Mark Leach is an attorney with a Master's in Bioethics, focusing on health law and public contracts. His interest in bioethics concerns the issues surrounding prenatal testing and Down syndrome.

The Parent’s Guide to Down Syndrome: A Review

There's a new resource for parents of children with Down syndrome. It may be just right for you. Continue Reading

Ohio’s Down Syndrome Fact Sheet: Revision Needed

At the end of 2014, Ohio joined the states in passing the Down Syndrome Information Act (DSIA). Almost a year later, its Department of Health has issued the fact sheet to be provided all patients. Let's take a look at it. Continue Reading

Obstetricians’ 2016 Resolutions for Prenatal Genetic Testing

With the start of 2016, obstetricians, like everyone else, are making their New Year's resolutions. Here are their resolutions for counseling their patients about prenatal genetic testing.  Continue Reading

2015 Down Syndrome Prenatal Testing Year in Review

Here are the top five posts posted in 2015: Continue Reading

Our story: A compliment at Chick-fil-A

A stop on a roadtrip, and the simplest of compliments, reminded me of how good some people can be towards others, particularly those who happen to have Down syndrome. Continue Reading

ISIS issues fatwa to kill children with Down syndrome: is that wrong?

The Islamic State in Iraq & Syria (ISIS) has issued a fatwa to kill children with disabilities, including those with Down syndrome. Is this wrong? Continue Reading

Will the FDA regulate Sequenom (and other cfDNA labs)?

Sequenom launched its MaterniT21 cell free DNA screen on the marketplace in October 2011. Four years later, screens like Sequenom's remain largely unregulated. The FDA is moving to change that. Continue Reading

A&E’s Born This Way: Down syndrome meets The Real World

On Tuesday, December 8, 2015, at 10 pm on A&E, individuals with Down syndrome break down another barrier: they star in a reality-TV show called Born This Way.  Continue Reading

The ABLE Act: changing the cost of a life with Down syndrome

Since the House of Representatives passed the ABLE Act in December 2014, it has gone on to be enacted into law with dozens of states already enacting enabling legislation for the ABLE savings accounts and the Treasury Department finalizing regulations for these accounts. A thought occurred on the impact these savings accounts will also have on prenatal genetic testing. Continue Reading