Rare Connection
HCU & NF1: Mathew’s Story...
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What happens when signs of a second rare condition are dismissed because a child already has one diagnosis?
For HCU Awareness Month, Joanna Ball welcomes Joseph, a father from the United Kingdom, to share the story of his 14-year-old son, Mathew. The youngest of five children, Mathew is nonverbal and lives with Classical Homocystinuria (HCU) and neurofibromatosis type 1…