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Using The New Format


bella

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bella Newbie

I have not been on in months,when did this change? I am having a really hard time getting around this new format. I will be the first to say I don't know what I am doing HELP!! :(


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gf4life Enthusiast

Hi Bella,

The new board switched over at the end of December. It takes a bit of getting used to, but the new features are good. I think the best feature for me is being able to send e-mails or personal messages directly to other people on the board. It is certainly a lot easier than it used to be. If you have any specific questions and need help, please post them and we will try to help you out. Welcome back! :)

God bless,

Mariann

Connie R-E Apprentice

:) What is the easiest way to "send e-mails or personal messages directly to other people on the board."?

Thanks!

Connie

JsBaby-G Newbie

Connie,

Below everyone's post you will see the Email and PM button. Just press those!!

Connie R-E Apprentice

Duh! Thanks Crystal!! :lol:

Connie

  • 1 month later...
hadafish Newbie

I still cannot get all of the messages, I only see about 2/3rds of each message and

cannot see the introductory message of the topics. I am so sad because I loved this

board and wth wonderful people on it. I will keep trying. hadafish, formerly known

as glowmore. Jan, Marin, California

judy04 Rookie

Jan,

Don't feel bad I had a lot of problems at first. When you said you could only see

2/3 of the message, you probably need to center it by pushing the right arrow

at the bottom of the window, that's what I have to do. Hope this helps!

I think you will like it when you get used to it...


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hadafish Newbie

Hi Judy, thank you. I do push that button all the way over and still I only see only

one third of the original message and two thirds of the replies. I don't have this

problem on any other site. I am on an Imac. My husband says I have to get a PC

for it to work and true enough if I use his computer it is fine. His is for

business and I rarely get to be on. However, I am pleased that I can post and

that you can see my reply. Thanks again. This is better than not being here at all! I

love the site. Jan, Caifornia.

  • 2 weeks later...
warpspeed Newbie

I've never been on a message board at all and am writing this to be sure this is how you post something.

gf4life Enthusiast

Warpspeed, welcome to the site! It worked fine. Now you can look around and post any questions, answers or topics. It helps to look around first and see if there is already a topic you are interested in, and add to that. Again, welcome.

See you around the site!

God bless,

Mariann :)

  • 3 weeks later...
honeybee Apprentice

How do you post events to the calendar??? Every time I try to "Add and Event", I get the message "This menu is disabled" - there must be a way because I see that other people have posted events, such as Celiac Walks and Support Group Meetings. Please help.

Paula :unsure:

gf4life Enthusiast

Hi Paula,

I have never tried to add an event to the calendar, but it seems to me that it would have to be cleared with the sites administrator before being added. I would suggest when you get to the disables menu page that says you don't have access to that feature, then click on the "contact site administrator" link and ask what you need to do to add an event.

Good luck,

Mariann

  • 3 months later...
balanc Newbie

Why are some (most) postings signified as "Pinned"? I have been a member for a year or so, although I have written just a few messages. Some of the messages I did send I never saw posted. Thanks.

Flo

celiac3270 Collaborator

Flo,

When you post a new topic on the board, it goes to one of the last few pages, which may be why you don't see it. When a moderator sees it they have a decision to move it to another section of the board (for example, if you posted a recipe under the Coping section) or they can "pin" it. If a moderator pins something, it shows that they've read it and it's important and good to read. Pinning a topic also makes it so it cannot be moved. All unpinned topics stay on the last pages of the forum along with any "moved" topics....pinned topics are towards the front in order of date. Hope this helps.... :)

-celiac3270

A Celiac.com moderator

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  • Posts

    • captaincrab55
      Imemsm, Most of us have experienced discontinued, not currently available or products that suddenly become seasonal.   My biggest fear about relocating from Maryland to Florida 5 years ago, was being able to find gluten-free foods that fit my restricted diet.  I soon found out that the Win Dixie and Publix supper markets actually has 99% of their gluten-free foods tagged, next to the price.  The gluten-free tags opened up a  lot of foods that aren't actually marked gluten-free by the manufacture.  Now I only need to check for my other dietary restrictions.  Where my son lives in New Hartford, New York there's a Hannaford Supermarket that also has a gluten-free tag next to the price tag.  Hopefully you can locate a Supermarket within a reasonable travel distance that you can learn what foods to check out at a Supermarket close to you.  I have dermatitis herpetiformis too and I'm very sensitive to gluten and the three stores I named were very gluten-free friendly.  Good Luck 
    • rei.b
      Okay well the info about TTG-A actually makes a lot of sense and I wish the PA had explained that to me. But yes, I would assume I would have intestinal damage from eating a lot of gluten for 32 years while having all these symptoms. As far as avoiding gluten foods - I was definitely not doing that. Bread, pasta, quesadillas (with flour tortillas) and crackers are my 4 favorite foods and I ate at least one of those things multiple times a day e.g. breakfast with eggs and toast, a cheese quesadilla for lunch, and pasta for dinner, and crackers and cheese as a before bed snack. I'm not even kidding.  I'm not really big on sugar, so I don't really do sweets. I don't have any of those conditions.  I am not sure if I have the genes or not. When the geneticist did my genetic testing for EDS this year, I didn't think to ask for him to request the celiac genes so they didn't test for them, unfortunately.  I guess another expectation I had is  that if gluten was the issue, the gluten-free diet would make me feel better, and I'm 3 months in and that hasn't been the case. I am being very careful and reading every label because I didn't want to screw this up and have to do gluten-free for longer than necessary if I end up not having celiac. I'm literally checking everything, even tea and anything else prepacked like caramel dip. Honestly its making me anxious 😅
    • 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.  
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