Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Tracie: I suffered in pain for weeks waiting for my Rheumy appointment. I was shocked when my Rheumy told me she didn't prescribe triplicate (narcotic) medications. I had to make another appointment to see my GP, and wait to get into see him at a later date. After that huge run- around, I was finally prescribed the pain patch. I too have trouble with my stomach, so am limited as to what I can take for oral medications. I found that the patch did provide relief and I had the weakest dose. It didn't cover all the pain, but it was way better than any other pain killer I'd tried previously. I find that when I am in the middle of a flare, I can become so fatigued because of the non-stop pain my body is in. Try your best to get a pain prescription that works for you ASAP. You need your rest to stay healthy and get through this latest flare. Take care, > As you know I am trying to get started on the Humira, but came down > with bronchitis so had to hold off on that. I am on the MTX and > Prednisone right now, but still have awful pain. I have been on > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > for about six weeks and my PCP is all paranoid about the narcotic > thing and I am very, very careful with it. She wants to switch me to > Mobic, but I have horrible stomach problems and am already on Nexium > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > a lot of you are on chronic pain meds, but some doctors are sooooo > paranoid about it. Should I go to my rheumy about it? Should I ask > to see a Pain Management specialist until they get my RA stabilized? > I am housebound literally between the walking cast and the pain. I go > nowhere other than the doctors and am having a hard time getting > around. At this point, I don't care if I have to take the medicine > for the rest of my life if it means I can at least putter and sleep > somewhat pain free. Has anyone else run into this or am I some kind > of freak? You know you can email me and I will try to check for > responses, but please, I am begging you for advice here. Tracie in > Maine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Tracie: I suffered in pain for weeks waiting for my Rheumy appointment. I was shocked when my Rheumy told me she didn't prescribe triplicate (narcotic) medications. I had to make another appointment to see my GP, and wait to get into see him at a later date. After that huge run- around, I was finally prescribed the pain patch. I too have trouble with my stomach, so am limited as to what I can take for oral medications. I found that the patch did provide relief and I had the weakest dose. It didn't cover all the pain, but it was way better than any other pain killer I'd tried previously. I find that when I am in the middle of a flare, I can become so fatigued because of the non-stop pain my body is in. Try your best to get a pain prescription that works for you ASAP. You need your rest to stay healthy and get through this latest flare. Take care, > As you know I am trying to get started on the Humira, but came down > with bronchitis so had to hold off on that. I am on the MTX and > Prednisone right now, but still have awful pain. I have been on > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > for about six weeks and my PCP is all paranoid about the narcotic > thing and I am very, very careful with it. She wants to switch me to > Mobic, but I have horrible stomach problems and am already on Nexium > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > a lot of you are on chronic pain meds, but some doctors are sooooo > paranoid about it. Should I go to my rheumy about it? Should I ask > to see a Pain Management specialist until they get my RA stabilized? > I am housebound literally between the walking cast and the pain. I go > nowhere other than the doctors and am having a hard time getting > around. At this point, I don't care if I have to take the medicine > for the rest of my life if it means I can at least putter and sleep > somewhat pain free. Has anyone else run into this or am I some kind > of freak? You know you can email me and I will try to check for > responses, but please, I am begging you for advice here. Tracie in > Maine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Tracie, You're not the only one with problems getting pain meds. My old rheumy wouldn't prescribe narcotics. I went to 3 different ones, and none would treat my pain. Then I moved to another state, and the first rheumy I went to wouldn't prescribe narcotics. He wanted me to go to a pain management clinic. I went to another rheumy instead, and this one has no problem prescribing narcotic pain meds. Untreated pain has health consequences, so please try to find a doctor that will help you. I hope you find one and get some relief. a On Jun 2, 2005, at 11:36 AM, tracierae143 wrote: > As you know I am trying to get started on the Humira, but came down > with bronchitis so had to hold off on that. I am on the MTX and > Prednisone right now, but still have awful pain. I have been on > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > for about six weeks and my PCP is all paranoid about the narcotic > thing and I am very, very careful with it. She wants to switch me to > Mobic, but I have horrible stomach problems and am already on Nexium > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > a lot of you are on chronic pain meds, but some doctors are sooooo > paranoid about it. Should I go to my rheumy about it? Should I ask > to see a Pain Management specialist until they get my RA stabilized? > I am housebound literally between the walking cast and the pain. I go > nowhere other than the doctors and am having a hard time getting > around. At this point, I don't care if I have to take the medicine > for the rest of my life if it means I can at least putter and sleep > somewhat pain free. Has anyone else run into this or am I some kind > of freak? You know you can email me