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

Question For Those With Lyme


DingoGirl

Recommended Posts

DingoGirl Enthusiast

Hi everyone,

I have a friend of a friend who's fought a long battle with MS, but I suspect he may have Lyme.

As I recall from my reading here over the years, there is only one lab that can accurately test all the bands for Lyme and etc.

Can anyone give me quickly the name of that lab?

Thanks so much. :)


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



Celiac.com Sponsor (A8-M):



nikki-uk Enthusiast
Hi everyone,

I have a friend of a friend who's fought a long battle with MS, but I suspect he may have Lyme.

As I recall from my reading here over the years, there is only one lab that can accurately test all the bands for Lyme and etc.

Can anyone give me quickly the name of that lab?

Thanks so much. :)

Pretty sure it was Igenex

Open Original Shared Link

I'm sure one of the Lymies will verify.....

DingoGirl Enthusiast
Pretty sure it was Igenex

Open Original Shared Link

I'm sure one of the Lymies will verify.....

that's IT! and the Brit gets it right!!

thanks, Nik :)

  • 3 weeks later...
still tiredofdoctors Rookie

Susie,

IgeneX caught all four of my tick diseases: Lyme, Babesia, Bartonella and Erlichia.

Oddly, my veterinarian told the MD's YEARS ago that I needed to have the type of testing that they do -- he mentioned specifically the Erlichia because of the way I was walking.

Please tell your friend that it is important to use a laboratory such as IgeneX because of the dual-testing protocol they have. In the very beginning, I was (reluctantly) given a generic "is there any Lyme in the blood" test which returned a false negative -- which will up until two years after initial disease contraction.

You know my history . . . which so STRONGLY mimicked MS. Best of luck to your friend.

Lynnie

Jestgar Rising Star
Oddly, my veterinarian told the MD's YEARS ago that I needed to have the type of testing that they do -- he mentioned specifically the Erlichia because of the way I was walking.

Lynne, how could he tell? What about your walking tipped him off?

Judyin Philly Enthusiast
Lynne, how could he tell? What about your walking tipped him off?

Great question Jess? I'd love to know too

Lynne, i didn't know you had lyme? When in the heck did you get that dx?

Judy

still tiredofdoctors Rookie

Honest to goodness, I don't KNOW how he knew by my walking! I forgot to ask him! I was to the point of using the walker - not in the wheelchair yet - and while, yes, I definitely had a typical "widened" cerebellar gait, I did have some unusual characteristics to it. My doctor and I once joked that it was a cross between "Herman Munster" and a "Royal Lippizon Stallion"! Maybe that was it . . .

I was finally diagnosed when I saw Mtndog's doctor in NYC in December. He said just recently that had I not seen him when I did, I probably would not have seen this last birthday in March. I was having seizures 3-5 times per day, each lasting 20 minutes. He said eventually my heart would have stopped during one of them. Scary stuff, huh?

Because I seroconverted to the neurogenic Celiac (because of the Lyme), I'll always have to be gluten-free. There's no getting around that. He has discussed that with me, also. We have toxic mold in our house and are living with my mother until we can get SOMETHING figured out with regard to the house (it has to be burned to the ground), but the mycotoxicosis I developed (again because the Lyme took away my ability to fight it) is what caused the white spots on the gray matter of my brain.


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



Celiac.com Sponsor (A8-M):



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 Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    2. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    3. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    4. - Ello replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

    5. - trents replied to Ello's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      7

      Small Bowel Resection 12 inches

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

    • Total Members
      132,833
    • Most Online (within 30 mins)
      7,748

    Grandma13
    Newest Member
    Grandma13
    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)

  • Upcoming Events

  • Posts

    • trents
      You might consider asking for a referral to a RD (Registered Dietician) to help with food choices and planning a diet. Even apart from any gluten issues, you will likely find there are some foods you need to avoid because of the shorter bowel but you may also find that your system may make adjustments over time and that symptoms may improve.
    • Ello
      I wish Dr’s would have these discussions with their patients. So frustrating but will continue to do research. Absolutely love this website. I will post any updates on my testing and results.  Thank you
    • trents
      Losing 12" of your small bowel is going to present challenges for you in nutritional uptake because you are losing a significant amount of nutritional absorption surface area. You will need to focus on consuming foods that are nutritionally dense and also probably look at some good supplements. If indeed you are having issues with gluten you will need to educate yourself as to how gluten is hidden in the food supply. There's more to it than just avoiding the major sources of gluten like bread and pasta. It is hidden in so many things you would never expect to find it in like canned tomato soup and soy sauce just to name a few. It can be in pills and medications.  Also, your "yellow diarrhea, constipation and bloating" though these are classic signs of a gluten disorder, could also be related to the post surgical shorter length of your small bowel causing incomplete processing/digestion of food.
    • Ello
      Yes this information helps. I will continue to be pro active with this issues I am having. More testing to be done. Thank you so much for your response. 
    • trents
      There are two gluten-related disorders that share many of the same symptoms but differ in nature from each other. One is known as celiac disease or "gluten intolerance". By nature, it is an autoimmune disorder, meaning the ingestion of gluten triggers the body to attack it's own tissues, specifically the lining of the small bowel. This attack causes inflammation and produces antibodies that can be detected in the blood by specific tests like the TTG-IGA test you had. Over time, if gluten is not withheld, this inflammation can cause severe damage to the lining of the small bowel and even result in nutrient deficiency related health issues since the small bowel lining is organ where all the nutrition found in our food is absorbed.  The other is NCGS (Non Celiac Gluten Sensitivity or just "gluten sensitivity") which we know less about and are unsure of the exact mechanism of action. It is not an autoimmune disorder and unlike celiac disease it does not damage the lining of the small bowel, though, like celiac disease, it can cause GI distress and it can also do other kinds of damage to the body. It is thought to be more common than celiac disease. Currently, we cannot test for NCGS. Celiac disease must first be ruled out to arrive at a diagnosis of NCGS. Both disorders require elimination of gluten from the diet.  Either of these disorders can find their onset at any stage of life. We know that celiac disease has a genetic component but the genes are inactive until awakened by some stress event. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% develop active celiac disease. The incidence of NCGS is thought to be considerably higher. I hope this helps.
×
×
  • 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.