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

Two Weeks Gluten Free


vickiguerra

Recommended Posts

vickiguerra Rookie

and I am still bloated???


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



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master

I bet your doctor failed to tell you that patience (besides avioiding gluten) is your best tool for healing?

It took me six weeks before I felt a little bit better. Two months in to heal two vertabrae fractures. Six months to resolve my anemia. A year to resolve most food intolerances. YWO YEARS to finally feel better! That is about the average around here.

Why all the delay? There is a huge learning curve in avoiding gluten. Each glutening can start the autoimmune destructin process that can last for weeks. I feel lucky that it has only taken me two years and I sarted with a Marsh Stage IIIB which translates into moderate to severe damage.

Hang in there! The bloating will soon go away!

Hugs!

kareng Grand Master

There is a huge learning curve like Cycling said. And it can take a long time for the damage to heal. But there is also the fact that, even if the villi heal, the whole system may take a long time ( months or years) to get back to good working order. Also, when people change thier diet drastically, they may be eating more fiber, less fiber, more gassy veggies, etc than before.

I don't know if you are eating lactose, but you might want to cut that out for a few months. The part of the intestines that are damaged by Celic are the parts that "digest" lactose. Even without Celiac, many adult humans are lactose intolerant.

vickiguerra Rookie

About 5 months ago I just bloated up out of the blue....ever since then I eat 2 or 3 bites and am so full it's not even funny.

 

All my gastro said was..you have celiac disease and you need to talk to a nutritionist...that was it.

 

For two weeks I have had coffee and gluten free cream.  Tortilla chips, rice cakes, peanut butter, grits, cheese, rice crackers, bananas, apples, ground meat, beans, rice, avocados.....that's it.

 

I had tendinitis last week and a GP told me to take ibuprofin, when I told him I had just found out I have celiac and had not taken any kind of medication for the pain.....he kind of mumbled something....I got the impression he doesn't believe celiac is a sickness.  Makes me really wonder too.

 

Thank you all for your input. :) 

kareng Grand Master

About 5 months ago I just bloated up out of the blue....ever since then I eat 2 or 3 bites and am so full it's not even funny.

All my gastro said was..you have celiac disease and you need to talk to a nutritionist...that was it.

For two weeks I have had coffee and gluten free cream. Tortilla chips, rice cakes, peanut butter, grits, cheese, rice crackers, bananas, apples, ground meat, beans, rice, avocados.....that's it.

I had tendinitis last week and a GP told me to take ibuprofin, when I told him I had just found out I have celiac and had not taken any kind of medication for the pain.....he kind of mumbled something....I got the impression he doesn't believe celiac is a sickness. Makes me really wonder too.

Thank you all for your input. :)

"For two weeks I have had coffee and gluten free cream. Tortilla chips, rice cakes, peanut butter, grits, cheese, rice crackers, bananas, apples, ground meat, beans, rice, avocados.....that's it."

There's part of your answer! :)

cyclinglady Grand Master

The ends of the villi are the first to go and that is where the enzymes to help digest lactose (milk sugars) are released and the place to absorb iron occurs. So, like Karen said, avoid milk products for the first six months. Then add back in yogurt or cheese as though products have been fermented resulting in less lactose.

If you have not seen improvement in six weeks, try keeping a food journal. Lots of folks develop intolerances to corn and other foods as a result of a damaged gut. This seems to improve with healing.

Finally, keep those foods simple and easy to digest. Cooking fruits and veggies is helpful.

nvsmom Community Regular

Ditto the others.  Unfortunately, two weeks is nothing in a celiac's recovery.  Most celiacs will not have even stopped making autoantibodies yet, so recovery isn't even an option at this point.  Hang in there and be patient.  I'm sure you'll be feeling much better by the autumn.

 

I know... waiting is easier said than done.  ;)


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



Celiac.com Sponsor (A8-M):



vickiguerra Rookie

 

 

"For two weeks I have had coffee and gluten free cream. Tortilla chips, rice cakes, peanut butter, grits, cheese, rice crackers, bananas, apples, ground meat, beans, rice, avocados.....that's it."

There's part of your answer!  :) 

Ok, so I take out the dairy.  Is the rest ok to eat?

vickiguerra Rookie

Take out the corn too?

cyclinglady Grand Master

Just try the dairy first. Like a week. Then see about other food intolerances if you do not notice a difference. But dairy is a problem for most celiacs. At least until healing is done.

sreese68 Enthusiast

Beans are also hard on the gut.  I'd take them out for a bit. Then try them again with a small serving size.

 

With a food journal, record gut symptoms but also mood and energy level and anything out of the ordinary.  Keep in mind that a reaction to food may take anywhere from a few hours to two days.  For me, the big C takes two days.  D is usually overnight.  I can handle some foods if I eat them once a week, but if I eat them a few days in a row, I get symptoms.

 

And recovery does take time.  It took 8 months for my anxiety and brain fog to go away.  My nerves still aren't healed after 4 years, but they are much, much, much better.  My continued gut problems are unusual and may be partially caused by another syndrome/disorder I'm seeking a diagnosis for, so I may not be able to heal my gut completely.

vickiguerra Rookie

Thank you all. :)

notme Experienced

i agree:  food journal - and be nice to your intestines!  lolz - you can't see them, but if you have celiac, the poor things are a mess.  just keep writing down everything you eat in relation to how you are feeling.  if something doesn't digest well, remove the offending food for now.  it's a boring diet eating just safe stuff (lolz my 'go to' is turkey sandwich on udi's bread, which i ate for about 2 weeks straight) but after your gut has calmed down, you should be able to add some things back in.  trial & error & yes, patience.  ibuprofen should be ok just make sure it's gluten free.  i try not to overdo it with them because they contain iodine, which irritates dh rash.  (my skin never forgets, i guess...)

vickiguerra Rookie

The thing with me is I have not ever felt bad, just bloated.  Eating doesn't bother me....my symptoms are not as severe as some of y'alls sound.

 

Also I figured out last night that I obviously have been celiac since around 2003....I was having tongue issues.....no one caught it back then.

 

I am absolutely miserable trying to figure out what to eat and what not to eat....plus I am not supposed to be stressing about anything as I have heart palpitations too.  

 

Thank you all for your kind word and encouragement.  Just not sure about any of this at all.

Gemini Experienced

vicki....are you taking digestive enzymes?  That should help digest your food and ease the bloating.  What you listed as eating was dairy heavy and fat heavy....even though avocado is a good fat, fat is fat as far as digestion is concerned.  Maybe eat more chicken and fish, along with fruits and veggies that are well tolerated? 

vickiguerra Rookie

No, I didn't know about digestive enzymes.  Thank you 

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,960
    • Most Online (within 30 mins)
      7,748

    Noa
    Newest Member
    Noa
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.