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Omg...i Might Be On To Something


Rachel--24

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CarlaB Enthusiast
Does anyone have a rebounder?

I do. I used to get pain in my lymph nodes afterward. I've carried five babies, so I can't do more than about 50 jumps .... my bladder can't take it, LOL.

That's awesome you and Chloe can eat gluten again, you guys didn't have the genes? Or are you just going by symptoms?

We neither had the gene. I tested negative by biopsy and blood test, too, not that that means anything.

Beer made me very very sick. I didn't do well with alcohol in general, I think we talked about this way back when in the thread. Even if I could tolerate it I wouldn't be a drinker anyway I don't think so no loss there for me.

I could never tolerate a lot, but I did like to have a couple drinks once in a while. I could sometimes get hungover from just a couple, but usually two was okay.

found myself watching Kate and Leopold until it was over
I LOVE that movie!!! I especially like the scene where the dog poops and the cop is telling him he needs to pick it up! Almost everyone in our house can quote that scene verbatim.

hence the very early morning comment Carla, lol.
I didn't notice the time! LOL I used to have that every night, so my doc made me start taking Ambien after all the natural stuff didn't work. I also take 5 HTP. The Ambien gets me to sleep, the 5 HTP keeps me asleep. Last night I was out of 5 HTP and the same thing happened as last time, woke up and couldn't get back to sleep.
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confusedks Enthusiast
Does anyone have a rebounder? Julie I know you have one. When you use it do you get jarring headaches afterwards? Anyone? I do and I feel moody. :angry:

Also I got diarrhea today. I had some organic animal cookies on Sunday. I don't know if maybe it was a real, real long delayed reaction? Dumb, dumb, dumb, dumb, dumb..........

I have a rebounder. It does give me headaches. I don't go on it often because I think it just drains my lymphs too much...I can't tolerate it.

You had animal cookies....are you gluten free? Were they gluten free? I have nightmares about being forced to eat gluten, lol. I am SO sensitive to it I can't imagine it!

Actually...on this subject, does anyone know how to say gluten or wheat, rye, barley and oats in Spanish? I am at my Uncles house and they have a house keeper...she speaks some English, but considering most people who speak PERFECT English don't know what gluten is, I thought I'd have a better chance if I told her I can't have gluten in Spanish.

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Green12 Enthusiast
I LOVE that movie!!! I especially like the scene where the dog poops and the cop is telling him he needs to pick it up! Almost everyone in our house can quote that scene verbatim.

I didn't notice the time! LOL I used to have that every night, so my doc made me start taking Ambien after all the natural stuff didn't work. I also take 5 HTP. The Ambien gets me to sleep, the 5 HTP keeps me asleep. Last night I was out of 5 HTP and the same thing happened as last time, woke up and couldn't get back to sleep.

I love K & L too, that is a very funny scene.

Thank goodness it doesn't happen to me every night. I get that a few times a year, but last night was just extreme, the rate at which my mind was racing was a little alarming, I was writing pages and pages of lists. I decorated my sister-in-law's entire house in my mind, I visualized it. Major creativity was pouring out. :unsure: I was a Martha Stewart Rain Man.

Actually...on this subject, does anyone know how to say gluten or wheat, rye, barley and oats in Spanish? I am at my Uncles house and they have a house keeper...she speaks some English, but considering most people who speak PERFECT English don't know what gluten is, I thought I'd have a better chance if I told her I can't have gluten in Spanish.

I believe trigo is wheat, harina is flour....let me go get my dictionary and I'll get back to you on the other words.

My Spanish isn't perfect but it might be, No puedo comer trigo/harina (I am not able to eat wheat/flour)

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Green12 Enthusiast
Actually...on this subject, does anyone know how to say gluten or wheat, rye, barley and oats in Spanish? I am at my Uncles house and they have a house keeper...she speaks some English, but considering most people who speak PERFECT English don't know what gluten is, I thought I'd have a better chance if I told her I can't have gluten in Spanish.

Ok, oats is avena, barley is cebada, rye is centeno.

Gluten isn't even in my little dictionary, lol.

You are friends with Molly, right? She would be a good one to ask, she knows a lot of Spanish.

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tom Contributor
Well said Sherry.

Thanks for this book mention, sounds interesting. I am going to look into it.

Yes, I think I could use a book like that these days.

Already checked closest library, but they don't have it.

