Over 90 % of parents of children with hearing loss have normal hearing.
For many parents, your child is the first person with hearing loss that you have ever met.
The diagnosis of hearing loss at birth is almost never anticipated by parents. The confirmation of permanent hearing loss that comes with follow up testing can be devastating. As an audiologist, informing parents that their child has hearing loss is the most difficult aspect of the profession. However, it is most rewarding to see the many positive outcomes that happen because we are able to identify hearing loss and intervene so early in life.
The problem is, parents often find they have entered a world they are unfamiliar with and know nothing about -not to mention they came completely unprepared. I see this Support Group as a way for parents to educate themselves on everything they need to know in order to create the best situation for their child. Getting information may be difficult if you don't know where to look. Now that you're here, you have a start.
I'm also hoping this Support Group will provide a means for parents that have already been through the early, difficult days to be able to share their experiences with parents of newly identified children. Some of the best support comes from other parents who have gone through the very same thing.
From my perspective, it's easy for me to see that you are not alone. However without actually meeting other parents, you may not realize that you are not alone until you gather as a group. If you are a parent of a child with permanent hearing loss and would like some information and support, we look forward to meeting you!
-Megan D. Ford, Au.D.
Audiologist, Founder of Hear My Dreams Support Group
~ Hear My Dreams currently operates solely through volunteer efforts and pro bono services. It is not a non-profit organization and is not affiliated with a hospital, organization or business. ~