Forum of lupus bloggers & groups express passionate thoughts on disease, body, mind & spirit. Info Hub to share resources, articles & media.
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The Courage Award is being given to you for your public contributions in raising awareness, as well as your demonstration to other's as a fellow patient. Lupus Warriors are people who have overcome many challenges, who have walked through experiences having gained a renewed spirit and determination to thrive. Have gained the spirit of endurance through their difficulties and have in turn help other patients. You exemplify the inner strength of a Lupus Warrior and an empathy that makes your service work to other's rooted in compassion. Sincerely, The Lupus MCTD Foundation Team
Posted by Ruste Jill Vallerie on November 3, 2009 at 4:47pm — 1 Comment
Posted by Angie on November 2, 2009 at 1:28pm
Posted by Margaret Auchampaugh on October 28, 2009 at 1:43pm — 1 Comment
Posted by APSFA on October 23, 2009 at 6:09pm — 2 Comments
Posted by 3sisters on October 19, 2009 at 7:30pm — 2 Comments
Posted by Amy Domestico on October 10, 2009 at 1:21pm — 1 Comment
Posted by cookie on October 7, 2009 at 2:31pm
Posted by Ruste Jill Vallerie on October 6, 2009 at 10:33am — 8 Comments
Posted by 3sisters on October 3, 2009 at 9:30am
Posted by Maria on September 22, 2009 at 2:24pm
Posted by Angie on September 18, 2009 at 10:00pm — 1 Comment
Posted by Margaret Auchampaugh on September 4, 2009 at 8:30pm — 1 Comment
Posted by Ellen S on September 2, 2009 at 3:22pm
Posted by Maria on August 24, 2009 at 11:18am — 4 Comments
Posted by Jamica Cropper-Pam on August 21, 2009 at 10:34pm — 2 Comments
Posted by Angie on August 18, 2009 at 11:00pm
Posted by APSFA on August 17, 2009 at 1:11pm — 4 Comments
Posted by Maria on August 12, 2009 at 5:15pm — 2 Comments
Posted by wrightrs on August 12, 2009 at 12:05pm — 3 Comments
Discussions that maintain network objectives, but are not categorized by any of the network themes, The Disease, The Body, The Mind, or The Spirit.
7 discussions
This Salon is dedicated to broad issues, network policy and objectives. Survivors address issues, ask questions or make suggestions directly to me instead of my inbox. Other members may have the same issues and can benefit from open discussion. Members are still encouraged to use my inbox for private communication. Don't be shy about either. Initiate any issue you desire in this Q&A.
1 discussions
"The Disease" focuses on medical facts and scientific information specific to lupus, fibromyalgia, and APS. Join The Disease Group to collaborate on Network projects focused on this theme.
3 discussions
"The Body" focuses on non-pharmaceutical management of the symptoms of lupus, fibromyalgia and APS. Join The Disease Group to collaborate on Network projects focused on this theme.
3 discussions
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