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