July 2024

Listen to this Article I have had the pleasure of knowing Jim and his family for nearly 15 years since our kids first became friends. I have always known him to be someone who is kind, knowledgeable and passionate about advocacy. Jim Teneycke was born with spondyloepiphyseal dysplasia congenita (SEDc), a form of dwarfism. He […]

Listen to this Article Marie Trottier was born with achondroplasia, the most common form of dwarfism. She is the International Liaison with Little People of America (LPA) where she volunteers much of her time. She grew up with the organization and has a deep fondness for it. Marie currently works as the Outreach and Engagement

Listen to this article Kai Rivas is an incredible 15-year old athlete currently enrolled in high school in Arizona, U.S. He is a dedicated power wheelchair soccer player who recently travelled to Montreal, Canada for a soccer tournament with his team.  One key theme emerging from my conversation with Kai who was born with diastrophic

Listen to this Article I had the pleasure of interviewing my long-time friend Jesse Nichols in early May for this issue. Jesse, a seasoned traveller was born with a form of dwarfism called diastrophic dysplasia. Known for often saying “pack your patience,” by sharing his travel experience Jesse raises awareness and provides learning opportunities for

Listen to this Article Travelling holds a special allure for many, offering the promise of exploration, adventure and unforgettable experiences. Yet, for individuals born with dwarfism, embarking on a journey can unveil a distinct set of challenges, barriers and opportunities which shape the way we experience the world.  I have come up with a few