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

Vertigo


JaneWhoLovesRain

Recommended Posts

JaneWhoLovesRain Enthusiast

Do any of you suffer from vertigo or off balace feelings as part of your celiac disease? I started having severe vertigo attacks about 4+ years ago and have been unable to get a firm diagnosis for this because while my symptoms fit some parts of all the dizzy disorders they don't fit enough of any one to give a firm diagnosis. For instance, the vertigo is severe enough that one would think I have Meniere's but my hearing is barely affected. I've had several tests and I end up with a lot of shoulder shrugging from the doctors. I have also suffered my entire life from extreme motion sickness (and not just from being in a moving vehicle, but any kind of movement can make me feel sick). I've been eating gluten-free for about 2 years and have noticed an improvement but I'm definitely not feeling 100% yet. However, I'm not 100% gluten-free either, maybe 98%.

Now I am trying to figure out if celiac might be my problem because last night I came across something I never heard of. I've had a weird rash since December, started slow on my neck but in the last couple of weeks it has spread and now I have it on my elbows, hips and backs of knees. Very symmetrical and very itchy. In trying to figure out what this is I came across dermatitis herp.... (can't remember the spelling) which really seems to fit the pattern of my rash.

BTW, my intestines seem fine, so I'm stumped!!


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



Celiac.com Sponsor (A8-M):



youwillrise Rookie

I don't have a celiac diagnosis as of now...but I have been experiencing vertigo and dizziness amongst all the other symptoms. I've also been prone to motion sickness since I was young, though I didn't consider that as a possible sign...hmmm...now that I think of it, though, I've considered myself a healthy person most of my life...I realize now that I have had a lot of sensitivities and intolerances that I haven't really put into perspective until recently. I've thought of them separately, but I never thought of them as being parts of a bigger issue. Hmmm

I'm sure someone more knowledgeable will chime in! Your post just made me think some more about my own history.

Bubba's Mom Enthusiast

Do any of you suffer from vertigo or off balace feelings as part of your celiac disease? I started having severe vertigo attacks about 4+ years ago and have been unable to get a firm diagnosis for this because while my symptoms fit some parts of all the dizzy disorders they don't fit enough of any one to give a firm diagnosis. For instance, the vertigo is severe enough that one would think I have Meniere's but my hearing is barely affected. I've had several tests and I end up with a lot of shoulder shrugging from the doctors. I have also suffered my entire life from extreme motion sickness (and not just from being in a moving vehicle, but any kind of movement can make me feel sick). I've been eating gluten-free for about 2 years and have noticed an improvement but I'm definitely not feeling 100% yet. However, I'm not 100% gluten-free either, maybe 98%.

Now I am trying to figure out if celiac might be my problem because last night I came across something I never heard of. I've had a weird rash since December, started slow on my neck but in the last couple of weeks it has spread and now I have it on my elbows, hips and backs of knees. Very symmetrical and very itchy. In trying to figure out what this is I came across dermatitis herp.... (can't remember the spelling) which really seems to fit the pattern of my rash.

BTW, my intestines seem fine, so I'm stumped!!

I get dizzy and off balance from gluten. I went 100% gluten-free last July. I accidently got "glutened" and the symptoms came back stronger than ever. Some Celiacs don't get GI symptoms, and some of us get neurological AND GI issues.

The rash you are now experiencing sounds like it could be DH? If you can get in and have a biopsy, which is taken from the skin right next to the rash, you may have your DX?

AVR1962 Collaborator

Do any of you suffer from vertigo or off balace feelings as part of your celiac disease? I started having severe vertigo attacks about 4+ years ago and have been unable to get a firm diagnosis for this because while my symptoms fit some parts of all the dizzy disorders they don't fit enough of any one to give a firm diagnosis. For instance, the vertigo is severe enough that one would think I have Meniere's but my hearing is barely affected. I've had several tests and I end up with a lot of shoulder shrugging from the doctors. I have also suffered my entire life from extreme motion sickness (and not just from being in a moving vehicle, but any kind of movement can make me feel sick). I've been eating gluten-free for about 2 years and have noticed an improvement but I'm definitely not feeling 100% yet. However, I'm not 100% gluten-free either, maybe 98%.

Now I am trying to figure out if celiac might be my problem because last night I came across something I never heard of. I've had a weird rash since December, started slow on my neck but in the last couple of weeks it has spread and now I have it on my elbows, hips and backs of knees. Very symmetrical and very itchy. In trying to figure out what this is I came across dermatitis herp.... (can't remember the spelling) which really seems to fit the pattern of my rash.

