Guest guest Posted February 9, 2007 Report Share Posted February 9, 2007 Ringworm is a fungus so it's no wonder the abx didn't work. Ozonated olive oil does though Nail fungus responds to colloidal silver and DMSO, and a bunch of other things. You still have a lot of carbs in your diet (rye oats potatoes); they will slow you down considerably and possibly prevent recovery and they may be causing the consipation, one symptom of dysbiosis. More p [syllium, inulin, and if the constipation is very bad, a dose of epsom salts. Salt is fine but please make it NOT table salt for general health reasons. Duncan > > Hello, > > This is my first time in treating my candidiasis. I've had a number > of nail fungal infections in the past and now have ring worm that > was resistant to antibiotics, so now am trying the natural route. > Minus bloating that comes from yogurt and milk, I have not noticed > too many physical symptoms from my previous diet, but do know I have > felt better when I've stuck to more natural foods. > > Currently, I have taken out of my diet: wheat, gluten, sugar (of all > kinds), fruit, dairy, coffee and caffeine, alcohol, and soda. My > diet now consists of meat and poultry, vege's (including potatoes), > legumes, rice (including pasta and cakes), rye, oatmeal, and > cammomile and rosehip tea. > > I have also started taking borage oil, EPA, Capryl, Bentonite, and > Psyllium powder. > > A few questions: > > 1. I have been constipated since I started the supplements and never > have been before in my life. Is this common and what may be the > reason(s)? I'm curious about the effects of the Psyllium and > Bentonite. > 2. What about salt? Does that exacerbate candida? I haven't > removed that? > 3. What about rye and potatoes? > > Any input would be greatly appreciated Thanking you in advance > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 10, 2007 Report Share Posted February 10, 2007 Duncan, Thank you for your response. One more question, re: the epsom salts (which I have and have not used yet) do you mean to take as a laxative? Thank you, Lulu Duncan Crow <duncancrow@...> wrote: Ringworm is a fungus so it's no wonder the abx didn't work. Ozonated olive oil does though Nail fungus responds to colloidal silver and DMSO, and a bunch of other things. You still have a lot of carbs in your diet (rye oats potatoes); they will slow you down considerably and possibly prevent recovery and they may be causing the consipation, one symptom of dysbiosis. More p [syllium, inulin, and if the constipation is very bad, a dose of epsom salts. Salt is fine but please make it NOT table salt for general health reasons. Duncan > > Hello, > > This is my first time in treating my candidiasis. I've had a number > of nail fungal infections in the past and now have ring worm that > was resistant to antibiotics, so now am trying the natural route. > Minus bloating that comes from yogurt and milk, I have not noticed > too many physical symptoms from my previous diet, but do know I have > felt better when I've stuck to more natural foods. > > Currently, I have taken out of my diet: wheat, gluten, sugar (of all > kinds), fruit, dairy, coffee and caffeine, alcohol, and soda. My > diet now consists of meat and poultry, vege's (including potatoes), > legumes, rice (including pasta and cakes), rye, oatmeal, and > cammomile and rosehip tea. > > I have also started taking borage oil, EPA, Capryl, Bentonite, and > Psyllium powder. > > A few questions: > > 1. I have been constipated since I started the supplements and never > have been before in my life. Is this common and what may be the > reason(s)? I'm curious about the effects of the Psyllium and > Bentonite. > 2. What about salt? Does that exacerbate candida? I haven't > removed that? > 3. What about rye and potatoes? > > Any input would be greatly appreciated Thanking you in advance > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 10, 2007 Report Share Posted February 10, 2007 Right , epsom salts is a laxative; it also relaxes the hepatic ducts and bile duct to allow liver and gallstones to pass more easily; it's part of the liver/gallbladder flush for that reason. Duncan > > > > Hello, > > > > This is my first time in treating my candidiasis. I've had a > number > > of nail fungal infections in the past and now have ring worm that > > was resistant to antibiotics, so now am trying the natural route. > > Minus bloating that comes from yogurt and milk, I have not noticed > > too many physical symptoms from my previous diet, but do know I > have > > felt better when I've stuck to more natural foods. > > > > Currently, I have taken out of my diet: wheat, gluten, sugar (of > all > > kinds), fruit, dairy, coffee and caffeine, alcohol, and soda. My > > diet now consists of meat and poultry, vege's (including potatoes), > > legumes, rice (including pasta and cakes), rye, oatmeal, and > > cammomile and rosehip tea. > > > > I have also started taking borage oil, EPA, Capryl, Bentonite, and > > Psyllium powder. > > > > A few questions: > > > > 1. I have been constipated since I started the supplements and > never > > have