Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Rainbow Lite Vitamins


gretchen

Recommended Posts

gretchen Rookie

Hi,

I am wondering if anyone has ever researched Rainbow light vitamins? I bought the mulitvite for my husband who has celiac disease. The label states it is gluten free. I question the % of daily value on some of the vitamins for example vitamin B6 is 1250%, B2 1471%, B1 1667%, and K is 125%. All the daily values seem to be extremely high. I have been researching celiac disease ever since my husbands diagnosis and what I have found is the best source of infomation is gleaned from reading this forum. My husbands family doctor does not seem to have much knowledge on celiac disease. In fact, as a nurse, I requested he test my husband for celiac disease. When the blood tests came back negative I insisted on a biopsy. Although the GI doc who did this procedure specializes in celiac spru, I can not get any of the doctors to address the fact that my husband needs to have labs drawm to monitored for such deficiencies as iron, calcium, etc. I requested a consult with a nutritionist and she provided us with some great resources (this web site). When I discussed the need for my husband to take some kind of multivite she suggested we speak with his doctor regarding a "safe choice." Through my research, I have learned we need to read labels and contact manufactures to find out if any product/food is safe. The lists on this web site have been very helpful but I have not found any consistant research regarding what is the best mulivitamin to address the lack of absorption a person recovering from years of damage to the intestine by eating gluten while waiting for a diagnosis. I would think these vitamins are safe for him as they are labeled as "potent, scientific safe, and guarenteed to be gluten free." If anyone can provide me with any information regarding which vitamin deficiencies are common with celiac disease I will be very greatful. My husband was diagnosed approximately 3 months ago and had been doing well since beginning the gluten free diet. Recently he has become ill again and we are now monitoring his food intake much closer and pretty much having him eat fruit, veggies and meats. I do worry, with the amount of vomitting he has done, about the lack of absorbtion of essential vitamins. He has become very fatigued as well. All common syptoms, I know. Again, since I ahve found this forum to be the best source of information, I am turning to the experts for some advice. I thank you in advance for any information you share.

Gretchen


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



tarnalberry Community Regular

from what I have read, and seen here, there isn't a "if you have celiac, you're almost certainly deficient in this". it varies from person to person. while b12, iron, calcium, and magnesium are big hitters, they're just some obvious ones. he can't know without running a blood panel what he's short on, if anything (and it might be none of the above, not all celiacs - even symptomatic ones - are). I use the rainbow light women's multi-vit and food-based calcium, myself, for what it's worth.

missy'smom Collaborator

Rainbow Light products have worked very well for me. I took their Food For Life plant based supplement for years before gluten-free and have been taking the Healthy Family Mulit-vitamin Powder since I went gluten-free.

Lizz7711 Apprentice

If you can't get the doctor to run basic things like iron and B12, time for a new doctor! I'd try to find a holistic MD. Hormones are also important to check on as celiac disease puts extra stress on adrenal and thyroid glands.

I wouldn't worry about B vitamins being high...RDI's are set too low anyway, and if his absorption isnt' good he needs extra anyway. The only one to watch is B6...over 100 -200mg per day some people (like me) can experience numb hands/feet which means you're getting too much. If his B12 and /or iron/ferritin is low...i'd recommend B12 injections (again, ya need a holistic MD).

I'm just now starting to research leaky gut syndrome... I think that is key to healing first and foremost so you may want to also research that....healing the holes in the intestine will help stop the extreme reactions he's having.

take care and good luck,

Liz

Hi,

I am wondering if anyone has ever researched Rainbow light vitamins? I bought the mulitvite for my husband who has celiac disease. The label states it is gluten free. I question the % of daily value on some of the vitamins for example vitamin B6 is 1250%, B2 1471%, B1 1667%, and K is 125%. All the daily values seem to be extremely high. I have been researching celiac disease ever since my husbands diagnosis and what I have found is the best source of infomation is gleaned from reading this forum. My husbands family doctor does not seem to have much knowledge on celiac disease. In fact, as a nurse, I requested he test my husband for celiac disease. When the blood tests came back negative I insisted on a biopsy. Although the GI doc who did this procedure specializes in celiac spru, I can not get any of the doctors to address the fact that my husband needs to have labs drawm to monitored for such deficiencies as iron, calcium, etc. I requested a consult with a nutritionist and she provided us with some great resources (this web site). When I discussed the need for my husband to take some kind of multivite she suggested we speak with his doctor regarding a "safe choice." Through my research, I have learned we need to read labels and contact manufactures to find out if any product/food is safe. The lists on this web site have been very helpful but I have not found any consistant research regarding what is the best mulivitamin to address the lack of absorption a person recovering from years of damage to the intestine by eating gluten while waiting for a diagnosis. I would think these vitamins are safe for him as they are labeled as "potent, scientific safe, and guarenteed to be gluten free." If anyone can provide me with any information regarding which vitamin deficiencies are common with celiac disease I will be very greatful. My husband was diagnosed approximately 3 months ago and had been doing well since beginning the gluten free diet. Recently he has become ill again and we are now monitoring his food intake much closer and pretty much having him eat fruit, veggies and meats. I do worry, with the amount of vomitting he has done, about the lack of absorbtion of essential vitamins. He has become very fatigued as well. All common syptoms, I know. Again, since I ahve found this forum to be the best source of information, I am turning to the experts for some advice. I thank you in advance for any information you share.

