I started the Butrans Patch 4 days ago (10mg) patch and suffer from back issues as well as fibromyalgia and raynards - which effect your extremities. Today, I have notice a drastic improvement with my extremities, my hands, feet and calves do feel a bit better. It's noticeable, however, I am not so sure that my back is feeling better at all, as a matter of fact, I know it is hurting much worse. I think it from the stimulator that the Dr gave me. It is supposed to send off electronic pulses to interrupt pain signals, which it feels "ok" when I use it but with out it, dear gosh. I can't wear it forever, afterawhile it starts to hurt me.
I have been on Lortab for 3 years now and hate it, hate it hate it. First, it's not effective, secondly I hate to take pills all day long, I can't tell I'm taking it anymore but when I try to stop taking it I get very jittery and I know it's a form of withdrawl. I really had high hopes for this medication. I have only been on 10 mg and put it on Wed afternoon - it's now Sat. Should I call my Dr and request a higher dose? My biggest fear is that someone won't take me seriously. I have my MRI report stating the degenerative disk disease in L4-L5 and am set up for a nerve block appointment, but like the last post said, thanks to 'junkies' I feel like I am scared my Dr will think I am just trying to get more pain medicine since it has been only 4 days. I just keep thinking that, if it takes 3 days to get in to your system, I am looking at another few days of pain.
FYI, as you can see - I am sensitive to what others think of me, I got it from overly aggressive parents....
Can anyone give me any advice? I like the way this doesn't sedate me though, again, it is so much better than traditional meds like loratab. I have other spinal issues except the degenertive disk disease but I don't have the MRI infront of me so I am not sure how to pronouce it. Please advise.
PS.... I don't have spell check and know I'm a bad speller.