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

How Long Did It Take For Detox Symptoms To Go Away,


CGally81

Recommended Posts

CGally81 Enthusiast

I'm really hoping my detox symptoms, which have gotten pretty nasty in the past week or so (but are also somewhat dying down, thankfully), go away soon. Along with the super hunger, but that actually is noticably (slowly) decreasing too.

Anyway, before I went gluten-free, or figured out what was up with tons of internet searches and self-diagnosis, I had the GI symptoms for like ~5 months. I know for a fact it happened this year, because I remember feeling great during Christmas vacation 2008, so I definitely got the symptoms this year. Just don't remember when, but I'd say I was having GI symptoms for less than 6 months.

Well, since I only had overt symptoms for 6 months at most, I'm hoping my detox period should be short. I'm 28 years old, so if I'd actually been having more covert symptoms for years (i.e. gut damage, which is possible, as I developed fructose malabsorption last year and had to give up apples) and not realized it, then I'm probably in for a longer detox than I'd think before I get back to feeling normal again.

So, how about the rest of you guys? How long did you have your symptoms before you went gluten-free? And how long did it take after going gluten-free to feel normal again?

It would be interesting to see the relationship between the two values.

EDIT: Oops! Wrong board! This belongs on the post-diagnosis board, I think. Could an admin move this there? I'm sorry.


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



Celiac.com Sponsor (A8-M):



ang1e0251 Contributor

My earliest clue might have been lactose intolerance in high school which took me a few years to figure out. I started having the brain fog, fatigue, insomnia and a much harder time concentrating about 5th grade. I don't know if that's related or no.

I didn't have any trouble with my stomach until my daughter was about 2 YO, I was about 32. After that, things went downhill. I self diagnosed at age 49 so that's long time if it's all related.

GottaSki Mentor

Since being diagnosed just over 5 months ago, I have discovered that I had celiac symptoms most of my life. I'm 44.

Except for a few teen years where I was eating next to nothing I've always been slightly bloated and had periodic unexplained stomach trouble/flu like symptoms which included achy joints etc. When I'd go to the doctor I'd complain of general fatigue, soreness and occasional upset stomach. Episodes got worse, but livable. I continued to tell the docs that I eat a very balanced diet and get A LOT of exercise, yet I have had unexplained weight gain for years...docs could never find anything except anemia - and made it clear they thought it was all in my head.

The past 8 years symptoms increased until in 2008 I was extremely bloated and sick all the time, especially in the warmer months. I kept on my doctor because it was obvious something was going on -- there was a hit on low Vitamin D and finally after 50 blood tests she ran my tTG -- only slightly positive but positive. I was given referral to GI and told to ask for someone that "wants a Celiac Sprue case". Turns out we have one of the best Celiac facilities right here at UCSD, unfortunately it took 26 years of UCSD primary docs to get me pointed in the right direction. My biopsy confirmed moderate to severe damage from Celiac Disease.

I've been gluten-free for 5 months and my digestive system has improved...I hardly bloat anymore. I was really hungry for about the first two months. Unfortunately my fatigue, joint pain and heat intolerance have become much worse. Still looking into other possibilities for some of my symptoms, but remain hopeful that gluten-free time will bring more healing and I'll be able to claim a solid timeline for how long it took to heal.

Each time I read of someone being diagnosed much younger than I it makes me very happy and grateful that some doctors seem to be getting better training to look for Celiac -- although there is a long way to go on that front.

Improved health to you!

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Wheatwacked replied to GlutenFreeChef's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      12

      Blood Test for Celiac wheat type matters?

    2. - trents replied to JudyLou's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    3. - JudyLou posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Seeking advice on potential gluten challenge

    4. - marzian commented on Scott Adams's article in Diagnosis, Testing & Treatment
      5

      A Future Beyond the Gluten-Free Diet? Scientists Test a New Cell Therapy for Celiac Disease (+Video)

    5. - Jmartes71 posted a topic in Related Issues & Disorders
      0

      Medications

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,142
    • Most Online (within 30 mins)
      7,748

