Guest guest Posted October 26, 2005 Report Share Posted October 26, 2005 Kathe, Thank you for your kind words. I am hopeful with the prednisone even though I really do not want to take it. I will be seeing my new pcp on the 17th and getting the referral for the new rheumy. I have heard good things about him but no matter- he is the last one in the book. I just want someone to help me. Just because I " dont fit the profile " and it is a bit hard to figure out stuff for me doesnt mean I dont deserve help. I have lost all confidence in doctors at this point. I am almost 34 years old and life looks so bleak. I really do try to be positive and hopeful but at times it is so hard. Today I was diagnosed with plurisy. This is my 4th bout with it over the last 3 1/2 years. again I am just disgusted. Hope you are feeling well. Thanks again Sandie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2005 Report Share Posted October 26, 2005 Kathe, Thank you for your kind words. I am hopeful with the prednisone even though I really do not want to take it. I will be seeing my new pcp on the 17th and getting the referral for the new rheumy. I have heard good things about him but no matter- he is the last one in the book. I just want someone to help me. Just because I " dont fit the profile " and it is a bit hard to figure out stuff for me doesnt mean I dont deserve help. I have lost all confidence in doctors at this point. I am almost 34 years old and life looks so bleak. I really do try to be positive and hopeful but at times it is so hard. Today I was diagnosed with plurisy. This is my 4th bout with it over the last 3 1/2 years. again I am just disgusted. Hope you are feeling well. Thanks again Sandie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2005 Report Share Posted October 26, 2005 Hi Sandie: Well, that seems a bit extreme to stop all medications cold turkey, but at least he is giving you Prednisone. I have been in a severe flare for about a week now and finally cried uncle, called my rheumy, and asked for Prednisone for a couple of weeks until the Enbrel kicks in. I started taking it 10 mg. a day yesterday and can already feel a difference. There is still pain, but a bit less, and I am hopefull that each day that goes by will give me more relief. That stuff is remarkable in that it works so fast for me, but it does make me a bit wacky lol. I'm glad that you will be going to a new rheumy, hopefully it won't take you too long to get in and he will be better than the jerk you have now. " Don't let it ruin your night " ?? They just don't get it do they? Well, we do! Hope that you have better days soon - Kathe in CA --- slmcc93@... wrote: > Well, Today I went back to my rheumy. I told him the > MTX doesn't seem to be > working anymore as I have more pain in my hands and > feet and basically all > over. I told him when the pain hits my toes and > fingers it is hot and throbbing > and actually hits with such intensity that it turns > my stomach. What did he say > - nothing. He then told me to forget going to the > oncologist and took me off > all my meds. No more plaquenil, mtx and folic acid. > He said we " will do an > experiment with prednisone. " I will be taking the > prednisone for 3 weeks 20 mg a > day for two weeks and then tapering off slowly. if > that works to help me with > the pain he will put me on a mtx typ drug again. if > that doesnt work he is > done with me. He said i " fall in the gray zone. my > blood work doesnt show the RA > per say so there is nothing else he can do for me. " > He suggested a pain > management doc or my pcp to prescribe pain meds for > me but that is it. He does say I > have psoriatic arthritis. > I am completely disgusted. I am in constant pain- > and he doesnt seem to care. > My worry is that I DO have RA and if left untreated > I will have a host of > problems later in life and he of course will be long > gone. as far as I am > concerned I am done with this doctor(and i use that > term loosely) I will however take > the prednisone for the next 3 weeks and see him but > that is it. I have his > appointment on the 15th and my new pcp on the 17th. > Things coundt have worked > out better there. so I will then take my records and > get a referral for the last > rheumy in my insurance plan. Help everyone has > anyone had this type of thing > happen to them and if yes what have you done? any > and all advice is greatly > appreciated. I am at the end of my rope at 34years > old. I cant take it anymore. > i jsut want to not have pain. The only good thing > this guy did was give me a > script for the lortab and 2 refills. but ven there I > am just tired of the pain > meds as they dont even give much relief. > sorry to complain so much i am just so tired. then > dear hubby said " you > shouldnt let it ruin your night " UGH!!!!!!! I will > not even get into that! > > hugs to all > sandie > > > [Non-text portions of this message have been > removed] > > Kathe in CA __________________________________ FareChase: Search multiple travel sites in one click. http://farechase. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 26, 2005 Report Share Posted October 26, 2005 Hi Sandie: Well, that seems a bit extreme to stop all medications cold turkey, but at least he is giving you Prednisone. I have been in a severe flare for about a week now and finally cried uncle, called my rheumy, and asked for Prednisone for a couple of weeks until the Enbrel kicks in. I started taking it 10 mg. a day yesterday and can already feel a difference. There is still pain, but a bit less, and I am hopefull that each day that goes by will give me more relief. That stuff is remarkable in that it works so fast for me, but it does make me a bit wacky lol. I'm glad that you will be going to a new rheumy, hopefully it won't take you too long to get in and he will be better than the jerk you have now. " Don't let it ruin your night " ?? They just don't get it do they? Well, we do! Hope that you have better days soon - Kathe in CA --- slmcc93@... wrote: > Well, Today I went back to my rheumy. I told him the > MTX doesn't seem to be > working anymore as I have more pain in my hands and > feet and basically all > over. I told him when the pain hits my toes and > fingers it is hot and throbbing > and actually hits with such intensity that it turns > my stomach. What did he say > - nothing. He then told me to forget going to the > oncologist and took me off > all my meds. No more plaquenil, mtx and folic acid. > He said we " will do an > experiment with prednisone. " I will be taking the > prednisone for 3 weeks 20 mg a > day for two weeks and then tapering off slowly. if > that works to help me with > the pain he will put me on a mtx typ drug again. if > that doesnt work he is > done with me. He said i " fall in the gray zone. my > blood work doesnt show the RA > per say so there is nothing else he can do for me. " > He suggested a pain > management doc or my pcp to prescribe pain meds for > me but that is it. He does say I > have psoriatic arthritis. > I am completely disgusted. I am in constant pain- > and he doesnt seem to care. > My worry is that I DO have RA and if left untreated > I will have a host of > problems later in life and he of course will be long > gone. as far as I am > concerned I am done with this doctor(and i use that > term loosely) I will however take > the prednisone for the next 3 weeks and see him but > that is it. I have his > appointment on the 15th and my new pcp on the 17th. > Things coundt have worked > out better there. so I will then take my records and > get a referral for the last > rheumy in my insurance plan. Help everyone has > anyone had this type of thing > happen to them and if yes what have you done? any > and all advice is greatly > appreciated. I am at the end of my rope at 34years > old. I cant take it anymore. > i jsut want to not have pain. The only good thing > this guy did was give me a > script for the lortab and 2 refills. but ven there I > am just tired of the pain > meds as they dont even give much relief. > sorry to complain so much i am just so tired. then > dear hubby said " you > shouldnt let it ruin your night " UGH!!!!!!! I will > not even get into that! > > hugs to all > sandie > > > [Non-text portions of this message have been > removed] > > Kathe in CA __________________________________ FareChase: Search multiple travel sites in one click. http://farechase. Quote Link to comment Share on other sites More sharing options...
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