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“Rare is Everywhere” Author Partners with ThinkGenetic

November 29, 2017 Ruth O'Keefe Leave a Comment

Deborah Katz, health practitioner, author, illustrator, and founder of Rare is Everywhere Global Productions, has officially partnered with ThinkGenetic to support those living with rare genetic disorders. In November 2016,… CONTINUE

Filed Under: Partners Tagged With: Deborah Katz, Len Barker, Rare Disease Foundation, Rare is Everywhere, Rare is Everywhere Global Productions

Connecting, Collaborating, and Activating at the Vibrant 2017 RARE Patient Advocacy Summit

September 28, 2017 Dawn Laney, MS, CGC, CCRC | ThinkGenetic Co-Founder Leave a Comment

While many of our ThinkGenetic teammates helped others “harness their inner power” at the National Society of Genetic Counselors Annual Conference in Columbus, Ohio, ThinkGenetic CEO, Dave Jacob and I… CONTINUE

Filed Under: Events Tagged With: advocacy, Dave Jacob, Dawn Laney, Deborah Katz, Dekel Gelbman, Face2Gene, FDNA, genetic counselor, genetic disease, Global Genes, Rare Disease, summit, SymptomMatcher

Rare is Everywhere – A Children’s Book to Inspire Our Differences

November 3, 2016 thinkgenetic 2 Comments

deborah-katz

by Deborah Katz, RN, MSN, Guest Contributor My new children’s book RARE IS EVERYWHERE is a book showcasing genetically rare animals like white tigers, blue lobsters, black jaguars and other amazing creatures to… CONTINUE

Filed Under: Education Tagged With: Deborah Katz, kickstarter, promo code, Rare Disease Foundation, Rare is Everywhere

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