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      Frequently Asked Questions About Celiac Disease   04/24/2018

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to Celiac.com's FREE weekly eNewsletter   What is Celiac Disease and the Gluten-Free Diet? What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease?  Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes
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precious831

Looking For SCD'ers Here, Need Support

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Hi, I posted before I'm grain-free and now I'm trying to do SCD, I would like to connect with those that are also on the same path. I know there was at least one person here. Let me know, thanks!

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Hi, I posted before I'm grain-free and now I'm trying to do SCD, I would like to connect with those that are also on the same path. I know there was at least one person here. Let me know, thanks!

This thread is a couple of years old, but may still be relevant:

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Former SCD now recovered to where I can do some grain carbohydrates.

Eating more (good) fat to act as a slow burning fuel so you don't crash and burn as often, as well as the protein and vegetables, is the trick to this.

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Hi there--you are not alone. I know there are many others here like us. I'm 99% on a grain free diet. I participated with AliBi's thread for 10 months or so. I only eat some rice when nothing else is available. I do eat summer squash and now and then a little winter squash. I can't handle sweets of any kind except stevia--so my diet is actually more restricted than a strict scd that doesn't use stevia but does eat fruit and honey. I am allergic to all nuts too--so for pancakes I use ground up sunflower seeds and pumpkin seeds mixed with shredded zucchini. I eat a lot of vegetables and some meat. No eggs either since I am allergic to them too unfortunately... At least my boyfriend says I look great and overall I feel good too except for this darn condition of flaky ears and part of my nethers. It gets worse if I eat any fruit it seems, even lemons--not to speak of grains and anything really starchy. Aach! Fortunately the 24 hour yogurt works quite well for me and I enjoy making soups and stir frys and such and greatly enjoy using fresh spices so there are things I can eat...

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Former SCD now recovered to where I can do some grain carbohydrates.

Eating more (good) fat to act as a slow burning fuel so you don't crash and burn as often, as well as the protein and vegetables, is the trick to this.

How long were you on the SCD before you started to improve?

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This thread is a couple of years old, but may still be relevant:

Thanks I'll check it out!

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Hi there--you are not alone. I know there are many others here like us. I'm 99% on a grain free diet. I participated with AliBi's thread for 10 months or so. I only eat some rice when nothing else is available. I do eat summer squash and now and then a little winter squash. I can't handle sweets of any kind except stevia--so my diet is actually more restricted than a strict scd that doesn't use stevia but does eat fruit and honey. I am allergic to all nuts too--so for pancakes I use ground up sunflower seeds and pumpkin seeds mixed with shredded zucchini. I eat a lot of vegetables and some meat. No eggs either since I am allergic to them too unfortunately... At least my boyfriend says I look great and overall I feel good too except for this darn condition of flaky ears and part of my nethers. It gets worse if I eat any fruit it seems, even lemons--not to speak of grains and anything really starchy. Aach! Fortunately the 24 hour yogurt works quite well for me and I enjoy making soups and stir frys and such and greatly enjoy using fresh spices so there are things I can eat...

I'm just starting and I'm a little confused about the legal foods. I can eat pretty much anything on the legal list. I've only used honey, though I have stevia, I haven't used that on baking.

What stage are you? You must be advanced if you're able to use sunflower and pumpkin seeds...is that SCD legal?

I miss starchy foods and I've cheated, lol.

Now I want to try SCD on my 3 yr old and her pediatric GI is very optimistic about this diet but I'm just not sure what she will eat. She's allergic to a lot of meats and other things, plus she's still on Alimentum RTF liquid which has tapioca starch and carageenan and those are not SCD legal. She can't do dairy, and I thought the yogurt is for later stages, especially because she's intolerant to dairy too. Confused about the yogurt part, when to introduce it. My DD needs the formula because her diet is so limited. Anyway she's getting (Company Name Removed - They Spammed This Forum and are Banned) and a comprehensive stool test from Great Lakes Labs and then the GI and I will decide our next action from there.

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I looked but I'm not sure - what does SCD stand for?

Thanks.

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There were/are a lot of things I did and do that aren't completely in line with scd mainly due to the fact I have so many food intolerances.

Stevia is not really part of their diet. It is a member of the sunflower family actually. Why that should be a problem I never really figured out. There was a big scare about stevia years ago that was completely unfounded--mainly put out there by the artifcial sweetner companies (whose products really are not safe). Due to my ongoing difficulty with sugars its the only sweet I can tolerate and I refuse to give it up. The diet is supposed to help a person, not be something one slavishly follows to one's detriment.

If you and your daughter can tolerate the honey, however, so much the better!

The low carb muffins and pancakes etc. the scd'ers use which are made using almond meal did not work for me since I am severely allergic to almonds as well as other nuts--and eggs. I now can tolerate thoroughly rinsed walnuts say once every week but that is all. Thus I use the sunflower seeds and yogurt rather than eat meat for every meal...I think however its possible the almond meal is nicer. Especially if you can add an egg or two. If not, then you need to add ground up flax seed and think of using other non scd stuff like xanthum gum to hold your concoction together.

And yes, CC can be a problem for many here. So I suggest you make your own almond meal or whatever--rinse the almonds well and dry them out before grinding them. Its actually cost effective and in many ways more convenient than trying to chase down truly gluten-free almond meal (or sunflower and pumpkin seed meal in my case...) that hasn't been CC'd.

The yogurt as said works out well for me since I am not casein intolerant.. I am otherwise intolerant of all dairy (except butter) --but fortunately its just the lactose that really is the problem -- though I don't tolerate cheeses or kefir either.

I make the yogurt by using an improvised double boiler ( a large double handled cooking pot set on top of another yet larger double handled cooking pot with a small metal base underneath to separate the pots. I used canning lids as an improvised base for a long time. I now have a round shallow stainless steel grater I use since the canning lids were starting to rust. I scald (to 185 degrees F.) the milk and then cool it down (to 90 t o 100 degrees F) and then mix in 2 or 3 tablespoons of fresh yogurt in it. I then set the pot on a warm heating pad with a towel on top for 24 hours. By fermenting it that long or a little longer it gets rid of all the lactose. I only use organic milk to avoid the chemicals and antibiotics they put into the cows which thus also gets into the cows milk. I suggest you also consider this when it comes to meats too.

There is also an acidophilous fermented cabbage drink people make --especially used by those who are casein intolerant that is also listed on AliBi's scd thread. I never did try it yet though I am still interested. You can probably just google it on the site for directions. There is a wealth of information on it--including many recipes using zucchini.

Good luck Hope some of this helps.

Bea

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There were/are a lot of things I did and do that aren't completely in line with scd mainly due to the fact I have so many food intolerances.

