Is There Anything I Can Do To Not Trigger Celiac In Newborn?
#1
Posted 15 August 2009 - 06:25 PM
I'm currently 9 weeks pregnant. I actually don't know if I have Celiacs or not (long story, but stupid Dr.'s don't want to test me they claim it's not genetic and I have no need since I have no symptoms. Keep in mind I'm 5'9" and 115lbs soaking wet! But I don't have diarrhea.... LOL!) but my daughter does. She is also DQ2 positive, so obviously it's genetic. My husband and I are pretty darn sure it's from my side of the family and not his (we fit the background, he doesn't, my brother and mother are miraculous "better" after going gluten-free, after my daughter did and they had the same symptoms, etc).
So anyway, my question is, I have 3 kids, 2 are seemingly fine (didn't have it on the standard blood test but we didn't have the genetic test done for them yet) but 1 child has had Celiac since birth. So something triggered it. Was it something I ate? Her birth?
Should I be eating gluten free? Would that make her LESS likely to be born with active Celiac even if she has the gene? Just curious! I wonder b/c my 3rd daughter, when I was pg with her it was when everything started going Whole Grain. I ate TONS of whole wheat, everything was whole grain, etc. With my other 2 I ate whatever the heck I wanted and pretty badly - definetly not overloading on whole wheat everything! I always wonder if that did it?
Thanks for any insight!
Linda
#2
Posted 15 August 2009 - 06:56 PM
The difference is that I'm already gluten free, as it seems my son, who is 4, triggered my celiac in the first place. From what I've researched, babies should be introduced to gluten around 6 months.(American Pediatric Association) However, this is currently being studied by Dr Fasano, to see if waiting longer in children that are at risk for celiac disease helps to prevent it.
http://clinicaltrials.gov/ct2/show/NCT0081...ase&rank=10
My son seems to be fine; is tall for his age, very healthy, etc. I'm probably going to do the same with this one as I did with him... solids around 5/6 months, gradually adding in things. He didn't have gluten until 6 mos at least, not because of celiac (wasn't a thought in my mind), but because of how we added food.
I hope that helps a little
Oh, and celiac is a very common genetic disorder. What is your doctor talking about?????
Oscar Wilde
Gluten free November 2007
IgA Deficient, Neg Bloodwork, Double DQ2 Positive
Dietary and Genetic Diagnosis June 2, 2008
Soy free Jan 09
Celiac.com - Celiac Disease Board Moderator
#3
Posted 16 August 2009 - 03:18 AM
What's funny/interesting about my DD with Celiac is, she reacted to it through my breastmilk. She was a projectile vomiter and I did the elimination diet. Nothing seemed to work. Finally one day my mom said "You know why not try cutting out wheat, I hear some babies are sensitive to it. I did that and BOOM she stopped vomiting. But if I'd have one piece of toast, one slice of pizza she's SCREAM for hours on end and projectile vomit. She was so skinny and got FTT. Needless to say she went on formula at 3 months old and she thrived. Then when we introduced solids she became like she was as a newborn. Losing weight, screaming, vomiting, etc. Anyway, my point being, delaying solids wouldn't have worked with her b/c she is so sensitive just getting it through my breastmilk tore her up!
Honestly, I think I might just bottle feed this if I see ANY signs of projectile vomiting again!
#4
Posted 16 August 2009 - 05:08 PM
- 2005-2007 - 5 miscarriages, no live births
10/2007 - diagnosed with immune system issues + gene related to B/K vitamin malabsorbtion
12/2007 - After 2w gluten-free trial in Nov, back on gluten to complete bloodwork and endoscopy. Bloodwork negative. Endoscopy showed severe inflammation but no flat villi. Went gluten-free for life without "official" celiac diagnosis.
9/2008 - 6th pregnancy ends at 10 due to down syndome. First pregnancy with normal growth on ultrasounds.
