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Stories by Illness: Main List, Linear/Morphea, Systemic Scleroderma, By Symptoms
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Stories in English: A
Adriana: Daughter of Scleroderma Patient My mother is the most beautiful woman I know...
Aileen: CREST Scleroderma Oh, the wonderful feeling to have a doctor sit there and tell you that you are not imagining things...
Ainhoa: Morphea I do not have most of the apparent and most common symptoms...
AJ Miller: Linear Scleroderma I have had Linear Scleroderma since 1968, when I was 7 years old...
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
Alegria: Fibromyalgia (Israel) My hands, legs and shoulders hurt in a very distinctive manner; my fingers are paralyzed with pain, and sometimes I get strong headaches...
Alex: Localised Scleroderma (Italy) I am a 34-year-old woman and I have been suffering from localised scleroderma for about 20 years...
Alex: Mother of Daughter with Morphea My seven year old daughter has been diagnosed with Morphea...
Alicia: Linear Scleroderma My doctor said the people who are looking at me and seeing the scars are the ones who need healing, and that I should pray for them...
Alicia B: Localized Morphea with possible Parry Romberg Syndrome The doctor kept saying something had eaten away at all the fatty tissue and the muscles which left it just skin, blood, bone, and nerve so when you look at it, it looks like I have dirt on my face and a gaping hole to go with it...
Alina: Scleroderma CREST Syndrome This site is very helpful as I have been reading articles of people with my condition and can relate to what they are going through...
Allen's Mom: Son has Scleroderma With his tightness of skin he has a very hard time bending, walking up the stairs and for the most part he cannot walk for more than a few minutes without his legs giving out...
Amanda: Diffuse Scleroderma Systemic Sclerosis I am thirty-nine years old and was diagnosed with diffuse scleroderma systemic sclerosis in August 2007...
Amber: Morphea with Possible Systemic Sclerosis My story with Morphea started two years ago. I went to a tanning salon...
A.M. Keyes: Surviving Daughter My father died on February 9, 2002 from pulmonary fibrosis, a complication of scleroderma...
Amy: Daughter of Systemic Sclerosis Patient: What is Scleroderma? Imagine for me if you would that in certain areas of your body the skin has begun to thicken and harden...
Amy B: Limited Scleroderma with CREST I am a full time pharmacist in a pediatric hospital. In February or March of this year, I began to be very intolerable of the cold...
Ana Lucia: Diffuse Scleroderma I am twenty years old and I was diagnosed with diffuse systemic scleroderma a year and a half ago...
Anastasia: Surviving Granddaughter of a Diffuse Scleroderma Patient Traveling to a different hospital finally we heard scleroderma...
Andie Friend: Morphea I want to share my story with scleroderma that is nearly eighteen years old now...
Andi P: UCTD and Possible Scleroderma It is believed that I do have an autoimmune disease they are not sure if it is systemic or not, but I know what I live through on a daily basis...
Andrea: Girlfriend with Raynaud's Syndrome (Italy) It started a few months ago when my girlfriend started finding strange spots on her hands when it was cold, they would turn purple...
Andrea H: Mother of Son with Facial Morphea I am the mother of a six year old boy called Alex who is suffering from facial scleroderma...
Andy Markman: Systemic Sclerosis I am a 42 year old male. I have had scleroderma for two and a half years. It was first diagnosed as an "atypical phenomena"...
Ang: Morphea and Fibromyalgia I was diagnosed with morphea in February 2002, but had this for a year prior to that without knowing exactly what the diagnosis was...
Angel: Linear Scleroderma I have linear scleroderma. I have had it for a little over five years and I am only twelve...
Angela: Mother of Linear Scleroderma Patient We are in search of others who know how to handle the pain and muscle spasms in her legs...
Angela M: Diffuse Scleroderma The rheumatologist that treats me says it is due to the illness, but my orthopedist says it is a problem that should be operated...
Angela S: Overlap Syndrome I am twenty-five years old and I was diagnosed with polymyositis and scleroderma, rheumatoid arthritis, mitral valve prolapse, a heart murmur, and pericarditis...
Angiola: Progressive Systemic Scleroderma (Italy) I would very much like to find other people that find themselves in a similar situation...