Stevia is not really part of their diet. It is a member of the sunflower family actually. Why that should be a problem I never really figured out. There was a big scare about stevia years ago that was completely unfounded--mainly put out there by the artifcial sweetner companies (whose products really are not safe). Due to my ongoing difficulty with sugars its the only sweet I can tolerate and I refuse to give it up. The diet is supposed to help a person, not be something one slavishly follows to one's detriment.

If you and your daughter can tolerate the honey, however, so much the better!

The low carb muffins and pancakes etc. the scd'ers use which are made using almond meal did not work for me since I am severely allergic to almonds as well as other nuts--and eggs. I now can tolerate thoroughly rinsed walnuts say once every week but that is all. Thus I use the sunflower seeds and yogurt rather than eat meat for every meal...I think however its possible the almond meal is nicer. Especially if you can add an egg or two. If not, then you need to add ground up flax seed and think of using other non scd stuff like xanthum gum to hold your concoction together.

And yes, CC can be a problem for many here. So I suggest you make your own almond meal or whatever--rinse the almonds well and dry them out before grinding them. Its actually cost effective and in many ways more convenient than trying to chase down truly gluten-free almond meal (or sunflower and pumpkin seed meal in my case...) that hasn't been CC'd.

The yogurt as said works out well for me since I am not casein intolerant.. I am otherwise intolerant of all dairy (except butter) --but fortunately its just the lactose that really is the problem -- though I don't tolerate cheeses or kefir either.

I make the yogurt by using an improvised double boiler ( a large double handled cooking pot set on top of another yet larger double handled cooking pot with a small metal base underneath to separate the pots. I used canning lids as an improvised base for a long time. I now have a round shallow stainless steel grater I use since the canning lids were starting to rust. I scald (to 185 degrees F.) the milk and then cool it down (to 90 t o 100 degrees F) and then mix in 2 or 3 tablespoons of fresh yogurt in it. I then set the pot on a warm heating pad with a towel on top for 24 hours. By fermenting it that long or a little longer it gets rid of all the lactose. I only use organic milk to avoid the chemicals and antibiotics they put into the cows which thus also gets into the cows milk. I suggest you also consider this when it comes to meats too.

There is also an acidophilous fermented cabbage drink people make --especially used by those who are casein intolerant that is also listed on AliBi's scd thread. I never did try it yet though I am still interested. You can probably just google it on the site for directions. There is a wealth of information on it--including many recipes using zucchini.

Good luck Hope some of this helps.

Bea

Thanks, I buy the almond flour from an SCD website and no problems with them, it's great! I know about that acidophilus drink, you mean kombucha? I don't like that at all, I don't like kimchi either. I've not tried to do anything with kefir grains yet but I'm thinking about it. I grew up w/ my dad making those fermented vegetable and he always tried to get me to eat them, never liked them.

Eventually I'll start grinding my own almonds into meal and/or flour.

Well it's funny you said that because I've looked a the other support groups and even in the book it's so strict. That's why I was like holy cow I don't know how I'm gonna do this with my daughter, she's 3 and her diet is already so limited. You know what though, sticking with the diet makes a whole world of difference for me! First of all I no longer crave sugar like I used to, that itself is amazing! LOL, I used to be a sugar addict, I ate tons of candy, drank soda, I mean name it. I did go through a really bad withdrawal with the sugar but now I'm fine w/out it. And like I said I'm no longer pre-diabetic and also my blood pressure is now normal, not high like it was before. The dramatic improvements were my GI symptoms.

I used to make coconut yogurt, I bought a dairy-free yogurt starter, expensive but it was great yogurt. I have a yogurt maker. However I kind of want to do the goat milk too as suggested and before I only cured the yogurt for 12 hrs, this time it has to be 24 hrs. I react to the casein, this is a huge problem for me, a real bummer.

I am a real health nut so I make most of the foods we eat from scratch, I only buy organic meats, veggies, everything so don't have to worry about that. I take a bunch of supplements they seem to be ok with the SCD, they don't contain any of the forbidden stuff.

Where do you get your almonds? I need one that is certified gluten-free. My sis bought me one fr Trader Joes and it says it's processed in shared equipment, I don't even want to take a risk with that. The ones at Whole Foods are the same, processed equipment.

Thanks!

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I looked but I'm not sure - what does SCD stand for?

Thanks.

Hi, SCD stands for the Specific Carbohydrate Diet. There is a wonderful book called "Breaking the Vicious Cycle" that details it but you can also find a lot of info online.

HTH

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Thanks, I buy the almond flour from an SCD website and no problems with them, it's great! I know about that acidophilus drink, you mean kombucha? I don't like that at all, I don't like kimchi either. I've not tried to do anything with kefir grains yet but I'm thinking about it. I grew up w/ my dad making those fermented vegetable and he always tried to get me to eat them, never liked them.

Eventually I'll start grinding my own almonds into meal and/or flour.

Well it's funny you said that because I've looked a the other support groups and even in the book it's so strict. That's why I was like holy cow I don't know how I'm gonna do this with my daughter, she's 3 and her diet is already so limited. You know what though, sticking with the diet makes a whole world of difference for me! First of all I no longer crave sugar like I used to, that itself is amazing! LOL, I used to be a sugar addict, I ate tons of candy, drank soda, I mean name it. I did go through a really bad withdrawal with the sugar but now I'm fine w/out it. And like I said I'm no longer pre-diabetic and also my blood pressure is now normal, not high like it was before. The dramatic improvements were my GI symptoms.

I used to make coconut yogurt, I bought a dairy-free yogurt starter, expensive but it was great yogurt. I have a yogurt maker. However I kind of want to do the goat milk too as suggested and before I only cured the yogurt for 12 hrs, this time it has to be 24 hrs. I react to the casein, this is a huge problem for me, a real bummer.

I am a real health nut so I make most of the foods we eat from scratch, I only buy organic meats, veggies, everything so don't have to worry about that. I take a bunch of supplements they seem to be ok with the SCD, they don't contain any of the forbidden stuff.

Where do you get your almonds? I need one that is certified gluten-free. My sis bought me one fr Trader Joes and it says it's processed in shared equipment, I don't even want to take a risk with that. The ones at Whole Foods are the same, processed equipment.

Thanks!

I am so glad to hear the scd diet is helping you so much. Bravo for you! Given your family history with your dad's concoctions, you probably aren't the only ones in your genetic lineup to have this and similar conditions. though honestly the standard american diet is not very good for anyone...and does create cravings for carbs and sugars.

As far as being strict with the scd diet, well I think it all depends on how well the diet works for you. If it does, fine. If there are glitches you need to adjust. The book was written for this woman's daughter in mind who had a specific intestinal condition which is not the same as celiac.

