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Our mission is to reclaim the quality of life stolen by Lupus. To do so by providing an establishment staffed with a permanent, compassionate and knowledgeable workforce to ensure continuous and sustainable support for those diagnosed with Lupus. CLICK HERE TO FIND US ON FACEBOOK! http://www.facebook.com/?sk=2361831622#!/group.php?gid=160646573694
The list of Top 3 TV Shows in 2010. I am great fan of tv shows and love to watch and download online tv shows. Here is the the list of top tv shows that one can hardly missed out. Glee EpisodesGlee is one of the famous tv show represented by Fox. All the Glee Episodes are worth watching and currently season 1 of glee is airing high these days. Reba TV show This program ran for five seasons before The WB merged with UPN to form The CW Television Network and it ran on The CW for its final season. Watching Reba TV Show is real fun and no one wants to miss out such a great television series.Late Night with jimmy FallonLate Night with jimmy fallon is one of the incridible talk show. Jimmy Fallon, who is well known for his energetic, humorous and tricky attitude is the one, who is behind the success of this show.
Let us as christians stand on the word. God wants us to be whole and well. This group is for prayer requests and to uphold our Lupus friends in prayer. Romans 8:28
Let us as christians stand on the word. God wants us to be whole and well. This group is for prayer requests and to uphold our Lupus friends in prayer. Romans 8:28
Fashion Show ('09) We are BACK!!! Full force :) ... to raise awareness for Lupus and other autoimmune diseases.(check out www.lupus.org and www.aarda.org)And now we have our own website too! www.careforautoimmunity.info. You can purchase your tickets here. Please do so early, so that you can get whichever section you desire. We also hope to raise funds for Anteaters Against Autoimmunity... an organization at UCI that attempts to educate the public about this group of diseases and to help those affected by them. If we are able to raise enough money (please buy your tickets now and donate :) ), we will be donating a percentage of our profits to Alliance for Lupus Research, a percentage to LupusLA, and maybe even some to the Lupus Foundation of America!The show will be at the Pacific Ballroom, Student Center, UCIrvine, Irvine, CA 92697-1225 on Saturday, October 3rd, 2009.Keep in mind, this is a "black tie" event. Arrivals start at 5pm; Refreshments and Musical Performances from 5:30-6:30pm; Runway from 6:30-9:00pm.PEOPLE HELPING:Anteaters Against AutoimmunityAND::::::::::Host and Headliner: Comedian Jonny Loquasto(
Created by Anteaters Against Autoimmunity
Members: 3
A group for Aussies on here to be in touch with one another for support and information.
My Life Works Today! is a Pacific Northwest (Oregon and SW Washington) health networking project designed to act as a resource and service 'hub' for patients living with lupus and lupus-related conditions, diseases, and syndromes. Even though participation in the local workshops, presentations and community forums are available for those of us living here, we offer anyone in this Ning community to join in on our goals to connect, celebrate and aim for lives on our own terms.
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.
The primary function of Lupus International is to alleviate suffering for lupus patients through patient services, including education, early detection of undiagnosed cases through awareness promotion, and to eradicate lupus by supporting lupus research. There is hope. Since 1983, we have provided thousands of people with educational and supportive services. We assist those affected by lupus to live fuller, more productive lives.
Lupus affects well over a 1.5 million people in North America, and is said to affect over 10 million people worldwide, yet Lupus is far from the household name that say Breast Cancer or HIV is for example. This community is for us to get together and work out what we can do together to raise awareness for a condition that affects so many people.
The major problem in discussing the role of diet is that there are so many factors involved.People living with lupus are individuals with different backgrounds, habits and medical histories, who respond to substances differently at different times. It is difficult to evaluate whether any specific dietary change is responsible for exacerbating the symptoms of lupus. The addition or elimination of one substance from the diet can be the remedy for one person and the culprit for another. There is certainly no harm in exploring how diet impacts symptoms, as long as your overall health is not compromised.This community is for all of us to share ideas, tips and experiences with diet and nutrition in the management of lupus symptoms.
This group is for those who want to share, learn or hear more about caring for those with Lupus. Engage in conversation with those who you might learn something from, share your tips and insights about what might help out those caring for individuals living with Lupus.
FInd out all the most up to date information on Lupus 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!
Lupus Foundation Of America, Inc.- With nearly 300 chapters, branches and support groups in 32 states, the Lupus Foundation of America (LFA) is the nation's leading non-profit voluntary health organization dedicated to finding the causes and cure for lupus. Our mission is to improve the diagnosis and treatment of lupus, support individuals and families affected by the disease, increase awareness of lupus among health professionals and the public, and find the causes and cure. Research, education, and patient services are at the heart of LFA's programs.
The Lupus Research Institute leads the way to a cure for lupus by unleashing the scientific community’s creativity, championing innovation, and exploring uncharted territory in lupus research. The LRI recognizes that most major breakthroughs come from unexpected directions, and supports only the highest-ranked new science to prevent, treat, and cure this chronic autoimmune disease. Mission: Life without lupus.