Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

The Lyme Disease Thread


CarlaB

Recommended Posts

Rpm999 Contributor

it's definite if it was positive right? must be something strong for it to, but wow i knew i wasn't going crazy with my 30 million symptoms :lol: i guess there


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



Celiac.com Sponsor (A8-M):



  • Replies 886
  • Created
  • Last Reply
dlp252 Apprentice
it's definite if it was positive right? must be something strong for it to, but wow i knew i wasn't going crazy with my 30 million symptoms :lol: i guess there

I don't here too often of doctors saying it's positive if it isn't. :) Usually, one would have the opposite problem...they would say it wasn't sometimes even if it was positive. :P

Rpm999 Contributor

no not the doctor, i mean the test, cause it isn't the big fancy igenex one

CarlaB Enthusiast
holy poop, lyme came back positive....like i said, i just know the test is a western blot one but it wasn't like it was a false negative or anything so i guess i definately have lyme, or something similiar

Congratulations on a diagnosis!!!!!!

Yep, if it came back positive and you have symptoms, it's positive. It's false negatives you have to worry about! You have a lot of work ahead of you, but at least now you know the nature of what you're fighting. Keep us posted!

dlp252 Apprentice
no not the doctor, i mean the test, cause it isn't the big fancy igenex one

Even MORE SO then, lol. The Igenix is usually the more sensitive, so if you've got a positive test by another method then you can be sure you have it.

Rpm999 Contributor

horray! it's crazy because i don't remember any bite, and never have pulled a tick out in my life...so almost every person with lyme has heavy metals i hear? how does that work, do infections have some sort of strange chemistry with them? glad lyme came up because it seems like everyone with lyme has other issues cause of it so i'm sure treating/finding out all these things will be weight lifted from my chest

CarlaB Enthusiast

I am convinced that Lyme does not exist alone. After all, it weakens the immune system, so other problems are bound to be there, how can they not be?

Everything you do to take more of the burden off your body will help.


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



Celiac.com Sponsor (A8-M):



truthsearcher Rookie

Rpm999,

Just wanted to chime in and say I'm glad your getting to the root of the problem. It was a relief to me as well.

I'm just waiting till March to see the LLMD

April,

No I don't test well for Apple pectin, the stuff just plugs me right up.

I take all that you listed except for the Molybedenum, and NAC.

I juice just about everyday as well :D

A note about my kids....

I had their blood drawn today. They handled it very well.

Bad news, I did not realize the lab did not spin the blood before giving it back to me to send Fed Ex.

I called IgeneX..... they said maybe they could spin it out. Otherwise I have to get two more kits and redo UGGGGGGH.

Let's hope it will spin out. THey said they would not charge me for two more kits but would have to pay for the Fed EX shipping. I was like OHHHHH NOOOOOOOO after I realized they had spinned my blood in November.You would think the lab should have known this ??????

So...... A WARNING for all who get the Western Blots.... Make sure they spin your blood before you leave that lab.

Take care everyone.

Rpm999 Contributor

i think i have most of this figured out...i believe i had lyme for a while, and that bad attack i had weakened my system severely and allowed lyme to sink in...before i had that attack, i had mini ones which i should have went to a GI for because it was throat swallowing based which i can't see being complicated, and me being careless led up to a big one that wasn't so easy...before i had the attack, nothing bothered me, i had a very strong immune and was fighting off lyme probably, but it all went downhill when my system became distressed...almost everything bothers me now and rachels story sounds so similiar...the root of the problem is the key plus when you're immune has gone to hell, allergies/intolerances always come up...it reminds me of when i was younger, everything bothered me but when i cured my severe athsma, it all went away because it caused immune distress...i believe a lot of people on here have a deeper problem, because what's the hardest things on your system? gluten, dairy and soy..when your immune is having problems because of sickness, what do you think will give the most issues? it all makes sense, but i know some people have had issues with those things constantly, but before i was sick luckily nothing bothered me in anyway so i think it's all because of what my immunes gone through and the attacks allowed, then lyme allowed (parasites, infections, ect.)....a lot to juggle but maybe it's good in a way when you tie it all together...it's all a detox problem too i'm sure which it seems like lyme always gives and just makes it all hard to handle and get rid of and that alone throws off your body chemistry...what do you think carla? i just don't have natural food allergies/intolerances and i know it, the pieces just didn't fit and thankfully i've stood asking questions and found out a main cause...when your body goes to hell that bad, there's always something hidden going crazy i bet...you can eliminate all you want, but why when something simple could be causing it all? i think we all underestimate how complex the immune can be and want to think it's all simple answers, and suffer in ways because of that...i feel bad for people stuck on strict diets and suffering, but oh well just some random thought :D

and what do you mean spin your blood?

truthsearcher Rookie

Rpm999,

Spinning the blood separates the serum or plasma form the the whole blood sample.

If it is not spinned the sample will start to coagulate and get thick and clumpy.

I really don't know if the samples I sent are going to be viable when Igenex gets them.