The TJ bags of raw almonds my bf has says its made on same equipment as other tree nuts, not wheat etc. I'd still wash them though. I don't know more than that since I am allergic to all nuts as said...and haven't really looked into it. The raw sunflower seeds and raw pumpkin seeds from TJs seem fine. Nevertheless I would check out sources on the internet if you have any problems with TJ's or WF. I am betting you could order a bag from a grower if needs be. You could also check out the source of the scd almond meal perhaps.

I would be interested in your coconut yogurt recipe for a friend of mine who also has celiac and is going off milk.

If you are truly casein intolerant then any milk is probably not so great. Though I do recall goats milk casein being a little different so you never know. For me actually I am More allergic to goats milk so go figure. I also seem to be allergic to goat and sheep meat...as well as tuna.

With us folks who have celiac or severe gluten intolerance the problem is usually having too many "holes" in the intestines causing leaky gut syndrome, not that there aren't enough. We actually in my opinion sometimes need these so called "gucky substances" to help our intestines heal if we have just been "glutened" (such as marshmallow root and/or slippery elm--both strictly non scd by the way!!). For celiacs our auto immune reacts to gluten; it attacks the villi and basically either flatten or destroys them which then causes inflammation which makes the whole thing worse. Marshmallow root and slippery elm take down the inflammation and soothe the intestines. Once healed enough one can go off them. The gluten attack and resultant flattened villi and inflammation creates some scar tissue yes but overall creates too much permeability in the intestinal membrane. This then allows undigested proteins into the blood stream which our bodies then treat as foreign invaders, creating inflammation. This then creates toxicity and blockages in the liver and the lymphatic system. When this happens I get out my trusty herbs like dandelion root and cleavers to the rescue as well as marshmallow root, acidophilous and a variety of other things.

Oh I am rambling. Sorry.

Meanwhile i am very glad you are finding things that are working for you and your daughter.

For myself I am an inveterate inquisitive and doubter of all things truly fixed. I like structure, but am inclined to play with it to see what is real or not and what does or does not work for me.

I thus combine things I learned from scd with the paleo diet and my own experience and those of others I have observed, which can improve and change over time...

Bea

It also creates and environment where it is very difficult to absorb basic oil soluble nutrients like vitamins b, d, a and e and the like as well as most minerals. B vitamin absorption also becomes difficult I think in part due to the liver being so overwhelmed--which is why I take co-enzyme B vitamins since they absorb into the blood stream right away (on an empty stomach), thus by passing the need to go through the liver.

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I am so glad to hear the scd diet is helping you so much. Bravo for you! Given your family history with your dad's concoctions, you probably aren't the only ones in your genetic lineup to have this and similar conditions. though honestly the standard american diet is not very good for anyone...and does create cravings for carbs and sugars.

As far as being strict with the scd diet, well I think it all depends on how well the diet works for you. If it does, fine. If there are glitches you need to adjust. The book was written for this woman's daughter in mind who had a specific intestinal condition which is not the same as celiac.

The TJ bags of raw almonds my bf has says its made on same equipment as other tree nuts, not wheat etc. I'd still wash them though. I don't know more than that since I am allergic to all nuts as said...and haven't really looked into it. The raw sunflower seeds and raw pumpkin seeds from TJs seem fine. Nevertheless I would check out sources on the internet if you have any problems with TJ's or WF. I am betting you could order a bag from a grower if needs be. You could also check out the source of the scd almond meal perhaps.

I would be interested in your coconut yogurt recipe for a friend of mine who also has celiac and is going off milk.

If you are truly casein intolerant then any milk is probably not so great. Though I do recall goats milk casein being a little different so you never know. For me actually I am More allergic to goats milk so go figure. I also seem to be allergic to goat and sheep meat...as well as tuna.

With us folks who have celiac or severe gluten intolerance the problem is usually having too many "holes" in the intestines causing leaky gut syndrome, not that there aren't enough. We actually in my opinion sometimes need these so called "gucky substances" to help our intestines heal if we have just been "glutened" (such as marshmallow root and/or slippery elm--both strictly non scd by the way!!). For celiacs our auto immune reacts to gluten; it attacks the villi and basically either flatten or destroys them which then causes inflammation which makes the whole thing worse. Marshmallow root and slippery elm take down the inflammation and soothe the intestines. Once healed enough one can go off them. The gluten attack and resultant flattened villi and inflammation creates some scar tissue yes but overall creates too much permeability in the intestinal membrane. This then allows undigested proteins into the blood stream which our bodies then treat as foreign invaders, creating inflammation. This then creates toxicity and blockages in the liver and the lymphatic system. When this happens I get out my trusty herbs like dandelion root and cleavers to the rescue as well as marshmallow root, acidophilous and a variety of other things.

Oh I am rambling. Sorry.

Meanwhile i am very glad you are finding things that are working for you and your daughter.

For myself I am an inveterate inquisitive and doubter of all things truly fixed. I like structure, but am inclined to play with it to see what is real or not and what does or does not work for me.

I thus combine things I learned from scd with the paleo diet and my own experience and those of others I have observed, which can improve and change over time...

Bea

It also creates and environment where it is very difficult to absorb basic oil soluble nutrients like vitamins b, d, a and e and the like as well as most minerals. B vitamin absorption also becomes difficult I think in part due to the liver being so overwhelmed--which is why I take co-enzyme B vitamins since they absorb into the blood stream right away (on an empty stomach), thus by passing the need to go through the liver.

Thanks for all the info, I'll look for the coconut yogurt, it's been a while since I made it. I actually got it off someone's site so it's not really my recipe. It was really easy to make.

I'm changing GI drs because the last one is no help really,we disagree on a lot of stuff. He said I might have "ulcerative colitis" he did the colonoscopy and wants to do it again to make sure. I just got it done and I'm not about to go get it done again! I hope the new GI is better.

I don't know yet about SCD and my DD, like I said she hasn't tried it yet, it's just me doing it.

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A very sensitive celiac I know buys her nuts on-line from either anuts.com or nutsonline.com

I have yet to try these, and I believe they are unshelled (?), but she seems to have success with these ones. :)

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A very sensitive celiac I know buys her nuts on-line from either anuts.com or nutsonline.com

I have yet to try these, and I believe they are unshelled (?), but she seems to have success with these ones. :)

Thanks, one of them sounds familiar and I have it bookmarked.

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I feel good too except for this darn condition of flaky ears and part of my nethers. It gets worse if I eat any fruit it seems, even lemons--not to speak of grains and anything really starchy.

This sounds almost entirely like a yeast infection, have you been tested?

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This sounds almost entirely like a yeast infection, have you been tested?

