Guest guest Posted September 14, 2001 Report Share Posted September 14, 2001 Hi Rob, Welcome to the group. I am currently between cleanses, haven't decided which one I'm going to start. I'm oscillating between the Sonne's cleanse and the master cleanse. I have a few extra pounds that I'd like to shed, which is my reason for the cleanse at this point in time. I have been cleansing for many, many years. Tried most of them on the market. I rotate through them, I don't like to stay on the same products for more than four months at a time. ¸..· ´¨¨)) -:¦:- ¸.·´ .·´¨¨)) ((¸¸.·´ ..·´ -:¦:- Karma -:¦:- ((¸¸.·´* http://loaves-n-fishes.com http://www.karma.awarenesshealth.com New to the group! Hi guys! I am new to the group and have lots to share. I am currently on day 11 of a juice fast and have not set a finish date. I juice fresh fruits in the morning..follow the master cleanser all day..then fresh veggies at nite. Also taking dr. christopher's herbs and psyllium. Have seen some gunk but it's been a little slow lately. Could share tons on my journey to sickness and my journey back.. look forward to chatting also. rob L Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2001 Report Share Posted September 15, 2001 Through your experience, what advice can you give to someone who is truly cleansing for the first time? My road to illness was totally diet related...carb fanatic, sugary weight gain shakes, overly enervating workouts, stress, the whole nine yards..about 30 years worth. Have been on the road to health for over a year and a half..I've overcome a systemic fungal infection...parasites..total dysbiosis...will be a raw foods vegan for life...am undertaking my first real cleanse now. Patience is the most difficult thing for me but a juice cleanse is the ultimate teacher. I think what's important is not to set a finish date in advance. Spiritually, I feel like I've been told to go until I know. I've already seen some of the gunk that's inside and don't want to cut it short like most do. Look forward to learning from you and others. Also, I am pursuing a diploma of Natural Hygiene as helping others learn about the causes of health will be a focus of my life! rob L Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2002 Report Share Posted April 29, 2002 Hello and welcome You will find alot of support here. I understand your stress in the begining fo this illness. God prayers to you.. Information most of the time, will help with the anxiety over this dragon. Here is alot of good information. The depression is something I understand too. Remember that this is a slow progressive illness. What tests have you had so far? I look at this as a personal challenge and a teaching expereince ( for both me and others) I have up and down days too I guess that I feel luck to be in todays medical world that there are ways to help with all this stuff. There are alot of treatments on the horizon and some now. I deal with treatment and the dragon by prayer and online support. My family isn't to bad either. (sometimes LOL) actually the best friend I have during this has been my dog. ( poodle) he cuddles me on days that I feel bad and loves me no matterwhat. Now is time for you to care about YOU. Your needs come first and that includes Laughter. IF you want to talk anytime mom0244@... God bless > hi, just joined yesterday. having a hard time dealing with this > disease. i'm confused about this illness and am looking for some type > of support. all suggestions about how one deals with this illness > would be very helpful. > i've been feeling very depressed and feel like my life is over before > it started! nothing really matters to me anymore. i shouldn't say > this because i have a ten year old son and a wife that i want to be > here for. > would like to hear from others that feel the same. thanks,izy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 29, 2002 Report Share Posted April 29, 2002 Hello and welcome You will find alot of support here. I understand your stress in the begining fo this illness. God prayers to you.. Information most of the time, will help with the anxiety over this dragon. Here is alot of good information. The depression is something I understand too. Remember that this is a slow progressive illness. What tests have you had so far? I look at this as a personal challenge and a teaching expereince ( for both me and others) I have up and down days too I guess that I feel luck to be in todays medical world that there are ways to help with all this stuff. There are alot of treatments on the horizon and some now. I deal with treatment and the dragon by prayer and online support. My family isn't to bad either. (sometimes LOL) actually the best friend I have during this has been my dog. ( poodle) he cuddles me on days that I feel bad and loves me no matterwhat. Now is time for you to care about YOU. Your needs come first and that includes Laughter. IF you want to talk anytime mom0244@... God bless > hi, just joined yesterday. having a hard time dealing with