New here..........OMG am I GLAD to find this site!! I've been looking for an RA forum where people actually POST once in a while. Last one I went to, the last post was in 2002. I have a question. Does anyone take the methatrexate injectible? If so - does it REALLY work better than the pills? I've been taking it in pill form for over 7 years... now my doctor seems to think that injecting it will work better. about me......... So - right now, I'm worse now than I ever have been. It seems I can literally FEEL my joints deteriorating...(if that's possible). EVERY single joint in my body hurts all the time........ morning stiffness lasts all day... every day. I have ZERO energy...and what really kills me is that even prednisone isn't helping. Usually, prednisone gives me atleast that nervous energy... nada now. and it's NOT helping the pain or inflammation at all. I'm sick of it - and it's nice to know there's a forum with PEOPLE on it that understand. I thought about starting my own message board, but I dont have the patience to figure it out. Are there any other message boards that are active like this for RA??? Thanks for listening to my rant. I plan to be sticking around for a while.... woobie
Woobie, Glad you came to this site. I came in April of last year, I think. We have lots of posts. I found this board and have stuck with with. I don't know if there are any more but I am sure there are. For the most part, we help and support each other. I haven't been online for a while, today is the first day in quite some time. I take the pills, 6 a week. I can't help you about the injections but I am sure someone will respond to you. I must be having a flare up, yesterday no energy, hip hurting and especially my hands and wrists. May I ask you, seeing as you have been on mtx, have you noticed any facial hair? I took pred. for 3 days, as directed. But when the dosage for mtx was increased, I have noticed the hair. I can't find any info on that. Stick around and you will learn and get support from all the others. Mailady LOL yes. I did notice that my mustache and whiskers grow a lot quicker. Dont know if it's all the prednisone, or the MTX.... but I never used to be a man before. I have to get waxed every week...
peace great place with lots of supportive people. I don't have experience with mtx injectable, but just wanted to say 'hi' and that I'm so sorry to hear you are feeling so bad. You will be in my thoughts and prayers today. Hang in there. The mtx injectable may be just what you need. And again, welcome!!!  Welcome Woobie. I'm glad you're here. We're very close in age....actually I'm a little older. 35; can't quite get use to saying that yet I was dx'ed with RA about 12 years ago. I take 25mg & Humira weekly. If your doctor hasn't considered weekly verses bi-weekly you might want to suggest it to him. Especially if you were getting good results from Humira at first. For me after about 6 months I wasn't making it the full 14 days...maybe a good 9 days then it sort of "Petered Out" does that make sense? Welcome again. Another site many of us are members at is www.rafriends.com Please ignore some of the recent behavior on here and references to this site I mentioned. I'd love for you to come over and judge for yourself. There seems to have been some really inappropreate behavior here the past few days; but it's honestly only between two people and I ask you please do not judge the groups as a whole. I personally am embarrashed by it and I know others feel the same way. Hope to hear more from you in the future. Lovie OH - and another question.... and this is personal - but it's been bothering me..... Husband and I have been together for over 18 years. He loves me and he helps me more than I deserve, I bet. Little things like putting on my socks, squeezing my toothpaste. I havent done dishes in a couple years.... but - well - SEX. It hurts me. He is gentle - and he feels horrible that it hurts me - so we never do it anymore. Sometimes.. ya just GOTTA. But then I pay for it - for a week. I'm 33 - My sex drive it increasing - and I cant DO anything about it. Is it over for me?? Am I DONE? Woobie I too, want to blame the drugs!!! Its the whiskers I see!!! I wax the other. Lovie is right, some posts haven't been nice, but please stay here. Lovie, thanks for the other site. I may go over there myself. Mailady Hi and welcome, Woobie.. Hmmm...as far as the sex question goes..for me I feel better after sex, so I'm not sure. I would suggest you ask your doctor, maybe there is something else that's going on. Do you mean your joints hurt after sex? Thanks guys - you sure are QUICK! Lovie - I registered over there - same name - woobie. but i have to go lay down... I'll look at it and post on it later. I spend 4 hours on here today, and i have to get up.........But - I will, for sure. Thanks. I think 2 places will be enough for now. I 'm just glad to find people. At my wits end, ya know? yes, you do... thanks .......... [QUOTE=kelstev] Hi and welcome, Woobie.. Hmmm...as far as the sex question goes..for me I feel better after sex, so I'm not sure. I would suggest you ask your doctor, maybe there is something else that's going on. Do you mean your joints hurt after sex? [/QUOTE] Oh I feel awesome after sex. Then my husband feels horrible. Then he wont touch me. Then I feel bad that he feels bad and we're laying around feeling bad. it's not good. woobie oh yea. he has no answers. his answers are increasing my meds and giving me pain pills that dont work. he says that nothing is going to get better until we get the RA "under control". wonder how long that takes - it's been years so far. woobie i have to go to bed now - been on here for more than 4 hours.. hee hee it's WAY passed my bedtime. Well that's not good at all. Trying not to get too personal here...but have you tried different positions? Plus, if it's intercourse that has been the cause of the sore joints, then maybe other things hee hee I'm sorry .......... I really believe that sex has to be a problem for a lot of us. I mean, maybe it's not talked about - but i cannot be the ONLY ONE. It's a very real problem for me....for my husband too... altho he wont complain... at least not to me. and i'm a very blunt person - so even tho it's my first day here, i am just gonna come out with it - --- I guess. I dont know how Loose this forum is....... so I'll behave today. I'm really going to bed now - promise. woobie
Welcome woobie. Hope you found a new home here...You'll love the folks on this board...Great people. Looking forward to reading your post. Have a wonderful weekend and make sure you do something special for yourself. Toni Welcome Woobie -
Ok Maybe you don't feel like partying but I do know how it feels to find relief in finding others that understand your frustration and pain. This board was truly a lifesaver for me when I was diagnosed last May. I was miserable like you sound for months until I got on Enbrel. I do not tolerate mtx so have to only take low doses. Never had injectable. Right now I am well but fingers crossed, knock on wood, prayers and chants that the Enbrel never stops working. I hope that some of the new biologics may be helpful to you. I did want to tell you that my doctor changed my pain med to Talwin. It is not codeine based and it has helped me more with the pain. You may want to try it. I am sorry you are so miserable - ra is a monster but hopefully positive changes will be coming soon. RA is so unpredictable. Keep in touch and let us know how you are doing. PS Sex is a good discussion.  I'm sick of pain but I'm tough so I get thru it. I've been lucky... I am only on plaquenil, vicodin as needed. I do have a terrible time sleeping not just because of pain I just wake up constantly.As I said once before Hormones cause it all!!! I hate hormones. I have been having alot of trouble with dry eye and mouth too. Anti depressants can effect your sex drive big time. I'm also on celexa. They have come out with a couple that don't effect it so much. Hope you feel better keep posting. Pat  Thank you for all the kind welcomes.... I like it here... I think I will stay! |
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can be done....I dunno...I'm sure you've tried everything you can think of
RA does change things. I had a great sex drive and it has not been so good lately. I am wondering if it is the antidepressants I am on. I do know that when we do have sex I ask myself - NOW WHY AM I NOT DOING THAT MORE OFTEN