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

Marmite!


Mateto

Recommended Posts

Mateto Enthusiast

...and of course Irish.

How do you enjoy it? Or better yet....CAN you eat it? It's supposed to be gluten-free, and it doesn't bother me....yet, but how 'bout you?

  • 2 weeks later...

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



Celiac.com Sponsor (A8-M):



anabananakins Explorer

I'm australian and therefore used to be a happy little vegemite... alas, no more (vegemite is not gluten free) I'm not bothering witht the gluten free versions because in my experience, the type of spread you eat (marmite, vegemite etc) depends on what you were given as a little kid and all the others taste awful! I used to love it on vita wheat biscuits with butter, when you squeezed them together they made little worms ;-) I also loved it on toast. Vegemite is now one of those childhood things that I'll never ever have again... but I have fond memories so I'm ok about it :P

Mateto Enthusiast

Vegemite isn't gluten free? That's another difference from Marmite. Marmite is, at least as far as I know. But I know what you mean. For me, just looking at the marmite picture brings a lot of nostalgia!

anabananakins Explorer

I'm pretty sure it's an extract from barley. There is a gluten free version though (made by another company)

Mateto Enthusiast

I thought they were both yeast extracts...so Vegemite is not. I have to look for the gluten free version, now I'm curious!

Saz Explorer

I thought they were both yeast extracts...so Vegemite is not. I have to look for the gluten free version, now I'm curious!

I'm not sure where you are from but you need to be very very careful with MARMITE. Marmite sold in Australia made by sanitarium is NOT gluten free, this version is sold in a large jar with a orange lid. However the English version of Marmite which is sold in some supermarkets here is gluten free. This version is in a small boulbus shaped jar with a yellow lid. To avoid confusion with the other sort, the english one has been rebranded as Our Mate in most Australian stores. There are however some shops, such as lolly shops who it labeled marmite.

There is a gluten-free spread called mightymite which is meant to be like vegemite. Personally I buy the english marmite becuse I like it better.

Hope I haven't made this more confusing for anyone.

Greyhound Rookie

Spread THICKLY :D

Haven't tried it since going gluten free but I've heard it's fine.


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



Celiac.com Sponsor (A8-M):



auzzi Newbie

Freedom Foods Vege Spread is a gluten-free vegemite replacement.

Three333Threes Mightymite is a gluten-free vegemite replacement.

Vegemite is made from yeast grown on barley and barley malt extract.

Marmite contains derivatives of barley and wheat.

Greyhound Rookie
Marmite contains derivatives of barley and wheat.

I thought Marmite was gluten free in the UK but I might be wrong. I must buy a copy of the food directory.

Saz Explorer

I thought Marmite was gluten free in the UK but I might be wrong. I must buy a copy of the food directory.

Unless it has changed in the last month or two it is. As I mentioned in a previous post there is a product sold in Australia called Marmite but this slightly different to the UK version and not gluten free.

Remember when posting about a particular product it is often helful to add in which country you are in. This helps to avoid confusion as in the above case there can be different products that share the same name, or the product may different ingredients in another country. A good example of this is M&Ms been gluten free in the US but not in Australia.

beebs Enthusiast

I am a promite girl, it is the only thing I truly miss, with sweet and sour rye, lashings of butter and just a thing spread of promite - my all time favourite comfort food:(

beebs Enthusiast

This thread just inspired me to email masterfoods about promite - haha!

anabananakins Explorer

Beebs, are you from Victoria? In my family the NSW raised kids were vegemite kids, but the victorian branch of the family were promite kids.

I hope for you that it's gluten free!

beebs Enthusiast

NSW!

mushroom Proficient

Thank goodness I could never stomach any of the "mites" as a kid - a cheese and marmite sandwich was an automatic trade :rolleyes:

  • 2 weeks later...
Mateto Enthusiast

I'm not sure where you are from but you need to be very very careful with MARMITE. Marmite sold in Australia made by sanitarium is NOT gluten free, this version is sold in a large jar with a orange lid. However the English version of Marmite which is sold in some supermarkets here is gluten free. This version is in a small boulbus shaped jar with a yellow lid. To avoid confusion with the other sort, the english one has been rebranded as Our Mate in most Australian stores. There are however some shops, such as lolly shops who it labeled marmite.

There is a gluten-free spread called mightymite which is meant to be like vegemite. Personally I buy the english marmite becuse I like it better.

Hope I haven't made this more confusing for anyone.

Ah, I see :)

You can't get Vegemite here, so I dunna haveta worry. I do buy the one with yellow lid, pot-belly.

But I love it, though it does take a while to finish off a jar, because I like it subtly, not thickly, though if I did spread it thickly I wouldn't complain :P

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    2. - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

    3. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

    4. - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

    5. - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748

    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • cristiana
      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac. (This was the same GP who said Dad didn't have dementia, when months before one of his colleagues suspected it and told me Dad must be diagnosed).  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.