The AJBQ believes strongly in the need to inform the public about stuttering. At present there are many prejudices and myths that make everyday situations difficult for those who stutter. The AJBQ endeavours to inform the public about the nature of stuttering through the media (television programs that focus on family issues) and by taking part in conferences (eg: ABC-CAPS 1999). In addition, the AJBQ prepares a special conference for International Stuttering Awareness Day on October 22. In order to better inform the public, the AJBQ also offers free information about stuttering. We are very proud of a1999 booklet designed especially for teachers, people who are instrumental in helping children who stutter yet often do not know how to interact with a pupil who stutters. In addition to information about the nature of stuttering, this booklet explains what the teacher should do when interacting with the child or teenager who stutters and offers consultations for class presentations.
Regarding services offered directly to young stutterers and to their families, the AJBQ takes time to answer any questions. By providing accurate information and offering guidance to the young stutterer and the family we are able to reduce concerns . The AJBQ also offers evening informational meetings intended for the parents waiting for speech therapy services or whose children are currently receiving therapy.
Additional services are also offered to the members of association. We publish a newsletter five times each year and offer special rates for our conferences and other special activities where children who stutter and their families to get together. The Association also offers a special program connecting young stutterers with volunteers who are studying to be speech-language pathologists. This program consists of weekly telephone meetings, thus making it possible for young people anywhere in Quebec to participate. The purpose of this program is to make it possible for the young person to continue to practice therapy techniques and to be supported by another person in addition to their family.
In summary, the AJBQ is an association ready to do everything for the greater comfort of children who stutter and their families. Our watchwords are information, sensitizing and support. We know that children who stutter have a lot to say, in spite of their stuttering. For this reason we want to say to them: " Just say what you want, we will listen. "