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Dear Kim,

NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her daddy has it; she has it. She has some of the major symptoms -- bloating and gastric distress! Start her on the GF diet IMMEDIATELY.

LOTS of doctors are just catching up on this thing. We know more than many of them at this point. Trust your instincts. You don't want her to suffer any more!

Gail in Houston

-- Any advice??

I had my 6 year old to the ER for all of last night. She had intense stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-ray and her colon was taking up the entire left side of her abdomen. Thinking a blockage they did a cat scan, which showed no blockage, just an enormous amount of gas. Doctor brought in 5 other doctors to consult as he thought he was missing something, cause he had never seen an xray like hers with no blockage. I had mentioned my hubby has CD to him, he mentioned following up with my ped and starting her on a GF diet. Arent you suppose to wait for diagnose to go GF? Also he said CD symptoms have to be brought on by eating GF and she wouldnt tolerate bread, etc. My hubby was diagnosed after coming up anemic in routine blood work, in hindsight we saw some signs but nothing severe. Looking back over the past year my daughter has had GI problems frequently and says she is tired alot, but I never thought CD because she Doesn't "look" the part. Should I start her on the CD, or wait? Since my hubby is biopsy diagnosed, would a blood test be sufficent to make a diagnosis in her?? Anyone who has advice I would love to hear it. Sorry I seem to ramble. KIm

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Dear Kim,

NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her daddy has it; she has it. She has some of the major symptoms -- bloating and gastric distress! Start her on the GF diet IMMEDIATELY.

LOTS of doctors are just catching up on this thing. We know more than many of them at this point. Trust your instincts. You don't want her to suffer any more!

Gail in Houston

-- Any advice??

I had my 6 year old to the ER for all of last night. She had intense stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-ray and her colon was taking up the entire left side of her abdomen. Thinking a blockage they did a cat scan, which showed no blockage, just an enormous amount of gas. Doctor brought in 5 other doctors to consult as he thought he was missing something, cause he had never seen an xray like hers with no blockage. I had mentioned my hubby has CD to him, he mentioned following up with my ped and starting her on a GF diet. Arent you suppose to wait for diagnose to go GF? Also he said CD symptoms have to be brought on by eating GF and she wouldnt tolerate bread, etc. My hubby was diagnosed after coming up anemic in routine blood work, in hindsight we saw some signs but nothing severe. Looking back over the past year my daughter has had GI problems frequently and says she is tired alot, but I never thought CD because she Doesn't "look" the part. Should I start her on the CD, or wait? Since my hubby is biopsy diagnosed, would a blood test be sufficent to make a diagnosis in her?? Anyone who has advice I would love to hear it. Sorry I seem to ramble. KIm

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Dear Kim,

NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her daddy has it; she has it. She has some of the major symptoms -- bloating and gastric distress! Start her on the GF diet IMMEDIATELY.

LOTS of doctors are just catching up on this thing. We know more than many of them at this point. Trust your instincts. You don't want her to suffer any more!

Gail in Houston

-- Any advice??

I had my 6 year old to the ER for all of last night. She had intense stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-ray and her colon was taking up the entire left side of her abdomen. Thinking a blockage they did a cat scan, which showed no blockage, just an enormous amount of gas. Doctor brought in 5 other doctors to consult as he thought he was missing something, cause he had never seen an xray like hers with no blockage. I had mentioned my hubby has CD to him, he mentioned following up with my ped and starting her on a GF diet. Arent you suppose to wait for diagnose to go GF? Also he said CD symptoms have to be brought on by eating GF and she wouldnt tolerate bread, etc. My hubby was diagnosed after coming up anemic in routine blood work, in hindsight we saw some signs but nothing severe. Looking back over the past year my daughter has had GI problems frequently and says she is tired alot, but I never thought CD because she Doesn't "look" the part. Should I start her on the CD, or wait? Since my hubby is biopsy diagnosed, would a blood test be sufficent to make a diagnosis in her?? Anyone who has advice I would love to hear it. Sorry I seem to ramble. KIm

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Hi Kim - Your DD sounds just like mine. She started having severe

cramping and we did the ER route several times. Never got very far

on " why's " with that approach. She also had severe fatigue. We

didn't feel the need for a full celiac diagnosis but did test thru

enterolab for gluten sensitivity. She tested positive. GF resulted

in a huge improvement for her. No more GI issues. Her mood is much

more upbeat. She rarely feels the need to sleep past 9 am on the

weekends (I used to have to drag her out of bed by 11am). The best

part is she loves how she feels when off gluten.

