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

Rachel--24 Collaborator
I suspect it might be why Igenex sends out a copy of the results to each person who is tested.

Yes....its VERY important to request and review all lab results to make sure the Dr. is interpreting the results correctly. NEVER take the doctors "word" for it. <_<


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



Celiac.com Sponsor (A8-M):



  • Replies 33.4k
  • Created
  • Last Reply
rinne Apprentice

Miamia, when were these tests done?

I wish I had been on earlier.

Does anyone else know?

Rachel--24 Collaborator
Rachel, I do try to resist. :lol:

:P

:lol::lol::lol:

I havent noticed the "resistance" part yet. :lol:

:P

Miamia, when were these tests done?

I wish I had been on earlier.

Does anyone else know?

I dont know...I asked the same thing. I'm thinking they were done awhile back....before the Lyme clan came to be. :unsure:

Does anyone know how long miamia has been sick?? Rinne is it longer than us (4 years) or shorter??

rinne Apprentice

I don't know but it has been for quite a while I think. :(

AndreaB Contributor
I suspect it might be why Igenex sends out a copy of the results to each person who is tested.

That's a pretty good idea on their part.

I don't know how long she's been sick. :( Hopefully she'll be on tonight and can fill us in, as well as when she had these done.

Why do I have a feeling they were done awhile ago? :(

happygirl Collaborator

x

CarlaB Enthusiast
:lol::lol::lol:

I havent noticed the "resistance" part yet. :lol:

Me either! :lol:


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

My goodness. This is a sin if the doctor had the results that Rachel and Rinne say are positive and didn't follow up.

Miamia--I don't mean to speak about you while you're not here, it's just that I feel so bad about this. I hope that this revelation is the beginning of your recovery :)

DingoGirl Enthusiast

oh my gaaaawd!!!!!!! :o:o:o Another one....Miamia, I"m actually not shocked. I just hope you can get some treatment and really start to feel better....the same thing that I hope for all of you.

So, The Dr's R have diagnosed this :P Why don't you two just hang up a shingle, and we'll come and see you? :o:lol: You guys DO seem to know more than the doctors.....that is really scary.

happygirl Collaborator

x

CarlaB Enthusiast
can i voice that i am apprehensive about carlas...and potentially mine...and anyone elses results... sigh :(

The only thing I'm apprehensive about is that the results will be unclear. I am really starting to believe this has to be my problem, it just makes too much sense. I hope the Igenex results are clear .... I'm afraid of being uncertain -- either positive or negative.

I feel like in going to an LLMD that I will get diagnosed. But I have reservations about it, too. Do they diagnose everyone who has these problems with Lyme? Maybe that's because everyone with these problems might have Lyme (or at the very least another bacteria that acts similarly and responds similarly).

I wouldn't be surprised if it was your problem, too, Laura. I actually think Lyme would be less difficult than EOS, too ... EOS sounds very scary ... such a limited diet! I hope your results come back negative on that one!!! You'll do fine with it if it's positive, I am sure ... Either way it's a chronic illness we have to deal with forever, I just hope to know soon what the illness is ... and I hope you find out soon, too.

happygirl Collaborator

x

miamia Rookie
Andrea, there are three people, but the numbers are four across, I'm confused.

Miamia, let me know if you want the name of the doctor. He's in Hyde Park and is Lyme Literate.

carla that would be great

DingoGirl Enthusiast

Oh good, I see Mia - - she can tell us everything, but thank you Laura for the briefing! :)

can i voice that i am apprehensive about carlas...and potentially mine...and anyone elses results... sigh :(

Yes, I would be very apprehensive too. :(

What brought all of you together here, it seems, was the fact that some of you were not getting significantly better (or permanently better) by gluten removal, for one, and also that there are still SO many intolerances, not to mention aches, pains, and general overall continual malais and decline, despite your best efforts, and still reacting to so many foods or losing lots of weight....it sounds like that's what Lyme does (in some cases - I know it's stealthy). So I am thinking that Laura, Bev, Carla and Julie may actually have Lyme also....who else?

I had something profound to say, the thought just plain dingo'd itself :( I am totally off today.....Rinne will express what I wanted to say quite eloquently, I am sure.