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CarlaB Enthusiast
:)
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Green12 Enthusiast
This is from the Triumph dining card --

"No puedo comer trigo, avena, cebada, centeno ni nada preparado con estos alientos incluyendo harina, pan, pasta, hotcakes, tortillas de harina, pasteles, comidas empanizadas o capeadas, crutones, avena. Ni, aunque parezca extrano, salsa de soya, teriyaki, blue cheese, o cerveza."

Muy excellente!

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Rachel--24 Collaborator

I've got more scientificness on molybdenum. :)

Function

The biological form of molybdenum, present in almost all molybdenum-containing enzymes (molybdoenzymes), is an organic molecule known as the molybdenum cofactor . In humans, molybdenum is known to function as a cofactor for three enzymes:

Sulfite oxidase catalyzes the transformation of sulfite to sulfate, a reaction that is necessary for the metabolism of sulfur-containing amino acids (methionine and cysteine).

Xanthine oxidase catalyzes the breakdown of nucleotides (precursors to DNA and RNA) to form uric acid, which contributes to the plasma antioxidant capacity of the blood.

Aldehyde oxidase and xanthine oxidase catalyze hydroxylation reactions that involve a number of different molecules with similar chemical structures. Xanthine oxidase and aldehyde oxidase also play a role in the metabolism of drugs and toxins .

Of these three enzymes, only sulfite oxidase is known to be crucial for human health .

I'm guessing I'm having problems with all 3 of these enzymes because..

#1. I'm reacting to sulfur and phenols.

#2 I've had low uric acid

#3 Reacting to lots of perfumes and other scents.

The aldehyde oxidase enzyme protects us from toxic "aldehydes".....this includes the toxins produced by candida. So if this enzyme is down....yeast toxins will make us sick. Usually if this enzyme is deficient there will be increased sensitivity to fragrances and other environmental toxins.

As it relates to Candida, those of you who have read the work of Dr. Orion Truss, or who have seen quotes by others from his work, will already have been alerted to his assertion that much of the harm done by Candida results from its waste product, acetaldehyde, which in turn can affect the metabolic, neurological, endocrine, and immune systems.

Further, that few chemicals can create so much havoc in the body as acetaldehyde can. It may interfere with the receptors for acetylcholine which is supposedly the major neurotransmitter in the corpus callosum.

Formaldehyde, obviously then, is related to acetaldehyde in the aldehyde chain of chemicals.

Chemical aldehydes are best known as fragrances." "Chemical aldehydess are best known as fragrances.... Ethanol, or drinking alcohol, is also precessed to acetaldehyde. ...the body has an enzyme which breaks down the aldehydes to less toxic substances.

This enzyme is aldehyde oxidase, or sometimes, aldehyde dehydrogenase. Aldehydes encountered dietarily or environmentally or produced in the body must be handled by aldehyde oxidase metabolic pathways.

Acetaldehyde is a paraticularly toxic substance which, in addition to being produced by threonine and ethanol, is a product of the metabolism (i.e. fermentation) of carbohydrate in yeast -- hence the Candida connection.

Acetaldehyde is thought to be the major source of tissue damage in alcoholics rather than ethanol itself. The conversion of acetaldehyde into acetic acid" for this reaction to occur, threonine to acetaldehyde to acetic acid to acetyl coenzyme A, NAD (niacine amide) is required, and aldehyde oxidase is dependent of riboflavin, iron, and molybdenum.

These forgoing nutrients could be helpful to Candida albicans patients, and others who are sensitive to various fragrances and airborne odors. Those patients with aldehyde sensitivity are incredibly sensitive to any type of fragrance.

In my book on mercury toxicity it states that these 3 enzymes are often impaired in mercury intoxication. Molybdenum is the main cofactor for these enzymes and supplementing it may improve their function.

Another interesting thing I learned is that both copper and Tungsten are antagonists of molybdenum. Too much of either one can cause a deficiency of molybdenum.

Tungsten is a toxic metal and it was the metal that I had the highest levels of on my first provoked urine challenge.

I've had off the charts copper on both of my tests but this is considered normal since DMPS preferentially pulls copper out. Of course I could have elevated copper anyway but I havent had any test to confirm this.

I was less sensitive and tolerating more foods early in the year and I'm still wondering why that was. I'm wondering if the DMPS was helping by pulling out the tungsten and the copper.