I can certainly see the reasons for a definitive diagnosis in

certain cases. It would certainly seem to me that a blood test

would be sufficient for your DD since your hubby is diagnosed. It's

really a personal decision in the end. If you think it will help

her stay on the diet, or if a diagnosis would help you in dealing

with her school or something, then hang in a little longer and do

some testing.

Good luck

Sue in Denver

>

> I had my 6 year old to the ER for all of last night. She had

intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did

an x-

> ray and her colon was taking up the entire left side of her

abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage,

just

> an enormous amount of gas. Doctor brought in 5 other doctors to

consult

> as he thought he was missing something, cause he had never seen an

xray

> like hers with no blockage. I had mentioned my hubby has CD to

him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt

tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in

routine

> blood work, in hindsight we saw some signs but nothing severe.

Looking

> back over the past year my daughter has had GI problems frequently

and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

Since

> my hubby is biopsy diagnosed, would a blood test be sufficent to

make a

> diagnosis in her?? Anyone who has advice I would love to hear

it.

> Sorry I seem to ramble. KIm

>

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Hi Kim - Your DD sounds just like mine. She started having severe

cramping and we did the ER route several times. Never got very far

on " why's " with that approach. She also had severe fatigue. We

didn't feel the need for a full celiac diagnosis but did test thru

enterolab for gluten sensitivity. She tested positive. GF resulted

in a huge improvement for her. No more GI issues. Her mood is much

more upbeat. She rarely feels the need to sleep past 9 am on the

weekends (I used to have to drag her out of bed by 11am). The best

part is she loves how she feels when off gluten.

I can certainly see the reasons for a definitive diagnosis in

certain cases. It would certainly seem to me that a blood test

would be sufficient for your DD since your hubby is diagnosed. It's

really a personal decision in the end. If you think it will help

her stay on the diet, or if a diagnosis would help you in dealing

with her school or something, then hang in a little longer and do

some testing.

Good luck

Sue in Denver

>

> I had my 6 year old to the ER for all of last night. She had

intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did

an x-

> ray and her colon was taking up the entire left side of her

abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage,

just

> an enormous amount of gas. Doctor brought in 5 other doctors to

consult

> as he thought he was missing something, cause he had never seen an

xray

> like hers with no blockage. I had mentioned my hubby has CD to

him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt

tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in

routine

> blood work, in hindsight we saw some signs but nothing severe.

Looking

> back over the past year my daughter has had GI problems frequently

and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

Since

> my hubby is biopsy diagnosed, would a blood test be sufficent to

make a

> diagnosis in her?? Anyone who has advice I would love to hear

it.

> Sorry I seem to ramble. KIm

>

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Share on other sites

Hi Kim - Your DD sounds just like mine. She started having severe

cramping and we did the ER route several times. Never got very far

on " why's " with that approach. She also had severe fatigue. We

didn't feel the need for a full celiac diagnosis but did test thru

enterolab for gluten sensitivity. She tested positive. GF resulted

in a huge improvement for her. No more GI issues. Her mood is much

more upbeat. She rarely feels the need to sleep past 9 am on the

weekends (I used to have to drag her out of bed by 11am). The best

part is she loves how she feels when off gluten.

I can certainly see the reasons for a definitive diagnosis in

certain cases. It would certainly seem to me that a blood test

would be sufficient for your DD since your hubby is diagnosed. It's

really a personal decision in the end. If you think it will help

her stay on the diet, or if a diagnosis would help you in dealing

with her school or something, then hang in a little longer and do

some testing.

Good luck

Sue in Denver

>

> I had my 6 year old to the ER for all of last night. She had

intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did

an x-

> ray and her colon was taking up the entire left side of her

abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage,

just

> an enormous amount of gas. Doctor brought in 5 other doctors to

consult

> as he thought he was missing something, cause he had never seen an

xray

> like hers with no blockage. I had mentioned my hubby has CD to

him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt

tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in

routine

> blood work, in hindsight we saw some signs but nothing severe.