been before in my life. Is this common and what may be the > > reason(s)? I'm curious about the effects of the Psyllium and > > Bentonite. > > 2. What about salt? Does that exacerbate candida? I haven't > > removed that? > > 3. What about rye and potatoes? > > > > Any input would be greatly appreciated Thanking you in advance > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 10, 2007 Report Share Posted February 10, 2007 Oh Duncan, I love all this stuff you write. I'm learning so much from reading your posts and saving them all. Bonnie Re: New Member Right , epsom salts is a laxative; it also relaxes the hepatic ducts and bile duct to allow liver and gallstones to pass more easily; it's part of the liver/gallbladder flush for that reason. Duncan > > > > Hello, > > > > This is my first time in treating my candidiasis. I've had a > number > > of nail fungal infections in the past and now have ring worm that > > was resistant to antibiotics, so now am trying the natural route. > > Minus bloating that comes from yogurt and milk, I have not noticed > > too many physical symptoms from my previous diet, but do know I > have > > felt better when I've stuck to more natural foods. > > > > Currently, I have taken out of my diet: wheat, gluten, sugar (of > all > > kinds), fruit, dairy, coffee and caffeine, alcohol, and soda. My > > diet now consists of meat and poultry, vege's (including potatoes), > > legumes, rice (including pasta and cakes), rye, oatmeal, and > > cammomile and rosehip tea. > > > > I have also started taking borage oil, EPA, Capryl, Bentonite, and > > Psyllium powder. > > > > A few questions: > > > > 1. I have been constipated since I started the supplements and > never > > have been before in my life. Is this common and what may be the > > reason(s)? I'm curious about the effects of the Psyllium and > > Bentonite. > > 2. What about salt? Does that exacerbate candida? I haven't > > removed that? > > 3. What about rye and potatoes? > > > > Any input would be greatly appreciated Thanking you in advance > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2007 Report Share Posted February 14, 2007 Hi everyone, I am new to the group - I did try to mail you all before but my message failed as it was not sent in plain text. Anyway if you care to scroll down you will see my own details and my reasons for joining. I very much appreciate all your help and advice. Duncan - firstly thank you very much for your earlier feedback which is very exciting to me. I have a few more specific questions I would appreciate yours or others feedback on, 1) as previously, we are thinking seriously of going full steam ahead with the BED diet for our son, Inulin does play a part in the diet and I will be sure to add this in - given that my four year old son is eating a lot of high inuline veg. as part of his anti-candida diet - what dosing should we be thinking about (12-15 grams??) - could you have a look at the BED diet inulin product (Ecobloom - see https://shop.bodyecology.com/ ), and give me your feedback on same, seems very similar to the NOW Inulin product 2) while I'm asking about inulin - still a bit confused about FOS - the Now GR-8 probiotic you mention seems to contain FOS - we have been very careful to avoid probiotics containing FOS - so is the FOS in the GR-8 product strictly Inulin or is it ok to use and why so? 3) we did a CDSA (stool analysis) with Great Smokies lab back in August 2005 on my then almost 3 year old son and it showed up dysbiosis - i.e. No growth for Lactobacillus and more significantly from all you say No growth for Bifidobacterium -- we have been dosing with probiotics on and off for many months now (e.g. a lot from Klaires Lab prothera range) at dosages of about 100 bn cfu's daily - what do you think of this - would you suggest we just supplement with the inulin while keeping at least some bifido. probiotics going - i.e. the inulin should kick start new growth and take care of the everything else 4) the attraction of the BED was that we can give the Inulin and indeed the whey, both of which are recommended on the diet (what do you think of the undenatured product, see https://shop.bodyecology.com/prodinfo.asp?number=WW004 - again seems to fit your recommendations fully) while also introducing the probiotic fermented foods (cultured vegetables, coconut water kefir using Vita CoCo product, raw butter, good animal based proteins). 5) Regarding the grains (seeds really) allowed on the BED, we are currently giving quinoa, buckwheat, millet and flax seeds - should we stop these altogether - are veg. carbs the only carbs allowed 6) finally could you give a brief summary of the general diet we should be following to support the Inulin, Whey and Selenium protocol - right now we would seem to have plenty of all the ok veg, have started making and using cultured veg. (i.e. sauerkraut) also, quality eggs, fish, chicken and some lean red meat, some of the right type of olive oil, and just today some pumpkin seed oil, some coconut oil for sauteeing, some butter, and then of course the grains which we give as simple water only added porridge. Apologies for the length of the mail but am very anxious to get on the right path as soon as possible so would really appreciate any feebback, Thanks very much, From: Duncan Crow <duncancrow@...