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 Does Healing Take! So Frustrated!


Maryw88

Recommended Posts

Maryw88 Apprentice

Hi all,

I am so fed up. I am trying to be patient but I don't know what to do. I went VERY gluten free about 1 month ago but have been gluten light for 1 1/2 years (I thought I was gluten-free....I didn't know better). So, I haven't been 100% gluten-free for very long. I also figured out about 6 months ago I react to soy, and 2 months ago I react to caesin. I also have a problem with nightshades, vinegar, beans, corn, rice, quinoa. EVERYTHING! I seem to do ok with many leafy veggies and fruits. Red meat, fish, and shellfish. Thats about it.

I am currently trying to do the GAPS diet and am even reacting with that. Apparently chicken and chicken broth are intolerances as well. I can't handle the 1 tsp. of fermented veggie juice. I get D with that too. I have no idea what to do. This diet is terrible and not actually helping.

I have terrible stomach pains, burning pains. alternating C and D depending on the food. I get tingling and numbness in my mouth and arms if I eat an offending food. I can't afford to continue the intro to GAPS honestly and its not helping.

SO, what to do!? Do I just need to be more patient. How long did it take for those of you with similar issues to see changes? I really don't want to do GAPS or SCD. They are miserable and ineffective for me. Is it related to stress? I feel like I am so focused and stressed about all food. Any ideas or suggestions are welcome. I honestly do not know what I would do without this forum. It has been so nice to see others making this work and reading about your experiences.

Thanks everyone


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



Celiac.com Sponsor (A8-M):



shadowicewolf Proficient

numbness in mouth indicates an allergy :/ Be careful please.

It takes time, some people take up to two years to get back to something "normal".

It took me over a year.

GottaSki Mentor

I seem to do ok with many leafy veggies and fruits. Red meat, fish, and shellfish.

This is what you want to stick to for a while. Paleo recipes can help make things a bit more interesting. Who knew you could make a decent fried rice with cauliflower? I certainly didn't a year ago. There are many recipes for bread/muffins that can be made with almond or coconut flour.

I completely understand your frustration. Unfortunately it can take months and even years to heal. Give yourself time to process this. Progress can often be followed by set-backs. Try to be patient - you can't be patient all the time, but as you start to feel better it will become easier.

Try to hang with the foods you listed for at least six months before trialing any of the foods you know are causing problems. When you do trial them wait at least three days between trials to monitor for reactions. If you still react, remove them and trial at six month intervals.

Hang in there - your time completely gluten-free is very brief - adding all the other intolerance may make it seem like you have been at this forever.

I was able to do the broth of GAPS, but was unable to tolerate any of the fermented items so I've gone back to my basic diet of meat, fish, selected fruits and vegies. Don't forget healthy fats...avocado, nuts (if you can tolerate them), coconut oil, etc.

Oh...Small Intestine Bacterial Overgrowth (SIBO) can trigger multiple intolerances, so you might want to research or talk to your doc about it.

Hang in there!

deb445 Rookie

I think that Paleo diet will likely help. I am inclined to question diet, when healing is not happening at the rate you would expect. It sounds like you are pretty in tune with your body, and listening to the signals you're receiving. I don't remember now, the exact link, but there is a doctor ( Doc Osborne ? sp? ) who has some videos on youtube, and he discusses cutting out cereals and grains and legumes to attain optimal health. Perhaps worth a look, and it might provide you some freedom from pain. Freedom from pain, and freedom to make menu choices that serve you well. His website has some good recipes also. Best of luck!

1desperateladysaved Proficient

I have been grain free for since May. I know what you mean about the diet and confusion about healing. I use almond, coconut, buckwheat and bean flours instead of grains. I have used the Gluten-Free Society for recipes. That is Dr. Osborne mentioned above. Anyway I haven't found food that I don't really like. I thought I was reacting to chicken at one time, but I believe now that I don't. It is confusing, but I think it is just about healing. There isn't always an explanation in what I just ate, but sometimes my body is just making profound changes. I feel certain that mine still is.

Make sure you are doing all you can. I cut foods that bother me, take supplements, and only eat the food cooked at my food. Then hang on for the rollar coaster ride. Enjoy the changes as they occur. There is hope for better days.

Get well soon, *******

Diana

inducedjoy Newbie

Hi all,

I am so fed up. I am trying to be patient but I don't know what to do. I went VERY gluten free about 1 month ago but have been gluten light for 1 1/2 years (I thought I was gluten-free....I didn't know better). So, I haven't been 100% gluten-free for very long. I also figured out about 6 months ago I react to soy, and 2 months ago I react to caesin. I also have a problem with nightshades, vinegar, beans, corn, rice, quinoa. EVERYTHING! I seem to do ok with many leafy veggies and fruits. Red meat, fish, and shellfish. Thats about it.

I am currently trying to do the GAPS diet and am even reacting with that. Apparently chicken and chicken broth are intolerances as well. I can't handle the 1 tsp. of fermented veggie juice. I get D with that too. I have no idea what to do. This diet is terrible and not actually helping.

