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

My Diet Sucks - Major Vent


julandjo

Recommended Posts

julandjo Explorer

So I've been gluten free for 13 months now. I've reacted to more and more foods as I go along, and at this point I'm back down to 7 foods plus a few spices. I was up to 9 foods, but the 2 I gained (rice and strawberries) proved to be failures after all. I'M GOING CRAZY on this diet. I've been at or near this level of restriction for almost 6 months now. When does this get any better??

In January I went to see a new doctor who specializes in Celiac and she could not help me, so she sent me to a dietician. The dietician had me start glutamine supplements - my reaction to that nearly landed me in the hospital (turns out anyone with a sensitivity to MSG should avoid glutamine - nothing like finding out by dumping 2000mg into your body!). She was also completely baffled by my situation, and when I expressed my growing hopelessness she joked that maybe I'm "one of the lucky few people who go their whole lives like this"! Was that supposed to be funny?! So now I'm being referred to a nationally-renowned (or so they say) Intestinal Rehab Program. When I spoke w/the nurse coordinator today it sounds like they plan to run a few days' worth of tests (all of which I've had done in the past year already), and then have me meet with a team including a GI specialist, dietician, therapist, etc. I'm seriously questioning whether this is worth my time and money. What on earth can they do for me?

I sat down with my food & symptom journal a few weeks ago and just read through the past year. Even though it's hard to see in my day-to-day struggles, I rejoiced to see that I've come a LONG way. Things that used to be part of my daily life - high blood pressure, joint pain, left-sided chest pain, lethargy, neuropathy - are just GONE. My vitamin/mineral levels have drastically improved, as has my cholesterol. For the first time in my life I feel my age (31), instead of someone much much older. I enjoy my life and my kids much more now and feel truly blessed to have made such a physical recovery. But this level of restriction is extremely difficult. There is zero leeway; the consequences last for days and make me miserable to be around which is unfair to my family.

Ughhh... sorry for the sobfest. It's just a rough week.

Julie


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



Celiac.com Sponsor (A8-M):



Katie B Apprentice

Hi Julie,

I can definitely relate. What is the Intestinal Rehab Program that you mention?

Have you heard of the low FODMAP diet? I'm not sure if it is of any interest to you but I've tried it with much success (tried the SCDiet previously and it didn't work this time around). I use this diet + gluten-free + low-carb and it seems to be working well. You can get the low FODMAP diet booklet from Monash Unviersity (there is a lot of conflicting info. on the web) and Sue Shepherd (Shepherd Works) and Jaci Barrett (Diet Solutions) are the main dieticians working on the project.

Hope this helps!

Katie

julandjo Explorer

Hi Julie,

I can definitely relate. What is the Intestinal Rehab Program that you mention?

Have you heard of the low FODMAP diet? I'm not sure if it is of any interest to you but I've tried it with much success (tried the SCDiet previously and it didn't work this time around). I use this diet + gluten-free + low-carb and it seems to be working well. You can get the low FODMAP diet booklet from Monash Unviersity (there is a lot of conflicting info. on the web) and Sue Shepherd (Shepherd Works) and Jaci Barrett (Diet Solutions) are the main dieticians working on the project.

Hope this helps!

Katie

I really don't understand what the program entails, just that I'll be working with a whole team of specialists to try to get answers, versus the one-doctor route I've been going so far. This program specializes in people who have a whole variety of intestinal disorders or injuries/transplants. I have to assume that these people, if anyone, will know what to make of my predicament.

As far as FODMAP or any other specialized diet, there's nothing I can do. I'm only eating 7 foods (chicken, beef, turkey, carrots, sweet potatoes, apples and blueberries. Oh and olive oil.) and have not successfully added anything. As long as I stick to those foods I feel great; any deviation and I'm in physical hell. My diet IS an eating disorder. :(

cahill Collaborator

I'm only eating 7 foods (chicken, beef, turkey, carrots, sweet potatoes, apples and blueberries. Oh and olive oil.) and have not successfully added anything. As long as I stick to those foods I feel great; any deviation and I'm in physical hell. My diet IS an eating disorder. :(

I can eat a couple more foods than you do, sweet potatoes,lamb,turkey,pork,beef ,carrots,peas,broccoli,olive oil,peaches and blueberries .. I have been eating rice and NOW I am starting to wonder about it,

May I just say THIS SUCKS!I have reacted to almost everything I have tried to add back ((since starting my elimination diet in Jan.))

I try to stay positive, really I do ,, But I am tried of fighting and I am tired of feeling like crap.