> Quinlan <mkldc@...> Subject: Re: FW: New member Date: Sun, 11 Feb 2007 17:15:29 -0800 >Hi , > >You CAN get enough inulin from the diet, but this entails using >the high-inulin foods as staples foods, which most people can not >do. Several high-inulin foods are in the chart on my inulin page: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2007 Report Share Posted February 15, 2007 Hi , For a four-year-old I think one tsp four times daily, about 6 grams daily should be about right; going higher presents no hazard at all. The Ecobloom inulin is 3x the price of the Now inulin but otherwise the same thing. The Body Ecology site writers aren't too bright. the description calls it " fructooleosaccharides " ; there's no such thing. Each capsule of GR8 Dophilus contains 8 billion organisms so there's little room left for FOS, less than the natural amount present in a tbsp of native inulin. This isn't enough to materially contribute to the program either way. FOS ferments more quickly, fermenting more in the proximal colon, and causing more discomfort in humans, but there is no reason for caution. You wouldn't want to use FOS instead of inulin at 12 grams per day though. 100 bn cfus daily is a fine starter culter proposal but without the inulin you haven't made lactobacilli and bifidobacteria a viable part of the ecology. Yes, continue with it and adding the inulin will start to make a difference. The RenewPro whey is a good product but I note it's 6 times the price of the equivalent, Source Naturals' True whey http://tinyurl.com/2w8koq and 13 times the price of the Jarrow Whey http://tinyurl.com/yj8nop The price may deter your use of 30 grams or so per person. Quinoa buckweat millet and flax on the Body Ecology diet are high- carbohydrate foods. As you guessed I would suggest avoiding them. A brief summary is to avoid carbohydrate intake, use lots of low- carb, high-fiber veggies and whey protein, probiotics, inulin, a mineral supplement, selenium, vitamin C, E, D, A, and cod-liver or wild fish EPA/DHA oil. Duncan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2007 Report Share Posted February 15, 2007 Hi Duncan, Thanks for that clear advice. Only starting out with the inulin and whey but cost, as always is a factor and I will bear the significant price differences in mind when ordering future supplies. We are living in Ireland and regularly get stuff from the States and Canada. I'm assuming I can order the Now products from your referenced sites and that even after shipping costs the price would still be as good as there is out there. Thanks again for all the advice. >From: " Duncan Crow " <duncancrow@...> >Reply-candidiasis >candidiasis >Subject: Re: FW: New member >Date: Thu, 15 Feb 2007 16:56:41 -0000 > >Hi , >For a four-year-old I think one tsp four times daily, about 6 grams >daily should be about right; going higher presents no hazard at all. > >The Ecobloom inulin is 3x the price of the Now inulin but otherwise >the same thing. The Body Ecology site writers aren't too bright. the >description calls it " fructooleosaccharides " ; there's no such thing. >Each capsule of GR8 Dophilus contains 8 billion organisms so there's >little room left for FOS, less than the natural amount present in a >tbsp of native inulin. This isn't enough to materially contribute to >the program either way. FOS ferments more quickly, fermenting more >in the proximal colon, and causing more discomfort in humans, but >there is no reason for caution. You wouldn't want to use FOS instead >of inulin at 12 grams per day though. > >100 bn cfus daily is a fine starter culter proposal but without the >inulin you haven't made lactobacilli and bifidobacteria a viable part >of the ecology. Yes, continue with it and adding the inulin will >start to make a difference. > >The RenewPro whey is a good product but I note it's 6 times the price >of the equivalent, >Source Naturals' True whey http://tinyurl.com/2w8koq >and 13 times the price of the >Jarrow Whey http://tinyurl.com/yj8nop > >The price may deter your use of 30 grams or so per person. > >Quinoa buckweat millet and flax on the Body Ecology diet are high- >carbohydrate foods. As you guessed I would suggest avoiding them. > >A brief summary is to avoid carbohydrate intake, use lots of low- >carb, high-fiber veggies and whey protein, probiotics, inulin, a >mineral supplement, selenium, vitamin C, E, D, A, and cod-liver or >wild fish EPA/DHA oil. > >Duncan > _________________________________________________________________ Discover the magic of RSS feeds at MSN Ireland! http://ie.msn.com/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2007 Report Share Posted February 23, 2007 Hi Will, The foundaton of our bowel health therapy is inulin, high vegetables, reasonable protein and saturated fat, low-carbing, undenatured whey and selenium. In your case especially the bowel lining can be glutathione-depleted, so the undenatured whey and selenium