Recent Posts

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Eye Issues / Re: Double Vision following surgery
« Last post by Mark F. on May 14, 2026, 10:41:27 AM »
I know this is an old thread, but if you are still checking out the site Cheryl.  I have some experience with that.   It may not be exactly what you want to hear.  Immediately following my surgery I had side by side double vision all the time for several weeks.  I wore an eyepatch over one eye when I was reading or watching TV because then I only saw one image instead of two.   Now total disclosure, I had double vision for 2 weeks about a month before my surgery that resolved itself, but after surgery it lasted much longer all the time.   I say all the time because I am one year post op now and I actually still have instances of double vision though not everyday and not for long periods of time.   It comes and goes.  The positives of my surgery far outweigh the negatives so I hesitated to respond because I don't want to make anyone change their mind.  Overall I couldn't be more pleased with my progress. 
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Post-Treatment / 1 year post -op
« Last post by Mark F. on May 13, 2026, 08:04:19 PM »
Just updating.  Today 5/13/2026 marks one year post-op for me.  Things have gone very well for me this past year.  I quickly regained balance, dizziness is gone, headaches which used to be a 24 hour a day thing are now only occasional and a lot milder than before.  I used to think that regaining my hearing would be important, well I am single side deaf, and I can honestly say it doesn't bother me.  If I had known how much better I would feel I wouldn't have placed such a high value on hearing out of the left side again.   I even set a new personal best 5k time this past year, since I no longer have balance issues.   This past year since my surgery has actually been the best year I've had in a long time.   I hope it continues, and that the tumor is truly gone forever now.   Thank you to all my friends on here for being there when things were very dark.   I really wonder sometimes how people without a support system make it through mental health wise.   

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Post-Treatment / Re: 2.5 Year Update
« Last post by Mark F. on April 28, 2026, 03:38:42 PM »
Michelle, Glad to hear you have been pain free.   
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Post-Treatment / Re: 2.5 Year Update
« Last post by mwatto on April 27, 2026, 10:44:46 PM »
Hi Mark - you are right! I bought an extra pillow to relive pain plus I got a pillow with a hole in the middle for a while for that side (in the end I didnt really use it much). The elevation now with my extra pillow has made a bg difference- plus I got rid of my latex pillow as way too firm which increased the pressure. In fact CatGPT suggested the same- that the pressure from lying on firm pillow and less elevated was the cause. Have had no pain at all past two weeks!
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Post-Treatment / Re: 2.5 Year Update
« Last post by Mark F. on April 22, 2026, 08:19:34 PM »
Hey Michelle,
Glad you found relief.  Those pains can be pretty bad.   You ever try sleeping slightly elevated?  I noticed quite a difference when I came home from the hospital between laying flat on the bed and the elevated position I had with the hospital bed.   My first night at home I got really sick from laying flat.   After a couple  days I was fine laying flat, but if your getting pressure laying down I just thought it might help.  Just a thought. 
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Post-Treatment / Re: 2.5 Year Update
« Last post by mwatto on April 22, 2026, 08:10:09 PM »
Thanks Dan! Actually its gone away at the moment and I feel great! Sleeping deeply on just a hot magnesium bath before bed (was on medical cannabis which kind of helped). Anyway will let you know how MRI goes- at least the audiology report was excellent.
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Post-Treatment / Re: 2.5 Year Update
« Last post by DanFouratt on April 21, 2026, 07:35:23 PM »
Michelle,  Sorry to hear you are suffering from this. I hope your MRI goes well. If I recall you are a non contrast person.

Take care,
Dan
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Post-Treatment / Re: 2.5 Year Update
« Last post by mwatto on April 20, 2026, 03:53:42 AM »
Hey Dan- am abt to get my 7th MRI after CK and will post. Hearing stable no change. But I continue to get geniculate neuralgia and it affects my sleep. I think maybe an artery compressing nervus intermdius in ear. like trigeminal pain. nyway will report back after MRI. Havent had a goodnights sleep for 7 years. No pain in day- only when lying on that side.
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Quote
ANA Patient Education Event
Hosted by Northwestern Medicine
Saturday, September 20, 2025
8:00 am - 4:00 pm CT

Location:
Northwestern Memorial Hospital
Conference Room L, 3rd Floor
Prentice Women’s Hospital
250 E Superior St, Chicago, IL 60611

Please join the Acoustic Neuroma Association and the team from Northwestern Medicine for a day of patient education, networking, and support. This in-person event will include presentations from distinguished medical professionals working with acoustic neuroma patients, as well as time for Q&A and networking.

Scheduled Topics Include:
Treatment Options
Mock Tumor Board
Facial Physical Therapy
Quality of Life - Balance, Dizziness, Headaches
Ocular Recovery
Hearing Restoration Options
and more!

More information at https://www.anausa.org/programs/patient-event-northwestern
Register at: https://interland3.donorperfect.net/weblink/weblink.aspx?name=E199564&id=782 geometry dash lite

Questions? Contact stephanierommer@anausa.org

Hope to see you there,

The ANA Team
This looks like a really valuable event—great mix of medical insight and patient support. The mock tumor board and quality-of-life sessions sound especially helpful.
Thanks for sharing the details and links. Hope it’s a great turnout!
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Post-Treatment / Re: 2.5 Year Update
« Last post by Mark F. on April 19, 2026, 06:35:16 PM »
Hey Dan,

Glad you had a positive follow-up.  I too had a tough time before treatment partially because of the lack of positive results being posted. I'm glad you stuck around on here.  I knew as soon as I found this website that I was going to stick around after treatment and try to be a  positive influence for all those scared people who were searching for answers like I was.  There are some people on here who have become kind of like an extended family because of our shared experiences.  Although I have never met any of them, and I may never meet any of you in person, I feel like we are all friends, brought together through an unfortunate coincidence.  I value each one of you, and even though there are relatively few posts made on this forum, I stop by almost every day to check in and see if anyone has questions or follow-up reports.   Stay well my friend. 
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