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

The Lyme Disease Thread


CarlaB

Recommended Posts

CarlaB Enthusiast

Thanks Patti. :)


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



Celiac.com Sponsor (A8-M):



  • Replies 886
  • Created
  • Last Reply
lizard00 Enthusiast

Hi everyone!

So a quick update: ALL of my bloodwork came back normal; I don't have copies yet, but I'll get them soon. I have been feeling pretty good these past couple of weeks, so maybe it's just getting over the initial damage by gluten. I am going to another GI in a few weeks, so we'll see what comes of that. But until then, I am going to continue to monitor changes in how I feel and go from there. I'm kind of sick of being tested at the moment, and since I'm feeling much better, I'm taking a brief rest. I haven't ruled anything out, but I'm kind of stepping back from everything for a bit to see what comes to be. Thanks to all of you for your help and information.

I have been reading the posts and saw the new info about the review of the panel of DRs who say chronic lyme is nonexistant. What an amazing victory!!!

Here is an article that was in our paper today. I'm not very good at linking things, so I'll give it a shot. Hope it works!

Open Original Shared Link

CarlaB Enthusiast

Lizard, I hope you do get copies of your results ..... my doctor told me my blood work was normal, too, when it was clearly a positive test. <_<

Plus, the CDC standards for a positive test for their tracking purposes is much more strict than diagnostic standards should be ... though for reasons you already know due to the political climate surrounding Lyme, most doctors use those standards that the CDC never intended to be used for diagnostic purposes. Lyme docs will treat you if you have a positive Lyme specific band along with symptoms ..... well, even symptoms alone since it's a clinical diagnosis, but a Lyme specific band is confirmation of the diagnosis.

My daughter was treated with a negative test .... her diagnosis was confirmed by her reaction to the meds.

I'm glad you're feeling better lately!

Thanks for the link.

Ridgewalker Contributor

My mom pulled a tick off Ezra today. :(Yeeeargh!

AndreaB Contributor
My mom pulled a tick off Ezra today. :(Yeeeargh!

Uh-oh! :ph34r::(

What a handsome little boy he is. :)

susieg-1 Apprentice

Lizard, I hope you do get copies of your results ..... my doctor told me my blood work was normal, too, when it was clearly a positive test. <_<

Plus, the CDC standards for a positive test for their tracking purposes is much more strict than diagnostic standards should be ... though for reasons you already know due to the political climate surrounding Lyme, most doctors use those standards that the CDC never intended to be used for diagnostic purposes. Lyme docs will treat you if you have a positive Lyme specific band along with symptoms ..... well, even symptoms alone since it's a clinical diagnosis, but a Lyme specific band is confirmation of the diagnosis.

My daughter was treated with a negative test .... her diagnosis was confirmed by her reaction to the meds.

I'm glad you're feeling better lately!

Thanks for the link.

Carla, Laurie

I have a signed IGeneX lab slip !!!!! I will do bloodwork tomarrow and get FedX to ship to CA!!! Will post results for your input in a couple weeks Yahooooooooooo!!!!!!

truthsearcher Rookie

Sarah,

Sorry about Ezra. Definetly get treatment right away to erradicate it quickly. It can be done if treated very promptly.

Susie, Yeah! You got the lab slip signed! Wow good news! Keep us posted! If you don't hear in two weeks give your Dr. a call because if they thing it's negative they may never call you. And make sure you get copies, both the IgG and IgM.

Take Care


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



Celiac.com Sponsor (A8-M):



CarlaB Enthusiast
My mom pulled a tick off Ezra today. :(Yeeeargh!

Sarah,

Sorry about Ezra. Definetly get treatment right away to erradicate it quickly. It can be done if treated very promptly.

That is what I'd do!!!

Susie, YAY!! Keep us posted!

Ridgewalker Contributor

Seriously?! The tick was just on him yesterday-- there's no way to tell if the tick was even a carrier unless he shows symptoms, right?

I mean... everyone I know has been bitten by ticks, literally. We're in a bad area for them. But that doesn't mean they all have Lyme, right?

I am keeping an eye on him, though, of course, for any rash, fever etc...

CarlaB Enthusiast

No, they don't all have Lyme. But after what I've experienced, I would rather do antibiotics than wait till they get sick .... but everyone has to do what they think is right. :)

Rachel--24 Collaborator
Seriously?! The tick was just on him yesterday-- there's no way to tell if the tick was even a carrier unless he shows symptoms, right?

I mean... everyone I know has been bitten by ticks, literally. We're in a bad area for them. But that doesn't mean they all have Lyme, right?

I know its too late now but you can actually keep the tick and send it off to be tested. That would tell you whether or not the tick is a carrier.

It might take years for symptoms to develop. Lyme can live in the body without causing symptoms. Its an opportunistic bug....the immune system may be able to keep it in check for the time being but when the immune system is under stress the Lyme can become more of an issue.

I dont know that I would treat in the absence of symptoms but you should definately be aware that those symptoms can appear years from now. Many times people dont make the connection because the tick bite is long forgotten.

fedora Enthusiast

I contacted IgeneX. Oh my...the test they recommended is $450. It is the complete panel. Is this what you recommend?

