Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 She might be referreing to taking the pressure off the nerve. I have a nerve entrapment in my elbow, and sometimes it makes my wrist hurt, so I wrap it in an ace bandage, to take the pressure off the nerve, and it helps. Don't you hate when doctors don't explain things! I have had doctors like that - hate it! My doctor explains things, but I can't understand him because of his heavy accent. I have to go back to my PCP, and get him to interpret the notes and explain it to me, and since he is not a Rhematologist, sometimes he doesn't get it. Being in the dark sucks. Try getting a copy of your dr's notes. Call the nurse and have it faxed. Hopefully you can read the handwritting. I always get a copy of the notes. Helps a little, when I can read them (my old rheumy dictated them, and the staff typed them out - that was awesome!). Maybe yours does too. Hope you get help with this. - > > Hi everyone! > Today I made the long roundtrip of 6.5 hours in the car to see the rheumatologist in the high heat and humidity. My visit wasn't as long or as thorough as most. She checked my knees just from the chair I was sitting in. I've a new problem for over the past week. My elbow is extremely sore with sharp radiating pain, near the bone, if I touch it the bone hurts. She checked my arm all the way down and whenever she asked if it hurt where she touched, it did. She said she could give me a cortisone shot if it prevails or even today could have given me one. She suggested I get a brace for the forearm to take the pressure off of it. She thought this might help. I'm not sure what is wrong as it wasn't explained to me? Take the pressure off of what exactly? Has anyone had any experience with this? > > She stopped my plaquenil last visit and now said that at the next visit if I am doing ok we will be reducing my Sulfasalazine. I used to take 1500mgs a day, but had a bad flare and was upped to the maximum dose of 3000mgs. Does this sound normal? I'm so frustrated with not ever knowing what is wrong, and all of the labs being ok except for the SED and CRP and WESTEGREN. Today she did a urinalysis although I have no idea why, also ordered my normal CBC with differentials to monitor the sulfasalazine and also did a metabolic panel. > > Thank you all for any advice! Hope you all are hanging in there:) > Gentle Hugs to you all > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2008 Report Share Posted July 29, 2008 Hi ! I know I sooo hate when they don't explain things! She did ask me if I have any numbness going down the arm so I wonder if she was checking for a nerve too. I told her that the actual bone hurts. That their is radiating pain like when my knees are inflammed with the inflammatory arthritis. I thought it was going to get blamed on the Fibromyalgia because there is a trigger point near there, but it wasn't that which was a good thing...U of M always types my notes on a computer and sends them to my PCP. I think I am going to fill out a form to get my records from a little over the past year. They are talking about decreasing my Sulfasalazine and that is the only dmard I am on! So I am hoping that means taking me down to the minimum dose (that is if I stay doing ok) on 1500 mgs instead of the maximum 3000mgs. She did offer to give a steroid or cortisone shot in the elbow..I'm thinking today I probably should have gotten it then:) From: laurenrosepeters <laurenrosepeters@...> Subject: [ ] Re: Elbow Pain-Help Date: Tuesday, July 29, 2008, 2:22 PM She might be referreing to taking the pressure off the nerve. I have a nerve entrapment in my elbow, and sometimes it makes my wrist hurt, so I wrap it in an ace bandage, to take the pressure off the nerve, and it helps. Don't you hate when doctors don't explain things! I have had doctors like that - hate it! My doctor explains things, but I can't understand him because of his heavy accent. I have to go back to my PCP, and get him to interpret the notes and explain it to me, and since he is not a Rhematologist, sometimes he doesn't get it. Being in the dark sucks. Try getting a copy of your dr's notes. Call the nurse and have it faxed. Hopefully you can read the handwritting. I always get a copy of the notes. Helps a little, when I can read them (my old rheumy dictated them, and the staff typed them out - that was awesome!). Maybe yours does too. Hope you get help with this. - > > Hi everyone! > Today I made the long roundtrip of 6.5 hours in the car to see the rheumatologist in the high heat and humidity. My visit wasn't as long or as thorough as most. She checked my knees just from the chair I was sitting in. I've a new problem for over the past week. My elbow is extremely sore with sharp radiating pain, near the bone, if I touch it the bone hurts. She checked my arm all the way down and whenever she asked if it hurt where she touched, it did. She said she could give me a cortisone shot if it prevails or even today could have given me one. She suggested I get a brace for the forearm to take the pressure off of it. She thought this might help. I'm not sure what is wrong as it wasn't explained to me? Take the pressure off of what exactly? Has anyone had any experience with this? > > She stopped my plaquenil last visit and now said that at the next visit if I am doing ok we will be reducing my Sulfasalazine. I used to take 1500mgs a day, but had a bad flare and was upped to the maximum dose of 3000mgs. Does this sound normal? I'm so frustrated with not ever knowing what is wrong, and all of the labs being ok except for the SED and CRP and WESTEGREN. Today she did a urinalysis although I have no idea why, also ordered my normal CBC with differentials to monitor the sulfasalazine and also did a metabolic panel. > > Thank you all for any advice! Hope you all are hanging in there:) > Gentle Hugs to you all > > > > > Quote Link to comment Share on other sites More sharing options...
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