I am also new to this forum. I had been surfing around trying to get info on Humira when I came across this
site. I had been reading the posts and found it to be informative.
I suffer from RA and have been having a pretty tough time of it lately. Sounds like everyone is in the same boat
here.
Here's hoping for better days ahead!
Spondylolithesis III
Alleycat - are you on any meds to help with the pain?
caprie - have you started on humira or is your rheumy thinking of putting you on it? There are a lot of people here that are on it...
I hope you two continue to post often... Best of luck to you and let us know how you are doing..
Duck
Diagnosed January 2005 - Psoriatic Arthritis/Spondylitis
Diagnosed May 1998 - Graves Disease
-Complete Thyroidectomy September 1998 - While 11 weeks pregnant
Other Complications - GERD/Scoliosis/Hiatal Hernia/Graves Disease of the Eyes
Welcome you two!
I'm sorry we have to meet on such 'painful' circumstances. I hope you can find some solace here with the people on HW. They are a great bunch!
Degenerative spinal arthritis
Hi Caprie,
Thanks so much for the welcome!
To Ducky- I should be starting the Humira as soon as approved by my insurance. Possibly by end of this week. I have to admit that I am not happy about going on it. I have reservations because it seems to me if you have to be that careful about getting an infection while on it, then it must be pretty harsh on your system as far as affecting your immunity which has already turned against you. I just worry that the meds can make you worse down the road even though they temporarily help. Doctor asked which one i wanted to take- Remicade, Enbrel, Humira. How do you choose? Didn't like the infusion choice so I asked why someone would pick the Enbrel (once a wk shot) over the Humira (every other week). He didn't really have an answer. I chose Humira. He said their all about the same, but I really believe everyone will react differently and it's pot luck as to what will help. So, I am nervous about it but am hoping it will help and praying I don't eventually end up worse.
To Michelle- I have been off and on Methotrexate for years. I did very well on it for years but its not working well for me now. No side effects from it other than a little queasiness day after taking it but nothing to keep me from going on with my day. I hope you do well on it. It really had made a difference for me.
Alley cat- I am sorry you are still in such pain. I hope someone has some good advice for you as I am not familiar with your diagnosis. Hang in there!
Again, thanks everyone for your welcome!
Caprie
Hi everyone-
I'm another newcomer, but an oldtime RA sufferer, for over 18 years. Even with meds I have the occasional flare up, so I truly can sympathize with anyone out there who suffers from PAIN. I had tried most meds without much success (though methotrexate seemed to help for a while and I know others who do well with it) until Enbrel came along. I even tried bee sting therapy for over a year-yep-bee stings, over 1,500. I'm on Enbrel, two x a week (though I only do one shot a week if I can get by with it), and Arava. I don't like to think about side effects, but dwell on quality of life at present. The hardest thing is to keep moving, but it makes a difference.
I check out a great book on arthritis-Strong Women and Men Beat Arthritis. I have found that exercise and strength training have done me a world of good the past 8 years.
I just got a new puppy who makes me smile, but whew, it's hard to get the joints moving fast enough to get him out the door when he needs to go!
A lousy way to make connections, but great to be able to talk about it....I'll be back!
From Moderator: Your post was edited due to Forum Rule #4 listed below:
- Advertising or Spam is defined as posting a link for the purpose of selling, soliciting or promoting by someone that has ownership or other "vested interest" to the web site involved, including efforts to promote other online forums or web sites by web site owners.
- If you are a web site owner and have a link that fits into this category that you want to share, please submit it to our resource directory and we will review your submission.
- Posts and links about fundraising (including nonprofit fundraisers) are NOT permitted.
- Only links to personal home pages are allowed in signatures and member profiles.
- Links to helpful web sites (commercial or otherwise) are allowed when they are posted by someone without any "vested interest" AND whose purpose is NOT to solicit, advertise, promote, fundraise, etc.
Post Edited By Moderator (Ducky) : 5/10/2006 10:54:51 AM (GMT-6)
Caprie...Thanks so much for the reply. I'm glad to hear that methotrexate worked for you, even though it was in the past. And good to hear that you didn't suffer side effects from it, other than a little queasiness the following day. I hope I can do as well on it.
Eliznel...I just read your post, and understand methotrexate also worked for you for awhile. I know you've had RA for a long time, and I'm very sorry to hear that. You sound like a fighter, and that's what all of us here have to be. I'm beginning methotrexate in a couple of days, and would be interested in hearing how you tolerated it. I think my main fear is infection. I already have diabetes, and have struggled with infection because of my compromised immune system. Any info you could give me on how well you tolerated it would be helpful.
To everyone here...it's great being able to come here, read the posts, and know that others are here for support...people that know, and understand, and are fighting for better lives...or better quality of life. Good luck to all of you...Michelle
Michelle-I was able to tolerate Methotrexate fairly well, with no side effects, much like Caprie. It was several years ago-If I recall correctly-I did have to go in to the lab quite often for blood work. I really hope you find some relief. Chronic pain is no fun, and the depression that comes with it. I had no problems with infection. Let us know how it goes.
-Eliznel