Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Grain free and low FODmap anti itchy eczema


YoloGx

Recommended Posts

YoloGx Rookie

Hi, I am re- discovering that a grain free diet is helping my eczema go away plus hits making me able to sleep way better. That along with a lower FODMap diet is reducing my bloating.
 

I realize this could be considered a controversial topic—however it’s really helping me even though I’ve had no great need to lose weight. Just getting rid of the itchy eczema is beneficial enough. Now I can sleep way better not being itchy. It also seems to be improving my nerves. Plus now I can eat more non grain foods. 
 

I have been completely gluten free since the end of 2007– and previous to that I had reduced gluten greatly for many years (I had erroneously thought it was just an allergy).
 

Being strictly gluten free simply hasn’t been enough. Even the pseudo grains bother me  unfortunately. 
 

Being grain free is actually reducing my other food sensitivities. Now I can eat eggs and peanut butter amazingly— both of which have been verboten for some years.
 

I was initially diagnosed with celiac when I was less than a year old. I was exposed to radiation from Hanford’s infamous Green Run experiments. I became ill with terrible bronchitis plus i stopped growing. This went on for several months.

Fortunately the doctor was from a research hospital back East. He figured out after I was put in isolation and got better after being taken off gluten and high fat milk. My mother had celiac but thought she had “grown out of it”— which no doubt gave the good doctor an important clue. I got way better being gluten free. Back then I ate a lot of Uncle Ben’s Rice. 

Unfortunately I was put back onto eating gluten grains when I turned five due to the ignorance of the 1950’s. At that time the docs figured one could grow out of it.

My mother also wanted to spare me the experience of appearing different at school etc— as she was forced to have a gluten free diet by her parents. 

The problem is that being severely sensitive to gluten all those years didn’t help my intestinal villi any. I thus still have leaky gut even though it probably isn’t as bad as it was ten or fifteen years ago. 

I am now eating more low FODMap squashes —mainly summer squash and delicati with small portions of Kabocha (which I am more sensitive to) as well as some root vegetables for my starch. Fortunately rutabagas work well for me. I also eat a bit of yams—after I peel, slice and boil them and then throw out the water to reduce oxalates. I’m allergic to carrots so I avoid them and their cousin parsnips.

I’ve yet to fully figure out which high FODmaps are ok for me—though onion and garlic appear to be fine. 

I’ve reintroduced chia seed pudding sweetened with stevia. And am glad to report I am fine adding a couple of tablespoons of ground sunflower seeds to it along with two tablespoons of blueberries—for now my one allowable fruit given how sensitive I am to fruit in general. 
 

so this is my journey. I’m wondering if there’s others here experiencing and exploring similar healing effects being grain free and perhaps low FODMap.

YoloGx


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



YoloGx Rookie

I’m actually wondering if scar tissue from a traumatic accident when I was six could have also created intestinal adhesions. I take serrapeptase regularly to counteract scar tissue. However it seems like I get bloated no matter what I eat, though some things like eating more than just a smidgen of cabbage or an excess of almond flour are worse.

Meanwhile despite all I’m going to try out having a very small amount (1/4 cup) of organic canned garbanzo beans. I used to cook up my own after a day of letting it soak and then cooking it extra—given all that there was no problem. This was also while I was eating grain free. So I’m hopeful.

I think eating the pseudo grains may have also contributed towards my having severe histamine sensitivity since it appears I wasn’t so awfully sensitive to eating lactose free yogurt in the past while also grain free—YoloGx

 

knitty kitty Grand Master

@YoloGx,

Welcome to the forum!

I followed the Autoimmune Protocol Diet and found more health improvements than when I followed the Low fodmap diet.  

https://www.healthline.com/nutrition/aip-diet-autoimmune-protocol-diet

Dr. Sarah Ballantyne, herself a Celiac, developed the diet for herself and her Celiac family.  scientific studies have shown this diet does help heal the small intestine.  Once healed and feeling better, you can include more foods.  

Nuts and beans are eliminated because they have hard to digest Lectins.  

Cabbage is a cruciferous vegetable like broccoli and cauliflower.  They produce lots of gas during digestion, so those are best avoided.  

