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Vitamins

mouth

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mouth Enthusiast
mouth
Posted

My daughter has just graduated from kids vitamins and now i need a regular multi vitamin. Her peds. said to use 1 a day, but i heard that it IS NOT gluten-free.

Can somebody please help me?

I would greatly appreciate it.

thank you so much

lynn

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lfij Newbie
lfij
Posted

My daughter has just graduated from kids vitamins and now i need a regular multi vitamin. Her peds. said to use 1 a day, but i heard that it IS NOT gluten-free.

Can somebody please help me?

I would greatly appreciate it.

thank you so much

lynn

i will get back to you but centrum makes one that is gluten-free i just dont have the bottle in front of me to tell you which one it is (I take it), and im' sure there are tons of others. i will reply tommorow and im sure others will before me.

tarnalberry Community Regular
tarnalberry
Posted

I've been using Rainbow Light's women's formula, which I'm happy with, but it might be a bit big for your daughter.

tiffjake Enthusiast
tiffjake
Posted

Not sure if they have one for kids, but all of the GNC stuff that I get is gluten-free and most is cf too.

mouth Enthusiast
mouth
Posted
  • Author
i will get back to you but centrum makes one that is gluten-free i just dont have the bottle in front of me to tell you which one it is (I take it), and im' sure there are tons of others. i will reply tommorow and im sure others will before me.

Thanks very much for your help. she is 13 but very small. But dr says reg. vitamins are ok

mouth Enthusiast
mouth
Posted
  • Author
Not sure if they have one for kids, but all of the GNC stuff that I get is gluten-free and most is cf too.

On another connected subject, do you have a contact address, phone or email for Entero Labs? I can not seem to get one here in NY and my daughters blood work was never sent there!!!!

They have been doing it in house at the hospital, and the #'s aren't even exact!

Thanks much

:D

Lynn

jmd3 Contributor
jmd3
Posted

My daughter has just graduated from kids vitamins and now i need a regular multi vitamin. Her peds. said to use 1 a day, but i heard that it IS NOT gluten-free.

Can somebody please help me?

I would greatly appreciate it.

thank you so much

lynn

My daughter takes Ar*bonne gluten free vitamin chews for teens, but they also have a special gluten free one for small children - called

ASN HYBRIDS - Daily Powder Punch for Kids A great-tasting power punch drink mix for kids.

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mouth Enthusiast
mouth
Posted
  • Author
My daughter takes Ar*bonne gluten free vitamin chews for teens, but they also have a special gluten free one for small children - called

ASN HYBRIDS - Daily Powder Punch for Kids A great-tasting power punch drink mix for kids.

Ok, where can I get the Ar*bonne gluten-free vitamins. she is a teen just small for her size. dr had said one a day but they are gluten..

You have some side things on the bottom that I have, but my blood work was negative the drs said. may do more testing.. we also do not know where in the family or which side it came from... We do not talk to her fathers side of the family at all.. One friend of mine said that it is prevalant in Irish blood lines, if that is the case it came from her fathers side. There are alot of med problems in his side of the family inc: MS, autism, learning problems, asmatha, A.D.H.D. AND A.D.D.

GL. and tyvm

what is Hashimoto's? gl

lynn

tiffjake Enthusiast
tiffjake
Posted
On another connected subject, do you have a contact address, phone or email for Entero Labs? I can not seem to get one here in NY and my daughters blood work was never sent there!!!!

They have been doing it in house at the hospital, and the #'s aren't even exact!

Thanks much

:D

Lynn

I went through their website, enterolab.com. It is not a blood test, it is a stool sample test (and cheek swab for the genetic test). My doctors office messed up the blood work too...so I understand that. :)

mouth Enthusiast
mouth
Posted
  • Author
I went through their website, enterolab.com. It is not a blood test, it is a stool sample test (and cheek swab for the genetic test). My doctors office messed up the blood work too...so I understand that. :)

Oh I didn't know that. It wasn't that they made mistakes, it is just that like her number was over a hundred and instead of an exact number they just said over 100. stupid..

ok, i will look into the samples and how to get them there.

thanx much

lynn

codetalker Contributor
codetalker
Posted

Due to additional intolerances, I've been using multi-vitamins and calcium from Kirkman Labs.

