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

Omg...i Might Be On To Something


Rachel--24

Recommended Posts

CarlaB Enthusiast
Dear CarlaB,

Thanks a lot! I think I have been on Lyme net before. You know, it is amazing how much you can find! I recall a medical mysteries special I took notes on the other week about a teen suffering from excruciating chronic pain. It turned out it was Lyme, though she had been tested for it previously.

The results had been negative, but after seeing a specific doctor named by another girl she met with the exact same symptoms, and a similar story, she convinced her parents to contact him. I wrote his name down. I will check my notes. The caffeine is something I can do on my own. You see, I also eat chocolate pretty much daily. I need to start watching it! That should help!

Sincerely,

NoGluGirl

NoGluGirl, you might try supplementing magnesium to get off the chocolate. Chocolate cravings are a sign of a magnesium deficiency. It won't hurt you to take it, so you might try it. It helped my daughter with her chocolate cravings.


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
MissMeliss169 Newbie
Miss Meliss:

If you are super sensitive, note that veggies and meat aren't necessarily safe. Even organic foods can be sprayed with corn derivatives (organic, of course!). I didn't realize that and kept reacting. So make sure to rinse and scrub everything :)

Even many rices are enriched with corn but Lundberg farms Rice is safe.

The sites that Donna posted are great. I was corn free for a few months and it was really helpful.

Thanks for the tips, I am getting a lot of great responses here and that is so wonderful. I am hoping that someday I will be able to introduce some of these things back into my diet, they want me to stay on this hypo-allergenic diet for atleast 6 months. Who knows, maybe by then I won't even miss all the other stuff that I can't eat right now =)

CarlaB Enthusiast

Rachel, I read a comment on Lymenet yesterday that made me think of you. It said that if a person went to an LLMD, the doc would rule out everything before diagnosing Lyme. It's not like they diagnose everyone with Lyme as some people claim.

Even though my test was VERY positive, I'm still getting tested for thyroid, heavy metals, cortisol, etc. They are thorough.

After reading that, I thought that's what your doctor is doing ... just being thorough. He has to rule out everything else since your test was not positive, but there were significant bands.

I don't have joint pain either. I DID have it, but now it only pops up once in a while, but not often. I do get muscle cramping though, and severe brain fog (from the babesia I would imagine).

Just a note about avocados .... you cannot feed a bird and avocado because the fleshy part near the seed and near the skin have a poison that will kill the bird. Maybe that's what you're reacting to. Chocolate is the other no-no for birds.

dlp252 Apprentice
Hey does anyone eat the food for life brown rice tortillas I am thinking about trying them

I think I might be the only one who didn't love these, lol. I think I just didn't figure out how to prepare them correctly though. I may still have some in the freezer, but it will be a while now before I can try one again. :(

Rachel-

don't expect him to coddle me but god I could use some cooddling right now

So sorry your appointment didn't go better! I wish doctors had a sixth sense about these kinds of things. I think even the best intentioned doctors are so focused sometimes that they just can't see what we really need or hear what we are really saying.

Thanks for the tips, I am getting a lot of great responses here and that is so wonderful. I am hoping that someday I will be able to introduce some of these things back into my diet, they want me to stay on this hypo-allergenic diet for atleast 6 months. Who knows, maybe by then I won't even miss all the other stuff that I can't eat right now =)

I think all of us have that same hope, lol!!! I am really hopeful that someday I can at least eat avocados again!! :lol:

Very interesting BioSET installment!! ART sounds really great, and it's great that Scott can do the testing...I wonder how long his list is....

Well, today is day 5 of the candida diet, and I have to say that I feel pretty good. I haven't had any die off symptoms yet, but I'm also not taking any anti-fungals either. I wanted to get the diet down first then I'll add in a couple of natural anti-fungals. I've lost 5 pounds since Friday (this is not a bad thing for me though, lol), probably mostly water, but I'll take it. I DO expect that once I start antifungals I'll probably have some bad days...right now my worst symptom is a little achyness behind the eyes.

