> Harvey,
> How are you doing? Do you think the med is kicking in? I think it has
[quoted text clipped - 3 lines]
>
> Kelly
Ohhh, I keep getting into so much trouble with the program but I do feel
better. A person is not suppose to change anything or take any new medicine
or change the amounts of medicine a person takes. They want to know what
there medicine is doing with my body and nothing else.
Ok,,,,ok,,, I understand that but I have this catch 22 that I deal
with,,,,, prednisone. A person can not take 10 mg or more and be in the
program. At the very start I was living on pred. and Naprosyn while I
lived through 30 days of getting Enbril out of my system. I was taking 10
mg at the very start....only my RD kept me in. Then,,,, when I was feeling
better,,, I lowered the pred to 7.5 because the more pred I take the worse
my shingles are. The lady got soooo mad at me that I was nearly washed out
again because I changed an amount of anything I take. I can take being
chewed out as well as the next guy but she went on and on and on. I
finally put my hand up and said,,,, I fully understand your point and
nothing I could say would change the fact that I changed the amount of
something I take,,,, can we move on now?
The shots I take are a pretty big shot,,,,,two of them. It seemed to
me that she gave them to me a little fast which hurts like hell. I asked
her when I was going to be able to give myself my shots or shot. Her
eyebrows went up and I thought she was going to start in on me again....LOL
I just smiled at her and she said,,,, soon.
I know that they are building up the medicine in my system but what I
have not told them,,,,,,,, is that I have started to itch in my lower back
like I did with Remicade. I think it will be OK when I cut back to one
shot every two weeks. So it goes.
Harv
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