Ischemic colitis...Tex?

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Leah
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Ischemic colitis...Tex?

Post by Leah »

Hi Tex Long time, huh? Things are going so well with my MC and I have been so busy at work, I haven't had time to check in. How are things going?

I have a friend who just was DX with Ischemic Colitis. Does the same diet restrictions apply?

Leah
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tex
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Post by tex »

Hi Leah,

It's good to see some posts from you again, and it's great to see that you're doing well. The family here is continuing to grow, and I've had to add soy, peanuts, and agar to my own list of sensitivities.

About 2 weeks ago I had to move the forum to a new hosting service when the old one abruptly announced that they were going out of business. :roll: I made the mistake of letting the "tech experts" at the new hosting service move the files to the new server and they made the dumb mistake of forgetting to import the database from the old server, so the board was down for 3 days over the weekend before they got around to correcting their mistake. :sigh: But other than that everything seems to be percolating along OK.

Ischemic colitis is a horse of a different color. It's caused by a restriction of blood flow to a section of the intestines, and it can be a very serious, even life-threatening condition if the restriction is severe enough to cause cells to die. It's commonly associated with long-distance running (such as marathons) and it can also be caused by problems with the mesentary that attaches the intestines to the back of the abdominal wall. If the intestines somehow become twisted due to inadequate support, or a section flips because of certain maneuvers, the blood supply to that section can be cut off or severely restricted, causing ischemic colitis.

The reason why ischemic colitis is a risk for runners is because if the body is pushed too far beyond it's limits while running, a primordial human reflex can take over to cut off the blood supply to the intestines as part of the original fight or flight response.

Most cases are resolved without major consequences, but the warning must not be ignored because it will often occur again, under similar circumstances.

I'm not aware that any food sensitivities are categorically involved with IC, but a bland, easy-to-digest diet may be helpful during recovery.

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.
Leah
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Post by Leah »

Thanks Tex. Sorry to hear about your new sensitivities. I am actually able to eat a bit of everything now! I don't overdo any indulgences and I stay away from gluten almost always ( I did have a couple slices of pizza a week ago with no ill effect) I now take probiotics ( PEFECT BIOTICS) that make my daily BM "picture perfect" . I think my gut no longer "leaks" and not having IgA antibodies helps in this particular way :)

Leah
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tex
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Post by tex »

Interesting. I wonder if the probiotics might be beneficial because they might help to make up for your IgA deficiency.

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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Erica P-G
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Post by Erica P-G »

So glad to hear you are doing well and enjoying life Leah!

That is my aim one of these days :wink:
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jlbattin
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Post by jlbattin »

Leah,

It's good to hear that you are doing so well and very encouraging that you can eat so much without a lot of restrictions (but moderation). I'm hoping to be there one of these days soon! :)
Jari


Diagnosed with Collagenous Colitis, June 29th, 2015
Gluten free, Dairy free, and Soy free since July 3rd, 2015
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humbird753
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Post by humbird753 »

It's good to hear from you Leah, and to hear you're doing so well.

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Vanessa
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Post by Vanessa »

Leah, good to see you doing well! Hey, just wondered if you ever re tested your IgA deficiency as mine is now normal....I suppose I could do more enterolab testing in the future to weed out the bugs if need be! It was deficicient when I was first diagnosed, then went way high after a year of diet changes, and now is in the normal range. Hmmmmm......the process of healing an inflamed immune system would be my guess.
Vanessa
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Post by Marcia K »

Pizza! Oh my goodness that would be aswesome. It hasn't bothered me too much but they had some at work the other day and it smelled out of this world! Glad you're doing so well!
Marcia
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tex
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Post by tex »

Vanessa wrote:Leah, good to see you doing well! Hey, just wondered if you ever re tested your IgA deficiency as mine is now normal....I suppose I could do more enterolab testing in the future to weed out the bugs if need be! It was deficicient when I was first diagnosed, then went way high after a year of diet changes, and now is in the normal range. Hmmmmm......the process of healing an inflamed immune system would be my guess.
Now that's mighty interesting. I always just assumed that selective IgA deficiency was a permanent genetic condition. I searched, and I can't find any connection with magnesium deficiency. But now I'm wondering if that might be because no one has ever had the insight to make the connection before.

Have you by any chance had the 23andme testing? Supposedly their testing is able to identify 3 genes in the HLA region that are linked to Selective IgA deficiency.

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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Vanessa
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Post by Vanessa »

Hey Tex,

I thought it was permanent also. But I re-tested when I was feeling so poorly checking everything I could think of and was confused when it was off the charts high. I did do the 23 and me. I'll have to check my results. If I have the genes associated with the deficiency, the only conclusion is that the magnesium I started around the same time was trying to normalize it. Now thats some woo woo stuff going on here, my chanting must have worked. :lol:
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Gabes-Apg
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Post by Gabes-Apg »

Vanessa/Tex
I am no scientist or expert, my feeling is that it is a combo of things

the right magnesium levels will mean that the Vit D receptor is working properly
and I have a feeling that a balanced methylation cycle (right B levels etc) will also contribute

keep in mind that we may have genetic SNP's but their function can turn on and off depending on our 'overall health'
Gabes Ryan

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Gabes-Apg
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Post by Gabes-Apg »

ohh - another lightbulb

the theory that intolerance's/inflammation are linked to excess toxins
as you reduce toxins (via healthy cells and magnesium, good methylation cycle) the inflammation and intensity of reactions will reduce

Vanessa, your success stories post and all the various things you did to reduce toxins, maybe they had more of an influence than you first thought...
Gabes Ryan

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Leah
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Post by Leah »

No, I haven't re=tested for the IgA deficiency, but when my daughter started having gut issues and colds that wouldn't go away, I had her tested ... and she is also Deficient! I have a feeling that mine is permanent, but I don't know for sure.

Thanks to all of you who remember me :)

Leah
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Vanessa
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Post by Vanessa »

Leah,

I can't forget you, that picture is gorge! Interesting about your daughter, definitely a genetic component.

Gabes,

I think your onto something. I think stress is a major player in lowering IgA, thus reducing toxic and mental overload had to have some effect.
Vanessa
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