I started increasing my mineral IV's and I'm wondering if that might have set me back. It was only certain minerals that were increased....copper was doubled but molybdenum was not increased. So I'm wondering if I was improving enzyme function by chelating tungsten and copper...but then went backward by increasing the copper in my mineral IV's. <_<

I dunno...all I know is that I was less sensitive and I was eating more foods! And now I'm eating beef and peas again. :rolleyes:

I think I have to figure out a way to improve the function of these 3 enzymes....especially the sulfur oxidase enzyme.

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Rachel--24 Collaborator

Julie,

I think you asked if my hair analysis showed elevated copper?

Unfortunately, it was not included in the test. So...I have no idea either way.

It would probably be good for me to have a more updated hair analysis since that one was from about 4 years ago.

When I first got sick I bought this book on mercury toxicity...at that time I seriously couldnt understand most of the info...it was WAY to scientific for me. :blink:

Now I'm actually familiar with alot of what is discussed in the book and I've found it to be very helpful. I still wouldnt consider it an easy read though. Its not good for days when my brain has the dumb. :P

Anyways, its got good info. about copper toxicity and how to reduce copper in the body. It also talks about how to tell the difference from mercury toxicity and true copper toxicity.

I think in my case mercury is the real problem but copper is probably high as a result of that. Even though low copper can also cause problems it says that since it interacts with mercury its best to keep the copper somewhat low (but obviously not too low) when mercury is an issue.

Molybdenum is one of the things that can bring copper levels down so maybe it will do me some good.

I think I can get some idea about whether or not I have elevated copper by doing an unprovoked urine challenge.

DMPS is really good at removing copper (DMSA isnt) so once I get back on it that should help as well. If I get back on the mineral IV's I'll see if they can leave the copper out...or at least reduce it.

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mftnchn Explorer
I didn't notice the time! LOL I used to have that every night, so my doc made me start taking Ambien after all the natural stuff didn't work. I also take 5 HTP. The Ambien gets me to sleep, the 5 HTP keeps me asleep. Last night I was out of 5 HTP and the same thing happened as last time, woke up and couldn't get back to sleep.

I am really amazed at how well the Travacor (neurotransmitter support) is helping me sleep. Night 4 last night post time zone change, and I slept 6 hours with ambien until 5 am. That hasn't happened in several years usually it takes me 9-10 days on Ambien every night to switch. I think the Natural Calm (an easily absorbed magnesium) is also helping.

Sherry

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mftnchn Explorer
Yes, I think I could use a book like that these days.

Already checked closest library, but they don't have it.

My used copy bought online was cheap, it's an older book and very small. Published in '95

Sherry

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mftnchn Explorer

Someone just mentioned they were staring Nattokinase--sorry, I forgot who? I just wanted to update you because I started this in mid-February. The ART testing showed I would benefit and had the fibrin problem common with lyme with poor lyme flow and the erlichia was plugging the lymph too. I take the Nattokinase for the fibrin issue (and maybe something else?), and poke root for the lymph and erlichia issue. March ART showed improvement in this.

Anyway, another confirmation of this improvement was that today I did the gua sha which I wasn't doing while in the USA. I had very little "sha" compared to last time, there was a HUGE difference! So apparently the stagnation problem has really improved.

So, the expensive nattokinase is worth it I guess. I am taking the lowest dose recommended by ART because of the expense. I use Jarrow, 1-3 in the afternoon and evening.

Sherry

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AndreaB Contributor
Anyway, another confirmation of this improvement was that today I did the gua sha which I wasn't doing while in the USA. I had very little "sha" compared to last time, there was a HUGE difference! So apparently the stagnation problem has really improved.

Great news Sherry! :D

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mftnchn Explorer

Thanks. Can't wait to get the R/O water filter working to see if that helps too.

Rachel, the scientificness is going over my head for now...but trying to at least recall that the info is here.

Lots of fatigue for me lately too, but better yesterday and today.

I wrote Dr. E after I read on the forum here that herbal tinctures often use grain based alcohol. I am supposed to be corn free and one of mine says right on it that it has corn-based alcohol..., haven't heard back from her on that one. Worse than that would be if they are barley or wheat derived. :ph34r:

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CarlaB Enthusiast
I am really amazed at how well the Travacor (neurotransmitter support) is helping me sleep. Night 4 last night post time zone change, and I slept 6 hours with ambien until 5 am. That hasn't happened in several years usually it takes me 9-10 days on Ambien every night to switch. I think the Natural Calm (an easily absorbed magnesium) is also helping.

