Guest guest Posted February 8, 2004 Report Share Posted February 8, 2004 Uh ohhh.....this will no doubt peeve the toxic flushers in the crowd and before you know it coffee enemas are front and center again. But it was good to finally read about the basis for the eight cups. Not familiar with this Mirkin guy, but he and I are on the same page on this. I also believe that everybody's needs are probably very different depending on conditions, activity, diet, metabolism, etc., so pinning a number on it probably isn't all that useful, but if we gotta have a number..... I personally don't keep track, but am usually drinking throughout the day anyway. Jeff Original Message Follows---- From: " Mark Holmes " <mholmes@...> Reply- " Mark Holmes " <markholmes@...> <rheumatic > Subject: rheumatic HOW MUCH WATER DO YOU NEED?.htm Date: Sun, 8 Feb 2004 16:16:39 -0500 I know this is sometimes discussed in this group. Noticed this on Dr. Mirkin's site and thought I'd pass it along. Will no doubt stir debate (that's healthy, right? http://www.drmirkin.com/nutrition/9942.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 8, 2004 Report Share Posted February 8, 2004 Mark, you've been on this list long enough to have heard the importance of proper hydration to health and particularly it's use in this therapy. It's inexcusable for you to post this and try to confuse people on this list trying to get well. For Dr. Mirkin to put something like this on his site shows absolute ignorance on the subject. Just note his source. This is not a subject for debate. Ethel rheumatic HOW MUCH WATER DO YOU NEED?.htm > I know this is sometimes discussed in this group. Noticed this on Dr. Mirkin's site and thought I'd pass it along. Will no doubt stir debate (that's healthy, right? > http://www.drmirkin.com/nutrition/9942.html > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 10, 2004 Report Share Posted February 10, 2004 I am totally baffled by this article. And to tell you the truth, I don't care what kind of 'research' was done for this. I just know that when I drink more water, I feel better. Ya know, it's not just about digestion and poop. I think they might be missing part of the picture here! Just my opinion, Mel rheumatic HOW MUCH WATER DO YOU NEED?.htm > I know this is sometimes discussed in this group. Noticed this on Dr. Mirkin's site and thought I'd pass it along. Will no doubt stir debate (that's healthy, right? > http://www.drmirkin.com/nutrition/9942.html > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Mark, I am glad that Methotrexate works for you. And I hope that you do not exhaust your immune system should you need it one day. DMARDs are immune depressants, as you well know by this time. Immune suppression is not a side effect; It is what DMARDS are created to do. I am not saying that sometimes other means are not necessary. But, I think the majority of us would like to save our immune systems just in case we need them in the future. I continue with my sulfasalazine (a less ghastly poison), just to keep my disease in check while I am on the AP. However, I know that it will cause damage in the long run. I hope to ween off of it in the near future. But, we cannot deny that the DMARDs poison our bodies and diminish our immune systems that we all need in order to survive. I am not trying to offend anyone. I do not judge others for continuing or starting DMARDs, as I do so myself. But we cannot sugar coat the fact that they are poisons. On a side note, I am not suggesting that anyone should " exist on aspirin alone " , nor do I believe that the antibiotic therapy fails anyone. Each person is different and may need a different combination of medications, supplements, and healthy lifestyle (including diet and exercise) in order to repair their bodies. And some people take longer to heal and detoxify than others. I know it is a long, difficult road to recovery....but I do not believe that one should discontinue the AP because it does not appear to work. Maybe that person just needs to find the right combination for himself/herself. I wish everyone the best and hope that we can all be pain-free one day. God Bless! Mel Re: HOW MUCH WATER DO YOU NEED?.htm Mel, Glad that more water works for you. I think it depends on the individual. We're all different. I posted the article because I found it interesting in view of all the input I found here about large intakes of water. Despite Ethel's viewpoint that it was inexcusable that I post this, I thought this was a forum to discuss the antibiotic therapy and side therapies associated with it. There appears to be an extraordinary number of variations of the antibiotic therapy, so I don't think a different viewpoint of the amount of water one intakes, is, or should be contentious. It is certainly debateable. I can not comment or confirm Dr. Mirkin's sources - I trust him to evaluate those before posting and you can form your own judgment, just as I do in regards to Ethel's sources. Incidentally, I too, have been a patient of Dr. Kempf's myself. I would not recommend him as an AP doc. Whereas he prescribed it for me, it was apparent he did not really believe in it. Like many traditional docs, he is most likely inclined to follow the road that leads to the least lawsuits. On a side note, I think " ghastly poisons " when referring to Enbrel and Remicade may be a bit strong, as they are continually shown to be of significant benefit to many (http://www.medscape.com/viewprogram/2785). I realize that the antibiotic forum is a forum for those who wish to avoid the medical establishment's normal prescriptions, but I would hate to see someone decide to exist on aspirin alone, should the antibiotic therapy for whatever reason, fail them. Personally, I have been on a regimen of methotrexate for 5 years now (after a year on AP) and much to the surprise, no doubt of many here, I'm not dead yet. (knock on wood). I consider myself fortunate that there was an alternative for myself and one that was affordable. I'll still switch to any alternative that appears safer, if I feel that it can be of benefit. I admire those of you who tough it out over the years through many herxes - I didn't like the progress of the radiological erosions I experienced while on it and for me personally, felt it was time to change. I still have minor progression of erosion, but slowed considerably. You may have no progression and may be doing fine and I think that is wonderful. Despite not currently taking AP, I do pay attention to postings and am interested in new approaches or new studies involving it. I am also interested in Bab's chicken collagen stories, which are also a bit removed from the AP. I hope one of these days, we'll here more from the human genome project. But, mostly I'm interested in whatever works and hope that you feel the same. Mark Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 13, 2004 Report Share Posted February 13, 2004 Mel, I am glad you wrote what you did. I was