Author Topic: 14 month MRI  (Read 2781 times)

Tod

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14 month MRI
« on: April 11, 2011, 02:42:32 pm »

No change. Back again in six months. Neurosurgeon wants to maintain a careful watch so that when growth does occur we have a good sense of growth rate. This was MRI #9 in 15 months and while it is a stretch to say I enjoy them, I do find it somewhat restful...especially given the stress of the week leading up to an MRI. I think most of us know what that is like.

My neuro is slightly puzzled by my current facial issues as he has never seen them  quite like this before. The cheek muscle is spasming pulling things one way, while other muscles are pulling the nostril closed. Basically he is seeing it as a form of synkinesis, or perhaps a combination of re-enervation of the nerves and partially atrophied muscles, or both. Anyhow, he suggests that I start working at making faces doing basic facial retraining for awhile.

So, life continues to be pretty sweet. My voice is continuing to return, slowly, but returning. It was also nice to be in a meeting and hear the people on my left side, courtesy of my new Baha.


-Tod

Bob the tumor: 4.4cm x 3.9cm x 4.1 cm.
Trans-Lab and Retro-sigmoid at MCV on 2/12/2010.

Removed 90-95% in a 32 hour surgery. Two weeks in ICU.  SSD Left.

http://randomdatablog.com

BAHA implant 1/25/11.

28 Sessions of FSR @ MCV ended 2/9/12.

Jim Scott

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Re: 14 month MRI
« Reply #1 on: April 11, 2011, 03:00:50 pm »
Tod ~

Thanks for the positive MRI update.  Like many, I can relate to the irony of the 'restfulness' aspect of an MRI scanning procedure.  

It appears as if, despite the facial issues you're experiencing, your recovery is moving forward, which is great.  I trust the facial problems will eventually be resolved.  That the enhanced hearing now present with your new BAHA is proving to be a real benefit for you is not unexpected - but just as welcome.  Good news is always pleasant to read so thanks, again.  

Jim
« Last Edit: April 11, 2011, 04:10:08 pm by Jim Scott »
4.5 cm AN diagnosed 5/06.  Retrosigmoid surgery 6/06.  Follow-up FSR completed 10/06.  Tumor shrinkage & necrosis noted on last MRI.  Life is good. 

Life is not the way it's supposed to be. It's the way it is.  The way we cope with it is what makes the difference.

Kaybo

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Re: 14 month MRI
« Reply #2 on: April 11, 2011, 03:54:13 pm »
Great news, Tod!

K ;D
Translab 12/95@Houston Methodist(Baylor College of Medicine)for "HUGE" tumor-no size specified
25 yrs then-14 hour surgery-stroke
12/7 Graft 1/97
Gold Weight x 5
SSD
Facial Paralysis-R(no movement or feelings in face,mouth,eye)
T3-3/08
Great life!

CHD63

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Re: 14 month MRI
« Reply #3 on: April 11, 2011, 04:59:37 pm »
Good to hear this, Tod!!

Clarice
Right MVD for trigeminal neuralgia, 1994, Pittsburgh, PA
Left retrosigmoid 2.6 cm AN removal, February, 2008, Duke U
Tumor regrew to 1.3 cm in February, 2011
Translab AN removal, May, 2011 at HEI, Friedman & Schwartz
Oticon Ponto Pro abutment implant at same time; processor added August, 2011

kkl

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Re: 14 month MRI
« Reply #4 on: April 12, 2011, 07:04:07 am »
Great news...Congrats again!  Am sure the facial issues will resolve in no time.  I felt some twitching on my left cheeks last week but it's gone this week.  Other than that, my smile is like 90% there  ;D

yardtick

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Re: 14 month MRI
« Reply #5 on: April 14, 2011, 12:13:23 am »
Todd,

Your face does the same thing mine does and it gets damn sore, like tonight!  Isn't breathing such fun???  Well I see the specialist June 29 about my nose job.  My doctor feels I need valve augmentation surgery with autogenous cartilage and turbinale reduction, he claims this will help my breathing.  Wonder if I can have a tummy tuck and lipo while he's at it  ::)

Anne Marie
Sept 8/06 Translab
Post surgical headaches, hemifacial spasms and a scar neuroma. 
Our we having fun YET!!! 
Watch & Wait for more fun & games