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Medical Forum / Diseases and Disorders / Arthritis / March 2005Dairy spurs flare-ups.
Dairy exacerbates flare-ups. Years ago I fasted for three days. I broke my fast with yogurt before going to bed for the night. The next morning my whole body was swollen with an abnormal accumulation of fluid (edema). I also was barely able to move. The next time I went to the rheumatologist I told her about my experience. She had recently returned from a rheumatology conference. One of the doctors there had done a test of RA patients, according to a paper which he handed out, which showed that dairy does exacerbate flares. I also, in breaking the fast. ate scrambled eggs the next day and then proceeded to suffer a whopping migraine headache. I had been experiencing severe migraines (with violent vomiting) for years. Very horrible misery, migraines. Have been eating vegan ever since, with no more migraines. Of course the abrasion of the joints continued, due to existing mechanical deformities, but no more extra pain from dairy. I love soy products now. Still, some people are allergic to soy. Jan2 Dairy helps me out when I am feeling badly and inflamed. It helps my swelling in my hands. and it helps edema. I think to each his own. I do know that beans cause me flare up I dont want to hear any gassy jokes either...... > Dairy exacerbates flare-ups. > [quoted text clipped - 17 lines] > deformities, but no more extra pain from dairy. I love soy products now. > Still, some people are allergic to soy. Jan2 > Dairy helps me out when I am feeling badly and inflamed. It helps my > swelling in my hands. and it helps edema. I think to each his own. I do [quoted text clipped - 22 lines] >> deformities, but no more extra pain from dairy. I love soy products now. >> Still, some people are allergic to soy. Jan2 Hi Rhonda! Yes I agree, [that each with an autoimmune disease is unique in his/her experience of it.] It helped me feel better about my life in researching the available therapies, including the orthodox treatments. My first couple of rheumatologists almost killed me with drugs and lied to me about the steroids. I will relate the details if you want them, but it would take a lot of reading on your part. I finally asked myself, Why do they give me all these drugs if there is no stopping the joints from being destroyed? -- drugs which destroy vital organs like, liver, heart veins, bowel function, nervous system, and also teeth, bone, etc? My hair was falling out on methotrexate. That's the first time I heard of that." my doctor said. Yeah--right! And it drove my BP to a very dangerous level. The drug was working and she still increased my dose. Thank you for replying to my post. Jan2 Why do they give me all these drugs if there is no stopping the joints from being > destroyed? -- drugs which destroy vital organs like, liver, heart veins, > bowel function, nervous system, and also teeth, bone, etc? My hair was > falling out on methotrexate. That's the first time I heard of that." my > doctor said. Yeah--right! And it drove my BP to a very dangerous level. > The drug was working and she still increased my dose. Thank you for > replying to my post. Jan2 Hi Jan, I want to try to get you not to be your own worst enemy. It is not our medicines fault that we have inflam.arth. It is not the doctors fault that you have inflam.arth. We must try to control our immune system. Methx usually has to get up to 15mg a week before it really even starts to control inflam.arth. Please understand that if it is not controlled the damage to our system and our joints is on going. I first came down with RA when I was 38 and 45 before I saw a RD. Like many people here, I took Methx for 7 or 8 years and it did its job for me in almost all of those years at 17.5 mg and at the end when it was not working too well,,,, 20mg by shot and then it was stopped and I moved on to Arava for a year. Most of those years with Methx, I took 5mg of prednisone and 10 mg a day for the first year with steroid shots in my knees, ankles, feet, and shoulders By the way, grape seed extract and/or biotin will help with the loss of hair. Please find you a RD that you can talk to and feel at ease with. Accept that you have a disease that can not be cured at this time and people like me that have had RA for over 25 years do control it and live a good life. I have had both shoulders shot with steroids this year while in a bad flare. We nearly all have what we call flares and it is in this time when the most RA damage takes place,,,, IMO. It could be that one of the newer medicines for RA will be your answer and I hope you have good insurance if you do. We all come here for support and other peoples opinion of what has taken place with them. I want you to remember that we need to believe in our doctors and our medicine because the mind controls a great deal of how bad inflam.arth is for a person. We must also remember that inflam.arth does more damage to our system and joints than the medicine does. You are lucky that in these days we have choices in what works best for us and there are new medicines coming out. About blood pressure,, that is a problem for all of us and we can cause a great deal of the problem. Please be positive and read in this newsgroup how many different types of people deal with what we have. Tomorrow is going to be better and you are going to help make it that way. Harv I am beginning to wonder if there is any point in my posting here. You are the third...forth here who misread my post, the one that enraged spambuster. I posted about s-p-e-c-i-f-i-c experiences of m-y o-w-n, sharing my own experience with dairy, yet spambuster did not like that I was not generalizing. I set my own boundaries. Others can read into my words whatever spirit the need to see. They can set their boundaries too. They may not set mine. If I get many more high handed replies from any other person needing to dishonor me by assuming dominance over me, and finding insult where there was none intended by me, then I will be certain that the spirit in here is not to look up, but to look down with no hope. I still don't understand what in my words are so threatening to the few who keep trying to get me to accept that they know my heart. I treat others as equals, until they give me reason not to. What does my life have to do with yours? Why do you need to read into my posts "a need to speak for others." It was information, period. Jan2 > Why do > they give me all these drugs if there is no stopping the joints from being [quoted text clipped - 41 lines] > Tomorrow is going to be better and you are going to help make it that way. > Harv Hi Jan,,,, I have made my last post with you for quite awhile. You have a great deal of anger and a need to slap someone when it is not required or needed. No one is really speaking with you in a harsh manner but you take it that way and have a need to lash out at someone that is trying to help you with the truth as they know it. Its not about personalities as much as it is a need to accept the disease you have. Please read my post again. There is a great deal in it that had to be learned the hard way and the reason it was put here is to help to deal with it all. So it goes. Harv >I am beginning to wonder if there is any point in my posting here. You are >the third...forth here who misread my post, the one that enraged [quoted text clipped - 59 lines] >> way. >> Harv >I am beginning to wonder if there is any point in my posting here. Probably not when you insist on extreme overreaction to even a polite expression of good wishes that you had found a solution for yourself. Jo > I I get many more high handed replies from any other person > needing to dishonor me by assuming dominance over me, You'll get nowhere with your tirades and false accusations. Calm down. Visit your shrink if you haven't lately. |
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