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

Several Doc Visits And Need Help!


nuttmegs17

Recommended Posts

nuttmegs17 Apprentice

Hi

i have had severe stomach pains for the last 3 years...my symptons are

1. gas and extreme bloating (to the point where - no exaggeration - I GO UP at least a size within the hour and have taken to only wearing skirts as I never know when i'm going to have an "Attack"..When it's really bad, my stomach is out far enough to mistake being pregnant!)

2. constipation

3. distended bowels

4. painful stomach (due to gass/bloating)

5. weight stagnation (havn't gained a lot of weight but am someone who generally drops weight super easy when busy and despite working out and being active my weight is no longer fluctuating)...my face also looks fuller

6. Swelling in my body - breasts, arms around shoulders and back

7. can pin down when my attacks(Extreme bloating/swelling) occur...sometimes all I will have eaten is an apple and I swell up, other times its a glass of milk or often times I have a glass of water! But I hear allergies can sometimes show up a day later or several hours later so perhaps that is why?

I suspected food allergies and/or autoimmune problems (I've had graves disease in the past).

I have been to my main doc several times - she has run CT scans and Ultrasounds to no avail (think she was trying to rule out things). I kept food diaries and cut back on gluton. The only time I got any relief was when I would do a juice fast for 3 days. Seemed to get me running again and I experienced little pain. However, that is expensive and not a sustainable way to live (at least for me) whenever I would go back to normal all the symptons would return and it has definitely interferred with my life: having to call into work, canceling plans with friends, dates, etc Both my doc and i are frustarted. At this point it is outside her area of expertise so she referred me to what is supposed to be a very good GI doc. I have waited a while to see him: made my appt in Jan and will finally see him at the end of March (!)....b/c I am waiting so long to see him, I really want to make the most of the appt bc who knows when he will have an opening again!. Any advice? My main worry is being blown off (As i have been in the past). I really want to make this visit count.

To take matters in my own hand in the meantime I have elimated dairy, soy (although I have noticed it still sneaks in) and wheat....Since making these drastic cuts even my boyfriend has noticed improvements. I still get gassy and bloated but not nearly to the extend it was before - not debilitating, only annoying from time to time. However cutting all these food groups out is more than challenging. I sincerely hope they can help me determine what my allergies are (hopefully not all of the above!).

ugh. this is very frustrating and I suspect this will take a while to sort out. I hear that for instance, if my allergy is lactose, that it can be hard to determine what amounts/types I have issues with (ie, some people tolerate yogurts and cooked cheeses but cannot process cheese or plain milk, some can tolerate a half a cup of milk every other day but a whole cup every day would result in lot of issues!) luckily i eat very clean whole foods mostly anyways, but it's made it a pain when I go out with friends or eat at someones house.

So to sum up

Does this sound familiar to anyone?

Suggestions to make the most of my GI visit

Thank you for your time!


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

The main thing I am going to tell you is to not stop eating gluten before your appointment or your testing will come back negative for sure. Add wheat back in to your diet if you have cut it out. Hopefully since you haven't been fully gluten free if you add it back in the tests will show an accurate result. Once you are done with all celiac related testing do give the diet a strict try for at least a couple of months even if you tests are negative. Your in the right place to learn how to follow the lifestyle strictly. Welcome to the board and I hope you are feeling better soon.

MsCurious Enthusiast

Ditto what Raven said. DON'T stop eating gluten until you have been tested. Painful as it is... keep lots of it in your diet until the blood tests and/or biopsy are done, or your test results will possibly be a false negative. You have a LOT of the same symptoms that I have, and I know how uncomfortable/painful and NOT FUN it is to keep eating things that you suspect are making you ill, but it will soon be over. Once the tests are done you can stop eating gluten.

I have a few more days to go, and then hopefully I am off the hook, and I can't wait! In the mean time... I'm putting up with the headaches, fatigue, tummy aches, bloating, gas and all the fun digestive issues but it will be worth it to have an answer. They suspect food allergies with me as well, so I have tests in progress as we speak. Hopefully, results tomorrow. Have they done any of those for you?

I have a ton of allergies that run in my family, and I have the genetic DQ2.5 marker for Celiac, so I really have no idea at this point exactly what is causing the issues. So they are testing for both. I read yesterday that the two highest risk factors for celiac are 1. if a first degree family member has it (diagnosed) 2. if you have DQ2.5 marker, then it goes on from there, but who knows. They are still doing research and finding new information all the time.