Gretchen

Lizz7711 Apprentice
Hi,

I am wondering if anyone has ever researched Rainbow light vitamins? I bought the mulitvite for my husband who has celiac disease.

I've never heard of them, but just looked at some of the products and to me they look pretty good with the amounts of nutrients and types (i.e. using vitamin E with mixed tocopherols, using D3 which is better absorbed that D2). My only problem is they use cyanocobalamin for B12. The best vitamins use methylcobalamin (more expensive to process) because that is the form the body uses it...so it doens't have to be converted from cyanocobalamin to methylcobalamin. One company i'm looking into to buy Gluten-free Casein-free vitamins is Pioneer (saw them on this website)...they use methylcobalamin and other amounts etc. look similar to Rainbow.

I do have a question though...on Pioneer's B-complex, labeled as Gluten free...they have barley grass as an ingredient. Is this ok since it is the grass only...especially since they are advertising gluten free it seems like it must be...but just thought i'd ask!

thanks,

Liz

ravenwoodglass Mentor
I do have a question though...on Pioneer's B-complex, labeled as Gluten free...they have barley grass as an ingredient. Is this ok since it is the grass only...especially since they are advertising gluten free it seems like it must be...but just thought i'd ask!

thanks,

Liz

I know I wouldn't touch it. I think we had a discussion on barley grass not too long ago, you may want to do a search to help you make up your mind.

gretchen Rookie

Thank you all for your responses. I am feeling better about having my husband take these vitamins just knowing others have had success with them.

I am very appreciative of this forum. I have been reading a lot of the posts and have learned a ton. I feel so helpless sometimes when my husband becomes sick and I can not find the source of gluten. There are many challenges to overcome when beginning this diet and I can see how it can take many months to learn all there is to know.

Gretchen


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



holiday16 Enthusiast
Hi,

I am wondering if anyone has ever researched Rainbow light vitamins? I bought the mulitvite for my husband who has celiac disease. The label states it is gluten free. I question the % of daily value on some of the vitamins for example vitamin B6 is 1250%, B2 1471%, B1 1667%, and K is 125%. All the daily values seem to be extremely high. I have been researching celiac disease ever since my husbands diagnosis and what I have found is the best source of infomation is gleaned from reading this forum. My husbands family doctor does not seem to have much knowledge on celiac disease. In fact, as a nurse, I requested he test my husband for celiac disease. When the blood tests came back negative I insisted on a biopsy. Although the GI doc who did this procedure specializes in celiac spru, I can not get any of the doctors to address the fact that my husband needs to have labs drawm to monitored for such deficiencies as iron, calcium, etc. I requested a consult with a nutritionist and she provided us with some great resources (this web site). When I discussed the need for my husband to take some kind of multivite she suggested we speak with his doctor regarding a "safe choice." Through my research, I have learned we need to read labels and contact manufactures to find out if any product/food is safe. The lists on this web site have been very helpful but I have not found any consistant research regarding what is the best mulivitamin to address the lack of absorption a person recovering from years of damage to the intestine by eating gluten while waiting for a diagnosis. I would think these vitamins are safe for him as they are labeled as "potent, scientific safe, and guarenteed to be gluten free." If anyone can provide me with any information regarding which vitamin deficiencies are common with celiac disease I will be very greatful. My husband was diagnosed approximately 3 months ago and had been doing well since beginning the gluten free diet. Recently he has become ill again and we are now monitoring his food intake much closer and pretty much having him eat fruit, veggies and meats. I do worry, with the amount of vomitting he has done, about the lack of absorbtion of essential vitamins. He has become very fatigued as well. All common syptoms, I know. Again, since I ahve found this forum to be the best source of information, I am turning to the experts for some advice. I thank you in advance for any information you share.

Gretchen

The really high RDA's are actually a red flag that the product is synthetic. Basically it falls in the category of using either D2 or D3. While similar the body does not treat them the same. I heard it explained once as it being a mirror image and it's like trying to put a left handed glove on your right hand. Just doesn't fit. Also, one of the key things to look for to see if a vitamin is of good quality is check the Biotin. It's one of the more expensive supplements and if it's not listed at 100% that's a good screening test to see if the vitamin is high quality or not. If you want to contact me from my profile I think I still have some of this information in my files on my computer I could send along to you.

Paulette

Lizz7711 Apprentice

Having worked in a health food store with many "natural" vitamin companies...i've learned that almost all companies, even the most natural among them, use some synthetic vitamins, and there is not necessarily anything wrong with that. However, you do want the best quality, synthetic or not, so you want D3, you want methylcobalamin B12, you want mixed tocopherols for vitamin E, etc.

