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

Family Doctor Not Acting On Results


Josina

Recommended Posts

Josina Newbie

Hello everyone!

I am very new here. I have been battling gluten and lactose intolerance now for the past 8 years. I just learned about Celiac Disease from a neighbour in the past few years. I have been asking my doctor for most of the past 8 years if I could be tested for food allergies. I was very grateful to learn that I was not going crazy. (family not very supportive). I was finally tested for Celiac Disease by blood and my results came back positive. I believe that I have been battling this disease for most of my life. My doctor still believes it is no big deal! After reading on the net and this site, I am realizing that this is very much a big deal.

Would someone please tell me what my next step should be. I have put myself on a Gluten free diet. I know in the past that has worked. I did not realize that shampoo and soaps etc. can harm me. What kind of doctor do I have to see next, and do I really have to have more testing? It seems really insane to have to keep eating foods that will continue to harm me and make me feel horrible?

I also would like to know, does this disease effect moods and depression etc. There seems to be so much info that I am unable to find on the sites that I have been to. I have learned more here than anywhere else. I read that 1 out of 133 North Americans suffer from Celiac Disease!

Thank you!


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



Celiac.com Sponsor (A8-M):



mouse Enthusiast

Welcome to the forum and here is to your future good health.

I was only diagnosed with a blood test as I was literally almost dead by the time I was diagnosed. I was to sick for the endoscopy and my GP wanted me to go gluten free right then. He said another two weeks and I would have had no recovery. So, if I had been told to keep eating gluten and wait for the endo, I would not have done so. It just was not an option for me.

As far as depression, I had very little, but I had unbelivable mood swings. In that I could throw such a temper tantrum that would scare anybody, including myself. I used to break things, even things I loved during these tantrums. I would be telling myself to calm down and shut up, but there was no way I could. They just had to play themselves out. After I went gluten free, they went away. I can still get mad at something, but it is calm and with rational thinking.

You will notice many changes in the coming months both physical and mental. Welcome to a good new life.

AndreaB Contributor

The next step would be biospy if you want to do that. It's certainly not necessary in my opinion though. If you are comfortable going gluten free based on the blood test and diet response then go ahead.

If you want the "gold" standard diagnosis by biopsy then you'll need to stay on gluten until that is over with.

Murph Newbie
I read that 1 out of 133 North Americans suffer from Celiac Disease!

Ya, that's not really SUFFER suffer. I think it's that there is data that 1 in 133 have the genes to *potentially* have celiac disease activated. And even among those w/ active celiac, the magnitude of the effect on their lives varies drastically.

That being said - best of luck in finding a better Dr. They ARE out there! Being gluten-free is tough and frustrating for a while, but you'll get used to both the diet and the feeling good!!

aikiducky Apprentice

Murpf, it really is 1 in 133 with active celiac. As to the genes, about 40% of the population have the genes to potentially have celiac activated, but as you see, about 1%-and-a-bit actually get celiac. It's really much more common than people think!

I'm not saying that you were advocating not going gluten free...just wanted to clarify in case someone new read this: Some celiacs can be asymptomatic and so not notice a big effect on their lives immediately, but the tricky thing is that if one doesn't go gluten free, no one can predict who's going to get the really bad problems later in life, like damage from severe vitamin deficiencies, neurological symptoms, or cancer.

Pauliina

Karen B. Explorer
Ya, that's not really SUFFER suffer. I think it's that there is data that 1 in 133 have the genes to *potentially* have celiac disease activated. And even among those w/ active celiac, the magnitude of the effect on their lives varies drastically.

That being said - best of luck in finding a better Dr. They ARE out there! Being gluten-free is tough and frustrating for a while, but you'll get used to both the diet and the feeling good!!

https://www.celiac.com/st_prod.html?p_prodi...-19107121139.04

Celiac.com 04/10/2005 - Celiac disease is, by definition, a condition in which the intestinal wall is damaged as a result of eating gluten. It is a chronic illness in which the symptoms wax and wane1 for reasons that are not yet understood. Celiac disease is the result of genetic and environmental factors. We now know two HLA markers (DQ2 and DQ8) for the predisposition for celiac disease2. One environmental factor is, of course, the consumption of gluten, but there may be other environmental contributors. Recent research reveals that about 1% of the population suffers from this condition although most remain undiagnosed.

No, that's 1 in 133 that actually have it. When you consider the number of ads for reflux drugs, IBS drugs, diarrhea drugs and osteoporsis drugs, you'll see where some of those people might be hiding. Since there is no drug for Celiac, it's not nearly as well known but I suspect we provide a great market for all of these products before we finally find our way to a diagnosis. I know I took Prevacid for 5 years before finding out I have Celiac. Haven't needed it since going gluten-free.

Karen B. Explorer
Hello everyone!

I am very new here. I have been battling gluten and lactose intolerance now for the past 8 years. I just learned about Celiac Disease from a neighbour in the past few years. I have been asking my doctor for most of the past 8 years if I could be tested for food allergies. I was very grateful to learn that I was not going crazy. (family not very supportive). I was finally tested for Celiac Disease by blood and my results came back positive. I believe that I have been battling this disease for most of my life. My doctor still believes it is no big deal! After reading on the net and this site, I am realizing that this is very much a big deal.

Would someone please tell me what my next step should be. I have put myself on a Gluten free diet. I know in the past that has worked. I did not realize that shampoo and soaps etc. can harm me. What kind of doctor do I have to see next, and do I really have to have more testing? It seems really insane to have to keep eating foods that will continue to harm me and make me feel horrible?

