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

Heart Palpitations And Fatigue


Guest Laurie anne

Recommended Posts

Guest Laurie anne

:unsure: I was first told i had IBS and just cut out pasta and bread, but the last 2 weeks I developed a itchy,blistery rash and severe fatigue and heart flutters,

I have not had any test done yet , but I found an article in readers digest and it fit me to a tee. so i started experminting with not eating anything with modified food starch or wheat flour or gluten. is this normal when first starting to not eat wheat?


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



Celiac.com Sponsor (A8-M):



Lily Rookie

Laurie anne,

If you are seriously going to be tested for Celiac you can't go off wheat yet, because it can cause a false positive. I had been off but they made me go back on for the biopsy and to be honest after being off gluten for 3 months, I was even more sensitive :(. If you don't care about the diagnosis then by all means, stay off the gluten, dairy may be sensitive for you too. If you have flattened villi, you are lactose intolerant until those little buggers grow back.

I too have the heart fluttering and am exhausted all the time. Not having the nutrients your body needs really throws everything out of whack.

Hope you feel better soon :)

Lily

Guest Loribop

Hi,

I am in the same boat as you are. I went off gluten, felt better and now am back on gluten for the biopsy (Tuesday.) My gastro Dr said my allergist shouldn't have taken me off gluten until the biopsy, but it's too late now. My fatigue was much better after 6 weeks gluten free. Even if the biopsy comes back negative, I have the gliadin antibodies so I guess it gluten free for me.

Good luck in your diagnosis. It's hard going back to foods that you think are making you sick. I wish there was a better way for us. :blink:

Guest Laurie anne

B)

Hi thanks for the advice I don't see my doctor until wednesday and i don't have insurance so I don't know what test he will do. My biggest concern now is i'm not eating much and I'am taking vitamins but I itch on my neck sometimes it wakes me up at night and i almost scratch till i bleed, and suggestions on what to put on it??????????? I've tried beneadryl cream, cortizone, gold bond and neosporin. any other suggestions on what to do or what is causing this. I feel almost worse since i stopped eating things with gluten or modified food starch , i did'nt have the heart palpitaions or the heavy bone melting fatigue, i'm also irritilble.

how do other people deal with this. my husband tries to understand but my kids just know mommy is sick. I've tried almost all of the antidepressants out there.

I'm on clozampane now. Laurie anne

VAGuy Apprentice

re: Skin problems

I have been having terrible skin problems for years and I wonder if they are related to celiac disease -

1 - I have developed an extreme sensitivity to anything alkalai, such as soaps, this carries over to the water supply here, ph was at 8.2 at end of summer, 7.5 in the fall, I only use Poland spring water on my face, neck, and scalp, ph 5.5, and it helps -

2 - My skin will not tolerate the vehicle or base in most ointments and creams - causes horrible problems - I read one in three people are sensitive to Neosporin - I can use Johnson and Johnson First Aid Cream - I can use Vaseline Intensive Care Lotion if skin not broken

3 - The neck (if you can use soap) gets soap, runoff from shampoo, Shaving cream (guys), and shower spray - 4 alkaline substances I was exposing myself to - not good

4 - I was prescribed anti-depressants a couple years ago and the potential side effects sounded really scary so I didn't take them - could they be a problem?

5 - Look into relaxation techniques - I did a BioFeedback program a couple years ago and it really helps. Sometimes I just unplug phone, put on my noise suppresion muffs, or headphones and classical music, blanket to keep warm, get comfortable, and either try to blank my mind or think of something calming - it really helps, pulse and pressure go down, respiration down, calm down - you can be wide awake, but when you end the session I always feel like I just woke up, was warned to take it easy for a few minutes after rather than jumping right up -if you have children, a husband, and celiac disease you need a little quiet time - when I described a floating feeling to the therapist she said it was a common description, sometimes it's like I am not aware of my body being in contact with the recliner I'm sitting in

6 - I've noticed since going gluten-free (7 or 8 weeks) I'm a lotless antsy/irritable - are you better feeling taking meds than you were before?

Good luck on your test - I'm in the same boat - gluten-free prior to test, no insurance

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,959
    • Most Online (within 30 mins)
      7,748

    jenny44
    Newest Member
    jenny44
    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.