this > disease. i'm confused about this illness and am looking for some type > of support. all suggestions about how one deals with this illness > would be very helpful. > i've been feeling very depressed and feel like my life is over before > it started! nothing really matters to me anymore. i shouldn't say > this because i have a ten year old son and a wife that i want to be > here for. > would like to hear from others that feel the same. thanks,izy Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2002 Report Share Posted October 9, 2002 Marcy: I too was diagnosed with PBC only nine months ago. I am 50 and at age 48, I had to have triple bypass and was already showing slight symptoms. It went dowhill from there. I also have microscopic colitis, and suffer from pancreaitis. These darn autoimmune diseases are the pits. Still going strong, working full-time and fortunately for me I am the office manager for my family physician, so she is trying to help my specialist all she can to keep me going strong. I do have spells of feeling totally wasted like most who suffer from any liver disease, but my doctor lets me take provigil twice a day, one when I get up in the morning, along with a couple of ultratram to help the joint pain, and then about 5:00 another provigil and I do pretty good until bed time. Have had a couple of pancreaitis attacks and they are quite painful, but most of the time I just suffer discomfort from the fluid build up in my abdomen. My liver doc does not think I am yet to the stage where I am retaining fluid from the liver, but thinks it is from the colitis. However, I am only 5'1" with a thin body and a big belly. Just having to learn to live with that and I cannot say I like it. Hopefully there will come a time when they will drain some of the fluid. Keep a good attitude and be your own judge on what helps you feel better. It is extremely hard for me to follow any kind of diet, so I mostly just eat very light meals, soup, cereal, etc., but with the multiple gastro illnesses I suffer from some foods are better for the liver, but worse for the colon, so I just improvise and eat what I can. I, like you, would really like to hear from others that have suffered the BPH and how long we have before we cannot work, etc. I hope to just keep on with my life as is, but am quite anxious about what the future holds. I wish you lots of good luck and look forward to hearing from you. By the way, I am not 52 (of course a very young 52). Lots of Luck Carolyn D Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 9, 2002 Report Share Posted October 9, 2002 marcy welcome to the group.... i love your "contagious"humor...your letter made me feel good this morning .... take care karen s.carolina Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 10, 2002 Report Share Posted October 10, 2002 Marcy..... welcome to the group! You sound like my king of woman.... (but then all women are my kind of woman) I love a sense of humor..... If you can write to this site then you ain't dead and that is alwys a good sign... hugs jerry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Grace, It's scary, sorry you have to go through this. My 4.5 yr old just started seizures in March so this whole thing is new for me too. I can't offer you much except to say you've typed the right group, it's full of wonderful knowledgeable people. Hang in there. Barb [ ] New to the group! > Hello, > > I am new to this group so I am going to start off by telling you > about my situation. I have a daughter who is developmentally delayed > and began having seizures when she turned 12 yo. She is now 13. I > have never seen anyone have a seizure so you can imagine what shock > it was to me when I first saw her having one. All I could think is > that my baby was dying. She began having petit and grand mal > seizures. In a little over a year she's had three petit and three > grand mal seizures and they are months apart of each other. I just > find it very strange that she just began having them at this age. I > feel that something is causing them but I don't know what. She had > two EEGs done which came back abnormal so the neuro put her on > Trileptal. She began taking .75 mg once a day for four days > then .75mg twice a day, but when she began this dose, two weeks later > she had two seizures within 10 hours but these seizures were > different from the others, so the doctor put her back on just .75mg > once a day and told me to keep an eye on her and that if she began > having them again to put her back on .75mg twice a day. I can handle > the petit seizures, but It terrifies me to go in her room at night > and find her having a grand mal because of the convulsions. I'm > hoping that someone in this group can give me some advice on what to > do and how to deal with it. Thanks for listening. > > Grace > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2003 Report Share Posted October 6, 2003 Thanks Barb. Grace On Mon, 6 Oct 2003 01:19:33 -0600 " Barb Hunte " <gbhunte@...