several years on mtx befre AP. It damaged my immune system( bone marrow suppression) irreparably! I have been on AP for 7 1/2 yrs and have had to try to rebuild with many alt txs what the mtx did. I am up to a 3.1 white count from a 1.8! Trust me with a low white count..you go NO WHERE!!! I agree too that we need dietary changes and to approach allegies as they impact the immune system as well( I do naet). I am doing hormone supplements (natural) and you need thyroid testing as well It all works togther. Also, dmards allow yeast to have a field day as it is suppressing your immunity and the yeast is allowed to run wild.Its been my main problem even now as I have such a poor defense system. Ap saved my life and yes I have had to scramble to find a right combo for me but it has been totally worthwhile. Love Marge > Mark, > > I am glad that Methotrexate works for you. And I hope that you do not exhaust your immune system should you need it one day. DMARDs are immune depressants, as you well know by this time. Immune suppression is not a side effect; It is what DMARDS are created to do. I am not saying that sometimes other means are not necessary. But, I think the majority of us would like to save our immune systems just in case we need them in the future. I continue with my sulfasalazine (a less ghastly poison), just to keep my disease in check while I am on the AP. However, I know that it will cause damage in the long run. I hope to ween off of it in the near future. But, we cannot deny that the DMARDs poison our bodies and diminish our immune systems that we all need in order to survive. I am not trying to offend anyone. I do not judge others for continuing or starting DMARDs, as I do so myself. But we cannot sugar coat the fact that they are poisons. > > On a side note, I am not suggesting that anyone should " exist on aspirin alone " , nor do I believe that the antibiotic therapy fails anyone. Each person is different and may need a different combination of medications, supplements, and healthy lifestyle (including diet and exercise) in order to repair their bodies. And some people take longer to heal and detoxify than others. I know it is a long, difficult road to recovery....but I do not believe that one should discontinue the AP because it does not appear to work. Maybe that person just needs to find the right combination for himself/herself. > > I wish everyone the best and hope that we can all be pain-free one day. God Bless! > > Mel > Re: HOW MUCH WATER DO YOU NEED?.htm > > > Mel, > Glad that more water works for you. I think it depends on the individual. We're all different. I posted the article because I found it interesting in view of all the input I found here about large intakes of water. Despite Ethel's viewpoint that it was inexcusable that I post this, I thought this was a forum to discuss the antibiotic therapy and side therapies associated with it. There appears to be an extraordinary number of variations of the antibiotic therapy, so I don't think a different viewpoint of the amount of water one intakes, is, or should be contentious. It is certainly debateable. I can not comment or confirm Dr. Mirkin's sources - I trust him to evaluate those before posting and you can form your own judgment, just as I do in regards to Ethel's sources. > > Incidentally, I too, have been a patient of Dr. Kempf's myself. I would not recommend him as an AP doc. Whereas he prescribed it for me, it was apparent he did not really believe in it. Like many traditional docs, he is most likely inclined to follow the road that leads to the least lawsuits. > > On a side note, I think " ghastly poisons " when referring to Enbrel and Remicade may be a bit strong, as they are continually shown to be of significant benefit to many (http://www.medscape.com/viewprogram/2785). I realize that the antibiotic forum is a forum for those who wish to avoid the medical establishment's normal prescriptions, but I would hate to see someone decide to exist on aspirin alone, should the antibiotic therapy for whatever reason, fail them. Personally, I have been on a regimen of methotrexate for 5 years now (after a year on AP) and much to the surprise, no doubt of many here, I'm not dead yet. (knock on wood). I consider myself fortunate that there was an alternative for myself and one that was affordable. I'll still switch to any alternative that appears safer, if I feel that it can be of benefit. I admire those of you who tough it out over the years through many herxes - I didn't like the progress of the radiological erosions I experienced while on it and for me personally, felt it was time to change. I still have minor progression of erosion, but slowed considerably. You may have no progression and may be doing fine and I think that is wonderful. > > Despite not currently taking AP, I do pay attention to postings and am interested in new approaches or new studies involving it. I am also interested in Bab's chicken collagen stories, which are also a bit removed from the AP. I hope one of these days, we'll here more from the human genome project. But, mostly I'm interested in whatever works and hope that you feel the same. > > Mark > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2004 Report Share Posted February 14, 2004 Geoff here. Mark wrote: > I hope one of these days, we'll here [sic] > more from the human genome project. Thus far the evidence points toward using genetics to (a) identify those who have a higher than average probability of developing the disease and ( selectively shutting down those immune system functions that create the symptoms, e.g., swelling, thick blood (high SED rate), etc. Our first taste of the common use of genetics occurred many years ago as pregnant women began to be tested to see if their baby __might__ have Down's Syndrome. If the test is positive, the mother-to-be is commonly advised to kill the child before it is born via abortion. Keep in mind, the positive test is not a guarantee that Down's will present, nor of its severity if it does; just that the marker is factually present. The prospects are... exciting. Excitement, however, is not always a good thing. BTW, adequate water to defecate does not equate to adequate water to flush the kidneys, perspirate toxins, expel sinoid irritants, etc. IMO, Mirkin's perspective is valuable only to those confronted with the specter (real or imagined) of death through dehydration; At times such as that, his words would be invaluable. Absent that, he's all wet. Drink enough to run clear, or nearly clear, and you're good to go. All puns intended. :-) Geoff soli Deo gloria www.HealingYou.org - Your nonprofit source for remedies and aids in fighting these diseases, information on weaning from drugs, and nutritional kits for repairing adrenal damage; 100% volunteer staffed. (Courtesy: Captain Cook's www.800-800-cruise.com) Quote Link to comment Share on other sites More sharing options...
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