I have terrible stomach pains, burning pains. alternating C and D depending on the food. I get tingling and numbness in my mouth and arms if I eat an offending food. I can't afford to continue the intro to GAPS honestly and its not helping.

SO, what to do!? Do I just need to be more patient. How long did it take for those of you with similar issues to see changes? I really don't want to do GAPS or SCD. They are miserable and ineffective for me. Is it related to stress? I feel like I am so focused and stressed about all food. Any ideas or suggestions are welcome. I honestly do not know what I would do without this forum. It has been so nice to see others making this work and reading about your experiences.

Thanks everyone

Unfortunately, the simple answer is yes, you just need to be more patient.

Healing from celiac disease is different for everyone. People go undiagnosed for years and the severity of it differs greatly from one individual to another. Healing can be anywhere from 6 months to 2 years, maybe even more, according to what my GI has told me. My advice is to stick to the foods you know won't cause a reaction, even if that means severely limiting your diet. The very sad reality of having celiac disease or any other food intolerance/allergy is that we can't just be "fed up with it." You will have this forever. It was hard for me to come to terms with it, but it's a fact of reality. It's frustrating and upsetting to not be able to eat the way you once did, and waiting for healing to happen can be lengthy and painful when you're still dealing with intense symptoms. However, nothing you do can speed things up. You can only continue to eat a healthy, COMPLETELY gluten free diet and wait for the healing to happen. I hope you find relief soon, it took me over a year of being completely gluten free to stop having symptoms. Even now, almost two years after being diagnosed, I still have symptoms every once in while (mind you, i had an extremely heavy case of celiac, and I had it for almost my entire life before finding out). With all of this said, patience is the key, and you can rely on your family and friends when the going gets tough. It's difficult to accept it and to be patient with your body, but it will pay off once you're healthy again.

GFinDC Veteran

Hi Mary,

You are right, 1 month gluten-free is not very long. All the time spent gluten light would not stop the auto-immune reaction. Being totally gluten-free should stop it in time though. Your small intestine is around 20 to 22 feet long, so that is a lot of damaged tissue to heal. Making it easy for your gut to digest food is a good idea. You can do that by sticking to foods that don't cause symptoms for now, and taking pro-biotics and digestive enzymes. Avoiding sugar and spicy foods can help also. Cooked veggies are easier to digest than raw.

Avoiding dairy is also helpful, if you aren't doing that already. Some people find changing their hair care products to gluten-free versions helps. Remember to check your vitamin pills and meds for gluten also, and avoid cross contamination.

The early part of the diet change is about healing and learning to eat gluten-free. There is also a lot of change going on in your gut as it tries to heal the damage. That can involve bacterial imbalances and the probiotics and avoiding sugar can relieve that some.

A simple diet is the best way to go, and whole foods only. Adding in gluten-free baked goods after you are feeling better is ok, just go slow on it.


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



Celiac.com Sponsor (A8-M):



T.H. Community Regular

The bowel stuff, yea, you may just need to be patient. It can take a long time to get better.

The tingling and numbness? That needs a new approach, because that does not sound like gluten intolerance or celiac disease but rather an allergy.

I would go get checked with an allergist, ASAP. Also, I'm sitting here trying to think of something that can causing tingling and numbness but would cause you to react to multiple foods. Better to have one allergen than many, yeah?

1. Corn - this is in freaking everything. It is often in vinegars, sprayed on tomatoes as a ripening spray, on rice with vitamins added, in dairy as vitamin fortification, and so on. However, meat can sometimes be a problem, too, so that seems like it might not quite fit.

2. Sulfites - this is hard to get tested for, because it doesn't test well with allergies. The big kicker for this one is wine. If wine makes you very sick, that may be a sign that sulfites are the problem. Processed corn is often soaked in a sulfited bath, so many of the corn products are ALSO sulfite issues. Fermented foods have sulfite as a natural by-product produced by the yeast, so some sulfite sensitive folks get very sick from vinegars. This one is a problem of mine and I used to describe how I felt sometimes as this tingling 'heavy' feeling in my arms and head. I felt very dizzy and spacy too, but the symptoms for this vary. (good website: Open Original Shared Link)

3. I wonder if yeast could be an issue, or SIBO (bacterial overgrowth)? I don't know as much about these two, but I think both can actually make it so that fermented foods do not do so well. Might be worth looking at, anyway. I don't, however, think these cause burning or numbness, although an ALLERGY to yeast might cause that. That's not very common, but I know of one gal who has this and it was pretty awful. If you DID have this, you would be very prone to extremely nasty yeast infections anywhere in the body, and even native yeast levels on produce could have an affect.

4. I DON'T think you are having fructose malabsorption, problems with tyramine, histamine intolerance, or salicylate sensitivity. I don't know a lot about these, to be honest, but from what I remember, these almost all involve a lot of fruits and veggies causing problems, which doesn't seem to be the case for you so much.

