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

What Has Helped You Heal?


BRCoats

Recommended Posts

BRCoats Enthusiast

Just curious as to what foods, supplements, etc. have helped you heal? My doc has me on some glutamine, which is supposed to be great for healing the gut. Also, bananas seem to soothe my system better than any other food. Other than that, I haven't found much that sits exceptionally well. Admittedly, I haven't been gluten-free for that long. I'd love to hear what has proven to be successful for the more experienced gluten-free eaters!!

Brenda


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



Celiac.com Sponsor (A8-M):



hthorvald Rookie

I'd be interested in learning what works for others, too. I think my stomach is worse now than before my diagnosis. What about supplements? I haven't heard of glutamine, but have heard of probiotics. Where does one find this stuff? What about gluten free vitamins? Liquid vs. pill. Perhaps the iron I'm taking is part of the problem. But, I need it to build up my iron stores.

Processed or packaged, gluten-free foods don't sit well at all. I realize that everyone is individual with their reactions, but any input will be welcomed.

H.

tarnalberry Community Regular

Being careful to deal with the hypoglycemic tendencies has been the most important. That and doing the elimination diet to learn that I need to avoid all dairy.

CoolCat1 Rookie

I had to get iron injections because the iron pills gave me really bad diarrhea. Ask about this.

calico jo Rookie

BOY do I have a lot to contribute on this, I hope.

I've been gluten free for almost 3 years now and it doesn't seem like it's been that long, really. It's always a challenge and I've found things that help me get better quickly in case of accidental contamination. Believe me, I've experimented with many diff. supplements and things.

When I was first diagnosed, I found a few safe "staples" and didn't eat anything BUT those things, but in addition I started taking digestive enzymes prior to even knowing what was wrong and it helped from the very beginning. Be careful that you start out slowly with any kind of supplement because THEY can upset your stomach as well. Whenever I tell any docs that I take those they always say it's a good idea, no matter what, especially as we get older our bodies stop producing as many enzymes. It helps utilyze your foods more efficiently and therefore will make you feel better. Also find a good gluten-free vitamin. The better your body feels and gets what it needs, the better it can heal ITSELF, even.

I also take liquid chlorophyll. Sounds odd, but it's like getting pure oxygen directly into your blood. It helps your cells heal and regenerate. You can also take a pill of something similar called chlorella. They are both made from an algae. Look up info on the internet, you'll see that some countries give it to cancer patients because it regulates red and white blood cells.

Get lots of sleep if you can. Your body heals better when it's resting. Drink lots of spring water.

I've been feeling better, for the most extended period of time right now, than since this all began for me. I faithfully take my vitamins and supplements and certain "mandatory" foods per day....pineapple for the bromelein, an apple for the pectin and fiber, and carrots for the beta carotein and antioxidants.

Enough of a ramble of my diet...I guess I'm just saying to do research and experiment with what makes you feel good, be patient.

Take care. :)

BRCoats Enthusiast

I have considered chlorophyll before. What brand do you use?

Brenda

kschmitz Newbie

Hi,

Whole Foods Markets carry a house brand of supplements called 365 that are free of wheat, gluten corn, yeast, fish, egg, dairy and lactose, no artificial colors, flavors or preservatives. I started taking the multi-vitamin, calcium and glucosamine & chondroitin for my osteoporosis, and vitamin E. I recently discovered that the iron supplement that I was taking for my anemia contains gluten - Feosol. So now I take Slo-Fe. I also must take several prescription drugs for conditions caused by celiac disease - GERD, low thyroid function. Fortunately, the medications are gluten free. Hopefully, now gluten-free for two weeks, my intestines will heal and the rest of my body will return to better health.

ks


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



Celiac.com Sponsor (A8-M):



hthorvald Rookie

To Calico Jo, thanks for your detailed account of what you take. Can you tell me the brand name of the vitamins? I realize that each person has their own personal reaction to the supplements they take, but the Centrum Silver I was told to take does not sit well with me. In fact, I discontinued taking them about two weeks after starting.

All I take now is Ferro-Sequels for the iron, Viactiv for calcium (I have osteopenia as a result of celiac disease), and my Levoxyl for my thyroid (which is not a supplement). I understand that these three are gluten free, but I think the iron still upsets my stomach.

Thanks also to kschmitz with her recommendation of the 365 brand of supplements. I practically live at Whole Foods and will check it out.

H.

Pam Newbie

calico jo, when you said that you had a few "safe" staples, what did that include?

calico jo Rookie

The vitamins I'm currently taking I buy at Kroger. They're "Nature Made" I've also found Rexall vitamins suit me well and they are gluten-free. The liquid chlorophyll I take is by Nature's Sunshine and many of the other supplements I buy are Nature's Sunshine brand. I find them at herb stores. Remember that our bodies only absorb about 30-50% of what we ingest as vitamins so the %it says you get from each vitamin isn't what you actually get. Liquid vitamins are better, but I have yet to find some.