Sorry :unsure: , some days, like today, it just gets to me ,, just want to say,I do understand (( HUGS))

gary'sgirl Explorer

I had a very similar situation happen once I went gluten free. I was down to no meats only a few veggies and blueberries and raspberries - I couldn't eat apples - I think there was something else, but I'm drawing a blank right now. Anyway, the same thing was happening - one by one I had to keep taking more and more out of my diet until it seemed i couldn't eat anything.

I still wasn't feeling well, though and in desperation I was looking around at all the different diets and things that others had tried to heal their gut.

I stumbled across the Specific Carbohydrate Diet and ordered the book so I could get more detailed info as to why it was supposed to help and it really made sense to me. I started it and within a couple of weeks I could eat a little meat and have been able to gradually add more and more into my diet as the months have gone by (I started the diet the end of September 2010). I am not completely better yet, but am noticing little by little improvements in how I feel - not to mention it's great to have more in my diet. I had been gluten free for one year when I started the diet.

I just thought I would suggest looking into it, because you are already almost on the diet with what you are eating. The only thing you eat that you wouldn't be able to eat while on the diet is the sweet potatoes. I thought it might be worth looking into, anyway.

I hope the best for you - that you will be led to do what will help you to heal. This can be such a discouraging journey! Please post if you find something that you think will help - whether or not it ends up being that program you mentioned.

gary'sgirl Explorer

Oh, I also wanted to mention that some people use the Gaps diet, which is very similar to the SCD, but with the same idea in mind.

Katie B Apprentice

Thanks Julie - where is the program? What is it called?


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



Celiac.com Sponsor (A8-M):



julandjo Explorer

Thanks Julie - where is the program? What is it called?

It's called the Intestinal Rehab Program. It's at a transplant center in Nebraska.

cassP Contributor

I really don't understand what the program entails, just that I'll be working with a whole team of specialists to try to get answers, versus the one-doctor route I've been going so far. This program specializes in people who have a whole variety of intestinal disorders or injuries/transplants. I have to assume that these people, if anyone, will know what to make of my predicament.

As far as FODMAP or any other specialized diet, there's nothing I can do. I'm only eating 7 foods (chicken, beef, turkey, carrots, sweet potatoes, apples and blueberries. Oh and olive oil.) and have not successfully added anything. As long as I stick to those foods I feel great; any deviation and I'm in physical hell. My diet IS an eating disorder. :(

if you can eat apples and feel fine, you probably dont have an issue with fructose (part of the FODmap diet)- BUT i honestly have to say- that in the past i could SOMETIMES get away with an apple- but a pear would give me so much pain, i would wish i could have an epidural.

im sorry you're having to stick to so few foods... im wondering IF part of the problem is that you're not getting enough fruits & veggies that have natural digestive enzymes in them to help you digest?? idk...

have you considered JUICING?? for some people- the actual pulverization of the different fruits & veggies make them easier for a compromised body to digest... i however with my fructose problem cant do some of the juices... but the ones i can really help me feel better (i can do spinach/pineapple/beet)-> actually a beet and pineapple before a meal could help u maybe ****Just dont ever drink beet on it's own.. because beet juice is very comparable to actual stomach acid- if you dont mix it with something- it will burn your esophagus. i learned this the hard way.

also- black cherry juice can help with digestion.. drinkin a little before a meal.. or even marinating a steak or lamb in it over night can make it easier to digest.

ok, i'll shut up now. hope you can add more foods soon

GFinDC Veteran

Have you tried not eating the carrots? Carrots are no friend of mine. Just a thot.

cassP Contributor

Have you tried not eating the carrots? Carrots are no friend of mine. Just a thot.

SO interesting... i never had a prob with carrots EVER... and now, since going gluten free, i have developed an allergy to raw carrots!!! what the h is up with that??? so weird

julandjo Explorer

Have you tried not eating the carrots? Carrots are no friend of mine. Just a thot.

I have gone a few days without carrots, and it hasn't made any difference it seems. And if I stay on just those foods I feel pretty awesome.

I wanted to tell you too - you were who suggested I give up the white potatoes I was clinging so hard to a few months back. Well I gave those up, as well as peas. And guess what? Within a few weeks, the chest pain that had been CONSTANT over the past few years disappeared. Completely. Talk about life-changing! :)

julandjo Explorer

if you can eat apples and feel fine, you probably dont have an issue with fructose (part of the FODmap diet)- BUT i honestly have to say- that in the past i could SOMETIMES get away with an apple- but a pear would give me so much pain, i would wish i could have an epidural.

im sorry you're having to stick to so few foods... im wondering IF part of the problem is that you're not getting enough fruits & veggies that have natural digestive enzymes in them to help you digest?? idk...

