HME – Patient Worthy

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A Journey to Self-Empowerment: What Kandise Has Learned from Life with Hereditary Multiple Exostoses (HME) (Pt. 1)

Post author:Jessica Lynn
Post published:February 24, 2023
Post category:Hereditary Multiple Osteochondromas Timely

When Kandise MacLeod was twelve years old, she began noticing various growths and tumors popping up on her bones. These sometimes caused pain or discomfort; in one case, Kandise even…

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A New Hope for Rare Bone Disease

Post author:Andres Rovira
Post published:September 28, 2017
Post category:Hereditary Multiple Osteochondromas Rare Disease

It's called Hereditary multiple exostoses (HME). Yes, quite the mouthful. Our friendly neighborhood scientists at Children's Hospital of Philly (CHOP) have been working diligently to study this rare bone disease…

A Journey to Self-Empowerment: What Kandise Has Learned from Life with Hereditary Multiple Exostoses (HME) (Pt. 1)

A New Hope for Rare Bone Disease

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