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
      126,060
    • Most Online (within 30 mins)
      7,748

    Laura Conley
    Newest Member
    Laura Conley
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.1k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Staci, take note of the forms of magnesium and zinc I recommended. With some of the vitamins and minerals, the formulation can be very important in how well they are absorbed. Many of the vitamin and mineral products on supermarket shelves are in a form that maximizes shelf life rather than bioavailability which, in your case, would seem to be a critical issue. And with magnesium, if you use the typical over the counter form (magnesium oxide) you may find it has a definite laxative effect (think, "milk of magnesia") simply because it isn't well absorbed and draws water into the colon. Spend some extra money and get quality vitamin and mineral products and research the issue of bioavailability. There are forum members who are knowledgeable in this area who may have recommendations. Do you have Costco stores where you live? Is Amazon available to you?
    • Kathleen JJ
      And yes, of course it's better to know and we will adjust.  It's just, he's 7 and in our house we can control what he gets. But he plays soccer 3 times a week and in the changing room the boys share candies. I can and will tell him not to accept them any more, but "mistakes" will be made.   I'm really burdened by the potential social impact for him. He so loves to go to a restaurant as a family - I'll guess that's finished. Going to birthday parties at another kids house? I am reading about Coeliacs and apparently the fact that something as much as TOUCHED something with wheat is enough, even if he doesn't feel the symptoms - how can we control that bar from keeping him locked up?    And the worst worry of all: how do you tell a little boy to do all of this to not have symptoms that he does not have. If he'd been having horrible diarrhea or feeling really tired, we could tell him 'see, you feel so much better now, that kind of food was just not good for your body', but now, what will our argument be? For clarity: of course we will put him on the diet, I am not saying I don't believe in the necessity of that, it is just that it will be quite a stretch to 'sell' it to him 😞
    • StaciField
      I’m 41. You have helped me achieve the goals of finding a way of getting nutrients into my body so I will see how it works for me. Thank you so much.
    • Kathleen JJ
      Thank you for your reaction. The reference values are both "<10", although I found a medical paper from Netherlands (I'm Belgian) who use the same values and there the see a positive daignosis as twice more then 200 and a positive biopsie. I didn't see how to change this in my original message, sorry...
    • cristiana
      Hi Kathleen Welcome to the forum. I am based in the UK so I am just picking this post up before our US based moderators appear.  I think they will want to know the lab values of both of the figures you have provided us with (min/max reading) as they tend to vary - could you post those for us, please? We see a lot of coeliacs who also have helicobacter pylori on this forum.  I am not sure how that would reflect in the blood results so I will leave this to be answered by my more experienced colleagues @trents or @Scott Adams. Obviously, you won't really know for sure where things stand until you have your meeting with the consultant.  I am sorry that you have to wait, but it will be worth knowing one way or another.  Apart from his recent gastric issues, it is fantastic to know that your son is otherwise a picture of health.  But it is worth bearing in mind that undiagnosed coeliac disease can cause health issues in the longer term, so far better to know now if he does turn out to have coeliac disease and adapt your son's diet accordingly, before other health issues have a chance to appear. Cristiana  
×
×
  • Create New...