Author Topic: 13 months Post Middle Fossa  (Read 3971 times)

Pharm925

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13 months Post Middle Fossa
« on: June 03, 2015, 10:13:07 am »
I'm so happy to report that I had my 1 year post-middle fossa MRI and I just found out that it was clean!!! No regrowth of the tumor and I couldn't be happier!! If you're still in the pre-op stages, have hope. I had to post this because I know when I was there I lived to see happy reports like this. I forget about my (now lack of) tumor most of the time now, which is great since before I thought about it constantly. I can hear some ringing in the ear, but mainly only when I think about it. It's louder after leaving a loud room/area. I only notice some hearing loss when I lay down with my good ear down to the pillow. Life is great and I hope someone finds some glimmer of hope from this post. Feel free to message me with any questions!!
Diagnosed 9/2012 - 8mm
5/2013- no growth- 8mm
4/2014- no growth- 8mm
Surgery on 4/16/2014 by Dr. Vrabec at Methodist in Houston-100% removed via Middle Fossa approach
6/6/2014- Hearing test done and AN ear hearing mostly saved!!!
4/2015- MRI 1 year post-op- clean of AN!!! :)

michellef08

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Re: 13 months Post Middle Fossa
« Reply #1 on: June 03, 2015, 12:20:34 pm »
Great report!! As we just figured out - we have very similar stories. We were both 27 when we had our surgeries, which is rare! I am now 2 years post-op with an amazing outcome as well - hearing was saved, no facial or balances issues.

I also hope this post gives some hope to anyone who is struggling. The entire ordeal is very confusing and scary. Here is my humble advice - do as much research as you can handle and make sure you make the right decision for you. We are lucky enough that the tumor is normally slow-growing so you can take your time and see as many specialists as you can. Whatever route you choose - choose a doctor who is experienced with an AN. It is a rare tumor, and cannot be treated successfully by just any local doctor. Then once you have made a decision, maintain a positive attitude. There are many people who have great outcomes, and they are out there living completely normal lives now!
Diagnosed Dec 2012: AN 1.4 cm with mild hearing loss and tinnitus. Surgery: Middle Fossa at House with Schwartz/Friedman on April 10, 2013. Entire tumor removed, no facial issues, no balance issues, and they preserved my hearing!! Co-leader of the Washington, DC ANA support group since 2016.

ANGuy

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Re: 13 months Post Middle Fossa
« Reply #2 on: June 03, 2015, 04:00:31 pm »
As a WW'er, I do find your posts encouraging.  So, if I get the surgery, I'll be 27 again? ;D
Diagnosed June 2014 1cm AN at 47 years of age.  Had fluctuating symptoms since 2006.    6 mos MRI (Dec 2014) showed no growth, MRI  in July 2015 showed no growth.  MRI Jan 2016 showed no growth.  MRI Aug 2016 showed no growth.  I'm gonna ride the WW train as long as I can.

Pharm925

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Re: 13 months Post Middle Fossa
« Reply #3 on: June 04, 2015, 09:08:53 am »
Yea, it's rare to find someone else my age with this! Definitely good advice to research and take your time. I was lucky enough to be living in Houston with the largest medical center in the country. My ENT was amazing and I highly recommend him. I thankfully didn't have a large tumor, so the neurosurgeon didn't have a lot to do in my case, but he was great as well, they have been doing these surgeries together for I believe it was like 15 years.

Michellef08---did you also have middle fossa approach? My AN is my right ear too!

Hang in there ANGuy! Yes, if you have the surgery you'll be 27 again! :)
Diagnosed 9/2012 - 8mm
5/2013- no growth- 8mm
4/2014- no growth- 8mm
Surgery on 4/16/2014 by Dr. Vrabec at Methodist in Houston-100% removed via Middle Fossa approach
6/6/2014- Hearing test done and AN ear hearing mostly saved!!!
4/2015- MRI 1 year post-op- clean of AN!!! :)

michellef08

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Re: 13 months Post Middle Fossa
« Reply #4 on: June 25, 2015, 07:41:25 am »
Yes, I had Middle Fossa too!
Diagnosed Dec 2012: AN 1.4 cm with mild hearing loss and tinnitus. Surgery: Middle Fossa at House with Schwartz/Friedman on April 10, 2013. Entire tumor removed, no facial issues, no balance issues, and they preserved my hearing!! Co-leader of the Washington, DC ANA support group since 2016.

bethtretrault

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Re: 13 months Post Middle Fossa
« Reply #5 on: June 25, 2015, 04:58:40 pm »
Having retrosigmoid in November. Looking forward to being 27 again! Thank-you, thank-you, thank-you for the positive posts. That is all I want to see now.
beth
12/2013 5mmx4mmx4mm left
tinnitus, w&w
5/2015 7mm-louder tinnitus, occasional dizziness
retro sigmoid 11/2015