Humira it is . . . .

Earlier this week I FINALLY saw my GI, even though it was only for 5 minutes. .The PA and my GI both agreed that the next step of my treatment is Humira.  Since I’ve been bleeding for the past month and the low dosage of prednisone has had no effect, and Apriso has never worked (I believe), they believe Humira is the next best thing.  My application has been submitted and I assume I just wait to hear from my GI office to pick it up or it’s being shipped to me? Of course I’m confused as always. I’ll send an email to followup.

In the meantime I was given a practice pen and a pamphlet to read, still haven’t read it just tossed it to the side. . . I really should care, but I’m not excited.  To be honest, I rather take pills any day over an injection. It’s like my condition is at a new level when pills are no longer working, its scary.   The PA highly suggested that I come in for my first injection but of course her earliest time is 8:30am, I need to be at work by 8:30 . . . so I said that’s not going to work.  I can’t take time off right now. I’ve been at this new job for 6 weeks and they know nothing about my illness. I would like to keep it that way for as long as I can.   Also, I don’t believe its smart to get an injection of a new drug and go straight to work, I might have bad side effects. I’ll just have to be a big girl and do it myself, I think I’ll be fine. Also, I have been playing phone tag with my Humira Ambassador. I plan to take time to actually speak with her, but its difficult to have any private conversations at this new job . . I’ll have to figure it out.

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