I also would like to know, does this disease effect moods and depression etc. There seems to be so much info that I am unable to find on the sites that I have been to. I have learned more here than anywhere else. I read that 1 out of 133 North Americans suffer from Celiac Disease!

Thank you!

The next step I'd take, if I were you, is finding a local supprt group because they could recommend a doctor that is knowledgeable about Celiac issues and will listen to you. They'll also be a great source of information about what to expect, where the best sources are locally for gluten-free food and supprt for where you are now.

https://www.celiac.com/st_prod.html?p_prodi...-49107235539.b0

Also, the Celiac.com website is definitely my first "go to" place for Celiac info online. But you may find Clan Thompson handy (Open Original Shared Link) and there are others out there that are very informative, helpful and some are downright entertaining.


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



Celiac.com Sponsor (A8-M):



little-c Contributor

I'm newly diagnosed also. I did have a positive biopsy, so no question with me. My next step was to see a dietician to get tips on how to follow a gluten free diet. You need to be sure that it's a dietician that knows about celiac.

I also recommend that you read "Celiac Disease: A Hidden Epidemic" by Peter H.R. Green and Rory Jones. Dr. Green is the foremost expert on celiac disease. I just finished reading it. There's an explanation of the disease, the diagnosis process, how to cope, how to read labels, etc, pretty much any angle you can think of. I checked it out from the library.

And, the internet has tons of information. This site in particular has great info and this forum has helped me cope.

You'll need to do an inventory of your kitchen foods and cookware. Out with the old, in with the gluten free. And, you'll need to find sources for gluten free food. This site is a good one, also Whole Foods has bakery if there's one near you. I've also found that there are quite a few mail order bakeries for gluten free stuff if you just search. Hopefully you live in a celiac friendly area. If you don't the internet will be a godsend.

Good luck in adjusting to your new lifestyle. It takes time and patience. The good news is you'll feel much better.

Josina Newbie

Thanks everyone!!!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,645
    • Most Online (within 30 mins)
      7,748

    MaryLou N
    Newest Member
    MaryLou N
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      I agree, there can be contamination at many points--milling is another possible source of contamination for any flours.
    • trents
      Keep in mind that with manufactured food products, "gluten free" doesn't equate to no gluten. Things that are naturally gluten free can be cross-contaminated with gluten in the field, in shipping and in processing. In the U.S. companies can use the gluten free label as long as the product doesn't exceed 20ppm of gluten. That amount still may cause a reaction in some people.
    • deanna1ynne
      Dd10 was tested for celiac four years ago bc two siblings were dx’d (positive labs and biopsies). Her results at the time were positive ema  and ttg (7x the UL), but a negative biopsy. We checked again three months later and her ttg was still positive (4x the UL), but ema and biopsy were negative. Doc said it was “potential celiac” and to keep eating gluten, but we were concerned about harming her growth and development while young and had her go gluten-free because we felt the labs and ema in particular were very suggestive of early celiac, despite the negative biopsies. She also had stomach aches and lethargy when eating it. We just felt it’d be better to be safe than sorry. Now, four years later, she doesn’t want to be gluten-free if she doesn’t “have to be,” so underwent a 12 week gluten challenge. She had labs done before starting and all looked great (celiac panel all negative, as expected.) Surprisingly, she experienced no noticeable symptoms when she began eating gluten again, which we felt was a positive sign. However, 12 weeks in, her labs are positive again (ttg 4x the UL and ema positive again as well). Doc says that since she feels fine and her previous two biopsies showed nothing, she can just keep eating gluten and we could maybe biopsy again in two years. I was looking up the ema test and the probability of having not just one but two false positives, and it seems ridiculously low.  Any advice? Would you biopsy again? She’s old enough at this point that I really feel I need her buy-in to keep her gluten-free, and she feels that if the doc says it’s fine, then that’s the final word — which makes me inclined to biopsy again and hope that it actually shows damage this time (not because I want her to have celiac like her sisters, but because I kind of think she already does have it, and seeing the damage now would save her more severe damage in the long run that would come from just continuing to eat gluten for a few more years before testing again.)  Our doc is great - we really like him. But we are very confused and want to protect her. One of her older sibs stopped growing and has lots of teeth problems and all that jazz from not catching the celiac disease sooner, and we don’t want to get to that point with the younger sis. fwiw- she doesn’t mind the biopsy at all. It’s at a children’s hospital and she thinks it’s kind of fun. So it’s not like that would stress her out or anything.
    • Inkie
      Thanks for the replies. I already use a gluten-free brand of buckwheat flakes I occasionally get itchy bumps. I'm still reviewing all my food products. I occasionally eat prepackaged gluten-free crackers and cookies, so I'll stop using those. I use buckwheat flakes and Doves Farm flour as a base for baking. Would you recommend eliminating those as well? It's a constant search.
    • Wheatwacked
      Gluten free food is not fortified with vitamins and minerals as regular food is.  Vitamin deficiencies are common especially in recently diagnosed persons,  Get a 25(OH)Vitamin D blood test. And work on raising it.  The safe upper blood level is around 200 nmol/L.    "Low serum levels of 25(OH)D have been associated with increased risk of autoimmune disease onset and/or high disease activity. The role of vitamin D in autoimmune diseases   🏋️‍♂️Good job!   I find the commercial milk will give me mild stomach burn at night, while pasture/grassfed only milk does not bother me at all.  While you are healing, listen to your body.  If it hurts to eat something, eat something else.  You may be able to eat it later, or maybe it is just not good for you.  Lower your Omega 6 to 3 ratio of what you eat.  Most omega 6 fatty acids are inflammation causing.    The standard american diet omega 6:3 ratio is estimated at upward of 14:1.  Thats why fish oil works
×
×
  • 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.