Sherry

That's wonderful!

I wrote Dr. E after I read on the forum here that herbal tinctures often use grain based alcohol. I am supposed to be corn free and one of mine says right on it that it has corn-based alcohol..., haven't heard back from her on that one. Worse than that would be if they are barley or wheat derived. :ph34r:

I would think it was distilled alcohol, so it's probably okay. Even if it were derived from wheat or barley, there will be no gluten left after distillation. Now if you had a corn allergy, I don't know how that would work. I guess it depends on what part of the corn you are allergic to.

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aprilh Apprentice
Someone just mentioned they were staring Nattokinase--sorry, I forgot who? I just wanted to update you because I started this in mid-February. The ART testing showed I would benefit and had the fibrin problem common with lyme with poor lyme flow and the erlichia was plugging the lymph too. I take the Nattokinase for the fibrin issue (and maybe something else?), and poke root for the lymph and erlichia issue. March ART showed improvement in this.

Anyway, another confirmation of this improvement was that today I did the gua sha which I wasn't doing while in the USA. I had very little "sha" compared to last time, there was a HUGE difference! So apparently the stagnation problem has really improved.

So, the expensive nattokinase is worth it I guess. I am taking the lowest dose recommended by ART because of the expense. I use Jarrow, 1-3 in the afternoon and evening.

Sherry

Hi Sherry,

I am taking Nattokinase. I did a lot of research on it, but am always scared to try new things, so I put it off for a long time. I actually feel really good on this supplement!

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aprilh Apprentice

Rachel,

Zinc also balances copper.

We had high copper and tungsten in our household. I didn't know molybdenum helped with that.

I couldn't figure out where my son's tungsten was coming from. Did you know that its found in those toaster oven lamp things??!! I am sure there are other sources.

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Green12 Enthusiast

Rachel, thanks for all the scientificness. It's a little over my head right now, I need to read it through again and try to focus.

My hair analysis was actually quite revealing, and the way my practitioner explained everything made sense. Copper toxicity showed up and she touched on the elevated copper and fungal/yeast issues. Most significant for me was my patossium/sodium ratio, extremely low, which means adrenal burnout, the inability to fight off infections (like lyme), etc.

Her approach with me was to build up the adrenals, bring up the potassium/sodium ratio, detox the copper. When the adrenals are stronger, potassium/sodium ratio balanced, and copper detoxed the yeast and fungal issues will normalize.

My practitioner said the sauna would help detox the copper, I was also taking kelp to bind with the copper, and she had me on selenium for added protection against the copper and other metals. Unfortunately the sauna was too strong for me and I had to take a break, but I hope to be able to get back in it again.

Someone just mentioned they were staring Nattokinase--sorry, I forgot who? I just wanted to update you because I started this in mid-February. The ART testing showed I would benefit and had the fibrin problem common with lyme with poor lyme flow and the erlichia was plugging the lymph too. I take the Nattokinase for the fibrin issue (and maybe something else?), and poke root for the lymph and erlichia issue. March ART showed improvement in this.

Anyway, another confirmation of this improvement was that today I did the gua sha which I wasn't doing while in the USA. I had very little "sha" compared to last time, there was a HUGE difference! So apparently the stagnation problem has really improved.

So, the expensive nattokinase is worth it I guess. I am taking the lowest dose recommended by ART because of the expense. I use Jarrow, 1-3 in the afternoon and evening.

Great news Sherry.

It's nice to hear about results, sometimes we take stuff and never really know if it is making a difference or if it's worth it. I am sure having the confirmation that you have had improvement with the gua sha is reassuring.

Hi Sherry,

I am taking Nattokinase. I did a lot of research on it, but am always scared to try new things, so I put it off for a long time. I actually feel really good on this supplement!

I might be put on nattokinase, or something similar, soon for the fibrin. From what you and Sherry say about it here I'm encouraged about it.

Kassandra, I got my LEAP test kit. I can't really tell you much about it now other than it is a blood draw, they take 4 vials. You have to check boxes on a page about all the foods you don't eat or that give you known reactions.

I will be able to tell you more when I get the results and the Dr goes over them with me and explains more about it and what it's supposed to do.

