Tonight I started my IV that I will be on for a year. I
guess it didn’t really hit me how hard it is going to be to do antibiotics and
a IV every day at the same time, cover my port everyday for a shower, access
and de-access my port weekly, change my dressing weekly, get blood drawn
bi-weekly, make sure I’m not having any symptoms or side effects, and make sure
I’m not eating anything that would react with the antibiotics.
After I started the IV tonight I only felt a little
nauseated. Once my body gets used to the meds I should be fine. If I do get
more nauseated the doctor gave me some medicine to help with it that won’t
knock me out at the same time. I pray that this treatment works, and that I
don’t have to switch things up. The doc said this was the easiest thing to
start out with, so hopefully it works. I can’t imagine doing more antibiotics
or more times a day than this.
My home health nurse was really cool. It really makes a
difference in your care when you have someone you like. It doesn’t matter how
good a nurse is, if you don’t like them, its still not good care. If they don’t
have compassion and sympathy then it makes a world of difference.
I will be tough, I will do what I have to do, and I will
kick this. No matter how hard it will be, I have the best friends and family to
help me get through this. I have the last name that proves to be strong and
hardheaded.
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