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

Doctor Search


gracie1

Recommended Posts

gracie1 Newbie

We live by Ft Wayne, Indiana and I am looking for a Doctor who specializes in Celiac Disease for my 23 year old daughter who is not doing well. Considering Mayo Clinic, Cleveland Clinic, and Celiac Disease Center in Chicago. If anyone has any thoughts or suggestions, they would be greatly appreciated. She was diagnosed locally, but I think with her not thriving and feeling worn out all the time we need further help. Thank you


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



Celiac.com Sponsor (A8-M):



Cypressmyst Explorer

Open Original Shared Link

Try finding a Functional Medicine Doctor in your area. They will treat the whole her and should know about Gluten and Celiac and how to handle recovery, you may still want to ask when you call though as I can't be 100% sure for every Doc on there. :)

Best of luck!

  • 2 weeks later...
T.H. Community Regular

So sorry she's having trouble. :-(

I don't have a recommendation for a doctor, but until you are able to get her in to see someone, some ideas that might help at least a little, that you can do on your own.

1. Have a doctor test her for vitamin and mineral deficiencies - that is often a problem for Celiacs.

2. A food journal, recording everything she eats and reactions - including brands of what she eats - can be VERY helpful in case she has another food sensitivity or allergy. It can help you track it down - there can be a delay for up to 48 hours, though, so you have to do it for a while sometimes before you see a pattern. And remember - ANYTHING can be an issue, with processing today. For example, iodized salt has corn in it to stabilize the iodine, and can have other chemicals added to keep it from clumping. So if she had, say, a sensitivity to the chemical used, she'd react to everything she put the salt into. So - every last ingredient needs to be written down on one of these journals.

By the way, allergy tests are only so-so in reliability (and this info came from my allergist!), otherwise I'd recommend one. But if she can find a pattern between eating and feeling crummy, who cares what it is, as long as it stops hurting her because she stops eating it, yeah?

3. See if she's willing to drop processed foods, pretty much. If she doesn't already know - Gluten Free does not mean 'zero gluten.' It's actually a legal definition of how much gluten a product can contain, and it's not even regulated yet! The gov't can't decide how much gluten they think will be 'okay' to have in gluten free foods. Now, most celiacs can have gluten free foods and seem fine, but sometimes, a celiac is more sensitive and they react to the low levels of gluten. So they never heal. Also, because these products (the gluten-free crackers, cereal, etc...) are 'low' gluten, if your daughter eats a lot of them, she may still be getting too much gluten. My daughter, for example, can eat maybe one bowl of gluten-free cereal that has less gluten than the norm (5ppm), and that's her gluten-free product for the day. Any more than that and she's ill - and we're still trying to see if this is too much or not - it's hard in the beginning to track it all down and make sure the diet is safe.

Fruits and veggies are the safest options. Olive oils are generally less of a contamination risk than nut, seed, and grain oils (the nuts, seeds, and grains get minor CC during harvesting and production, often). gluten-free grains are pretty easily contaminated (and they still get to call themselves gluten free,ugh) so she may want to limit them severely for a couple weeks to see if it helps. Whole meats are better than processed ones, and getting them frozen from the slaughterhouse is usually safer than getting them at the butcher counter where they were cut up next to the other meats that were getting gluten coatings put on them. Dairy is iffy, as many healing celiacs are lactose intolerant (the damaged part of the villi is where lactose is digested). So she might want to skip dairy until she's better.

If this helps, and she starts to feel better, she can always slowly add in foods and figure out what works for her, and what doesn't.

4. It may help to check out other issues that are common to celiacs. Hypothyroidism, diabetes,and Hashimoto's disease are possibilities, depending on her issues. Fructose malabsorption, histamine sensitivity, and sulfite sensitivity may also be problems, if she's having general issues, or lots of trouble with what she eats. H. Pylori infection could be a problem. I have heard of yeast overgrowth, as well, although I don't know a lot about it, just that some celiacs have reported suffering from it. Also Crohn's disease can occur in Celiacs more often, too.

Again, if she's not well or improving, it sounds like you have the right idea in hunting down someone. But if it is taking a while, some of the above might help her some while she's waiting.

Good luck to you and her both in the coming year!

We live by Ft Wayne, Indiana and I am looking for a Doctor who specializes in Celiac Disease for my 23 year old daughter who is not doing well. Considering Mayo Clinic, Cleveland Clinic, and Celiac Disease Center in Chicago. If anyone has any thoughts or suggestions, they would be greatly appreciated. She was diagnosed locally, but I think with her not thriving and feeling worn out all the time we need further help. Thank you

  • 2 months later...
healthuser Newbie

I suggest you to go to doctor search websites such as Open Original Shared Link and find a relative doctor in your area.

NateJ Contributor

I'm sorry but what is a functional Dr.? i've never heard of that.

  • 2 weeks later...
Tyson Holly MD Newbie

I am a traditional western medicine doc who was treated so poorly by my colleagues that I went to a chiropractor who specialized in nutrition and homeopathic medicine. I was hella skeptical but he is brilliant and knew so much more about food intolerances than any of the THREE GI specialists I'd seen. You may give them a try. If not, I can highly recommend the University of Chicago's celiac center. I did my training there and unfortunately didn't know I was celiac at the time, but I was always impressed with how cutting edge they were.