Looking

> back over the past year my daughter has had GI problems frequently

and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

Since

> my hubby is biopsy diagnosed, would a blood test be sufficent to

make a

> diagnosis in her?? Anyone who has advice I would love to hear

it.

> Sorry I seem to ramble. KIm

>

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She needs to stay on gluten until diagnosis - but call the ped's office and

tell them you need a blood draw for the blood test immediately (a visit

isn't needed for this, tell the nurse the ER doc referred you back to them).

Ask for a referral to a pediatric GI at the same time -- this can take some

time to get, but once you have any date, call that office to get on the

standby/cancellation list. It is possible to get hthis all done in a week

or two -- or to let them put you off with thinking it isn't urgent and spend

several months on it, even when you know what tests need to be run.

With kids - if any test is positive and any symptoms present, a biopsy

should be done if a parent is diagnosed (antibody tests have too many false

negatives to use them alone). However, if the test is a very high positive

(TTG over 100), some new research shows that this corresponds almost 100% to

a positive biopsy. The problem is that if she needs a positive biopsy to

keep her gf 5,10,15 or 40 years from now -- this is your one shot at doing

so.

> -----Original Message-----

>

>

> I had my 6 year old to the ER for all of last night. She had intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

> ray and her colon was taking up the entire left side of her abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage, just

> an enormous amount of gas. Doctor brought in 5 other doctors to consult

> as he thought he was missing something, cause he had never seen an xray

> like hers with no blockage. I had mentioned my hubby has CD to him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in routine

> blood work, in hindsight we saw some signs but nothing severe. Looking

> back over the past year my daughter has had GI problems frequently and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

---

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She needs to stay on gluten until diagnosis - but call the ped's office and

tell them you need a blood draw for the blood test immediately (a visit

isn't needed for this, tell the nurse the ER doc referred you back to them).

Ask for a referral to a pediatric GI at the same time -- this can take some

time to get, but once you have any date, call that office to get on the

standby/cancellation list. It is possible to get hthis all done in a week

or two -- or to let them put you off with thinking it isn't urgent and spend

several months on it, even when you know what tests need to be run.

With kids - if any test is positive and any symptoms present, a biopsy

should be done if a parent is diagnosed (antibody tests have too many false

negatives to use them alone). However, if the test is a very high positive

(TTG over 100), some new research shows that this corresponds almost 100% to

a positive biopsy. The problem is that if she needs a positive biopsy to

keep her gf 5,10,15 or 40 years from now -- this is your one shot at doing

so.

> -----Original Message-----

>

>

> I had my 6 year old to the ER for all of last night. She had intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

> ray and her colon was taking up the entire left side of her abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage, just

> an enormous amount of gas. Doctor brought in 5 other doctors to consult

> as he thought he was missing something, cause he had never seen an xray

> like hers with no blockage. I had mentioned my hubby has CD to him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in routine

> blood work, in hindsight we saw some signs but nothing severe. Looking

> back over the past year my daughter has had GI problems frequently and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

---

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She needs to stay on gluten until diagnosis - but call the ped's office and

tell them you need a blood draw for the blood test immediately (a visit

isn't needed for this, tell the nurse the ER doc referred you back to them).

Ask for a referral to a pediatric GI at the same time -- this can take some

time to get, but once you have any date, call that office to get on the

standby/cancellation list. It is possible to get hthis all done in a week

or two -- or to let them put you off with thinking it isn't urgent and spend

several months on it, even when you know what tests need to be run.

With kids - if any test is positive and any symptoms present, a biopsy

should be done if a parent is diagnosed (antibody tests have too many false

negatives to use them alone). However, if the test is a very high positive

(TTG over 100), some new research shows that this corresponds almost 100% to

a positive biopsy. The problem is that if she needs a positive biopsy to

keep her gf 5,10,15 or 40 years from now -- this is your one shot at doing

so.

> -----Original Message-----

>

>

> I had my 6 year old to the ER for all of last night. She had intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

> ray and her colon was taking up the entire left side of her abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage, just

> an enormous amount of gas. Doctor brought in 5 other doctors to consult

> as he thought he was missing something, cause he had never seen an xray

> like hers with no blockage. I had mentioned my hubby has CD to him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in routine

> blood work, in hindsight we saw some signs but nothing severe. Looking

> back over the past year my daughter has had GI problems frequently and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

---

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Even if the tests are negative, you know its in the family, and if a gf

diets solves some of the problems, the tests are irrelevant.

