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Celiac, Colitis, Ibs And Diverticulitis... What Can I Eat?


WitchyWoman

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WitchyWoman Rookie

Hi~~~~

This is my first time on this forum. I have had severe Diverticulitis and IBS for 14 years. I have had multiple abdominal surgeries removing the sigmoid, transverse and transending colon. I have been in a catch 22 of every time they do surgery I have worse adhesions, so they do more surgery and it results in more adhesions ect. I have suffered with severe abdominal pain and D for years. I recently went to John Hopkin's and was diagnosed with Celiac Disease and Colitis as well as an infection in the stomach and in the intestines. I go back to the Dr on March 10th to discuss antibiotics and a new regimine of RX. Unfortunately my insurance does not cover a dietician to assist me in selecting foods that will work with all 4 diagnosis and I can't afford $500 per hour for a dietician. Is there anyone else out there with similar multiple diagnosis that could assist with what Not to eat or as resource that may assist me? It has been very difficult dealing with the Diverticulitis and IBS and now I just really feel overwhelmed with the addition of two more diagnosis.

Thanks in advance!!!

WitchyWoman


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captaincrab55 Collaborator

Witchy Woman, Whats your Doctor's name from Hopkins ???

T.H. Community Regular

So, so sorry you're having such trouble.

It's highly likely you will end up with less diagnoses by the end of this. Which is good, really good, but you may want to prepare for potential frustration and anger over how long it took to be diagnosed. I could be wrong - obviously I don't know your health - but IBS has a good chance of being missed Celiac Disease. :( Diverticulitis can be a complication from Celiac Disease, too, or actually WAS Celiac Disease.

"...Recognizing celiac disease can be difficult because some of its symptoms are similar to those of other diseases. Celiac disease can be confused with irritable bowel syndrome, iron-deficiency anemia caused by menstrual blood loss, inflammatory bowel disease, diverticulitis, intestinal infections, and chronic fatigue syndrome. As a result, celiac disease has long been underdiagnosed or misdiagnosed. As doctors become more aware of the many varied symptoms of the disease and reliable blood tests become more available, diagnosis rates are increasing..."

( from Open Original Shared Link )

Colitis can also be a result of untreated Celiac Disease, although it can be something else, too (I believe Crohn's Disease, at times).

There is a good list here on celiac.com what ingredients you need to avoid on a gluten free diet if you do a small search (unsafe ingredient list for things to avoid, and a safe ingredient list for what you can eat). I'd try to avoid most obvious dairy, too, as many celiacs are lactose intolerant until they are healed up (a few months, at least), and it sounds like you've had gut trouble for quite some time. With the antibiotics, I would also try to find some probiotics, because Celiac guts need all the help we can get, and the antibiotics will make that even more vital, ya know? Liquid probiotic is better. Capsule or pill ones are pretty much a waste of money as no food for the bacteria cultures mean they are dying off as soon as they are encapsulated. <_<

A book I found recently that might help with trying to come up with your own diet is "Nutrition for Dummies." It just has some of the basics you want to think about in your nutrition, and along with the gluten free lists here, I think it might help you get at least a fairly good diet for your condition.

Wishing you good luck, and hoping that Celiac Disease is THE answer that can get you back on the road to better health.

YoloGx Rookie

I agree with Shauna. I wish you much good luck! Finding out you have celiac will no doubt prove to be a blessing which can help you finally be on the healing path and heal your gut much better than any surgeries etc.

In addition however, in order to speed up your healing you might want to consider going on a basic diet of meat, veggies, squash, brown rice and the like rather than eat pre-prepared foods. At first you should avoid raw vegetables since they probably are too irritating for your system right now. If you crave sweets, consider using powdered stevia instead of sugar, especially while you are healing. Some people find honey better than sugar, but for many sweet carbs are not good in any quantity.

Taking things like bromelain/papain and pancreatic enzymes could be important at first to improve your digestion in your intestines. If you can tolerate pineapple and/or papaya, so much the better since that is what the bromelain/papain come from.

Taking nattokinase or some other fibronylitic enzymes on an empty stomach should help counteract the scar tissue from all those surgeries. I suggest you Google it and find out more about it. Taking marshmallow root powder regularly to soothe and heal your intestines might also be a good idea at first.

Many folks here are also allergic to other things like, as mentioned, milk products, especially at first. Nevertheless many here can tolerate plain yogurt, especially if it is home made and cultured 24 hours to get rid of the lactose. It also greatly increases the probiotic content.