I have been experimenting with food. I may be corn intolerant :( I took it out and then brought it back in. I hurt more now than when I was not eatin it. I will test it more. I am off soy, and nightshads( but messed up there so have to go longer without them) I figured I should check what I can on my own.

CarlaB Enthusiast

Just get the two Western Blots and it will be $190.

fedora Enthusiast

Hey, the two western blots are the IgM and IgG right?

$190 is much better.

CarlaB Enthusiast
Hey, the two western blots are the IgM and IgG right?

$190 is much better.

yes

  • 3 weeks later...
mftnchn Explorer

Hi, does anyone have any information about what CBC blood tests might show in lyme or the co-infections?

I have slightly elevated monocytes (could be chronic inflammation, parasites, viral or bacterial infection is what I found).

Also have in increase is large sized RBC (might be anemia) and large sized platelets and platelet distribution width (might indicate increased active platelet release).

Just wondering if this might be helpful to know what is active.

Also I had this blood draw the morning of my bad herx/flare day, so I am especially curious.

Sherry

CarlaB Enthusiast

Sorry, Sherry, I don't know.

dlp252 Apprentice

Sherry, I don't know either, but the last two years my lymphocytes were very low (lower than the lowest number in the range), and this year my neutrophils were high. Last year I did some searching for low lymphocytes and came up with the same thing you did...inflamation, virus, etc. So, I don't know if it's connected to the lyme, but I have an intestinal thing going on now, lol.

confusedks Enthusiast

I have no idea either Sherry. Sorry. I don't think CBC's show anything as far as Lyme...hence people going for so long undiagnosed.

dollamasgetceliac? Explorer

I have a question, I hope someone can help. I have been very ill in the last 5 years, It started out with Migraines every day, Neuropathy and then shoulder and pains all over. Then it turned into severe abdominal pain. Have been hospitalized etc.. developed all these new allergies to everything.

Tested positive for Celiac disease recently but my doctor is not sure. I have been on gluten-free diet and feel a lot better.

The question I have is that I seem to have many of the symptoms mentioned above, I had asked a Neurologist to test me for Lyme disease and he said I do not have the symptoms. I recently asked my Doctor he is a regular practitioner and he too said no reason to believe you have Lyme.

I do have a tick bite and was exposed to ticks throughout my life.

Why would he refuse the test? Is it expensive?

Another question about exposure to Mercury how do they test that and who tests it? And who treats Lyme is it a Neurologist?

CarlaB Enthusiast

Oh, difficult questions, and it's late. I'll look back tomorrow and be more detailed if no one else gets back to you ....

Lyme is a politically charged battle within the medical field so not many doctors at all, except those who specialize in Lyme only, will test for it properly or treat it. That is why your docs won't test you .... they are either ignorant, or don't want to treat it.

If you go to lymenet (.org), you will find a lot of info on this. Also www.ilads.org. At Lymenet you can also find doctors in your area on the message board.

There is a lot of info buried in this thread, too.

I'll check back tomorrow.

susieg-1 Apprentice
Oh, difficult questions, and it's late. I'll look back tomorrow and be more detailed if no one else gets back to you ....

Lyme is a politically charged battle within the medical field so not many doctors at all, except those who specialize in Lyme only, will test for it properly or treat it. That is why your docs won't test you .... they are either ignorant, or don't want to treat it.

If you go to lymenet (.org), you will find a lot of info on this. Also www.ilads.org. At Lymenet you can also find doctors in your area on the message board.

There is a lot of info buried in this thread, too.

I'll check back tomorrow.

On that note, My Dr. office is insisting that my Lyme test results from IGeneX labs have not yet arrived although IGeneX tells me they were sent one week ago. I know snail mail can be slow especially around holidays but, IGeneX offered to fax results when I called two days ago but needed my Dr to sign faxed form first saying OK to having lab results faxed. So far nothing!!! This is the typical runaround that you will get regarding Lyme disease with most Dr.s. I signed on with a new medical practice and am changing primary care physician and I have no intention of discussing Lyme with new Dr. So my advice is to order the IgG and IgM western blot test kit from IGeneX lab (their website has 800 # to call) the cost is 190 bucks plus any draw fees. If you can get one of your Dr.'s to sign the lab slip you will be ahead of the game as that is probably the most help a conventional Dr will give you on the topic of Lyme. Then you need to get a copy of the results from IGeneX and post results here for help understanding the report. CarlaB is the resident expert and can give you great advice Keep us posted :rolleyes:

susieg-1 Apprentice
Oh, difficult questions, and it's late. I'll look back tomorrow and be more detailed if no one else gets back to you ....

Lyme is a politically charged battle within the medical field so not many doctors at all, except those who specialize in Lyme only, will test for it properly or treat it. That is why your docs won't test you .... they are either ignorant, or don't want to treat it.

If you go to lymenet (.org), you will find a lot of info on this. Also www.ilads.org. At Lymenet you can also find doctors in your area on the message board.

There is a lot of info buried in this thread, too.

