Here is what my MRI report says:
Technique: Multiplanar, multi-sequence pre and post contrast images were obtained through the IAC's.
LEFT: At the level of the opening of the IAC, there is a 5mm oblong focus of signal abnormality which is hypointense on TI weighted images and lies between the facial nerve and vestibulocochlear nerve. Post contrast images demonstrate mild enhancement of the small focus of soft tissue suggesting a small or early acoustic schwannoma. Adjacent to this focus of signal abnormality runs a tortuous left anteroinferior cerebellar artery. My ENT read the report, looked at me and said, "looks like you have a tumor" and then proceeded to tell me how he would recommend surgery over any other option.
I was never shown my MRI by the dr. I came home looked up MRI films online and searched pics that showed tumors. Then I went to radiology and obtained copies of my MRI myself and compared. This one of my images I compared and thought this might be the one showing the tumor (hope this link works)
http://i853.photobucket.com/albums/ab100/tgillesp1/MRI.jpgOf course I don't really know what I'm looking for, and I know most of you won't either. So my biggest question is if that blob is not a tumor then what is it? And now that I have Dr. Chang saying I have no mass, I'm back to square one on what is causing my hearing loss and tinnitus. So anyway, I have a followup with my ENT on Tuesday and I am going to ask him to refer me to a neurotologist because I have so many unanswered questions. My hearing aides (Siemans OTC) are not doing as well as I need them. My biggest problem is speech recognition. I can hear noise (especially background), so teaching in a classroom environment is killing me. The hearing aides amplify all the noise to a headache level everyday and make tinnitus worse, and I'm still having to ask students to repeat themselves over and over. I didn't want an AN, but at least I felt I finally had a cause. So I do still hope Dr. Chang is correct, and I will find out soon from House. However, I would still like to address my hearing situation and try to get help for that. If I can't find some help, then I just can't see myself continuing as a teacher in a noisy classroom for much longer.
Jan, I've joined Cochlear community and have been reading, but I don't see where any of the implants would be helpful to me yet since I'm not SSD. Do you know if there are any other solutions to improving my hearing situation or anything I should ask the neurotologist about?
Thanks