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Eli: Sclerodermia and Raynaud's Syndrome


Lavender Flowers by Ione Bridgman, ISN ArtistIt began in 1995, when I was diagnosed with Raynaud's Syndrome, but it wasn't given any importance, and I could not be cured.

With each passing year I added symptoms in several parts of my body, with multiple calcifications, so much so that I had to have three surgeries in a very short time. Nobody had ever understood what I went through nor helped me so I always took a turn for the worse.

Now I have perhaps found a good rheumatologist in Milano who could help me recover since finally, after thirteen years of suffering, he has given me a diagnosis and a cure, before it is too late…I hope.

To Contact the Author

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

Eli: Sclerodermia e Sindrome di Raynaud
Cos'è la Sclerodermia
Sistemica: Sindrome di CREST
Tipi di Sclerodermia: Limitata

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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 Eliza: Daughter-in-Law of Morphea Patient

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