I hope to go Monday or Tuesday for the bood draw, I figured I would do both the LEAP test and the additional tests that my ART pratitioner ordered and get them both over in one trip.

I so dread the blood draw, I have a small window of time I can get it done, if I have an outbreak I will react to the needle stick and break out more :( So I hope Monday/Tuesday comes and goes quickly.

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AndreaB Contributor
I hope to go Monday or Tuesday for the bood draw, I figured I would do both the LEAP test and the additional tests that my ART pratitioner ordered and get them both over in one trip.

I so dread the blood draw, I have a small window of time I can get it done, if I have an outbreak I will react to the needle stick and break out more :( So I hope Monday/Tuesday comes and goes quickly.

Hope all works out smoothly, with no outbreaks!

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Rachel--24 Collaborator
I couldn't figure out where my son's tungsten was coming from. Did you know that its found in those toaster oven lamp things??!! I am sure there are other sources.

I had never even heard of tungsten until I saw it on my lab results. I tried to find info online but didnt find anything significant. When I asked my Dr. about it he said that he wasnt concerned with the tungsten....he said the main concern was the mercury...along with cadmium and lead.

I'm thinking that tungsten isnt likely to cause problems on its own...under normal circumstances the body probably has no problems detoxing it.

If mercury wreaks havoc and interferes with the pathways..then some of these other metals are building up as a result.

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Rachel--24 Collaborator
Rachel, thanks for all the scientificness. It's a little over my head right now, I need to read it through again and try to focus.

I think the pathway stuff can be really complicated. I havent had alot of brainfog lately and I think some of this stuff is actually sinking in...and it makes sense to me! :blink:

I so dread the blood draw, I have a small window of time I can get it done, if I have an outbreak I will react to the needle stick and break out more :( So I hope Monday/Tuesday comes and goes quickly.

Good luck with this Julie! Hopefully there will be NO outbreak to cause problems. :)

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tabasco32 Apprentice
Muy excellente!

:lol::lol:

You guys are to much. I know I shouldn't laugh it's just cute and funny. Not only do we come to learn about all the scientificness but also some spanish lessons. My grandma and mom eat avena everyday..

Oh and those organic animal cookies were not gluten free. I guess I just wanted to test them out. They were starring me in the face saying eat me, eat me. <_<

I have nightmares about gluten too! I want to eat the pizza in my dream but then my family comes and gobbles it all up before I can have any. :(

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confusedks Enthusiast
Kassandra, I got my LEAP test kit. I can't really tell you much about it now other than it is a blood draw, they take 4 vials. You have to check boxes on a page about all the foods you don't eat or that give you known reactions.

I will be able to tell you more when I get the results and the Dr goes over them with me and explains more about it and what it's supposed to do.

Julie...do you know how much it will cost to have done? You can PM me if you'd like. I am seeing Dr H this weekend and I want to ask him about these kinds of tests.

Everyone,

I made an appt. with a Naturopath Dr for this coming Wednesday. I figured this way I will be able to have her test stuff that Dr H puts me on this weekend.

I am excited...she does some sort of muscle testing, I don't know if it's ART or what it is. She will be testing me for all the supplements I'm taking and some foods I want tested. Actually, I might just do that instead of a blood test. I would love to have a session of just foods, where we test all kinds of things.

She specializes in nutrition and homeopathy, so she will be able to help me figure out a good meal plan...since I'm ALWAYS running out of food ideas. :)

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mftnchn Explorer

Kassandra, this sounds good, hope she works out really well.

Sherry

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Green12 Enthusiast
Lots of fatigue for me lately too, but better yesterday and today.

I wrote Dr. E after I read on the forum here that herbal tinctures often use grain based alcohol. I am supposed to be corn free and one of mine says right on it that it has corn-based alcohol..., haven't heard back from her on that one. Worse than that would be if they are barley or wheat derived. :ph34r:

Sorry, I must have missed this Sherry.

Do you think the fatigue is travel related? Glad it is better today.

I don't know about the corn based grain alcohol, I hope you get some answers. Let us know what you find out.

I think the pathway stuff can be really complicated. I havent had alot of brainfog lately and I think some of this stuff is actually sinking in...and it makes sense to me! :blink:

Good luck with this Julie! Hopefully there will be NO outbreak to cause problems. :)

Thanks Rachel, Andrea too.