I have been tested though its been a while since I was. Supposedly I don't have candida overgrowth. Its hard to believe since I also get gunk on my tongue in the morning when I have eaten an offending item. I thus have treated myself for fungal infection using herbs from time to time as well as topical creams. I was treated with nystatin years ago by a rather decent AMA doc. down in San Diego (though I also went on a "cave man" diet at the time). And also lefenuron more recently--which helped my tongue but did not do the complete thing with my ears etc.

However even more recently I have found vitamin C is also a culprit.

Many moons ago a naturopath told me I was allergic to fructose--he did muscle testing using vials of various things... which of course I did not want to believe. I really should have listened to him. I did on other items, but I thought the fruit thing was going too far. I went on eating fruit for a long time but eventually it seems it may have caught up. So... am thinking it may be more of an allergy to all fruit and vit. C with some fungal overtones since sugars are a definite no too.

Some years ago I reacted badly to carrots so I avoid that family too. It is a true allergy with welts (if I eat them often enough) plus more commonly causes mental confusion and depression.

I should go on a complete elimination diet (i.e., no food for five days before reintroducing foods one at a time every other day) but hate to do that due to weak kidneys and a bad experience in that regard years ago. So I've just been doing trials by avoiding and keeping my diet simple and then reintroduce what I think may be the offending element. Early last week I went without lemons (as well as avoiding the sugars and fruit and starchy stuff) for instance and then reintroduced a lemon and the flakiness reappeared in spades. I thought lemons would be OK but this does not bode well for that thought...

Am also avoiding tomatoes and potatoes--since I could also have an allergy to the nightshade family--like my dad did. If so, I might need to avoid peppers too though I hate to... Am still playing with that possibility. I had peppers in some stew I made last night. I had my bf add in his tomatoes separately. I got some flakiness, though it could also be the fact I had a little brown rice yesterday. I should avoid both and reintroduce one item at a time later on.

What a bother, but having this condition could otherwise become serious since it degrades my skin in places that could get bacterial infections.

At least I am not allergic to pollen like some members of my family.

Another naturopath tested me a few years ago and told me I have difficulty absorbing Vit. B1. So I take co-enzyme B vitamins--which have helped a lot since, within two weeks, the con-enzyme B's stopped my heart from racing etc.

Despite all, my body seems to manufacture plenty of vit. C from all the veggies I eat... Just makes for a less than inspiring diet at times... Thank heavens for fresh spices and herbs--and a good ability to improvise--like with the sunflower seeds and zucchini.

I saw a regular AMA doc about a year ago concerning my ears and he gave me antibiotics that really knocked me out and made me quite ill last Fall. He seemed to have a nice personality but the effect of his treatment was disastrous.

I have had very bad luck with the AMA and at this point overall just try to stay away from them unless I get a kidney infection that needs antibiotics--which fortunately at this point rarely happens. Usually if my kidneys act up I successfully treat them with herbs and diet...which is what I have been doing successfully for years.

The last time they acted up badly was when I first went off all trace gluten and got CC several times in the spring of 2008. I contracted a bacterial infection that went into my lungs and then progressed to my kidneys. I seem to be one of those celiacs that gets inflammation in my respiratory system and kidneys from gluten if it happens often enough. My herbs helped somewhat but just couldn't get rid of the infection entirely. So yes then the antibiotics were a great help and saved me from crossing over in an untimely fashion...

I have been told I should have a regular care from a doctor, but I have yet to find one that really can understand my condition--or even wants to. I have at various times been called "too sensitive" even by that naturopath who called himself a health detective and gave me stuff that had gluten in it to detox. Go figure! This was after I told him I might have celiac. Unfortunately I didn't realize that the things he was giving me were making me ill until several months passed. He ended up not liking me I was told. Well, I didn't particularly like what he did to me although some of the lab tests he had done were helpful and I am grateful at least for that since he was the one that discovered I am low on B1.

So over the years I have gleaned what I could from various healing professionals. I now as said just avoid them in general when I can... and have become my own best doctor and overall am in great condition--whereas the opposite was the case when I was younger. I am experiencing the blessing of having a very healthy and vital beginning of my sixties. I just have this flakiness that at this point comes and goes. That is good news since it seems I will be able to treat it by learning what I am allergic to and avoiding the offending items. Sometimes this is what we have to do--heal ourselves in spite of the limited medical system out there when it comes to celiac, sensitivities, and allergies...

Bea

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Best of luck with the peppers issue, losing those too would certainly be rough. I mentioned yeast infection largely because I was experiencing the same flaky ear thing along with around the corners of my nose, my elbows, knee caps and bottom of my feet. I treated it for some time with miconazole and initially experienced a severe herxheimer reaction most markedly in my ears. I think that reaction is most noticeable there because of the decreased circulation of the ear which was slightly helped out by frequent massage/rubbing/stretching of the cartilage. Unfortunately even when the severity of it started to diminish I ended up right back where I started once I discontinued use of the fungicides. The flare-ups ended up being directly linked to days of high carbohydrate consumption. So far I'm on week 2 of that "cave man" diet and even without the fungicides the severity of the flaking is greatly diminishing.

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Best of luck with the peppers issue, losing those too would certainly be rough. I mentioned yeast infection largely because I was experiencing the same flaky ear thing along with around the corners of my nose, my elbows, knee caps and bottom of my feet. I treated it for some time with miconazole and initially experienced a severe herxheimer reaction most markedly in my ears. I think that reaction is most noticeable there because of the decreased circulation of the ear which was slightly helped out by frequent massage/rubbing/stretching of the cartilage. Unfortunately even when the severity of it started to diminish I ended up right back where I started once I discontinued use of the fungicides. The flare-ups ended up being directly linked to days of high carbohydrate consumption. So far I'm on week 2 of that "cave man" diet and even without the fungicides the severity of the flaking is greatly diminishing.

Am glad to hear the cave man diet is working for you. It mostly does for me too -- its just that it is complicated by allergies which I also seem to have. Years ago I used to get cracking around my lips and the outside top and bottom of my ears. I think that was both allergies and malabsorption of minerals and vitamins caused by celiac etc.

The flaking in my nethers is probably more subject to problems due to scar tissue from an accident involving scalding hot apple cider when I was a kid (it fell in my lap and I got a nasty burn there on one side).

The ear thing can drive one a little batty. So I am glad to hear (lol!) someone else is getting good results on the cave man diet. I also throw in a few pointers from the scd and thus avoid winter squash for the most part and instead rely on summer squash etc. And eat the 24 hour yogurt. You get the picture.

Unfortunately like what you experienced the fungicides seem to be of limited use. They are hard on a body to take and then the effect doesn't last. You might want to look into lefenuron. It changes the fungi so they no long have a chitonous shell and are thus easier to kill afterwards using more natural methods. My bf found out about it online. I tried it this summer and it has helped overall with internal fungi problems though not so much with the ear thing. The same people have another product called pythium oligandrum. Its supposed to be very good against foot and elbow fungi. It helped me somewhat but again I still have to avoid the carbs and the things I am allergic to. I need to pack my ears with cotton drenched with the liquid (water mixed with the pythium oligandrum) again for three nights. It was a bother to do the first time but I have to admit it really helped for a while.