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grantschoep Contributor
grantschoep
Posted

I used to buy Centrium, but started reading that they have some chemicals in them that are considered toxic. I can't find the source for that now, so random things on the web, but there was a page about it for awhile. Anyways, I always buy Nature Made. A bit more expensive, but the grocery store here always has the "multi's for Men, multi's for Women" at 2 for 1 price. So I just grab one of each for my wife and I.

jmd3 Contributor
jmd3
Posted
Ok, where can I get the Ar*bonne gluten-free vitamins. she is a teen just small for her size. dr had said one a day but they are gluten..

You have some side things on the bottom that I have, but my blood work was negative the drs said. may do more testing.. we also do not know where in the family or which side it came from... We do not talk to her fathers side of the family at all.. One friend of mine said that it is prevalant in Irish blood lines, if that is the case it came from her fathers side. There are alot of med problems in his side of the family inc: MS, autism, learning problems, asmatha, A.D.H.D. AND A.D.D.

GL. and tyvm

what is Hashimoto's? gl

lynn

It is a thyroid problem, sometimes associated with celiac...however she has not tested postive for celiac, she does better without the gluten.

I can send you an instant message about the vitamins

Both of my parents say it is not them with the gene for celiac...neither will get tested. Dad is diabetic, and mom has auto immune on her side - lupos, lymphoma, etc.... but can't express to them enough to get tested.

mouth Enthusiast
mouth
Posted
  • Author
It is a thyroid problem, sometimes associated with celiac...however she has not tested postive for celiac, she does better without the gluten.

I can send you an instant message about the vitamins

Both of my parents say it is not them with the gene for celiac...neither will get tested. Dad is diabetic, and mom has auto immune on her side - lupos, lymphoma, etc.... but can't express to them enough to get tested.

I'm sorry to hear about your parents. You can email me also. same name @ aol. tyvm lynn

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    • cococo
      11 yo waiting for diagnosis

      By cococo · Posted

      Thanks @trents I'll keep that in mind.
    • trents
      11 yo waiting for diagnosis

      By trents · Posted

      One thing to be aware of is that reactions to gluten can sometimes be more severe after having been gluten free for a significant period of time. Something to think about in connection with a gluten challenge.
    • cococo
      11 yo waiting for diagnosis

      By cococo · Posted

      Hi @trents Thanks for your reply and the clarification on terminology—most appreciated. My GP has referred us to a Paediatric Gastroenterologist, and we're waiting for an appointment. She mentioned they might want to do an endoscopy or run further testing. But that often with children they try to avoid scoping them.  She also said it could take months to get an appointment, which is why she recommended starting a gluten-free diet immediately to see if there's any improvement in his symptoms, growth, and blood tests. I have an appointment in 5 weeks with the Paediatrician (who ordered all the tests)—not the Gastroenterologist. I expect the Paediatrician will also recommend a Gastroenterologist referral for further testing and diagnosis. I understand the reasons for confirming with biopsies. I'm just eager to help him feel better and I don't want to keep him eating gluten for months while waiting for a specialist when it's clearly affecting him. I really appreciate your input on this, especially your thoughts about this pointing to celiac rather than NCGS. Intuitively, it feels that way—he's always been incredibly healthy and strong, but he's suddenly wasting away. We're in Australia, so I'm not sure about benefits, etc. and needing a formal diagnosis. I’ll have to investigate.  If necessary to do a gluten challenge down the track for confirmation I'm happy to cross that bridge when I come to it. Thanks so much for your advice!
    • trents
      11 yo waiting for diagnosis

