Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Help I'm Sick!


IndigoRose

Recommended Posts

IndigoRose Newbie

For the past 5 years my health has been declining, I have been passed from doctor to doctor and had test after test. I began feeling fatigue, weekness and lack of endurance, signs of 'IBS' or maybe "lactose intolorance", constipation, none of which were helped by any medications or showed anything serious on scopes or tests.

I ran a low grade fever and my white count was slightly elevated on every blood test, but no disease, they just kept telling me it was a virus! but I never got better... for 1 1/2 years until I went to the emergency room with a kidney stone and they found a tumor on my left overy! I had that removed and then proceded to pass 4 more stones...

I felt a little better but my symptoms were still present and in addition the migraine headaches that I had suffered with had increased to daily and so severe sometimes I could not even stand. I have been hospitalized several times because of them. Also my body is so acidic I have sores in my mouth despite taking Lysine 1000mg a day.

I have removed all tyrizine, MSG and soy from my diet, but am still sick. Two days ago I went to the doctor that took my tumor out and he suggested I be tested for Celiac Disease. He is an excellent doctor, (I don't say that often) but I would still like to know more about this?

My symptoms seem to fit, yet seem extreme too? Does anyone have migraines like this?

Also I am trying to go completely glutin free, it is a bit confusing, any SIMPLE advice?

I could sure use some encouragement, I have been sick for SOOOO long, I have been ready to give up!

Thank you...


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



Celiac.com Sponsor (A8-M):



dbmamaz Explorer

I dropped gluten and dairy 2 months ago, because i'd reacted to them as an infant, and just thought I might feel healthier, but i had no major complaints. However, all my minor complaints (headaches 4/wk, frequent bouts of fatigue, depression and anxiety, and iffy bowels) have all cleared up. I saw a woman on youtube who said she got rid of canker sores from going off gluten, and I'm pretty sure headaches are a common one.

I'm waiting on my celiac test (done after i'd been off for 6 wks, so likely to be negative), but if i can come up with any positive results, I'm going to encourage my sister to try also. She's been sick like you for years - chronic fatigue, fibromyalgia, headaches, plus hallucinations and bouts of being suicidal, more recently her hands have been swelling up and she's had fevers. My mother has been parading her past every specialist she can find in boston, and no one knows what's wrong. I'm afraid to talk to her about food sensitivities (she also has an allergy to corn, which honestly they say is harder ot avoid than gluten), because she thinks I'm a hypochondriac who's always trying to label everyone else with what I think I have.

Anyways, the simplest way to get off of gluten is to eat whole, unprocessed foods. Roast a chicken and some potatoes and steam some veggies, and eat the leftovers the next day. I was eating plain grits with a fried egg. But at first, rather than hoping various things are gluten free, just eat very plain food. Even rice crispies have hidden gluten in the form of barley malt flavoring.

However, you might want to wait until you have your dx back from your doctor, becuase if they want to do a biopsy, going off gluten now can affect your biopsy.

I sure hope gluten is your answer - so many people on this site seemed to have been brought back from death's door by dropping the gluten. Good luck!

lizard00 Enthusiast

THe headaches, mouth sores and chronic fatigue are definitely symptoms/signs of Celiac. Sounds like you found a keeper for your doc!! I hope your test is soon and gives you some answers. Remeber though, they are not always conclusive, so regardless of the result, you should go gluten-free for a few weeks to see if you feel any relief. But make sure you stay on gluten until then, or you could get a false negative.

It seems very overwhelming at first, but there is a safe foods list and an unsafe list on this website, and many manufacturers are very clear, I know Kraft is great about not hiding ingredients. But at first, the easiet way is just what dbmamaz said, fresh meats, fruits and veggies. Leftovers for lunch, and then as it gets easier and you don't feel so overwhelmed, move on to different things. You'd be really surprised at how much is gluten-free. Also, if you have a whole foods nearby, they have a list of everything in their store that is gluten-free. You can print it off the internet, or they will give you a list at the service desk.