For those who still have a problem with yogurt, fermented cabbage inoculated with probiotics is another alternative. You can find instructions about it by looking at the old SCD thread (specific carbohydrate diet) here on celiac.com.

For me the SCD did not help me, however it does help many. I discovered just recently that I have salicylic acid sensitivity that makes eating things like zucchini and honey a real no no and that for the likes of people like me brown rice is actually very healing. Just goes to show that we are all different.

Other common allergens are soy, corn, the nightshade family, nuts, citrus. Though with leaky gut syndrome (often caused by damage to the villi from celiac), one can become sensitive to most anything. Again, when you heal more, its likely you will become less reactive to so many things (in case you are to begin with that is...).

Again, welcome and good luck!

Bea

Nor-TX Enthusiast

I also have multiple digestive issues. I have Colitis, IBS, GERD, Reflux, Hiatal Hernia, Gluten intolerance, Dairy and Lactose intolerance, Egg intolerance, and Peanut Butter gives me Angelina Jollie lips although no formal diagnosis.

I am facing possible whole Thyroid gland and/or nodule surgery. My Vitamin D and iron are low and every 5 weeks I get Remicade infusions along with lots of drugs to stave off reactions. I have arthritis in my knees and may not be able to have a total knee replacement because I have had an allergic response to both nickel and titanium.

So I know exactly what you are going through. I was at a loss what to eat until I decided the only one who could come up with an appropriate list of foods to eat was me. I didn't have a dietition and relied on my body and the research I did on the Internet.

I made a page of paper for every digestive/medical issue I was going through and proceeded to list those foods that I could NOT tolerate for one reason or another and the list of foods I COULD eat. Then I cross referenced each of the pages and made a master list of what I could eat.

When I found out about a new food, I would add it to the list in pencil until I ate it a few times and it could be permanently added to my master list.

The list was very spare at the beginning. Some foods have gotten onto the list and have been deleted from the list such as: Chex cereal (I thought it was wonderful at the beginning, but my stomach didn't) When I try a new food I make a note of how I felt immediately after eating, and later that day. If I get a couple of negative comments I just figure it is something else I cannot tolerate.

I have just added sardines to my list and so far everything is going great. I have tried them several different ways and tried both the mustard and plain packed in water. This one food has helped me so much when I just want to grab something to take to work and not have to do alot of preparing.

For me, having these food issues makes it all about me. I have to make a concious decision on everything I eat. I plan my days meals the night before. It's alot of work for sure, but now I have my "go to" foods. I've just discovered haddock frozen fillets and have made them a few different ways. I have always loved fish but turned away because DH doesn't eat fish. Lately though, I am back to this favorite food with great results.

Keep your food journal and sooner rather than later, a pattern of "safe foods" will emerge and you will have your own little database of acceptable foods that meet the needs of all your health issues.

WitchyWoman Rookie

Witchy Woman, Whats your Doctor's name from Hopkins ???

I had Dr. Milligan but he fell and broke his hip and retired. He did all of my testing but now I start all over next week with a new Dr...... Dr. Stien

WitchyWoman Rookie

So, so sorry you're having such trouble.

It's highly likely you will end up with less diagnoses by the end of this. Which is good, really good, but you may want to prepare for potential frustration and anger over how long it took to be diagnosed. I could be wrong - obviously I don't know your health - but IBS has a good chance of being missed Celiac Disease. :( Diverticulitis can be a complication from Celiac Disease, too, or actually WAS Celiac Disease.

"...Recognizing celiac disease can be difficult because some of its symptoms are similar to those of other diseases. Celiac disease can be confused with irritable bowel syndrome, iron-deficiency anemia caused by menstrual blood loss, inflammatory bowel disease, diverticulitis, intestinal infections, and chronic fatigue syndrome. As a result, celiac disease has long been underdiagnosed or misdiagnosed. As doctors become more aware of the many varied symptoms of the disease and reliable blood tests become more available, diagnosis rates are increasing..."

( from Open Original Shared Link )

Colitis can also be a result of untreated Celiac Disease, although it can be something else, too (I believe Crohn's Disease, at times).