Bottom line--there seems to be no magic pill. Exercise and diet remain the best treatments. And using herbs like olive leaf and oregano oil and garlic etc. long term seems best.

Bea

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I've been using the SCD for about 2 years and it has been helpful. The book gave me a better understanding of the problems as I have both celiac disease and Leaky Gut Syndrome. I can add a few of the grains for a short time but then begin reacting again. People who suspect or know they have gall stones or bile insufficiency are warned not to use stevia. I don't tolerate goat's milk very well so only use kefir occasionally for the probiotics. I can tolerate sprouted quinona and am going to try out sprouted grains sometime.

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I've been using the SCD for about 2 years and it has been helpful. The book gave me a better understanding of the problems as I have both celiac disease and Leaky Gut Syndrome. I can add a few of the grains for a short time but then begin reacting again. People who suspect or know they have gall stones or bile insufficiency are warned not to use stevia. I don't tolerate goat's milk very well so only use kefir occasionally for the probiotics. I can tolerate sprouted quinona and am going to try out sprouted grains sometime.

Do you know when you're supposed to introduce other nuts? I can't seem to find that in the book. Thanks.

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Do you know when you're supposed to introduce other nuts? I can't seem to find that in the book. Thanks.

I've been on the SCD diet for 7 months and follow it strictly (no cheating). Even after 2.5 years gluten-free, I had severe reactions to food and couldn't figure out the culprits because I randomly got sick, so I decided to do the diet and eliminate everything and then add 1 thing back every 4 days. I feel wonderful! Like you, I had a major junk-food addiction which has now disappeared. That was a shock for me because I never thought I could go without chocolate.

I'm committed to the diet for a year, then will introduce the most common offending foods. Funny thing about the diet - I've found that I can't tolerate strawberries, grapes, Parmesan cheese, and pineapple. I would never know that if I didn't follow the diet to a T.

Here are some resources for you:

http://pecanbread.com (good for introducing a child to SCD - also gives suggestions on introducing foods into the diet)

http://scdrecipe.com/ (great recipes! and a legal/illegal list of foods - also has a bunch of links to other SCD sites)

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I know this is an older thread, but I am hoping that someone can help me out and answer a question or two for me ,,,

For those who can NOT tolerate dairy ,,, can you tolerate regular yogurt and /or kefir??

I am truly not sure what I can tolerate any more, I seem to react to everything.

I believe I have a yeast thing <_< going on,,, white on the back of my tongue and burning in the back of my throat,,I have an appointment with my doctor on Thursday,, if she prescribes medication (( what do they prescribe for yeast?? ) should I start a SCD diet then or wait until after the course of medication??

What happens when the yeast dies off?? How will my body react ??

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This sounds almost entirely like a yeast infection, have you been tested?

How do they test for an yeast infection ??

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  • Who's Online   9 Members, 1 Anonymous, 244 Guests (See full list)

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    Jefferson Adams
    Celiac.com 04/26/2018 - Emily Dickson is one of Canada’s top athletes. As a world-class competitor in the biathlon, the event that combines cross-country skiing with shooting marksmanship, Emily Dickson was familiar with a demanding routine of training and competition. After discovering she had celiac disease, Dickson is using her diagnosis and gluten-free diet a fuel to help her get her mojo back.
    Just a few years ago, Dickson dominated her peers nationally and won a gold medal at Canada Games for both pursuit and team relay. She also won silver in the sprint and bronze in the individual race. But just as she was set to reach her peak, Dickson found herself in an agonizing battle. She was suffering a mysterious loss of strength and endurance, which itself caused huge anxiety for Dickson. As a result of these physical and mental pressures, Dickson slipped from her perch as one of Canada's most promising young biathletes.
    Eventually, in September 2016, she was diagnosed with celiac disease. Before the diagnosis, Dickson said, she had “a lot of fatigue, I just felt tired in training all the time and I wasn't responding to my training and I wasn't recovering well and I had a few things going on, but nothing that pointed to celiac.”
    It took a little over a year for Dickson to eliminate gluten, and begin to heal her body. She still hasn’t fully recovered, which makes competing more of a challenge, but, she says improving steadily, and expects to be fully recovered in the next few months. Dickson’s diagnosis was prompted when her older sister Kate tested positive for celiac, which carries a hereditary component. "Once we figured out it was celiac and we looked at all the symptoms it all made sense,” said Dickson.
    Dickson’s own positive test proved to be both a revelation and a catalyst for her own goals as an athlete. Armed with there new diagnosis, a gluten-free diet, and a body that is steadily healing, Dickson is looking to reap the benefits of improved strength, recovery and endurance to ramp up her training and competition results.
    Keep your eyes open for the 20-year-old native of Burns Lake, British Columbia. Next season, she will be competing internationally, making a big jump to the senior ranks, and hopefully a regular next on the IBU Cup tour.
    Read more at princegeorgecitizen.com

    Jefferson Adams
    Celiac.com 04/25/2018 - A team of Yale University researchers discovered that bacteria in the small intestine can travel to other organs and trigger an autoimmune response. In this case, they looked at Enterococcus gallinarum, which can travel beyond the gut to the spleen, lymph nodes, and liver. The research could be helpful for treating type 1 diabetes, lupus, and celiac disease.
    In autoimmune diseases, such as type 1 diabetes, lupus, and celiac disease, the body’s immune system mistakenly attacks healthy cells and tissues. Autoimmune disease affects nearly 24 million people in the United States. 
    In their study, a team of Yale University researchers discovered that bacteria in the small intestine can travel to other organs and trigger an autoimmune response. In this case, they looked at Enterococcus gallinarum, which can travel beyond the gut to the spleen, lymph nodes, and liver. They found that E. gallinarum triggered an autoimmune response in the mice when it traveled beyond the gut.
    They also found that the response can be countered by using antibiotics or vaccines to suppress the autoimmune reaction and prevent the bacterium from growing. The researchers were able to duplicate this mechanism using cultured human liver cells, and they also found the bacteria E. gallinarum in the livers of people with autoimmune disease.
    The team found that administering an antibiotic or vaccine to target E. gallinarum suppressed the autoimmune reaction in the mice and prevented the bacterium from growing. "When we blocked the pathway leading to inflammation," says senior study author Martin Kriegel, "we could reverse the effect of this bug on autoimmunity."
    Team research team plans to further investigate the biological mechanisms that are associated with E. gallinarum, along with the potential implications for systemic lupus and autoimmune liver disease.
    This study indicates that gut bacteria may be the key to treating chronic autoimmune conditions such as systemic lupus and autoimmune liver disease. Numerous autoimmune conditions have been linked to gut bacteria.
    Read the full study in Science.