Hope you start feeling better soon!!

IndigoRose Newbie
THe headaches, mouth sores and chronic fatigue are definitely symptoms/signs of Celiac. Sounds like you found a keeper for your doc!! I hope your test is soon and gives you some answers. Remeber though, they are not always conclusive, so regardless of the result, you should go gluten-free for a few weeks to see if you feel any relief. But make sure you stay on gluten until then, or you could get a false negative.

It seems very overwhelming at first, but there is a safe foods list and an unsafe list on this website, and many manufacturers are very clear, I know Kraft is great about not hiding ingredients. But at first, the easiet way is just what dbmamaz said, fresh meats, fruits and veggies. Leftovers for lunch, and then as it gets easier and you don't feel so overwhelmed, move on to different things. You'd be really surprised at how much is gluten-free. Also, if you have a whole foods nearby, they have a list of everything in their store that is gluten-free. You can print it off the internet, or they will give you a list at the service desk.

Hope you start feeling better soon!!

thank you so much for your response! I am beside myself I do not know if I can still continue to eat gluten knowing this may be the cause, I have stopped eating all products for one full day now, I still do not feel great but am hoping there will be a change. I am willing to try anything! I am desperate!!!

Thank you for the SIMPLE food suggestions, they were most helpful. fresh meats, fruits and veggies. I can do that! I understand reading food labels but the gluten thing was sooo confusing and I was already so frustrated with the whole soy and soy bi-product issue.

One last question? Can I eat yogert? Drink milk? Dairy Products? Are they safe? I do not think I am lactose intolerent, I think my symptoms are from Celiac Disease.

Thank you again....

lizard00 Enthusiast

The dairy thing is difficult to answer. Some people find that they need to go off dairy for a bit while they are healing. I have seen many recommendations from this site. There are also just as many who say give it a try and see how it makes you feel. If you find you can tolerate dairy products with no problem, I say go for it.

If you do find that dairy bothers you, cut it out for a while. You can always try it again a few months down the road when your body is doing better. If you've been eating dairy this long, chances are you probably aren't lactose intolerant, but if your digestive system is out of whack, lactose can be an issue until things are better. So, experiment, ask your doc, and go from there.

Hope that helped!

Liz

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      127,862
    • Most Online (within 30 mins)
      7,748