But now - what , five of you? - - have Lyme, and you all had such similar symptoms.......and longterm misery.... :o:ph34r::o

miamia Rookie
OMG miamia. :o

I have to say....I CANNOT believe your Dr. dismissed these results. I just dont know what to say. You really need to see a Dr. who is familiar with Lyme. These results are VERY much looking like you have Lyme Disease. Much more than mine and Rinnes results. I'm serious Miamia....you need to pursue this. If your Dr. dismissed these results he's not the right Dr. for you...not for Lyme anyway.

I'm pre-posting so I dont know if Rinne has seen these results are not or if anyone else has commented. If these were my results I would be much more certain that I have Lyme.

Thank God you found these results....I really think they mean something and further testing needs to be done or a Dr. who knows about Lyme needs to take a look at these results. Igenix clearly states on the results that IND's have clinical significance on double starred bands and further testing should be done. This would apply for only ONE indeterminate on a double starred band....you have SEVERAL. :blink:

You basically have a positive or weak positive on EVERY critical band indicating Lyme. I think your test is more positive then mine and Rinnes put together. :o

I am just dumbfounded that your Dr. would order these tests and then ignore the results. There should have been some follow up with results like this....even though they are "technically" negative. I would go so far as to say I'm more than 90% sure you have Lyme Disease based on these results. I dont know whether you have any Lyme Literate M.D.'s in your area but I would reccommend finding out and seeing a different Dr.

I cant even believe this....how long ago did you take this test??

Those Indeterminates mean that they found something....its a "weak" positive but the band was not dark enough to register as a +.

Its highly possible that if you started treatment those Indeterminates would then come back positive. Every single one of them are on the bands that are most specific for Lyme Disease. You have a high positive on band 41...if any ONE of those Indeterminates would have been a little stronger in intensity you would have had a positive test for Lyme Disease.

OMG...I'm sorry Miamia but right now I feel like I want to punch your Dr. for letting this go. The only thing I can think of is that he doesnt know anything about Lyme or how to read these test results. The thing that most bothers me is that it *says* right on the test that results like these (even if negative) need to be further pursued because the IND'S on double starred bands have clinical significance.

So yeah.....I want to punch him. :ph34r:

Rachel-

this is why I was so overwhelmed when I got them today. I immediatly got on line and posted - especially since on the results it says- "Diagnosis should not be based on lab tests alone. Results should be interpreted in conjunction with clinical symptoms and patient history" and something else about the low assay of this test and recommending further testing. I guess when I first got the results I didn;t really look ove rthem I just excepted I didn't have it. I have a doctors appt. on WEdnesday and I am bringing these and if he dosen't want to pursue it I will just go to another source, becaue it defintly looks a bit fishy to me. I am so happy you agree and I'm not crazy

Miamia

Ditto!!! Maybe I should practice some of my ant relocation techniques on him! Unbelievable!

I love you donna

I don't know but it has been for quite a while I think. :(

I just checked and this test was done in MAY!!!! I feel stupid right now for not looking at it closer. I am a little bit overwhelmed here- The meds I am taking for candida are giving me major brain fog and I can't think straight already but now trying to figure this out is insane. Thank you everyone - god I feel like I ahve such a wonderful support system- it means so much to me!!!!

I have been sick for 4 years now- but I got sick when I was younger and they thought it was just reflux finally I was able to control it but then 4 years ago after going on birth control which I reacted very strongly to I was never the same again- the thing is when I first got sick I spent the summer doing some traveling and I had stayed at ahouse that was pretty rustic- bugs everywhere type of thing- makes you wonder........

AndreaB Contributor
can i voice that i am apprehensive about carlas...and potentially mine...and anyone elses results... sigh :(

Carla's seemingly had hers awhile so I'll be real curious about her test results. I am really curious about you too. Seems like those with high intolerances, chemical sensitivities etc are testing positive.

So I am thinking that Laura, Bev, Carla and Julie may actually have Lyme also....who else?

Julie's already said she has it based on her bioscan and now she's got to find a doctor who will sign the note for the Igenix test.

I also think Judy may still have problems with lyme.

But now - what , five of you? - - have Lyme, and you all had such similar symptoms.......and longterm misery.... :o:ph34r::o

Rachel, Rinne, Julie and Mia. More than likely Carla.

