New and looking for support/advice

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boney
Posts: 1
Joined: Thu Aug 29, 2024 3:10 pm

New and looking for support/advice

Post by boney »

Hello all,
This may be a bit long and personal, but I'd like to explain my story with this illness so far. Like I said in the title, I'm here in search of support and advice. I'm new, so please be patient with me. :wave:

I've been reading this forum for the past week because my doctors aren't giving me enough information about my disease. I've had chronic/active Lymphocytic Colitis from Celiac Disease for about 7-9 years. Initially, I was incorrectly told to just "deal with" LC after my diagnosis at a pediatric hospital. I became blind to it and "pushed through" my symptoms beyond what is normal, but now I realize it's not normal or healthy to struggle with basic tasks.

I've turned down several jobs because I can't focus or do simple things due to symptoms. I'm considering contacting a disability lawyer. Being in my 20s, I'm unsure of my chances and doubt my doctors will help. Managing my health feels like a full-time job with 2-4 appointments monthly, and accepting I may be unable to work for now has greatly affected my mental health.

I had a colonoscopy/endoscopy earlier this year, still positive for Lymphocytic Colitis, but no major/current damage from Celiac. My blood tests showed low in iron, vitamin D, and some fat soluble vitamins. I've been taking iron and D3 for a few months but haven't felt much improvement with my nutrients.

As for treatments I've tried so far,
- My treatment with budesonide 9mg worked for the first month, then stopped immediately after the first taper to 6mg. It was great to have normal BMs for a month after 7 years of active LC.
- Now I'm on Colesevelam for LC and gallbladder issues, but I haven't noticed any improvement.
- Changing my diet hasn't improved my LC. I notice more BMs with lactose, but it's not significant. I've tried many diets, including elimination/reintroduction, with no change. I mainly eat rice and vegetables.

I average 5-10 urgent BMs a day, which may be low for many with MC, but I feel fatigued, have brain fog, and knee/leg pain. I struggle to stand for long periods, bend, or squat without feeling faint. I have urgent BMs every 1-3 hours for about 15 minutes at a time, often seeing undigested food, which my doctors have no comment on. I'm dealing with nausea, near-incontinence, and lack of appetite, and only eating enough to take my medications. This all keeps me from leaving the house most days, and I haven't been social in a while.

Anyway, I'm not really sure what to do now or where to go from here, but I have a few questions:
- What are the worthwhile next steps after Budesonide / Colesevelam ? I'm concerned about taking immunosuppresants. Does anyone have any positive experiences with it, or should I decline if offered?
- Any suggestions for things should I mention at my next GI doctor appointment?
- My LC feels so resistant to treatment, and I know I haven't tried everything, but is it possible for LC to be permanently treatment resistant? My doctors all suggest LC can be cured/managed.
- Is it true that it becomes worse/harder to treat over time? Over the years, I've had periods of "better days" (3-4 BMs) and periods of "worse days" (8-15 BMs), but it's never gone away besides the one month on 9mg Budesonide.

Thank you for reading. Sorry if I sound ignorant about anything, it's my first time posting and I'm only just now starting to learn more about my condition. Thank you in advance for any advice! It's nice that there's a forum full of people I can relate to. :music:
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tex
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Posts: 35068
Joined: Tue May 24, 2005 9:00 am
Location: Central Texas

Re: New and looking for support/advice

Post by tex »

Welcome to the group. Since you seem to favor long posts, here's a long response that should get you up to speed regarding the basics of this disease. You're probably already well aware of most of this information, especially the part about gluten sensitivity, but it's very important to understand this, so just in case some of this information might be critical for your recovery, here goes:

Medical treatments for MC typically focus on the use of anti-inflammatory medications, and doctors either minimize, or totally avoid treatments that properly incorporate dietary changes. Medications are only temporary treatments. They only address the symptoms, not the cause of MC. To stop the inflammation from recurring with each meal, we have to avoid every food or medication antigen that causes our immune system to produce antibodies. Some gastroenterologists are beginning to learn this, but many of them are still way behind on the learning curve and they incorrectly insist that diet has nothing to do with the disease. In fact, it has everything to do with not only microscopic colitis, but all inflammatory bowel diseases. Claiming that food has nothing to do with digestive diseases is a lot like claiming that breathing polluted air has nothing to do with respiratory diseases like asthma, COPD, and lung cancer.

For example, we've always recommended a low fiber diet, at least when trying to recover from microscopic colitis, to achieve remission. The medical community has continued to recommend fiber, although it's clearly contraindicated for treating an IBD. Recently, medical researchers have finally published some research data which proves that fiber increases the inflammation level, and therefore the severity of the disease, for patients who have an IBD. So probably, in about 10 years, most gastroenterologists will begin to recognize that fiber should not be recommended when treating inflammatory bowel diseases.