> writes: > Grace, > > It's scary, sorry you have to go through this. My 4.5 yr old just > started > seizures in March so this whole thing is new for me too. I can't > offer you > much except to say you've typed the right group, it's full of > wonderful > knowledgeable people. Hang in there. > > Barb > [ ] New to the group! > > > > Hello, > > > > I am new to this group so I am going to start off by telling you > > about my situation. I have a daughter who is developmentally > delayed > > and began having seizures when she turned 12 yo. She is now 13. > I > > have never seen anyone have a seizure so you can imagine what > shock > > it was to me when I first saw her having one. All I could think is > > that my baby was dying. She began having petit and grand mal > > seizures. In a little over a year she's had three petit and three > > grand mal seizures and they are months apart of each other. I > just > > find it very strange that she just began having them at this age. > I > > feel that something is causing them but I don't know what. She had > > two EEGs done which came back abnormal so the neuro put her on > > Trileptal. She began taking .75 mg once a day for four days > > then .75mg twice a day, but when she began this dose, two weeks > later > > she had two seizures within 10 hours but these seizures were > > different from the others, so the doctor put her back on just > .75mg > > once a day and told me to keep an eye on her and that if she began > > having them again to put her back on .75mg twice a day. I can > handle > > the petit seizures, but It terrifies me to go in her room at night > > and find her having a grand mal because of the convulsions. I'm > > hoping that someone in this group can give me some advice on what > to > > do and how to deal with it. Thanks for listening. > > > > Grace > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2004 Report Share Posted September 9, 2004 Hi Jeri Just wanted to say hello and welcome,...congradulations and best of luck with your lap band.We will look forward to hearing about your triumphs and your frustrations, and your new life here. Thanks for sharing Stay well Jeri Armistead <jerifromor@...> wrote: Hi, My name is Jeri. I'm very excited about getting the Lap-Band surgery. We got the loan and I can't believe how things are moving along. I have been trying for years to get help as i'm sure you all have. Now there is hope, the saying "when God closes a door, he opens a window" it never really struck me how true that is. I'm looking forward to having a new relationship with food. It should be an interesting ride. Jeri Do you ?New and Improved - 100MB free storage! __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 10, 2004 Report Share Posted September 10, 2004 Jeri, So glad to see you here. Are you having the surgery with Dr Aceves? When is your surgery date? I had my surgery August 21. I am going back in October for a fill. Good luck! Maggie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2006 Report Share Posted August 2, 2006 Welcome to the group , so glad you joined us. Please ask any questions you can think of - there are no stupid questions here - I have plenty of stupid answers...lol Best of luck with the rest of the evaluation and please let us know how it goes... Regards, Mike " Ears Hopin " P > > Hi everyone! I am new to this group and this is my first post. My > name is , I'm from NC, and I am 30 years old. I am married and > have a 5 yr old daughter. > > I went Monday for my CI evaluation and the dr. says it looks like I > am a good candidate for it. I go back this month on th 23rd for the > CT scan of my ears to see which would be better to implant. > > I was started losing my hearing at the age of 10 due to a severe case > of the chicken pox accompanied by a high fever. I had them really > bad in my throat and ears. I started noticing the tinnitus around > the age of 10, which sounded like loud crickets chirping. I had my > first hearing test at age 12 at school, in which I failed. This was > the first time my mother realized I had hearing loss. Being the age > I was, she thought I just wasn't paying attention or had my nose > stuck too far in the t.v.! So, I got hearing aids (BTE's) then. The > aids made everything louder, but not clearer and I still couldn't > understand speech unless I was looking at someone and still couldn't > hear high pitches. When I was 15 yrs. old. in 1990, my mom took me > to Duke Univesity in Durham, NC to see if anything else could be done > then. After spending two days there and much testing, they told us > there was nothing more they could do for me since the nerves were > already damaged, and the aids were my best alternative. Just this > year I started hearing more and more about CI's and started reading > testimonials about them. I called Carolina Ear and Hearing Center in > Raleigh, NC after reading about them in one woman's story. The > doctor really eased my nervousness about everything. I am so excited > about it, but still just don't know what to fully expect yet. > > That's my story. Hope to talk with some of you soon! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2006 Report Share Posted August 2, 2006 Hi , Welcome to the group! I'm pretty new too. We'll try to answer any questions you may have. I was implanted in 2001 with the Advanced Bionics CII. Having a CI is great. You'll see lots of posts about things we can hear now.like my wife running the mixer in the kitchen.cookies in process! Doug _____ From: [mailto: ] On Behalf Of Sent: Wednesday, August 02, 2006 1:25 PM Subject: New to the group! Hi everyone! I am new to this group and this is my first post. My name is , I'm from NC, and I am 30 years old. I am married and have a 5 yr old daughter. I went Monday for my CI evaluation and the dr. says it looks like I am a good candidate for it. I go back this month on th 23rd for the CT scan of my ears to see which would be better to implant. I was started losing my hearing at the age of 10 due to a severe case of the chicken pox accompanied by a high fever. I had them really bad in my throat and ears. I started noticing the tinnitus around the age of 10, which sounded like loud crickets chirping. I had my first hearing test at age 12 at school, in which I failed. This was the first time my mother realized I had hearing loss. Being the age I was, she thought I just wasn't paying attention or had my nose stuck too far in the t.v.! So, I got hearing aids (BTE's) then. The aids made everything louder, but not clearer and I still couldn't understand speech unless I was looking at someone and still couldn't hear high pitches. When I was 15 yrs. old. in 1990, my mom took me to Duke Univesity in Durham, NC to see if anything else could be done then. After spending two days there and much testing, they told us there was nothing more they could do for me since the nerves were already damaged, and the aids were my best alternative. Just this year I started hearing more and more about CI's and started reading testimonials about them. I called Carolina Ear and Hearing Center in Raleigh, NC after reading about them in one woman's story. The doctor really eased my nervousness about everything. I am so excited about it, but still just don't know what to fully expect yet. That's my story. Hope to talk with some of you soon! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 3, 2006 Report Share Posted August 3, 2006 Welcome, of NC! Good luck in your journey back to hearing. As you read more here and on the website, you will see that everyone's result is different. Almost everyone gets sound. Some get voice distinction from the first day of activation, and some (like me) take months with lots of practice before they can truely say they are glad they did it. Most (I say, most!) say that the CI has brought them much improvement in their hearing over what they had. I have met people who seem not to be hearing at all with their CI and many, many more who seem to be hearing as well as any hearing person I know. I'm sure your audi and surgeon will tell you the same. Just know that, chances are, that you WILL have a good outcome. Feel free to ask any and all question here. Good luck! ) Jackie Implanted - right ear - Oct.2002 - Nucleus 24/3G Reimplanted - right ear - Jan.2005 - Nucleus 24C/3G Implanted - left ear - Sept.2005 - Nucleus-Freedom Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2006 Report Share Posted August 18, 2006 welcome to the group, actually, you brought up an interesting question about the likelyhood of your children having it... I kinda hope when I have kids one of them does since but I doubt it since I wasn't born with it in the first place. I just think it's such a unique feature to have. I made a lot of friends with my eyes since I'm shy and some people would approach me first to ask about them. If you're interested http://health.ph./group/heterochromia/photos/browse/4ba 6 Those are mine. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2006 Report Share Posted August 18, 2006 Thank you! The different coloured eyes can indeed be an ice-breaker sometimes. It's also meant that I pay particular attention to everyone's eyes - does anyone else do that? I mean I'm sure I could recognise anyone I've already met just by their eyes. I thought it was normal until I realised that my husband doesn't even know what colour of eyes any of our friends have (although he does know his parents and sisters' colours. I suppose having unusual eyes makes you pay more attention to tother people's. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2006 Report Share Posted August 18, 2006 Not sure about that.... I have had heterochromia since borths (over 51 years ago) and I rarely notice others' eye colours unless they are striking. Possibly, it is a gender thing that females notice and pay attention to eye colour more than males do. This would probably make a good poll question... Do females pay attention to eye colour more than males do? > > Thank you! The different coloured eyes can indeed be an ice- breaker > sometimes. It's also meant that I pay particular attention to > everyone's eyes - does anyone else do that? I mean I'm sure I could > recognise anyone I've already met just by their eyes. I thought it > was normal until I realised that my husband doesn't even know what > colour of eyes any of our friends have (although he does know his > parents and sisters' colours. I suppose having unusual eyes makes you > pay more attention to tother people's. