Welcome to Connect, @jillshaw12.
I'm tagging @tracylynnedaley72 on this message in the hopes that she'll a new member from Omaha has joined the acoustic neuroma group. I see @donna3 also mentioned that she was seeing a specialist in Omaha.

I second your opinion that finding an experienced neurosurgeon is important. I'm not sure if Mayo Clinic is an option for you. At Mayo Clinic, we offer appointments within 48 hours through the the Brain Tumor 48-access program. Experts at the Mayo Clinic can help you navigate your healthcare journey, answer your questions and guide you through the treatment plan. Here is the online form and contact numbers for our 3 campuses in AZ, FL and MN http://mayocl.in/1mtmR63 Be sure to mention the Brain Tumor 48-access program.

I'd also like to tag other Connect members who have had surgery for an acoustic neuroma to share their experiences with you. Please meet @cynaburst @jjennings @sepdvm @ccubed @estherhg and @dnonnie to name a few. You'll read about their stories in this discussion.
Jill, what questions do you have for the group?

Ask away !???

JILL
My tumor was 2.5cm I had surgery 6 months ago , I feel great w some limitations I had surgery at Jefferson. Neuro hospital in Phila Pa

Thank you for the Mayo Clinic resources. I am meeting with my primary doctor on Friday to ask her questions about my MRI and what to expect. I want to learn more about Dr. Moore and his experience treating ANs. I am praying that when I meet with him next week I get a good vibe and that he is capable and greatly skilled. If I do not feel comfortable my next steps will be to contact the Mayo Clinic using the information you have provided.
Having a response from you touches my heart and makes me feel like I am not alone. Crazy how just having you reach out to me and to know there are resources and great people who do not even know me willing and able to answer my questions is so comforting.
I am still in the not even sure what to ask stage. I am sure I will have many questions as I progress through this journey (that I do not really want to take).
One of my biggest concerns right now is that I am a teacher and a planner. I feel I need to have a plan in place asap so that I can get a sub to cover for me. How long recovery will take is a huge concern. How much to share with my 5th grade students, parents, colleagues, administrators are all running through my mind.
i do not want to become the teacher with the brain tumor! I do not want parents to worry that their 5th grader is worried about their teacher. I know my teaching team love me and will be supportive but I am not sure if the administrators will think that I am in any way unable to be an effective teacher due to having a brain tumor. I pray that my effectiveness and my passion to teach are not lost through this ordeal. I am a very positive person but this diagnosis is really tearing me down. Any advice from AN post surgery teachers would be much appreciated.

How soon were you able to return to work and more of your routine? How did you pick your surgeons?
Which type of surgery?
I see the neurosurgeon that my ENT suggested tomorrow. I am hoping it goes well

Hope your visit helped ! I was back driving in 8 weeks , and back to part time working at a computer desk job in 8 weeks I was not able to return to my full time job yet due to the standing , and multitasking as a high school school nurse of 1600 students . If you are young you may bounce back even quicker ! You will realize everyone recovers differently I am in Vestibular PT and it had really helped a lot .