I think my adrenals are starting to come back too. Yesterday I had so much energy left after a walk on the treadmill that it surprised me...that hasn't happened in a long time (excess energy AFTER a workout).

So yesterday I added a tiny bit of coconut oil to my green beans as they cooked...I felt a bit of gassyness and some noisy bowels after dinner (I ate what I've been eating all week for dinner, so nothing new except the coconut oil). I started thinking mild die-off...then this morning my BM had some "tissue" looking stuff...kind of mucusy I guess. Could that be die-off??? I don't remember that happening when I did the diet a few years ago, and really, I didn't eat very much coconut oil...maybe half a tablespoon, cuz I'm trying to keep my fats down until I get treated for them at BioSET.

happygirl Collaborator

x

dlp252 Apprentice
x?

Sorry, I've seen this discussed a couple of times in my reading over the last couple of days, but I couldn't find a link. It's mostly in discussions I've read regarding candida and mercury...I'll post one if I can find it.

dlp252 Apprentice

You probably found these already, but I thought I'd post anyway:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



happygirl Collaborator

Thanks, Donna! :)

AndreaB Contributor

Mia,

Hugs!

Rachel,

I didn't finish reading last night as the little one woke up. I did read about your appointment, not the ART. I hope Scott will be able to get you worked in and tested.

Donna,

Glad you are getting some energy back!

Hi to everyone else! I'm still reading along.

My dad has a mass in his abdomin that needs to be biopsied. Don't know when that will happen. Other than that things are going pretty much the same. Still need to work on not being up so late. :)

dlp252 Apprentice
My dad has a mass in his abdomin that needs to be biopsied. Don't know when that will happen. Other than that things are going pretty much the same. Still need to work on not being up so late. :)

Gosh, I'm sorry to hear that! Will pray it's nothing serious!

Rachel--24 Collaborator
Rachel, I read a comment on Lymenet yesterday that made me think of you. It said that if a person went to an LLMD, the doc would rule out everything before diagnosing Lyme. It's not like they diagnose everyone with Lyme as some people claim.

Carla, By the time I went to the LLMD....there wasnt really much left to rule out. Basically just Lyme and Mercury.

I've had every test imaginable over the last 4 years....of course never finding anything wrong. <_<

As far as mercury...I'd had hair analysis, bloodwork, urine testing and antibody testing. My levels were always normal. :huh:

The hair analysis showed elevated cadmium. I think that could be creating alot of my toxicity. I smoked for alot of years and probably wasnt detoxing well after I got Lyme and things started building up.

I had a whole stack of test results.....(both traditional and non-traditional)....when I went to my first appt. He was really happy that so many tests had been done....it was helpful and allowed for us to move forward. He was confidant that its not cancer or anything like that.

So thats why he was able to focus on the stuff that *doesnt* show up in mainstream tests .....everything had already been ruled out.

I think this is the case for *most* patients that the LLMD sees....they've already made the rounds and by the time the LLMD sees them.....most things have been ruled out.

So far the only other testing the LLMD has done was for vit/min deficiencies and the tests for viruses and other infections.

Rachel--24 Collaborator
After reading that, I thought that's what your doctor is doing ... just being thorough. He has to rule out everything else since your test was not positive, but there were significant bands.

The Dr. isnt trying to rule anything else out. He says I have Lyme. I guess I'm the only one who's doubtful and wants more proof. <_<

The Dr. already said back in October that I have Lyme.....he just wont put me on antibiotics until other problems are addressed and I'm in better shape with my liver.

Just a note about avocados .... you cannot feed a bird and avocado because the fleshy part near the seed and near the skin have a poison that will kill the bird. Maybe that's what you're reacting to. Chocolate is the other no-no for birds.

I know you have birds (what kind?).....I have a Sun Conure.

Yeah....its true that chocolate and avocado will kill a bird...I never knew exactly why though. :unsure:

When I first got my bird I was told to never give her either of those but they never told me why.