Microscopic colitis (MC) is caused by chronic inflammation. There are two ways the symptoms can be controlled.

1. Medications such as budesonide, or immune system suppressants. Unfortunately, not all patients respond to budesonide, and published medical research shows that 85% of patients who respond to budesonide, relapse soon after the treatment is ended. And other research shows that budesonide becomes less effective each time a treatment is stopped and restarted, so that it eventually becomes ineffective. Therefore, medications are only temporary treatments. They only address the symptoms, not the cause of MC. So-called "biologics" are not what they're claimed to be. Although biologics are very risky for long-term health, many doctors prescribe one of the biologics after budesonide fails to provide long-term relief. Published research shows that only a relatively small percentage of MC patients are actually helped by this class of drugs, and their efficacy is usually short to medium term. The Microscopic Colitis Foundation (MCF) published a newsletter on May 1, 2022 that analyzed the possible use of these drugs for treating MC. For your convenience, here's a link where you can either read or download a copy of that newsletter:

https://www.microscopiccolitisfoundatio ... fcb80f.pdf

2. Diet changes that eliminate the foods that are causing the inflammation. This is the only way of which we're aware, to safely provide reliable, long-term control of the disease. Diet changes can be used with or without medications. Diet changes are what I used to completely control my symptoms. I have never taken any medications to treat my MC. All my clinical symptoms slowly faded away, after I changed my diet. But, I managed to track down and eliminate every food that was causing my immune system to produce antibodies. This is important, because if we overlook a single allergen, (even trace amounts) the inflammation, and therefore the disease, will continue, regardless of what else we might do.

The disease is caused by chronic inflammation of the mucosal lining of the intestines, but in many cases, the inflammation can be found at any point in the digestive tract, from mouth to anus, including any and all organs in the digestive system. The initial inflammation can be caused by infection, parasites, stress, certain medications, and a few other things. Research shows that the inflammation triggers increased intestinal porosity (leaky gut), and leaky gut leads to the development of food sensitivities. Once the inflammation triggers the disease, then the disease tends to perpetuate itself, due to the food sensitivities that are created as a result of the inflammation. To stop the inflammation from recurring with each meal, we have to avoid every food, medication, and supplement that's causing our immune system to produce antibodies. MC, including collagenous colitis (CC), lymphocytic colitis (LC), and at least 10 other known types of the disease, is usually not caused by food sensitivities, but food sensitivities tend to develop after the disease begins. The molecules of which food is composed, are long chains of amino acids. Normally, proper digestion reduces those long chains of amino acids to individual amino acids, or short chains of them, so that our body can then use them as nutrition, or building materials for new cells.

Peptides are simply medium-length chains of amino acids that are the result of incomplete digestion of a food molecule. No one can completely digest gluten. And when gluten is digested, the process results in the creation of hundreds of peptides. But although no one can completely digest gluten, that usually that doesn't matter. It only matters if a person has one or both of the genes that predispose to celiac disease (DQ2 and DQ8), or increased intestinal permeability (commonly known as leaky gut). But research shows that gluten sensitivity can cause leaky gut and this can allow partially-digested peptides from certain foods to enter the bloodstream, which provokes an immune system response (because those peptides are obviously not supposed to be in the blood). The immune system then begins to react to certain proteins in those foods every time they are eaten, thus causing chronic inflammation . This is why some of the foods that we have been eating for most of our life can suddenly begin to cause chronic inflammation by provoking our immune system to produce antibodies against them. Because of the inability to digest gluten, leaky gut makes all of us with this condition sensitive to gluten, which means that we have to totally avoid all foods that contain wheat, rye, barley, and for most of us, also oats. About two-thirds of us are also sensitive to cow's milk, which means that we have to avoid all dairy products. Over half of us are sensitive to soy and/or chicken eggs.

note that while lactose is a problem, it only causes poor digestion, it doesn't cause the immune system to produce antibodies. The reason most of us have to avoid all dairy products is because all dairy products contain the protein casein. And note that we react to many of the proteins in the common foods that we have eaten all our lives. Interestingly, we rarely react to the proteins in foods that we have rarely eaten prior to developing MC.

Similar to food sensitivities, certain drugs can also cause the immune system to produce antibodies that trigger MC symptoms. In some cases, just stopping the use of those drugs can bring remission of the MC symptoms. These drugs include antibiotics, NSAIDs, PPIs, SSRIs, SNRIs, statins, bisphosphonates, ACE inhibitors, beta blockers, and others. But in many cases, food sensitivities develop before the use of the drug is stopped, so the diet must also be changed in addition to avoiding the drug that causes the inflammation. But the bottom line is that if we stop the antibodies from being produced by totally avoiding the offending foods or drugs, then we can stop the inflammation from being produced and the symptoms will begin to fade away, as our digestive system heals. And the symptoms will stay away as long as we are very careful with our diet (and the medications we use).

