Guest guest Posted August 31, 2006 Report Share Posted August 31, 2006 Lee Ann, If at your next appointment in two months this rheumatologist does not put you on a DMARD, you need to find another rheumy. A DMARD such as plaquenil or methotrexate can stop the progression of RA, while prednisone and Celebrex cannot. You are right to be cautious about prednisone. It can make you feel wonderful, but it has so many adverse side effects. Sometimes prednisone is prescribed to hold you over until a DMARD takes effect, but he didn't even prescribe a DMARD, so I don't know what he has in mind. Keep us posted. Sue On Thursday, August 31, 2006, at 10:50 AM, Leeann King wrote: > > I had my first visit to the rheumatologist. He examined me and went > over my > history and felt fairly certain that I have seronegative RA. He put > me on > prednisone 5mg a day and Celebrex to begin with. I got a steroid > injection > and had blood work and x-rays and was sent on my way with another appt > in > 2months. I'm not excited about steroid therapy. He wasn't much of a > talker. This morning I felt much better than I've felt in months. > BUT....the steroid side affects scare me. I'd love some feedback from > you > guys because I know you all have been through everything. Thanks a > bunch, Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 4, 2007 Report Share Posted January 4, 2007 I have my first appointment with a rheumatologist on the 17th and I am so nervous. Can anyone suggest what questions would be good to ask and what I should expect from the visit? My husband seems to think that I'll walk out with a prescription and feel better the next day, but I don't want to hope for anything even remotely close to that. I do not have any extreme swelling of joints or deformities so part of me is very much afraid of being told there is nothing wrong with me. And sometimes the pain goes away for a few days, and if I'm not in a lot of pain I might not be taken seriously. I will also need to get my rheumatologist in contact with my endocrinologist. A lot of people are telling me that I am too young to have arthritis (I'm 20), so that is very discouraging. I am currently battling hypothyroidism, hypoglycemia, Mitral Valve Prolapse, Raynaud's Phenomenon (not threatening but very uncomfortable), and now Rheumatoid Arthritis. Sometimes the fatigue is so severe I feel like a ton of bricks is sitting in my lap and I can hardly move. This makes work VERY difficult despite having a desk job. My finger joints aren't always happy with me either due to all the typing I do. Sorry, I need to seriously vent. My husband's response is that other people have to deal with it too, so I should just suck it up and get over it. He has his sensative moments but I think it's too much for him to deal with so he just blocks it all out. Everyone's posts are very helpful, so thanks to you all! Any suggestions for my first rheumatologist visit would be greatly appreciated. Also, any pep-talks or some sort of encouragement. We had a miscarriage scare earlier this week, but it turns out I wasn't pregnant to begin with so that's good. Thanks to all for listening! Lyndsay S. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 4, 2007 Report Share Posted January 4, 2007 Can your husband go to your rheumy appt with you? I found this very helpful, both in that he understands better, and he's very good at taking notes and remembering things. I have enough trouble remembering what I have to ask (i make a list, and just hand to my rheumy), and it's really hard to take notes while you're being poked and prodded. But, if you're like me, and hubby can't go, take a notebook and pen, and just insist that you have to take time to write everything down right away. It took a while, but my hubby finally understands that I can't just " suck it up " . Now he watches for signs that I'm overdoing it, and sometimes infuriates me when he makes me stop and rest! Since I have Polymialga Rheumatica, not RA, I can't say exactly what your rheumy will be looking for. Give him a complete history, including all the meds you take. If he's like my rheumy, it will be important to him to find out what else you're being treated for, there's a lot of overlap often. My sister has both RA and Reynauds, a lot of people have both. Not as familiar with the others. He'll surely want to do some blood work, maybe some images. Depending on what he sees, he may start you on medication right away, or wait for the test results. Even if you do walk out with a prescription, it can take weeks before finding the right combo of meds and for them to be really effective. Hopefully your rheumy will take the time to talk to you, and explain RA and the various treatment possibilities. What do you want to know? Make a list, and ask. Like the fact that RA is no respecter of age, lots of RA patients are young women! Just check out many of the posters here. I happen to be in my 50s, but my daughter who is 22 has had psoriasis, another auto immune disorder, since she was about 14. Good luck, and let us know what happens! On 1/4/07, Mrs. Castro <chocolatewookie@...