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

Recovery Question


Cornhusker

Recommended Posts

Cornhusker Apprentice

I've been on the diet for 4 weeks now. The first two weeks went really well. I'm confident I've removed all sources of gluten (haven't eaten out or done anything risky).

At the start of week 3 things began to go sour. Moderate to severe nausea. Difficulty eating enough. Stools have gone soft (not really D, not more than twice a day). I had started taking some Advil to treat some elbow tendinitis. My doc thought this might have been a mistake. Irritated my stomach. Gave me some Prevacid to calm things back down.

Since starting the Prevacid the long lasting nausea has gone away. I've been able to up my caloric intake (I'm pushing hard to gain weight) to my target levels. However a more low-grade of nausea has replaced the previous issues. After I eat (lasts about 1 hour) I experience nausea (but no vomitting, and it doesn't seem to build into anything else). My stools are still soft (they were strangely perfect for the first two weeks after months of D), but it's still not D. My appetite returns for the next snack/meal, but after eating...nausea again. I've stopped the Prevacid, hoping that's the cause. I've been on Bentyl, Advil, and Prevacid one after the other for the past 2 weeks. So there is a strong feeling on my part that the meds are keeping me from feeling my best.

I guess I'm looking for some recovery guidance. Is the nausea part of the healing process? What was the 1st couple months like for some of you veterans? I'm keeping a food log, more to track calories than anything else, but I'm not seeing any correlation between foods and effects. Nothing I'm eating is making me feel worse than I did before diagnosis, so maybe I just need to develop some patience (something I'm not good at).

Thanks.


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



Celiac.com Sponsor (A8-M):



BRUMI1968 Collaborator

I did not have nausea as part of my healing, though I have had what you describe in the past, before going off gluten.

The only thing that helped was valium, so I think in my case I was just getting really wound up about the mild nausea, and it would become more severe. I ended up losing a bunch of weight because I never wanted to eat. After a week or so on the valium, I went back to eating and all was well. HOWEVER.....

I wouldn't guess that was someone else's problem. (I have mental issues about stomach aches thanks to undiagnosed Celiac for 37 years tormenting my childhood.)

I might try, if I were you, PRE biotics. I use DigestGold. It has all the enzymes in it you can possibly imagine. That way, if your pancreas is unable to make enough digestive good stuff, this will help.

Peppermint tea should also help you -- just make sure it is gluten-free. Some herbal teas are not gluten free.

Then I don't know...is there anything you do at EVERY meal that is remotely suspect?

Guhlia Rising Star

Just a thought... Your body may be going through gluten withdrawal. When I went gluten free I got well very quickly, then got sick again, then got well again and stayed well. This may be the case for you too. I would try and go med free for a few days and see if that helps. Your body may just be screaming at you for cutting gluten (a very addictive substance) out of your diet.

Cornhusker Apprentice
Just a thought... Your body may be going through gluten withdrawal. When I went gluten free I got well very quickly, then got sick again, then got well again and stayed well. This may be the case for you too. I would try and go med free for a few days and see if that helps. Your body may just be screaming at you for cutting gluten (a very addictive substance) out of your diet.

When did the 'stayed well' phase start for you? I know everyone is different, but it's a question I like to ask.

I can't take credit for my diagnosis, my GI doc discovered it through biopsy before I had a chance to figure it out (really didn't think celiac fit, but in retrospect it makes perfect sense). But before diagnosis I was actively 'searching' for a solution. It's just really tough at this phase to accept that this is IT, and 'you will get better'. I'm having a hard time stopping my 'search'.

jesscarmel Enthusiast

For the first few months on the diet (2 to3) i felt nauseus all the time and still get it once in a while. i was taking reglan to help it and still take if i need it. also lately when im nauseous i drink ginger aid tea by traditional medicinals. i also take culturelle a probiotic which seems to have helped.....

Jess

jerseyangel Proficient

I've been gluten-free for a little over a year.

The first 3-4 months for me were kind of rough. I had nausea--not after every meal, but often enough. I guess it was related more to the D I was still having.

I was put on Prevacid, and only took it for 3 weeks before stopping. I had side effects from it--the worst of which was vertigo.

