Season 4, Episode 4: Hypophosphatasia - Meg Barker

Meg Barker, a teen advocate joins me on the podcast today.

We discuss Meg's journey into advocacy within the rare disease community. From a young age, Meg felt compelled to amplify voices in the rare disease space due to their mother's battle with Hypophosphatasia; a condition that affects the mineralization of bones and teeth.

Despite their youth, Meg has found their place at the advocacy table, tirelessly advocating for awareness and support in this often overlooked area of healthcare.

In our discussion, we delve into the significance of raising our voices, regardless of volume, and how small conversations can ignite meaningful change. Tune in to discover how you can utilize your voice to effect change in every room you enter.

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