Today was my first day back to work since being in the hospital. Tiring. That's the only way I can describe how my day was. I really am glad that I have such an understanding boss and co-workers. I feel as if I really matter to them. I am lucky in this aspect as I know their are other places that would have been less understanding. I try to do a full 8 hour shift, but at this point I am so tired. By the 6th hour I start stumbling, my walking becomes slower, my speech begins to slur and my right eye starts seeing everything double and blurred. Rather frustrating, but what can I do. What is really funny is that I forget how to speak Spanish, which I am fluent in normally. I sort of begin to stutter over my words. I think I expect too much of myself, after all it has only been a week since I was discharged from the hospital.
I need to learn to give myself a break, to let my body rest, heal. It's just that I get so bored. I like being busy, helping people. Makes me feel like I can contribute to society. It's hard for me to let go, even if it's just for a little while.
One of my dreams, hopes before this illness was to join a mission with Doctor's Without Borders. I wanted to help those people who were not able to help themselves due to poverty, politics or other obstacles beyond their control. That is not going to be a reality for me now, I have to come to terms with it. I just feel in my heart that I need to help people, I only wish I knew how I can help now.
http://www.doctorswithoutborders.org/
Title pretty much says it all. Journal of dealing with this very confusing condition on a daily/weekly basis. Sharing laughter, frustrations, and all the emotions that come with Multiple Sclerosis.
Welcome
Welcome to all who visit this Blog whether you suffer from Multiple Sclerosis or have a loved one who does. Hopefully this will help all who read understand that they are not alone even though MS affects us all in very different ways. Maybe it can help open eyes of those around who do not know the unpredictability of daily life with MS.
The purpose of this blog is to offer support and inspiration. Please feel free to share any useful information that you have gathered along your journey and words of inspiration. It is hard to overcome all the obstacles we must face and it is nice to hear ways people have adapted. Inspirational stories and anectedotes are especially sought after.
If you post and suffer from Vision disabilities you are welcome to post in all capitals and no one will think that you are shouting.
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