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In this episode, Lara Erekson shares the health journey of her daughter Whitney. It was only after many years of symptoms and distressing experiences and procedures and testing that she finally received the diagnosis: a rare genetic condition known as KDM5C. Their story sheds light on the challenges faced by individuals with this condition, as well as the emotional and practical difficulties parents experience while seeking answers and care.
Information about the KARES foundation: https://kares.foundation
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In this episode, Lara Erekson shares the health journey of her daughter Whitney. It was only after many years of symptoms and distressing experiences and procedures and testing that she finally received the diagnosis: a rare genetic condition known as KDM5C. Their story sheds light on the challenges faced by individuals with this condition, as well as the emotional and practical difficulties parents experience while seeking answers and care.
Information about the KARES foundation: https://kares.foundation
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