I'm glad all the scientifcness is sinking in for you and making sense, that's a good thing!

When do you meet with your Drs/practitioners again? I'm excited to hear what you all come up with when you put your heads together.

I'm totally bummed, apparently Jenny McCarthy was on Larry King Live again last night with another Autism panel and I missed it! I am always interested in what they say.

My grandma and mom eat avena everyday..

Oh and those organic animal cookies were not gluten free. I guess I just wanted to test them out. They were starring me in the face saying eat me, eat me. <_<

Boy do I wish I could eat avena everyday Lisa. I'm jealous of your grandma and mom. Out of everything I think I miss oats the most, oatmeal, oatmeal cookies were 2 of my most favorite foods. There really isn't any replacement for it, quinoa flakes just don't cut it.

Did you have anymore reactions to the gluten filled animal cookies? I hope you don't get too sick and can bounce back quickly.

Everyone,

I made an appt. with a Naturopath Dr for this coming Wednesday. I figured this way I will be able to have her test stuff that Dr H puts me on this weekend.

I am excited...she does some sort of muscle testing, I don't know if it's ART or what it is. She will be testing me for all the supplements I'm taking and some foods I want tested. Actually, I might just do that instead of a blood test. I would love to have a session of just foods, where we test all kinds of things.

She specializes in nutrition and homeopathy, so she will be able to help me figure out a good meal plan...since I'm ALWAYS running out of food ideas. :)

She sounds very promising, I hope she is able to help you with foods!

