Guest guest Posted July 28, 2004 Report Share Posted July 28, 2004 Hi , Food-related arthritis flare-ups seem to happen within 12 hours. I discovered one reaction by eating a lot of peanuts one night, after not having any for ages [_raw_ peanuts - hey, maybe that had something to do with it], and next morning woke up extremely debilitated. The only recent [couple of days] change in my diet had been the peanuts, so I knew they were the cause. So you should try keeping a food diary, or at least try to remember what you've been eating in the last 24 hours. On the other hand, if it's a food you have all the time, your body will adapt to a certain extent, so the condition seems constant rather than flaring. [This is just my experience and supposition, not based on any scientific studies.] Stress and fatigue may also be factors, but I don't know much about that area. Neil > I have a question for you : some have reported that such and such > causes a flare in the PA. I'm used to thinking of just P and the > slow onset of any change in conditon, due to the nature of the > maturing skin. Do PA flares happen so fast that you can definitely > assign some cause to them? [/snip] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2004 Report Share Posted July 29, 2004 My experience with PA is that my hands will hurt for a few days then the next day I will be ok. So it comes and goes fast. It seems to be unrelated to any diet or environmental event. I have tried all the supplements that suppposedly help with inflamation, but can not establish any cause and effect. Recently I have noticed that I have one flare per month that last for 4 or 5 days.(Is it the moon?) I keep a diary of what is happening so I can give the doctor good feedback. My most recent X-rays show changes in the joints " consistent with PA. " I am taking 20 mg of MTX per week, 400 mg of Celebrex per day.The doctor may start a biologic next month. Mike -- In , " castlinga " <mcqueenm46@m...> wrote: > HI this is from in WF..I'm the one who had a late diagnosis in > January, saw the rheumy in March and have been on mtx since Jan, > (injections since March) and Enbrel for 8 weeks now. I have been > declining since January with additional joints in one hand being > affected and my lower back starting to " feel weak " making standing > painful. I did get some improvement in toe and fingernails. > Have seen the rheumy twice and talk to her main nurse when I feel I > need some advice/support. > I had been taking flaxseed oil for cholesterol purposes and when I > read about the 1 tablespoon dosage, I upped my intake over this past > weekend. For three days, I've had less pain in my really swollen > left knee, back and sore feet. I've had an energy boost as well so > am wondering - weather, meds, flaxseed oil???? who knows what's > helping. I also stopped taking Lipitor since I hadn't known about > the side effect of loss of muscle use before. > I self-inject and have no problems and don't think I have much in > side effects except fatigue. I have had some swellings; a boil in > my neck, some glands in my jaw which went down, some underarm > swellings which remind me of the boil, so I ignore them at the > moment. > I have a question for you : some have reported that such and such > causes a flare in the PA. I'm used ot thinking of just P and the > slow onset of any change in conditon, due to the nature of the > maturing skin. Do PA flares happen so fast that you can definitely > assign some cause to them? > > Thanks in advance, (just for being here - when I'm working fulltime > I often don't have the strength to even read the newsletters > regularly. > > in WF, TX Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2004 Report Share Posted July 30, 2004 > HI this is from in WF..I'm the one who had a late diagnosis in > January, saw the rheumy in March and have been on mtx since Jan, > (injections since March) and Enbrel for 8 weeks now. > > in WF, TX Hi , I'm new on this board, but old to P.A. I also have Hep C, so there aren't many of the drugs I can take. I have to be carefull of anything that could effect my liver. I spend alot of time searching the internet for all the drug info I can find. I know that the doctors, for what erver reason, don't always tell us everything they know about the drugs that they are asking people to take. I noticed ENBREL, in your post. Here's a government site I found on Metacrawler.com; http://www.fda.gov/bbs/topics/ANSWERS/ANS00954.html We have to look out for ourselves, cuz nobody else is as effected by the drugs, as ourselves. Be carefull out there, it's a dangerous world..... Carl Portland,Or. 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.