It is almost always heart-wrenching for hearing parents to find out that their child is deaf. We all have our own stories. My husband told me that his entire family was distraught, except for his great-grandmother who said: “Don’t worry, he’ll be fine.”

Erin Himmelman’s recent blog, “Take One Away and What Are You Left With“, left me wondering how differently each of our parents reacted when first discovering our deafness. I don’t need to cite sources to tell you that exceptional and devoted parents truly make all the difference or that socioeconomics very likely play a huge factor in the deaf child’s academic and social development.

Well, what about cultural backgrounds? Do they influence a parents’ reaction to their child’s newfound disability, and subsequently determine the path that their child takes in life?

Yale University conducted a fascinating research project, “National Culture and Risk Survey” that used two separate scales of cultural orientation (hierarchy-egalitarianism and individualism-solidarism) to gauge responses among participants. The researchers were able to conclude that cultural factors may play a factor in one’s attitudinal outlook toward risk. Ultimately, there is “no such thing as a generalized attitude toward risk”. They found that people tend to trust those who share their cultural views.

Just how does this relate to deafness? A child born with a disability leads to a perceived risk for the family. There’s uncertainty and fear of the unknown. It even affects family dynamics; there are higher rates of divorce among parents of a child with a disability. Out of every 1,000 newborns, about two or three are deaf or hard-of-hearing, and ninety-percent of those babies are born to hearing parents. With approximately four million babies born in 2005, that’s ten thousand deaf or hard-of-hearing babies! Obviously, all of these families come from widely diverse backgrounds and cultural upbringings. So there are probably thousands of different reactions toward the news of hearing loss. Is it always perceived as a ‘risk’? This depends on the family’s inherent outlook on people with disabilities.

For example, I married into a large Jewish family. Aside from learning that there are no holiday recipes for Yom Kippur and one does not serve challah during Passover, my family and I have come to appreciate a rather unique outlook on life through the eyes of my husband’s family. I was surprised to learn that Jewish temples generally do not provide interpreters, unlike the Christian-based churches that I attended while growing up. The latter operates on the principle that all must be saved so deaf children should not be excluded while learning the Truth about Christ. On the other hand, the Jewish religion is generally exclusive and does not often focus on expanding their reach. Would a Christian be more likely to seek ‘medical miracles’ for the child compared to his/her Jewish counterpart?

Keep in mind that the above is a very particular example and should not be interpreted as a distorted view of all Jewish and all Christians. My intent is to highlight different perspectives according to cultural background.

Latin Americans like eye contact. One of my personal flaws (or advantages, as a poker player might think) is that I do not maintain eye contact. If a parent of Hispanic origin had a conversation with me, they might sense dishonesty. Accordingly, that person would not absorb my information as well as another person who maintained eye contact. With whom would that Hispanic parent feel comfortable discussing sensitive medical issues involving the deaf child?

Cultural differences influence the way doctors handle their patients. According to this article (hat tip to Silent Cacophony),

Men, Christian doctors and physicians with the strongest religious beliefs were most likely to say it is permissible to withhold information and not help a patient find another source of controversial care.

If we understand that some families will naturally either entrust (or distrust) medical authorities of different cultural backgrounds, then we need to modify our approaches accordingly. We also need to keep in mind that some may prefer to rely solely on word of mouth, rather than visiting the Internet. Sometimes parents will want to “fix” their child’s deafness or leave as is. It is for these reasons that organizations need a universal presentation of materials to encompass cultural differences. How do we present educational materials to diverse parents from different cultural backgrounds who wish to learn more about their child’s deafness?

That’s why I heartily support the recent efforts of DeafDC.com participants to contact two organizations, Hand and Voices (www.handsandvoices.org) and American Society for Deaf Children (www.deafchildren.org). Together, these two organizations can take the lead effort in promoting culturally-sensitive materials that will have an equal impact on all families of deaf and hard of hearing children.


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