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Our CMV Story - The George Family
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Throughout CMV Awareness Month, we will be highlighting families across Canada and sharing their journeys with #CMV
About the George Family
Mike George's son, Ben, was born with congenital Cytomegalovirus (CMV). Doctors told them that he may never walk, talk or go to school. But Mike and his wife, Jan, never gave up hope and today, Ben is a university graduate.
Mike and Jan run Soaring Families, an organization that supports families impacted by disability. They are based out of Saint John, New Brunswick.
As of June 2, 2021, no province-wide CMV screening protocols exist in New Brunswick, Canada. It's time to change that! It's time to #screen4cmv
About the George Family
Mike George's son, Ben, was born with congenital Cytomegalovirus (CMV). Doctors told them that he may never walk, talk or go to school. But Mike and his wife, Jan, never gave up hope and today, Ben is a university graduate.
Mike and Jan run Soaring Families, an organization that supports families impacted by disability. They are based out of Saint John, New Brunswick.
As of June 2, 2021, no province-wide CMV screening protocols exist in New Brunswick, Canada. It's time to change that! It's time to #screen4cmv
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