I'm hoping for the best, I want to spare the kids from getting poked again. Again I don't understand why the lab couldn't figure it out, and I was so caught up in not having the kids freak out about getting poked that we practically ran out the lab door when we were finished.

Oh well. Live and learn. I can't be too upset or my Lyme really flares.

Rpm999 Contributor

guess i don't have to worry since they came positive but yeah, silly mistakes people make can screw it all up huh?

CarlaB Enthusiast
...what do you think carla?

I think you really seem to have a good handle of what's going on with you. :)

I recently viewed online a talk giving by Dr. B. He said that on it's own, babesia will clear out in about 6 weeks. Bart is also self-resolving. However, when Lyme weakens the immune system, these two diseases cause major problems.

I know that stress has triggered my Lyme symptoms each of the four times it has really disabled me. The other three times more or less resolved themselves with eating right and heavy exercise.

I think the immune system is designed to handle this, but with all the burdens put on our systems today, it can't.

I also agree that many people on here, the ones who do not have celiac disease, might have something else going on underlying their intolerances, ie their intolerances are a symptom. At least that was the case for me.

I think that as you are working on it from all angles -- Lyme, parasites, metals, toxins, etc. -- you will get better.

dlp252 Apprentice

Yeah, I don't know when I got lyme either, but I do believe severe stress in 1995-1996 caused everything to be too much for my immune system!

truthsearcher Rookie

Well said Carla

And like Donna, whenever there was an upheaval in my life Lyme took over.

I think eating as clean and healthy as I can and not letting stress effect me keeps my lyme symptoms (tolerable).

I believe I've had lyme for a long, long time and I'm only 36 but when I got pregnant at 27 everything changed for me, I can't even handle misplacing a pencil now.

aprilh Apprentice

I got my blood taken today for the lyme tests. They send off to igenex. I asked the lady what testing they do but I didn't know what I was talking about to be specific. The testing was $400 but someone said that probably didn't include ???

I guess I'll know more when it comes back. Does anyone have an idea how long for igenex to return the results?

Rpm999 Contributor

and what's the way to find out if you definately have celiac perminately by genetics or whatever? i'd be shocked if i did since i had no issues before, i had some blood test and it just came up slightly abnormal...everything bothers me which would make sense with what my immunes gone through

CarlaB Enthusiast

Well, all my celiac tests were negative, but I felt better on the gluten-free diet and would react when I ate gluten. So, I did not test positive for celiac. If someone tested positive, that would mean they had it for life.

Which blood test came up abnormal for you?

dlp252 Apprentice
I got my blood taken today for the lyme tests. They send off to igenex. I asked the lady what testing they do but I didn't know what I was talking about to be specific. The testing was $400 but someone said that probably didn't include ???

I guess I'll know more when it comes back. Does anyone have an idea how long for igenex to return the results?

I'm not sure what all that covered. I know I didn't spend $400 for the western blots (only $190 in California, but that was last year), but I know it's more expensive in some areas and the price may have gone up. I think the co-infections testing is a lot more than that, so I'm thinking it doesn't include that. Probably the two western blots, maybe a PCR test, and I'm not sure what else.

dlp252 Apprentice

Oh, and maybe they took extra blood for another kind of test? I had 7 vials drawn...some of that went to Igenix and some went to other labs for mold toxicity testing, etc.

aprilh Apprentice
Oh, and maybe they took extra blood for another kind of test? I had 7 vials drawn...some of that went to Igenix and some went to other labs for mold toxicity testing, etc.

What kind of mold toxicity testing did you do? This may be something I need to do.

Rpm999 Contributor

i'll have to find out...but even if it came up, it could just be because of everything else going on, right? isn't the only way to find out if it's genetic through something on enterolab? i assume it's attacking my body and bothering me, but i want to know if it's the genetic disease that i'm now stuck with, which like i said would shock me...but do you have any clue what the blood test they do tests for? never really found out

aprilh Apprentice
i'll have to find out...but even if it came up, it could just be because of everything else going on, right? isn't the only way to find out if it's genetic through something on enterolab? i assume it's attacking my body and bothering me, but i want to know if it's the genetic disease that i'm now stuck with, which like i said would shock me...but do you have any clue what the blood test they do tests for? never really found out

You could retest yourself once you deal with lyme and your underlying issues. You will be surprised how many people are gluten intolerant because of those type issues and not necessarily because they are "celiac". A Year ago I could not handle the tinyest bit of gluten and now after healing leaky gut, treating a systemic candida overgrowth (fungal infection) I can handle "some" gluten now.

I predict that once I find out IF I have lyme and also deal with the underlying toxicity issue, I will be back to eating a "normal" diet.

dlp252 Apprentice
What kind of mold toxicity testing did you do? This may be something I need to do.