NateJ Contributor

I am a traditional western medicine doc who was treated so poorly by my colleagues that I went to a chiropractor who specialized in nutrition and homeopathic medicine. I was hella skeptical but he is brilliant and knew so much more about food intolerances than any of the THREE GI specialists I'd seen. You may give them a try. If not, I can highly recommend the University of Chicago's celiac center. I did my training there and unfortunately didn't know I was celiac at the time, but I was always impressed with how cutting edge they were.

that is completely unnerving to hear a Dr say that. I really think there is something completely wrong with the healthcare system. not just talking about insurance but the whole thing in general.

My insurance won't pay for a holistic Dr. or at least the only one I found searching the link in this thread says they don't take insurance and the Dr. doesn't practice at a hospital at all.

So, since I'm not in a financial position to pay for visits out of my own pocket. i guess i'm just SOL like the

other 350 million people who have to rely on Drs trained in foreign countries who come here and are handicapped by our insurance system to treat us.


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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,925
    • Most Online (within 30 mins)
      7,748

    Linda Stark
    Newest Member
    Linda Stark
    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

    • Hmart
      I was not taking any medications previous to this. I was a healthy 49 yo with some mild stomach discomfort. I noticed the onset of tinnitus earlier this year and I had Covid at the end of June. My first ‘flare-up’ with these symptoms was in August and I was eating gluten like normal. I had another flare-up in September and then got an upper endo at the end of September that showed possible celiac. My blood test came a week later. While I didn’t stop eating gluten before I had the blood test, I had cut back on food and gluten both. I had a flare-up with this symptoms after one week of gluten free but wasn’t being crazy careful. Then I had another flare-up this week. I think it might have been caused by Trader Joe’s baked tofu which I didn’t realize had wheat. But I don’t know if these flare-ups are caused by gluten or if there’s something else going on. I am food journaling and tracking all symptoms. I have lost 7 pounds in the last 10 days. 
    • trents
      Welcome to the forum, @Hmart! There are other medical conditions besides celiac disease that can cause villous atrophy as well as some medications and for some people, the dairy protein casein. So, your question is a valid one. Especially in view of the fact that your antibody testing was negative, though there are also some seronegative celiacs. So, do you get reactions every time you consume gluten? If you were to purposely consume a slice of bread would you be certain to develop the symptoms you describe?
    • klmgarland
    • DebJ14
      I only went on the multi vitamin AFTER a couple of year of high dose, targeted supplementation resolved most of my deficiencies.  I was on quite a cocktail of vitamins that was changed every 6 months as my deficiencies resolved.  Those that were determined to be genetic are still addressed with specific doses of those vitamins, minerals and amino acids. I have an update on my husband and his A Fib.  He ended up in the hospital in August 2025 when his A Fib would not convert.  He took the maximum dose of Flecainide allowed within a 24 hour period.  It was a nightmare experience!  They took him into the ER immediately.  They put in a line, drew blood, did an EKG and chest Xray all within minutes.  Never saw another human for 6 hours.  Never got any results, but obviously we could see he was still in A fib by watching the monitor.  They have the family sign up for text alerts at the ER desk.  So glad I did.  That is the only way we found out that he was being admitted.  About an hour after that text someone came to take him to his room on an observation floor.  We were there two hours before we saw another human being and believe it or not that was by zoom on the TV in the room.  It was admissions wanting to know his vaccine status and confirming his insurance, which we provided at the ER desk.  They said someone would be in and finally a nurse arrived.  He was told a hospitalist was in charge of his case.  Finally the NP for the hospitalist showed up and my husband literally blew his stack.  He got so angry and yelled at this poor woman, but it was exactly what he needed to convert himself to sinus rhythm while she was there.  They got an EKG machine and confirmed it.  She told him that they wanted to keep him overnight and would do an echo in the morning and they were concerned about a wound on his leg and wanted to do a doppler to make sure he did not have a DVT.  He agreed.  The echo showed everything fine, just as it was at his annual check up in June and there was no DVT.  A cardiologist finally showed up to discharge him and after reviewing his history said the A Fib was due to the Amoxicillan prescribed for his leg wound.  It both triggers A Fib and prevents the Flecainide from working.  His conversion coincided with the last dose of antibiotic getting out of his system.  So, make sure your PCP understands what antibiotics you can or cannot take if susceptible to A Fib.  This cardiologist (not his regular) wanted him on Metoprolol 25 mg and Pradaxa.  My husband told him that his cardiologist axed the idea of a beta blocker because his heart rate is already low.  Sure enough, it dropped to 42 on the Metoprolol and my husband felt horrible.  The pradaxa gave him a full body rash!  He went back to his cardiologist for follow up and his BP was fine and heart rate in the mid 50's.  He also axed the Pradaxa since my husband has low platelets, bruises easily and gets bloody noses just from Fish Oil  He suggested he take Black Cumin Seed Oil for inflammation.  He discovered that by taking the Black Seed oil, he can eat carbs and not go into A Fib, since it does such a good job of reducing inflammation.   Oh and I forgot to say the hospital bill was over $26,000.  Houston Methodist!  
    • Hmart
      The symptoms that led to my diagnosis were stomach pain, diarrhea, nausea, body/nerve tingling and burning and chills. It went away after about four days but led me to a gastro who did an upper endo and found I had marsh 3b. I did the blood test for celiac and it came back negative.  I have gone gluten free. In week 1 I had a flare-up that was similar to my original symptoms. I got more careful/serious. Now at the end of week 2 I had another flare-up. These symptoms seem to get more intense. My questions:  1. How do I know if I have celiac and not something else? 2. Are these symptoms what others experience from gluten?  When I have a flare-up it’s completely debilitating. Can’t sleep, can’t eat, can’t move. Body just shakes. I have lost 10 pounds since going gluten free in the last two weeks.
×
×
  • 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.