I would suggest that you stop the Advil and Prevacid for a week or so and see if it makes any difference. Also during that time, stick to plain, whole, natural foods like meat (if you eat it), veggies, fruits, pure water.

Montana Julie Newbie

Good discussion - I am interested in hearing more.

Like the Husker Fan that started this conversation, I went gluten-free and did great for 3+ weeks and then got symptoms again - D and the works - but only at weird intervals that could maybe be attributed to contamination as I get my diet figured out.

Looking forward to that "getting well" and "staying well". Good to hear that this may just be a phase that we all will go through...

Montana Julie


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient
Good discussion - I am interested in hearing more.

Like the Husker Fan that started this conversation, I went gluten-free and did great for 3+ weeks and then got symptoms again - D and the works - but only at weird intervals that could maybe be attributed to contamination as I get my diet figured out.

Looking forward to that "getting well" and "staying well". Good to hear that this may just be a phase that we all will go through...

Montana Julie

Hi Julie--

Yes, we tend to go through a phase at the beginning that's kind of uneven. What with learning which foods and ingredients are safe, the inevitable mistakes and the healing process itself--it takes some of us a little time before we begin to feel any results.

Healing and recovery are different for everyone--keep at it, it will be worth it--I promise :D

Lollie Enthusiast

Hi all! I wanted to through in my experience! I have been gluten free since January, about 8 months.... I have had mostly ups. I had the same kind of thing with the nausea, and still do sometimes. But for me, i feel like the up times are far more often then the bad times. I found out at about the one month stage that I couldn't eat soy..... Sometimes as the gluten is eleminated other intolerences come to the surface. I always eat rice when I feel sick. It is what I always fall back on. I also advice getting rid of the prevacid. I was on antiacid meds for 10 years before figureing out this gluten thing. I quit them cold turkey. If you take them for a long time and then stop they actually increase your acid production.....I figure I will deal with what ever comes my way as naturally as I can. I also drink tons of sparkling mineral water. I feel like it flushes out my system and helps anytime I feel sick again. I think that since the D has not come back you are probably on the right track and would encourage you to keep to it. I understand the feeling of still looking. I thought getting rid of gluten was just too easy, but I can honestly say it has changed my life in a way I wouldn't have hoped for!

Hang in there, it does get better!

Lollie

Aerin328 Apprentice

Cornhusker, I am in a very similar situation. I have been gluten-free for 1 month now and the symptoms continually roller coaster in and out. Nausea is only occasional for me, but the other symptoms really seem to come and go with a vengeance. The good news is the good times are starting now to get better, so I hope to reach a better/ more reliable state over the next few months. From what I read time and again on this forum is that it takes a long TIME for sustainable healing to take place. For now eat simple yummy healthy foods and have patience - you will heal in time, and all on this site will be here for you! :) (I may be preaching to myself on the patience part- gosh it's frustrating. lol ;) )

jknnej Collaborator

I had so much nausea I lost 20 lbs. right away. But it gets better. Now I rarely have it although it does creep up sometimes. I also found out I had acid reflux a few months after going gluten free and once I started on Nexium the nausea disappeared. I tried going off Nexium and it returned....my dr. says 25% of reflux patients do NOT present with heartburn; they get nausea instead.

If you do have reflux and you tried Prevacid remember, as my dr. told me, that ALL of the reflux meds can have nausea as a side effect....it just so happens that Nexium is the one for me personally that doesn't cause it. I tried Prevacid and Prilosec OTC first. Prevacid was OK but Prilosec made me terribly nauseated, even worse than I already was.

Even if it is not reflux, it will get better. You are going through gluten withdrawls. My dr. told me that I never should have gone OFF gluten so fast....I should have weaned off instead of stopping all at once. I was dizzy, nauseated, etc. for a while because of this.

It will get better!!!

angel-jd1 Community Regular
I am NOT a celiac. I have Celiac Disease, but it is not who I am.

I noticed that on your replies today. I LOVE that you have put that up. I cringe each time that I read on the board somebody saying "my little celiac" or She's/He's a celiac......blah!! :blink:

In college I took courses for special education. We were always taught to use person first language. Meaning.....put the person infront of the disability. Instead of saying the dislexic girl you would say a girl with dislexia. Etc.

Anyways...........thank you for putting that out there for people to read. I think that sometimes we forget!!