and I will try to check for > responses, but please, I am begging you for advice here. Tracie in > Maine > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Tracie, You're not the only one with problems getting pain meds. My old rheumy wouldn't prescribe narcotics. I went to 3 different ones, and none would treat my pain. Then I moved to another state, and the first rheumy I went to wouldn't prescribe narcotics. He wanted me to go to a pain management clinic. I went to another rheumy instead, and this one has no problem prescribing narcotic pain meds. Untreated pain has health consequences, so please try to find a doctor that will help you. I hope you find one and get some relief. a On Jun 2, 2005, at 11:36 AM, tracierae143 wrote: > As you know I am trying to get started on the Humira, but came down > with bronchitis so had to hold off on that. I am on the MTX and > Prednisone right now, but still have awful pain. I have been on > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > for about six weeks and my PCP is all paranoid about the narcotic > thing and I am very, very careful with it. She wants to switch me to > Mobic, but I have horrible stomach problems and am already on Nexium > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > a lot of you are on chronic pain meds, but some doctors are sooooo > paranoid about it. Should I go to my rheumy about it? Should I ask > to see a Pain Management specialist until they get my RA stabilized? > I am housebound literally between the walking cast and the pain. I go > nowhere other than the doctors and am having a hard time getting > around. At this point, I don't care if I have to take the medicine > for the rest of my life if it means I can at least putter and sleep > somewhat pain free. Has anyone else run into this or am I some kind > of freak? You know you can email me and I will try to check for > responses, but please, I am begging you for advice here. Tracie in > Maine > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 a, Thank you for your support. I was feeling so alone, but I see now that this is a major problem for RA patients. It is totally ridiculous and makes me angry when I stop and think about it. If the doctors were in our shoes, I think they would think a whole lot differently about it. I will persist with my rheumy and switch if I have to. I just won't take no for an answer. I don't want to get high or anything, I just want to be able to function. I am not even asking to be completely pain free, but I need to move around a little. It is not good for me to be this immobile either. Thanks again to you and everyone who emailed me. Tracie > > > As you know I am trying to get started on the Humira, but came down > > with bronchitis so had to hold off on that. I am on the MTX and > > Prednisone right now, but still have awful pain. I have been on > > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > > for about six weeks and my PCP is all paranoid about the narcotic > > thing and I am very, very careful with it. She wants to switch me to > > Mobic, but I have horrible stomach problems and am already on Nexium > > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > > a lot of you are on chronic pain meds, but some doctors are sooooo > > paranoid about it. Should I go to my rheumy about it? Should I ask > > to see a Pain Management specialist until they get my RA stabilized? > > I am housebound literally between the walking cast and the pain. I go > > nowhere other than the doctors and am having a hard time getting > > around. At this point, I don't care if I have to take the medicine > > for the rest of my life if it means I can at least putter and sleep > > somewhat pain free. Has anyone else run into this or am I some kind > > of freak? You know you can email me and I will try to check for > > responses, but please, I am begging you for advice here. Tracie in > > Maine > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 a, Thank you for your support. I was feeling so alone, but I see now that this is a major problem for RA patients. It is totally ridiculous and makes me angry when I stop and think about it. If the doctors were in our shoes, I think they would think a whole lot differently about it. I will persist with my rheumy and switch if I have to. I just won't take no for an answer. I don't want to get high or anything, I just want to be able to function. I am not even asking to be completely pain free, but I need to move around a little. It is not good for me to be this immobile either. Thanks again to you and everyone who emailed me. Tracie > > > As you know I am trying to get started on the Humira, but came down > > with bronchitis so had to hold off on that. I am on the MTX and > > Prednisone right now, but still have awful pain. I have been on > > Vicoprofen (which is like Vicodin except ibuprofen instead of Tylenol) > > for about six weeks and my PCP is all paranoid about the narcotic > > thing and I am very, very careful with it. She wants to switch me to > > Mobic, but I have horrible stomach problems and am already on Nexium > > 40 mg a day. I am allergic to sulfa so cannot take Celebrex. I know > > a lot of you are on chronic pain meds, but some doctors are sooooo > > paranoid about it. Should I go to my rheumy about it? Should I ask > > to see a Pain Management specialist until they get my RA stabilized? > > I am housebound literally between the walking cast and the pain. I go > > nowhere other than the doctors and am having a hard time getting > > around. At this point, I don't care if I have to take the medicine > > for the rest of my life if it means I can at least putter and sleep > > somewhat pain free. Has anyone else run into this or am I some kind > > of freak? You know you can email me and I will try to check for > > responses, but please, I am begging you for advice here. Tracie in > > Maine > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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