Lisa,
I think just the diagnoses of acoustic, facial or trimengial neuroma is enough to change anyone's attitude. Its a shock to the system. Some of us have no say in the treatment, they are just rushed into surgery. Others have time to decide what treatment option they want to under go. The decision is not on easy one.
It is a life altering event. Some of us have many complications and were not prepared for them. Dealing with dizziness, headaches, swallowing issues, eye issues and facial paralysis is not a walk in the park. It is great some bounce back so quickly, but those that do not it just adds to the change in attitude.
I cringe every time I see someone much younger than myself join the forum. I know how problematic my facial neuroma has been. It breaks my heart to read about Satman's latest issues, Taylor's new fight and now Lisa you are only 27 and I feel you should not be going through this. I had my first son at 27. I admire Kaybo, her journey started when she was 24 and she has gone on to have 3 gorgeous daughter. She a hero in my eyes. Actually if one really stops and things we are all heros. We are here and alive.
My attitude this past summer has been I do not care about a dam thing except, I care about my immediate family, those close to me who try to understand what I'm going through and everything else is irrelevant. Oh I enjoy reading a good book, a long hot bubble bath, the occasional glass of wine and I love following the US elections. (I'm Canadian and I find yours so much more interesting.) I also care about this forum. It has been a blessing, I know I've said this a lot in my postings, but it's true.
You cannot go through something like AN and not have a different attitude. I am grateful though, this is all I have is to deal with. My issues from my facial neurona are painful, and annoying but I also know it can always be much worse.
Hang in there Lisa, I know you been through a battle but you have won.
Anne Marie