Andy P: Surviving Son of Fibrosing Alveolitis Sufferer The hospital is blaming the fibrosing alveolitis, which they say entered an aggressive phase two days before his death...
Anita: Lichen Sclerosus et Atrophicus My concern is that it is spreading all over my body: both legs, my back, my neck and moving toward my face...
Anita G: Localized Scleroderma This all started as a small spot that I thought was insignificant, but as time went on, it grew, along with my symptoms...
Anna: Linear Scleroderma (Poland) I realised that it is not worthwhile to give up, even during the most difficult moments; it is necessary to fight and to believe that it will be better. If I had not believed I would not have been alive now...
Anna B: Morphea My Morphea started as bruise-like marks on the backs of my legs about three years ago, after I had just fought cervical cancer and won...
Annabella: Mother of Daughter with Linear/Morphea Scleroderma A mother's intuition never fails. When I first noticed the marks on my little girl's left thigh during bath time last summer, I got a sick feeling in my stomach...
Annette: Diffuse Scleroderma (Illinois) I can see where having friends who understand what I am going through would be a big help...
Annette G: MCTD, Systemic Scleroderma, Chronic Kidney Disease, CFS, Fibromyalgia, Trigeminal Neuralgia, TMJ People think that because I am a nurse I have all the answers. Well guess what? I don't...
(Italiano) Antea: La Sindrome di Sjogren Sono Angela dalla provincia di pesaro, ho 29 anni e da ieri ho scoperto di avere la Sindrome di Sjogren...
Archie Bailey: Scleroderma: Sue's Story Time has passed since Sue's death. Only those who have experienced the grieving process can understand...
Arianna: Early LcSSc with lung involvement, recent alveolitis, and grade II esophagitis with hiatus hernia (Italy) What I want is to struggle against this disease to stop it from beating me...
Ariel: Linear Morphea Luckily, it only affects my skin, so I can still dance and play the piano...
Ariel D: Pansclerotic Morphea My first treatment was chemotherapy, then steroids, then light treatment...
Ariel M-S: Linear Morphea Within six months, the morphea had eaten away almost all of the fat on my arm and I have developed nerve and muscle pains that do not go away...
Ashlin: Localized Scleroderma It took me five months to realize that I needed to go to the doctor, and now I feel that I should not have waited so long...
Audley: Mother of Linear Morphea (en coup de sabre) Patient After one diagnosis of Vitiligo, my motherly intuition told me that the diagnosis was not correct...
Aurora: Linear Scleroderma I am always very tired, and I suffer from pain that will not go away no matter what I do...
Avril: Morphea The consultants in Nottingham, United Kingdom, have all shaken their heads in shock and said that they cannot provide treatment to me...
Awilda: CREST and Morphea Scleroderma In 1971, I had the first symptoms of Raynaud's. I'm 53 years old and live in Puerto Rico...
Aziz: Surviving Son of Gangrene Patient (India) What I am writing now is something even more horrible than what you might have read in a Stephen King's scariest of novels. My father died of gangrene...
(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
New Personal Stories
Mila: Morphea Now I am twenty-five years old, and that spot has grown throughout my right leg and on one side of my belly button...
(Español/Spanish) Mila: Morfea Hoy en día tengo 25 años y esa mancha está en toda mi pierna derecha y al lado de mi ombligo...
(Español/Spanish) (Update) Jeins: Esclerodermia Sistemica Difusa y Dermatopolimiositis Ya había escrito mi historia hace 3 años cuando recién estaba pasando por la enfermedad. Para quienes no lo saben tengo esclerodermia y dermatomiositis desde los 19 años.
Alana: Scleroderma (Peru) I cannot open my mouth completely, I have lost strength in my hands, I have breathing problems, my face looks different, my skin is really tight and I have lost my appetite...
(Español/Spanish) Alana: Paciente Nuevo con Esclerodermia (Peru) Le dije que ya no podía abrir la boca completamente, he perdido la fuerza de las manos, tengo problemas respiratorios, mi rosto está diferente, mi piel está dura y he perdido casi el apetito...
Kristy C: Generalized Morphea The only place where I do not have any morphea is my face, which I am very thankful for...
(Update) Raymond: Surviving Son of Scleroderma Patient On October 19th, the Herbert family lost another member of the family to scleroderma. My uncle Edmond has passed on...
More New Stories: November 2008
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