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Stuttering Foundation of America
American nonprofit organization From Wikipedia, the free encyclopedia
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The Stuttering Foundation of America provides free online resources, services and support to those who stutter and their families, as well as support for research into the causes of stuttering. A 501(c)(3) nonprofit organization, The Stuttering Foundation was established by Malcolm Fraser in 1947 in Memphis, Tennessee.[1] The Stuttering Foundation provides a toll-free helpline, free printed and online resources including books, pamphlets, videos, posters, referral services, support and information for people who stutter and their families, and research into the causes of stuttering.[2]
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Malcolm Fraser's daughter, Jane Fraser, is president of the Foundation.
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History
Summarize
Perspective
In 1947, Malcolm Fraser, a man from Memphis, Tennessee, knew about stuttering from personal, often painful experience.[3] He met with Dr. Charles Van Riper, a prominent stuttering speech therapist at the time, to discuss founding a nonprofit charitable organization. The organization Fraser founded became today's Stuttering Foundation of America. Its goal was to provide the best and most up-to-date information and help available for the prevention of stuttering in young children and the most effective treatment available for teenagers and adults.
Founder
Malcolm Fraser was a person who stuttered. His introduction to stuttering corrective procedures first came at the age of fifteen under the direction of Frederick Martin, M.D., who at that time was Superintendent of Speech Correction for the New York City schools. A few years later, he worked with J. Stanley Smith, L.L.D., a stutterer and philanthropist, who founded the Kingsley Clubs in Philadelphia and New York that were named after the English author Charles Kingsley, who also stuttered.
In 1928, Fraser joined his brother Carlyle, who founded the NAPA Genuine Parts Company that year in Atlanta, Georgia. In 1947, Fraser founded the Stuttering Foundation of America. In subsequent years, he added $20 million to the endowment.[4]
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Mission
Research
Neuroimaging studies for the potential to understand brain-behavior relationships in complex behaviors such as speech and language. [5] The Foundation was involved in projects by Dr. Dennis Drayna[6] of the National Institute on Deafness and other Communicative Disorders searching for genetic markers.[7]
Education
The Foundation discusses questions and provides information surrounding stuttering. This includes:
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Public awareness
Press releases have resulted in stories in print and segments on stuttering in the broadcast media, including CBS This Morning, The Today Show, CNN,[11] NPR,[12] and AP wire stories.[citation needed]
The Foundation's toll-free line is accessed by more than 20,000 callers each year.[citation needed]
Global outreach
In an alliance to help children who stutter through research, treatment and training programs, the Stuttering Foundation and the Michael Palin Centre for Stammering Children joined forces in 2006.[13] The Michael Palin Centre based in London.[14]
Honors and awards
In 1978, American Speech-Language-Hearing Association gave a Distinguished Service Award to the Foundation.[15] The NCCD, a council of 32 national organizations, recognized the Foundation's efforts in "adding to stutterers, parents, clinicians, and the public's awareness and ability to deal constructively with stuttering."[citation needed]
References
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