• Ads by Google:
     




    Get email alerts Celiac.com E-Newsletter

    Ads by Google:



       Get email alertsCeliac.com E-Newsletter

  • Announcements

    • admin

      Frequently Asked Questions About Celiac Disease   09/30/2015

      This Celiac.com FAQ on celiac disease will guide you to all of the basic information you will need to know about the disease, its diagnosis, testing methods, a gluten-free diet, etc.   Subscribe to FREE Celiac.com email alerts   What are the major symptoms of celiac disease? Celiac Disease Symptoms What testing is available for celiac disease? - list blood tests, endo with biopsy, genetic test and enterolab (not diagnostic) Celiac Disease Screening Interpretation of Celiac Disease Blood Test Results Can I be tested even though I am eating gluten free? How long must gluten be taken for the serological tests to be meaningful? The Gluten-Free Diet 101 - A Beginner's Guide to Going Gluten-Free Is celiac inherited? Should my children be tested? Ten Facts About Celiac Disease Genetic Testing Is there a link between celiac and other autoimmune diseases? Celiac Disease Research: Associated Diseases and Disorders Is there a list of gluten foods to avoid? Unsafe Gluten-Free Food List (Unsafe Ingredients) Is there a list of gluten free foods? Safe Gluten-Free Food List (Safe Ingredients) Gluten-Free Alcoholic Beverages Distilled Spirits (Grain Alcohols) and Vinegar: Are they Gluten-Free? Where does gluten hide? Additional Things to Beware of to Maintain a 100% Gluten-Free Diet What if my doctor won't listen to me? An Open Letter to Skeptical Health Care Practitioners Gluten-Free recipes: Gluten-Free Recipes Where can I buy gluten-free stuff? Support this site by shopping at The Celiac.com Store.

Nutrametrix Supplements
0

3 posts in this topic

Recommended Posts

greed2109    0

Hello, 

 

I recently just joined and find this forum to be very helpful. After two long years of all sorts of weird issues (joint pain, numbness and tingling, acid reflux) and thousands of dollars in medical bills with no answers for my symptoms turns out about 3 weeks ago monday my biopsy and blood test came back positive for Celiac Disease.. FINALLY looks like i may have an answer. 

 

Long story short my doctor is having me take Nutrametrix supplements ( ORAC, OPC-3, B-Complex, Might-a-mins, Aloe Vera Juice, and a Probiotic) To treat the nausea and burning sensation in my gut. Have any of you taken these supplements? Have they helped you? 

 

ORAC

OPC-3                             2x daily empty stomach

Activated-B Complex

 

Nutriclean Probiotic     2x daily before meals 

 

Might-a-mins      after/or before meals or PRN (as needed)

 

Aloe Juice natural flavor     2oz 4-5x as PRN 

Share this post


Link to post
Share on other sites
Ads by Google:
Ads by Google:


Adalaide    361

I'm glad you have an answer, and welcome.

 

After looking up those supplements, my first thought is what stake does your doctor have in the company? If you purchase the cheapest way possible, 90 pills at a time, that is $200 for 45 days of supplements. And that's just the supplements, not the rest! Another $70 for probiotics, plus however many of the others you take. And at $26 a bottle for that aloe juice and 16  2oz servings you'll go through two bottles a week if that means 4-5 times a day as needed. I can tell you what I'd tell my doctor, no matter if I had the money to spend on it or not.

 

There are a lot of supplements and probiotics on the market. Your doctor having a financial stake in the company shouldn't influence which you choose to take. Have you been tested for vitamin deficiencies before you start taking anything or is your doctor just advising a random catch-all? A good B complex is something I see a significant number of people here say they take because they were deficient in B something or other. The ORAC and OPC-3 don't seem to offer any actual benefit, did the doctor provide sound medical reasoning on why you should be taking each of these? They both really seem an awful lot like snake oil to be perfectly honest.

 

I'm sure there will be people along with more knowledge of probiotics and supplements than I have. I have never taken mine in liquid form, I've always taken pills when I take them. I take ones with a USP stamp on them, which means they are independently reviewed by an outside source for quality. Nature Made is a good company and will label on their bottle if they are gluten free or not. It is my go-to company for supplements. I don't take a probiotic so I don't really have any advice on that one.

Share this post


Link to post
Share on other sites
greed2109    0

Thanks for the reply!

 

It was my doctors nurse practitioner who suggested I take those supplements. She was the first person I saw since being diagnosed and my symptoms included joint pain, headaches, numbness tingling, and bad stomach pains from dull to sharp. My GI told me my stomach was severely inflamed and would probably take about 6 months to heal.. Ill assume thats why I'm taking the Aloe Vera? My B-12 is also low at 300 not critical but for someone my age who eats healthy anyway should be around 550-700. The pro biotic and stomach enzymes are to help with digestion and stomach pain (is what i was told) As for the OPC and ORAC.. Looks like body cleansing and maybe some joint relief? I got blood drawn that day and don't understand most of the results but I do know I am not anemic I will get the results Thursday. I was told the Vili being dull and not being able to "pluck" nutrients that solid pills for vitamins would not be a good choice this early on for me. 