    Mark Conway
    Newest Member
    Mark Conway
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • Wheatwacked
      no argument. Never take the pills sold for Nuclear events, except in a nuclear event when instructed to by authorities.  Some of these go up to 130 milligrams per pill. 5000 times the strength of the dietary supplement.  130 times the safe upper limit.  130 mg = 130,000 mcg. Dietary supplements like Lugol's Solution and Liquid Iodine are 50 micrograms per drop.  It takes 20 drops to reach the safe upper limit. In the US the Safe upper limit is 1100 mcg.  In Europe 600 mcg and in Japan 3000 mcg ( 3 mg).
    • trents
      Welcome to the celiac.com community, @JudyLou! There are a couple of things you might consider to help you in your decision that would not require you to do a gluten challenge. The first, that is if you have not had this test run already, is to request a "total IGA" test to be run. One of the reasons that celiac blood antibody tests can be negative, apart from not having celiac disease, that is, is because of IGA deficiency. If a person is IGA deficient, they will not respond accurately to the celiac disease blood antibody tests (such as the commonly run TTG-IGA). The total IGA test is designed to check for IGA deficiency. The total IGA test is not a celiac antibody test so I wouldn't think that a gluten challenge is necessary. The second is to have genetic testing done to determine if you have the genetic potential to develop celiac disease. About 30-40% of  the general population have the genetic potential but only about 1% actually develop celiac disease. So, genetic testing cannot be used to diagnose celiac disease but it can be used to rule it out. Those who don't have the genetic potential but still have reaction to gluten would not be diagnosed with celiac disease but with NCGS (Non Celiac Gluten Sensitivity).  Another possibility is that you do have celiac disease but are in remission. We do see this but often it doesn't last.
    • JudyLou
      Hi there, I’m debating whether to consider a gluten challenge and I’m hoping someone here can help with that decision (so far, none of the doctors have been helpful). I have a history of breaking out in a horrible, burning/itchy somewhat blistering rash about every 8 years. This started when I was in my early 30’s and at that point it started at the ankles and went about to my knees. Every time I had the rash it would cover more of my body, so my arms and part of my torso were impacted as well, and it was always symmetrical. First I was told it was an allergic reaction to a bug bite. Next I was told it was eczema (after a biopsy of the lesion - not the skin near the lesion) and given a steroid injection (didn’t help). I took myself off of gluten about 3 weeks before seeing an allergist, just to see if it would help (it didn’t in that time period). He thought the rash looked like dermatitis herpetiformis and told me to eat some bread the night before my blood tests, which I did, and the tests came back negative. I’ve since learned from this forum that I needed to be eating gluten daily for at least a month in order to get an accurate test result. I’m grateful to the allergist as he found that 5 mg of doxepin daily will eliminate the rash within about 10 days (previously it lasted for months whether I was eating gluten or not). I have been gluten free for about 25 years as a precaution and recommendation from my doctor, and the pattern of breaking out every 8 years or so remains the same except once I broke out after just one year (was not glutened as far as I know), and now it’s been over 9 years. What’s confusing to me, is that there have been 3 times in the past 2 years when I’ve accidentally eaten gluten, and I haven’t had any reaction at all. Once someone made pancakes (they said they were gluten-free, they were not) and I ate several. I need to decide whether to do a gluten challenge and get another blood test. If I do, are these tests really accurate? I’m also concerned that I could damage my gut in that process if I do have celiac disease. My brother and cousin both had lymphoma so that’s a concern regarding a challenge as well, though there is a lot of cancer in various forms in my family so there may be no gluten connection there. Sorry for the ramble, I’m just doubting the need to remain gluten free if I don’t have any reaction to eating it and haven’t had a positive test (other than testing positive for one of the genes, though it sounds like that’s pretty common). I’d appreciate any thoughts or advice! 
    • Jmartes71
      Hello, just popped in my head to ask this question about medications and celiac? I have always had refurse reaction to meds since I can remember  of what little meds my body is able to tolerate. I was taking gabapentin 300mg for a week,  in past I believe 150? Any ways it amps me up not able to sleep, though very tired.However I did notice it helped with my bloating sibo belly.I hate that my body is that sensitive and medical doesn't seem to take seriously. Im STILL healing with my skin, eye, and now ms or meningioma ( will know in April  which)and dealing with this limbo nightmare. I did write my name, address ect on the reclamation but im not tech savvy and not sure if went through properly. I called my city representative in Stanislaus County and asked if theres a physical paper i can sign for proclamation for celiac and she had no clue about what I was saying, so I just said I'll go back on website. 
    • Scott Adams
      I'm not saying that some celiacs won't need it, but it should be done under a doctor's supervision because it can cause lots of problems in some people.
×
×
  • 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.