    Tammy Rhodes
    Celiac.com 04/24/2018 - Did you know in 2017 alone, the United States had OVER TENS OF THOUSANDS of people evacuate their homes due to natural disasters such as fires, floods, hurricanes, tornadoes and tsunamis? Most evacuation sites are not equipped to feed your family the safe gluten free foods that are required to stay healthy.  Are you prepared in case of an emergency? Do you have your Gluten Free Emergency Food Bag ready to grab and go?  
    I have already lived through two natural disasters. Neither of which I ever want to experience again, but they taught me a very valuable lesson, which is why I created a Gluten Free Emergency Food Bag (see link below). Here’s my story. If you’ve ever lived in or visited the Los Angeles area, you’re probably familiar with the Santa Ana winds and how bitter sweet they are. Sweet for cleaning the air and leaving the skies a brilliant crystal blue, and bitter for the power outages and potential brush fires that might ensue.  It was one of those bitter nights where the Santa Ana winds were howling, and we had subsequently lost our power. We had to drive over an hour just to find a restaurant so we could eat dinner. I remember vividly seeing the glow of a brush fire on the upper hillside of the San Gabriel Mountains, a good distance from our neighborhood. I really didn’t think much of it, given that it seemed so far from where we lived, and I was hungry! After we ate, we headed back home to a very dark house and called it a night. 
    That’s where the story takes a dangerous turn….about 3:15am. I awoke to the TV blaring loudly, along with the lights shining brightly. Our power was back on! I proceeded to walk throughout the house turning everything off at exactly the same time our neighbor, who was told to evacuate our street, saw me through our window, assuming I knew that our hillside was ablaze with flames. Flames that were shooting 50 feet into the air. I went back to bed and fell fast asleep. The fire department was assured we had left because our house was dark and quiet again. Two hours had passed.  I suddenly awoke to screams coming from a family member yelling, “fire, fire, fire”! Flames were shooting straight up into the sky, just blocks from our house. We lived on a private drive with only one way in and one way out.  The entrance to our street was full of smoke and the fire fighters were doing their best to save our neighbors homes. We literally had enough time to grab our dogs, pile into the car, and speed to safety. As we were coming down our street, fire trucks passed us with sirens blaring, and I wondered if I would ever see my house and our possessions ever again. Where do we go? Who do we turn to? Are shelters a safe option? 
    When our daughter was almost three years old, we left the West Coast and relocated to Northern Illinois. A place where severe weather is a common occurrence. Since the age of two, I noticed that my daughter appeared gaunt, had an incredibly distended belly, along with gas, stomach pain, low weight, slow growth, unusual looking stool, and a dislike for pizza, hotdog buns, crackers, Toast, etc. The phone call from our doctor overwhelmed me.  She was diagnosed with Celiac Disease. I broke down into tears sobbing. What am I going to feed my child? Gluten is everywhere.
    After being scoped at Children's Hospital of Chicago, and my daughters Celiac Disease officially confirmed, I worried about her getting all the nutrients her under nourished body so desperately needed. I already knew she had a peanut allergy from blood tests, but just assumed she would be safe with other nuts. I was so horribly wrong. After feeding her a small bite of a pistachio, which she immediately spit out, nuts would become her enemy. Her anaphylactic reaction came within minutes of taking a bite of that pistachio. She was complaining of horrible stomach cramps when the vomiting set in. She then went limp and starting welting. We called 911.
    Now we never leave home without our Epipens and our gluten free food supplies. We analyze every food label. We are hyper vigilant about cross contamination. We are constantly looking for welts and praying for no stomach pain. We are always prepared and on guard. It's just what we do now. Anything to protect our child, our love...like so many other parents out there have to do every moment of ever day!  
    Then, my second brush with a natural disaster happened, without any notice, leaving us once again scrambling to find a safe place to shelter. It was a warm and muggy summer morning, and my husband was away on a business trip leaving my young daughter and me to enjoy our summer day. Our Severe Weather Alert Radio was going off, again, as I continued getting our daughter ready for gymnastics.  Having gotten used to the (what seemed to be daily) “Severe Thunderstorm warning,” I didn’t pay much attention to it. I continued downstairs with my daughter and our dog, when I caught a glimpse out the window of an incredibly black looking cloud. By the time I got downstairs, I saw the cover to our grill literally shoot straight up into the air. Because we didn’t have a fenced in yard, I quickly ran outside and chased the cover, when subsequently, I saw my neighbor’s lawn furniture blow pass me. I quickly realized I made a big mistake going outside. As I ran back inside, I heard debris hitting the front of our home.  Our dog was the first one to the basement door! As we sat huddled in the dark corner of our basement, I was once again thinking where are we going to go if our house is destroyed. I was not prepared, and I should have been. I should have learned my lesson the first time. Once the storm passed, we quickly realized we were without power and most of our trees were destroyed. We were lucky that our house had minimal damage, but that wasn’t true for most of the area surrounding us.  We were without power for five days. We lost most of our food - our gluten free food.
    That is when I knew we had to be prepared. No more winging it. We couldn’t take a chance like that ever again. We were “lucky” one too many times. We were very fortunate that we did not lose our home to the Los Angeles wildfire, and only had minimal damage from the severe storm which hit our home in Illinois.
      
    In 2017 alone, FEMA (Federal Emergency Management Agency) had 137 natural disasters declared within the United States. According to FEMA, around 50% of the United States population isn’t prepared for a natural disaster. These disasters can happen anywhere, anytime and some without notice. It’s hard enough being a parent, let alone being a parent of a gluten free family member. Now, add a natural disaster on top of that. Are you prepared?
    You can find my Gluten Free Emergency Food Bags and other useful products at www.allergynavigator.com.  

