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Do you share celiac with other family members? (parents, grandparents, children, grandchildren, etc)Ideas, tips, suggestion, for doing LIFE together!
The 4th of July is around the corner, which normally means all sorts of fun: BBQ's!! Fireworks!! Parades!! Friends & Family!! All topped with a great appreciation for the U.S.A.!With this fun comes some great photos - so go ahead and share your good times with the community!To submit a photo, first become a member of the 4th of July Fun! Community:Once you're a member, you're also set to start submitting photos! But be sure and read the below submission guidelines. Five Simple Rules (Submission Guidelines)1. No inappropriateness.2. You can submit up to five (5) photos per contest.3. You, a family member, or a friend must have taken the photo (no scouring the web for cool photos)!4. You must fully own rights to the photo (again, no scouring the web for cool photos).5. Your photo must fit the contest theme (above).If you have any questions please post them below in the comments section.Have fun! We can't wait to see your entries.
Discussion on restaurants, grocery stores and hotels suitable for celiacs. Help for those who will travel and need to know about gf options in a city or country.
Please join us for the Second Annual Bowling Bash for Celiac Disease to benefit the Celiac Disease Center at Columbia University. This event is hosted by Randi & Rob Albertelli…Date: Sunday, March 22, 2009Time: 1:00 – 4:00 pmLocation: AMF Syosset Lanes111 Eileen Way, Syosset, NY 11791 Unlimited bowling, gluten-free refreshments, fabulous gifts, silent auction (including sports memorabilia from Steiner Sports) and lots of fun!!!Adults $50Children $30 (12 & under)Please register in advance by completing the attached form and mail to:Randi Albertelli15 John DriveOld Bethpage, NY 11804For additional information, please contact: Randi Albertelli, email: r******@optonline.netWe look forward to seeing you on Sunday, March 22!Cynthia BeckmanDirector of DevelopmentCeliac Disease Center at Columbia UniversityHarkness Pavilion180 Fort Washington AvenueSuite 934New York, NY 10032Tel 212.342.4529Cell 646.812.1212Fax 212.342.0447email:cb2280@columbia.eduwww.celiacdiseasecenter.org
Please join the L. Lodico Walk for Celaic Disease, May 31st, 2009!
The 411 for Portland, Oregon. To help Empower, Educate and inform you & those around you. For tips, tricks & a little bit of bitchin'-but NO whining allowed. Links-awareness, restaurants, suggestions, actions.
Once the diagnosis of celiac disease (CD) has been confirmed, treatment can begin immediately. It does not require surgery. It does not require an unending dependence on medication. It does not even require repeated visits to the doctor's office. The best and only known treatment for CD is simply this: a lifelong elimination of "gluten". Use this community to come and find out more about what you can do to manage the symptoms of CD.
Find out all the most up to date information on Celiac Disease right here! From news articles to interesting videos and podcasts, have your morning coffee and click through the news! Feel free to submit anything you find of interest!
Check out the blog: www.glutenfreefortwayne.blogspot.com You can also "like" Gluten Free Fort Wayne on Facebook: www.facebook.com/glutenfreefortwayne I hope to unite gluten-free people in Fort Wayne, with the support of other celiacs and camaraderie of others in Fort Wayne. When I first started my gluten-free journey, I knew nobody with Celiac Disease. I only knew a couple of people who were gluten-free, but I quickly learned that it was only as a trendy thing to do, and only when it was convenient. My health depends on this. I cannot "cheat". Ever. I hope that by having a page for gluten-free people in Fort Wayne, I can eventually bring together a supportive group of local celiacs. Perhaps someday we can even have some influence in the community to increase awareness and open up more opportunities for us in grocery shopping and dining out. This page is open to all celiacs, not just locals. I want to share the resources I have found on the internet- these are all linked on sides and bottom of the blog page- and maintain a supportive community of celiacs. I welcome and encourage friends from the local area as well- celiac or not- for increased awareness, education, and networking. I am not doing this to make a profit; I am not a medical professional. Please use good judgement when following anyone's advice online.