The "staples" I ate ....(that sounded funny :P ) that made me feel good in the beginning were roast beef, mashed potatoes and apples. I practically lived on those three things. Breaksfast, lunch and dinner. I CRAVED red meat which was funny because I had almost become a vegatarian up to that point and didn't care much for red meat. I still drool over a good roast.

The "staples" NOW are what I mentioned...pineapple, carrots, apples, and all kinds of other fruits. BUT I need to add, that until I seemed to get my stomach in order I was having trouble digesting fruits and vegetables so I don't suggest diving right into a lot of raw foods if your stomach is still "off". Eating a lot of fruits has made me not seem to need the digestive supplements any more.

I've been hearing some research regarding GERD and acid reflux, and that we actually are not OVER producing acid in those cases, but our bodies are not producing enough. (Thus the need for digestive enzymes.) When our bodies sense the lack of, it begins to overproduce. Also the prescriptions for acid problems neutralizes ALL the acid, and our bodies say, "hey,....I need that acid" and will THEN start to overproduce making a vicious cycle of requiring the prescription to offset it, which is subsequently causing the problem to be worse. Just exactly what the pharmaceutical companies want; dependency on their medication.

A test you can do for this is, the next time you are feeling acid, take a spoonful of vinegar and WAIT. See if your stomach starts to feel better. If so, you are NOT getting ENOUGH acid and you ought to try digestive enzymes instead. Doctors don't want us to know that we can use natural alternatives.

This is similar to bodies that produce calcium based kidney stones. It's not because we have too much calcium, but not enough. When we have a deficit of something, our bodies try to produce it and generally causes a problem. For years, farmers knew that when their cows got kidney stones they needed to give them calcium. It remedied the problem. Why human doctors told people to lay off calcium when they got kidney stones for YEARS is a puzzle.

My testament to the liquid chlorophyll: I had a stress fracture on my right foot that was refusing to heal after almost a year. I also had a complete hysterectomy about 8 years ago and have struggled with the "normal" side affects that causes because I do not wish to take estrogen replacement (soy combinations don't quite do the trick for me either) Less than 1 month after taking the chlorophyll 2X a day my foot got 90% better and my post menopausal symptoms have improved dramatically. I'm certain my cells have healed themselves. I also had some rashy, itchy bumps on my arms and sides (from the gluten intolerance, I believe) and those have dramatically improved, even the scars that I've donned for years. Do I have any medical proof? No. But my body tells me all I need to know.

BRCoats Enthusiast

calico jo,

Thanks for all the info you posted. I thought the acid info was particularly interesting. I have terrible acid problems with my stomach....but if I eat vinegar, (pickles), it just makes it worse. However, I haven't eaten pickles since going gluten-free....so maybe it was the gluten?? I'm so sensitive, I'm scared to try just taking a swig of vinegar! :o Do you have any info on the net that I could read about this? Would taking Betaine HCL help? Seems like a dumb thing to do if I'm already on Aciphex. :unsure: ??

I will definitely try some chlorophyll. I seem to be low on my estrogen - even though I'm only 32, but very high on the progesterone (ovarian cyst problem). Had no clue chlorophyll could help that. Thanks again for the info!!!

Brenda

burdee Enthusiast

I've been waiting to answer this one on a day I FELT like I was healing (no lingering reactions from slips). :o So tracking back to when I first suspected I had celiac disease, these helped me heal:

Digestive enzymes (Udo's Choice Enzyme Blend) and Probiotics (Ethical Nutrients Intestinal Care DF include 6 billion active bacteria each of acidophilus and bifidobacterium per capsule);

VERY supportive friends, esp. an ex-next door neighbor, whose husband was diagnosed 6 years previously, who told me to begin avoiding gluten ASAP. She also told me what containined gluten, what was safe, where to order gluten-free product guide books and where to find celiac disease websites, as well as answering all my frantic questions.

A local celiac support group, but especially the leader who became a close friend and listened to me vent when I had slips (as well as answered my venting emails);

All the supportive posts and friends I have met on this website;

My CSA gluten-free mainstream product guidebook and my Gluten-free Casein-free diet shopping guide which helped me choose 'safe' foods;

Our local GIG list of 'celiac friendly' restaurants in the Seattle area (and which entrees were safe), but esp. Kaili's Kitchen, a local totally gluten-free restaurant where I could always eat without fear of contamination;

My Enterolab Test results which revealed I also have casein (as well as gluten) intolerance and corroborated my suspicions about celiac disease, esp. with their gene test, and Dr. Fine who patiently answered all my questions, esp. when I suspected soy;

Learning to respect and obey my body cues: If I felt bad or experienced celiac symptoms, I learned to gluten/dairy/soy 'sleuth' to find the culprit and avoid that to prevent future slips;

Peppermint tea, hot water, yoga positions, and long walks (on noisy trails) to soothe cramps and relieve gas and bloating from reactions;

My husband who was willing to buy me any gluten-free/DF/SF supplies I wanted and agreed to eat up all the contaminated gluten containing food to eventually go gluten-free with me, as cancel our plans on a moment's notice when I suffered 'symptoms';

Above all, prayer when I was confused, hopeless, frustrated and scared.