BTW, my intestines seem fine, so I'm stumped!!

I was stumped too as my symptoms were not so much digestive initially. I was having some visual issues, very tired and then I became off balance. I could tip over if I were leaning to water a plant. Not spining in my head but more of an inability to keep myself steady. I would trip on my toes, my coordination was way off from normal. I did decide to go off gluten just to see what would happen. I tried for 3 weeks, went back to eating gluten and then is when I noticed the digestive issues. So I really cleaned up my diet, took all the gluten out, cleaned up my kitchen, cookware, etc. In 4 weeks of having no gluten all the dizzines stopped. I lived with the balance issues for 9 months.

The other issues I found too was that I was having vertigo (spinning) in reaction to other foods, however the reaction would not last as long, maybe 3 days. I kept a food journal and looked at all labels. I could not eat any gums like xanthan, caraageenan or high fructose. I also found I was lactose intolerant. Big changes at 48 and I wondered what in the world happened to me. The more I read the more I realized my intestines were a ship wreck and that's why I was haviong so many issues.

I have been gluten-free 11 months now. What I can say is it is a slow process and I at times in this I have questioned if this is really what is going on but I think I have to look at the obvious.....I have come a long way in less than a year.

I hope that helps!

YoloGx Rookie

I used to always wake up dizzy and had to be careful standing up from a sitting position so I would not faint. My dear bf has had the same problem, especially getting up out of bed. Sometimes even having had to crawl on the floor! My bp has always been low, and years ago I was diagnosed as having a condition where my bp would fall 30 points when I would get up. This was after I had fainted and broken 2 teeth and then fainted again and severely messed up my left foot which had caught under a stairwell.

I now don't faint anymore. It is like a miracle!!

I also have fewer problems with not being able to remember the names of things etc. etc.

I ascribe this to having gone off gluten, as well as, for me, going off high to medium salicylate foods. My bf has improved greatly too just going off the gluten.

So yes, you are not nuts. Neither are we. They call it gluten ataxia. Please be careful in the meantime; and its likely best to continue to stay off the gluten. Maybe try being 100% gluten-free?

I would meanwhile look into the rash. Sounds like DH to me. Though you never know, you could be unlucky and have a salicylate or some other allergy problem like me. The symmetry however and the locations make one think DH as the most likely cause. DH is a lot easier to diagnose by the way than classic celiac. They check the area immediately next to the rash/blisters.

Bea

deinanthe Newbie

Yes, vertigo is one of my main symptoms as a celiac. It is one of the ways I can tell if I've been getting into anything gluten contaminated, as the vertigo starts to come back. However, if I am 100% gluten free, I am also 100% vertigo free. If I were only 98% gluten free as you say you are, I would have vertigo all the time still. Get yourself to 100% gluten free and give yourself some time to heal, you may be pleasantly surprised to see your vertigo is gone completely.

Takala Enthusiast

For me this "vertigo" is caused by gluten ataxia. I also had other neurological symptoms which the doctors blew off or attempted to attribute to other diseases, which I then would not have, when they bothered to test me.

Most of it has resolved by sticking to a strict gluten free diet. I self diagnosed as at least gluten intolerant after the Neurologist From Hell


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



Celiac.com Sponsor (A8-M):



JaneWhoLovesRain Enthusiast

Thank you all for your responses. While I don't want celiac I am kind of hoping this rash is DH and that I will then successfully go 100% gluten-free and both the rash and vertigo problems will clear up. I'm going back to the dermatologist Tuesday. My first visit a couple of weeks ago wasn't real productive. Since that time my rash has increased greatly so maybe he will actually do something about it this time.

I've been reading what I can about gluten ataxia but there doesn't seem to be a lot of info on it. Do doctors generally recognize this part of celiac or is it the sort of thing that they brush off?

Jane

IrishHeart Veteran

Vertigo, among several other NASTY and persistent neuro issues, (ataxia, burning nerves, parasthesia, memory issues, muscle atrophy, etc. ) were among my symptoms of celiac.

Listen to TAKALA and insist upon that biopsy.

People with DH are celiacs, in most medical opinions. Period.

Actually, there is quite a bit written about gluten ataxia.

here you go:

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

also, check the website called THE GLUTEN FILE--that person has generously complied MANY articles there.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,860
    • Most Online (within 30 mins)
      7,748

    Rena Celiac
    Newest Member
    Rena Celiac
    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.