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07-20-2009, 01:28 PM | #1 | |||
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I was formally diagnosed with PD in May 2006. I had been "treated" for Essential Tremor since 1998....I was 35.
I worked in law enforcement for many years, then medically retired due to an injury unrelated to PD jn 1994. I went to work in healthcare as an ER Supervisor. My neuro & pysch both warned me that stress and fatigue are the enemy. I lasted four more months before I had to admit they were right, between work and my son having nearly died in a suicide bombing in Iraq (July 2006), I went out on disability in October 2006. I mourned those losses for awhile, then I picked myself up, gave YOPD the middle finger and went back to figure skating, working out at the gym, took up quilting and crochet. I try to spend my time focused on my abilities and gains, not the losses.
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Kimberly M. Fowler Each player must accept the cards life deals him or her: but once they are in hand, he or she alone must decide how to play the cards in order to win the game. -- Voltaire dx'ed w/Young Onset Parkinson's Disease May 2006 at age 43. Symptomatic since 1997 or earlier. DBS June 22, 2010 dx'ed w/TN on right side 2007. GK x4, last GK 02/2013 |
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"Thanks for this!" says: | RLSmi (07-23-2009) |
07-21-2009, 03:51 PM | #2 | |||
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Senior Member
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Quote:
Those are my sentiments exactly. Though I'd still love to contribute to my profession and feel that I can to an extent, I'm just not sure that I can do it full-time. What makes it difficult for me is the need to hide my symptoms; I am currently seeking a position and have to make it through interviews while my meds are not predictably working for me- I have seen my neuro but tweaking things takes time. Some days, I'm incapacitated by dizziness that I attribute to Mirapex; I actually have to lie down for an hour before it goes away. If I felt I was in control and making the choice, I wouldn't mourn having to give up my career. Since I feel it's the PD making decisions for me, I feel out of control and that drives me batty. Peony- Welcome to the forum. I enjoyed reading your experience. Oddly, a few studies show educational and medical professionals have a higher rate of PD. Who knows? Please, I hope you continue to share with us. -Laura |
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07-21-2009, 05:56 PM | #3 | ||
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In Remembrance
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this is a wonderful thread. got behind in reading.
i taught for 8 years after diagnosis; 11-12 with symptoms. Special education. i quit when i had no energy left to recover from work. paula pkell i'm so happy to see you're here.
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paula "Time is not neutral for those who have pd or for those who will get it." |
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07-22-2009, 12:52 PM | #4 | ||
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Thank you Paula, it's nice to be remembered. Lots of water under the bridge.
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