Lactose in meds

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Bifcus16
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Lactose in meds

Post by Bifcus16 »

Think I might have worked out what was causing my flare. :grin:

My HRT contains lactose. Soon as I stopped taking it, I started to come good. Doctor has got me on patches instead.

I started taking this med in September and the D didn't get serious until March. I didn't have an immediate reaction at all. However, around October I started having the odd bad day when I didn't think I had eaten anything risky but still had D. Just the odd day or three, weeks apart, but gradually becoming more frequent, until it flared non stop for a month.

I don't think the quantity of lactose actually increased, I think it was just that initially my body could cope with a small amount. After continually subjecting it to that small amount it became less able to cope until it finally gave up. Now I have some more healing to do before I get back to 'textbook' perfect colour, frequency etc, but I am producing formed stools. Fingers still swelling slightly, but not bad. I have no D, wind, discomfort, no problems at all, and I have reintroduced most foods - still got the high fibre things like beans to go and a couple of supplements I have been off for weeks.

I think there is a lesson in here. If we are doing well we may not have problems with small amounts of irritants, but keep doing it and they'll get you every time. No more slips up on the meds for me.


Lyn
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Post by Polly »

Hi Lyn,

Interesting........but don't forget that HRT itself is a cause of MC. I first learned of this from Dr. Fine. I'm glad that the flare is subsiding!

Love,

Polly
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tex
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Post by tex »

Polly,

Excellent point. Obviously, Dr. Fine was not only correct, but he was way ahead of the pack, (which is not surprising, since he seems to have been, (and still is), light years ahead of the pack, in diagnosing and treating MC, celiac disease, and gluten sensitivity in general. Here is an abstract of an article recently published in the American Journal of Gastroenterology, (September, 2008), showing evidence of an association between the use of oral contraceptive agents, and the risk of development of an IBD:

http://www.citeulike.org/user/Zephyrus/article/3179846

To confuse the issue, here is an article showing how HRT can be protective of IBD flares, in post-menopausal women:

http://www.nature.com/ajg/journal/v103/ ... 8239a.html

However, I don't see any mention in this abstract, of the form of HRT used in this trial. Obviously, if transdermal patches were used to administer the HRT, that would preclude the direct effects on the GI tract, caused by oral treatment.

Like you, my guess is that the oral treatment was the problem, rather than the lactose. Here's why I feel that way: Pharmaceutical lactose is pure, which should preempt the possibility that it might contain any casein. While it is true that we are "intolerant" of lactose, anytime that we have any enteritis originating in the small intestine or upstream of there, this is not the same type of intolerance as that caused by proteins. Instead, it is merely due to the incomplete digestion of lactose, because of a shortage of the lactase enzyme, which results in the undigested lactose passing into the colon, where it ferments, resulting in gas and bloating, (but not an autoimmune reaction, so no inflammation should be produced).

It is true, however, that this type of reaction can include diarrhea, so it is certainly possible that this was causing your problem, though typically, such small amounts shouldn't result in mal-digestion of lactose, since lactase production is usually just reduced, not stopped completely. A good clue to consider, in this case, would be whether or not any of the other typical MC symptoms were present, in addition to the D, (such as aches, pains, joint pains, stiffness, brain fog, etc.). The swollen fingers, for example, would suggest more than just a simple case of lactose intolerance. At least, that's my take on the situation.
Lyn wrote:I think there is a lesson in here. If we are doing well we may not have problems with small amounts of irritants, but keep doing it and they'll get you every time.
Truer words were never spoken. Gluten, especially, has a cumulative effect, and our bodies might ignore a small amount, (as long as it is below our threshold for a reaction), but our GI tract is like a production line, and if we continue to add small amounts of intolerants, on a regular basis, eventually, the accumulated amount that's in the system, at any given time, will be more than it can handle, and our immune system will begin to produce antibodies, and when they become numerous enough, we will find ourselves in a flare.

Good detective work, Lyn. Thanks for posting that information. I hope you have clear sailing from here on.

Tex
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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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Bifcus16
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Post by Bifcus16 »

Thank you for that information Polly and Tex.

I hadn't realised HRT or the OCP were involved in MC.

The effects of lactose intolerance vs MC symptoms is an important point. When I think about it, I had very little gas/bloating, but did have liquid D, general aches, swollen fingers & feet etc. So it could well have been the HRT rather than the lactose causing the problem. Though in that case I would have expected a slower resolution of the problem.

We'll see how I go with the patches. Doing without is not a good option for me at this stage. Whilst I would dearly love to just use a natural solution, nothing worked for me even though the naturopath tested for levels of the various hormones and tried to adjust treatment to suit precisely my hormone balance. Life was not worth living as I was having so many hot flashes I couldn't sleep or function properly and was getting depressed and making bad decisions. With other stresses in my life, I needed to do something. I've always planned to stay on it for as short a time as possible. My doc at the time felt a year or two for women under 50 was a reasonable risk to take.

Interesting that the MC originally hit about 6 months after I stopped taking the OCP. I was menopausal before then, but the OCP was partly masking it. The change in hormone levels seems to cause lots of problems to come out of the woodwork. :mad:

Lyn
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Post by tex »

Lyn,

Unlike the GF diet, (where the gut requires a significant amount of time to heal, due to the damage caused by gluten), when a med is causing a flare, the symptoms usually resolve rather quickly, once the offending medication is discontinued, (usually within a couple of weeks). That's usually true of the other food intolerances, also, (other than gluten). Of course, HRT is not exactly the equivalent of a med, but the effects on the body are probably close enough to fall into the same category, as far as recovery time is concerned,

That is indeed interesting, that your MC symptoms began about 6 months after discontinuing an OCP. I think you hit the nail on the head - hormonal changes can make life pretty tricky, sometimes.

Tex
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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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Post by Gloria »

I'm impressed that you were able to determine the cause of your flare, especially when there was a time span between the start of HRT and the onset of your flare. Good job!

You've also taught us a lesson. We may be able to eat a food intolerance now and then without a problem once we're healed, but we probably can't go back to eating it regularly.

Gloria
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