> wrote: > > I have my first appointment with a rheumatologist on the 17th and I > am so nervous. Can anyone suggest what questions would be good to ask > and what I should expect from the visit? My husband seems to think > that I'll walk out with a prescription and feel better the next day, > but I don't want to hope for anything even remotely close to that. I > do not have any extreme swelling of joints or deformities so part of > me is very much afraid of being told there is nothing wrong with me. > And sometimes the pain goes away for a few days, and if I'm not in a > lot of pain I might not be taken seriously. I will also need to get > my rheumatologist in contact with my endocrinologist. A lot of people > are telling me that I am too young to have arthritis (I'm 20), so > that is very discouraging. I am currently battling hypothyroidism, > hypoglycemia, Mitral Valve Prolapse, Raynaud's Phenomenon (not > threatening but very uncomfortable), and now Rheumatoid Arthritis. > Sometimes the fatigue is so severe I feel like a ton of bricks is > sitting in my lap and I can hardly move. This makes work VERY > difficult despite having a desk job. My finger joints aren't always > happy with me either due to all the typing I do. Sorry, I need to > seriously vent. My husband's response is that other people have to > deal with it too, so I should just suck it up and get over it. He has > his sensative moments but I think it's too much for him to deal with > so he just blocks it all out. Everyone's posts are very helpful, so > thanks to you all! Any suggestions for my first rheumatologist visit > would be greatly appreciated. Also, any pep-talks or some sort of > encouragement. We had a miscarriage scare earlier this week, but it > turns out I wasn't pregnant to begin with so that's good. > > Thanks to all for listening! > Lyndsay S. > > > -- Shoreview, MN, until April! brrrr! South Pasadena, CA You can see my galleries at http://www.pbase.com/arenared986 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 4, 2007 Report Share Posted January 4, 2007 Lyndsay I would just go in with a list of your meds and your complaints or symptoms to your doc and see what he or she wants to try first. Sometimes if they start you on meds you will have to get your blood checked every 4-6 weeks and they will probably tell you that some meds will take awhile to start working. They will probably take blood and maybe some other tests and xrays to begin with. Feel free to vent anytime that is why we all joined a group like this. Sometimes it is hard for some of us to talk to our loved ones if they don't understand so we are here to help each other out. Joy " Mrs. Castro " <chocolatewookie@...> wrote: I have my first appointment with a rheumatologist on the 17th and I am so nervous. Can anyone suggest what questions would be good to ask and what I should expect from the visit? My husband seems to think that I'll walk out with a prescription and feel better the next day, but I don't want to hope for anything even remotely close to that. I do not have any extreme swelling of joints or deformities so part of me is very much afraid of being told there is nothing wrong with me. And sometimes the pain goes away for a few days, and if I'm not in a lot of pain I might not be taken seriously. I will also need to get my rheumatologist in contact with my endocrinologist. A lot of people are telling me that I am too young to have arthritis (I'm 20), so that is very discouraging. I am currently battling hypothyroidism, hypoglycemia, Mitral Valve Prolapse, Raynaud's Phenomenon (not threatening but very uncomfortable), and now Rheumatoid Arthritis. Sometimes the fatigue is so severe I feel like a ton of bricks is sitting in my lap and I can hardly move. This makes work VERY difficult despite having a desk job. My finger joints aren't always happy with me either due to all the typing I do. Sorry, I need to seriously vent. My husband's response is that other people have to deal with it too, so I should just suck it up and get over it. He has his sensative moments but I think it's too much for him to deal with so he just blocks it all out. Everyone's posts are very helpful, so thanks to you all! Any suggestions for my first rheumatologist visit would be greatly appreciated. Also, any pep-talks or some sort of encouragement. We had a miscarriage scare earlier this week, but it turns out I wasn't pregnant to begin with so that's good. Thanks to all for listening! Lyndsay S. Joy ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Visit Joy's Homepage and Reading Room! http://jhoormann-ivil.tripod.com Come see My Dog Salsa! http://www.geocities.com/jhoorm01/Salsa.