I think like people say on here.. get tested. If positive ... GREAT .. you know what to do.. gluten free diet. If negative... give gluten free diet a good try and if you feel better... that's your answer... you're gluten intolerant. If that doesn't seem to do the trick for you... you probably have other food intolerances or allergies that you need to track down. Like my husband says, its like opening up a big puzzle box of 2000 pieces of a picture of the ocean ! LOL :P Not an easy task, but just keep at it and dont' get discouraged. This forum is a great source of support, suggestions and resources. Good luck! And hope you feel better really soon!

nuttmegs17 Apprentice

Ditto what Raven said. DON'T stop eating gluten until you have been tested. Painful as it is... keep lots of it in your diet until the blood tests and/or biopsy are done, or your test results will possibly be a false negative. You have a LOT of the same symptoms that I have, and I know how uncomfortable/painful and NOT FUN it is to keep eating things that you suspect are making you ill, but it will soon be over. Once the tests are done you can stop eating gluten.

I have a few more days to go, and then hopefully I am off the hook, and I can't wait! In the mean time... I'm putting up with the headaches, fatigue, tummy aches, bloating, gas and all the fun digestive issues but it will be worth it to have an answer. They suspect food allergies with me as well, so I have tests in progress as we speak. Hopefully, results tomorrow. Have they done any of those for you?

I have a ton of allergies that run in my family, and I have the genetic DQ2.5 marker for Celiac, so I really have no idea at this point exactly what is causing the issues. So they are testing for both. I read yesterday that the two highest risk factors for celiac are 1. if a first degree family member has it (diagnosed) 2. if you have DQ2.5 marker, then it goes on from there, but who knows. They are still doing research and finding new information all the time.

I think like people say on here.. get tested. If positive ... GREAT .. you know what to do.. gluten free diet. If negative... give gluten free diet a good try and if you feel better... that's your answer... you're gluten intolerant. If that doesn't seem to do the trick for you... you probably have other food intolerances or allergies that you need to track down. Like my husband says, its like opening up a big puzzle box of 2000 pieces of a picture of the ocean ! LOL :P Not an easy task, but just keep at it and dont' get discouraged. This forum is a great source of support, suggestions and resources. Good luck! And hope you feel better really soon!

WOw that is interesting that you both said that...I mentioned the same concern to my current doc, and in fact before I went gluten-free and begged her for the blood test b/c of the exact reason you outlined above (neg test results)...I figured I could have the test, and then follow a gluten-free diet before I say him . However, she told me to elimintate it for the time being and if I feel better, that helps with the diagnosis. eek. Soooo confusing.

I just don't get the swelling part of all this (Arms back breasts) after eating so strange (and uncomfortable)

Are there any specific tests (for allergies) I might want to ask for?

nuttmegs17 Apprentice

Oh and one other question

When you say to add gluten back into my diet prior to seeing the doc, how much gluten are we talking about? A serving every day? A serving every meal?

ravenwoodglass Mentor

Oh and one other question

When you say to add gluten back into my diet prior to seeing the doc, how much gluten are we talking about? A serving every day? A serving every meal?

At least 3 servings a day or the equivalent of 4 slices of bread. While feeling better on the diet is pretty diagnostic in itself if you are going to try to get a diagnosis based on the endoscopy then you have to keep eating gluten. If you are able to stict strictly with the diet without the biopsy then skip the biopsy and just go with the diet. As to allergy testing being helpful with a celiac diagnosis, no it won't be. Celiac is not an allergic reaction it is an autoimmune reaction and will not show up in allergy testing. Some of us are allergic and celiac both though.

Takala Enthusiast

I will puff up sometimes after eating a commercially made gluten free product. Only it's more generalized, and it includes my ankles.

Nobody can give me an explanation. I know what an allergy feels like, and this doesn't feel like anything. It's not gluten, either, I can tell when that happens as I go neuro reactive. I'm not sure if it is xanthan gum, guar gum, tapioca, or mystery ingredient yet to be determined. It is so annoying.

I did get really suspicious about some powdered garlic which was sourced from China, but .... what about the other times this has happened.

I've even eaten a complex gluten free meal out at a restaurant, and it DOESN'T happen.

