Their Story Matters with Sara Troy and her guest Serafina Sammarco aired from August 2nd
Her drive was sparked by her daughter’s diagnosis of a genetic blood disorder at the age of 8 months and her death at 14 years of age.
She is the founder and president of The Vancouver Thalassemia Society, which she started after her daughter’s passing.
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Who is affected by it?
Diagnoses & Treatment
When Did I first learn about Thalassemia
How did my family handle it
Led the way to new treatment /
law (Isabella’s involvement)
Her Treatment and experiments
Forming a support Group after her passing
(The Vancouver Thalassemia Society of BC)
Face Book –serafina sammarco
Telephone # 604-274-1052
More on your host Sara Troy’s shows, their-story-matters
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