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

Need Some Direction... I'm Suffering Every Day And Not Sure Where To Head


Trademarked

Recommended Posts

Trademarked Newbie

I'll summarize my situation that I described in a previous post. I've had severe itching all over my body for 8 months. In the last 3 months additional symptoms have become present. They include: rash, hives on butt/hands/feet/eblows (and sudden, but quick, pains where they are forming), hot skin, blurry vision, new headaches, stomach discomfort/gas, aching/swelling joints, loose stool (but not diarrhea). The symptoms all increase/decrease at the same time. It's rare to get only one.

I've CONFIRMED multiple reactions to peanuts, ALMOST SURE I've had reactions to dairy, and POSSIBLE reactions to soy. I've been avoiding all of them, including gluten of course, and I tend to get better for a day or two, but I almost always slip up and ingest one of them. I'm going to continue removing them all from my diet, but being a vegetarian of 15 years it is very challenging to find protein without dairy, soy, and peanuts. I felt better when I removed gluten from my diet, but I haven't noticed a sudden reaction like with the foods mentioned above.

I've been to a dermatologist who couldn't tell what the rash was, and suggested the next step to be a biopsy. (I have to pay out of pocket) I've been to an allergist who found nothing on a prick test, and nothing on a blood test (not sure what this blood test actually tested for). He suggested the next step being a biopsy of the intestine (endoscopy? again... have to pay out of pocket). I've been to a holistic doctor that suggested an (Company Name Removed - They Spammed This Forum and are Banned) test, but I didn't do it yet due to the allergist's lack of support and trust in the test. I've been to 2 general doctors who had blood tests done, with no deficiencies (worth noting I've always ate a diet rich in vegetables high in vitamins and minerals), and they state that since the allergist turned up nothing that I must not have celiac, and that it must be mental. I meditate often and even in the most relaxed state I still feel the sudden sharp pains where the hives are forming, so I've ruled out latent stress or anxiety. It's very frustrating that I have to become a medical researcher to solve my problems, but I'll bet many of you feel the same way.

What I'm looking for is direction. Where would you go next if you were in my shoes? Of course, I'm avoiding these foods as well as I can, but I really need peace of mind that I'm doing the right thing. So far I see my options as 1) Endoscopy, 2) Skin biopsy, 3) (Company Name Removed - They Spammed This Forum and are Banned) test, 4) Stomach doctor. What would YOU do?


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



Celiac.com Sponsor (A8-M):



Pac Apprentice

I can't help with the tests, but if you suspect soy, dairy or peanuts to be a problem, then avoid them strictly for at least a few weeks (4-6). If the symptoms disappear, add them back one at a time.

You don't really need any of those three to get enough protein. Just (nixtamal) corn and beans alone will provide you with enough protein and all important amino acids. Can you eat beans, chickpeas, green/yellow peas, lentils, potatoes, corn, mushroom, other nuts? I'm a rather strict carnivore but those are my stapples when I can't get any fish, meat or eggs. Do you eat eggs?

Trademarked Newbie

I can't help with the tests, but if you suspect soy, dairy or peanuts to be a problem, then avoid them strictly for at least a few weeks (4-6). If the symptoms disappear, add them back one at a time.

You don't really need any of those three to get enough protein. Just (nixtamal) corn and beans alone will provide you with enough protein and all important amino acids. Can you eat beans, chickpeas, green/yellow peas, lentils, potatoes, corn, mushroom, other nuts? I'm a rather strict carnivore but those are my stapples when I can't get any fish, meat or eggs. Do you eat eggs?

I've eliminated soy and dairy for about a week now, and peanuts for about 5 days. Do beans or other nuts cause cross reactions?

Skylark Collaborator

Well, what I did was an elimination diet. Allergy testing is unreliable, doctors are mostly useless when it comes to sensitivities, and nobody knows your body better than you do. I would not waste money on mail order allergy testing or subject myself to invasive procedures.