>

>Reply-To: SillyYaks

>To: <SillyYaks >

>Subject: Re: Any advice??

>Date: Sat, 24 Dec 2005 20:30:40 -0600 (Central Standard Time)

>

>Dear Kim,

> NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her

>daddy has it; she has it. She has some of the major symptoms -- bloating

>and

>gastric distress! Start her on the GF diet IMMEDIATELY.

>

> LOTS of doctors are just catching up on this thing. We know more than

>many

>of them at this point. Trust your instincts. You don't want her to suffer

>any more!

>

>Gail in Houston

>

>

>

>-- Any advice??

>

>I had my 6 year old to the ER for all of last night. She had intense

>stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

>ray and her colon was taking up the entire left side of her abdomen.

>Thinking a blockage they did a cat scan, which showed no blockage, just

>an enormous amount of gas. Doctor brought in 5 other doctors to consult

>as he thought he was missing something, cause he had never seen an xray

>like hers with no blockage. I had mentioned my hubby has CD to him, he

>mentioned following up with my ped and starting her on a GF diet.

>Arent you suppose to wait for diagnose to go GF? Also he said CD

>symptoms have to be brought on by eating GF and she wouldnt tolerate

>bread, etc. My hubby was diagnosed after coming up anemic in routine

>blood work, in hindsight we saw some signs but nothing severe. Looking

>back over the past year my daughter has had GI problems frequently and

>says she is tired alot, but I never thought CD because she

>Doesn't " look " the part. Should I start her on the CD, or wait? Since

>my hubby is biopsy diagnosed, would a blood test be sufficent to make a

>diagnosis in her?? Anyone who has advice I would love to hear it.

>Sorry I seem to ramble. KIm

>

>

>

>

>

>

>

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Share on other sites

Even if the tests are negative, you know its in the family, and if a gf

diets solves some of the problems, the tests are irrelevant.

>

>Reply-To: SillyYaks

>To: <SillyYaks >

>Subject: Re: Any advice??

>Date: Sat, 24 Dec 2005 20:30:40 -0600 (Central Standard Time)

>

>Dear Kim,

> NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her

>daddy has it; she has it. She has some of the major symptoms -- bloating

>and

>gastric distress! Start her on the GF diet IMMEDIATELY.

>

> LOTS of doctors are just catching up on this thing. We know more than

>many

>of them at this point. Trust your instincts. You don't want her to suffer

>any more!

>

>Gail in Houston

>

>

>

>-- Any advice??

>

>I had my 6 year old to the ER for all of last night. She had intense

>stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

>ray and her colon was taking up the entire left side of her abdomen.

>Thinking a blockage they did a cat scan, which showed no blockage, just

>an enormous amount of gas. Doctor brought in 5 other doctors to consult

>as he thought he was missing something, cause he had never seen an xray

>like hers with no blockage. I had mentioned my hubby has CD to him, he

>mentioned following up with my ped and starting her on a GF diet.

>Arent you suppose to wait for diagnose to go GF? Also he said CD

>symptoms have to be brought on by eating GF and she wouldnt tolerate

>bread, etc. My hubby was diagnosed after coming up anemic in routine

>blood work, in hindsight we saw some signs but nothing severe. Looking

>back over the past year my daughter has had GI problems frequently and

>says she is tired alot, but I never thought CD because she

>Doesn't " look " the part. Should I start her on the CD, or wait? Since

>my hubby is biopsy diagnosed, would a blood test be sufficent to make a

>diagnosis in her?? Anyone who has advice I would love to hear it.

>Sorry I seem to ramble. KIm

>

>

>

>

>

>

>

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Share on other sites

Even if the tests are negative, you know its in the family, and if a gf

diets solves some of the problems, the tests are irrelevant.

>

>Reply-To: SillyYaks

>To: <SillyYaks >

>Subject: Re: Any advice??

>Date: Sat, 24 Dec 2005 20:30:40 -0600 (Central Standard Time)

>

>Dear Kim,

> NO! Don't WAIT for a diagnosis! You do NOT need it; it's hereditary. Her

>daddy has it; she has it. She has some of the major symptoms -- bloating

>and

>gastric distress! Start her on the GF diet IMMEDIATELY.

