A few of the young people associated with the Scleroderma Foundation. Go to the Scleroderma Foundation's home page.

 

Medical Articles
Camps
My Space

Books

Overlapping Diseases
Juvenile Home
my space
Alivia Watson

Feeling Better

By Alivia Watson

Hi! My name is Alivia Watson, and I am 10 years old. I am in the fifth grade. I have two little brothers named Tanner and Riley. Sometimes I wish I had a little sister. I really like the movie "High School Musical." For my birthday, my mom redecorated my room in all "High School Musical" bedding and accessories. I have a karaoke machine, and I put on “concerts” for my family, performing all the songs from "High School Musical 1" and "2," and Hannah Montana songs. Sometimes I even make my little brothers be in the concerts. My dad and my cousins and I sing together in church all the time. My favorite animal is a cat. I like horses, too. We have two quarter horses, and a pony. I’m kind of a tom boy, because I love to play outside! My favorite thing to do is ride four wheelers and go-karts through the mud. In the summertime I play softball and tennis. I don’t get to play outside very much in the winter because it’s so cold outside. I have Raynaud’s, and the cold makes my hands hurt too much to be outside for very long.

I was diagnosed with Raynaud’s when I was 4. My doctor told my mom and dad that I may have scleroderma. He kept a good watch on me for three years, and when I was 7 he told my mom and dad that I had systemic sclerosis. I had to start taking lots of medicine every night, and my mom had to give me a shot every week. I hate needles! Also, I spent the night in the hospital once a month to get some special IV medicine. I was a little bit scared, and confused because I didn’t feel bad ALL the time. Sometimes I felt tired, and my hands and wrists hurt. My mom told me why I had to do all these things, and I tried to be strong. But sometimes it was hard. One time I asked my mom if I was going to die. She told me that my life was in God’s hands, and He would take good care of me.

For two years I took all my medicine and shots just like my doctor said. I had tests every three months to make sure my lungs and heart were okay. My mom and dad and all my family and friends prayed that God would take care of me. Eventually, I started to feel better. My hands and wrists didn’t hurt anymore, and my doctor said I could stop taking some of my medicine. He told my mom that I looked so good he wanted me to go see a special doctor in Pittsburgh, Pa. In July, my mom and dad and I fl ew to Pittsburgh for my appointment. It was the first time I ever got to fly! I was so nervous I almost threw up on the plane! The doctor was really nice. He examined me and asked me and my parents lots of questions. After a long visit he told us that my scleroderma is in the limited category. He said I could stop taking all my medicine! No more needles every week! I was so excited! When we got home every one was so happy to see us. My grandparents took the whole family out for a big dinner to celebrate!

My life has changed a lot since the doctor told me that my scleroderma is limited. I don’t have to take so much medicine anymore. And I feel so much better. I only have to go the hospital a couple times a year for tests instead of every month.

I still can’t play outside in the cold weather, and I always have to stay inside for recess in the wintertime. My friends at school don’t always understand. They ask questions, and I don’t always know how to answer them. My mom helps me figure out what to say. It used to embarrass me when people asked questions, but now I don’t mind because I feel so much better. Now I just tell people that God takes care of me, just like my family and friends always told me He would.

To reach Alivia, send an e-mail to cwatson@carington.com.

300 Rosewood Drive, Suite 105, Danvers, MA 01923 · Phone 978-463-5843 · 800-722-HOPE (4673)
Home  | Donate | Contact UsFree eLetter | Membership | National Conference | Message BoardStoreCalendar
Careers
Search Site

© Copyright 2001-2008 Scleroderma Foundation. All Rights Reserved. Disclaimer. Privacy Policy.

Last Updated 11/21/08

Webmaster