1/2009 - 7th pregnancy. So far so good (as of May 2009, amnio clear, it's a girl!) edd 10/28/09
#5
Posted 16 August 2009 - 06:41 PM
1989: I am diagnosed with IBS.
3/08: 8-year-old son diagnosed with Celiac (blood test and biopsy) and allergies to corn, egg whites, soy, peanuts, walnuts, wheat, and clam.
6/08: My Celiac test is negative.
7/08: I go completely gluten free despite negative test and NO MORE IBS SYMPTOMS!!
7/09: My Enterolab gluten sensitivity gene testing results indicate I have one Celiac gene and one gluten sensitivity gene.
8/09: I am diagnosed with Celiac based on gene testing results and positive response to diet.
#6
Posted 16 August 2009 - 07:04 PM
Amyleigh0007, on Aug 16 2009, 06:41 PM, said:
I agree with Amy! If it is in the family and there's even a CHANCE the child could develop celiac down the road, I feel it my duty as a parent to prevent that as much as I possibly can. The diet is scary, and hard at first, but if you're already on it or someone in your house, I would not give the child gluten. I feel it is way easier on a child to be reared without gluten, than for a 33 yo like myself to give it up after a lifetime with it! Once you're used to the diet and the social ramifications of it, it's really no bid deal! Just think of it as preventing eminant (sp?) cancer......why wouldn't you? Up the road, if your child wants the genetic test, or you want them to have it, them you could do that.
Myself: Neg blood tests despite myriad of life-long symptoms. Enterolab testing positive for gluten sensitivity: DQ5DQ5. Currently gluten, dairy, grain, & sugar free and on rotation diet.
5yo dd diagnosed celiac by blood test/biopsy Oct/Nov 2007: DQ2DQ5
7yo dd: neg blood tests, DQ5DQ6
3yo ds: neg blood tests, IgA deficient, DQ5DQ6
21mo dd: DQ2DQ5
DH: Neg blood tests, by deductive reasoning: DQ2DQ6.
#7
Posted 16 August 2009 - 07:29 PM
#8
Posted 16 August 2009 - 08:48 PM
sandy_b, on Aug 16 2009, 07:29 PM, said:
This is an interesting article. There are lots of percentages about the likeliness of a child developing celiac depending on different variables regarding breastfeeding & other feeding patterns, and how early or late gluten was introduced.
My point is that there is 100% chance that your child will NEVER develop celiac disease if you NEVER introduce gluten.
I breastfed my celiac dd for 12 months (gluten containing breastmilk-it DOES get through!), and held off on solids until after she was 6 months old. At that time I had never even heard of the word gluten. She developed celiac. Although she wasn't diagnosed until 2 1/2, I guarantee that she was reacting to gluten from night one in the hospital. She was labeled as "colicky" and when the "colic" didn't subside we were told by the ped that just because she was not like our #1 dd (an angel!), that did not mean something was wrong with her (actually made me feel guilty for wondering) and that this was probably just her "temperament". The ped even joked about her being "stubborn" when she wouldn't eat as an infant & had bouts of constapation when we were trying to potty train her. It is really sad, that she now at 4 still suffers from behvioral issues, I believe all stemming from her first two horrific years of life. She has really good days too, so I am hoping the bad ones will become less and less, and the good ones eventually out-number the bad ones. The effects of gluten makes life really hard for the whole family. This is something, trust me, that you NEVER want to go through. Don't even take the chance. The diet is NOTHING compared to the ramifications of gluten on a potentially sensitive child. I wish I had known about our genes ahead of time for her.
PS I am a HUGE breastfeeding advocate, just make it gluten free milk
Myself: Neg blood tests despite myriad of life-long symptoms. Enterolab testing positive for gluten sensitivity: DQ5DQ5. Currently gluten, dairy, grain, & sugar free and on rotation diet.
