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 issues get weirder


ironictruth

Recommended Posts

ironictruth Proficient

Back in March I started getting some skipped beats, a bit unnerving but I figured I was just developing PVCs. In July I actually had some kind of arrhythmia at the gym. I had 2 stress tests, monitors and an ultrasound of the heart and all looks good except for some PVCs. They never caught the arrhythmia.

Fast forward 3 months from my cardiologist making me cry, I am finding that my heart acts very weird after eating. My stomach pain has increased since late August and my heart is much weirder then it was in the previous months. It seems to speed up and skip a lot and go out of rhythm after some meals. I can feel it stop in the pulse in my neck, then speed up, then go back to normal and it will do it again.  Usually begins 20-60 minutes after a meal or a coffee or tea (I am on low acid coffee).

Has anyone experienced this?  I know I had some inflammation in the intestine in late August which I thought would be better by now and I am wondering if perhaps when the food hits the inflammation it does something wacky to the heart? I am just waiting for it to go out of synch and not got back! And why does it NOT do it for my doctors? Argh.

My upper stomach is tender and I have not been able to lie on my right side for sometime due to pressure in the upper right area.

But this heart stuff is freaking me out. Just when I think I was bothered by symptoms before, they get worse!

 

 


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

Hi IronicT,

I haven't had those symptoms exactly.  I've had faster heart rate at times, and feeling my heart beat against the inside of my chest.  I've even had my heart go all a flutter when seeing a pretty girl or a shiny new gun! :)

If your symptoms don't cooperate when you are at the doctor, maybe they can equip you with a monitor to record heart events.

Not being able to lay on your right side seems like it should point the doctors at something pretty quick IMHO.  At least it should give them a general area to examine.

I hope you get some  answers soon.

 

ironictruth Proficient
19 hours ago, GFinDC said:

Hi IronicT,

I haven't had those symptoms exactly.  I've had faster heart rate at times, and feeling my heart beat against the inside of my chest.  I've even had my heart go all a flutter when seeing a pretty girl or a shiny new gun! :)

If your symptoms don't cooperate when you are at the doctor, maybe they can equip you with a monitor to record heart events.

Not being able to lay on your right side seems like it should point the doctors at something pretty quick IMHO.  At least it should give them a general area to examine.

I hope you get some  answers soon.

 

Thank you. We did a monitor months ago, just some pvcs. But things are nuch worse. 

obesiac Newbie

Yes ! before self diagnosis I had full on magnesium defieceny symptoms. Palpitations, insomia, Increased heart rate, I couldnt eat. Found out about deficiency online. Took some magnesium and my heartrate went from 114 to 70 within a half an hour. 

Of course something like this is serious and needs to be looked into. Being celiac is complicated . Each case is different. Someone who has gone undiagnosed for a long time has to really take care of themselves and be vigilant about their nutrition. 

I have been battling the particular palpitation issues since self diagnosis, 15 years. When the palpitation episodes increased I took magnesium regularly.  And other supplements. I have made progress as now I hardly get them ( palpitations).

ironictruth Proficient

Thank you. I do take magnesium

frieze Community Regular

ironic, what form of magnesium do you take, and how much?  are you on a PPI?  or other acid inhibitor?

ironictruth Proficient

I was on a ppi for a couple of months in the fall. I did not want to take it but figured i would give it a shot. I was told to discontinue it and a GERD PH test revealed normal acid. So I have been off of it for about 2 months. Some zantac or pepcid following d/c of ppi and now totally off everything. 

400 mg mag oxide at bedtime since early August. 


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



Celiac.com Sponsor (A8-M):



Caroles Newbie

The funny thing with me, 2008 I had the fundoplication  done, where they tie your stomach closer to your esphagus. Last year I had an endoscopy done and I was definite celiac. Sometimes I wonder if it from the acid reflux operation. I do not take any medications for acid reflux because they cause more harm than good. What I have been doing is using a product called "intestinew" in my local vitamin store. This is a powder that I mix with EmergencC, it helps...I also drink green tea with a few drops of frankincense. I feel wonderful! Please read up on the oil of frankincense. I also take a probiotic called THRIVE and I have to Magnesium (glycincate) 120 mg. I take the Magnesium 4 times a day all day. Make sure you take the Thrive at night because it gets all the old stuff out of there.

