Hello, I have previously posted a few questions here, leading up to my decision to have CyberKnife treatments for a right-side AN. The first of my 5 treatments is tomorrow, April 13, 2017. They start on a Thursday, skip the weekend, and end next Wednesday (Th-F-M-Tue-W). I found it helpful to read the posts here where people posted updates as they went through their AN journey, so I thought I would post an on-going thread as I progress through the treatments and the months afterwards. Hopefully it will be helpful to someone at some point in the future, just as the posts of others have been helpful to me.
First the background.
I experienced sudden, unexplained hearing loss in my right ear about 3 years ago (can't remember exactly when). I called my ENT group for an appointment but the ENT doctor I have seen in the past for allergies and sinus infections, and whom I like and trust, was booked up, so I was given an appointment with the first available doctor. That ENT told me the loss was caused by a virus and would be permanent - nothing can be done about it. He gave me a prescription for prednisone but said it probably wouldn't help. (He was right about that. It didn't help. So I accepted the hearing loss and life went on.)
About a year or year-and-a-half later, in September 2015, I saw my regular ENT doctor for something unrelated, and during the visit he studied my chart and history, and kept saying "very interesting". I asked him what was interesting and he said "I don't think your hearing loss was caused by a virus. I think it may be neurological. We need to get an MRI." I got the MRI in October, 2015, and shortly afterwards he called me to tell me I have an acoustic neuroma on the right side. He explained a little about it, but said he is not a expert in these tumors and was referring me to a local neurotologist who is.
I met with the neurotologist later in the month. He told me the tumor was 16 mm x 9 mm, which would be near the low end of medium-sized. My only symptoms were hearing loss in the right ear of about 75% (based on their tests), and very mild tinnitus in that ear. (The left ear hearing is not 100% but is very serviceable.) We decided on watch and wait, and a followup MRI in 3 months.
The 3-month MRI was done in January 2016 and showed the tumor was now 15 mm x 6.7 mm, compared to 16 mm x 9 mm three months earlier. The neurotologist said that was probably just a measurement difference between the two radiologists who evaluated the two MRI's. He didn't think it actually shrunk. But it was encouraging that it didn't grow. We decided on further watch and wait. He scheduled another MRI for one year later (January 2017.)
I had that MRI in January 2017 and met with the neurotologist in February. He told me the new MRI showed the tumor was now 19 mm x 10 mm. A new hearing test showed a further loss of hearing in the right ear - now at about 90%. After some discussion, we decided on CyberKnife at Parkview Hospital in Fort Wayne, IN, which is where I live. I prefer to avoid surgery if possible, and my age (71 but quite healthy) may not be ideal for surgery. I met with a Radiation Oncologist at the Parkview CyberKnife center in early March and they scheduled the 5-fraction procedure for April.
I had the mask fitting, CT Scan, and MRI two days ago. This latest MRI shows the tumor is now 20 mm x 13 mm, which is quite an increase in just 3 months. I have 5 Decadron tablets. I am to take one tablet 1-hour before each of the 5 treatments. Nothing was mentioned about anti-nausea pills that many here mention that they got after each treatment. My pre-treatment symptoms are 90% hearing loss and very mild tinnitus on the right side. No noticeable balance or facial problems.
To summarize the tumor growth pattern:
October 2015: 16mm x 9 mm
January 2016: 15mm x 6.7 mm
January 2017: 19 mm x 10 mm
April 2017: 20 mm x 13 mm
I will post updates during the treatments, and thereafter will post when something significant occurs, but will also check-in with occasional updates even if nothing significant happens.