could help a lot. If you react at first to the inital gas from the inulin, bear with it; all it's doing is correcting a bad bowel ecology and that takes several days or so. Several people have told me that their bopwel has been better in ten days to a month than in the previous ten years. You'kll probably see a lot of comments along those lines from people on this list too. Duncan > > As a member of the CrohnsColitis group, I see a lot of cross > messaging with this group so I thought I would check it out. One of > your members (Bonnie) also suggested I give it a shot. > > Here's my story, the short version: > > I'm a male in my 50's with a history of Crohn's Disease since my > teens. I've had 8 abdomonal surgeries including 3 bowel resections > which left me with about 1/3 or less of my small intestine & about > 60% of my colon. My last surgery was in 1994 but my Crohn's Disease, > which was quiescent for 12 years, came back with a vengence in 2006. > > For most of my adult life I have had frequent bouts of severe > diarrhea. So much so, that a day with only 3-5 bowel movements is a > great day for me! Some days it gets up to 15-20 BM's a day. Those are > baaad days! > > Even when my Crohn's disease was inactive, I still had frequent > diarrhea which I always attributed to Short Bowel Syndrome. But > recently, I've been reading messages on group boards and I've started > thinking there might be more to it. And there might be something to > probiotics. > > I certainly qualify as a newbie in this field but I have an open mind > & I'm willing to listen & learn. Comments appreciated. > > Will > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 2, 2007 Report Share Posted March 2, 2007 Will, have you read Patient Heal Thyself by Jordan S. Rubin, N.M.D. Ph.D.? It's a very informative book, and you may find some real help in his experience. I've been reading it again, in regard to candidiasis, and have found it quite interesting. His story and pictures are very dramatic!!! Sue Will <xrman55@...> wrote: As a member of the CrohnsColitis group, I see a lot of cross messaging with this group so I thought I would check it out. One of your members (Bonnie) also suggested I give it a shot. Here's my story, the short version: I'm a male in my 50's with a history of Crohn's Disease since my teens. I've had 8 abdomonal surgeries including 3 bowel resections which left me with about 1/3 or less of my small intestine & about 60% of my colon. My last surgery was in 1994 but my Crohn's Disease, which was quiescent for 12 years, came back with a vengence in 2006. For most of my adult life I have had frequent bouts of severe diarrhea. So much so, that a day with only 3-5 bowel movements is a great day for me! Some days it gets up to 15-20 BM's a day. Those are baaad days! Even when my Crohn's disease was inactive, I still had frequent diarrhea which I always attributed to Short Bowel Syndrome. But recently, I've been reading messages on group boards and I've started thinking there might be more to it. And there might be something to probiotics. I certainly qualify as a newbie in this field but I have an open mind & I'm willing to listen & learn. Comments appreciated. Will --------------------------------- The fish are biting. Get more visitors on your site using Search Marketing. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2007 Report Share Posted March 3, 2007 Many people as well as Gastroenterology journal raise issues with the use of soil bacteria and bacteria associated with cancer (bacillus licheniformis) in a probiotic such as the one Jordan Rubin designed. A lot can be accomplished with bacteria that are normal for the human gut. Duncan > As a member of the CrohnsColitis group, I see a lot of cross > messaging with this group so I thought I would check it out. One of > your members (Bonnie) also suggested I give it a shot. > > Here's my story, the short version: > > I'm a male in my 50's with a history of Crohn's Disease since my > teens. I've had 8 abdomonal surgeries including 3 bowel resections > which left me with about 1/3 or less of my small intestine & about > 60% of my colon. My last surgery was in 1994 but my Crohn's Disease, > which was quiescent for 12 years, came back with a vengence in 2006. > > For most of my adult life I have had frequent bouts of severe > diarrhea. So much so, that a day with only 3-5 bowel movements is a > great day for me! Some days it gets up to 15-20 BM's a day. Those are > baaad days! > > Even when my Crohn's disease was inactive, I still had frequent > diarrhea which I always attributed to Short Bowel Syndrome. But > recently, I've been reading messages on group boards and I've started > thinking there might be more to it. And there might be something to > probiotics. > > I certainly qualify as a newbie in this field but I have an open mind > & I'm willing to listen & learn. Comments appreciated. > > Will > > > > > > > > --------------------------------- > The fish are biting. > Get more visitors on your site using Search Marketing. