Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 Hi Kathe, I'm new to this group and have been reading through the posts. After reading your letter I know exactly what you meant. I was diagnosed 2 years by my regular doctor who treated me with Celebrex. That worked up until a year ago November. Since then the joint pain and fatigue haven't gotten any better. I have now started seeing a specialist but of course he wants to check everything out before he changes any of the meds. Right now I'm on Methotraxate (6 pills a week) and the folic acid. I was on Effexor XR for a little while but, gained about 12 pounds and couldn't stand the weight gain. It did help dealing with the RA but I was beginning to think the weight gain was causing the pain to get worse. So now, I'm not taking anything like that. As far as this totally taking control of your live, I know that has mine. Even though I ty to keep doing the things I use to, I just can't. I use to love to do counted cross stitch pictures and haven't been able to do them for almost a year. Even when I'm feeling good, I keep thinking that by doing things like that, it's going to flare it up again. I was also the one around here who did all the decorating and fixing of things and gardening. I love doing all those things and it's the hardest thing to realize that I can't do things when I want to any more. They have to be done when I'm feeling up to it. I'm 46 and have two children. A daughter who just turned 22 and just opened her business in November and a son who is 19. I think it's even harder for them to understand this, because they are so use to " mom " being there and doing the things that needed to be done. My daughter had ideas that I would be there to help her whenever she needed me, which I would love to do but can't. She opened a copy center and some of the jobs require folding or stapling and I can't do it. Getting the store together required a lot of work and I did what I had to even with the pain because I wanted to do it for her. In my family, they see me doing certain things and assume that there's really nothing wrong with me. Even something as simple as letting the dog out, just having to get up and walk to the kitchen is sometimes the hardest thing I have to do, but they just ignore her and it's easier for me to get up and do it then to keep calling them. My husband is the same way. I just can't make them understand that I didn't ask for this and I hate having to depend on other people to do things for me. Now I'm waiting to go back to the specialist in 6 weeks and see what he's going to say. He put me on Prednisone 5mg daily until I see him and that's it. It hasn't made much difference at all. I can't believe how bad it's been for the last month and I know it could get a lot worse. I just keep telling the doctors that I know they can't make it go away but just make me feel like I did a year ago. Thanks so much for your letter it does make it a little easier to handle. Take Care in IL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2004 Report Share Posted February 3, 2004 i know how you feel i use to lift weights to keep in shape and now i can't. i have to ask my wife to open bottles for me. you just don't know how embarrasing that is. and when i try to do some stuff around the house like fix something i usally get mad . and then she thinks i'm mad at her. and i tell her i'm not mad at her i'm mad at myself because it's hard to do it... when you go from bench pressing 200 lbs. to can't even open a bottle that's VERY UPSETTING TO ME. thanks for hearing me out . i know i'm not the only one who has this problem. mike elmo826@... wrote:Hi Kathe, I'm new to this group and have been reading through the posts. After reading your letter I know exactly what you meant. I was diagnosed 2 years by my regular doctor who treated me with Celebrex. That worked up until a year ago November. Since then the joint pain and fatigue haven't gotten any better. I have now started seeing a specialist but of course he wants to check everything out before he changes any of the meds. Right now I'm on Methotraxate (6 pills a week) and the folic acid. I was on Effexor XR for a little while but, gained about 12 pounds and couldn't stand the weight gain. It did help dealing with the RA but I was beginning to think the weight gain was causing the pain to get worse. So now, I'm not taking anything like that. As far as this totally taking control of your live, I know that has mine. Even though I ty to keep doing the things I use to, I just can't. I use to love to do counted cross stitch pictures and haven't been able to do them for almost a year. Even when I'm feeling good, I keep thinking that by doing things like that, it's going to flare it up again. I was also the one around here who did all the decorating and fixing of things and gardening. I love doing all those things and it's the hardest thing to realize that I can't do things when I want to any more. They have to be done when I'm feeling up to it. I'm 46 and have two children. A daughter who just turned 22 and just opened her business in November and a son who is 19. I think it's even harder for them to understand this, because they are so use to " mom " being there and doing the things that needed to be done. My daughter had ideas that I would be there to help her whenever she needed me, which I would love to do but can't. She opened a copy center and some of the jobs require folding or stapling and I can't do it. Getting the store together required a lot of work and I did what I had to even with the pain because I wanted to do it for her. In my family, they see me doing certain things and assume that there's really nothing wrong with me. Even something as simple as letting the dog out, just having to get up and walk to the kitchen is sometimes the hardest thing I have to do, but they just ignore her and it's easier for me to get up and do it then to keep calling them. My husband is the same way. I just can't make them understand that I didn't ask for this and I hate having to depend on other people to do things for me. Now I'm waiting to go back to the specialist in 6 weeks and see what he's going to say. He put me on Prednisone 5mg daily until I see him and that's it. It hasn't made much difference at all. I can't believe how bad it's been for the last month and I know it could get a lot worse. I just keep telling the doctors that I know they can't make it go away but just make me feel like I did a year ago. Thanks so much for your letter it does make it a little easier to handle. Take Care in IL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2004 Report Share Posted February 3, 2004 no mike i am the same way im so glad ive got friends here who know what im dealing with god bless you all hugs from kansas cindy r Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2004 Report Share Posted February 4, 2004 you all have a friend in me. if thee is anything i can help anybody with i'd be glad to help. you guys have helped me alot too. love you all.........mike sweetcindy56@... wrote:no mike i am the same way im so glad ive got friends here who know what im dealing with god bless you all hugs from kansas cindy r Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.