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      It sounds like you've been through a lot with your son's health journey, and it's understandable that you're seeking answers and solutions. Given the complexity of his symptoms and medical history, it might be beneficial to explore a few avenues: Encourage your son to keep a detailed journal of his symptoms, including when they occur, their severity, any triggers or patterns, and how they impact his daily life. This information can be valuable during medical consultations and may help identify correlations or trends. Consider seeking opinions from specialized medical centers or academic hospitals that have multidisciplinary teams specializing in gastrointestinal disorders, especially those related to Celiac disease and Eosinophilic Esophagitis (EOE). These centers often have experts who deal with complex cases and can offer a comprehensive evaluation. Since you've already explored alternative medicine with a nutrition response doctor and a gut detox diet, you may want to consider consulting a functional medicine practitioner. They take a holistic approach to health, looking at underlying causes and imbalances that may contribute to symptoms. Given his low vitamin D levels and other nutritional markers, a thorough nutritional assessment by a registered dietitian or nutritionist specializing in gastrointestinal health could provide insights into any deficiencies or dietary adjustments that might help alleviate symptoms. In addition to routine tests, consider asking about more specialized tests that may not be part of standard screenings. These could include comprehensive stool analyses, food intolerance testing, allergy panels, or advanced imaging studies to assess gut health.
    • Nacina
      Hello, I am a 45 year old mom, who was diagnosed at 29 with Celiac. My now 14 year old son was diagnosed just before his 4th birthday. Needless to say, we are old pros with the diet. He was experiencing some issues, overall health took a major plummet a year ago, and through a bit of work, was diagnosed with EOE. Tried diet alone, but his follow up endoscopy didn't show the improvements his DR. wanted to see, so I tried the medication. (Steroid). He became extremely backed up, and they had him taking Miralax daily. His health plummeted. He is a straight A honor's 8th grader who plays club soccer very competitively. His health continued to decline and at 13 had a colonoscopy and another upper gi. (He was still compacted even with the prep). I finally pulled him off all meds and mira lax, after reading much negative literature online, and put him on a gut detox diet and took him to a nutrition response dr. Finally things have improved. However...over a year later and he is having relapse stomach pain, debilitating stomach pain. Missing a day of school a week, to three this week. This is where we downward spiral with him. He says it doesn't feel the same as when he has gotten backed up before. He is eating prunes, taking his supplements, drinking water...all of the things. Yet, he is feeling horrible. Pain is abdomen, headache, lethargy, diarrhea . He is on a strict gluten dairy, egg free diet. He has adapted well in regards to diet. But I feel like we are missing something here. He is too active, too outgoing to be feeling sick all of the time. His Bilirubin is constantly high. His white blood count always runs slightly low. His vitamin D was very low last time he ran tests, (last month) when he was sick for a week. His celiac markers show negative, so it isn't that. His last endoscopy showed no Eosinaphils in his esophagus.  I have taken him to multiple Ped. Gastro specialists. They run tests, and we get zero answers. I meticulously go through labs, hoping to make some sense and maybe catch something. Any thoughts or ideas would greatly be appreciated. 
    • trents
      But if you have been off of wheat for a period of weeks/months leading up to the testing it will likely turn out to be negative for celiac disease, even if you actually have celiac disease. Given your symptoms when consuming gluten, we certainly understand your reluctance to undergo  the "gluten challenge" before testing but you need to understand that the testing may be a waste of time if you don't. What are you going to do if it is negative for celiac disease? Are you going to go back to merrily eating wheat/barley/rye products while living in pain and destroying your health? You will be in a conundrum. Do I or do I not? And you will likely have a difficult time being consistent with your diet. Celiac disease causes inflammation to the small bowel villous lining when gluten containing grains are consumed. This inflammation produces certain antibodies that can be detected in the blood after they reach a certain level, which takes weeks or months after the onset of the disease. If gluten is stopped or drastically reduced, the inflammation begins to decrease and so do the antibodies. Before long, their low levels are not detectable by testing and the antibody blood tests done for diagnosing celiac disease will be negative. Over time, this inflammation wears down the billions of microscopic, finger-like projections that make up the lining and form the nutrient absorbing layer of the small bowel where all the nutrition in our food is absorbed. As the villi bet worn down, vitamin and mineral deficiencies typically develop because absorption is compromised. An endoscopy with biopsy of the small bowel lining to microscopically examine this damage is usually the second stage of celiac disease diagnosis. However, when people cut out gluten or cut back on it significantly ahead of time before the biopsy is done, the villous lining has already experienced some healing and the microscopic examination may be negative or inconclusive. I'm not trying to tell you what to do I just want you to understand what the consequences of going gluten free ahead of testing are as far as test results go so that you will either not waste your time in having the tests done or will be prepared for negative test results and the impact that will have on your dietary decisions. And, who are these "consultants" you keep talking about and what are their qualifications? You are in the unenviable position that many who joint this forum have found themselves in. Namely, having begun a gluten free diet before getting a proper diagnosis but unwilling to enter into the gluten challenge for valid testing because of the severity of the symptoms it would cause them.
    • Fluka66
      Thank you very much for your reply. I hadn't heard of celiac disease but began to notice a pattern of pain. I've been on the floor more than once with agonising pain but this was always put down to another abdominal problem consequently I've been on a roundabout of backwards and forwards with another consultant for many years. I originally questioned this diagnosis but was assured it was the reason for my pain. Many years later the consultant gave up and I had a new GP. I started to cut out certain food types ,reading packets then really started to cut out wheat and went lactose free. After a month I reintroduced these in one meal and ended screaming in agony the tearing and bloating pain. With this info and a swollen lymph node in my neck I went back to the GP.  I have a referral now . I have also found out that acidic food is causing the terrible pain . My thoughts are this is irritating any ulcers. I'm hoping that after a decade the outlook isn't all bad. My blood test came back with a high marker but I didn't catch what it was. My GP and I have agreed that I won't go back on wheat just for the test due to the pain , my swollen lymph node and blood test results.  Trying to remain calm for the referral and perhaps needed to be more forceful all those years ago but I'm not assertive and consultants can be overwhelming. Many thanks for your reply . Wishing you all the best.
    • Moodiefoodie
      Wow! Fascinating info. Thanks so much! I really appreciate the guidance. @Spacepanther Over the years I have had rheumatologists do full lab work ups on me. They told me they had screened me for arthritis, lupus, and Lyme disease (all negative). In addition to joint pain and stiffness I had swelling in both knees that later moved to my elbow as well.  I also experience stiffness and pain in my neck and shoulders when it flares. I vomited fairly often growing up, but there wasn’t a real pattern to it and I didn’t know it wasn’t normal (thought people caught stomach viruses often).  I don’t usually have stomach symptoms immediately after eating gluten that I notice.  The only other joint condition I know of is fibromyalgia. Good luck! Hope you can get it figured out. I only assumed my joint symptoms were due to the celiac’s because it is under control for the most part on a gluten-free diet.  The rheumatologist also mentioned that some inflammatory/autoimmune diseases can be slow-moving and not detectable until they progress.
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