Kelly you are exactly right on!! I couldn't agree more. If we let our condition get to us we only dig
ourselves in a deeper hole. Acceptance, and a attitude and we can live a life style again and be happy. I
found once I got to this point, and was up to me and me alone which side of the fence I wanted to be on, life
was so much easier. This came right down to the number of seizures I had and the ability to control them.
Good going and happy for you Kelly.
After all each day is a new day.
Julie
Julie Hope
epilepsyhealth@sasktel.net
http://www.2betrhealth.com
----- Original Message -----
From: "Kelly Porter" <kellyporter@frontiernet.net>
To: <epilepsy@yahoogroups.com>
Sent: Wednesday, September 22, 2010 11:56 AM
Subject: Re: [epilepsy] just staying in
Nearly 5 years ago my life was ripped out from under me because I became
so sick so fast. I didn't get a full diagnosis until just over a year
after that. Now I am at home. I leave to go to the store when my
husband takes me, and to go to church on Sunday. I do walk to my son's
school once a week to help out for 2 hours. I am at home now more then
ever, and I live in a small town of only 4000 with no public
transportation to take me anywhere. Unless my husband drives me I am at
home.
At first I climbed the walls. I would cry because I felt isolated. I
missed my active life which included a career I loved and volunteer
work. One day I decided that I refused to allow my diagnosis to effect
my attitude that much. My attitude is my decision and regardless of my
circumstance I could determine how I would respond to it, rather then
letting my circumstance control my attitude. Though iIstill don't go
very many places, I have found joy in the fact that I can support my
husband and son in all they do. Because I am home and on SSDI I can
accomplish the housework and the cooking without much suffering. I find
joy in the fact that I can put dinner on the table almost every night.
Simple things give me joy because I know 3 years ago i couldn't do even
those things. Rather then miss what I can't do and regret what I have
lost, I take joy in the fact that I am doing what I am capable of now
and that I have learned to accept this new life. Is it what i would
choose, no, but it is what I was given and i refuse to allow my
circumstance to rob me of my attitude and my joy.
Is it difficult to maintain that attitude? Yes. But each day I wake up
I have to decide what that day will be like, not think about what
yesterday was like. I have to wake up and say to myself "today I will
decide how well my day goes and how it ends and how I feel about it no
matter what".
Kelly P
musical612000 wrote:
> Hello, has anyone else discovered that aside from a few friends that actually UNDERSTAND and accept your
> condition, do you feel more content to just to stay at home, and involve yourself in activities that you can
> do at home?
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Yahoo! Groups Links
Thursday, September 23, 2010
Re: [epilepsy] just staying in
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