5yo dd diagnosed celiac by blood test/biopsy Oct/Nov 2007: DQ2DQ5
7yo dd: neg blood tests, DQ5DQ6
3yo ds: neg blood tests, IgA deficient, DQ5DQ6
21mo dd: DQ2DQ5
DH: Neg blood tests, by deductive reasoning: DQ2DQ6.
#9
Posted 17 August 2009 - 02:40 AM
Jackie - I TOTALLY agree with you about your daughter! You basically just described Violet's first year of life. She was MISERBLE. Labeled "colicy". Then they said she had reflux and we gave her so darn much Zantac. She is still *different* than my other kids. She's STILL clingier, she's STILL more attention needing and I really do think it was from being so miserable her first year of life.
I will definetly BF'd her gluten free for at least the first few months, but I'm not making any garuntees to go 2+ years like I did with my first 2 daughters. I'd say (since I'm not Celiac, that I know of) I'm gluten light. I do mainly eat gluten free but sometimes (b/c I have no reactions) I do get lazy and sometimes grab a sandwich or "real" cereal.....
#10
Posted 17 August 2009 - 04:26 AM
Yes, but there's also a 100 percent chance your child will eventually rebel and try pizza or cake or a Big Mac or whatever.
I'd never consider forcing a child to be gluten-free just because there's a chance he or she might develop celiac. The odds the child not NOT develop celiac are even higher. My youngest is 16 and neither one of mine had ever shown any signs.
richard
#11
Posted 17 August 2009 - 09:25 AM
lovegrov, on Aug 17 2009, 08:26 AM, said:
I'd never consider forcing a child to be gluten-free just because there's a chance he or she might develop celiac. The odds the child not NOT develop celiac are even higher.
richard
I couldn't agree more. Being the celiac in my house, I do know what gluten can do. I lived it. My husband knows what gluten can do. We don't wish it on our children, but I can't imagine trying to force a restricitve diet on my child with no medical/dietary basis. But, you can believe that at the first sign of anything, I would have my kid(s) go gluten-free in a second. It's a sticky situation and a tough decision to make.
Oscar Wilde
Gluten free November 2007
IgA Deficient, Neg Bloodwork, Double DQ2 Positive
Dietary and Genetic Diagnosis June 2, 2008
Soy free Jan 09
Celiac.com - Celiac Disease Board Moderator
#12
Posted 17 August 2009 - 06:32 PM
lizard00, on Aug 17 2009, 09:25 AM, said:
I do agree with what you two are saying about not forcing the diet on a teen-ager, I mean you probably couldn't anyway. I was more referring to when they are babies &/or elementary age children. I think it is our jobs as parents to make decisions for them until they are old enough to make informed decisions themselves. It just makes me nervous to wait for "the first sign" when there seem to be many that suffer in silence, or are asymptomatic. I wonder if a teenager would necessarily want to tell mom & dad or dr. that they have d or c.
Myself: Neg blood tests despite myriad of life-long symptoms. Enterolab testing positive for gluten sensitivity: DQ5DQ5. Currently gluten, dairy, grain, & sugar free and on rotation diet.
5yo dd diagnosed celiac by blood test/biopsy Oct/Nov 2007: DQ2DQ5
7yo dd: neg blood tests, DQ5DQ6
3yo ds: neg blood tests, IgA deficient, DQ5DQ6
21mo dd: DQ2DQ5
DH: Neg blood tests, by deductive reasoning: DQ2DQ6.
#13
Posted 31 January 2010 - 07:34 AM
lovegrov, on 17 August 2009 - 04:26 AM, said:
Yes, but there's also a 100 percent chance your child will eventually rebel and try pizza or cake or a Big Mac or whatever.
I'd never consider forcing a child to be gluten-free just because there's a chance he or she might develop celiac. The odds the child not NOT develop celiac are even higher. My youngest is 16 and neither one of mine had ever shown any signs.
richard
I completely disagree that there is a 100% chance the child would rebel. Why would they rebel if they never feel deprived? I've been gluten free for almost 4 years and honestly have found so many awesome gluten-free versions of foods I never thought I could eat again that most of the time the diet doesn't bother me. If the child is gluten-free from birth, they know nothing else. They'd be more likely to rebel or cheat if they ate gluten for a few years and then had to give it up. Sure maybe for some kids the curiosity would get the better of them, but you can't make that claim about every single child in the world.