      By trents · Posted

      Welcome to the forum, @cococo!  So. let me first clarify some terminology. Gluten intolerance is a general term that can refer either to celiac disease or NCGS (Non Celiac Gluten Sensitivity or "gluten sensitivity" for short). Having said that, in common, informal usage there is still a lot of mix up in the use of the terms "gluten sensitivity" and "gluten intolerance".  Elevated DGP-IGG can certainly indicate celiac disease but the IGG tests are considered not quite as specific for celiac disease as are the IGA tests, especially the TTG-IGA. If it were the TTG-IGA that gave a 250 score it would have been grounds for declaring an official diagnosis of celiac disease without further testing in the UK and many European countries. With children, however, because their immune systems are immature, we often see their celiac disease show up in the IGG tests rather than the IGA tests. Has their been any talk about an endoscopy with biopsy of the small bowel lining to confirm or disprove a diagnosis of celiac disease? The endoscopy/biopsy is considered the gold standard of celiac disease diagnosis. Physicians are not eager to do scoping on pediatric patients, however, and try to avoid that unless there is a very good reason for it.  I think to proceed with a gluten free diet experiment at this time is a reasonable approach. If there is improvement in labs, symptoms and growth then it is reasonable to assume that there is celiac disease to blame or at least NCGS. At the end of the day, both conditions require a gluten free diet anyway. But I would also have to say that when looking at the total body of evidence you present, it looks much more like celiac disease than NCGS.  One caution, however, and that is if you are in the UK there are certain government provided benefits that incur from a formal diagnosis of celiac disease. I mention that because some of your spelling suggests that to me.
    • cococo
      11 yo waiting for diagnosis

      By cococo · Posted

      Hi all, I'd love some feedback on my 11 year old son who is waiting for a diagnosis. He has been unwell for about 6 months. His symptoms include: early morning (4/5am) nausea and vomiting, loose bowels, fatigue, headaches, aching legs, persistent dermatitis on cheeks. Recently, I noticed he wasn't growing as expected. After measuring him, we found his height had dropped from above 50th percentile to 25th, and weight from 50th percentile to 5th. I took him to our GP who confirmed he only grew 2cm in the past year and lost weight, and subsequently referred us to a paediatrician. We saw the paediatrician who ordered extremely comprehensive tests (including urine and poo testing, x-ray on wrist, hormones, thyroid, liver, kidney, diabetes checks, etc). While waiting for all results, our GP received some preliminary findings indicating coeliac disease. The GP recommended starting a gluten-free diet and referred us to a paediatric gastroenterologist. Most test results are normal except: Iron levels:  18 (normal range 20-200) Anisocytosis and Microcytosis (abnormal sized red blood cells indicating iron deficiency anaemia) Coeliac-related results: DGP IgG:     >250 (normal <15) DGP IgA:      8 (normal <15) Tissue IgA:   1 (normal <15) Tissue IgG:   1 (normal <15) Genetic markers are present for coeliac A comment was made on the blood tests that total serum IgA would be tested and commented on if below 0.07. There was no comment so I assume it wasn’t that low. While I understand it could be coeliac disease, gluten intolerance, or wheat allergy, his significant growth issues suggest coeliac. The paediatrician won't see me for 5 more weeks (because he's waiting for one more test he did on his chromosomes), but I'm concerned about waiting that long given his symptoms. Clearly he shouldn't be eating gluten regardless of the diagnosis, and I'm keen to help him feel better and start growing again, especially with puberty approaching. The blood tests were extremely comprehensive and ruled out everything except coeliac disease or a strong gluten intolerance. My GP is adamant it must be coeliac because of his symptoms. My GP said, "Don't worry about the chromosome test—that's just precautionary. His blood tests, weight loss, lack of growth, iron deficiency, fatigue, dermatitis, and other symptoms all point to coeliac." Would starting a gluten-free diet now and doing a gluten challenge later be unreasonable? (I do understand the reason to wait for a clear diagnosis, I just want him to feel better. Also, he is homeschooled so I can very much be in control of his food to ensure no cross contamination, etc) Also, does anyone have experience with highly elevated DGP IgG (but normal other results) and testing positive for coeliac? For what its worth, I personally have had many checks for Coeliac over the years and the results are always "unclear". Apparently I'm a complicated case, so I just eat gluten-free. Thanks!
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