It still shocks me to say this, but we have officially left the Gray Area. I repeat, WE HAVE LEFT THE GRAY AREA! While I hated and resented the Gray Area, I had grown used to it. I had accepted that we would be stuck in this limbo for years, maybe forever. It was miserable and frustrating but it was what we knew. We'd resigned ourselves to it, agreed to stop talking about Cochlear Implants and evaluations and all those what if's (and yes I pretty much abandoned this blog) because it was too hard. I knew I couldn't get my hopes up yet again only to have them crushed. I couldn't go through that again. So I can't even describe the conflicted feelings I went through when everything changed a few months ago.
After the appointment with Dr. Awesome and Dr. Windsor last September,
we started working with a new audiologist, Beth, and a new speech-language
pathologist, Ariel. Like our previous team from three years ago,
Beth and Ariel thought that with a different brand of hearing aids and
extensive listening therapy, Brandt could significantly improve his speech
perception and would not need a Cochlear Implant. They felt that Oticon hearing aids have a
much better processing algorithm than his Phonaks, so they gave him a loaner
pair for an extended trial. We also
started doing listening therapy, both with Ariel and at home. Well, very long story short, six months with
the new hearing aids and listening therapy didn't help at all and our
communication was struggling more than ever.
The next theory was that he has Auditory Neuropathy, which Dr. Awesome and Dr. Windsor
had suggested last year. Beth conducted
an Auditory Brainstem Response (ABR) test, thinking that it would confirm
Neuropathy. I don't even know why we
were surprised, but the test came back as “probably no” on his right ear and
“inconclusive” on the left ear. She
retested the left ear twice and it would never cooperate.
In May, Brandt had another
appointment with Beth and Ariel. We
assumed it was just to return the loaner hearing aids, so I didn't bother going
with him. Having accepted that he wasn’t
a CI candidate and there was nothing more we could do to improve his speech
perception, we resigned ourselves to years more of struggling to
communicate. I was not at all prepared
for the text message I received an hour after he should have been home from the
appointment: “They say I am a candidate now. Want to get MRI and CT scan next.
I’m talking to their financial counselor now about insurance.” Umm,
what?! I just sat in stunned silence
for a few minutes, reading the text over and over. I thought he must have misunderstood what
they told him and cursed myself for not being there. It didn't start to sink in until he finally
got home and explained that they had retested his hearing with the Oticon
hearing aids and since he performed so much worse than ever before, he was now
eligible for a CI as long as the brain scans did not find anything abnormal. Another long story short, both scans came
back normal.
The next month, Brandt had his
appointment with Dr. Awesome. He entered
the room saying “Well, they finally approved you! All you have to do now is pick which ear and
which device you want.” Wait, hold on. ‘All’???
No. No no no. Not even close. With all due respect to Dr. Awesome—and
we respect him immensely—it’s not nearly that simple. Not anymore.
Not after years of getting our hopes up only to have them crushed, years
of emergency audiologist appointments to send back defective devices for the
umpteenth time, years of theories for how we might improve our situation that
never pan out. Years of heartache,
frustration, and disappointment. I told
Dr. Awesome that five years ago I would be jumping up and down crying happy
tears at this news, but it’s so complicated and seems so risky now, we don't
know what to think. He chuckled, having
heard this many times before apparently.
Brandt asked, “How can we know what is causing my hearing loss? And how can we know that a CI will actually
help?” Dr. Awesome said that we can't
know, his hearing loss is idiopathic
(unknown cause)—90% of hearing loss cases have an unknown cause. And there’s really no way to know if the CI
is going to help the way we want it to.
You just have to do it. Is this scary to anyone else??
Dr. Awesome said that it probably
would have been better if Brandt had been approved four years ago, because then
he wouldn't have had all this time to second-guess it. And I agree, it would have made it much
easier. There wouldn't have been a
question in my mind four years ago, I was SO sure that he would get approved
and that it was going to improve our lives immensely. I wished I could get that naiveté back, but
it’s long gone. We were weighing an option
that has the potential for high rewards, but that possibility comes with a high
risk.