Pare your diet down to a few foods and see if you feel better. Then you can get a much better idea of what's bothering you when you add foods back in. As Pac says, you can get by on corn/beans or corn/rice without soy or animal protein. It's a good point about eggs - they are a lovely protein source too. It also may be time to re-examine your vegetarian diet. Nobody on this board is really able to eat the way we would like. We are forced into certain diets to avoid getting sick.

As for the gluten, it can cause underlying intestinal inflammation that lets allergens from other foods through. I was sensitive to diary, soy, and shellfish on my elimination, as well as gluten. After about six months gluten-free I was able to eat the other foods again. You are not likely to lose the peanut allergy with soy cross-reactivity, but you may be able to eat dairy again if you go gluten-free for a while.

cassP Contributor

im assuming you dont have health insurance? or are you like me- i have catastrophic insurance which is basically the same thing... i just have a huge bill i pay off little by little every month..

if you're like me and you need some sort of diagnosis- the easiest thing may be to first post a pic of your rash here- if it looks like DH- then u could get a biopsy next to it-

or a blood test (complete celiac panel) with a GP.

if you dont need a dx, and just want to feel better now- i would follow suggestions above for elimination diet. of course i would eliminate gluten NOW... and possibly corn, dairy & soy.

those are the big ones... after that- some have issues with nightshades... others find relief somewhat following the FODMAP diet... and still- some of us feel best mostly grain free

good luck- hope u feel better soon!!!

Trademarked Newbie

Well, what I did was an elimination diet. Allergy testing is unreliable, doctors are mostly useless when it comes to sensitivities, and nobody knows your body better than you do. I would not waste money on mail order allergy testing or subject myself to invasive procedures.

Pare your diet down to a few foods and see if you feel better. Then you can get a much better idea of what's bothering you when you add foods back in. As Pac says, you can get by on corn/beans or corn/rice without soy or animal protein. It's a good point about eggs - they are a lovely protein source too. It also may be time to re-examine your vegetarian diet. Nobody on this board is really able to eat the way we would like. We are forced into certain diets to avoid getting sick.

As for the gluten, it can cause underlying intestinal inflammation that lets allergens from other foods through. I was sensitive to diary, soy, and shellfish on my elimination, as well as gluten. After about six months gluten-free I was able to eat the other foods again. You are not likely to lose the peanut allergy with soy cross-reactivity, but you may be able to eat dairy again if you go gluten-free for a while.

I think I will exactly this. I need to really crack down and avoid anything in question for a significant amount of time.

im assuming you dont have health insurance? or are you like me- i have catastrophic insurance which is basically the same thing... i just have a huge bill i pay off little by little every month..

if you're like me and you need some sort of diagnosis- the easiest thing may be to first post a pic of your rash here- if it looks like DH- then u could get a biopsy next to it-

or a blood test (complete celiac panel) with a GP.

if you dont need a dx, and just want to feel better now- i would follow suggestions above for elimination diet. of course i would eliminate gluten NOW... and possibly corn, dairy & soy.

those are the big ones... after that- some have issues with nightshades... others find relief somewhat following the FODMAP diet... and still- some of us feel best mostly grain free

good luck- hope u feel better soon!!!

I do have insurance, but I have a very high deductible. If I really need something I can afford to pay for it, but I just don't want to spend needlessly on a hunch, you know? As soon as the rash reappears (its too faint to see on a camera) I will post a photo.

What's a GP? I have my blood test results in front of me and they say negative for celiac on the test. It says celiac disease panel with a few items listed, and there are some other items, then f079-ige gluten. It says all are negative. Is that a reliable test? Does it test for intolerance?

starrytrekchic Apprentice

I would do an elimination diet. Just pick a few things (simple, unprocessed, like rice) you know you can eat and slowly add other things back in. Be sure you're actually gluten free--check all meds, supplements, foods, drinks, personal products, anything that could cross-contaminate you. You may need to be more strict with your gluten free diet--finding out if your food is made on the same equipment as wheat, etc.