There is a good list here on celiac.com what ingredients you need to avoid on a gluten free diet if you do a small search (unsafe ingredient list for things to avoid, and a safe ingredient list for what you can eat). I'd try to avoid most obvious dairy, too, as many celiacs are lactose intolerant until they are healed up (a few months, at least), and it sounds like you've had gut trouble for quite some time. With the antibiotics, I would also try to find some probiotics, because Celiac guts need all the help we can get, and the antibiotics will make that even more vital, ya know? Liquid probiotic is better. Capsule or pill ones are pretty much a waste of money as no food for the bacteria cultures mean they are dying off as soon as they are encapsulated. <_<

A book I found recently that might help with trying to come up with your own diet is "Nutrition for Dummies." It just has some of the basics you want to think about in your nutrition, and along with the gluten free lists here, I think it might help you get at least a fairly good diet for your condition.

Wishing you good luck, and hoping that Celiac Disease is THE answer that can get you back on the road to better health.

y

Thank you so much for the response!! It has been very frustrating over the years. It actually all started with my ovaries cystizing and rupturing in 1997...... They did emergency surgery and while I was in the local hospital I attained MRSA (what a gift!! LOL) and it set into my gut. The MRSA basically ate my intestines up form the outside in, causing the severe diverticulits. After months of IV antibiotics and numerous pain meds and three subsequent abdominal surgeries removing the sigmoid, transverse and transending colon (total of 5 abdominal surgeries from the breast bone down over a three year period..... ) The Dr's basically said you are going to just have to live with this... "D" ten times a day on a good day, bedridden on bad days, severe abdominal pain and too many RX to mention.

I took myself off of a lot of the meds and stopped eating raw vegtables, corn, popcorn, seeds, anything fried or hard to digest.... ect out of my diet and it helped...... but not enough, so I finally requested to see a big city hospital doctor LOL at John Hopkins. I only have a few inches of intestines left and I know, if I don't get whatever is going on under control, I will end up on a bag and I am willing to do anything to avoid that.

I go back up to John Hopkins on March 10th and they are supposed to start me on antibiotics and new RX's. With removing the above foods and then the gluten foods.... LOL it sounds like it leaves me with meats and expensive gluten free foods. I am hoping the Dr. will write a letter to my insurance company (I thought Blue Cross Blue Shield was a good insurance company LOL... they only cover seeing a dietician if you are diabetic)) to request a special exemption so that I can see a dietician, which would allieviate a lot of my concerns. So fingers crossed that the insurance company realizes that it is much cheaper $2000 to send me to a dietician that the $100,000's it will cost if I have to undergo surgery again.

Thank you so much for your advice!! I am open to any suggestions... I am just feeling a little overwhelmed at this point and I know it sounds strange but I am glad to finally have the Celiac diagnosis so that I can really fight back and my Dr's finally realize it was real pain.... Thanks again!!! :)


