Warm Hugs
Get a FREE warm hug today at
Search sclero.org:
 
The most important thing in the world to know about
scleroderma is sclero.org with 5,000+ pages in 23 languages!
 
Earn $50 for PAH Marketing Research Survey!
Home   Donate/Shop   Medical   News   *Sclero Forums*   Support   Languages/Countries
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
Stories in Other Languages: French | German | Greek | Italian | Polish | Romanian | Russian | Spanish | Turkish
Stories by Date Posted: 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010

Star S: Morphea and Systemic Scleroderma

They should think of how bad they feel when they get the flu and then think of about fifteen more conditions each with its own problems.

Vegetables for Star, by Shelley EnszI was diagnosed with morphea at age seven. Now at age thirty-three, I have recently developed systemic scleroderma with gastrointestinal manifestations, Sjogren's syndrome, inflammatory arthritis, malabsorption (celiac, ulcerative colitis, Crohns disease?), and many more. I have had secondary Raynaud's for years although recently it has gotten worse with digital ulcers.

I also have great difficulty with apthous mouth ulcers. They are always in my mouth although they flare up at times worse than others, they are extremely painful and I get cracks at the corners of my mouth and have bad dental problems. My mouth is getting tighter, I have difficulty with swallowing, talking and hoarseness. This makes it hard to eat and drink, and I am already very thin.

I have many other chronic diseases including chronic disabling migraines for seventeen years, fibromyalgia, depression, allergies, eczema, esophageal reflux, constipation, tendonitis, urinary incontinence, and restless legs syndrome. I have also experienced severe trauma and physical and emotional abuse.

When I was a kid I was often asked if my parents abused me because of the large bruise like areas on my hips and legs (especially during swimming), and even today at doctors I often am asked if my husband beats me.

Some of the most difficult things with any of my chronic diseases are not being able to do things for myself, having people not believe I'm sick ('you look okay') ,and accusing me of having an eating disorder. I also have a handicap sticker and get rude comments and looks constantly. Last of all, not being able to do things I love doing. I love to shop, travel, draw, write, read, go to concerts, etc. Unfortunately I get sick in the car so I can't travel far. My hands are so swollen and stiff that I can't open bottles, etc. It's extremely frustrating at this age as I wet my bed, I have urinary incontinence from my seventh pelvic surgery for severe endometriosis of ovaries, fallopian tubes, rectum, ureter, and bladder.

I also have adhesions from all my surgeries and these cause severe pain daily. My last surgery they took my last ovary so I am in menopause (no uterus, or ovaries left, or appendix).

I live near Madison Wisconsin if anyone is near by. I also would love to volunteer. I am especially interested in animal rights and have been a vegetarian for about seventeen years, something I am proud of.

I have been married for fourteen years, although we are separated at the moment. I raise my son mostly myself and I wish people would give me more credit. They should think of how bad they feel when they get the flu and then think of about fifteen more conditions each with its own problems. Every day, no breaks, raising a kid, keeping house, paying bills, it is very hard.

My son keeps me going , he is my star, he is so helpful. I don't know what I would do without him. He asked me a week ago if I was going to die because of all my illnesses?

All I can say is, if you have your health, cherish it. All the medications, doctors, pain, fatigue, and not knowing if tomorrow will be the day my kidneys shut down is a lot to handle. However, I enjoy each day to the fullest and am thankful every day. I don't blame or regret my illness, I just want to help others.

To Contact the Author
Star
Email: angelstar@charter.net
Story edited 08-10-08 JTD
Story posted 10-04-08 SLE
Story Artist: Shelley Ensz
Story Editor: Judith Thompson Devlin
LINKS
Bowel Involvement
Dental Involvement
Depression
Depression Stories
Digital Ulcers
Digital Ulcer Stories
Endometriosis
Fibromyalgia
Fibromyalgia Stories
Gastrointestinal Involvement
Heartburn (Reflux)
Heartburn (Reflux) Stories
Morphea Scleroderma
Morphea Stories
Raynaud's
Raynaud's Stories
Sjogren's Syndrome
Sjogren's Stories
Skeletal Involvement
Skeletal Involvement Stories
Systemic Sclerosis (Scleroderma)
Medical: Diseases and Symptoms
Scleroderma Experts (Worldwide)
Symptoms of Systemic Scleroderma
Types of Scleroderma
What is Scleroderma?
ISN Story Editor: Judith Thompson Devlin
Judith Rose ThompsonJudith 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!
New Personal Stories
Mars: Scleroderma with Full Gastrointestinal Involvement I finally started total parenteral nutrition (TPN, or tubal feeding) in May 2010 and it was an absolute success...
Sonya D: Surviving Daughter of Systemic Scleroderma Patient (Portugal) She had difficulty eating, drinking and digesting her food, but yet doctors had no clue...
Hazel: Morphea Scleroderma In 1962 when I was just twelve years old, my mother took me to our family doctor with what looked like a blister under my right eye...
Angela R: Linear Morphea Scleroderma I am twenty-five now and only have the two spots that I deal with pretty easily. I just hope it doesn't get worse...
Heather A: Scleroderma (South Africa) My fingers started to curl up and I could not wear any rings on my fingers anymore as they were so swollen...
More New Stories: May-July 2010
Submit Your Patient, Caregiver or Survivor Story in:
Arabic  | Dutch  | English  | Español  | Deutsche (German)
Italiano  | Polski  | Russian  | Spanish  | Turkish  | Other Languages
We will edit your story, create original artwork to decorate it, prepare it for the web, and post it on this site. Just fill out our simple Story Submission Form for your story, updates, or email address changes.
 
Go to Stefan: Progressive Systemic Sclerosis
 
SCLERO.ORG is brought to you by the nonprofit International Scleroderma Network (ISN). The ISN is a full-service nonprofit scleroderma charitable foundation providing stellar research, support, education and awareness for scleroderma and related illnesses, such as pulmonary hypertension.
  1. Post a message in Sclero Forums
  2. Email: isn@sclero.org
  3. English Email Form
  4. Español Email Form
  5. Italiano Email Form
International Scleroderma Network (ISN)
7455 France Ave So #266
Edina, MN 55435-4702
United States

This website is certified by Health On the Net Foundation. Click to verify.
This site complies with the HONcode standard for trustworthy health information: verify here.

Toll Free Hotline in U.S.
Hours: 9am-3pm CST only.
Please leave a complete message, in English.
1-800-564-7099
Direct Line
1-952-583-5735
We are also known as the Scleroderma from A to Z web site.
Privacy Policy, Financial Disclosure, and Disclaimer.
© Copyright 1998-2010 International Scleroderma Network
All Rights Reserved
 
Home   Donate   Medical   News   *Sclero Forums*   Support   Translations   Search