I still have problems with alternative grains.  I recently came to the conclusion that buckwheat is a problem.  

Which alternative grains were problematic for you?  What prompted you to go grain free? 

YoloGx Rookie

Hi Knitty,

 I’m glad to hear that the autoimmune protocol diet has helped you. It really is good for a lot of people.

Unfortunately I developed severe histamine intolerance when I tried following that diet years ago. I was loving making sauerkraut and bone broth but it didn’t last long. It ended up increasing my histamine intolerance and thus migraines and insomnia etc. 

Since then I haven’t been able to eat fermented foods without getting a migraine. Am hoping that will eventually change by my being off the grains again. 

Years ago I was on an anti Candida diet— and found great relief following the so called Cave Man diet. Basically we ate everything made from scratch plus no grains or sugar etc. And instead we ate lots of vegetables including squash and roots as well as meat and fish. The one kind of fermented food I tolerated was home made yogurt.

I also finally had my silver amalgam fillings removed which both helped and for a time hindered me due to the mercury that got stirred up. My detox herbs really helped me slowly get past that plus taking food grade bentonite clay slaked in water regularly.

I reverted later on and began eating rice again after I was supposedly cured of candida overgrowth. At that time I thought I was allergic to gluten containing grains and thus mostly avoided them. 

so I had this old experience of eating grain free and feeling a lot better. And I now realize from reading an old post of mine from 2009 here on celiac.com that I briefly tried eating grain free again and felt way healthier—plus my eczema went away.

However I was going through an extremely stressful period of time right after the initial eczema free experience—so it came back. 

After that I soon went back to eating rice and started exploring using pseudo grains. In the process of all that I eventually discovered I had celiac rather than just an allergy to wheat and oats etc. 

The last three years I wasn’t eating any rice and instead just ate pseudo grains plus lots of vegetables and home made chicken soup.

Recently the eczema got really bad however and it finally occurred to me I should try out that old Cave man diet without even the pseudo grains again. 

So far it seems to be really working! The eczema is nearly gone. 

I’m also just now starting to experiment with sprouting legumes—so far so good! Though it’s just at the beginning stage now. Whereas otherwise I’ve had issues with legumes previously. 

similarly I now can eat pure peanut butter and also  eggs. I haven’t tolerated either in years.

The low FODMap diet in addition seems to be helping reduce my bloating and helps against insomnia. Thus I’m finding it’s ok for me to eat half a cup of broccoli but no more. Ditto with cabbage. But Bok Choi, kale and collard greens are just fine for instance.

Am excited since so far it seems that lactose free yogurt may turn out to be  fine for me.

And now by having blueberries only in small portions I am able to eat a little fruit again. I plan on trying out a little honeydew next. The idea is to freeze the rest in serving sizes. 

I’ve also just figured out that I am not only intolerant to all nuts but also to coconut—even the oil as well as the milk etc.

I plan to try out sprouting quinoa and maybe buckwheat. My hope is that by getting rid of the anti-nutrients I’ll be able to eat the sprouted grains (much like the sprouted legumes) without getting the itchy eczema back again. Or migraines. Or insomnia and jerky legs at night. So we’ll see by trial and error.

of course walking and yoga helps a lot too. And my kidney, liver, lymphatic balancing herbs

It’s still in the experimental stage. But so far it seems very promising.

my friend G is being helped by this combination diet too — though he feels like he’s getting too skinny. So he’s going to experiment and try out eating some buckwheat noodles again.

He seems to have more FODMap sensitivity than I do. He’s had terrible IBS with severe nausea. That is amazingly going away! Plus he’s sleeping a lot better. But it may be that the low FODMap diet has been helping him the most. His body will surely let him know if it’s ok for  him to eat the pseudo grains or not. Plus of course he intends to stay gluten free. 

My hope is that eating sprouted pseudo grains and legumes will make all the difference for me. 

So are you still on the elemental diet or have you gone more paleo or?

