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

Well, It Figures!

Canadian Karen

Recommended Posts

Canadian Karen Community Regular
Canadian Karen
Posted

I posted before about the one thing that I most mourned when I had to go gluten free was Clamato Juice because I used to LOVE having my weekend Caesar (it's a Canadian concoction with vodka, clamato juice, worshesthire sauce, tabasco sauce and celery salt, sounds weird, but it is delicious!!!!) Anyway, I almost cried when I e-mailed Motts and they replied that it was NOT gluten free. :(

I was at the A & P supermarket a couple of weeks ago and read the ingredients on their name brand clam juice. It was different than Motts so I thought, "Hey, maybe........." :rolleyes: I e-mail them and this is a reply:

Dear Mrs.

Our Corporate Brands Department has informed us that the Master Choice Tomato Clam Cocktail Regular does not contain "Gluten" 1.89L. :lol::lol::lol: But, the product will be updated shortly and unfortunately the recipe will contain gluten. The label will be updated at that time to reflect the formulation change. :angry:

Thank you for your patience.

Regards,

Karen Knight

Customer Care Specialist

A&P Canada

1-877-763-7374

:angry:

I have gone out and purchased a supply of bottles so at least I can have Caesars for awhile!!!!!

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

Celiac.com Sponsor (A8-M):


celiac3270 Collaborator
celiac3270
Posted

I don't get it...why do they have to change the formula? It just doesn't make sense to me that they have to add wheat or another form of gluten to the product. Oh, well...stock up! Maybe temporarily clear out one of the kids' bedrooms so you can stack it up :lol:

FaithInScienceToo Contributor
FaithInScienceToo
Posted

Hi there, Karen,

I just wanted to tell you that I enjoyed reading your post...seems that you are in touch with your feelings about all of this...

One thing I am learning is that I MUST keep applauding myself for continuing to accept that liife is diffferent now...

I am different...healthier...and that's all that matters...

Food is food...there will always be some great things that I can eat...

But, health is health...

Food now only REALLY matters to me if I know it won't hurt me...

I'm glad that you will get a little 'withdrawal time' from your favorite drink...perhaps you can find a new favorite that is 100% safe for you? Maybe even someone you'll like even more?

Love, Gina

:)

Canadian Karen Community Regular
Canadian Karen
Posted
  • Author

Hi Gina!

Well, the way I figure it, ranting and raving over the unfairness of this disease is not going to change one crumb..... and since one of my continuing symptoms is fatigue (some days much worse than others......), I am not going to use up any energy in being angry at the situation - I don't have much energy to go around!!!!

:D

Actually, I have pretty well gotten used to this diet - I don't even think twice about things I used to have all the time before (except my Caesar, that is!!!!) <_<

Karen

stef-the-kicking-cuty Enthusiast
stef-the-kicking-cuty
Posted

@ Karen, maybe you could stock up a lot of these bottles. Then buy the ingredients and try to mix it on your own. And then just always go back and forward and compare, until you mixed it with the "right" taste of the original. I know, things like that can make you angry. It would have made me a lot angry, too. But isn't that a good idea?

Hugs, Stef

Canadian Karen Community Regular
Canadian Karen
Posted
  • Author

I'm already a pro (I am a Caesar connoisseur :D ) But because of the fact that the main ingredient (the clam juice) was off limits to me, I could no longer make my beloved "weekend drink"..... After a long week, there was nothing better than having a weekend bbq in the backyard and have a nice cold Caesar drink with it!! B)

Oh well, at least I should be able to stock up enough to last me through this summer (I wonder how long of a shelf life they have, how long can I store it before it is no good any more :huh: )

Hey celiac3270, now that we have moved to a house where the girls can have their own rooms, things are much more peaceful in the household..... :P If I put them back together again, there would be World War III for sure!! :o Eileen is into AC/DC and Pink Floyd, guitar lessons, etc. and Rhiannon is still in the Dora the Explorer stage...... Nope, the two don't mix!!!! :lol: Even if the drink was the elixir of life, it's wouldn't be worth it!!!! ;) I can store a bunch in the basement though..... :D

Karen

Archived

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

Go to topic listing

  • 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. knitty kitty
      - knitty kitty replied to Jmartes71's topic in Doctors
      9

      Second chance

      @Jmartes71, Have you tried a naturopathic or holistic doctor? Some posters in the past have commented theirs were more helpful than mainstream doctors.
    2. knitty kitty
      - knitty kitty replied to HectorConvector's topic in Related Issues & Disorders
      330

      Terrible Neurological Symptoms

      @HectorConvector, Have you tried taking 500 mg of the Thiamine Mononitrate that you have left? Thiamine Mononitrate may not be as helpful as other forms of thiamine, but since that's what you have on hand. Thiamine is safe and nontoxic even at high doses needed to correct thiamine deficiency. No harm in trying it. Neuroplastic...
    3. HectorConvector
      - HectorConvector replied to HectorConvector's topic in Related Issues & Disorders
      330

      Terrible Neurological Symptoms

      This may seem non-relevant but I thought I'd add it here anyway to see what anyone thinks. Many might dismiss it but that's OK. I went through the entire history of this condition from its onset in 2010 or so, including the things that flare it up, and the timeline of what made it worse, the medications that worked and didn't, in ChatGPT (rolleyes I...
    4. HectorConvector
      - HectorConvector replied to HectorConvector's topic in Related Issues & Disorders
      330

      Terrible Neurological Symptoms

      So I've been eatin no carbs in the evening and only a bit for my lunch so a big reduction. Well, made no difference, in fact it's actually got even worse. So everything I do makes it get worse. I said this to the doctor. He said he definitely thinks it's a neuroplastic pain condition where I've sensitized my nerves to max volume and now the pain has outgrown...
    5. Jmartes71
      - Jmartes71 replied to Jmartes71's topic in Doctors
      9

      Second chance

      Im not a doctor and my term isnt right.All I know is I had what ever lovely procedure I know I had it in down the throat and the bottom biopsy. Im tired of and not feeling well and my blood looks fabulous though STULL HLA-DQ2 Positive and past biopsy Positive. Dealing with this is literally insane im begging for help.im at the point where just what ever
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      133,671
    • Most Online (within 30 mins)
      7,748
    brad Mccarroll
    Newest Member
    brad Mccarroll
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):

  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):

  • Who's Online (See full list)

    • There are no registered users currently online

  • Upcoming Events

  • Posts

    • knitty kitty
      Second chance

      By knitty kitty · Posted

      @Jmartes71, Have you tried a naturopathic or holistic doctor?  Some posters in the past have commented theirs were more helpful than mainstream doctors.  
    • knitty kitty
      Terrible Neurological Symptoms

      By knitty kitty · Posted

      @HectorConvector,  Have you tried taking 500 mg of the Thiamine Mononitrate that you have left?   Thiamine Mononitrate may not be as helpful as other forms of thiamine, but since that's what you have on hand.    Thiamine is safe and nontoxic even at high doses needed to correct thiamine deficiency.   No harm in trying it. Neuroplastic changes in the brain may be caused by thiamine deficiency.   These changes can be seen in Wernicke's encephalopathy and Korsakoff's syndrome, Alzheimer's and Parkinson's. I googled "Neuroplastic Sensitization syndrome and thiamine pubmed" and see for yourself what it says.   Try taking 500 mg Thiamine Mononitrate and look for health changes.
    • HectorConvector
      Terrible Neurological Symptoms

      By HectorConvector · Posted

      This may seem non-relevant but I thought I'd add it here anyway to see what anyone thinks. Many might dismiss it but that's OK. I went through the entire history of this condition from its onset in 2010 or so, including the things that flare it up, and the timeline of what made it worse, the medications that worked and didn't, in ChatGPT (rolleyes I know lol)  and supplied it with all the clinical evidence I've had from tests etc.... After hours of "discussing" with it and finding research it "concluded" it's a chronic neuroplastic sensitization syndrome but of course said I should only get a proper diagnosis from a  doctor. When I saw the doctor on 9th February because this got worse he looked through all my medical history and the course of the "condition". I didn't tell him I'd used ChatGPT or mention what I thought it is because I still don't really know until I have a formal diagnosis. He came with the same conclusion as ChatGPT. Just thought it was an interesting co-incidence perhaps. As for myself, I'm not forming any conclusions til I can really know exactly what's happening and why and what stops it. Only then can I truly know.
    • HectorConvector
      Terrible Neurological Symptoms

      By HectorConvector · Posted

      So I've been eatin no carbs in the evening and only a bit for my lunch so a big reduction. Well, made no difference, in fact it's actually got even worse. So everything I do makes it get worse. I said this to the doctor. He said he definitely thinks it's a neuroplastic pain condition where I've sensitized my nerves to max volume and now the pain has outgrown the medication max dose even though there is nothing physically wrong with my body. A bit earlier I had violent shocking evil burning nerve pain that made me nearly pass out and want to die again, also noticed this seems to be associated with sudden water retention. I've made hardly any pee in nearly 12 hours and despite drinking loads. Mouth is super dry. I am getting the "correct" sort of this when I've finished the current ones, so not long now. Can only get it on the internet here. Then I can say how it might change anything.
    • Jmartes71
      Second chance

      By Jmartes71 · Posted

      Im not a doctor and my term isnt right.All I know is I had what ever lovely procedure I know I had it in down the throat and the bottom biopsy. Im tired of and not feeling well and my blood looks fabulous though STULL HLA-DQ2 Positive and past biopsy Positive. Dealing with this is literally insane im begging for help.im at the point where just what ever 
×
×
  • 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.