    Jefferson Adams
    Celiac.com 04/23/2018 - A team of researchers recently set out to learn whether celiac disease patients commonly suffer cognitive impairment at the time they are diagnosed, and to compare their cognitive performance with non-celiac subjects with similar chronic symptoms and to a group of healthy control subjects.
    The research team included G Longarini, P Richly, MP Temprano, AF Costa, H Vázquez, ML Moreno, S Niveloni, P López, E Smecuol, R Mazure, A González, E Mauriño, and JC Bai. They are variously associated with the Small Bowel Section, Department of Medicine, Dr. C. Bonorino Udaondo Gastroenterology Hospital; Neurocience Cognitive and Traslational Institute (INECO), Favaloro Fundation, CONICET, Buenos Aires; the Brain Health Center (CESAL), Quilmes, Argentina; the Research Council, MSAL, CABA; and with the Research Institute, School of Medicine, Universidad del Salvador.
    The team enrolled fifty adults with symptoms and indications of celiac disease in a prospective cohort without regard to the final diagnosis.  At baseline, all individuals underwent cognitive functional and psychological evaluation. The team then compared celiac disease patients with subjects without celiac disease, and with healthy controls matched by sex, age, and education.
    Celiac disease patients had similar cognitive performance and anxiety, but no significant differences in depression scores compared with disease controls.
    A total of thirty-three subjects were diagnosed with celiac disease. Compared with the 26 healthy control subjects, the 17 celiac disease subjects, and the 17 disease control subjects, who mostly had irritable bowel syndrome, showed impaired cognitive performance (P=0.02 and P=0.04, respectively), functional impairment (P<0.01), and higher depression (P<0.01). 
    From their data, the team noted that any abnormal cognitive functions they saw in adults with newly diagnosed celiac disease did not seem not to be a result of the disease itself. 
    Their results indicate that cognitive dysfunction in celiac patients could be related to long-term symptoms from chronic disease, in general.
    Source:
    J Clin Gastroenterol. 2018 Mar 1. doi: 10.1097/MCG.0000000000001018.

    Connie Sarros
    Celiac.com 04/21/2018 - Dear Friends and Readers,
    I have been writing articles for Scott Adams since the 2002 Summer Issue of the Scott-Free Press. The Scott-Free Press evolved into the Journal of Gluten Sensitivity. I felt honored when Scott asked me ten years ago to contribute to his quarterly journal and it's been a privilege to write articles for his publication ever since.
    Due to personal health reasons and restrictions, I find that I need to retire. My husband and I can no longer travel the country speaking at conferences and to support groups (which we dearly loved to do) nor can I commit to writing more books, articles, or menus. Consequently, I will no longer be contributing articles to the Journal of Gluten Sensitivity. 
    My following books will still be available at Amazon.com:
    Gluten-free Cooking for Dummies Student's Vegetarian Cookbook for Dummies Wheat-free Gluten-free Dessert Cookbook Wheat-free Gluten-free Reduced Calorie Cookbook Wheat-free Gluten-free Cookbook for Kids and Busy Adults (revised version) My first book was published in 1996. My journey since then has been incredible. I have met so many in the celiac community and I feel blessed to be able to call you friends. Many of you have told me that I helped to change your life – let me assure you that your kind words, your phone calls, your thoughtful notes, and your feedback throughout the years have had a vital impact on my life, too. Thank you for all of your support through these years.