 

knitty kitty Grand Master

@YoloGx,

Yes, I had histamine intolerance, too, when doing the Autoimmune Protocol Diet, so I skipped the high histamine bone broth and fermented foods.  I skipped the kefir, too, due to casein allergy.

How does the AIP diet without the high histamine foods differ from the Cave man diet?  The AIP diet cuts out sugar and all grains.  

Vitamins for skin health include Vitamin A, Vitamin C, iron, and niacin (the kind that flushes).  Healthy fats, omega threes, like flaxseed oil, are helpful, too.  

Thiamine (Benfotiamine and Allithiamine/Thiamax) helps with insomnia.  Tryptophan, magnesium, Pyridoxine B6, and L-Theanine help with insomnia, too. 

I'm so glad you're feeling better!

 

YoloGx Rookie

Knitty, wow—our experience with the histamine is so similar! That diet made me worse. What is it that you’ve done since?

But yes for me the last three years my diet was otherwise very like the autoimmune diet.  I’ve eaten an awful lot of zucchini and lettuce and cucumbers for instance. However I was also eating those pseudo grains every day. Plus coconut which I was eating almost every day apparently is a no no for me. It appears to keep awake plus makes me bloated —and who knows what else. 

I think it’s also helped that I avoided high oxalate foods for nearly four years. Now I can eat cruciferous vegetables again —though not in excess. 

I just tried out eating Green Valley lactose free yogurt and found it really agreed with me. It seemed to calm me down and allowed me to finally sleep after I had reacted to the coconut some hours before. It’s obviously too early to really tell but I’m speculating that my problem with milk has been the lactose and not the casein.

Interestingly Lactaid milk makes me feel ill. However I just learned there’s different ways they create lactose free milk. Lactose intolerance apparently can be a FODMap issue. I think that the way I used to make homemade yogurt may have reduced the lactose in it. 

It’s also possible that going off the pseudo grains and the coconut (which I’ve done this last month) is reducing my inflammation—thus allowing me to eat more foods. 

no matter what it’s all rather complicated. However I’m finally appearing to successfully thread the needle!
 

YoloGx Rookie
On 11/23/2022 at 2:44 AM, knitty kitty said:

@YoloGx,

Welcome to the forum!

I followed the Autoimmune Protocol Diet and found more health improvements than when I followed the Low fodmap diet.  

https://www.healthline.com/nutrition/aip-diet-autoimmune-protocol-diet

Dr. Sarah Ballantyne, herself a Celiac, developed the diet for herself and her Celiac family.  scientific studies have shown this diet does help heal the small intestine.  Once healed and feeling better, you can include more foods.  

Nuts and beans are eliminated because they have hard to digest Lectins.  

Cabbage is a cruciferous vegetable like broccoli and cauliflower.  They produce lots of gas during digestion, so those are best avoided.  

I still have problems with alternative grains.  I recently came to the conclusion that buckwheat is a problem.  

Which alternative grains were problematic for you?  What prompted you to go grain free? 

Hi Knitty, I hope you survived Thanksgiving ok. I ended up getting a migraine from eating lactose free yogurt that also had sugar etc in it. I thought it’d be ok but clearly it wasn’t!!

you might want to consider sprouting your pseudo grains or at least soaking them overnight. It’s supposed to help get rid of a lot of the often offending excess phytates. Ditto with legumes (which apparently also digest better with greens and a little meat). Of course legumes also have other hard to digest lectins and saponins. Which again are reduced by sprouting —I think.

Am I right? For me fermenting my food seems to be no longer an option. 

Check out the Weston Price Foundation for more information. 

I am giving it a try. So am soaking a serving of hulled whole millet to cook up tomorrow.  

Right now am eating home grown mung bean sprouts with my greens, zucchini and liver. I made some up the other day and had no issues with the sprouts! 

Bea


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - marion wheaton replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    2. - trents replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    3. - BlessedinBoston replied to marion wheaton's topic in Gluten-Free Foods, Products, Shopping & Medications
      3

      Are Lindt chocolate balls gluten free?

    4. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      14

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,414
    • Most Online (within 30 mins)
      7,748

    Jane Margaret
    Newest Member
    Jane Margaret
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.