Oy ya not until this morning did I realize I responded to the same post twice – and both in one day. Must have been all that celebrating of the 6 month mark and winking at everyone- had me not-too-with-it by the late evening (I was also typing while family were all chatting around me) … you all must think me a
loony tune…
A mistake I just got to laugh at. I thought I was responding to this post
http://anausa.org/forum/index.php?topic=5910.0- and must have had 2 windows open at once. I am holding my ground that “
this AN tumor has NOT affected my cognitive ability� - but obviously late on a Friday night with people talking all around me while I typed - my multi-tasking skills were
sliding. Oy ya- my apologies for not reading after I posted… until this morning… Oops
So anyway I too am curios as to what time frame, post op, people started getting their blink back. Crooked-smile has asked a
very valid question here to which I too would be curious to learn from.
Kate and Marie- thanks for your encouraging words.
Crooked-smile- I have read back on your posts and see that you are at the 7 month mark and your complications are from something different than an acoustic neuroma tumor. I was told, by a physician, that the Bell’s palsy can take anywhere from 3 months to 3 years to resolve (I gasped at the “years!?� too). Have you gone to this website for help?
http://www.bellspalsy.ws/I find that the “facial retraining exercises�
http://www.bellspalsy.ws/exercise.htm…are actually helping with my facial tone. In fact after I started these- it seemed the recovery expedited - these past weeks. We have others contributing on the forum who did NOT have an acoustic neuroma but other medical issues with similar symptoms- to which here they are finding support here (i.e. facial neuroma, other tumors etc). I have found the contributors to this forum are very supportive and it is nice to have a discussion forum with good moderators - keeping us ion track. I hope you have found some answers- as I have.
Keep moving forward,
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