So we went ahead and set the surgery date, September 11, with the understanding that we might back out at any time. Brandt chose his company--Advanced Bionics, because its technology has the most connectivity, and his ear--the right one, since it had better data from the ABR test. Then we decided to get a second opinion, because we were so on the fence about this decision. I kept saying, "flip a coin, because I seriously don't know if I want you to go through with this or not." We thought we had our CI center picked out for the second opinion, but after a series of problems over the course of 6 weeks, it fell through. We didn't know if we could get another appointment before September 11, and the next available surgery date was in November, which was not going to work with our schedule. It was 4:02 in the afternoon when I just started googling CI centers within a two-state radius and called them up. Some were already closed for the day, others didn't have appointments until late September. The first one to answer and have an appointment was UT Southwestern in Dallas. Brandt faxed his medical records to them on his way home from work, and first thing the next morning he had an appointment for August 29. Thirteen days before surgery.
We packed up and drove (and drove, and drove, and drove) to Dallas. We made it through the thick traffic and construction and got to the appointment early. First we met with an audiologist, who reviewed Brandt's tall stack of medical records: hearing tests, MRI, CT, ABR, notes from three evaluations and months of listening therapy. She didn't do any tests of her own, since we already had plenty of data. She said that she didn't think he has Neuropathy, and she thought he was a good candidate for a CI. "On paper, I think you would do pretty well with an implant...but you do have a lot to lose, so it is a crapshoot. I say go for it, if you can accept the possibility that it could or couldn't work. It probably will, but it's still a shot in the dark." This was actually much more positive than I was expecting, I honestly thought she would say something like 'Why are y'all even here, he obviously should not be a candidate and you're just going to have to suffer with hearing aids until you go deaf.' Seriously, that's what I expected. We had to wait two hours until the appointment with the otolaryngologist (I could barely eat my lunch) but it was well worth the wait! He was a very upbeat doctor with a loud, booming voice. He agreed that it doesn't sound like Neuropathy, just a "typical hereditary pattern with a dip" (which we discovered is called a "cookie bite," a term we had never heard before). He told us, "I think an implant is a good idea for you, you're within both the FDA and Medicaid criteria--and Medicaid is more stringent than the FDA. You have a much better chance to do better with a CI, because adults with progressive hearing loss do best. It's a leap of faith, but you are struggling with these hearing aids. I think you'll do very well, I say go for it!" We left the appointment in a daze, and on our long drive back home, we discussed preparations for before and after surgery.
Brandt decided, "I'm going to have to do it eventually, my hearing is just going to keep getting worse, so I might as well do it now." No more flipping coins, we were really out of that %#&*$@ Gray Area, jumping into the fire.
We packed up and drove (and drove, and drove, and drove) to Dallas. We made it through the thick traffic and construction and got to the appointment early. First we met with an audiologist, who reviewed Brandt's tall stack of medical records: hearing tests, MRI, CT, ABR, notes from three evaluations and months of listening therapy. She didn't do any tests of her own, since we already had plenty of data. She said that she didn't think he has Neuropathy, and she thought he was a good candidate for a CI. "On paper, I think you would do pretty well with an implant...but you do have a lot to lose, so it is a crapshoot. I say go for it, if you can accept the possibility that it could or couldn't work. It probably will, but it's still a shot in the dark." This was actually much more positive than I was expecting, I honestly thought she would say something like 'Why are y'all even here, he obviously should not be a candidate and you're just going to have to suffer with hearing aids until you go deaf.' Seriously, that's what I expected. We had to wait two hours until the appointment with the otolaryngologist (I could barely eat my lunch) but it was well worth the wait! He was a very upbeat doctor with a loud, booming voice. He agreed that it doesn't sound like Neuropathy, just a "typical hereditary pattern with a dip" (which we discovered is called a "cookie bite," a term we had never heard before). He told us, "I think an implant is a good idea for you, you're within both the FDA and Medicaid criteria--and Medicaid is more stringent than the FDA. You have a much better chance to do better with a CI, because adults with progressive hearing loss do best. It's a leap of faith, but you are struggling with these hearing aids. I think you'll do very well, I say go for it!" We left the appointment in a daze, and on our long drive back home, we discussed preparations for before and after surgery.
Brandt decided, "I'm going to have to do it eventually, my hearing is just going to keep getting worse, so I might as well do it now." No more flipping coins, we were really out of that %#&*$@ Gray Area, jumping into the fire.
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