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

Newly Diagnosed - Having New Symptoms


Jodi399

Recommended Posts

Jodi399 Newbie

Hi,

After 10 years of migrains, heart palpatations, IBS like symptoms, and various other odd symptoms, I finally switched to a great doctor who took the time with me to diagnose Celiacs. She recommended I go to a GI for a formal diagnosis with a slew of tests involved. I made the appointment with the GI, but then cancelled it because after a month of a strick gluten-free diet I feel tons better. And the thought of going back on gluten just to get a positive diagnosis is terrifying to me. I haven't had a heart palpatation since the day I went gluten-free ( I was having them every single day for 10 years), my migrains have also gotten much less frequent, and my IBS like symptoms have gotten a bit better, although not a lot. I have been gluten-free now for a month and a half.

Here's my delema.... I'm having new symptoms, which I've never had before. I've read on this forum that these are normal symptoms of Celiacs, but why would I be getting them now after being gluten-free for a month and a half? I'm having awful muscle aches. I feel very fatigued, foggy headed, and achy mostly in my arms, but a little in my legs too. Also, my heart feels like it's pounding. Not like a palpatation, or like my heart is beating fast, just like it's beating hard.

I've been vegetarian for over 3 years, so now with this gluten-free diet, I'm concerned that I'm not getting enough of some vitamin or nutrient that is making me feel this way. I take a daily multi-vitamin, and I have a very healthy diet, eating mostly fruits, veggies, and a lot of tofu. However I have now started eating gluten-free pasta, gluten-free waffles, gluten-free pizza crust, and gluten-free cereal. Is there any possibility that these gluten-free foods actually contain some sort of Gluten which might be making me feel this way? Honestly, this gluten-free diet wasn't that hard for me to get used to. But now with these new symptoms happening I'm feeling a bit defeated and depressed.

Any help would be appreciated.


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

I think vitamin deficiencies from the Celiac and your restrictive diet should be investigated. Maybe you could get your doc to test for those?

ciamarie Rookie

It's also quite possible there's some other ingredient that's bothering you, which might take a bit of detective work to figure out. You might want to keep track in a food diary, along with ingredients of what you're eating. Or check the items you eat frequently and see if they have one or more ingredients in common.

The best bet may be to figure out what single-ingredient foods you do o.k. with and just eat those for a few days, then introduce one of the other items and see what happens. (Elimination diet, basically) I've been on a gluten-free diet for about 3.5 months now, and I'm still trying to work out what works for me and what doesn't. It can get frustrating, but overall I'm feeling so much better that I just keep plugging along and taking notes.

Editing to add, one thing I've found helpful is to do a search using the search box at the top of the forums page, or on your favorite search engine, and enter the brand and item name with gluten-free and see if anything comes up. Some companies are better than others at labeling, and some make products in dedicated gluten-free facilities and some share facilities where gluten products are made, which sometimes makes a difference if you're pretty sensitive. Also read the FAQ's linked at the top of the forum topic page.

Lastly, make sure your multivitamin and any other supplements are gluten-free. And check their other ingredients too, just in case.

Jodi399 Newbie

Thank you for the helpful hints, I will try the food diary, as well as the elimination diet. I've also made an appointment with my PCP to request a test for any deficiencies.

Takala Enthusiast

Some brands and individual batches of a few kinds of "gluten free" foods may be cross contaminated with either gluten or another ingredient that you may be reacting to - if you ask, "how can this be ?" :blink: remember if you are in the U.S. we have no labeling standards at this time (Feb 2012) and everything re: gluten status disclosure is voluntary. Hence you may find yourself feeling "off" after consuming a 'gluten free' item, while feeling better after eating a regular item with a better manufacturer who is disclosing what is actually in the product., or what it was exposed to during manufacturing. I have had to give up some brands of alleged "gluten free" foods, and go with a non gluten free regular item, with a manufacturer which is saying "run on lines that also ran xxxx," as a result.

You may be one of the few people who also reacts poorly to oats, even gluten free oats, for example. Other common problems are too much soy not agreeing with your thyroid, etc.

Remember that everything that goes into your mouth needs to be gluten free, supplements, etc. Some people are so sensitive, they need to switch out personal care products, especially if they have long hair or use a lot of lotion. Also, if you have indoor pets, their food might be cross contaminating you, if they lick you or drool. Your spouse or boyfriend can also be a great accidental vector.

Also, if I were you, I would be searching for "gluten free vegetarian" blogs on the internet, to get some ideas. Eating a lot of grain based foods high on the refined carbohydrates, along with fruits and just tofu for protein, can really not work well sometimes for our individual metabolisms, even if we have been told that is is "healthier."

lucia Enthusiast

I was a pescetarian (vegetarian + fish) for over a decade, and my husband is still vegetarian. I have no problem creating nutritious, balanced, gluten-free, vegetarian meals at home. Not that I eat just tofu. My diet includes a variety of cheeses, dairy, nuts, beans and eggs, as well as, occasionally, soy. I have had a nutritionist review my diet to make sure that I was eating well.

That said, when I was first recovering from gluten intolerance/celiac, my acupuncturist strongly recommended adding meat back into my diet. I did, and found that drinking chicken broth daily for 4-5 days had a big effect on my energy. Interestingly, I discovered at that time that historically even in culturally vegetarian parts of India, the very young, elderly, and sick were all given bits of meat in their diet. I pass that advice on to you, and you can make your own decisions around it. (My husband is vegetarian for cultural/religious reasons, so I know vegetarianism can be a strongly-held belief. I also think that skewing towards a vegetarian diet is healthier for us all and for our planet.)

I'm happy now to have meat back in my diet though since it opens up possibilities when ordering in restaurants or when other people cook for me. I've eaten at restaurants where there was only a single meat dish on offer as a gluten-free alternative. I can't eat at Indian restaurants every time I go out!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,949
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    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

    • 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
    • DebJ14
×
×
  • 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.