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Finnish Scleroderma Association

(Finnish) ISN: Suomen Skleroderma Yhdistys ry

We are an affiliate of the nonprofit International Scleroderma Network (sclero.org). Scleroderma patients and their family members/caregivers are invited to these support groups. Meetings are free. You don't have to be a member to attend.

Contact

Group Leader is Maria Paiho-Vartiainen
Phone: +358447393312
Email: [email protected]

Finnish Website

Suomen Skleroderma Yhdistys ry (Finnish Scleroderma Association).

Finnish Association News

Finnish is ISN's 23rd Language!

(Suomi/Finnish) Mitä skleroderma on? (What is Scleroderma?) by ISN Finnish Translator, Emmi Myohanen, launches the 23rd language for the nonprofit International Scleroderma Network's SCLERO.ORG website. (Finnish) Skleroderma on harvinaine, krooninen autoimmuunisairausa, joka koettelee arviolta 300 000 amerikkalaista, erityisesti naisia jotka ovat 30-50 vuotiaita sairauden puhjetessa. Yleisesti ottaen sitä esiintyy yhdellä tuhannesta amerikkalaisesti, ja nais-potilaiden suhde mies-potilaisiin on noin neljän suhde yhteen. (Also see Emmi Myohanen)

Tervetuloa Emmi Myohanen, ISN Kääntäjä (Suomi)

Emmi Myohanen: ISN kääntäjä (suomi). Hei, nimeni on Emmi ja olen opiskelija Suomesta, teidän ISN kääntäjänne (suomi). Minulla diagnosoitiin paikallinen skleroderma kun olin 6 vuotta vanha, 1996. Olen möys Suome skleroderma yhdistyksen sihteeri, joka on ISN:n yhteistyökumppani.

Welcome to Emmi Myohanen, ISN Finnish Translator

Emmi Myohanen: ISN Finnish Translator. Hi there, my name is Emmi and I'm a student from Finland, your ISN Finnish Translator. I was diagnosed with localized scleroderma when I was only six years old, in 1996. I am also the secretary of The Finnish Scleroderma Association, which is an ISN Affiliate. Posted 06/26/09.

Welcome New ISN Affiliate: Finnish Scleroderma Association

Welcome New ISN Affiliate: Finnish Scleroderma Association! The Finnish Scleroderma Association, Suomen Skleroderma Yhdistys ry, has become an affiliate of the nonprofit International Scleroderma Network. The association is led by Maria Paiho-Vartiainen. Posted 12/19/08.

SCLERO.ORG is the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses. We are a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team. Donations may also be mailed to: