I have no idea how to start this other than to say that we received some unhappy news in regards to Owen last week. The worries began back at the hospital, and last Tuesday our fears were realized. During any newborns stay in the hospital they are subjected to many tests, one of which is the hearing screening. Owen's results the first time through showed him passing in his right ear but his results were "Refer" on his left ear. Many times a failed test can be caused by fluid in the ear or any other number of issues from birth. They'd be back the next day to retest, no need to worry. The next day the hearing screener rolled her cart back in and wired Owen up once again. Right ear pass, left ear "Refer." Shit. We'd need to come back to the hospital about a week later for a rescreen.
This is about when the Googling started. The internet is an amazing tool and it provides a huge amount of information, some of which is even accurate. We read that about 1 in 1000 babies is born with a hearing loss. Most babies who fail their first test at the hospital are fine, only about 5~10% of those with a "Refer" test actually having hearing loss and they generally pass their rescreen test. A week later Sara took Owen back to the hospital for the rescreen. Right ear pass, left ear "Refer." Shit again. We would be contacted by an audiologist for further testing.
Again, back to the googling. What's an audiologist?? What sort of tests do they run?? What type of percentages are we looking at now? We were contacted within the next couple of weeks by the John Tracy Clinic in Long Beach to set up Owen's additional testing, which occurred on Tuesday morning. They ran three different tests while we were there. First, a tympanometry which revealed normal activity of the ear drum. Second, an ABR, or auditory brainstem response. They basically put an earphone into the ear and measure the activity on the auditory nerve. Right ear pass, left ear "Noisy." Sadness
This was basically the end of hope that it was something that would end up being fine. Owen was diagnosed a a severe/profound unilateral hearing loss. He cannot hear, and without much doubt will never be able to hear, out of his left ear. We are still struggling with this news and all of the implications. Again, the internet can be both amazing and terrifying. We know that we have a huge number of additional appointments in our future, that team sports will be more difficult for Owen because sound localization is going to be problematic, that it could present a safety issue (for instance, not being able to hear an approaching car while on a bicycle), that he is significantly more likely to have learning difficulties....There is a second side to this coin though. With one good ear he has every opportunity to grow up with a completely normal childhood, excel in whatever he strives for, have no difficulties in school, become the next Stephen Colbert - another who suffers from unilateral hearing loss. As I think Sara and I try to approach everything, we will continue to hope for the best and plan to prevent the worst.
We still have more questions than answers. The next steps appear to be the following:
- Make appointment with different audiologist who can help with any sort of appropriate treatment plan.
- Make appointment with ENT to ensure that there is nothing structurally wrong with the ear.
- Make appointment with Early Start Program through our school district to begin in home work for both Owen and the rest of the family.
- Start attending classes on how to best help Owen live and learn as any normal child would.
We are extraordinarily blessed by having two amazing little boys. We are still struggling with the sadness and the complications that this diagnosis has brought into our lives. Regardless, we move forward, figure out what the next steps are, and figure out how best to love and care for both Owen and Connor while understanding this new reality.