Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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
      127,491
    • Most Online (within 30 mins)
      7,748

    Kadellia
    Newest Member
    Kadellia
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121k
    • Total Posts
      70.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Soleihey
      @Scott Adams Recently got blood work back and TTG antibodies went from 168.8 to 16.7 and deaminated gliadin was 22 (was not measured the first time). Is this a good start for an 11 month time frame? Just having a hard time with why my symptoms seemed to be flaring up again when my blood work has improved. 
    • dublin555
      I’ve been through something similar recently, and I know how frustrating it can be when nothing seems to work. Based on what you’ve described, it might be worth considering dermatitis herpetiformis, especially with the family history of celiac disease. Testing could give you some answers, and while online kits aren’t as reliable as a GP, they’re a good start if appointments are hard to get. I also found relief through medical cannabis for my eczema, at Releaf, a clinic in the UK that offers eczema medical cannabis treatment. They start with a low dose, adjust weekly, and track progress through online consultations.
    • trents
      Welcome to the forum, @Jaylan! Almost all of the symptoms and medical conditions you describe have been found to be associated with celiac disease. But they can also be caused by other things as well. There certainly is enough circumstantial evidence in your list of medical problems to warrant being tested for celiac disease. Ask your physician to order a celiac panel consisting of, at the very minimum, these two blood antibody tests: total IGA and tTG-IGA. Please do not attempt to limit your gluten intake before the blood draw is taken or you will invalidate the testing. Incidentally, celiac disease is often misdiagnosed as IBS.
    • Jaylan
      Hi there!  I’ve recently been tested for celiac disease, along with other autoimmune diseases. My symptoms started back in 2018 with joint pain in my knees. Since then, it has progressively worsened. I now have joint pain in both knees, elbows, and sometimes my shoulders. The pain is almost unbearable. I feel so stiff in the mornings, and this stiffness can last the whole day. I also experience swelling and warmth around those areas.   Other symptoms include IBS (diagnosed at age 16), restless legs, chest pain, tiredness, miscarriages, bloating, and sharp pain on the right side of my stomach. In the past, I’ve also had problems with a vitamin D deficiency, and my serum folate levels recently came back very low.   My question is: How likely is it that I have celiac disease?    
    • Rebeccaj
×
×
  • Create New...