    Aracely
    Newest Member
    Aracely
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Villi damage is caused by celiac disease, which does not happen in NCGS, although some people with NCGS do have elevated antibody levels. Some people with NCGS who have the genes for celiac disease may end up developing celiac disease, so in some people NCGS may be a precursor to celiac disease, but more research needs to be done on NCGS. Both low iron and vitamin D are common symptoms of celiac disease. Also, regarding beer:  
    • Scott Adams
      It’s true that some vaccines contain small amounts of preservatives, stabilizers, or adjuvants to ensure their safety and effectiveness. For example: Thimerosal: A preservative that contains ethylmercury (not to be confused with methylmercury, which is toxic). Most routine vaccines no longer contain thimerosal, except for some flu vaccines in multi-dose vials. Aluminum: Used in very small amounts as an adjuvant to boost the immune response. The amount is far below levels considered harmful, but if you suspect an aluminum allergy, it’s worth discussing with your doctor. Sugar alcohols: These are sometimes used as stabilizers, but they are generally well-tolerated. If you have a known intolerance, you can ask about specific ingredients in each vaccine. Since you mentioned an intolerance to metals and jewelry, it’s a good idea to follow up with allergy testing, as you planned. This can help identify specific metals (e.g., nickel, aluminum) to avoid. Your doctor can then guide you on whether any vaccine ingredients might be a concern. Since the Mayo Clinic has already identified potential allergies, it might be helpful to consult an allergist or immunologist. They can review your medical history, perform tests, and provide personalized advice on vaccines and their ingredients. While it’s important to address your intolerances, it’s also worth considering the risks of not being vaccinated. Many vaccine-preventable diseases can have serious consequences, especially for those with underlying health conditions. 
    • knitty kitty
      @Manaan2, I was on Miralax for several months after I crushed three vertebrae and fractured my hip.  The compression fractures of my vertebrae affected the Vagus nerve that stimulates digestion and intestinal movement, peristalsis. Miralax just didn't relieve the constipation I was experiencing at all.  Nothing budged.  I tried Milk of Magnesia (magnesium oxide) which pulls water into the digestive tract, and found that rather harsh and dehydrating.   Bad idea. I was already taking thiamine in various forms, Benfotiamine, TTFD (tetrahydrofurfuryl  disulfude), Lipothiamine and Allithiamine.  Click on my name, then Activities in the pull down menu to get to my blog to learn more about my journey with thiamine.   Since we need more thiamine when we are physically ill and emotionally stressed, I decided to focus on TTFD,  Benfotiamine, and magnesium l-threonate.  Within a week of increasing my doses a bit, my constipation was gone.  It took several more months to heal the compressed nerve damage.  For pain, I take a combination of TTFD, Pyridoxine B 6, and  Cobalamine B12 which together have an analgesic effect.  I can't function with pharmaceutical pain killers, besides they cause constipation.   Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Yes, I did just stop the Miralax, but I wasn't on it as long as your daughter.  Yes, there's a difference between adults and children.  Yes, my circumstances were different than your daughter's, but thiamine deficiency does affect the nerves and the brain.  A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function (which activates the Vagus nerve and controls digestion).   I recommend you visit Dr. Chandler Marrs' website, hormonesmatter.com.  Dr. Marrs worked with Dr. Derrick Longsdale, a pioneer in thiamine research, specifically with children and autism spectrum disorders.  She has been very helpful to me when I reached out to her.  She would be better able to guide you about your daughter's care. https://hormonesmatter.com/sibo-ibs-constipation-thiamine-deficiency/#google_vignette Do stay in touch, please.  You can start another thread or personal message me any time.  My heart goes out to you, your husband, and especially your daughter.   Namaste
    • Manaan2
      @knitty kitty  The information you've provided is invaluable!  I have a lot more homework to do before we make the official switch but you have significantly increased my hope that we can get her off Miralax (she started at 3 years old and is almost 8!).  This weekend my husband and I plan to solidify all the details for a start point, then adjust as we go along.  I realize that everyone's body is different, then there's also the fact that she's a child but just out of curiosity if you don't mind sharing and if you'd rather not, no problem at all-how long did you take Miralax before switching and when you switched, did you just completely stop the Miralax or was there a period where you did Miralax and the supplements?  I plan to research that piece this weekend but just curious what you did.  
    • BIg Nodge
      Scott, thanks so much for the thoughtful replies. My doctor did actually just re-order thyroid labs to see what is going on with my TPOs. I agree that will be interesting information.  I think I know the answer to this, but as far as the biopsy . . .. that would be quite conclusive as far as celiac goes, but a negative result would not rule out NCGS, correct? Does NCGS also cause damage to the lower intestine/leaky gut?  I appreciate the thought that I should be open-minded to other causes. I did not have dysautonomia on my radar, so I will look into that. From a quick scan at the potential symptoms it seems like almost anyone could convince themselves they have it, very broad! I can see why that is a tricky one to diagnose. I did also show low vitamin D, I'm in New England so that is somewhat common. I have a memory of low iron on some lab result as well but I can't find it, so I'll look into that. My cholesterol is high too, so working on that.  While the initial adjustment was tough, I have actually adapted fairly well to going gluten-free at home. The tough part for me is I love eating out and traveling, so that has been a challenge. I suppose if the answer ends up being NCGS then I could maintain a mostly gluten-free diet but also experiment with the occasional splurges. Snowboarding just doesn't feel right without a beer in the lodge . . ... cider is just not the same!  Thanks again.  
×
×
  • Create New...