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

Flu Shot?


silly celiac

Recommended Posts

silly celiac Rookie

I just signed up to get a flu shot through work next month. It didn't hit me until later that perhaps it might not be safe...? This will be my first flu season gluten-free, so I hadn't even considered it until now! Does anyone know offhand if flu shots are gluten-free?


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



Celiac.com Sponsor (A8-M):



jerseyangel Proficient

Flu shots are gluten-free. :)

uclangel422 Apprentice

They do affect people who are sensitive to eggs though, so watch out for that.

silly celiac Rookie

YAY!!! Thank you! :D

silly celiac Rookie

Eggs aren't a problem for me... yet... that I know of....

Fiddle-Faddle Community Regular

Be aware that most flu shots contain MERCURY--a known neurotoxin that has been banned in all over-the-counter products for years, but is still present in some vaccines. There does seem to be a link with celiac and mercury toxicity.

You can request a mercury-free shot--it will come in an individual-dose ampule without preservatives, and it will be more expensive. If you are getting the shot through your place of work, or at your pharmacy, the mercury-free shot is not likely to be available. I believe they are only available through your doctor, but it never hurts to ask.

If they tell you that the shot does not contain thimerosal, but it comes out of a multi-use vial, then they are either wrong or lying. Same thing if they tell you it's too small an amount to be harmful.

bbuster Explorer

Last year my kids' school began offering the nasal spray flu vaccine (I think it is called FluMist) and in the instructions it said it was not recommended for persons with any autoimmune disorders. I checked with my son's pediatrician and she advised against the FluMist but said he could have a regular flu shot no problem, so that's what we did.


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular

There does seem to be quite a bit of controversy over whether vaccines ought to be recommended for people with autoimmune disorders, especially vaccines for diseases that are usually not dangerous.

I don't think it's an easy call, at least for really devastating illnesses like polio. There are valid arguments on both sides. But flu--??? I know it can be deadly for the weak and elderly--but it seems that that same group is highly susceptible to very bad reactions to the vaccines, too (as are people with autoimmune disorders).

The best I can say is, do LOTS of research, on both sides of the issue.

Franceen Explorer

Last year I got the FluMist from my place of work. I work for a military unit (but I'm a civilian) and they set up a table at the front entrance and everyone (I mean EVERYONE) got a FluMist. They didn't even ask for names or signatures. I found out later that it wasn't FDA approved for people over 45 (I'm 55 and the guy behind me had to be in his 60s). -I also researched it afterwards and found out that it's a live virus vaccine (versus a "killed virus") and that the rate of reactions to it is higher. Well, true. All the people in my group felt sickish the next day (headache-ish, fever-like, yukky) and also on the 2nd day. Some more than others (even young healthy males!).

I DID go ask about Gluten and it is gluten free and there were no FDA warnings for autoimmune disease people.

I felt fine the 3rd day and did not get the flu! So, if they make us do it again this year, I'd prefer the shot, but will do the FluMist without qualms.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,130
    • Most Online (within 30 mins)
      7,748

    Tony White
    Newest Member
    Tony White
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      So you're saying that you think you should have severe intestinal damage since you've had the symptoms so long?   DGP IgG antibodies are produced in response to a partial gluten molecule.  This is different than what tissue transglutaminase antibodies are  produced in response to.   TTg IgA antibodies are produced in the intestines in response to gluten.  The tTg IgA antibodies attack our own cells because a structural component in our cell membranes resembles a part of gluten.  There's a correlation between the level of intestinal damage with the level of tTg antibodies produced.  You are not producing a high number of tTg IgA antibodies, so your level of tissue damage in your intestines is not very bad.  Be thankful.   There may be reasons why you are not producing a high quantity of tTg IgA antibodies.  Consuming ten grams or more of gluten a day for two weeks to two months before blood tests are done is required to get sufficient antibody production and damage to the intestines.  Some undiagnosed people tend to subconsciously avoid lots of gluten.  Cookies and cakes do not contain as much gluten as artisan breads and thick chewy pizza crust.  Anemia, diabetes and thiamine deficiency can affect IgA antibody production as well.   Do you carry genes for Celiac?  They frequently go along with EDS.
    • rei.b
      I was tested for celiac at the same time, so I wasn't taking naltrexone yet. I say that, because I don't. The endoscopy showed some mild inflammation but was inconclusive as to celiac disease. They took several biopsies and that's all that was shown. I was not given a Marsh score.
    • knitty kitty
      Food and environmental allergies involve IgE antibodies.  IgE antibodies provoke histamine release from mast cells.   Celiac disease is not always visible to the naked eye during endoscopy.  Much of the damage is microscopic and patchy or out of reach of the scope.  Did they take any biopsies of your small intestine for a pathologist to examine?  Were you given a Marsh score? Why do you say you "don't have intestinal damage to correlate with lifelong undiagnosed celiac disease"?   Just curious.  
    • rei.b
      I was tested for food allergies and environmental allergies about 7 months before I started taking Naltrexone, so I don't think that is the cause for me, but that's interesting!  The main thing with the celiac thing that is throwing me off is these symptoms are lifelong, but I don't have intestinal damage to correlate with lifelong undiagnosed celiac disease.
    • trents
      Welcome to the forum, @Kara S! Warrior bread is a grain free bread product. Google it. There are commercial mixes available, I believe, Youtube videos and many recipes. 
×
×
  • 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.