The MCF has also published a newsletter with details on how to properly select a safe recovery diet. If you are interested in controlling your disease symptoms by diet changes, you might find the information in this newsletter to be helpful, for fine-tuning your diet. You can download or read a copy of that newsletter by clicking on the link below:

https://www.microscopiccolitisfoundatio ... 479987.pdf

And you may find the newsletter at the following link to be helpful if you're running out of treatment ideas:

https://www.microscopiccolitisfoundatio ... mplate.pdf

You might find other issues of the newsletter to be helpful. Newsletters are published monthly, on or about the first of the month. You can sign up to receive the newsletters in an email, or read, or download any of the back issues, on the newsletter page of our website. For your convenience, here's a direct link to that page:

https://www.microscopiccolitisfoundatio ... etter.html

I have a blog to which I post new articles about every two weeks. The articles discuss issues associated with MC that might also be of interest. For your convenience here's a direct link to that blog:

https://www.microscopiccolitisfoundation.org/blog

Also, there are diet guidelines posted on the discussion and support forum associated with the website at this location (in case you haven't already come across this information):

viewforum.php?f=79

There is no one-size-fits-all diet that will control the disease, but contrary to the claims of the medical "experts", virtually every MC patient is sensitive to gluten. For most, it's a form of non-celiac gluten sensitivity, so that the celiac screening tests used by doctors are worthless for detecting the type of gluten sensitivity that is typically associated with MC or other IBDs. But non-celiac gluten sensitivity causes basically the same symptoms as celiac disease. Every patient has to customize their diet to fit their own specific food sensitivities. And note that stress (whether physical, chemical, or mental/psychological) has a major effect on MC. Very intense stress, or in many cases, chronic stress. can even trigger a relapse of the disease, in most cases. Therefore it's also important to find ways to minimize stress, otherwise stress can perpetuate the symptoms.

Many, many doctors have mistakenly informed many, many MC patients that they are not sensitive to gluten based on a negative celiac blood test result. The claim that a negative celiac test result means that a patient cannot be sensitive to gluten simply is not true, because doctors have no way to officially diagnose non-celiac gluten sensitivity. A positive celiac test result can confirm gluten sensitivity, but a negative celiac test result cannot rule out gluten sensitivity. Many doctors mistakenly believe that a negative celiac blood test result rules out gluten sensitivity, but there is no medical justification for making that assumption, it's simply incorrect.

Not everyone loses weight because of MC, but it can cause severe weight loss for some patients. Regaining that weight is virtually impossible until the inflammation is brought under control. Once the inflammation is controlled, then healing will begin and it becomes much easier to gain weight.

To put the disease into remission we have to totally avoid (100%) all gluten, casein (the main protein in milk and all dairy products), soy, and chicken eggs. After we're in remission, we can experiment with dairy-based foods to see if we react to them, and if we don't react, they can be added back into our diet. The same can be done with products containing soy, and chicken eggs. But we have to test foods one at a time for three days, before we can judge them to be safe.

Here's a quote from The Microscopic Colitis Diet Book to give you an idea of safe foods that you should be able to eat without reacting:

Summary
When choosing foods for a recovery diet, ideally, we should choose one to three safe proteins, and one to three safe vegetables, from the lists below. Except in rare cases, these foods are usually safe for most of us. Significant amounts of protein are necessary for healing, so we need to make sure that our diet contains adequate protein. Adequate protein and fat in the diet are essential for good health, but carbohydrates are optional, not essential.

Recovery can be accomplished eating only meat, because meat contains all the essential amino acids that our body needs for good health. But if we choose to go this route, we need to select a fatty meat, or at least make sure that we're ingesting enough fat, so that we avoid the risk of developing the syndrome known as protein poisoning.

We should make sure that we avoid any foods that we were allergic to, or were otherwise sensitive to, before we developed MC. And obviously, if we know that we've become sensitive to any of these foods, since the development of MC, we should continue to avoid them.

Safe Proteins
•turkey
•quail
•duck
•goose
•emu
•lamb
•cabrito (kid goat)
•venison
•antelope
•rabbit
•shrimp
•muscles
•clams
•prawns
•lobsters
•crabs
•octopus

Safe vegetables
•carrots
•squash
•green beans
•Brussels sprouts
•kohlrabi
•rutabagas
•turnips
•parsnips
•sweet potatoes
•yams
•cassava
•broccoli
•cabbage
•cauliflower

I hope that some of this is helpful.

Tex
:cowboy:

It is suspected that some of the hardest material known to science can be found in the skulls of GI specialists who insist that diet has nothing to do with the treatment of microscopic colitis.
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