I have a doctors appt. on WEdnesday and I am bringing these and if he dosen't want to pursue it I will just go to another source, becaue it defintly looks a bit fishy to me. I am so happy you agree and I'm not crazy

Make sure you hang on to those. You don't want your doctor to "forget" to give them back either.

I'll be waiting for your update post.

miamia Rookie
Poor thing, she's been sick with multiple issues on-off....more so "on" in the past 9 years or so...more so in past 4-ish, too. reflux since a kid, then flared during her teens, continued on into early 20s... late early 20s is when things got much worse. gluten intolerance and candida, now other food intolerances....she's my age, i think (25).

m-hope you don't mind me trying to BRIEFLY sum it up for you sweet girl. trying to save your energy for the lyme posting. if you want me to take any of this down, let me know :)

Laura

I just posted some of this before I read your post- I don't mind at all!!

AndreaB Contributor
I just checked and this test was done in MAY!!!! I feel stupid right now for not looking at it closer.

Back around when this thread was started (in April). :o

Don't feel stupid. We are trained to trust our doctors. Unfortunately that is becoming a dangerous thing most times.

DingoGirl Enthusiast
Julie's already said she has it based on her bioscan and now she's got to find a doctor who will sign the note for the Igenix test.

I also think Judy may still have problems with lyme.

Duh, totally forgot about Julie....where is my brain today? I sent her a big email about her results a couple of days ago! Sheesh.

Yup, Judy too, I think. And I am convinced Bev has it.

You should all take a group trip to that doctor in Hyde Park. :)

Rachel--24 Collaborator

OMG.....my head is really spinning from all of this.

So maybe miamia *will* be getting a diagnosis for Xmas this year! :)

It looks like me, Rinne and miamia all went downhill about the same time....4 years ago. :(

Miamia,

Dont feel bad about not having looked at your tests....you trusted your Doctor. We've all been there. Its part of this whole process....somewhere along the line we've all had to stand up for ourselves and to take a more active role because we have that determination and strong desire to get better. Thats why we're all here on this thread....because we dont give up.

The main thing is that now you have a better understanding of the results and can go from there as far as getting to the bottom of this....and I know you will get to the bottom of it. :)

I'm really glad we all have each other...I dont know what I'd do without all of you guys.

((((((((((hugs)))))))))) for everyone :wub:

I'm proud of all of us for hanging in there.....it hasnt been easy but OMG....I think we are on to something! BIGTIME. :o

Love you guys :)

CarlaB Enthusiast

Uh, oh, another hug fest!! :lol:

I certainly don't feel ALONE in this!!! :wub::wub::wub:

Rachel--24 Collaborator
So, The Dr's R have diagnosed this :P Why don't you two just hang up a shingle, and we'll come and see you? :

Hang up a shingle??? :unsure:

But, apparently preference doesn't always work ;)

Nope..it doesnt. <_<

If I got to pick...I'd be a happy Celiac eating one of those "Down Under" desert thingys at the Outback.

But instead I'm eating the same 5 foods I've been eating every day the last 2 months.... :huh:

CarlaB Enthusiast
Hang up a shingle??? :unsure:

It means put up a sign (go into business). Old signs were like shingles, especially considering old roofs were made out of wood. I mean back in the old, old days!

Rachel--24 Collaborator
so---do you lyme ladies who know of people who tested "clearly positive" on igenix?

Yeah...many, many people on the Lyme Boards got diagnosed with a "clearly" positive test from Igenix. Other people who've been sick for awhile have had to go on antibiotics and then retake the test to get the IND's to show up positive.

I've read lots of "personal" stories all over the web too.....lots of people get a definate answer.....but lots of people also get equivocal's...which is the case for all of us here so far.

Equivocals can sometimes be pretty clear.....like with miamia's results. Mine....isnt clear enough to satisfy me right now. I want further testing.

This is what is said about Equivocal's...

Instead of ignoring these, they should be a red flag to keep pursuing a laboratory diagnosis. Giving patients 4 weeks of antibiotics (usually tetracycline, 500 mg, 3 times a day), will convert a negative or equivocal Western blot to positive in about 36% of cases.

If these positive blots are found by specialty labs (Igenix), over 99% of those patients will respond to antibiotics.

AndreaB Contributor
I'm really glad we all have each other...I dont know what I'd do without all of you guys.