have you considered JUICING?? for some people- the actual pulverization of the different fruits & veggies make them easier for a compromised body to digest... i however with my fructose problem cant do some of the juices... but the ones i can really help me feel better (i can do spinach/pineapple/beet)-> actually a beet and pineapple before a meal could help u maybe ****Just dont ever drink beet on it's own.. because beet juice is very comparable to actual stomach acid- if you dont mix it with something- it will burn your esophagus. i learned this the hard way.

also- black cherry juice can help with digestion.. drinkin a little before a meal.. or even marinating a steak or lamb in it over night can make it easier to digest.

ok, i'll shut up now. hope you can add more foods soon

Yeah see I agree - I don't think I have an issue with fructose. Most days I eat 2-3 apples, plus 8-12 ounces of unfiltered apple juice, without issue. Apple has been my main source of carbs. I've never tried juicing, that might be something to look into. Due to a latex allergy I have to avoid all tropical fruits, so that might be difficult. And I'm interested in cherries and cherry juice. I think that will be my next food trial!

Thank you everyone so much for your input and support! I love this board and this group of helpful folks!

Julie

Looking for answers Contributor

Have you been tested for SIBO, or small intenstinal bacteria overgrowth? My GI mentioned it to me lately and said when people seem to be intolerant to nearly everything, this is usually what they have...just a thought.

julandjo Explorer

Have you been tested for SIBO, or small intenstinal bacteria overgrowth? My GI mentioned it to me lately and said when people seem to be intolerant to nearly everything, this is usually what they have...just a thought.

I haven't been tested for this. Interesting... how does one get tested?

gary'sgirl Explorer

Have you been tested for SIBO, or small intenstinal bacteria overgrowth? My GI mentioned it to me lately and said when people seem to be intolerant to nearly everything, this is usually what they have...just a thought.

SIBO is basically what the SCD and GAPS diets address, because to some degree all people with intestinal problems also have a bacterial imbalance (at least that's what I understand from all my research and reading).

GFinDC Veteran

SO interesting... i never had a prob with carrots EVER... and now, since going gluten free, i have developed an allergy to raw carrots!!! what the h is up with that??? so weird

I used to eat lots of carrots. But on one of my elimination diet rounds I found they were a problem. Bummer, they are fun to eat with all that crunchiness. :)

Open Original Shared Link

If you are allergic to Birch pollen Ragweed pollen Grasses Mugwort pollen

You may also have a reaction to: Apples

Carrots

Celery

Hazelnuts

Peaches

Pears

Raw potatoes Bananas

Melons

(cantaloupe, honeydew and watermelon) Tomatoes

Tomatoes Apples

Carrots

Celery

Kiwi fruit

Peanuts

Some spices (caraway seeds, parsley, coriander, anise seeds, fennel seeds)

This is from a table on Mayo Clinic's site.

I have gone a few days without carrots, and it hasn't made any difference it seems. And if I stay on just those foods I feel pretty awesome.

I wanted to tell you too - you were who suggested I give up the white potatoes I was clinging so hard to a few months back. Well I gave those up, as well as peas. And guess what? Within a few weeks, the chest pain that had been CONSTANT over the past few years disappeared. Completely. Talk about life-changing! :)

Hey, that's great! Less pain is a good thing. I am glad it helped!

cahill Collaborator

I haven't been tested for this. Interesting... how does one get tested?

I second that question,, How is someone tested for SIBO and what would be the recommended course of treatment ?

jenngolightly Contributor

I was also very sick last year and couldn't eat many foods. I took on the specific carb diet and have been on it for 11 months. It's done wonders for me. I'm still very restricted on my diet, but I can eat about 50-60 foods/spices/oils/etc now.

One of the things it suggests is to cook all fruits and veggies (and to peel the fruits and veggies before eating). This helps with digesting them. So even if you don't want to do the diet, you might try that option.

irisheyes13 Newbie

Julie,

I'm new around these parts and other than this thread, I'm not familiar with what you have gone through but it sounds like a tough road. Have you ever had a colonscopy to check for microscopic colitis? I have MC and it goes hand in hand with multiple food intolerances. I'm not suggesting that you do have it but often times people with celiac disease who are gluten-free and still have problems can have MC.

There is a test called MRT which tests for food intolerances that seems to be helpful for people with multiple sensitivities and are having problems with introducing new foods. After having the blood test you work with a dietitian in your area who helps with introducing foods (LEAP diet) which you test safe for and slowly you introduce new foods. The test checks for about 150 foods/seasonings and the results are then correlated with what you already know you can have/not have. I have not had the testing done yet but plan to do it soon.

Here is a excerpt to an article by Scot Lewey giving a brief explanation as well as a link to the MRT site:

Food intolerance and sensitivity reactions that are not due to an allergy:

Certain foods, additives and chemicals are capable of triggering immune reactions that are not due to allergies. Chemicals mediators released by the immune system are capable of producing a variety of body reactions and symptoms. Avoiding foods that produce such reactions is suppose to resolve or at least significantly improve symptoms resulting from eating those foods. Mediator release (MRT) testing measures the release of chemical mediators from white blood cells and platelets in response to specific foods, additives or chemicals. Such chemical reactions presumably indicate sensitivity to these foods or additives.