 

As for a financial stake.. Their office does sell these products however I did not buy them from their office... I do realize they are very expensive but at this point dealing with pain for 2 years ill do anything to feel better especially since I just got a full time Fire Department job and will be taking my PAT test in a week! So there was Urgency on my part.. I know it wont go away tomorrow but any relief would be great.. 

 

I will be seeing my actual PCP for the first time this Thursday and a nutritionist this Wens. I will update after those appointments. 

 

Thank you,

 

Gregory

Share this post


Link to post
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now

0

  • Forum Statistics

    • Total Topics
      107,921
    • Total Posts
      938,703
  • Member Statistics

    • Total Members
      65,850
    • Most Online
      3,093

    Newest Member
    rachellelnd@gmail.com
    Joined
  • Popular Now

  • Topics

  • Posts

    • Ah yes... dry beans. I am fortunate to live near a plant that only processes beans, pulses and rice (Western Rice Mills if you're on the west coast). I doubt that they test, but I would suspect that the biggest part of the risk with that type of food is in the plant where they pack them, as things like barley pearls and wheat berries are often sold as dried goods and would probably be done on the same lines. I would agree that dry beans could be problematic depending on source. 
    • No, Armour has always been gluten free.  The formulation changed a few years back and during the switch, there was a shortage.  That has long since resolved.  Forest Pharmaceuticals (manufacturer of Armour) was bought out by Activas in 2015.  They increased the price!  Now it is comparable to synthetic.   Imtried to find a good and reputable source about the history of thyroid replacement.  Here is one link -- the story is pretty accurate, but the site is trying to sell you stuff.   https://thyroidpharmacist.com/articles/the-history-of-natural-desiccated-thyroid-medications/  
    • If she is now at a public school, accommodations can be made for disabilities.  Here is a link that explains a 504 plan and an IEP, but you will have to investigate based on your state.   https://www.foodallergy.org/education-awareness/advocacy-resources/section-504-and-written-management-plans https://www.understood.org/en/school-learning/special-services/504-plan/the-difference-between-ieps-and-504-plans http://kidshealth.org/en/parents/504-plans.html https://www2.ed.gov/about/offices/list/ocr/504faq.html i am not very knowledgeable about this subject, so I encourage you to contact your school district for help.  Your doctor might be a good resource too.   You might consider homeschooling until she has been diagnosed and has received treatment.  The Department of Education can direct you to homeschooling resources.  There are lots of wonderful programs out there and you can get financial support.   I wish you all well!  
    • You make a good point about being neurotic. I'm slowly getting better. I guess time will tell. But thank you for the insight.   As far as roommates go, that's a good idea. I've definitely been thinking about that. But these guys are my best friends and the process of getting a new roommate this late in my schooling might be hard. Although, I will keep my eye out for the opportunity. 
    • Hello I understand what you are going thru. My son almost died from going 27 years without figuring out it was gluten and then corn causing all the illness. I brought him to Drs, none of them figured out gluten intolerance. Oh they told us he had everything else. Then as time went on, he found out he has issues with corn. Corn has identical genetic make-up as gluten.  Corn is sneaky and everywhere. Contact the manufactures, ask them if there is a chance of contamination or corn ingredient in their products. My son gets neurological problems when gluten/cornized. Anxiety, obsessive thoughts, can not think. He had to be taken out of school and homeschooled. He just found out the digestive enzymes he was taking contain an enzyme that is grown on barley. Enzymedic basic.  My suggestions for you are, seriously go find another place to live. You need your mind and health to continue school. If you don't and continue living where you are, school will suffer. In your spare time, find out all you can about gluten and what other foods act like gluten in the body. Like I said, corn has the same genetic make up as gluten, some people can not eat rice either. This is something that is doable, it is just becoming very aware of what goes in the mouth. Please find another place to live. You don't need to deal with those jerks, you have enough going on with school and health. There might be other people in your school that are celiac or gluten sensitive. Find them, post notes up, start a newsletter about gluten free lifestyle. I bet there are many people that would welcome that newsletter.  You don't need to do this alone!   You are the most important person in your life, you deserve to feel good and be respected! Stay away from those that don't respect you. Search out those that will.  Eating out is something that can be done, find those places that will work with you. Ask to have burgers or meat cooked on aluminum foil. Fresh veggies, fruits all gluten free. Again, research restaurants in your area willing to work with you. Even call the manager and talk to them. All the best to you!  Hang in there.   
  • Upcoming Events