 

ironictruth Proficient
12 minutes ago, Caroles said:

The funny thing with me, 2008 I had the fundoplication  done, where they tie your stomach closer to your esphagus. Last year I had an endoscopy done and I was definite celiac. Sometimes I wonder if it from the acid reflux operation. I do not take any medications for acid reflux because they cause more harm than good. What I have been doing is using a product called "intestinew" in my local vitamin store. This is a powder that I mix with EmergencC, it helps...I also drink green tea with a few drops of frankincense. I feel wonderful! Please read up on the oil of frankincense. I also take a probiotic called THRIVE and I have to Magnesium (glycincate) 120 mg. I take the Magnesium 4 times a day all day. Make sure you take the Thrive at night because it gets all the old stuff out of there.

 

Thank you!

  • 3 weeks later...
aliciahere Apprentice

Wouldn't be a bad idea to get full bloodwork done. Cbcd, vitamins, thyroid, etc. Thyroid in particular, it can do funny things with your heart if it's low or high. 

ironictruth Proficient
10 hours ago, aliciahere said:

Wouldn't be a bad idea to get full bloodwork done. Cbcd, vitamins, thyroid, etc. Thyroid in particular, it can do funny things with your heart if it's low or high. 

Thank you. My thyroid was normal in August except a nodule and enlarged lymphnode. But I know it needs to be run again. Am waiting on an appointment with an endo. 

Estes Contributor

What problems were caused by the PPI?  

I have heart pain that I thought might be anemia since I have tiny red blood cells (caused by celiac and my malabsorption).  I end up very fatigued every year late January-March.  I sometimes wonder if it could be even be related to vitamin D since I live in a cold climate.  Always trying to heal myself.  I don't feel comfortable taking so many vitamins, I feel like I might OD on something.

I am strict gluten free and have been since last March when I was diagnosed.  I thought I would have it all figured out by now with acid, anemia, vitamin levels.  I am currently feeling fatigue again and wondering if it might be the PPI.  Any words of wisdom on that would be appreciated.

I am on the PPI also because I have eosinophilia esophagitis.  Likely caused by 40 years of eating gluten.  I would like to heal all that and go off the PPI if possible.

cyclinglady Grand Master
21 minutes ago, Estes said:

What problems were caused by the PPI?  

I have heart pain that I thought might be anemia since I have tiny red blood cells (caused by celiac and my malabsorption).  I end up very fatigued every year late January-March.  I sometimes wonder if it could be even be related to vitamin D since I live in a cold climate.  Always trying to heal myself.  I don't feel comfortable taking so many vitamins, I feel like I might OD on something.

I am strict gluten free and have been since last March when I was diagnosed.  I thought I would have it all figured out by now with acid, anemia, vitamin levels.  I am currently feeling fatigue again and wondering if it might be the PPI.  Any words of wisdom on that would be appreciated.

I am on the PPI also because I have eosinophilia esophagitis.  Likely caused by 40 years of eating gluten.  I would like to heal all that and go off the PPI if possible.

Tiny red blood cells may be related to Thalassemia (a genetic anemia which can produce minor symptoms in many cases).  I have Thals and had iron-deficiency anemia.  Was never an issue until I could not keep up with my iron stores (due to celiac disease and menopause)  and my normal hemoglobin levels (which are always slightly below range) dropped very low.  But bodies often adapt.  I just wasn't going to get an Olympic medal!  BTW, Iron will not help with Thalassemia.  Your doctor should run a vitamin panel on you.  Standard  follow-up care for celiacs (includes Celiac antibody testing to help see if you are dietary complaint too).  

I am not suggesting you have Thals.  Just something to consider.  

Open Original Shared Link

frieze Community Regular

mag oxide is the  cheapest and least utile of the magnesium preparations, try mag 64/ mag delay.  or mag citrate caps, or glycinate as some one else mentioned.

kenlove Rising Star

Glycinate always worked best for me

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,858
    • Most Online (within 30 mins)
      7,748

    Janet1234
    Newest Member
    Janet1234
    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

    • Rogol72
      Some interesting articles regarding the use of Zinc Carnosine to help heal gastric ulcers, gastritis and intestinal permeability. I would consult a medical professional about it's use. https://www.nature.com/articles/ncpgasthep0778 https://www.rupahealth.com/post/clinical-applications-of-zinc-carnosine---evidence-review https://pmc.ncbi.nlm.nih.gov/articles/PMC7146259/ https://www.fallbrookmedicalcenter.com/zinc-l-carnosine-benefits-dosage-and-safety/
    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
×
×
  • 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.