Don't laugh, but this is playing **** with how my ski boots fit, and I've learned to be super careful the night and morning before going anywhere, with what I eat, anticipating trying to get that one boot fastened, as I tend to be a bit bigger and stronger on my entire one side of my body, longer leg, bigger foot, etc., and it's the larger side that the puffiness shows up more. Because of my age, my already sturdy legs are getting the dreaded cankles effect.

Before I went gluten free, (coming up 8 years) I had so many wierdo symptoms that this would not have been unusual, but this has started post gluten free.

Alas, to get a chance of a positive blood test result you will have to keep snarfing down the gluten until the blood is drawn for the test. After you have completed all medical testing to the best of your ability, if they still blow you off, you would be well to seriously do your gluten free diet challenge anyway. You will know, if you stop eating it and go gluten free, and feel better, that it is a problem for you. (you can also do over the counter genetic testing to see if you carry the genes pre disposing you to gluten sensitivity or celiac, which puts you in the class of "could be." )

Don't worry about the lactose testing. This is simple. STOP eating it for awhile. Highly likely if you are an adult, anyway, that you are lactose intolerant, once you are past your early twenties. Being celiac or gluten intolerant, increases your chances. Going on a gluten free diet, and having your gut heal, makes it more likely you will be able to tolerate non lactose dairy again. Add back in the safest, lowest levels of potentially lactose containing foods to re test yourself. Add back in only one thing at a time, and small amounts. Hard, aged cheese has very little lactose. Eating a small amount of that for a few days should let you know. If that works, you can try a safe yogurt. Yogurt is much more tricky, as it can have fillers and gums and powdered milk added to it as thickeners, and not really be lactose free. You can use homemade yogurt or one of the plain, safer, high quality brands. I can eat cheese, but have to be careful with yogurts.

It's unlikely that you will be able to tolerate regular milk.

Soy is another common ingredient that celiacs and gluten intolerant people react to. Soy oil and lecithin might not make you react the same as soy beans or soy flours, or soy sauce or tofu. Or it may be a low level, hard to pin down, sort of bleah feeling, not easy to pinpoint.

You can also be allergic to other things, as well. BUT- in my case, most of my allergies went way down once gluten was removed.


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



Celiac.com Sponsor (A8-M):



Mari Contributor

The gas is being produced by bacteria and yeasts in your gut. When people have an unbalanced mixture of organisms in their intestine it is common for people to have lots of gas, especially if they eat too many carbohydrates, sugars and other foods these organisms thrive on. The gastroenterologist will do the tests necessary to find the underlying causes and may do some tests to identify which organisms are out of balance. Although you have had some tests done they might have missed gallstones or insufficient bile production that may also include pancreatic enzyme deficiency. These gas forming organisms thrive better when the food eaten is not being well digested. I have found that taking a balanced Vit B supplement is helpful, especially Vit B12. The Dr may also order parasite tests but they are not very helpful, a better test is like the Enteric Effects Panel offered by (Company Name Removed - They Spammed This Forum and are Banned) Labs. This test also looks for anti gliadin antibodies and is more sensitive than the blood tests for possible Celiac Disease.

Hope this helps.

nuttmegs17 Apprentice

This is very helpful - thank you all!

I did a CAT scan and an gallstone was present - just one. So odd as they are linked to high cholesteral but I eat soooo healthy (whole foods, very little processed, fruits /veggies/lean meats are staples)

nuttmegs17 Apprentice

I posted another string similar to this, but lately have noticed via photos and scale that I am now GAINING weight and my face is fuller (not just temporarily swelling up in my arms shoulders back, just a constant bloated look). No I am not a drinker or smoker :) I live a very healthy/active lifestyle and am so worn out from all of this

nuttmegs17 Apprentice

another gluten challenge question:

I was on gluten and had all those horrible symtpons, then went gluten-free for 2-3 weeks, now I'm incorporating gluten again....will those 2-3 weeks be crucial? Will I need to go on the Challenge for a full 3 months? or will they not count against my gluten challenge that much as I have been eating gluten all my life previously?

nuttmegs17 Apprentice

another gluten challenge question:

I was on gluten and had all those horrible symtpons, then went gluten-free for 2-3 weeks, now I'm incorporating gluten again....will those 2-3 weeks be crucial? Will I need to go on the Challenge for a full 3 months? or will they not count against my gluten challenge that much as I have been eating gluten all my life previously?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,962
    • Most Online (within 30 mins)
      7,748

    AlissaW
    Newest Member
    AlissaW
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.