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 Hi Duncan, I respect and agree with many of your posts, but have to chime in with my experience re: Primal Defense. I've taken PD now for the last five years or so and I am a SIX year cancer survivor. And I have had no recurrences. Best regards, Alison > > As a member of the CrohnsColitis group, I see a lot of > cross > > messaging with this group so I thought I would check it out. One of > > your members (Bonnie) also suggested I give it a shot. > > > > Here's my story, the short version: > > > > I'm a male in my 50's with a history of Crohn's Disease since my > > teens. I've had 8 abdomonal surgeries including 3 bowel resections > > which left me with about 1/3 or less of my small intestine & about > > 60% of my colon. My last surgery was in 1994 but my Crohn's > Disease, > > which was quiescent for 12 years, came back with a vengence in 2006. > > > > For most of my adult life I have had frequent bouts of severe > > diarrhea. So much so, that a day with only 3-5 bowel movements is a > > great day for me! Some days it gets up to 15-20 BM's a day. Those > are > > baaad days! > > > > Even when my Crohn's disease was inactive, I still had frequent > > diarrhea which I always attributed to Short Bowel Syndrome. But > > recently, I've been reading messages on group boards and I've > started > > thinking there might be more to it. And there might be something to > > probiotics. > > > > I certainly qualify as a newbie in this field but I have an open > mind > > & I'm willing to listen & learn. Comments appreciated. > > > > Will > > > > > > > > > > > > > > > > --------------------------------- > > The fish are biting. > > Get more visitors on your site using Search Marketing. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 Hi allison, congratulations on your six years! I was just diagnosed in nov 06 had surgery and now am going thru chemo. Do you think the PD helped you with the cancer? I tried threelac and did not have good results although i was not sure why. I beleive my body was trying to shed something foreign, which was the cancer while i was on the threelac. This was made me aware of something is not right here. ANy suggestions would be appreciated. Love Sue ________________________________________________________________________________\ ____ We won't tell. Get more on shows you hate to love (and love to hate): TV's Guilty Pleasures list. http://tv./collections/265 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 Alison, it was actually the presence in Primal Defense of the bacillus associated with cancer that affected my sensibilities more than the rest of the soil bacteria; I note that a similar concern might well appeal to others. The soil-based organism blend from Now Foods which does not contain the cancer organism bacillus licheniformis or its extracts, might resonate with people with this similar view. http://tinyurl.com/257bd2 Speaking of resonance, note that in the Rife forums, this particular bacteria is directly targeted in the cancer frequency sets. Duncan > > > As a member of the CrohnsColitis group, I see a lot of > > cross > > > messaging with this group so I thought I would check it out. One of > > > your members (Bonnie) also suggested I give it a shot. > > > > > > Here's my story, the short version: > > > > > > I'm a male in my 50's with a history of Crohn's Disease since my > > > teens. I've had 8 abdomonal surgeries including 3 bowel resections > > > which left me with about 1/3 or less of my small intestine & about > > > 60% of my colon. My last surgery was in 1994 but my Crohn's > > Disease, > > > which was quiescent for 12 years, came back with a vengence in 2006. > > > > > > For most of my adult life I have had frequent bouts of severe > > > diarrhea. So much so, that a day with only 3-5 bowel movements is a > > > great day for me! Some days it gets up to 15-20 BM's a day. Those > > are > > > baaad days! > > > > > > Even when my Crohn's disease was inactive, I still had frequent > > > diarrhea which I always attributed to Short Bowel Syndrome. But > > > recently, I've been reading messages on group boards and I've > > started > > > thinking there might be more to it. And there might be something to > > > probiotics. > > > > > > I certainly qualify as a newbie in this field but I have an open > > mind > > > & I'm willing to listen & learn. Comments appreciated. > > > > > > Will > > > > > > > > > > > > > > > > > > > > > > > > --------------------------------- > > > The fish are biting. > > > Get more visitors on your site using Search Marketing. