| Re: How many of you still work with your fibro?
I have lupus and fibro. I work full time and it is not easy. I miss alot of work. We get 15 days a year and my goal is to not go over those days. I thought I had it last year but had ended up in the hospital for a week the last week of November. It has gotten better though. When I first got sick I missed 30 days that year.
Working is hard, and that is that...but I really feel that if I stop working I won't continue to push myself. I know that if I did that I would go down hill fast. Alot of dealing with this is mental. I take pain meds along with my other meds and then the meds for the side effects of the meds... but I also know that mentally I am fighting with all that I have and frankly, that is the only way to get through this. I need to work for financial reasons as well as needing the health insurance well ...to live. But it also gives me something to take my mind off the pain and keep me feeling I am contributing. I had to move in with my mother last year because the chemo meds were kicking my butt. I worked through it, but that was all I had.
I still have days where I am not sure I will be able to drive home, I am in so much pain... but like I said, not working I think would be the end of me.
__________________
Erin
Dallas TX
|