That said, you have to keep in mind other illnesses. I'd keep researching the symptoms to see what else comes up. These symptoms may be food related, but they may not--they might not even be from the same thing. Have you been checked for something like Lyme Disease? It features a lot of what you're describing and can trigger Celiac, so Celiac and Lyme are sometimes found together.


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



Celiac.com Sponsor (A8-M):



GFinDC Veteran

There is a section of the board dedicated to DH (dermatitis herpetiformis). That could be what the rash is. Take a look and see if the symptoms match.

Trademarked Newbie

I would do an elimination diet. Just pick a few things (simple, unprocessed, like rice) you know you can eat and slowly add other things back in. Be sure you're actually gluten free--check all meds, supplements, foods, drinks, personal products, anything that could cross-contaminate you. You may need to be more strict with your gluten free diet--finding out if your food is made on the same equipment as wheat, etc.That said, you have to keep in mind other illnesses. I'd keep researching the symptoms to see what else comes up. These symptoms may be food related, but they may not--they might not even be from the same thing. Have you been checked for something like Lyme Disease? It features a lot of what you're describing and can trigger Celiac, so Celiac and Lyme are sometimes found together.

I haven't been checked for it, but I've read the symptoms a few times and while some are similar, the overall situation just doesn't feel like mine. My itching is my primary problem, and far outweighs any other symptoms. The joint pains and headaches are annoying, but the itching is driving me mad. If I had a regular job I would be out on disability months ago.

There is a section of the board dedicated to DH (dermatitis herpetiformis). That could be what the rash is. Take a look and see if the symptoms match.

I will take a look, thanks!!

mushroom Proficient

If you want to follow the formal diagnosis path, it would be interesting if you have copies of all your lab results and could post them here. There are a lot of people on this forum who are much better at reading the lab results than the doctors, and who could help you interpret what they mean. Doctors' interpretations of test results are often really off base; if you are low normal then there's no problem,; if you are a little too high, hey, that's not really a problem because it's just a little bit over. There is a reason these ranges are set, and they are normally set much wider than they should be (for fear of bringing in too many people into the abnormal range, I guess, when that is really where we belong :o ). At any rate, if you have these test results, and the ranges the lab uses, post them and let us have a look at them.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • 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    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
    • Scott Adams
      Is this the same restaurant? https://www.facebook.com/TheHappyTartFallsChurch/ Is it too late to take this up with your credit card company? Normally you have a few months to do a chargeback with them. It seems very odd that they are taking this approach with someone who is likely to be a regular customer--not a good business-minded way of handling things!
    • Scott Adams
      Many people with celiac disease, especially those who are in the 0-2 year range of their recovery, have additional food intolerance issues which could be temporary. To figure this out you may need to keep a food diary and do an elimination diet over a few months. Some common food intolerance issues are dairy/casein, eggs, corn, oats, and soy. The good news is that after your gut heals (for most people who are 100% gluten-free this will take several months to two years) you may be able to slowly add some these items back into your diet after the damaged villi heal. This article may be helpful: The most common nutrient deficiencies associated with celiac disease that may lead to testing for the condition include iron, vitamin D, folate (vitamin B9), vitamin B12, calcium, zinc, and magnesium.  Unfortunately many doctors, including my own doctor at the time, don't do extensive follow up testing for a broad range of nutrient deficiencies, nor recommend that those just diagnosed with celiac disease take a broad spectrum vitamin/mineral supplement, which would greatly benefit most, if not all, newly diagnosed celiacs. Because of this it took me decades to overcome a few long-standing issues I had that were associated with gluten ataxia, for example numbness and tingling in my feet, and muscle knots--especially in my shoulders an neck. Only long term extensive supplementation has helped me to resolve these issues.        
×
×
  • 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.