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

Possible Intolerance?

chuckerychick

Recommended Posts

chuckerychick Newbie
chuckerychick
Posted

I am a 22-year-old female who is considering the possibility of gluten intolerance or celiac as being one of my problems, and I was wondering if I explained my situation if anyone could advise me if my symptoms are consistent. Since I was 11, I have had digestive issues, with my most notable symptom being nausea; it feels like having the stomach flu several dozen times a year. Is it possible for nausea to be the foremost symptom of gluten intolerance? I also have had bloating, fatigue, loss of interest in life in general, and loss of hope. I also have cold hands and feet, and my skin is so dry it itches, despite my best effort to keep lotion on and such.

The past month I have been sticking to a gluten -free diet, at least as far as I know; I realize there can be hidden sources I may be missing. Within the first few days, my bloating and the uncomfortable feeling in my abdomen subsided and has stayed away. Last week, I was almost completely nausea free, but this week I am feeling ill again, as well as tired and very emotional, edgy, snippy, and feeling as though I may cry, and I am not a crier normally. I have kept my diet consistent, so I don't know of any sources that may have slipped in. Is any of this on par with anyone else's symptoms? Is it just going to take some time for this all to even out and my body to start functioning? Are these sort of "relapses" possible even if I am truly following the diet correctly? Thank you ahead of time to anyone who takes the time to read this and help me.

ChuckeryChick

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

Celiac.com Sponsor (A8-M):


AliB Enthusiast
AliB
Posted
I am a 22-year-old female who is considering the possibility of gluten intolerance or celiac as being one of my problems, and I was wondering if I explained my situation if anyone could advise me if my symptoms are consistent. Since I was 11, I have had digestive issues, with my most notable symptom being nausea; it feels like having the stomach flu several dozen times a year. Is it possible for nausea to be the foremost symptom of gluten intolerance? I also have had bloating, fatigue, loss of interest in life in general, and loss of hope. I also have cold hands and feet, and my skin is so dry it itches, despite my best effort to keep lotion on and such.

The past month I have been sticking to a gluten -free diet, at least as far as I know; I realize there can be hidden sources I may be missing. Within the first few days, my bloating and the uncomfortable feeling in my abdomen subsided and has stayed away. Last week, I was almost completely nausea free, but this week I am feeling ill again, as well as tired and very emotional, edgy, snippy, and feeling as though I may cry, and I am not a crier normally. I have kept my diet consistent, so I don't know of any sources that may have slipped in. Is any of this on par with anyone else's symptoms? Is it just going to take some time for this all to even out and my body to start functioning? Are these sort of "relapses" possible even if I am truly following the diet correctly? Thank you ahead of time to anyone who takes the time to read this and help me.

ChuckeryChick

Hi. Your symptoms sound quite likely as a marker certainly for Gluten Intolerance, if not Celiac.

I haven't got quite as far as you as I have only been on it a weeks, but I would not be surprised for there to be odd reactions here and there. Your body is going through quite a radical change. It may also be hitting stages from time to time where it is having a clear-out of some of the toxins that have been languishing in the cells. If you have Candida, it might even be due to a die-off reaction where the change in diet has started to get the little beggars under control!

If you can't think of any way you have been 'glutened' then this may be a possibility, even a kind of 'Withdrawal'. The other possibility is that you may have inadvertently eaten or been in contact with something else other than Gluten to which you are unknowingly sensitive.

I have a slight theory as I have found that whilst I generally feel a lot better, there are one or two things that seem to have got worse, temporarily I hope. I am wondering perhaps that because my body is now starting to function more effectively it is demanding more nutrition, and deficiencies that were background whilst I was ill are now beginning to become more obvious. You may find that this you are experiencing is a temporary withdrawal phase and will pass - a bit like getting a plateau when you are dieting!

Sorry I can't give you anything concrete as a suggestion, but we are all different and have different responses. Hopefully there may be someone out there who has experienced this and may be able to shed a bit more light. I hope you manage to get past this phase.

chuckerychick Newbie
chuckerychick
Posted
  • Author

Thank you. When you mentioned that "I am wondering perhaps that because my body is now starting to function more effectively it is demanding more nutrition, and deficiencies that were background whilst I was ill are now beginning to become more obvious", it also made me think that maybe the rather strong hunger I've been experiencing can also be a part of all this.

Archived

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

Go to topic listing
  • Celiac.com Sponsor (A19):


  • Member Statistics

    • Total Members
      127,865
    • Most Online (within 30 mins)
      7,748
    Atasha
    Newest Member
    Atasha
    Joined
  • Celiac.com Sponsor (A20):

  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.5k
  • Celiac.com Sponsor (A22):



  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • Captain173
      Confused with test results

      By Captain173 · Posted

      I received my ANA test results - negative.  I'm thinking it was infection, was put on antibiotics for suspected sibo at the time blood test was taken. Significant improvements from taking them even while eating gluten.
    • BIg Nodge
      Opinions on my test results/symptoms

      By BIg Nodge · Posted

      Thanks again. I've actually convinced my local butcher shop to start carrying Ghostfish gluten-free beer. It's not bad! But you won't often find it at a ski lodge. 
    • Scott Adams
      Opinions on my test results/symptoms

      By Scott Adams · Posted

      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
      Vaccines

      By Scott Adams · Posted

      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
      Hidden Gluten in distilled vinegar

      By knitty kitty · Posted

      @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
×
×
  • Create New...