>

> LOTS of doctors are just catching up on this thing. We know more than

>many

>of them at this point. Trust your instincts. You don't want her to suffer

>any more!

>

>Gail in Houston

>

>

>

>-- Any advice??

>

>I had my 6 year old to the ER for all of last night. She had intense

>stomach pain, diarrhea, vomiting. My husband is celiac. They did an x-

>ray and her colon was taking up the entire left side of her abdomen.

>Thinking a blockage they did a cat scan, which showed no blockage, just

>an enormous amount of gas. Doctor brought in 5 other doctors to consult

>as he thought he was missing something, cause he had never seen an xray

>like hers with no blockage. I had mentioned my hubby has CD to him, he

>mentioned following up with my ped and starting her on a GF diet.

>Arent you suppose to wait for diagnose to go GF? Also he said CD

>symptoms have to be brought on by eating GF and she wouldnt tolerate

>bread, etc. My hubby was diagnosed after coming up anemic in routine

>blood work, in hindsight we saw some signs but nothing severe. Looking

>back over the past year my daughter has had GI problems frequently and

>says she is tired alot, but I never thought CD because she

>Doesn't " look " the part. Should I start her on the CD, or wait? Since

>my hubby is biopsy diagnosed, would a blood test be sufficent to make a

>diagnosis in her?? Anyone who has advice I would love to hear it.

>Sorry I seem to ramble. KIm

>

>

>

>

>

>

>

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DO NOT WAIT! I had those exact same problems as a child. My Pediatricians kept saying it was IBS and I just had to wait it out. But I remember sitting in the bathroom curled up in a ball because the gas was building up and was extremely painful. My poor parents had no idea what to do. Had I known I was a celiac, I would have gotten on the diet IMMEDIATELY! Unfortunately I did not find out until I was 19 and went through A LOT of pain. Putting her on the diet can never hurt even though she has not been properly diagnosed. It is heriditary and its a good possibility that she has it if your husband does. My best wishes!KIM wrote: I had my 6 year old to the ER for all of last night. She had intense stomach pain, diarrhea, vomiting. My husband is

celiac. They did an x-ray and her colon was taking up the entire left side of her abdomen. Thinking a blockage they did a cat scan, which showed no blockage, just an enormous amount of gas. Doctor brought in 5 other doctors to consult as he thought he was missing something, cause he had never seen an xray like hers with no blockage. I had mentioned my hubby has CD to him, he mentioned following up with my ped and starting her on a GF diet. Arent you suppose to wait for diagnose to go GF? Also he said CD symptoms have to be brought on by eating GF and she wouldnt tolerate bread, etc. My hubby was diagnosed after coming up anemic in routine blood work, in hindsight we saw some signs but nothing severe. Looking back over the past year my daughter has had GI problems frequently and says she is tired alot, but I never thought CD because she doesnt "look" the part. Should I start her on the

CD, or wait? Since my hubby is biopsy diagnosed, would a blood test be sufficent to make a diagnosis in her?? Anyone who has advice I would love to hear it. Sorry I seem to ramble. KIm

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DO NOT WAIT! I had those exact same problems as a child. My Pediatricians kept saying it was IBS and I just had to wait it out. But I remember sitting in the bathroom curled up in a ball because the gas was building up and was extremely painful. My poor parents had no idea what to do. Had I known I was a celiac, I would have gotten on the diet IMMEDIATELY! Unfortunately I did not find out until I was 19 and went through A LOT of pain. Putting her on the diet can never hurt even though she has not been properly diagnosed. It is heriditary and its a good possibility that she has it if your husband does. My best wishes!KIM wrote: I had my 6 year old to the ER for all of last night. She had intense stomach pain, diarrhea, vomiting. My husband is

celiac. They did an x-ray and her colon was taking up the entire left side of her abdomen. Thinking a blockage they did a cat scan, which showed no blockage, just an enormous amount of gas. Doctor brought in 5 other doctors to consult as he thought he was missing something, cause he had never seen an xray like hers with no blockage. I had mentioned my hubby has CD to him, he mentioned following up with my ped and starting her on a GF diet. Arent you suppose to wait for diagnose to go GF? Also he said CD symptoms have to be brought on by eating GF and she wouldnt tolerate bread, etc. My hubby was diagnosed after coming up anemic in routine blood work, in hindsight we saw some signs but nothing severe. Looking back over the past year my daughter has had GI problems frequently and says she is tired alot, but I never thought CD because she doesnt "look" the part. Should I start her on the

