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Alek's Controllable Christmas Lights for Celiac Disease are Online!


Alek is at it again--raising money for celiacs!

Yes, it is the holiday season, and back online for 2010 are the Controllable Christmas Lights for Celiac Disease: http://www.komar.org/cgi-bin/christmas_webcam

Once again, three live webcams and X10 technology allows web surfers to not only view the action, but also *control* 20,000+ lights. New this year is the Santa Plane, Santa Helicopter, and even Santa Skiing down my roof ... which can all be inflated/deflated in addition to the giant 12' Santa, 15' Santa Balloon, Elmo, Frosty Family, SpongeBob SquarePants, and Homer Simpson - D'OH! 

The website is totally free (and totally fun) and is one of my zany ways of raising awareness & soliciting donations for Celiac Disease - http://www.celiaccenter.org/news_xmas.asp - my two sons have this condition, so it's personal for me. If folks are so inclined, you can make an optional donation directly to the University of Maryland Center for Celiac Research. Over $50,000 has been raised with ... holiday lights - pretty wild.

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While people around the world (157 countries last year) enjoy seeing the lights ON, environmentalists will be happy to know that they can turn the lights OFF with a click of the mouse. Better yet, this is the 7th year I'm using Wind Power and even though that is "clean" energy, I even did a Carbon Offset contribution for the 0.6 Tons of CO2 for the ~MegaWatt-Hour of power consumed - that's about the same as *one* cross-country airline trip. Finally, by providing viewing via webcam, you don't need to burn fossil fuels by driving around to see Christmas lights ... Al Gore would be proud!  

But HEY, the couple of bucks a day in electrical costs are well worth the joy it brings to people (especially the kids) when they see the display in person and/or on the web. There's even a Hi-Def option, so gather your family around the large screen and open up some Eggnog as the chestnuts are roasting on an open fire.

So surf on by, tell your friends, Blog/Facebook/Tweet/spread the word.
Merry Christmas and HO-HO-HO! 

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Celiac.com Celiac Disease & Gluten-Free Diet Forum - All Activity

Hi Allie and welcome First off, I know 3 years was a long wait, but at 17 you've figured out celiac way before many people do. That should make a big impact on minimising its effects and helping you with the diet, so, bizarrely enough, congratulations! A lot of good advice has been brought together in this thread: Don't worry that your symptoms are bad now. As you follow the diet your body will begin healing itself and you're still very young so hopefully this will go really smoothly. Think in terms of the next 6 months rather than weeks however, recovery will likely take a little time. Eat as healthily as you can, lots of whole foods and try to avoid the gluten free processed substitutes as your digestive system needs all the help it can get at this moment. You may want to avoid dairy as well for now and think about reintroducing it later. This site has been really helpful to me and others. I hope you find it just as useful. Best of luck! ps, your increased reaction to gluten during the challenge phase was perfectly normal. Many find that reintroducing it much worse than the initial affects and take some time to get over the challenge. That's why you'll see lots of posts here urging folks to 'stay on gluten' till their testing is complete!

Hi! My daughter is 19 was diagnosed at age 16. It took about 12-18 month s for her to fully heal from the damage and feel "normal" again. Also because of the damage done she had reactions to dairy, so you may want to try no or minimum dairy until youre fully healed. Just a suggestion. Hope you start feeling well soon!

Hi yall! New to this blog, but really glad it exists because I have lots of questions. First off, I'm Allie! I'm 17 and newly diagnosed Celiac after about 3 years of searching for answers. I initially went gluten-free on the recommendation of a friend, I felt better in about a month and then my pediatric gastroenterologist had me do the gluten challenge, and my symptoms were the worst they have ever been, and ones I barely noticed before became very present. I did the biopsy and was diagnosed, it's been about 2 weeks and my symptoms are still pretty bad, although my diet has no known sources of gluten or cross contamination. Wondering if anyone has any input on healing post gluten challenge, any tips or how long it took for you would be quite helpful! Thanks

Might want to look into a keto diet, I have UC on top of celiacs and keto is working great Yeah I have major nerve and brain issues with gluten, gluten ataxia with nerve issues and brain issues. Seems to cause my body to attack my brain and nerve system. My brain stumbles fogs, and starts looping, the confusion causes me to become really irritable, I call it going Mr Hyde. Like my mind will start looping constantly on thoughts and not move driving me literally mad, or it used to. Now days it is primary the numbness anger but the gut issues and sometimes random motor loss limit me motionless to the floor now days for the duration of the major anger effects. Used to be a lot more mental then painful gut. I did a mental trauma post on it on while back where I came out about all my mental issues with gluten.

^^^^^^ good info, tips and tricks^^^^^^^^^ yes, crumbs will make you sick. also, breathing flour/pancake mix, etc that is in the air because eventually, you're going to swallow some.