Filename 1989_Fall_NFPMAReport.pdf
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Category The CMTA Report

Prior to 1990, the CMTA was known as the National Foundation for Peroneal Muscular Atrophy, and the newsletter was published as The NFPMA Report. In this issue, you’ll find these articles and items of interest:

  • Living with a Rare Disorder:  Hope and Fear
  • CMT People: The Remarkable Rebecca Sand
  • “Gadgets, Catalogs, & Books”
  • 1989 in Review
  • More Progress in CMT Research
  • NFPMA Founder Harold Shapiro to Pursue New Interests