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 duncan is the PD not recommended for cancers? Love Sue ________________________________________________________________________________\ ____ No need to miss a message. Get email on-the-go with for Mobile. Get started. http://mobile./mail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 Hi sue, Best wishes for a VERY speedy recovery! Hope the chemo goes well. If you ever find you'd like an alternative, check out herbhealers.com and also bevanpotter.com. Herbhealers has been shut down by the US Gov't--they offer a cancer treatment that works, is cheap, and comes with a 100% money back guarantee. That says it all. I took their Cansema Tonic for 18 months at a slightly reduced dose since I am quite sensitive, and it killed the internal cancer. If you need to order something for the cancer, you can still do so through bevanpotter--the Cansema and other lines of things featuring graviola work quite well and at this point I'll say I was recommended to try these over chemo, as my immune system was already in shut-down from the Candida when I was diagnosed with big C. The PD I take specifically for my gut problems, and it has really made the difference. My gut--and I--are much healthier with no recurrence of cancer at all (internal or external). All the best, Alison :-) > > > Hi allison, > > congratulations on your six years! > > I was just diagnosed in nov 06 had surgery and now am > going thru chemo. > > Do you think the PD helped you with the cancer? I > tried threelac and did not have good results although > i was not sure why. I beleive my body was trying to > shed something foreign, which was the cancer while i > was on the threelac. This was made me aware of > something is not right here. > > ANy suggestions would be appreciated. > > > > Love > Sue > > > > > > ________________________________________________________________________________\ ____ > We won't tell. Get more on shows you hate to love > (and love to hate): TV's Guilty Pleasures list. > http://tv./collections/265 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2007 Report Share Posted March 4, 2007 Hi Duncan, Thanks for your $.02. I can only speak from experience. Everyone's different. But I've had a grand old time on Primal Defense. It has made a real difference for me! Alison :-) > > > > As a member of the CrohnsColitis group, I see a lot > of > > > cross > > > > messaging with this group so I thought I would check it out. > One of > > > > your members (Bonnie) also suggested I give it a shot. > > > > > > > > Here's my story, the short version: > > > > > > > > I'm a male in my 50's with a history of Crohn's Disease since > my > > > > teens. I've had 8 abdomonal surgeries including 3 bowel > resections > > > > which left me with about 1/3 or less of my small intestine & > about > > > > 60% of my colon. My last surgery was in 1994 but my Crohn's > > > Disease, > > > > which was quiescent for 12 years, came back with a vengence in > 2006. > > > > > > > > For most of my adult life I have had frequent bouts of severe > > > > diarrhea. So much so, that a day with only 3-5 bowel movements > is a > > > > great day for me! Some days it gets up to 15-20 BM's a day. > Those > > > are > > > > baaad days! > > > > > > > > Even when my Crohn's disease was inactive, I still had frequent > > > > diarrhea which I always attributed to Short Bowel Syndrome. But > > > > recently, I've been reading messages on group boards and I've > > > started > > > > thinking there might be more to it. And there might be > something to > > > > probiotics. > > > > > > > > I certainly qualify as a newbie in this field but I have an > open > > > mind > > > > & I'm willing to listen & learn. Comments appreciated. > > > > > > > > Will > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > --------------------------------- > > > > The fish are biting. > > > > Get more visitors on your site using Search Marketing. > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2007 Report Share Posted March 17, 2007 Hello I suggest you go to the files in the group and read Duncan's suggestions. A lot of info is on his website (search for Duncan Crow) I and many others have had major improvements taking Undenatured whey powder, Inulin and Selenium. Thanks NSW AU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 8, 2007 Report Share Posted June 8, 2007 -My 6 yr. old son has had seizures since he was a baby. About a year ago his seizures were worse than they'd ever been and nothing (almost every medication and combinations of meds, ketogenic diet, VNS) was controlling the seizures. We started hyperbaric oxygen treatments and his condition greatly improved. He still has seizures, but not nearly as often or as many as he did, and he's on much less medication. We have done 60 dives and plan to do more. you might look into it. best wishes. lisa -- In , " josephine7962 " <medicalmissionary@...> wrote: > > just wondering if anyone has had any luck with alternative therapy? > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 16, 2007 Report Share Posted July 16, 2007 " My son, age 44 has been diagnosed with PBC. Am I at the right place? " you are very welcome here; there are people with PBC here as well as with autoimmune hepatitis. You can also go to this website, http://pbcers.org/, for more PBC-specific information. The PBC Digest website is http://pbcers.org/digest.htm, and there is also a wonderful group for Family Members and Friends Of PBCers: JOIN the Family & Friends (Leave text box of e-mail blank) Our support group listbot is a wonderful source of help and support for family members and friends of those who suffer from Primary Biliary Cirrhosis (PBC). Please NO PBCers in