World Down Syndrome Day was bookended by two pieces of legislation. The week after 3/21, North Dakota enacted its law banning Down syndrome-selective abortion, which I wrote about at this post. The week before 3/21, Kentucky passed the Down Syndrome Information Act, requiring written materials and referral to parent support organizations with every Down syndrome diagnosis, prenatal or postnatal, which I wrote about here. In a recent column in TIME magazine, the two laws were discussed. Continue Reading
WDSD & The Down Syndrome Information Act on TV
WDRB 41 Louisville - News, Weather, Sports Community Thursday is World Down Syndrome Day (WDSD). March 21st was chosen as the numerical date, 3/21, reflects the genetic cause of Down syndrome, a triplicate of the 21st Chromosome. Today, a local news affiliate featured my local organization in preparation for WDSD. Watch the video to see self-advocate Chris getting ready to make our host breakfast and your blog's author interviewed about the recently-passed Down Syndrome Information Continue Reading
Kentucky joins Massachusetts in expanding information about Down syndrome
Yesterday, Governor Steve Beshear signed into law Senate Bill 34, referred to already as "The Down Syndrome Information Bill." The bill was patterned after a 2012 Massachusetts law. It requires that any health care professional or facility that delivers a Down syndrome diagnosis, prenatally or postnatally, also provide the family with up-to-date, evidence-based, written information and the contact information for national and local support programs and services, specifically listing Down Continue Reading
How to deliver a Down syndrome diagnosis?
With the advances in prenatal testing and guidelines recommending prenatal testing be offered to all expectant mothers, more Down syndrome diagnoses are being delivered than ever before. But how should a Down syndrome diagnosis be delivered? Fortunately, there is a very helpful resource that is also a professional guideline by those who should know best. Continue Reading
The need for care and support
This past weekend was the Down Syndrome Affiliates in Action conference. Consistent with past years, the schedule featured sharing sessions and breakouts on best practices for medical outreach and new and expectant parent support. With the advances being made in prenatal testing and research showing that the need for care and support is a key factor for expectant mothers making a decision following a prenatal diagnosis, this information is needed now more than ever. Continue Reading
Getting ready for the Down Syndrome Affiliates in Action conference
What should you do if you are attending the Down Syndrome Affiliates in Action Annual Conference? Continue Reading
Two birthdays with competing legacies
Ten score and four years ago today, Abraham Lincoln was born. That same day 204 years ago also was the birthday of Charles Darwin. The competing legacies of these two men twist through history like the spiraling parallel sides of the DNA molecule. Continue Reading
We Know Not What We May Be
During the winter break, I tried spending as much time as possible with my family. I treasure how, at the start of December, the day after we put the Christmas tree up, my daughter came downstairs, threw down both her hands, and, exasperated, said, "Daddy--where are all the presents?!" A recent post by Amy Juila Becker got me thinking about an ancient lesson revealed in this the holiday season. Amy Julia is an author, a blogger, and a mother of three. Her oldest, Penny, happens to have Down Continue Reading
Comments due on UK inquiry into abortion for disability
The United Kingdom's Parliament is re-examining the Abortion Act of 1967, specifically Ground E which permits abortion at any time on the basis of disability. Comments are due tomorrow, March 6, 2013, by 12 pm, EST. Read on for the link and how to receive a template for your comment. Continue Reading