CD, or wait? Since my hubby is biopsy diagnosed, would a blood test be sufficent to make a diagnosis in her?? Anyone who has advice I would love to hear it. Sorry I seem to ramble. KIm

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I totally agree!! I had the same exact problems as a child as

did. I too was told that I just had to wait it out...I was

just high strung and needed to relax. As I got older it continued

and I started having sever diarrhea issues. Again went to the Dr.

and was told the same old story. He wanted to put me on anti

anxiety medication because he said that he thought I just worried

too much. ????? I didn't listen, thank goodness. I was finally

diagnosed earlier this year and I am now 28. So, I wouldn't wait I

guess because of my situation. That's just my opinion. Good luck!

Rhiannon

I had my 6 year old to the ER for all of

last night. She had intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did

an x-

> ray and her colon was taking up the entire left side of her

abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage,

just

> an enormous amount of gas. Doctor brought in 5 other doctors to

consult

> as he thought he was missing something, cause he had never seen an

xray

> like hers with no blockage. I had mentioned my hubby has CD to

him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt

tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in

routine

> blood work, in hindsight we saw some signs but nothing severe.

Looking

> back over the past year my daughter has had GI problems frequently

and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

Since

> my hubby is biopsy diagnosed, would a blood test be sufficent to

make a

> diagnosis in her?? Anyone who has advice I would love to hear

it.

> Sorry I seem to ramble. KIm

>

>

>

>

>

>

>

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I totally agree!! I had the same exact problems as a child as

did. I too was told that I just had to wait it out...I was

just high strung and needed to relax. As I got older it continued

and I started having sever diarrhea issues. Again went to the Dr.

and was told the same old story. He wanted to put me on anti

anxiety medication because he said that he thought I just worried

too much. ????? I didn't listen, thank goodness. I was finally

diagnosed earlier this year and I am now 28. So, I wouldn't wait I

guess because of my situation. That's just my opinion. Good luck!

Rhiannon

I had my 6 year old to the ER for all of

last night. She had intense

> stomach pain, diarrhea, vomiting. My husband is celiac. They did

an x-

> ray and her colon was taking up the entire left side of her

abdomen.

> Thinking a blockage they did a cat scan, which showed no blockage,

just

> an enormous amount of gas. Doctor brought in 5 other doctors to

consult

> as he thought he was missing something, cause he had never seen an

xray

> like hers with no blockage. I had mentioned my hubby has CD to

him, he

> mentioned following up with my ped and starting her on a GF diet.

> Arent you suppose to wait for diagnose to go GF? Also he said CD

> symptoms have to be brought on by eating GF and she wouldnt

tolerate

> bread, etc. My hubby was diagnosed after coming up anemic in

routine

> blood work, in hindsight we saw some signs but nothing severe.

Looking

> back over the past year my daughter has had GI problems frequently

and

> says she is tired alot, but I never thought CD because she

> doesnt " look " the part. Should I start her on the CD, or wait?

Since

> my hubby is biopsy diagnosed, would a blood test be sufficent to

make a

> diagnosis in her?? Anyone who has advice I would love to hear

it.

> Sorry I seem to ramble. KIm

>

>

>

>

>

>

>

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Several posters have recommended that a person go on a gf diet with no

diagnosis due to CD being hereditary. Although it is true that the two

identified genes can be passed down, not all the genes involved have even

been identified. The main gene is one that 30% of the population has, while

only 1% has CD - so 29 of 30 with the gene don't have CD (and never will).

There are a number of other causes that should also be ruled out for CD like

symptoms (and it's possible that she has a bad case of the flue - some of

these last several weeks). Going gf without testing means it will be

practically impossible to get a diagnosis and if the child decides to go off

the diet as an adult (due to uncertainty of having CD), the risks of

complication before diagnosis as an adult are much higher (24% have other

autoimmune diseases if diagnosed as an adult, vs. 2% as children). Lifelong

consequences, such as osteoporosis, are also much more common in adults

diagnosed with CD.

-----Original Message-----

Putting her on the diet can never hurt even though she has not been properly

diagnosed. It is heriditary and its a good possibility that she has it if

your husband does.