That said, I always do prefer as organic, food based as possible. I just got a catalog from Dr Mercola (www.mercola.com), and he's got a multivitamin that looks excellent..whole food based, no allergens, no excessive amounts of anything, and most importantly, they are third party tested for integrity by NSF. This is voluntary on the part of the company to be tested by an independent company for quality assurance, and NSF is the best. So I plan myself on trying this multivitamin...might be something to look into.

Liz

The really high RDA's are actually a red flag that the product is synthetic. Basically it falls in the category of using either D2 or D3. While similar the body does not treat them the same. I heard it explained once as it being a mirror image and it's like trying to put a left handed glove on your right hand. Just doesn't fit. Also, one of the key things to look for to see if a vitamin is of good quality is check the Biotin. It's one of the more expensive supplements and if it's not listed at 100% that's a good screening test to see if the vitamin is high quality or not. If you want to contact me from my profile I think I still have some of this information in my files on my computer I could send along to you.

Paulette

  • 3 years later...
Here-we-go-again Newbie

Sooo, I started taking Rainbow Light Men's One. I am pretty sure I got a reaction out of it. Its says on the back "Contains no sugar, lactose/dairy. wheat. gluten or yeast." After reading this I thought it would be OK.

I started getting gas a few hours after I took it, that night I had stomach gurgles, and the next morning all the usual symptoms.

I watch my diet very closely, so I am pretty sure it couldn't have been anything else.

Any thoughts?

-Here_we_go_again...

Looking for answers Contributor

Having worked in a health food store with many "natural" vitamin companies...i've learned that almost all companies, even the most natural among them, use some synthetic vitamins, and there is not necessarily anything wrong with that. However, you do want the best quality, synthetic or not, so you want D3, you want methylcobalamin B12, you want mixed tocopherols for vitamin E, etc.

That said, I always do prefer as organic, food based as possible. I just got a catalog from Dr Mercola (www.mercola.com), and he's got a multivitamin that looks excellent..whole food based, no allergens, no excessive amounts of anything, and most importantly, they are third party tested for integrity by NSF. This is voluntary on the part of the company to be tested by an independent company for quality assurance, and NSF is the best. So I plan myself on trying this multivitamin...might be something to look into.

Liz

I buy a lot of Mercola's products, but never have purchased his vitamin line because they contain a grass...barley maybe? I tried to go look at the label just now so I could report back what was in it but the labels are no longer available. Just wanted to give you a head's up before you order. Yes, they say gluten-free but they still had a grass that concerned me. Just something to look into.

Wait, just found it...wheatgrass in the Multi Plus, nothing in the other. The other one must be new because I don't recall seeing it before. So, I guess one is safe and one is not. :rolleyes:

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,027
    • Most Online (within 30 mins)
      7,748

    EmmaGraceeee
    Newest Member
    EmmaGraceeee
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Scott Adams
      Your experience is both shocking and critically important for the community to hear, underscoring the terrifying reality that cross-contamination can extend into the most unexpected and invasive medical devices. It is absolutely devastating that you had to endure six months of sickness and ultimately sustain permanent vision loss because a doctor dismissed your legitimate, life-altering condition. Your relentless research and advocacy, from discovering the gluten in MMA acrylic to finding a compassionate prosthodontist, is a testament to your strength in a system that often fails celiac patients. While the scientific and medical consensus is that gluten cannot be absorbed through the skin or eyes (as the molecules are too large to pass through these barriers), your story highlights a terrifying gray area: what about a substance *permanently implanted inside the body*, where it could potentially shed microparticles or cause a localized immune reaction? Your powerful warning about acrylic lenses and the drastic difference with the silicone alternative is invaluable information. Thank you for sharing your harrowing journey and the specific, severe neurological symptoms you endure; it is a stark reminder that celiac is a systemic disease, and your advocacy is undoubtedly saving others from similar trauma.
    • Scott Adams
      Those are driving distance from me--I will try to check them out, thanks for sharing!
    • Scott Adams
      I am so sorry you're going through this bad experience--it's difficult when your own lived reality of cause and effect is dismissed by the very professionals meant to help you. You are absolutely right—your violent physical reactions are not "what you think," but undeniable data points, and it's a form of medical gaslighting to be told otherwise, especially when you have a positive HLA-DQ2 gene and a clear clinical picture. Since your current "celiac specialist" is not addressing the core issue or your related conditions like SIBO and chronic fatigue, it may be time for a strategic pivot. Instead of trying to "reprove" your celiac disease to unwilling ears, consider seeking out a new gastroenterologist or functional medicine doctor, and frame the conversation around managing the complications of a confirmed gluten-free diet for celiac disease. Go in and say, "I have celiac disease, am strictly gluten-free, but I am still suffering from these specific complications: SIBO, chronic fatigue, dermatological issues, and high blood pressure linked to pain. I need a partner to help me address these related conditions." This shifts the focus from a debate about your diagnosis to a collaborative plan for your current suffering, which is the help you truly need and deserve to work toward bouncing back.
    • NanCel
      Hello, no I had to have them re done and then used a liner over the top.  Many dentists are not aware of the celiac effects.  Best of luck.   There is other material, yet, very expensive.
    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.