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Scleroderma from A to Z by the nonprofit International Scleroderma Network
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Earl's Running for SCLERO.ORG!
Sponsor Earl Manns in Green Bay Marathon, May 18, 2008! I'm running in honor of my daughter Mya, and in memory of Sherrill Knaggs. Join the excitement! (Also see: Donate Now, Earl Manns: ISN Fundraiser, and In Memory of Sherrill Knaggs)

Patient & Caregiver Stories Main Menu
ENGLISH Stories by First Name: A  B  C  D  E  F  G  H  I  J  K  L  M  N  O  P  Q  R  S  T  U  V-Z
ENGLISH Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008
ENGLISH Stories by Illness: Main List, Linear/Morphea, Systemic, Symptoms
Stories by Language: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish
Stories by Month Posted
2008: Jan Feb-Apr
2007: Jan-May Jun Jul Aug Sep Oct-Dec
2006: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov-Dec
2005: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
2004: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
2003: Jan-Apr May Jun Jul Aug Sep Oct Nov Dec
2002: Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
2001, 2000, 1999

1999 Stories by Month Posted
We began tracking stories by date posted in Nov. 1999. Nov Dec

Nov-Dec 1999
Shirley: Progressive Systemic Sclerosis I found out about my Scleroderma on November 1, 1971 at 4pm. Difficulty swallowing was the thing which got my doctor's attention...
Flora - Sclerodermia Sistemica (Italiana) Sono una ragazza di 23 anni e nell' Agosto di quest'anno (1999), dopo un ricovero, presso l' Arcispedale S. Anna di Ferrara, mi hanno diagnosticato una sclerodermia sistemica...
Valeria - Scleroderma Sistemica (Italiana) Mi farebbe anche molto piacere sapere se esiste qualche centro, possibilmente non troppo lontano da Roma...
Naye: Systemic Scleroderma "I was looking in the mirror one morning when I noticed a pink discoloration around my nose. I thought maybe I had scratched myself..."
Krissy: Systemic Scleroderma/Stem Cell Transplant Candidate Our home is like a hospital. We have oxygen tanks for when I need extra help breathing, and a lovely kangaroo pump which is how I get my continuous feeding in me...
Speranza: Figlia di donna colpita da sclerodermia morphea Mia madre ne è affetta da circa 8 anni e fino ad ora è andata peggiorando di mese in mese... ISN Italiana
Amy: Daughter of Systemic Sclerosis Patient (This was written for an informative speech which I delivered in my Communications class.) Imagine for me if you would that in certain areas of your body the skin has begun to thicken and harden...
Sheri: CREST Syndrome In the winter of '97, my fingers and toes started turning white and numb in response to the cold weather...
Patient and Caregiver Stories (Master Listing)
New Personal Stories
Jaci: MCTD and Autoimmune Hepatitis Out of fear of going back to the doctors, I tried just to live with it, whatever it was. What I found strange was that nobody seemed to noticed how terrible I was feeling, not even the doctors...
Heather: Vitiligo, Hypothyroidism, and now Linear Morphea I am not too concerned about the other two conditions since there really is nothing you can do about the vitiligo, and the thyroid is under control. The morphea is what is bugging me...
Amanda: Diffuse Scleroderma Systemic Sclerosis I am thirty-nine years old and was diagnosed with diffuse scleroderma systemic sclerosis in August 2007...
More New Stories: April 2008
This is a great day to submit or update your story!
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