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SCD and IBS

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Hi all!

I'm fairly new to SCD and the group. My impression so far is that most folks

here suffer from Crohns/UC. My reason for going SCD is " IBS " ( a label I don't

much like because it's somewhat meaningless). Symptom-wise my problems for the

past 11 years have been big-time bloating (intestinal gas AND fluid retention in

reaction to eating) and constipation. (Not hard stools, just loss of peristalsis

without the use of laxatives). Before discovering SCD I had severly limited my

diet for a long time due to my inability to digest " anything " . SCD feels like a

get-out-of -jail card - you mean I can actually eat fruit and veggies at some

point ?? Whohoo!

I would be interested in the experience and success of anyone with a similar

symptom-picture with SCD, as I can't really relate to the difficulties with

diarrhea etc.

Also, I would assume that IBS would represent somewhat less severe intestinal

damage than a condition that includes bleeding, am I right? If so, could one

expect to advance through the stages a bit faster, and are there any special

considerations re: diet since diarrhea is not a problem but would actually be

welcome (in moderation, not diminishing the hardship of a condition that

includes severe D, of course)??

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I think it is relative. IBS does not damage the gut like IBD does, but the

symptoms can be as debilitating, IMHO. I think the SCD is an excellent approach

to IBS. My mother has wicked IBS as does my H, but neither of them are

interested in the dietary approach. I felt like SCD was my only hope, having

been diagnosed with UC. Maybe mine was more serious- for the bleeding, but they

are generally more symptomatic than I am because they eat whatever they want,

and something can set them off quickly.

My mom gave me one of her books " IBS NO MORE " which was based on the dietary

approach- very similar to SCD- limiting certain carbs to prevent " bad " bacterial

overgrowth. She had no interest in trying it.

I would say for you, treat the symptoms regardless of whether it is IBD or IBS.

The best approach to SCD is slow- keep a diary- and advance as tolerated- or

back up if you go to far. Your body will tell you. I don't think there is a

specific course for IBD vs IBS- we are all different. The point is for all of us

to feel better and heal in our own way.

PJ

>

> Hi all!

> I'm fairly new to SCD and the group. My impression so far is that most folks

here suffer from Crohns/UC. My reason for going SCD is " IBS " ( a label I don't

much like because it's somewhat meaningless). Symptom-wise my problems for the

past 11 years have been big-time bloating (intestinal gas AND fluid retention in

reaction to eating) and constipation. (Not hard stools, just loss of peristalsis

without the use of laxatives). Before discovering SCD I had severly limited my

diet for a long time due to my inability to digest " anything " . SCD feels like a

get-out-of -jail card - you mean I can actually eat fruit and veggies at some

point ?? Whohoo!

>

> I would be interested in the experience and success of anyone with a similar

symptom-picture with SCD, as I can't really relate to the difficulties with

diarrhea etc.

>

> Also, I would assume that IBS would represent somewhat less severe intestinal

damage than a condition that includes bleeding, am I right? If so, could one

expect to advance through the stages a bit faster, and are there any special

considerations re: diet since diarrhea is not a problem but would actually be

welcome (in moderation, not diminishing the hardship of a condition that

includes severe D, of course)??

>

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Hi all!

I'm fairly new to SCD and the group. My impression so far is that

most folks here suffer from Crohns/UC. My reason for going SCD is

" IBS " ( a label I don't much like because it's somewhat meaningless).

Symptom-wise my problems for the past 11 years have been big-time

bloating (intestinal gas AND fluid retention in reaction to eating)

and constipation. (Not hard stools, just loss of peristalsis without

the use of laxatives). Before discovering SCD I had severly limited

my diet for a long time due to my inability to digest " anything " . SCD

feels like a get-out-of -jail card - you mean I can actually eat

fruit and veggies at some point ?? Whohoo!

I would be interested in the experience and success of anyone with a

similar symptom-picture with SCD, as I can't really relate to the

difficulties with diarrhea etc.

I came to SCD from IBS and though I don't have exactly the variety

you do, I was mixed. Never knew if it would be a C day, or a " loose "

day though I've never had the runny D most people talk about. I,

too, pretty much had learned what I could eat except I was using rice

as a " bland base " to calm the IBS down, which it did not. Once I gave

up the rice things calmed down quite a lot and fairly soon. I eat a

ton of fruit. Doesn't seem reasonable with IBS but it's my best food

group. Fruit, salads, plain roasted or boiled poultry, olive oil,

almond butter and some nuts in my salads. Once in awhile I use winter

squash but I havent had squash for so long I tend to forget that I can.

Anyhow, things are definitely better, calmer, with SCD. I will,

however, be very slow about introducing new foods, and for me that

includes things like dairy and eggs that have given me trouble for a

long time. I don't see offhand why SCD wouldn't help you; seems like

it's worth a try.

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