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2006 Report Share Posted August 18, 2006 So, I created the poll at: heterochromia/surveys?id=2037881 Go ahead and vote... > > > > Thank you! The different coloured eyes can indeed be an ice- > breaker > > sometimes. It's also meant that I pay particular attention to > > everyone's eyes - does anyone else do that? I mean I'm sure I > could > > recognise anyone I've already met just by their eyes. I thought it > > was normal until I realised that my husband doesn't even know what > > colour of eyes any of our friends have (although he does know his > > parents and sisters' colours. I suppose having unusual eyes makes > you > > pay more attention to tother people's. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2006 Report Share Posted August 19, 2006 > > Not sure about that.... > > I have had heterochromia since borths (over 51 years ago) and I > rarely notice others' eye colours unless they are striking. > > Possibly, it is a gender thing that females notice and pay attention > to eye colour more than males do. > > This would probably make a good poll question... > > Do females pay attention to eye colour more than males do? > You might be right! Maybe women do pay more attention to such details... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 22, 2006 Report Share Posted November 22, 2006 Hi , How's you CI quest going? Doug CII 2001 _____ From: [mailto: ] On Behalf Of Sent: Wednesday, August 02, 2006 1:25 PM Subject: New to the group! Hi everyone! I am new to this group and this is my first post. My name is , I'm from NC, and I am 30 years old. I am married and have a 5 yr old daughter. I went Monday for my CI evaluation and the dr. says it looks like I am a good candidate for it. I go back this month on th 23rd for the CT scan of my ears to see which would be better to implant. I was started losing my hearing at the age of 10 due to a severe case of the chicken pox accompanied by a high fever. I had them really bad in my throat and ears. I started noticing the tinnitus around the age of 10, which sounded like loud crickets chirping. I had my first hearing test at age 12 at school, in which I failed. This was the first time my mother realized I had hearing loss. Being the age I was, she thought I just wasn't paying attention or had my nose stuck too far in the t.v.! So, I got hearing aids (BTE's) then. The aids made everything louder, but not clearer and I still couldn't understand speech unless I was looking at someone and still couldn't hear high pitches. When I was 15 yrs. old. in 1990, my mom took me to Duke Univesity in Durham, NC to see if anything else could be done then. After spending two days there and much testing, they told us there was nothing more they could do for me since the nerves were already damaged, and the aids were my best alternative. Just this year I started hearing more and more about CI's and started reading testimonials about them. I called Carolina Ear and Hearing Center in Raleigh, NC after reading about them in one woman's story. The doctor really eased my nervousness about everything. I am so excited about it, but still just don't know what to fully expect yet. That's my story. Hope to talk with some of you soon! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 23, 2007 Report Share Posted September 23, 2007 Hi Grace, Welcome to the group! The best way to get started is to read the information that you were sent when you joined the group. The article, " How to Successfully Overcome Candida " will tell you step by step how to work your way into this program. There is also a wealth of information in the Files section (in the left menu) of our group website. There are a couple of files with articles that will be of particular interest to you. They are, " Candida Treatments for Babies & Children " and " Candida's Connection to Autism, Cancer & Diabetes. " We also have a " Recipes " file with lots of recipes. Happy reading! jackie > > hi everyone! > I'm so glad to find this group specifically on treating candidiasis. > I'm trying to get into the candida treatment for my son who is in the > autistic spectrum. After watching Oprah last tuesday with > McCarthy, I was so inspired to really dig deeper in helping my son > (4)overcome the nasty yeast problems. > Any recomendations on a great protocol. Also if anybody would like to > share some great gfcf yeast free recipes that they've tried at home > with their kids will be much appreciated.... > Any other input or comment is very much appreciated... > > TIA, > Grace > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 24, 2007 Report Share Posted September 24, 2007 Grace, go low carb and don't listen to people who advocate any high- carb foods, and you'll deter it better. I realize you'll have a hard time trying to feed an autistic kid good food, but there you have it; you might have to starve him just a bit until it tastes better You can't do it without low-carbing. Duncan > > hi everyone! > > I'm so glad to have find a group specifically for treating the yeast > beast. I have been very inspired to really concentrate in addressing > my son's yeast who has autism, he's 4. I always have a hard time with > the diet and I always get confuse, some say avoid fruits and others > says it's okay to have the berries(blueberries, raspberries etc.). Is > it really very important to avoid fruit altogether or just limit it? > I would also like to hear from others about their yeast protocol that > is working and is efficient in targeting the yeast. > Please also share any gfcf yeast free recipes that they have tried at > home with their kids. Diet and thinking of what other food I can serve > is the hardest part of the deal so I would appreciate any tips, advice > and input.... > > TIA, > Grace > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 > > Hi, > My name is Amy and I'm excited about joining this group because, as I > am sure most of you have experienced, I am sick and tired of feeling > sick and tired. > I have wonderful M.D. who is also board certified in Environmental > Medicine. He has gone through the Candida protocal himself and I have > just started mine on April 1. > I am mostly looking for solid food and lifestyle answers. The internet > is too contradicting. Some sites say " soy is a yes " others say " soy is > a no " ..and on and on it goes. > I am hoping I can get some real advice from real people who have and > still are working on this type of " lifestyle " I also look forward to > helping others if I can. > My first question... Can you eat popcorn? I pop my own in a skillet > with coconut oil and use real butter. Of course I've read yes and no, > that the body breaks it down into a sugar. ==>Hi Amy. Welcome to our wonderful group. The best source of information about the many anti-nutrients soy contains, and how it damages the body is the Weston A. Price Foundation, which is a non- profit organization: www.westonaprice.org Also Dr. Mercola writes about it: www.mercola.com Traditional peoples and our ancestors " knew " soy was only fit for human consumption if it is was fermented for very long periods of time. Popcorn is not good for candida sufferers; it turns into sugar, like you write, since it is high in starch and sugars. That's where food processors get glucose they add to many foods. It is also one of the most difficult foods to digest (ever see corn kernels in your stools?). LOL! Cheers, Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 > My name is Amy and I'm excited about joining this group because, Hi Any and welcome to the group. > The internet is too contradicting. Some sites say " soy is a yes " others say " soy is > a no " ..and on and on it goes. Yes, I know. There is conflicting information about almost everything. But this is also why Bee's program is so good. You just stick to EXACTLY what the program suggests. It works best if it's followed as precisely as possible. It takes away some of that confusion and contradiction. Like if you want to do this, do this fully without too much interference of contradicting views. When in doubt I usually try to listen to my own body and what it's communicating. That is not always easy though when taking healing reactions into account, but it seems to be more convincing than online info can be. Btw, soy is a no no here. You'll find articles about soy in the files archives. > My first question... Can you eat popcorn? I pop my own in a skillet > with coconut oil and use real butter. You will find answers to most of your questions in Bee's basic getting started article. I can't recommend reading it enough. It's an amazing article with all information you'll ever need in one place. I have it printed out and go back to refresh my memory often on a weekly basis. You can find it under: Files Bee's Candida Articles and How to Get Started " How to Successfully overcome Candida " The short answer is, in my understanding, that pocporn is not only a grain (all grains need to be eliminated until candida is under control) it is actually in the group of foods containing mycotoxins " (a toxin produced by a fungus), especially found in corn and wheat " making it even worse for us. So you'll need to wait until you are well before eating it again and then only in very small amounts. Good luck and welcome again! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 Thank you for the warm greeting and helpful advice. I have a lot of reading to do Amy Quote Link to comment Share on other sites More sharing options...
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