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Dance With Mweyne Talks shares passions and stories of experiences in developing countries to inspire you to serve a cause bigger than yourself. We will be joined by community supporters of disability awareness, both leaders and philanthropists to discuss topics such as what sparked their transition into a service based life, what it's like living with or caring for a disability and what we can all do to create a lasting positive impact.
Learn more about how to get involved at DanceWithMweyne.org
Donate : DanceWithMweyne.org/Donate
More about Gia Cordaro:
Gia Cordaro is a Chicago native, aesthetic mentor in beauty and wellness, who's life took a turn when her first son, Jimmy, was born with two rare diseases Agenisis Corpus Callosum, a neurological disorder and Mitochondrial Disease, a genetic disorder. He was given a life expectancy of 1 year, but to Gia that was unacceptable. It is now 12 years later and Jimmy along with the rest of the family continues to thrive.
By Dance with Mweyne FoundationDance With Mweyne Talks shares passions and stories of experiences in developing countries to inspire you to serve a cause bigger than yourself. We will be joined by community supporters of disability awareness, both leaders and philanthropists to discuss topics such as what sparked their transition into a service based life, what it's like living with or caring for a disability and what we can all do to create a lasting positive impact.
Learn more about how to get involved at DanceWithMweyne.org
Donate : DanceWithMweyne.org/Donate
More about Gia Cordaro:
Gia Cordaro is a Chicago native, aesthetic mentor in beauty and wellness, who's life took a turn when her first son, Jimmy, was born with two rare diseases Agenisis Corpus Callosum, a neurological disorder and Mitochondrial Disease, a genetic disorder. He was given a life expectancy of 1 year, but to Gia that was unacceptable. It is now 12 years later and Jimmy along with the rest of the family continues to thrive.