I am a newly diagnosed member. My AN is 25 mm* 23mm * 20 mm. I have been discussing options with various doctors. One of the doctor I had consultation with is Dr Steven Chang who seems to have a really good reputation here in cyberknife treatment. He assured me that my tumour size is about the average size they treated and about half of the patients they treated are same or above my size. In Australia this size is on the larger side of the scale for radiation.
I am based in Australia and I weigh heavily on doctors%u2019 volume and experience in treating AN. I searched this forum and found a lot of good feedbacks.
1. If you also had cyberknife at Stanford with Dr Chang, could you comment on your experience, the good and the bad?
2. How was the post-treatment support?
3. Did you have to go through some unexpected complications?
4. Are there other doctors in US with similar or better experiences in this area?
5. Are there any information about the radiated tumour sitting in your brain for > 30 years? I am 42 years old. The two radiation specialists with whom I consulted both say if the growth is controlled, it will not cause further issues. I still feel a bit worried about the dead tumour continue to pressure the surrounding nerves for such long. With surgery, my consultation with Dr Friedman and Dr Schwartz at UCSD revealed that I will completely lose hearing and balance on the affected side. There is 1% chance of permanent facial nerve damage and 5% chance of transient facial weakness/paralysis, which I am reluctant to take on given radiation has 95% of chance to avoid most of these and > 60% chance to preserve my hearing (My hearing report shows I have near perfect hearing and I haven%u2019t noticed any balancing issue).
6. I talked to Stella who traveled from Sydney to US for cyber knife treatment with Dr Chang. Are there any other AU members who had similar experiences? How do you find the treatment and life after treatment?
Thanks a lot!
Claire