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    • You could very well have celiac disease, but there are 200 symptoms attributed to celiac disease and those often overlap with other illnesses.  You could get tested, but all celiac testing requires you to be on a full gluten diet for 8 to 12 weeks prior to a blood draw (it can take time for antibodies to ramp up and spill into the bloodstream).    You have been off for a month and it is possible that you could have healed.   Consider getting back on gluten and get tested.  Since you have Gastritis, maybe you can get a GI referral and an endoscopy to biopsy the stomach and the small intestine.  Only two weeks on a gluten diet is required for that procedure.      Learn more about testing: http://www.cureceliacdisease.org/screening/  
    • I'm a 30 year old female. All of my life I've had extreme bloating after eating. About 4 years ago I started having upper stomach pain. It's dead center below my rib cage where the diaphragm is located. As the years have passed the pain became more intense and more frequent until it was daily and affecting my ability to function. I had 2 drs say it was gastritis but prilosec did nothing to help. My head got to where it always hurt and I was exhausted constantly. If the pain and head fog wasn't already enough my joints started to hurt and swell making it hard to get out of bed. I'm 4ft 11 inches and was 130 pounds and my blood pressure was staying 160/105. I've always suffered with spells of constipation then episodes of D. I was getting mouth sores and had random rashes and itching mostly on my legs. I've also suffered anemia. When my stomach pain is at its worst I have foul smelling stools. All my liver and pancreas testing have come back normal. I tested negative for h pylori but am currently on carafate for ulcers. I'm going for another gallbladder ultrasound in 3 days as 9 years ago the ultrasound showed sludge so the dr is wanting to recheck. I've done research for a while now on gluten and have cut it out for over a month. I have noticed a significant improvement since stopping it and only have flare ups if I accidently consume gluten. So my question is does this sound like anything you've experienced and been positive for celiac? I also have numbness and tingling in my feet and hands 
    • Welcome!   With a sister who has celiac disease, you are at a much higher risk of developing it.  I would go for the complete 12 weeks.  Why?  Because doctors recommend anywhere from six to 12 weeks for the blood tests, but there has not been many long term studies to back up the claims.  Best to play it safe.  It sounds like you are not suffering too much (I had no GI symptoms and just anemia when I was diagnosed).  Ask your PCP to run the full panel, including  the DGP and EMA tests.  Why?  Not all celiacs test positive to the TTG, like me!  If your Kaiser doc refuses, please ask if you can be referred to a GI and select one who handles celiac patients.  Some celiacs are even seronegative!  In that case, going to an endoscopy is necessary.  Keep in mind that you might just be developing it or know that if everything negative now, you can still develop it in the future.  First-degree relatives should get tested every few years even if there are no symptoms.   What if your PCP refuses even after you show him the printed data supporting your claims (and the ones I made...so hit Dr. Google)? Get to another PCP or put your request in writing  via the patient portal or a registered letter.  Be nice.  Support your claims.  Ask for the full panel or to be referred to a GI.  In writing, they have to respond.   I do know that the TTG catches most celiacs, but not all.  If celiac disease is still suspected, you should move to the next series of celiac tests.  Unfortunately, to keep costs down, Kaiser just orders the TTG for initial screening.  You have to get around that.  I found that out when family  went in for testing and they had Kaiser.   Advocate for your health!  Document!  Save and print all test results and maintain file.   Take care!  
    • hi All, I had been getting so gradually sick that I don't know when it started, (but I am now assuming 1994).  In 2008, I succumbed to pressure from my insurance rep to get more insurance, and they would even come to my house to test my blood.  I was denied insurance and recommended to see my doctor, who told me I had the liver of a severe alcoholic.  I very rarely drink. I went for tests and the doctor was baffled.  He said I should lose weight.  He said it was likely fatty liver disease. That was 2008.  For the next few years I got tests, tried to eat healthy, and every so often I would see if it was helping my liver numbers. I got stomach aches when I ate toast or a sandwich, but didnt link it to the toast except later, in hindsight.  How could toast give me a stomach ache?  Anyway, on the advice of my doctor, I tried very hard to lose weight, so went lo-carb.  One day, I had had no breakfast and at church 'goodie-time' was unable to resist all the carbs.  Later that afternoon, I felt like someone had literally poisoned me. This was now 2011.  I decided to not eat or drink anything but almonds and organic cold pressed  apple juice in a glass jar, and ate only those things for the next 3-4 days while I looked for symptoms on the Internet. I narrowed it down to celiac disease and went to the doctor.  I refused to eat gluten to get the test.  I decided not to eat gluten and I got better. I then started a job in China.  I learned how to say things like "no soy sauce" since it's made from wheat.  I got so much better.  I knew what my reactions were to gluten, especially the one that happened first: I would get a shakiness inside, like my blood system was micro-vibrating. i got the flu and was in bed for three days straight eating only mandarin oranges and water.  After a couple of days, I got that shakiness, suddenly, lying in bed.  I was astounded, cause I had only water and oranges.  Then I remembered that I had taken two Advil, in the gel cap form.  I looked on the Internet, and sure enough, the gel caps contained gluten.  Wow.  Even that small amount in two gel caps set it off. I was very vigilant.  Then one day, back in Canada, I was making hot dogs for a four-year-old and I had fresh bakery buns.  I couldn't resist.  I guess I thought, well, it's been a couple of years gluten free, let's see what happens.  I ate one and a half huge bakery hot dog buns on impulse.  Big mistake. I got so, so sick.  I was sick for 6 weeks with various symptoms.  Spleen pain, liver pain, kidney pain, migraine headaches, stomach issues, constipation, dizziness, brain fog, irritability, etc.  This was 2013. After one week of still being sick, I thought it's probably too late, but I should get that celiac test to see if there are detectable antibodies.  I went to the doctor, who didn't think it was necessary and insisted it was fatty liver disease and not celiac.  He humoured me and gave me the requisition anyway.  It wasn't too late!  One week later. i was shocked to see that my antibody level was 99. ( If you have less than 20 you don't have Celiac. It is called tTg test).  If you have 100, they say you don't really need a biopsy and it's pretty much confirmed celiac.  The doctor was a little bit embarrassed and said, "looks like you've diagnosed yourself". So finally he shut up about fatty liver disease.   I got so much better living in China.  I occasionally slipped. I  then went back to canada for a year.  I developed DH, as I got these lesions starting on my thumb and then on my fingers and palms.  Finally after 6 months I cut out dairy.  I had heard it was also somehow bad for Celiacs from the Internet but I really didn't want to cut out dairy as it was bad enough without gluten.  I finally did and the DH cleared up.   Then back to China.  I would go back to Canada twice a year for the time off from spring and summer holidays.  It was really hard to be around western food temptations and I would get "glutened" even though I tried hard. I began to get a strange pain in my leg and the doctor in canada said it was likely arthritis in my hip.  i went for an xray but it didnt show anything.  it really killed me to get that pain in my leg and then in my hip.  i would cry out and have to sit down.  i started riding my bike to work in china cause it was painful to walk very far.  I had started to reintroduce dairy while in China and found that I could eat yogurt, which I love. I had heard that people blamed their gluten reactions on Roundup, or glyphosate, because they could eat flour products in other countries but not North America.  One day about six months ago I made cookies for my students.  I wore gloves and was very careful.  Before this, I wouldn't even be in the same room with flour.  But nothing happened.  Then I tasted a cookie.  Nothing happened!!  The next day, I ate a whole cookie. Nothing happened!!  I began to think there was something to the theory of North America and roundup.  I still avoided flour in general cause I didn't want to push it, but I started eating soy sauce and relaxed a bit - started going to restaurants in china, etc. instead of micromanaging food in my kitchen, cause I was evidently not reacting to gluten in China.  I then realized that the only episodes of pain I had had were when I was in Canada the previous summer and spring.  Very strange.  So.  I got back to Canada, last spring, had my usual gluten free meal on the airplane, and then visited my mother.  I ate only organic yogurt.  Nothing else, and a few hours later I was attacked by almost every gluten related pain I had ever had.  My hip was suddenly shooting pain and I cried out and limped to the couch.  My mother asked, what did you eat?  I said, nothing!  Only organic yogurt!   Of course after any glutening, it takes weeks for these pains to subside, and I endured pain stabs in my spleen for a while.  Then back to China, where I was able to eat normally.  No pains, nothing.  I ate yogurt, made myself with uht milk imported from Germany or Australia, and I was fine.     Until the day when I ate one of the chocolate bars I had brought from Canada as prizes for my students.  Instant reaction! Spleen pain!  I had heard that sugar cane was as bad as flour for being drenched in roundup.  Now I was convinced. It was definitely stuff from Canada that was the culprit.  Only farm products.  Yes, they say the yogurt is organic, but I'm sure they feed the milk cows hay that has been exposed to roundup.   Now I know exactly what I can eat and where.  I love the food here, and it's safe.  There are exceptions.  They use pesticides on fruit, cause I get a stomach ache when I eat certain fruits, but it's a different reaction that the gluten reaction,  I can eat flour products without a huge reaction, but I still have celiac, because I do get reactions even from Chinese flour, just not as bad as I did before.  A mild sick feeling, like something is off, kind of unbalanced, and of course the inevitable shakiness.  I react much worse to Canadian chocolate.  But there is a huge difference between food here and food there.  A very painful difference.  Hard to figure out, but I think I have. so here's my theory,  roundup actually causes the celiac disease, or whatever disease you might happen to be genetically susceptible to. (My uncle has arthritis in his hip). If you keep ingesting it, you will get gradually sicker and sicker and get some kind of disease.  If you stop eating roundup completely, you will heal with a healthy diet.  If you already have a disease like celiac or DH you can manage it and stay healthy if you are totally roundup free. My dad died of nonHodgkins lymphoma and he insisted it was the roundup the neighbor had been spraying on his farm, right next to my dads organic hobby farm.  Now I believe him. I wish I'd been able to piece this together a bit earlier.  Since 1994, many diseases have hugely increased.  That's when they started with the roundup and there is a one on one correspondence on the graphs with roundup use and  many diseases. sorry for the novel but I just can't keep this all to myself,  I'm like the canary in the mine.  But roundup is everywhere so I don't know if you can really avoid it in North America, sadly. My advice is to move elsewhere and figure it out like I did. i saw a youtube video by an MIT researcher that they are now figuring out that glyphosate actually takes up the place of the essential amino acid glycine in your body.  Because they are molecularly similar, glyphosate gets in there and stops glycine from being able to do it's job in your body.  So it causes all sorts of problems in a gradual way and eventually you will have trouble. i hope this helps!  Stay away from farm products!  I hope it's not true what the conspiracy theorists say (that they are spraying chemicals, chemtrails etc.  I don't know if they are spraying roundup) but if it is, that's the end of the world as we know it.  I don't really want to go there,  I just know what I know and I'm sharing it.   this is just the short version  but I've tried to include important info.  Anyone else have a similar story in any way?
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