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Faces of HPP

Hypophosphatasia is a rare genetic disorder that has one of the widest range of symptoms and severity, no two journeys look the same. In this webinar, you’ll hear directly from members of the Soft Bones community as they share what it’s like to live with different forms of HPP, from diagnosis to daily life, and treatment decisions. Whether you’re newly diagnosed, supporting a loved one, or a healthcare professional seeking patient perspectives, this webinar offers real stories, diverse experiences, and valuable insight into how HPP can affect individuals in very different ways. Learn more about hypophosphatasia and the resources available at www.SoftBones.org.