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German Scarcodiodosis Web Site
Die Deutsche Sarkoidose-Vereinigung gemeinnütziger e.V. ist der Zusammenschluß von Sarkoidose-Erkrankten und ihren Angehörigen. Sie setzt sich für die nachhaltige Verbesserung der Situation Sarkoidose-Kranker ein. Ihre Gemeinnützigkeit ist anerkannt.
My Life with Scarcodiodosis by Donna G
My name is "Donna" and my saga began in July 2000.
So many of you have asked me about my Sarcoidosis
I thought it time to tell you my story.
National Scarcoidosis Resource Center
Hi, my name is Sandra Conroy. I am the founder and president of the National Sarcoidosis Resource Center. The Resource Center offers help and information to anyone that seeks it. The Resource Center is located in Piscataway, NJ, USA. Please feel free to contact us
Norway - Sarkoidose, et mysterium!
Det har vært forsket på sarkoidose i over 100 år. Sykdommen kalles også for "Boeck’s sykdom" etter den norske hudlegen Cesar Boeck, som var en av de første som beskrev sarkoidose
i slutten av 1800-tallet. Den første som beskrev sarkoidose var engelskmannen Jonathan Hutchinson i 1877. Han kalte sykdommen for "Livid papillary psoriasis".
Sarcoid Newsletter
The online newsletter about sarcoidosis! Here you can see the most current information, issues and articles about sarcoidosis. Information about new medications, new treatments, new theories on the cause and cure of sarcoid. There are also schedules for sarcoidosis chats on AOL and computer tips to help you better use the Internet to research sarcoidosis.
Sarcoïdose/Besnier Boeck Schaumann (In Dutch)
Sarcoïdosis is de Latijnse naam voor Sarcoïdose en wordt vaak afgekort met Sarco op onze site!
Sarcoidosis Australian Support Group
The "Sarcoidosis Australian Support Group" (SASG) was convened by Australian sarcoidosis patient Bob Rumsey in April 1997 following discussion with the Australian Lung Foundation and prompting from other sarcoidosis patients.
Sarcoidosis Family Foundation
The goal of the Sarcoidosis Family Foundation is to provide patients and caregivers with information on the disease.
Swiss Scarcodiodosis Web Site
Am 8. Juli 1999 wurde die SSARV in Rheinfelden gegründet.
Unsere Ziele sind: Orientierung der Öffentlichkeit über die Sarkoidose aus der Sicht der Betroffenen
Gründung, Förderung und Unterstützung regionaler Selbsthilfegruppen in der ganzen Schweiz
Information für Patienten, Ärzte, Therapeuten
Interesse an der Forschung wecken
World Scarcodiodosis Society
The World Sarcoidosis SOCIETY, (previously known as the Canadian Sarcoidosis SOCIETY) has grown so rapidly!
and as such we are a FREE Web site dedicated to providing information regarding Sarcoidosis to those whom are in need and thus does not solicit nor accept donations.