She was cute....I was working at PetsMart part-time and she was one of the hand-fed babies we got in. I ended up buying her....she was all fuzzy cuz she was new. :)

Rachel--24 Collaborator
My dad has a mass in his abdomin that needs to be biopsied. Don't know when that will happen. Other than that things are going pretty much the same. Still need to work on not being up so late. :)

Andrea....sorry about your dad. :(

Hope everything turns out to be ok.

CarlaB Enthusiast
The Dr. isnt trying to rule anything else out. He says I have Lyme. I guess I'm the only one who's doubtful and wants more proof. <_<

:lol::lol::lol::lol::lol: I thought your doc still wasn't convinced either!!!

Rachel--24 Collaborator
Dear Rachel,

Since you have candida, I was wanting to ask you about a body odor issue. I recall your garlic sauna experience, LOL! My body odor is so strong, it actually smells like onion or garlic, even when I have not eaten any! My feet actually smell like vinegar! Is this common with candida? If not, what else could cause this? This is awful to deal with, because no matter how much I bathe, nothing seems to completely get rid of it. I am so afraid everyone will smell it on me!

It could be from the candida. Candida produces alot of toxins that overwhelm the liver. I used to have weird body odor but it cleared up after I switched to a clean diet. Some of the things your eating might be contributing.

Rachel--24 Collaborator
:lol::lol::lol::lol::lol: I thought your doc still wasn't convinced either!!!

Nope....its just me. :ph34r:

I'm not easily convinced...I need to *see* the spirochetes. Then I will believe. :P

CarlaB Enthusiast
I know you have birds (what kind?).....I have a Sun Conure.

Yeah....its true that chocolate and avocado will kill a bird...I never knew exactly why though. :unsure:

When I first got my bird I was told to never give her either of those but they never told me why.

She was cute....I was working at PetsMart part-time and she was one of the hand-fed babies we got in. I ended up buying her....she was all fuzzy cuz she was new. :)

Sun conures are beautiful!! Where does she live -- at your mom's or at your house?

I have a goffin cockatoo. He looks like Open Original Shared Link. Adam has a Hahn's Macaw that looks like Open Original Shared Link. My bird loves to be held and cuddled, which is why I got a cockatoo.

Two of my daughters have birds, too, a parakeet and a cockatiel. One daughter has a hampster. It's definately a full house!!

CarlaB Enthusiast

Andrea, how is your dad doing with the rest of his health issues?

CarlaB Enthusiast
Nope....its just me. :ph34r:

I'm not easily convinced...I need to *see* the spirochetes. Then I will believe. :P

Hmm, do they do that kind of testing?? :lol: There is a video of some spirochetes on canlyme that were filmed in someone's skin. I have no idea how they did that, but it's a pretty interesting video. I found it today ... I was trying to research what it means to be Igg positve, but Igm negative. I know it means I have Lyme, and from what I've read it's pretty rare ... one doctor said that out of over 1000 patients, only 3 or 4 have had that result. Dr. H. said usually Igm was the one that was usually positive, too.

diamondheart Newbie
I am avoiding corn too, but mostly because of a candida issue.

Welcome Melissa!

So, what's the connection between corn and candida, besides the carbs/starch :huh: ?

Hey does anyone eat the food for life brown rice tortillas I am thinking about trying them

I like them, but they took some getting used to. I usually put a little bit of water on them and heat them up in a pan. They taste better this way. I don't even like to eat corn tortillas anymore.

Miamia, sorry to hear about your doctor's appointment. I hate unsympathetic doctors :angry: .

The doctor did not say anything was abnormal other than a rapid heartbeat. Does that really mean anything? I am worried. Of course, it may be Lyme... Congenital heart defects (especially electrical ones) are very dangerous. I am surprised they did not decide to implant a pacemaker in you. I know nutritional deficiencies could be to blame.