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 18, 2008 Report Share Posted October 18, 2008 Leanne, I am thanful that you got a correct diagnosis. I hope you are feeling much better soon with no other problems added. Shirley > > Hi all! > > I went to a rheumy yesterday for the first time. He told me a few > things, including the fact that my diagnosis of Polymyalgia a year ago > was incorrect, that it really is RA. He ordered one more test to > confirm, a brand new blood test. I can't remember what he called it. > > I had to give several vials of blood, and had 15 xrays taken. I think > I should be glowing! > > He wants me to return next month to discuss everything. I am > currently on prednisone and plaquenil, and he's talking about starting > Methotrexate. I'm scared spitless. He also recommended taking two > Tylenol Arthritis every 8 hours. > > Because I have diabetes and kidney disease, I always worry about what > all these medications are doing to me. > > Anyone have any advice? Do you belong to support groups, and if so, > do they help? > > Thanks! > > Lost Leanne > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 19, 2008 Report Share Posted October 19, 2008 LeAnne and group- I have belonged to this and one other arthritis groups I consider them both support groups they have both been helpful. I also have diabetes and have had problems with My kidneys at times. Just recently I outlined My whole history for the group I am not sure how to look it up but I am sure can tell you. I know when I got them If you can't find them I will e-mail to you outside group because they were 2 long letters. I have type 2 diab etes and have been on Methoxrexate and am now on Enbrel. It's worth taking and the Doctors keep pretty good eye on you,. you need to get the flares under control. so you don't ended up as bad as or worse then some of us. If you run into problems scream for help! PatS. from Twincities ----- Forwarded Message ---- From: nana2livi <s.p5315@...> Sent: Saturday, October 18, 2008 10:07:17 PM Subject: [ ] Re: First visit to rheumy Leanne, I am thanful that you got a correct diagnosis. I hope you are feeling much better soon with no other problems added. Shirley > > Hi all! > > I went to a rheumy yesterday for the first time. He told me a few > things, including the fact that my diagnosis of Polymyalgia a year ago > was incorrect, that it really is RA. He ordered one more test to > confirm, a brand new blood test. I can't remember what he called it. > > I had to give several vials of blood, and had 15 xrays taken. I think > I should be glowing! > > He wants me to return next month to discuss everything. I am > currently on prednisone and plaquenil, and he's talking about starting > Methotrexate. I'm scared spitless. He also recommended taking two > Tylenol Arthritis every 8 hours. > > Because I have diabetes and kidney disease, I always worry about what > all these medications are doing to me. > > Anyone have any advice? Do you belong to support groups, and if so, > do they help? > > Thanks! > > Lost Leanne > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 19, 2008 Report Share Posted October 19, 2008 Leanne, You will have to have blood work done frequently to monitor any adverse effects that the medications are having on you. I have type 2 diabetes, but no kidney trouble, and no RA medications except prednisone have had any effect on the diabetes. Now prednisone can really do a number on BG's and has even been known to cause diabetes in some people. Sue On Saturday, October 18, 2008, at 08:36 PM, Leanne wrote: > > Because I have diabetes and kidney disease, I always worry about what > all these medications are doing to me. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 20, 2008 Report Share Posted October 20, 2008 Hi Pat and Group - I found out that if you copy the " User Name " located in the heading of a post - in this case pat_rose_city - and then paste it in the " Author " section of an " Advanced Search " , leaving all the other fields as is, and then click on " Search " , it will bring up all the posts by a particular member. Hope this helps.........Doreen LeAnne and group- I have belonged to this and one other arthritis groups I consider them both support groups they have both been helpful. I also have diabetes and have had problems with My kidneys at times. Just recently I outlined My whole history for the group I am not sure how to look it up but I am sure can tell you. I know when I got them If you can't find them I will e-mail to you outside group because they were 2 long letters. I have type 2 diab etes and have been on Methoxrexate and am now on Enbrel. It's worth taking and the Doctors keep pretty good eye on you,. you need to get the flares under control. so you don't ended up as bad as or worse then some of us. If you run into problems scream for help! PatS. from Twincities Quote Link to comment Share on other sites More sharing options...
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