It has been three months since I had my middle fossa at HEI. For those who don’t know, my neuroma turned out to be a facial nerve neruoma instead of an acoustic neuroma. It was relatively small, only 1cmX8mm. I have improved some, and am sure I will improve more. I have always been the type of person who is always on the move, always trying to get things done. Now I get a little upset because I can’t do as much as I did before. I am still dizzy, and my eye doesn’t tear, or close completely. It will close about 3/4 of the way, but it dries our very quickly. I wear a patch to keep moisture in as much as possible; it is a standard black patch. I wear a black one because the sun or bright lights hurt my eye. I was hit by mortar shrapnel in Iraq in 05, so the sensitivity has nothing to do with neuroma... my face moves around 30-40 percent, so it is not really noticeable unless I smile or something such, and when i blink, the left eye only closes 3/4 way, but with the patch on no one really sees it. I still have tinnitus, don’t think it will go away, I heard there was a med. that may help reduce that....If any one knows the name of that med, please let me know. Every day I have headaches. I wake every morning with a # 6-9 headache, and with perocette, or something such, it is not a good way to start the day. If anyone has had headaches for this long after surgery or longer I would like to hear about it.
Well this post is getting a little long, so I will go for now. Thanks everyone for listing to my situation, hope I didn’t bore anyone,
Thanks Danny
PS Lana, if you read this, please email me, or call. I lost your # and would like to know how you are.....