Today I was feeling sorry for myself but I got over it; there is too much turmoil in this country to be feeling sorry for myself. I’m grateful for the things I still have and can do, even though I’m bedridden I still have my arms, hands and fingers I can still use. Now, enough about my current situation; I’m going to tell you what happened to me while I was in the hospital for almost 3 months. Last New Year’s Eve I was admitted into the hospital with a UTI infection and I was treated with Intravenous brain blood barrier Antibiotics for a week. Then in February I ended up with another UTI infection and was treated for a whole week with the intravenous blood brain barrier antibiotics. Again in March, I became incoherent and had seizures and was once again admitted into the hospital for a septic infection for three weeks this time. Once again they treated me with a brain blood barrier antibiotic. All in all before all of this, I was constantly suffering with spasticity, muscle spasms, re...
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Change the affect.
I recently got my hair shaved! My MS has now made it impossible to brush my hair. I tell you, since, I never realized how much effort it took out of me for such a simple task and now it's amazing how much energy I have now that I don't have to deal with my hair. I'm bedridden now and it sucks. I still try to stay in tune with today's modern chic way of life. I'm only in my forties so I should maintain how I look even though I can't use my legs anymore. You ladies hear me right? Being overweight doesn't help either so you know I got to work harder to look good these days! Don't get me wrong, I'm not ashamed living large! BBW are everywhere and look great working what their mother gave them. Also, I've noticed that just making yourself look "pretty" makes you feel like getting outside and sharing your beauty! That's when I started selling AVON products from the comfort of my home. I can't go to the people so I bring them to me thr...
March 7, 2013 ~
I haven't been feeling myself these last few weeks and having to endure muscle spasticity along with MS hugs during those weeks, I began feeling down on my luck. I can't say I haven't been depressed lately but I recently received my own Q6 Edge power wheelchair which lifted my spirits. I began thinking of how my life has changed and the things I have accomplished. When I first learned about my diagnosis of MS back in April of 1998, I was weighing over 310lbs. Despite my weight, I went out to many places enjoying my life. Dancing was my favorite pass time, I also loved horseback riding and walking trails but when I heard "you have MS", it shocked me. 'Not me', I thought to myself. 'There goes my life', I said to myself. This news made me think sad thoughts of no longer being able to do the things I truly enjoyed. I now had to focus and figure out where I stood in life with my health and my weight. I knew in the long run, my weight was going to be ...
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