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Description

Rare disease patients experience many different symptoms and side effects from their disease and treatment plans. Patients are faced with questioning what they should share with their medical teams during their appointments.

In this week's episode, Taylor and Liz break apart what leads to these concerns and how they have benefited from connecting with their medical teams throughout their care journeys.

Looking for updates or a way to connect with Taylor and Liz? Look for us on Instagram at the NotSoRarePodcast as well as on Facebook at the NotSoRarePodcast. Also, feel free to message us at notsorarepodcast@gmail.com. We love to hear from all of you!

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