Resources- Specific Diagnosis Card Catalog- Wegener Granulomatosis

Who to Contact

Wegener's Granulomatosis Association
P.O. Box 28660
Kansas City, Missouri 64188-8660
800-277-WGSG (9474)
Phone/Fax 816-436-8211
Web: www.wgassociation.org

Wegener's Granulomatosis Association offers comfort and support to WG patients and families through education, awareness and research. The mission of WGA is to: Establish rapport with all known WG patients, to alleviate the isolation of having an uncommon, life-threatening disease; Assist WG patients and their families with clinical information and coping strategies, to help them gain a strong, positive outlook; Create greater awareness about WG within the medical community, as well as the general public; Support research efforts for the cause, treatment and cure for WG; To support WG patients and their families through education, awareness, and research.

Where to go to Chat with Others?

Wegener's Granulomatosis Mailing List

savvy
Savvy list provides info-resources, support and contact opportunities on the rare, inflammatory autoimmune illnesses. - Members present Churg-Strauss,Wegener's granulomatosis, Henoch-Schoenlein, Polyarteritis Nodosa, giant-cell or temporal arteritis, takayasu, polyangiitis, Microscopic polyangiitis, leukocytoclastic Vasculitis, and related auto immune, secondary and overlapping syndromes, such as Lupus, Cushing's, osteoporosis and other orphan, auto-immune illnesses.

Learn More About It

What is Wegener's Granulomatosis?

Wegener's Granulomatosis FAQ?

Wegener's Granulomatosis

Wegener's Granulomatosis, NIAID Fact Sheet

Wegener's Granulomatosis - From MedlinePlus

Links

Wegener's Granulomatosis Association

Wegener's Granulomatosis Support Group of Australia