this group. In the PBCers Family Members and Friends Support Group we: a.. Openly discusses the ups and downs of our PBC family member or friend. b.. Learn more about caring for our PBCer. c.. Learn more about PBC the disease and it's many symptoms. d.. Help our PBCer cope with depression and daily living. e.. Ask questions of the other members. f.. Share personal experiences. g.. Help one another cope with our own fears and insecurities of PBC. h.. Build lasting friendships. Kay_TX, AIH 1995 and AMA negative PBC, 1999, stage 2 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 17, 2007 Report Share Posted July 17, 2007 HI CHRIS, Welcome to the group. Kay probably has told you we're pretty diverse group (a bag of mixed nuts). I'm ne AKA SunE Birds Mom, or Geo. I'm the old lady of the group. I have AIH stage 3 and despite everything doing not so bad. I live in Broomfield Co. just out side Denver. I have 2 grown sons 40 and 35 and I'm 60. SunE is an Umbrella Cockatoo, my only child at home currently. I must go now the big mouth is screaming, Love and Peace, Geo and SunE Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 28, 2007 Report Share Posted August 28, 2007 In answer to --I too was dx for AIH at the Center for Liver Disease in Pittsburg. I became very ill in 8/03--extreme fatigue, jaundice, nausea etc..Was admitted to local hospital in upstate NY where I live and had every test you mentioned and then some but was released with no dx. My hep had me in for blood work for two months and finally said we know your liver is failing but don't know why so can't help you and suggested Pittsburg. My daughter (whose name is also ) contacted Pittsburg through their web-site, made an appt., gathered up all my medical records and we flew to Pittsburg. I was very impressed with the hep. He did a little more blood work and said I had AIH. He said it's a chronic disease but can be controlled " you will feel better but it will take a long time. " He was right on both counts. I was put on 20 mg of prednisone--had blood work done weekly and faxed to Pittsburg. By January I was feeling somewhat better and my liver tests were improving. He gradually tapered the pred to 5mg and added 50mg of azathioprine. To answer your question, you will get a lot of your energy back I am sure and willsoon feel a lot better. I have had a few flares and my main complaint is the side effects of going up and down on the pred. The people on this website are great and a real morale booster as well as having useful info. One thing that I have never seen mentioned that almost did me in was sleep deprivation. Don't know what your liver has to do with it but I was exhausted and could not sleep day or night and this was before I was on any meds. My PCP gave me some sleep meds and it really helped although I still have a problem with it. wishing you good health soon.Beulah ************************************** Get a sneak peek of the all-new AOL at http://discover.aol.com/memed/aolcom30tour Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 28, 2007 Report Share Posted August 28, 2007 Hi and welcome. I was diagnosed with AIH in 1996 at UPMC in the DDC. My doctor was Dr. Balan and he has since left. I also went through a lot of test before getting the dx of AIH. By that time my numbers were in the thousands and they weren't very hopeful for me. I have been on Prednisone on and off for the last 11yrs. I am right now on a tapering dose and am at 30 mg. I also take Imuran and am taking100mg daily. I will stay on this for maybe forever according to my G.I. Everytime I come off the meds I relapse. The prednisone causes different reactions in different people. Some get real jittery and hyper,can't sit still and can't sleep. At the time of my original dx I also was very tired and slept all the time. It was hard for me to even make the bed. As time went on and I improved so did my energy levels. I still quite often need to take a nap and get worn out easier than I used to. As I said we all react differently to the medicines we are on so I can only tell you how I did. I am sure others will tell you their stories. I also have gained over a 100lbs and am now being checked for type 2 diabetis. I will be glad to answer any questions you have if I can. I hope you feel better soon. the WV hillbilly nancymerlin <nmerlin@...> wrote: Hello to all, My name is and I am new to the group. I was just dx in March after two months of tests--80 vials of blood, ultrasound, doplar, MRI, CT and biopsy. In January by liver enzyme count was 700 and was over 1300 before I had a DX. (normal under 30) Two different paths read the biopsy and could not come up with a dx. I started with an endocrinologist who first did the test. I was dx with diabetes in November during a pre-op for gallbladder surgery. Liver was good in November. Next, sent to a GI who sent me to the Center for Liver Disease in Pittsburgh, PA. All the tests were coming back normal. I was in Europe for three weeks in Oct and they were even testing me for parasites from Eastern Europe!! That's how far they were stretching for a DX. My liver count was still