Many of those things did not directly affect me physically, but gave me knowledge, reassurance and peace of mind to get through tough days of the healing process.

BURDEE

  • 3 weeks later...
Tutahl75 Apprentice

For an iron supplement I take Pallafer. It is designed to limit stomach upset.

For my digestive health, I take omega fatty acids, b-vitamins complex and L-Glutamine (which is really good at healing the intestines and muscle recovery).

I've dabbled in meditation for the tough times and just recently started using a Magnesium Chelate to help me relax and get more sleep.

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. - trents replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      GI DX celiac despite neg serology and no biopsy

    2. - Roses8721 posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      gluten-free Oatmeal

    3. - Roses8721 replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      8

      GI DX celiac despite neg serology and no biopsy

    4. - Scott Adams replied to Ginger38's topic in Related Issues & Disorders
      5

      Shingles - Could It Be Related to Gluten/ Celiac

    5. - Scott Adams replied to Xravith's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      3

      Challenges eating gluten before biopsy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,473
    • Most Online (within 30 mins)
      7,748

    Kelly Hannon
    Newest Member
    Kelly Hannon
    Joined

  • Celiac.com Sponsor (A20):



  • Celiac.com Sponsor (A22):




  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A21):


  • Upcoming Events

  • Posts

    • trents
      Certainly, it would b wise to have a gene test done if your physician is open to it as it would provide some more data to understand what's going on. But keep in mind that the genetic test for celiac disease cannot be used as to diagnose celiac disease, only to establish the potential to develop active celiac disease. About 40% of the general population possess one or both of the primary genes known to be associated with the development of active celiac disease but only about 1% of the population actually develop active celiac disease. So, the gene test is an effective "rule out" tool but not an effective diagnostic tool.
    • Roses8721
      Had Quaker gluten-free oatmeal last night and my stomach is a mess today. NO flu but def stomach stuff. Anyone else?
    • Roses8721
      So you would be good with the diagnosis and not worry to check genetics etc etc? Appreciate your words!
    • Scott Adams
      As recommended by @Flash1970, you may want to get this: https://www.amazon.com/Curist-Lidocaine-Maximum-Strength-Topical/dp/B09DN7GR14/
    • Scott Adams
      For those who will likely remain gluten-free for life anyway due to well-known symptoms they have when eating gluten, my general advice is to ignore any doctors who push to go through a gluten challenge to get a formal diagnosis--and this is especially true for those who have severe symptoms when they eat gluten. It can take months, or even years to recover from such a challenge, so why do this if you already know that gluten is the culprit and you won't be eating it anyway?  Approximately 10x more people have non-celiac gluten sensitivity than have celiac disease, but there isn’t yet a test for NCGS. If your symptoms go away on a gluten-free diet it would likely signal NCGS--but those in this group will usually have negative tests, or at best, elevated antibodies that don't reach the level of official positive. Unfortunately test results for celiac disease are not always definitive, and many errors can be made when doing an endoscopy for celiac disease, and they can happen in many ways, for example not collecting the samples in the right areas, not collecting enough samples, or not interpreting the results properly and giving a Marsh score.  Many biopsy results can also be borderline, where there may be certain damage that could be associated with celiac disease, but it just doesn't quite reach the level necessary to make a formal diagnosis. The same is true for blood test results. Over the last 10 years or so a new "Weak Positive" range has been created by many labs for antibody results, which can simply lead to confusion (some doctors apparently believe that this means the patient can decide if they want more testing or to go gluten-free). There is no "Weak Negative" category, for example. Many patients are not told to eat gluten daily, lots of it, for the 6-8 week period leading up to their blood test, nor asked whether or not they've been eating gluten. Some patients even report to their doctors that they've been gluten-free for weeks or months before their blood tests, yet their doctors incorrectly say nothing to them about how this can affect their test, and create false negative results. Many people are not routinely given a total IGA blood test when doing a blood screening, which can lead to false negative interpretations if the patient has low IGA. We've seen on this forum many times that some doctors who are not fully up on how interpret the blood test results can tell patients that the don't need to follow a gluten-free diet or get more testing because only 1 of the 2 or 3 tests done in their panel is positive (wrong!), and the other 1 or 2 tests are negative.  Dermatologists often don't know how to do a proper skin biopsy for dermatitis herpetiformis, and when they do it wrongly their patient will continue to suffer with terrible DH itching, and all the risks associated with celiac disease. For many, the DH rash is the only presentation of celiac disease. These patients may end up on strong prescriptions for life to control their itching which also may have many negative side effects, for example Dapsone. Unfortunately many people will continue to suffer needlessly and eat gluten due to these errors in performing or interpreting celiac disease tests, but luckily some will find out about non-celiac gluten sensitivity on their own and go gluten-free and recover from their symptoms. Consider yourself lucky if you've figured out that gluten is the source of your health issues, and you've gone gluten-free, because many people will never figure this out.    
×
×
  • 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.