A Loss for Words: The Story of Deafness in a Family by Lou Ann Walker

A Loss for Words: The Story of Deafness in a Family



A Loss for Words: The Story of Deafness in a Family ebook download

A Loss for Words: The Story of Deafness in a Family Lou Ann Walker ebook
ISBN: 9780062129895
Page: 224
Publisher: HarperCollins Publishers
Format: pdf


There is no clear explanation why, but compared with individuals with normal hearing, those with hearing loss have an increased risk of developing dementia. I am part of the Heart of America Christian Writers Network and landed my editor and publisher for my book, Confessions of a Lip Reading Mom, from past HACWN writing Raised in a hearing family, Shanna traces her hearing loss to a genetic loss on the paternal side of her family. A Loss for Words:The Story of Deafness in a Family by Lou Ann Walker. I would like to read A Loss for Words The Story of Deafness in a Family By Lou Ann Walker. A Loss for Words: The Story of Deafness in a Family. At age 13 The patient does not have a history of seizures or any other neurological deficits, and there is also no family history of macrocephaly. However, children who are deaf and born to hearing parents generally start learning language later, and with less consistent and less useful experiences. From the time she was a toddler, Lou Ann Walker was the ears and voice for her deaf parents. Find 0 Sale, Discount and Low Cost items for Business Idea List Small - prices as low as $6.39. I love stories with a breath of history.. Lou Ann Walker is the oldest daughter of deaf parents. Such children do not share a native language with their family. Females with DIS Her language at age 13 months was appropriately limited to babbling and a few words. Nancyecdavis AT bellsouth DOT net. I would encourage you, if you haven't already done so, to join a local and/or online writing group. Sincerely, Full of Words Dear Words, That is exciting about your book-writing endeavors. Sensorineural hearing loss and male infertility (Deafness-Infertility Syndrome; DIS) is a contiguous gene deletion syndrome resulting from homozygous deletion of the CATSPER2 and STRC genes on chromosome 15q15.3.

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