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Member
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Join Date: Apr 2010
Location: GulfCoastSouth .... April 2014 rudely displanted to the cold wet windy gloomy NW coast.
Posts: 675
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Member
Join Date: Apr 2010
Location: GulfCoastSouth .... April 2014 rudely displanted to the cold wet windy gloomy NW coast.
Posts: 675
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Simply, as Mark stated in above post, "Tinnitus is very common with PCS. There is no way to predict if it will go away."
I'm now 4 years post-TBI, still dealing with PCS, and yes, tinnitus still is a fact of life.
Trust us, it's among the least of concerns to 'focus on', i.e. to fret over. It's a common part of life for many, many persons in life, with or without TBI, & common as adults grow older. As Mark said, you can choose to focus your attention on it or something else. It's for me now just part of my ordinary everyday life.
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50s Babyboomer; 2008 high-impact rear-ended/totalled-MVC, closed-head injury->pcs ... "Still dealing with it."
1993, Fell on black ice; first closed-head injury; life-altering. // 2014 Now dealing with Peripheral Neuropathy, tremors, shakiness, vestibular disorder, akithesia, anhedonia, yada yada, likely thanks to rx meds // 2014: uprooted to the cold wet gray NW coast, trying to find a way back home ... where it's blue sky and warm!
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Each and every day I am better and better. I affirm and give thanks that it is so. // 2014-This was still true for me last year, I truly felt this a year ago. Unfortunately it holds no meaning for me now. Odd, it was the Theta mantra for years. Change change change.
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