-Jessica :rolleyes:

loraleena Contributor

I was nauseous for at least a month or so after starting. It subsided after a while. Prevacid is really bad for you. It can cause more harm than good. Also advil destroyed my gut. I can't touch the stuff now. Try drinking ginger tea by traditional medicinals. I also took deglycerized licorice for a while. I helps sooth the gut. Make sure it is deglycerized licorice. Good luck

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,638
    • Most Online (within 30 mins)
      7,748

    Sheepeye
    Newest Member
    Sheepeye
    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

    • Scott Adams
      I agree, there can be contamination at many points--milling is another possible source of contamination for any flours.
    • trents
      Keep in mind that with manufactured food products, "gluten free" doesn't equate to no gluten. Things that are naturally gluten free can be cross-contaminated with gluten in the field, in shipping and in processing. In the U.S. companies can use the gluten free label as long as the product doesn't exceed 20ppm of gluten. That amount still may cause a reaction in some people.
    • deanna1ynne
      Dd10 was tested for celiac four years ago bc two siblings were dx’d (positive labs and biopsies). Her results at the time were positive ema  and ttg (7x the UL), but a negative biopsy. We checked again three months later and her ttg was still positive (4x the UL), but ema and biopsy were negative. Doc said it was “potential celiac” and to keep eating gluten, but we were concerned about harming her growth and development while young and had her go gluten-free because we felt the labs and ema in particular were very suggestive of early celiac, despite the negative biopsies. She also had stomach aches and lethargy when eating it. We just felt it’d be better to be safe than sorry. Now, four years later, she doesn’t want to be gluten-free if she doesn’t “have to be,” so underwent a 12 week gluten challenge. She had labs done before starting and all looked great (celiac panel all negative, as expected.) Surprisingly, she experienced no noticeable symptoms when she began eating gluten again, which we felt was a positive sign. However, 12 weeks in, her labs are positive again (ttg 4x the UL and ema positive again as well). Doc says that since she feels fine and her previous two biopsies showed nothing, she can just keep eating gluten and we could maybe biopsy again in two years. I was looking up the ema test and the probability of having not just one but two false positives, and it seems ridiculously low.  Any advice? Would you biopsy again? She’s old enough at this point that I really feel I need her buy-in to keep her gluten-free, and she feels that if the doc says it’s fine, then that’s the final word — which makes me inclined to biopsy again and hope that it actually shows damage this time (not because I want her to have celiac like her sisters, but because I kind of think she already does have it, and seeing the damage now would save her more severe damage in the long run that would come from just continuing to eat gluten for a few more years before testing again.)  Our doc is great - we really like him. But we are very confused and want to protect her. One of her older sibs stopped growing and has lots of teeth problems and all that jazz from not catching the celiac disease sooner, and we don’t want to get to that point with the younger sis. fwiw- she doesn’t mind the biopsy at all. It’s at a children’s hospital and she thinks it’s kind of fun. So it’s not like that would stress her out or anything.
    • Inkie
      Thanks for the replies. I already use a gluten-free brand of buckwheat flakes I occasionally get itchy bumps. I'm still reviewing all my food products. I occasionally eat prepackaged gluten-free crackers and cookies, so I'll stop using those. I use buckwheat flakes and Doves Farm flour as a base for baking. Would you recommend eliminating those as well? It's a constant search.
    • Wheatwacked
      Gluten free food is not fortified with vitamins and minerals as regular food is.  Vitamin deficiencies are common especially in recently diagnosed persons,  Get a 25(OH)Vitamin D blood test. And work on raising it.  The safe upper blood level is around 200 nmol/L.    "Low serum levels of 25(OH)D have been associated with increased risk of autoimmune disease onset and/or high disease activity. The role of vitamin D in autoimmune diseases   🏋️‍♂️Good job!   I find the commercial milk will give me mild stomach burn at night, while pasture/grassfed only milk does not bother me at all.  While you are healing, listen to your body.  If it hurts to eat something, eat something else.  You may be able to eat it later, or maybe it is just not good for you.  Lower your Omega 6 to 3 ratio of what you eat.  Most omega 6 fatty acids are inflammation causing.    The standard american diet omega 6:3 ratio is estimated at upward of 14:1.  Thats why fish oil works
×
×
  • 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.