#14
Posted 31 January 2010 - 07:53 AM
Those first few months (at 27 years old) were the hardest of my life. Not only was it difficult to learn the diet, but it was extremely difficult mentally and emotionally. I am desperate to protect my daughter from having to deal with that... at any age. I'm especially concerned she could develop it young where she wouldn't fully understand what was happening and why she suddenly wouldn't be able to eat her favorite things. Plus the physical symptoms of the disease are so horrible that I would NEVER want her to go through them. I'm kind of liking one idea someone mentioned in this thread about having the child be gluten free until they're much older and then give them the option of trying gluten. At least by that point they would understand it, and be able to make an informed decision. Plus, if they have a reaction, they could switch back to gluten-free without feeling that overwhelming sense of loss and deprivation because they would already know the diet.
Because I've been gluten-free for almost 4 years, I feel pretty well educated on what gluten-free options are out there now, and more restaurants and manufacturers are coming out with gluten-free versions of things all the time. I don't feel starting a child gluten-free from birth as a negative thing. I'm confident if I were to go this route, she would never be deprived of all the yummy treats her friends would have; she would just have a different version. I also think that since we'd be sharing this diet, it would be easier for her to accept and grasp. I would think a child having to be the only one in the family needing to change their diet would be very isolating and would make the transition much more difficult. I know, because isolation is a very common feeling when you're surrounded by family and friends who can eat whatever they want, and you have to sit there and just watch.
#15
Posted 31 January 2010 - 09:40 AM
Ange7894, on 31 January 2010 - 07:34 AM, said:
They'll rebel because they want to do what "they're not supposed to". It's nothing to do with feeling deprived or not, it's just the lure of the forbidden fruit. Sure, it probably won't happen until the tween or teen years, and yeah, maybe not 100% chance, but 99% (no, no, no particular study on this one, but I'm sure you can find studies on other forms of teen rebellion). Rebellion has nothing to do with deprivation - it has to do with kids (at different ages, there's a "rebellion" phase at two years old too!) trying to find out how much control and power they have over their own environment, how much power they have to make their own decisions. They will find something to rebel about, regardless of how not-deprived they feel.)
The thing is, you can have your kid be gluten free from birth, but their world will not be gluten free. They will see their friends have tasty looking, and tasty smelling, things that have gluten. They'll try them, and as they get older, they'll "rationalize" it by saying you don't know they have to eat gluten free. Again, every single one? No. But the odds are FAR more likely than not.
My current plan is to leave gluten out of the picture for at least a year. While studies so far suggest that the optimum time frame to introduce wheat is between 4 and 7 months, I don't plan on introducing solids that early, and I plan on introducing things slowly. I'd like the child to be able to communicate, in some fashion, how they feel in a manner other than crying or screaming. (I'm going to try to teach baby sign language, so perhaps that will let us communicate earlier, perhaps not. We'll see. Maybe it'll be around two years before I introduce it. I think it will really depend on the kid.)
But I also want to introduce it at a time when things are still *mostly* in my control. Waiting until after the kid has started school, or is regularly at friends' houses makes it nearly impossible to determine, through dietary testing, if gluten is really the problem - since the environments are completely uncontrolled. If I'm starting gluten free, and then try adding it later, I doubt there will ever be enough gluten in her body to register reliably on a test, unless she decides (along with us) to eat gluten long enough for a test. So, I anticipate dietary testing is going to be our main evidence for a while.
Inconclusive Blood Tests, Positive Dietary Results, No Endoscopy
G.F. - September 2003; C.F. - July 2004
Hiker, Yoga Teacher, Engineer, Painter, Be-er of Me
Bellevue, WA

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