Associations for support

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Veteran Member

Date Joined Jan 2013
Total Posts : 1037
   Posted 6/23/2013 1:38 AM (GMT -6)   
I know Lupus has and others. Do they help people with UCTD or are there any organization that do help people with UCTD similar to 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

Forum Moderator

Date Joined May 2005
Total Posts : 7673
   Posted 6/23/2013 10:05 AM (GMT -6)   
I can't imagine a Lupus group that would not welcome you!!
Lynnwood, Lupus & Sjogren's Moderator
"Life is far too important to be taken seriously" - Oscar Wilde

Elite Member

Date Joined Jul 2009
Total Posts : 14475
   Posted 6/23/2013 12:37 PM (GMT -6)   
There's no lupus support groups in my area so I go to a chronic illness support group.
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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