SCLERO.ORG
Search
ISN: Italian Version

Angela Abati, ISN Italian GuideCiao, sono Angela Abati, Guida Italiana per ISN. Gestisco la sezione italiana di sclero.org e correggo o traduco le pagine mediche. Mi sono laureata in Lingue e Letterature Straniere presso l'Università di Bologna, e mia madre ha la Sclerodermia. Alba León, Traduttore per ISN, traduce le nuove storie dei pazienti Italiani in Inglese. La mia email è [email protected]

Questa pagina viene visualizzata bene con il browser che codifica per il set di caratteri Occidentale [ISO-8859-1]. Dal menu Visualizza scegli Set di caratteri e quindi (Europa) Occidentale. [English: This page displays best with browser encoding (see View menu) set to Western European (Windows) or Windows-1252.]

Eli: Sclerodermia e Sindrome di Raynaud

Italia

Lavender Flowers by Ione Bridgman, ISN ArtistHo incominciato nel 1995 quando mi hanno diagnosticato la Sindrome di Raynaud ma non ne è stata data importanza e non sono stata curata. Poi ogni anno che passava mi si aggiungeva male da qualche parte sempre diversa con calcificazioni multiple nelle articolazioni tanto che ho subito 3 interventi chirurgici.

Nessuno mi ha mai capito e aiutato così sono sempre peggiorata.

Adesso forse ho trovato un bravo reumatologo a Milano che deve ricoverarmi perchè finalmente dopo 13 anni di sofferenza ho diritto anche io a una diagnosi e una cura,prima che sia troppo tardi. Spero…

To Contact the Author

Eli
Email: [email protected]
Story edited 12-09-08 JTD
Story posted 01-16-09 SLE

Story Artist: Ione Bridgman
Story Translator: Alba León
Story Editor: Judith Thompson Devlin

LINKS
Cos'è la Sclerodermia
Sistemica: Sindrome di CREST
Tipi di Sclerodermia: Limitata

English:
Eli: Sclerodermia and Raynaud's Syndrome
Calcinosis
Calcinosis Stories
CREST Syndrome
CREST Syndrome Stories
Limited Scleroderma
Limited Scleroderma Stories
Raynaud's
Raynaud's Stories
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Sclero Forums *Online Support Group!*
Symptoms of Systemic Scleroderma
Types of Scleroderma
What is Scleroderma?

ISN Artist: Ione Bridgman

Ione BridgmanISN Artist Ione Bridgman created original artwork to illustrate this page. She is 90 years old, and lives in New Zealand. Her lovely paintings illustrate many of our pages and the covers of our Voices of Scleroderma Book Series .

ISN Translator and Editor: Alba León

Alba LeonAlba León is the ISN Translator for this page. She is studying international relations in Mexico City.

ISN Story Editor: Judith Thompson Devlin

Photo of JudithJudith Thompson Devlin is the ISN Story Editor for this story. She is also lead editor of the ISN's wonderful Voices of Scleroderma book series!

Go to {nextpage}
 
Recent Donors
See ISN News for recent donors, including memorials for
Christine Kane, Joleen M. Cascaden.
 

SCLERO.ORG is the world leader for trustworthy research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension. We are a service of the nonprofit International Scleroderma Network (ISN), which is a 501(c)(3) U.S.-based public charitable foundation, established in 2002. Meet Our Team, or Volunteer. Donations may also be mailed to:

International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702 USA

Email [email protected] to request our Welcome email, or to report bad links or to update this page content.

TOLL FREE HOTLINE 1-800-564-7099
Free to U.S. and Canadian Callers. Ask for our Free Info Packet by mail or email!
Scleroderma, Pulmonary Arterial Hypertension, and related illnesses.
Privacy Policy.

 
The most important thing in the world to know about scleroderma is sclero.org!
Donate Now
Copyright 1998-2017, International Scleroderma Network. AKA Scleroderma from A to Z and SCLERO.ORG. All Rights Reserved.