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

National Celiac Organizations


Dwight Senne

Recommended Posts

Dwight Senne Rookie

In a post in this topic entitled "Leaving", some interest was expressed about a national celiac organization to get the word out about Celiac Disease to both doctors and potential patients.

While there are currently several "National" organizations, it is my opinion that they are not getting this job done - either because their focus is in other areas, or because they do not have enough resources.

Another contributing factor is the fact that there are SEVERAL of these organizations and they sometimes are in conflict with each other.

What are your thoughts about this? Do we need still another group? Or should we rally behind one particular group who has this as a primary mission? Is this issue (getting the word out) the main issue that needs attention?

Would greatly appreciate any input!


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



Celiac.com Sponsor (A8-M):



debmidge Rising Star

I think you're right and maybe the groups should merge and then make a TV commercial about celiac disease.

I've been thinking about writing a one page flier about celiac disease, just basic true medical text book info -- nothing but the facts -- and passing the flier out at the local supermarket parking lot, or under the wiper blades of cars (like the advertisements you get when you are in the store) or anywhere. I'd mention how one "gets" it, what tests are done for it, what you do for it (diet), why it's a difficult diet to follow and why you should be concerned (i.e., many people have it and don't know, it could lead to lymphoma of intestine, you can develop it at any point in life if you have the gene for it, and you or your loved ones could get it one day & then you'll want to be able to have resources, like gluten free foods, available).

All celiacs are Celiac Ambassadors to the world to inform and educate people. A little like evangelization of the masses.

  • 3 weeks later...
plantime Contributor

Diabetes, epilepsy, HIV, even penile erectile dysfunction get lots of good press. The organizations that are supposed to help and educate us need to get some public info out for the masses. The problem is, no pharmaceutical company can market a pill to correct celiac disease. Money greases the wheels, and motivates people most. Maybe some of the manufacturers we depend on for gluten-free food will be willing to upgrade their advertising? I didn't know these companies existed until I found this site.

  • 2 weeks later...
debmidge Rising Star

Hi All

I am doing what I can to get the celiac disease info out. I ordered "Full Life with celiac disease" from CSA, but I find it to be too long and boring for a non-celiac disease person to read. Well I ordered some of them and I have started leaving them in my doctor's offices (ob-gyn, X-Ray lab, chiropractor, etc.)

I have also written my own 1-page flier based on celiac disease info as found in CSA literature. I condensed it to one page and made it read like an advertisement. I've been leaving them in stores. I handed one to a mother of a Girl Scout who was selling cookies in front of our local supermarket. She didn't know what celiac disease was (I was explaining to her why I couldn't buy the kid's cookies).

Funny thing is that 99% of the people I speak to who were born in USA don't know what celiac disease is; but I spoke to the Polish lady next door who still has an accent and she knew right away what celiac is. Go figure!

It's up to us Celiac Ambassadors to enlighten the masses. It appears that all of the celiac disease non profit orgs are not going to do a commercial or magazine advertising any time soon. We have to "hit the streets" ourselves.

plantime Contributor

A wonderful lady that I love to visit with at church got an education on celiac disease at our ladies meeting last night. The only thing on the refreshment table that I could have was a cup of Sprite, and she asked why I wasn't eating anything. I make it a point to tell as many people as are willing to listen!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,762
    • Most Online (within 30 mins)
      7,748

    dangunderson
    Newest Member
    dangunderson
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • knitty kitty
      For back pain, I take a combination of Cobalamine B12, Pyridoxine B 6, and Thiamine B 1 (in the form Benfotiamine), which have an analgesic effect.  These three B vitamins together work way better than those over the counter pain relievers.  Theses are water soluble B vitamins that are easily excreted via the kidneys if not needed.  Thiamine will also help the nausea. Interesting Reading... Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/#:~:text=Some of these processes include,Analgesics
    • knitty kitty
      @stephaniekl, welcome to the forum, Is your daughter taking any nutritional supplements?   Weight loss and failure to thrive are two symptoms of thiamine insufficiency.  Thiamine deficiency symptoms are not recognized as such by doctors.   I experienced similar symptoms when I became malnourished.  Thiamine deficiency symptoms can become worse quickly, and can affect one emotionally and mentally.  Although blood tests for thiamine aren't accurate, do have your daughter checked for nutritional deficiencies.  Thiamine B 1 works with the other B vitamins and magnesium.  Thiamine and Niacin B 3 help improve Gerd.  All the B vitamins are frequently low due to malabsorption.  Vitamin D will help calm the immune system.  Thiamine helps the immune system fight off viruses like those tick borne illnesses.   Thiamine Mononitrate, which is in many vitamin supplements, is not bioavailable.  I was taking a multivitamin containing thiamine mononitrate and still became deficient in thiamine. Thiamine in the form Benfotiamine has been shown to promote intestinal healing.  A form called TTFD (tetrahydrofurfuryl disulfide) is also excellent for correcting thiamine deficiency.  A combination of Thiamine, Cobalamine B12, and Pyridoxine B 6 has analgesic properties.  I take it for back pain.   Keep us posted on your progress! Interesting Reading... The importance of thiamine (vitamin B1) in humans https://pmc.ncbi.nlm.nih.gov/articles/PMC10568373/#:~:text=Thiamine absorption in the jejunum,system [51–53].
    • trents
      Has prednisone or some other systemic steroid been tried that might quiet her immune system down for a while? I have two acquaintances with Lyme's disease. It is a wicked condition that has long fingers.
    • stephaniekl
      We have.  She is so limited as to what she can eat.  She has a nutritionist, but they are even at a loss.  Right now, her pain is so significant that she can only eat 5-10 bites a meal.   We just got some labs back today and she is hypoglycemia, anemic and her immune system is shot.  She also is positive for 3 tickborne illnesses.  Thanks for your help! 
    • RMJ
      A much better suggestion than that of the new doctor!
×
×
  • 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.