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

Gluten withdrawal help


Misscshell24

Recommended Posts

Misscshell24 Rookie

Hi, newly gluten free and looking for help, tips, advice during the withdrawal phase. Anything to speed up the process or help with symptoms and what to expect and for how long, please. Day two and have migraine, nausea, and dizzy.  Thanks!


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Make sure you are eating a balanced diet with protein and carbs.  Sometimes people drastically change the basics and that can mess you up.  For example if you ate a lot of bread, you may want to find other carb sources.  

Jensy Newbie
1 hour ago, Misscshell24 said:

Hi, newly gluten free and looking for help, tips, advice during the withdrawal phase. Anything to speed up the process or help with symptoms and what to expect and for how long, please. Day two and have migraine, nausea, and dizzy.  Thanks!

 

1 hour ago, kareng said:

Make sure you are eating a balanced diet with protein and carbs.  Sometimes people drastically change the basics and that can mess you up.  For example if you ate a lot of bread, you may want to find other carb sources.  

 

1 hour ago, kareng said:

Make sure you are eating a balanced diet with protein and carbs.  Sometimes people drastically change the basics and that can mess you up.  For example if you ate a lot of bread, you may want to find other carb sources.  

Hi!  I was diagnosed with Celiac Disease eight weeks ago.  I have been gluten free for about eight weeks.  The first 4 weeks were rough!  I was dizzy, experiencing vertigo (spinning sensations), headaches, and continuous diarrhea.  I asked my doctor about my symptoms and she said the body is trying to get used to not having gluten.  I was also a chronic migraine sufferer prior to going gluten-free.  I can honestly say that at about 5-6 weeks gluten-free, I was starting to feel better!  I am continuing to feel better each day!  Hang in there and be patient!  You will soon start to feel relief!  ?

Misscshell24 Rookie

Thank you. My son has celiac and with my symptoms it was expected, so have been tapering off while awaiting test results and finally got them Friday. It's been 9 years since my son was diagnosed and he was just three years old and non-verbal autism at the time (he's verbal now), so vaguely remember what it was like for him. I also was just diagnosed with hashimotos so doc is recommending stopping soy and dairy as well, and I'm a vegetarian. Not sure if I am going to do it all at once or one at a time, haven't been tapering off dairy or soy as that one was not expected. Thanks again for the tips and encouragement!

cyclinglady Grand Master
57 minutes ago, Jensy said:

 

 

Hi!  I was diagnosed with Celiac Disease eight weeks ago.  I have been gluten free for about eight weeks.  The first 4 weeks were rough!  I was dizzy, experiencing vertigo (spinning sensations), headaches, and continuous diarrhea.  I asked my doctor about my symptoms and she said the body is trying to get used to not having gluten.  I was also a chronic migraine sufferer prior to going gluten-free.  I can honestly say that at about 5-6 weeks gluten-free, I was starting to feel better!  I am continuing to feel better each day!  Hang in there and be patient!  You will soon start to feel relief!  ?

Welcome to the forum!  

cyclinglady Grand Master

The good news is that you have the gluten free diet down.  That is half the battle, so your recovery should be much faster than most.  Many celiacs commonly have isues with dairy.  I did.  But with intestinal healing, now I can eat any dairy.  You might not really have any dairy issues at all.  Everyone is different.  I spent 20 years consuming soy.  Not sure if it actually affected my thyroid, (I read lots of things against it, but since I could not consume dairy, I chose to remain on soy).  My thyroid (Hashi's) has healed (nodules are gone and my thyroid size is normal).  Not sure if it was due to being gluten-free or giving soy.  

Hope you feel better soon!

 

Misscshell24 Rookie

Thanks, Cyclinglady. Interesting. I've been reading up online and read hashi's and celiac often go hand in hand, so I was wondering if anyone else with the same might comment. I just started seeing a functional med doc and she said for sure no gluten or soy and with dairy it's 50/50, some do ok and some don't. So for sure no more gluten, then may finish eating what I already have in the house that's soy and dairy and not buy any more. I've been very ill for over two years so don't want to shock my system too much and also don't want to go through three withdrawals (gluten, soy, and dairy). Idk, we'll see. While I was tapering off gluten I also stopped eating processed foods and preservatives and also switched all my personal and household products to natural and gluten free, so over all think these are all changes for the best and hopefully I'll be feeling better soon. 


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



Celiac.com Sponsor (A8-M):



Alwayssomething Contributor

Misschell24 - I have both Hoshi and Celiac.   I have not given up soy it was never suggested and I don't seem to have a problem with it.   Dairy for me is iffy.  I am lactose intolerant, I use lactaid milk and if I do have icecream or something with milk in it I take a Lactaid chewable tablet first, and this seems to solve all my issues.     Of course going gluten free usually means a lot more whole foods and fewer processed foods, so maybe by default I am consuming less soy and dairy but I don't  go out of my way.    Please do whatever makes you feel better, I am just giving you my experience.  

 

Misscshell24 Rookie

Thank you very much every one that took the time to write, it is greatly appreciated. 

Alwayssomething, interesting about the lactose and lactaid, I will keep that in mind. I am a vegetarian so have quite a bit of soy. Yesterday my joint pain was gone for the first time in months, not sure why and it was amazing, but it is back today. Think I may try going off gluten, soy, and dairy for 3 months, of course stay off the gluten, but maybe re-add the soy and dairy one at a time and see if there's a difference. So much info on different diets and everyone reacts differently, it's hard to know what to do and may change the game plan a few times along the way, lol, but I'll get there. 

Anna Walker Newbie

Hang in there! It's such a misconception that you'll feel better instantly after cutting out gluten. It's super important to heal your damaged gut lining, too. I found acupuncture, naps and Epsom salt baths really helpful when I first went gluten-free. My poor body was so overwhelmed!

 

Forman337 Apprentice

Gluten withdraw can be rough, and is different for everyone, but hang in there and you will start feeling better! It took a few weeks for the bad symptoms to subside and I keep getting better as time goes on. Just be careful not to consume anything with gluten after going gluten-free. Never assume anything is gluten-free without checking the ingredients and doing the research. I made that mistake and had to go through the whole process again.

Drinking water helped me through it. It helped in multiple ways. I feel like it probably flushed out my system, it's good for you anyway, and I used it as kind of a placebo. I kept telling myself I'll feel better if I drink more water and eventually my brain made the connection and it works as kind of a soothing mechanism. 

Hope you feel better soon!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,545
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    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

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.