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It’s Presidents’ Day: which President did the most for individuals with intellectual and developmental disabilities?
Continue reading...A resource for information-seekers
My name is Mark W. Leach. I am an attorney with a Master's in Bioethics. I have presented at international, national, regional, and local conferences for obstetricians, medical geneticists, genetic counselors, bioethicists, and Down syndrome support organizations. I have been published in professional journals, national and local newspapers, and on-line blogs. This blog is a continuation of my efforts to provide perspective and resources for Continue Reading
It’s Presidents’ Day: which President did the most for individuals with intellectual and developmental disabilities?
Continue reading...Dickens wrote “it was the best of times, it was the worst of times”. In the past 48 hours, I’ve experienced when a system designed to support individuals with disabilities functions optimally and when it functions absurdly.
Continue reading...In New Delhi, India a baby received multiple injections of human embryonic stem cells as an experimental treatment for Down syndrome. Any ethical issues here?
Continue reading...For Martin Luther King, Jr.’s national holiday, my kids and I toured seven National Park Service sites. They illustrated the truth of Dr. King’s wisdom that the arc of the moral universe is long, but it bends towards justice.
Continue reading...I have a post at the Prenatal Information Research Consortium about a coalition of prenatal testing laboratories seeking increased insurance coverage for their cell free DNA screening tests. It addresses the possible issues raised by this coalition representing in its mission to provide useful information to providers and insurers, while also working to increase reimbursement […]
Continue reading...Research now shows that a child with Down syndrome costs less than $3 a day more in health expenses than a child without Down syndrome. This research should cause obstetricians, genetic counselors, expectant parents, and policymakers to revise their view of how costly a life with Down syndrome really is (or isn’t).
Continue reading...In 2013, researchers estimated that the total number of people living in the United States was 40% less than the historically cited number. Three years later, that estimate has been revised down further by 20%.
Continue reading...The American College of Medical Genetics & Genomics (ACMG) issued an updated statement on how cell free DNA screening should be done. It’s not clear, though, why cfDNA screening should be done.
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