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Good Golly Miss Molly – The Birth of a Mascot for Pompe Disease

September 12, 2018 Lauren Bailey Flueckinger, MS, CGC 5 Comments

Molly bobs around the clinic room, her strawberry blonde hair bouncing with every move. She has spread out her array of toys – stickers, books, a baby doll named Jack… CONTINUE

Filed Under: Advocacy, Education Tagged With: adult onset pompe, cardiorespiratory, diagnosis, difficult breathing, early diagnosis, enlarged heart, enzyme deficiency, enzyme replacement therapy, fatigue, genetic diagnosis, genetic disease, Harmony School of Business, Hope travels, infantile Pompe, Julie Garfield, late onset pompe, muscle condition, muscle weakness, newborn screening, Pompe, pompe awareness, pompe community, pompe disease, Universal Screening Panel

ThinkGenetic to Attend and Exhibit at 13th Annual WORLDSymposium™

January 27, 2017 Ruth O'Keefe Leave a Comment

ThinkGenetic is excited to be heading to sunny San Diego, California this February to participate in the annual Lysosomal Disease Network WORLDSymposium.  The Symposium is an interdisciplinary forum to explore,… CONTINUE

Filed Under: Events Tagged With: alpha mannosidosis, Carol Ogg, Dave Jacob, Dawn Laney, diagnosis, Fabry disease, Gaucher disease, Krabbe disease, LSD, lysosomal disease, lysosomes, Morgan Simmons, Mucolipidosis, Mucopolysaccharidosis, neuronal ceroid lipfuscinosis, pompe disease, Ruth O'Keefe, Sandhoff disease, Tay-sachs disease, WORLDSymposium, WORLDSyposia

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