One thing you might want to check, just in case? For some of the foods that you have a problem with, it might be worth growing them yourself. When I was reacting to SO many things, I eventually discovered that it was a contaminant ON these things that was the problem. Growing them myself, I was able to eat them. So that might be worth exploring. :-)

dilettantesteph Collaborator

It took me about 4 years to heal/develop my diet. I don't know if I would have healed faster if I had gone on the diet I am now on right away. I do know that if I go back to eating some of the things I used to eat, I get sick again. Periodically I'll try one of them just in case. I just kept reading and informing myself about trace gluten sources and eliminating more things. Eventually I got to a place where I was healthy enough to determine whether or not I could tolerate something by doing challenge/elimination studies of everything I ate. I try to only change one thing per week so that I will know what might be causing any problems I come up with. I keep track of everything. My health is so much better now that it has been worth every bit of time and effort.

Maryw88 Apprentice

Wow, Thank you everyone! I know 1 month doesn't sound like much but this has felt like a long time. I thought I was doing everything right, then oh...that has gluten. Thought I was doing it right...oh cross contamination. This has been a steep learning curve.

I will try to be more patient. I think I may just have to accept that my body will not be quite right for sometme. In the meantime I am going to stick to a simple diet. I am also going to look into the intolerances/allergies mentioned. I think something else is going on. All alcohol makes me sick actually.

The most confusing thing here is that I believe these are new allergies. I have a true wheat allergy as well but when tested nothing else showed up. (2 years ago). However, I have developed these intolerance or allergies (who knows what they are) over the last year. Maybe another trip to the allergist is in order. I have looked into leaky gut and believe this may be a part of my problem.

Thanks for letting me vent and talking me down. As you all know, this is incredibly frustrating and lonely! I feel insane! So, thank you! I will take your advice and at least be more patient.

GottaSki Mentor

I'm glad you found this place to vent - we all have a time or two ;)

Just wanted to add a note. I have severe intolerances that have all been identified or gotten worse in my time gluten-free. I have tested negative to ALL food allergies several times in both blood and scratch tests. During the past year my reactions became much more allergy-like. I even had anaphylactic reaction to sunflower seeds when I trialed them.

My primary ordered epi pens for me immediately after that severe reaction. I have had other serious reactions - have not had to use an epi pen yet, but do have them at home, each of my cars and my purse. These reactions escalate, so even if you don't test positive for an "allergy" ask your doc to prescribe epi-pens - far better to be safe.

I hope you never have a reaction that severe, but did want you to be aware of the possibility. My family and I were caught completely off guard when my reaction became that extreme - and they are very familiar with my reactions to food.

Again, welcome - ask questions - feel free to vent - take it a day at a time and you will improve - I just can't guarantee it will be quickly.

Hang in there!

ncdave Apprentice

Your small intestine is around 20 to 22 feet long, so that is a lot of damaged tissue to heal.

According to dr oz there"s enough area inside the small intestine to cover a tennis court, now that"s a lot of healing! Sounds like your on the right track Mary, it does take a lot of patience, but you"ll get there. I'm not well yet, but i will say after 9 months, my last 2 weeks have been wonderful.

L.J. Rookie

Hi Maryw88!

I too have some similar issues as you do. GottaSki gave you some great "starter advice". :D

I am still a Newbie here, but have found amazing information! For me, I stick with vegatables and "freshly cooked" meats that I make--restaurants are a scarey place for me still! :D

I also have severe food allergies--and I agree with ?? (darn, who said that info?)to watch out for allergic reactions! The mouth tingling is a definite signal to me. I too avoid milk and nuts!

Maybe try thinking of it this way...with the money you save on not buying "poison foods" (my name for the foods I can't eat :) you can afford to buy an extra steak--and then you will have "leftovers" to eat the next day! Imagine that! You get to eat steak more often. Yum! :P

Hang in there and keep using this amazing site! You will get more information and support than you can believe!!! :D

Hi all,

I am so fed up. I am trying to be patient but I don't know what to do. I went VERY gluten free about 1 month ago but have been gluten light for 1 1/2 years (I thought I was gluten-free....I didn't know better). So, I haven't been 100% gluten-free for very long. I also figured out about 6 months ago I react to soy, and 2 months ago I react to caesin. I also have a problem with nightshades, vinegar, beans, corn, rice, quinoa. EVERYTHING! I seem to do ok with many leafy veggies and fruits. Red meat, fish, and shellfish. Thats about it.

I am currently trying to do the GAPS diet and am even reacting with that. Apparently chicken and chicken broth are intolerances as well. I can't handle the 1 tsp. of fermented veggie juice. I get D with that too. I have no idea what to do. This diet is terrible and not actually helping.

I have terrible stomach pains, burning pains. alternating C and D depending on the food. I get tingling and numbness in my mouth and arms if I eat an offending food. I can't afford to continue the intro to GAPS honestly and its not helping.

SO, what to do!? Do I just need to be more patient. How long did it take for those of you with similar issues to see changes? I really don't want to do GAPS or SCD. They are miserable and ineffective for me. Is it related to stress? I feel like I am so focused and stressed about all food. Any ideas or suggestions are welcome. I honestly do not know what I would do without this forum. It has been so nice to see others making this work and reading about your experiences.

Thanks everyone

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • 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.