going up 100 to 200 a week. Finally the hep said he would look at the path slides himself. He knew what markers he was looking for. AIH was confirmed and he started me on 30 pred and 50 imuran in March 07. I am down to 10 pred and 50 imuran now. Hope to start lowering pred later this month. I would like to know how you feel now after you have been on the meds for awhile. What symptoms of the disease to you still have. I still get tired. My good time is 11 am to 3 pm. I do go to work during that time. I come home, rest, prepare dinner, rest, and mayabe do a load of laundry. Shopping makes me very tired. I do not like to drive far or after 7 at night. Sometimes just taking a shower just wears me out. Are these normal? Will my energy level every come back to normal? Has anyone in this group been treated at the Center for Liver Disease in Pittsburgh, PA? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2007 Report Share Posted September 21, 2007 -Hi anne and welcome.My name is a and my daughter Jordan was diagnosed 10 months ago with Systemic.We went through many months of not knowing what was wrong as we continued back and forth trips to the ER. Jordan as of now is only on Kineret, a daily injection.Awonder drug for us.The Dr.s want to start her on methotrexate so that there is something in place if the Kineret stops working.We have to wait to see the specialist for her Liver first before we start. I understand the alone feeling but I can tell you this is a great place to come when you are feeling alone and afraid. I have had some great advice given me on here when I had nowhere else to turn. Once again, welcome. a -- In , " jzngsmama " <davemarejz@...> wrote: > > ~I posted but don't see my message so I will try again. hello! I am the > Mom of a three year old systemic jra diagnosed son... feeling lost and > very very alone! Look forward to chatting with someone. > ann > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 I have not tried that diet but i think it would be worth a try. I am at Cleveland Clinic with Hannah as we speak, they are doing a multitude of tests on her and one I have requested is a blood test for celiac disease. I have a friend who had nonspecific tendon and joint pain for many years. She had the celiac disease test done and it was positive. She went on the gluten free diet and is pain free after 3 weeks. She said she is not said at all to give up wheat if she feels good. Just my thoughts. - Martha >From: " dwsmom1996 " <dwsmom1996@...> >Reply- > >Subject: [ ] New Member >Date: Fri, 28 Sep 2007 20:31:55 -0000 > > > > Hello All, > > I just joined the group and have a question. I have a 6 year old boy >who is Autistic and has ab seizures and on meds for it. After reading >some posts I wanted to ask if anyone goes to a Alternative Med doctor. >I take my kids to one and when I told him my son was having ab seizures >he said to do the gf/cf diet and eliminate sugar as well until we see >him again. Has anyone ever tried it? I asked why and he said the sugar >is causing the seizures. I'm just looking for advice and not to upset >anyone. > >Kathy > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2007 Report Share Posted October 9, 2007 Kathy, I would strongly encourage you to try gluten/casein and soy free[soy is a protein much like casein]. My 22 year old pdd-nos daughter has dealt with seizures since age 9. Meds did little for her. The ketogenic diet helped but I could not get family cooperation for it. She went through a celiac work up at age 11 - positive blood work but her biopsy was 'negative' so the advice was to eat as usual. At age 16 I came across the diet link through Seroussi's and ' books. She has been a good responder. She still will seize, usually 8-12 hours after she eats an offending food, of she gets any of above. Summer 2006 at camp they used a gluten containing sunscreen on her and she came home with lots of withdrawal seizures. When we began the gfcfsf pattern it was like dt withdrawals. She several days of multiple seizures. I was very scared. After day 5 the seizures were gone. We had a lot of sorting out to do to get her diet pure. Even tegretol, her med at the time, had a unlisted casein component. Chocolate, peanut, and some other foods will put her close to seizures. The gut and brain are quite related imo. Have you read Dr. McCandless' book - 'Children with Starving Brains'? She's a big advocate of gfcfsf. , " dwsmom1996 " <dwsmom1996@...> wrote: > > > > Hello All, > > I just joined the group and have a question. I have a 6 year old boy > who is Autistic and has ab seizures and on meds for it. After reading > some posts I wanted to ask if anyone goes to a Alternative Med doctor. > I take my kids to one and when I told him my son was having ab seizures > he said to do the gf/cf diet and eliminate sugar as well until we see > him again. Has anyone ever tried it? I asked why and he said the sugar > is causing the seizures. I'm just looking for advice and not to upset > anyone. > > Kathy > Quote Link to comment Share on other sites More sharing options...
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