Principles of commercially available mediator release testing (MRT):

Commercially available mediator release testing (MRT, Signet Diagnostic Corporation, Open Original Shared Link) is based on measuring in the blood the reaction of various immune mediator chemicals released into in response to a food or chemical to which you have become sensitive or intolerant. The result is that when exposed to such foods or chemicals your blood cells release various chemicals that cause an alteration of the ratio of solids (cells) to liquid (serum) in your blood that can be measured. The white blood cells and platelets shrink and the volume of the liquid increases. The degree of change can be measured and reported as mild or moderate to severe corresponding with the degree of sensitivity to that particular food, additive or chemical.

Test results of 150 foods and chemicals combined with elimination diet and counseling:

A panel of 150 food and chemicals (123 foods and 27 chemicals) is available. The foods or chemicals producing abnormal reactions are summarized in color tables provided along with a comprehensive report containing a result's based specific elimination diet plan supplemented with several hours of personalized counseling from a dietician.

Insurance coverage for MRT food sensitivity and intolerance testing:

Several insurance carriers pay for at least a portion of the cost of this testing however because it is considered "out of network" for most plans patients are usually responsible for payment of the service. Some carriers consider the testing "experimental" or not validated and therefore do not cover the testing.

Conditions benefited by MRT testing include migraines, IBS, fatigue and fibromyalgia:

Signet markets the testing for several conditions based on limited published research combined with their extensive clinical experience and patient testimonials. They claim success with reducing or eliminating a myriad of symptoms or conditions. These include migraines, headaches, autistic behavior, anxiety, depression, ADD, sinus and ear, nose and throat problems, irritable bowel syndrome, vomiting syndromes, Celiac, chronic stomachaches, bladder problems, fibromyalgia, arthritis, eczema, hives, and chronic fatigue syndrome.

Skeptical doctor and frustrated patients look for answers:

Initially, I was skeptical about MRT. However, I began advocating it several months ago because many of my patients had ongoing symptoms or findings that suggested an ongoing food intolerance or sensitivity but the testing available to us could not tell us what food or foods may be a problem. After reviewing the available research data I concluded MRT testing had adequate scientific basis to recommend it as an option to those who were interested and would consider making dietary changes based on the results.

Expert food allergy doctor and patients find MRT testing helpful and worthwhile:

So far, my experience is that most of those who have undergone the testing and implemented dietary changes as a result have noted significant improvement in a variety of digestive and non-digestive symptoms. I have also noted some very interesting patterns in people with other allergies. There appears to be a strong correlation with food-pollen cross reactions, more commonly known as the oral allergy syndrome (OAS). I am following this systematically and hope to report my observations formally in the future.

Previously available testing and diet interventions fail to provide relief in some patients:

All of my patients who have decided to undergo MRT testing have already been tested for Celiac disease and most have had food allergy testing as well as both upper and lower endoscopy exams with biopsies. All also had already tried dietary interventions. Some have had tests that confirmed one or more food allergies, Celiac disease or gluten sensitivity or have presence of mast cell enterocolitis; eosinophilic esophagitis, gastroenteritis or colitis; or lymphocytic enteritis. Though most had some improvement with dietary interventions based on their previous tests, many had ongoing symptoms with or without inconclusive or negative food allergy testing.

Get MRT testing and try an elimination diet:

I believe MRT testing is a helpful addition to the evaluation and treatment of food intolerance. The testing does require a doctor's order. If your doctor is not familiar with the testing they can learn more at Open Original Shared Link. If your doctor will not order the testing Signet can help you locate a doctor in your area or you can obtain the testing as part of an on-line consultation. An elimination diet based on specific foods to which you are intolerant but not necessarily allergic to may be the key to relief from a variety of symptoms and conditions. If you are suspecting a food intolerance, get tested today.

The Food Doc, Dr. Scot Lewey, is an expert medical doctor specializing in digestive diseases and food related illness, especially food allergies, celiac disease and colitis. Dr. Lewey's expert reputation as the Food Doc is established by a foundation of formal training in internal medicine, pediatrics, and gastroenterology (diseases of the digestive tract), his personal and family experience with gluten and milk sensitivity, and over two decades as a practicing physician, clinical researcher, author and speaker. Access this expert knowledge online today at www.thefooddoc.com

FWIW, I would have to agree that you may have better luck with vegetables and fruits if you peel and cook them. Good luck to you and I hope you are able to add some new foods soon!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • 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.