I'll have to look up the info later...all my papers are at home. It was a blood test that tested for the 3 biggies, aspergillus, and I can never remember the other two, lol. I think it was measured in antibodies, but I can't be sure. I'll also look up the lab.

i'll have to find out...but even if it came up, it could just be because of everything else going on, right? isn't the only way to find out if it's genetic through something on enterolab? i assume it's attacking my body and bothering me, but i want to know if it's the genetic disease that i'm now stuck with, which like i said would shock me...but do you have any clue what the blood test they do tests for? never really found out

I think you can have other types of genetic testing done, just not sure where. I had mine through enterolabs, it was a cheek swab. I am not sure if I am Celiac or not because when my conventional testing was done I had already been gluten free for several months, and before that was eating low carb, so wasn't getting a lot of gluten anyway. My doctor was reluctant to officially diagnose me with celiac, and I'm glad now that he didn't.

I do have a gene, so I suspect the possibility is always there, but I'll never know for sure. I did see improvement on the gluten free diet, just not enough. My hope though, is that when the rest of the health issues are taken care of, I'll be able to worry less about cross-contamination issues, and maybe have a little "treat" once in a while. I'll probably not ever go back to eating gluten on a regular basis though.

Ridgewalker Contributor

Quickie update...

Well, I had about convinced myself that I had nothing to worry about. (My rash was probably pinworm, I'm not horribly ill, etc.) Now I'm on antibiotics for a sinus infection and two symptoms that began over the summer- joint pain and neck stiffness/pain- have gotten significantly worse.

It may mean absolutely nothing more than a drop in barometric pressure, but it's enough to make me worry again. Argh!

CarlaB Enthusiast

Sarah, that can happen if you have Lyme ... symptoms can worsen when put on abx. It's stirs up the disease, plus the die-off can cause the symptoms.

Even if someone has the celiac genes, it still does not mean they will ever develop the disease. Thirty percent of the population has a celiac gene, but only 1 percent has celiac disease.

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Savannah Wert replied to Savannah Wert's topic in Coping with Celiac Disease
      2

      Hey all!

    2. - trents replied to Savannah Wert's topic in Coping with Celiac Disease
      2

      Hey all!

    3. - Savannah Wert posted a topic in Coping with Celiac Disease
      2

      Hey all!

    4. - glucel replied to Bindi's topic in Super Sensitive People
      36

      Refractory or super sensitive?

    5. - trents replied to Bindi's topic in Super Sensitive People
      36

      Refractory or super sensitive?


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      125,943
    • Most Online (within 30 mins)
      7,748

    sheridreghornn
    Newest Member
    sheridreghornn
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)

    • There are no registered users currently online

  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Savannah Wert
      Thank you! I’m currently the breadwinner as my husband is pursuing a finance degree so the nights that I am at work they can eat whatever my husband makes but when I am home we have gluten free meals and no complaints so far! I definitely don’t have a choice but to switch but I think slowly transitioning my family is good!😀
    • trents
      Welcome aboard, @Savannah Wert! There usually is a learning curve involved in arriving at a consistently gluten free diet since gluten is found in so many food products where you would never expect it to be. This article may be helpful:  It is good that you have identified some other foods that you cannot tolerate at this point as this is so common in the celiac population and it often goes unaddressed for years. You may find that the lactose intolerance disappears as your gut heals. No guarantee, though. Keep an eye out for the development of celiac symptoms in your children as the likelihood of first degree relatives developing active celiac disease is somewhere between 10% and almost 50%. Yes, the studies on this are all over the map. Is your home gluten free or will you be attempting to avoid CC (Cross Contamination) while fixing gluten-containing foods for your family members? It is always best for everyone in the home to commit to gluten free eating in the home environment when one member has celiac disease. 
    • Savannah Wert
      Hey everyone! I just joined and figured I’d introduce myself, my name is Savannah, I’ve been with my husband for over 8 years and we have 3 kids, a 7 year old, 5 year old, and 3 year old. I was diagnosed with celiac disease beginning of October along with microscopic colitis, lactose intolerance, and sucrose intolerance. I got sick the day before my 5th wedding anniversary and thought it was just the flu, which lasted over 3 months. I finally had a colonoscopy and endoscopy and was diagnosed. This has been such a hard transition and any tips are greatly appreciated!
    • glucel
      I don't react the same way to all of them but do react badly to many of them where others may not. I also have a touch of hypochondria so when the labs come back too high or makes me anxious. I am dismayed but not really surprised that I may be in the small group of people to suffer a particular side effect. I was originally on warfirin. I think that was the one where I had trouble with vitamin k numbers and or was anemic with low hemoglobin, red blood cells etc.  My blood pressure drops to very low numbers after taking something as simple as turmeric for a few weeks. My diastolic had touched 50 one day before I finally figured out that the herb was the problem. No intention to go for 40 so never looked back. I wanted to try benfothiamine but one of the listed side effects is bradycardia and other stuff that I am not going to challenge esp since I have had and still have to a lesser degree heart rhythm problems. 
    • trents
      What do you mean when you say, "blood thinners are all the same to me"? Do you mean you react negatively in the same way to all of them? Otherwise, they are not all the same. They work in different ways. Aspirin causes the platelets to be less sticky. Warfarin and related meds work by reducing the production of platelets. You might talk to your doctor about alternatives to aspirin. 
×
×
  • Create New...