based in Paris to bring specialized medical care to adults with Down syndrome.

Bella Health & Wellness, a practice based in the Denver suburb of Englewood, Colorado, announced at a Dec. 3 fundraiser that they will partner with the Jerome Lejeune Foundation, a French organization named for the pro-life doctor who discovered the genetic cause of Down syndrome in the 1950s.

Dede Chism, Bella’s co-founder and executive director, told CNA that the Lejeune Foundation was looking to partner with a medical practice in the United States that shared their ethos.

“The biggest thing is really believing in one another’s mission. We really believe in the mission of Lejeune and the mission of life…to be able to augment one another’s capacity to care by joining forces in any way that we can,” Chism told CNA.

Named for Servant of God Jérôme Lejeune, a French pediatrician and geneticist, the Lejeune Foundation aims to provide research, care, and advocacy for people with genetic intellectual disabilities. The foundation currently operates the largest medical center for people with Down syndrome in the world, located in Paris.

Bella opened in December 2014 as a non-profit medical practice, founded by Chism and her daughter Abby Sinnett, both of whom are nurse practitioners, with the goal of taking a holistic approach to caring for women in mind, body, and spirit.

The practice is run in full alignment with Church teaching, although it attracts non-Catholics as well, particularly those drawn to the clinic’s natural and scientific approach. Some areas of focus for the clinic include obstetrics, annual exams, gynecology, infertility treatment, menopause care, and abortion pill reversal.

Over the years, the practice has expanded its scope to offer care for men and children as well as for women, with services such as well child check ups, management of chronic illness, and COVID-19 testing.

One of the important facets of Bella’s work is care for pregnant mothers, and Chism said they are already adept at meeting the medical needs of mothers who are carrying babies with Down syndrome.

The new partnership will enable Bella to care for adult patients who have Down syndrome, she said. Bella will help Lejeune learn more about how medicine in the United States works, while the Foundation’s knowledge of how to care for people with Down syndrome, passed on to Bella’s staff through mentorships, will greatly benefit Bella’s medical practice.

“We know that there is an identified need, and we are going to be there to fill it,” she said.

Chism said they expect to begin serving their first patients with Down syndrome on March 21, 2021. March 21 has been marked as World Down Syndrome Day by the United Nations since 2012.

Dr. Lejeune, a devout Catholic, discovered the genetic cause for Down syndrome— an extra copy of chromosome 21— in 1958.

He spent the rest of his life researching treatments and cures for the condition— also known as trisomy 21— advocating strongly against the use of prenatal testing and the abortion of unborn children who were found to have Down syndrome.

Chism commented that before Lejeune’s discovery, people generally thought there was  something “missing” from people with Down syndrome, but Lejeune found that there was “nothing missing at all.” Rather, “God chose to write a second sentence in the DNA of Down syndrome people.”

Kieth Mason, executive director of the Jerome Lejeune Foundation USA, told CNA that the foundation chose Bella as their first medical practice partner in the United States because of a shared reverence for the dignity of the human person.

Denver is already home to the Anna and John J. Sie Center for Down Syndrome at Children’s Hospital Colorado, as well as the Global Down Syndrome Foundation, a major advocacy organization.

Currently however, Mason said, there is no freestanding medical center in the United States for people with Down syndrome older than 21. Most specialized clinics— of which there are about a dozen throughout the country— are pediatric. The partnership with Bella will aim to change that, he said.

The Lejeune Foundation operates the largest DNA database in the world, Mason said, and they base their specialized care for people with Down syndrome on many years of research. Research by the foundation is likely to yield positive results not only for people with Down syndrome, but for all people, he noted.

For example, it is very common for people with Down syndrome to get Alzheimers, so the foundation is doing a lot of research into how to lessen the impact of the disease. On the other hand, women with Down syndrome appear to be protected from contracting breast cancer, so research into this area could benefit all humanity, he said.

Mason said he fully expects Bella to attract interest from patients across the country, just as their clinic in Paris attracts patients from across Europe and the world.

Mason’s daughter Maria, who has Down syndrome, will be one of the first people to receive specialized medical care at the Denver clinic, he said.

“As we care for people with Down syndrome, they care for us. They minister to our hearts and show us what true joy is,” he commented.

Lejeune was a personal friend of Pope St. John Paul II. In 1994, the pope named him the first president of the then brand-new Pontifical Academy for Life.

Lejeune died of lung cancer on Easter Saturday 1994. His canonization cause was opened in 2007.

Madame Berthe Lejeune, Dr. Lejeune’s widow, has said her husband was heartbroken that many doctors and governments used his discovery to “screen out” babies with Down syndrome, targeting them for abortion.

“He thought that all doctors would be happy to find research to cure them,” Madame Lejeune told EWTN Pro-Life Weekly in 2017.

“But sadly, all government[s], not only in France, said: oh, it’s a wonderful discovery. You can detect these little sick children before they are born, and so take them away with an abortion.”

Madame Lejeune died in May 2020, also of lung cancer.

The UN Committee on the Rights of Persons with Disabilities has consistently criticized countries which provide for abortion on the basis of disability. In some countries, such as Denmark and Iceland, the abortion rate for babies found to have Down syndrome is close to 100%.

In the United States, there have been numerous attempts at the state level to ban abortions based on a diagnosis of Down syndrome.

Missouri lawmakers passed a law during 2019 that, in addition to banning all abortions after eight weeks, prohibits “selective” abortions following a medical diagnosis or disability such as Down syndrome, or on the basis of the race or sex of the baby. The law is currently blocked in the courts amid a legal challenge.

Ohio lawmakers attempted in 2017 to pass a ban on Down syndrome abortions, but a federal judge in 2019 blocked the legislation from taking effect.

Arkansas, Indiana, Kentucky, North Dakota, and Utah have all considered or passed similar bans.

At the federal level, the Down Syndrome Discrimination by Abortion Prohibition Act has been introduced in Congress, but has not yet been debated. The proposed law would ban doctors from “knowingly perform[ing] an abortion being sought because the baby has or may have Down syndrome.”


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The Dispatch

A blessing, not a burden

February 20, 2017 Jerry Salyer 0

“We like to think we live in the most tolerant society of all time,” Mike Michalak points out dryly. “But […] our answer in the 1950’s with my Uncle Ray [was to tell] my Grandma […]