You got some good ideas about cutting out caffeine and chocolate. I can't have any kind of stimulants of any kind. They make my heart beat fast! I have supraventricular tachycardia (just a fancy way of saying my heart beats fast sometimes) and maybe mitral valve prolapse. I've been to several cardiologists at a young age, which initially freaked me out. I've had this for over 20 years. My first episode was after I had a cigarette as a teenage, I think :rolleyes: . After I started taking magnesium regularly, the fast heartbeats cleared up. It's really not a big deal, and it's kind of a blessing in disguise. My heart is my barometer for when I'm not taking care of myself. When I've had other nutritional deficiencies, its also shown up as heart palpitations. Stress will also set it off. I'm just glad I don't have to take any medication for it anymore :) .

Then found out I have Sjogren's Syndrome.

Welcome! My aunt has Sjogren's syndrome too. I don't want to get it, and I think there is some kind of genetic link? Does the Sjogren's cause the food intolerances?

I gotta try to learn more about ART....

Rachel, interesting info about the mold. The only acronymn I know for ART is Advanced Reproductive Technology, which I'll be embarking on soon. Sure wish I could get pregnant the old fashion way <_< .

Claire

dlp252 Apprentice
So, what's the connection between corn and candida, besides the carbs/starch?

Mold I think. Besides the carbs/starch, corn has a mold issue thing like peanuts.

Rachel--24 Collaborator
Mold I think. Besides the carbs/starch, corn has a mold issue thing like peanuts.

Yup...corn is full of mold and mycotoxins. Actually all grains are but corn is the worst of the bunch.

Candida feeds off of molds and mycotoxins.

Here are some foods conatining alot of mycotoxins....

Mycotoxins

Aflatoxin: One of the most potent carcinogens known. It occurs in beer, peanuts, brazil nuts, bulk grains and bread (more than a few days old), overripe fruit and apple cider vinegar (is especially bad). One hefty dose of aflatoxin can debilitate the liver for years. Thus losing it's ability to detoxify.

Patulin: A deadly mycotoxin. That is associated with cancer. It occurs in overripe apples and other overripe fruits.

Zearalenone: A corn mold mycotoxin. It occurs in brown rice, popcorn, corn chips and other corn products.

Ergot: Associated with cancer and occurs in whole grain products, honey and alcoholic beverages.

The importance of the above-mentioned mycotoxins is they can further weaken your immune system. They are actually used as food by candida albicans thus making matters even worse. If you are sick. You should avoid these foods if at all possible.

Learning about mold/mycotoxins through my BioSET results has answered so many questions for me.

Now I know why I have such heinous reactions to honey, cheese, brown rice, nuts and so many other things. There had to be some sort of connection....now I know what it is. One more piece to the puzzle. :)

Rachel--24 Collaborator

The top 10 list of mycotoxin containing foods....

1. Alcoholic beverages

Alcohol is the mycotoxin of the Saccharomyces yeast--brewer

Rachel--24 Collaborator

YAY!!

I'm scheduled for the ART testing. :D

Scott (the betterhealthguy) just called me and I'm set for the 10th.....so not too long of a wait. :)

He said to bring all my supplements and prescriptions so that he can test them and also I cant take anything for 48 hrs. before the test....so that it doesnt interfere.

He's gonna email me next week with more info. He said he will be testing for lots of infections but we'll talk about stuff before we get started. COOL....the more I can learn about what is going on the better. I'm excited. :D

miamia Rookie
YAY!!

I'm scheduled for the ART testing. :D

Scott (the betterhealthguy) just called me and I'm set for the 10th.....so not too long of a wait. :)

He said to bring all my supplements and prescriptions so that he can test them and also I cant take anything for 48 hrs. before the test....so that it doesnt interfere.