---

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Several posters have recommended that a person go on a gf diet with no

diagnosis due to CD being hereditary. Although it is true that the two

identified genes can be passed down, not all the genes involved have even

been identified. The main gene is one that 30% of the population has, while

only 1% has CD - so 29 of 30 with the gene don't have CD (and never will).

There are a number of other causes that should also be ruled out for CD like

symptoms (and it's possible that she has a bad case of the flue - some of

these last several weeks). Going gf without testing means it will be

practically impossible to get a diagnosis and if the child decides to go off

the diet as an adult (due to uncertainty of having CD), the risks of

complication before diagnosis as an adult are much higher (24% have other

autoimmune diseases if diagnosed as an adult, vs. 2% as children). Lifelong

consequences, such as osteoporosis, are also much more common in adults

diagnosed with CD.

-----Original Message-----

Putting her on the diet can never hurt even though she has not been properly

diagnosed. It is heriditary and its a good possibility that she has it if

your husband does.

---

[This E-mail scanned for viruses by Declude Virus]

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Several posters have recommended that a person go on a gf diet with no

diagnosis due to CD being hereditary. Although it is true that the two

identified genes can be passed down, not all the genes involved have even

been identified. The main gene is one that 30% of the population has, while

only 1% has CD - so 29 of 30 with the gene don't have CD (and never will).

There are a number of other causes that should also be ruled out for CD like

symptoms (and it's possible that she has a bad case of the flue - some of

these last several weeks). Going gf without testing means it will be

practically impossible to get a diagnosis and if the child decides to go off

the diet as an adult (due to uncertainty of having CD), the risks of

complication before diagnosis as an adult are much higher (24% have other

autoimmune diseases if diagnosed as an adult, vs. 2% as children). Lifelong

consequences, such as osteoporosis, are also much more common in adults

diagnosed with CD.

-----Original Message-----

Putting her on the diet can never hurt even though she has not been properly

diagnosed. It is heriditary and its a good possibility that she has it if

your husband does.

---

[This E-mail scanned for viruses by Declude Virus]

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....I was finally

> diagnosed earlier this year and I am now 28. So, I wouldn't wait I

> guess because of my situation. That's just my opinion. Good luck!

>

> Rhiannon

Knowing nothing about you except your name, I would have guessed you

to be just about that age! It's amazing how many Rhiannons there are

that are probably your age as well.... :)

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Was that about the time Fleetwood Mac's song was popular? :o)

--Trudy San , CA "People who believe in absurdities will eventually commit atrocities." ~Voltaire

-------------- Original message -------------- ...I was finally > diagnosed earlier this year and I am now 28. So, I wouldn't wait I > guess because of my situation. That's just my opinion. Good luck!> > RhiannonKnowing nothing about you except your name, I would have guessed youto be just about that age! It's amazing how many Rhiannons there arethat are probably your age as well.... :)

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Was that about the time Fleetwood Mac's song was popular? :o)

--Trudy San , CA "People who believe in absurdities will eventually commit atrocities." ~Voltaire

-------------- Original message -------------- ...I was finally > diagnosed earlier this year and I am now 28. So, I wouldn't wait I > guess because of my situation. That's just my opinion. Good luck!> > RhiannonKnowing nothing about you except your name, I would have guessed youto be just about that age! It's amazing how many Rhiannons there arethat are probably your age as well.... :)

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Was that about the time Fleetwood Mac's song was popular? :o)

--Trudy San , CA "People who believe in absurdities will eventually commit atrocities." ~Voltaire

-------------- Original message -------------- ...I was finally > diagnosed earlier this year and I am now 28. So, I wouldn't wait I > guess because of my situation. That's just my opinion. Good luck!> > RhiannonKnowing nothing about you except your name, I would have guessed youto be just about that age! It's amazing how many Rhiannons there arethat are probably your age as well.... :)

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All of whom now have that evil song stuck in their heads for the day!!!

> -----Original Message-----

>

> You mustn't be asking people in the right age group. :)

>

> Sue in Denver

>

>

> > >

> > > Was that about the time Fleetwood Mac's song was popular? :o)

> > >

---

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All of whom now have that evil song stuck in their heads for the day!!!

> -----Original Message-----

>

> You mustn't be asking people in the right age group. :)

>

> Sue in Denver

>

>

> > >

> > > Was that about the time Fleetwood Mac's song was popular? :o)

> > >

---

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