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VIDEO: We were told there's 'no cure' for our son's rare disease, so our work is to find one
5:34
  • wellness
  • November 24, 2021

We were told there's 'no cure' for our son's rare disease, so our work is to find one

Iris and Brett Schultz started their nonprofit organization, Hunters CMT4B3 Research Foundation, after their 4-year-old son was diagnosed with an ultra rare neurodegenerative disease.

Video by Elisa Tang

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