He's gonna email me next week with more info. He said he will be testing for lots of infections but we'll talk about stuff before we get started. COOL....the more I can learn about what is going on the better. I'm excited. :D

ok rachel i was just gonna post that i called my doctor about the art test and the women who works fo rhim called me andsaid he thought it was a good idea for me. I am seeing him tomorrow for my shot and we are going to talk about it then. I got info on it and found someone close to me that does it and the main doc trained with the guy who invented it or whatever so it seems pretty reputable. Hopefully i will find out more info tomorrow. I am so glad you already have an appt set up.

Miamia

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,553
    • Most Online (within 30 mins)
      7,748

    Jennifer CCC
    Newest Member
    Jennifer CCC
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your post demonstrates the profound frustration and isolation that so many in the Celiac community feel, and I want to thank you for channeling that experience into advocacy. The medical gaslighting you endured for decades is an unacceptable and, sadly, a common story, and the fact that you now have to "school" your own GI specialist speaks volumes about the critical lack of consistent and updated education. Your idea to make Celiac Disease a reportable condition to public health authorities is a compelling and strategic one. This single action would force the system to formally acknowledge the prevalence and seriousness of the disease, creating a concrete dataset that could drive better research funding, shape medical school curricula, and validate the patient experience in a way that individual stories alone often cannot. It is an uphill battle, but contacting representatives, as you have done with Adam Gray, is exactly how change begins. By framing it as a public health necessity—a matter of patient safety and protection from misdiagnosis and neglect—you are building a powerful case. Your voice and your perseverance, forged through thirty years of struggle, are exactly what this community needs to ensure that no one else has to fight so hard just to be believed and properly cared for.
    • Scott Adams
      I had no idea there is a "Louisville" in Colorado!😉 I thought it was a typo because I always think of the Kentucky city--but good luck!
    • Scott Adams
      Navigating medication safety with Celiac disease can be incredibly stressful, especially when dealing with asthma and severe allergies on top of it. While I don't have personal experience with the HealthA2Z brand of cetirizine, your caution is absolutely warranted. The inactive ingredients in pills, known as excipients, are often where gluten can be hidden, and since the FDA does not require gluten-free labeling for prescription or over-the-counter drugs, the manufacturer's word is essential. The fact that you cannot get a clear answer from Allegiant Health is a significant red flag; a company that is confident its product is gluten-free will typically have a customer service protocol to answer that exact question. In situations like this, the safest course of action is to consider this product "guilty until proven innocent" and avoid it. A better alternative would be to ask your pharmacist or doctor to help you identify a major national brand of cetirizine (like Zyrtec) whose manufacturer has a verified, publicly stated gluten-free policy for that specific medication. It's not worth the risk to your health when reliable, verifiable options are almost certainly available to you. You can search this site for USA prescriptions medications, but will need to know the manufacturer/maker if there is more than one, especially if you use a generic version of the medication: To see the ingredients you will need to click on the correct version of the medication and maker in the results, then scroll down to "Ingredients and Appearance" and click it, and then look at "Inactive Ingredients," as any gluten ingredients would likely appear there, rather than in the Active Ingredients area. https://dailymed.nlm.nih.gov/dailymed/   
    • Scott Adams
      What you're describing is indeed familiar to many in the Celiac community, especially in the early stages of healing. When the intestinal villi are damaged from Celiac disease, they struggle to properly digest and absorb fats, a condition known as bile acid malabsorption. This can cause exactly the kind of cramping and spasms you're seeing, as undigested fats can irritate the sensitive gut lining. It is highly plausible that her reactions to dairy and eggs are linked to their higher fat content rather than the proteins, especially since she tolerates lean chicken breast. The great news is that for many, this does improve with time. As her gut continues to heal on a strict gluten-free diet, her ability to produce the necessary enzymes and bile to break down fats should gradually return, allowing her to slowly tolerate a wider variety of foods. It's a slow process of healing, but your careful approach of focusing on low-fat, nutrient-dense foods like seeds and avocado is providing her system the best possible environment to recover. Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: Thank you for sharing your story—it's a valuable insight for other parents navigating similar challenges.
    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
×
×
  • 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.