I'll check back tomorrow.

I had to post as I got a message on my machine this afternoon that IGeneX lab results are in and Dr. that signed lab slip wants me to call and make an appt to see her. This is the same Dr that said that there is no Lyme in NY!! I can only assume that she would not want me to make appt if test came back negative. Now I am freaking out waiting to call her office in the AM. I also changed my PCP the other day with my insurance company and won't be covered for the visit now but have not yet told her that I am changing to another practice. I was going to get copy of results and give her form at same time to transfer records to new Dr. Now What?? (rhetorical ?)

CarlaB Enthusiast

Great Susie, when is your appt?

The scenario you described about your trouble getting your results is SO typical. My doctor told me mine were negative when they were positive. <_< The thing is, if they admit that you have it, they have to ethically treat you for it. So most docs don't want to test or admit you have it when they do.

dlp252 Apprentice
I was going to get copy of results and give her form at same time to transfer records to new Dr. Now What?? (rhetorical ?)

Still make sure you get a copy! Sometimes even when you have a positive result they will say it is negative, so definitely get a copy of the reports. There should be one for IgM and one for IgG.

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. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      12

      Blood Test for Celiac wheat type matters?

    2. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    3. - JudyLou posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    4. - marzian commented on Scott Adams's article in Diagnosis, Testing & Treatment
      5

      A Future Beyond the Gluten-Free Diet? Scientists Test a New Cell Therapy for Celiac Disease (+Video)

    5. - Jmartes71 posted a topic in Related Issues & Disorders
      0

      Medications

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,142
    • Most Online (within 30 mins)
      7,748

    Mark Conway
    Newest Member
    Mark Conway
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Wheatwacked
      no argument. Never take the pills sold for Nuclear events, except in a nuclear event when instructed to by authorities.  Some of these go up to 130 milligrams per pill. 5000 times the strength of the dietary supplement.  130 times the safe upper limit.  130 mg = 130,000 mcg. Dietary supplements like Lugol's Solution and Liquid Iodine are 50 micrograms per drop.  It takes 20 drops to reach the safe upper limit. In the US the Safe upper limit is 1100 mcg.  In Europe 600 mcg and in Japan 3000 mcg ( 3 mg).
    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
    • JudyLou
      Hi there, I’m debating whether to consider a gluten challenge and I’m hoping someone here can help with that decision (so far, none of the doctors have been helpful). I have a history of breaking out in a horrible, burning/itchy somewhat blistering rash about every 8 years. This started when I was in my early 30’s and at that point it started at the ankles and went about to my knees. Every time I had the rash it would cover more of my body, so my arms and part of my torso were impacted as well, and it was always symmetrical. First I was told it was an allergic reaction to a bug bite. Next I was told it was eczema (after a biopsy of the lesion - not the skin near the lesion) and given a steroid injection (didn’t help). I took myself off of gluten about 3 weeks before seeing an allergist, just to see if it would help (it didn’t in that time period). He thought the rash looked like dermatitis herpetiformis and told me to eat some bread the night before my blood tests, which I did, and the tests came back negative. I’ve since learned from this forum that I needed to be eating gluten daily for at least a month in order to get an accurate test result. I’m grateful to the allergist as he found that 5 mg of doxepin daily will eliminate the rash within about 10 days (previously it lasted for months whether I was eating gluten or not). I have been gluten free for about 25 years as a precaution and recommendation from my doctor, and the pattern of breaking out every 8 years or so remains the same except once I broke out after just one year (was not glutened as far as I know), and now it’s been over 9 years. What’s confusing to me, is that there have been 3 times in the past 2 years when I’ve accidentally eaten gluten, and I haven’t had any reaction at all. Once someone made pancakes (they said they were gluten-free, they were not) and I ate several. I need to decide whether to do a gluten challenge and get another blood test. If I do, are these tests really accurate? I’m also concerned that I could damage my gut in that process if I do have celiac disease. My brother and cousin both had lymphoma so that’s a concern regarding a challenge as well, though there is a lot of cancer in various forms in my family so there may be no gluten connection there. Sorry for the ramble, I’m just doubting the need to remain gluten free if I don’t have any reaction to eating it and haven’t had a positive test (other than testing positive for one of the genes, though it sounds like that’s pretty common). I’d appreciate any thoughts or advice! 
    • Jmartes71
      Hello, just popped in my head to ask this question about medications and celiac? I have always had refurse reaction to meds since I can remember  of what little meds my body is able to tolerate. I was taking gabapentin 300mg for a week,  in past I believe 150? Any ways it amps me up not able to sleep, though very tired.However I did notice it helped with my bloating sibo belly.I hate that my body is that sensitive and medical doesn't seem to take seriously. Im STILL healing with my skin, eye, and now ms or meningioma ( will know in April  which)and dealing with this limbo nightmare. I did write my name, address ect on the reclamation but im not tech savvy and not sure if went through properly. I called my city representative in Stanislaus County and asked if theres a physical paper i can sign for proclamation for celiac and she had no clue about what I was saying, so I just said I'll go back on website. 
    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
×
×
  • 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.