Associations for support

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Teddtlove
Veteran Member


Date Joined Jan 2013
Total Posts : 1038
   Posted 6/23/2013 2:38 AM (GMT -6)   
I know Lupus has Lupus.org and others. Do they help people with UCTD or are there any organization that do help people with UCTD similar to lupus.org? I know people can post on the message boards there with UCTD but I mean something like getting leaflets or support groups. The lupus foundation has a support group in my city but I do not know how they feel about UCTD.
30 female. Sherrie, 2007 UC, 5/13UCTD, Hypothyroidism, Intercostal Neuralgia, Agoraphobia, Bipolar tendencies, Panic disorder, Acid reflux, Lactose intolerance, Eczema, Migraines, Degenerative disk, Hypertension, and Anemia.
Plaquenil, Lialda, Canasa, Hyoscyamine sulfa, digestive ad lactose defense, Cymbalta, Lyrica, Lomotil , klor-con20, VSL 3DS, Rainbow light, Vit D, started Humira 12/31

Lynnwood
Veteran Member


Date Joined May 2005
Total Posts : 7723
   Posted 6/23/2013 11:05 AM (GMT -6)   
I can't imagine a Lupus group that would not welcome you!!
Lynnwood, Lupus & Sjogren's Moderator
DIAGNOSING LUPUS & LUPUS RESOURCES
"Life is far too important to be taken seriously" - Oscar Wilde

couchtater
Elite Member


Date Joined Jul 2009
Total Posts : 14475
   Posted 6/23/2013 1:37 PM (GMT -6)   
There's no lupus support groups in my area so I go to a chronic illness support group.
Joy
Lupus, Fibromyalgia, Glaucoma, Asthma, Hypothyriodism, Sleep Apnea, OA, Depression, and Allergies

When life throws you lemons....
Pick them up and throw them right back at them! :))
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