((((((((((hugs)))))))))) for everyone :wub:

I'm proud of all of us for hanging in there.....it hasnt been easy but OMG....I think we are on to something! BIGTIME. :o

Love you guys :)

I love hug and love fests!!

(((((((HUGS)))))) :wub::wub::wub::wub::wub::wub:

Archived

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

  • 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. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    2. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      26

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to Russ H's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      KAN-101 Treatment for Coeliac Disease

    5. - Scott Adams replied to miguel54b's topic in Related Issues & Disorders
      1

      Body dysmorphia experience


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,152
    • Most Online (within 30 mins)
      7,748

    denise.milillo
    Newest Member
    denise.milillo
    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

    • trents
      This article does not address migraines at all.  Yes, red wine and sulfites are often mentioned in connection with migraine triggers. With me, any kind of alcoholic beverage in very modest amounts will reliably produce a migraine. Nitrous oxide generators, which are vaso dialators, also will give me migraines reliably. So, I think most of my migraines are tied to fluctuations vascular tension and blood flow to the brain. That's why the sumatriptan works so well. It is a vaso constrictor. 
    • knitty kitty
      Excessive dietary tyrosine can cause problems.  Everything in moderation.   Sulfites can also trigger migraines. Sulfites are found in fermented, pickled and aged foods, like cheese.  Sulfites cause a high histamine release.  High histamine levels are found in migraine.  Following a low histamine diet like the low histamine Autoimmune Protocol diet, a Paleo diet, helps immensely.    Sulfites and other migraine trigger foods can cause changes in the gut microbiome.  These bad bacteria can increase the incidence of migraines, increasing histamine and inflammation leading to increased gut permeability (leaky gut), SIBO, and higher systemic inflammation.   A Ketogenic diet can reduce the incidence of migraine.  A Paleo diet like the AIP diet, that restricts carbohydrates (like from starchy vegetables) becomes a ketogenic diet.  This diet also changes the microbiome, eliminating the bad bacteria and SIBO that cause an increase in histamine, inflammation and migraine.  Fewer bad bacteria reduces inflammation, lowers migraine frequency, and improves leaky gut. Since I started following the low histamine ketogenic AIP paleo diet, I rarely get migraine.  Yes, I do eat carbs occasionally now, rice or potato, but still no migraines.  Feed your body right, feed your intestinal bacteria right, you'll feel better.  Good intestinal bacteria actually make your mental health better, too.  I had to decide to change my diet drastically in order to feel better all the time, not just to satisfy my taste buds.  I chose to eat so I would feel better all the time.  I do like dark chocolate (a migraine trigger), but now I can indulge occasionally without a migraine after.   Microbiota alterations are related to migraine food triggers and inflammatory markers in chronic migraine patients with medication overuse headache https://pmc.ncbi.nlm.nih.gov/articles/PMC11546420/  
    • trents
      Then we would need to cut out all meat and fish as they are richer sources of tyrosine than nuts and cheese. Something else about certain tyrosine rich foods must be the actual culprit. 
    • Scott Adams
      I agree that KAN-101 looks promising, and hope the fast track is approved. From our article below: "KAN-101 shows promise as an immune tolerance therapy aiming to retrain the immune system, potentially allowing safe gluten exposure in the future, but more clinical data is needed to confirm long-term effects."  
    • Scott Adams
      Thank you so much for having the courage to share this incredibly vivid and personal experience; it's a powerful reminder of how physical ailments can disrupt our fundamental sense of self. What you're describing sounds less like a purely psychological body dysmorphia and more like a distinct neurological event, likely triggered by the immense physical stress and inflammation that uncontrolled celiac disease can inflict on the entire body, including the nervous system. It makes complete sense that the specific sensory input—the pressure points of your elbows on your knees—created a temporary, distorted body map in your brain, and the fact that it ceased once you adopted a gluten-free diet is a crucial detail. Your intuition to document this is absolutely right; it's not "crazy" but rather a significant anecdotal data point that underscores the mysterious and far-reaching ways gluten can affect individuals. Your theory about sensory triggers from the feet for others is also a thoughtful insight, and sharing this story could indeed be validating for others who have had similar, unexplainable sensory disturbances, helping them feel less alone in their journey.
×
×
  • 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.