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    • marion wheaton
      Thanks for responding. I researched further and Lindt Lindor chocolate balls do contain barely malt powder which contains gluten. I was surprised at all of the conflicting information I found when I checked online.
    • trents
      @BlessedinBoston, it is possible that in Canada the product in question is formulated differently than in the USA or at least processed in in a facility that precludes cross contamination. I assume from your user name that you are in the USA. And it is also possible that the product meets the FDA requirement of not more than 20ppm of gluten but you are a super sensitive celiac for whom that standard is insufficient. 
    • BlessedinBoston
      No,Lindt is not gluten free no matter what they say on their website. I found out the hard way when I was newly diagnosed in 2000. At that time the Lindt truffles were just becoming popular and were only sold in small specialty shops at the mall. You couldn't buy them in any stores like today and I was obsessed with them 😁. Took me a while to get around to checking them and was heartbroken when I saw they were absolutely not gluten free 😔. Felt the same when I realized Twizzlers weren't either. Took me a while to get my diet on order after being diagnosed. I was diagnosed with small bowel non Hodgkins lymphoma at the same time. So it was a very stressful time to say the least. Hope this helps 😁.
    • knitty kitty
      @Jmartes71, I understand your frustration and anger.  I've been in a similar situation where no doctor took me seriously, accused me of making things up, and eventually sent me home to suffer alone.   My doctors did not recognize nutritional deficiencies.  Doctors are trained in medical learning institutions that are funded by pharmaceutical companies.  They are taught which medications cover up which symptoms.  Doctors are required to take twenty  hours of nutritional education in seven years of medical training.  (They can earn nine hours in Nutrition by taking a three day weekend seminar.)  They are taught nutritional deficiencies are passe' and don't happen in our well fed Western society any more.  In Celiac Disease, the autoimmune response and inflammation affects the absorption of ALL the essential vitamins and minerals.  Correcting nutritional deficiencies caused by malabsorption is essential!  I begged my doctor to check my Vitamin D level, which he did only after making sure my insurance would cover it.  When my Vitamin D came back extremely low, my doctor was very surprised, but refused to test for further nutritional deficiencies because he "couldn't make money prescribing vitamins.". I believe it was beyond his knowledge, so he blamed me for making stuff up, and stormed out of the exam room.  I had studied Nutrition before earning a degree in Microbiology.  I switched because I was curious what vitamins from our food were doing in our bodies.  Vitamins are substances that our bodies cannot manufacture, so we must ingest them every day.  Without them, our bodies cannot manufacture life sustaining enzymes and we sicken and die.   At home alone, I could feel myself dying.  It's an unnerving feeling, to say the least, and, so, with nothing left to lose, I relied in my education in nutrition.  My symptoms of Thiamine deficiency were the worst, so I began taking high dose Thiamine.  I had health improvement within an hour.  It was magical.  I continued taking high dose thiamine with a B Complex, magnesium. and other essential nutrients.  The health improvements continued for months.  High doses of thiamine are required to correct a thiamine deficiency because thiamine affects every cell and mitochondria in our bodies.    A twenty percent increase in dietary thiamine causes an eighty percent increase in brain function.  The cerebellum of the brain is most affected.  The cerebellum controls things we don't have to consciously have to think about, like digestion, balance, breathing, blood pressure, heart rate, hormone regulation, and many more.  Thiamine is absorbed from the digestive tract and sent to the most important organs like the brain and the heart.  This leaves the digestive tract depleted of Thiamine and symptoms of Gastrointestinal Beriberi, a thiamine deficiency localized in the digestive system, begin to appear.  Symptoms of Gastrointestinal Beriberi include anxiety, depression, chronic fatigue, headaches, Gerd, acid reflux, gas, slow stomach emptying, gastroparesis, bloating, diarrhea and/or constipation, incontinence, abdominal pain, IBS,  SIBO, POTS, high blood pressure, heart rate changes like tachycardia, difficulty swallowing, Barrett's Esophagus, peripheral neuropathy, and more. Doctors are only taught about thiamine deficiency in alcoholism and look for the classic triad of symptoms (changes in gait, mental function, and nystagmus) but fail to realize that gastrointestinal symptoms can precede these symptoms by months.  All three classic triad of symptoms only appear in fifteen percent of patients, with most patients being diagnosed with thiamine deficiency post mortem.  I had all three but swore I didn't drink, so I was dismissed as "crazy" and sent home to die basically.   Yes, I understand how frustrating no answers from doctors can be.  I took OTC Thiamine Hydrochloride, and later thiamine in the forms TTFD (tetrahydrofurfuryl disulfide) and Benfotiamine to correct my thiamine deficiency.  I also took magnesium, needed by thiamine to make those life sustaining enzymes.  Thiamine interacts with each of the other B vitamins, so the other B vitamins must be supplemented as well.  Thiamine is safe and nontoxic even in high doses.   A doctor can administer high dose thiamine by IV along with the other B vitamins.  Again, Thiamine is safe and nontoxic even in high doses.  Thiamine should be given if only to rule Gastrointestinal Beriberi out as a cause of your symptoms.  If no improvement, no harm is done. Share the following link with your doctors.  Section Three is especially informative.  They need to be expand their knowledge about Thiamine and nutrition in Celiac Disease.  Ask for an Erythrocyte Transketolace Activity test for thiamine deficiency.  This test is more reliable than a blood test. Thiamine, gastrointestinal beriberi and acetylcholine signaling.  https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/ Best wishes!
    • Jmartes71
      I have been diagnosed with celiac in 1994, in remission not eating wheat and other foods not to consume  my household eats wheat.I have diagnosed sibo, hernia ibs, high blood pressure, menopause, chronic fatigue just to name a few oh yes and Barrett's esophagus which i forgot, I currently have bumps in back of my throat, one Dr stated we all have bumps in the back of our throat.Im in pain.Standford specialist really dismissed me and now im really in limbo and trying to get properly cared for.I found a new gi and new pcp but its still a mess and medical is making it look like im a disability chaser when Im actively not well I look and feel horrible and its adding anxiety and depression more so.Im angery my condition is affecting me and its being down played 
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