When I was seventeen I got three ridged circular marks on my arm, near the wrist. The marks were red, going pink, then lilac and white in the center. They eventually went away after about a year. My doctor could not diagnose it.
At twenty-one it is back on the same arm, only one mark this time, but bigger. It starts out solid, like eczema, then spreads out into a circle, until it fades and leaves a slight shadow, which fades to nothing. I asked my present doctor what it could be after explaining that my father has been a sufferer of morphea all his life and that another relative of ours also has morphea. The doctor looked up the symptoms on the Internet and told me it was probably morphea. If it had not been for my dad I would still be uncertain as to what the marks were.
I am very scared though, as I have heard and read so many worrisome things about morphea. I have not seen a dermatologist and my doctor knows nothing about the condition. I do not know whether it will get worse, what type it could be or if I can give it to any children I may have in the future. I get severe pains in the wrist where the morphea comes up and have problems with my joints. I would like to know if it is linked and where I should go now for help. I do not know if it will spread or come up in other places or if it effects other areas of health.
I did not know anyone else had morphea outside my family, so it is a relief to know I can ask for help from people who understand.
I would greatly appreciate any information anyone could give me about this, as it scares me. I do not even know what makes the marks come up. I know there is no treatment, but I would greatly thank anyone who can advise me about morphea.
I am thankful I now know what it is and that it is still not very serious.
Email: [email protected]
Story edited 09-13-04
Story posted 09-21-04 SLE
ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
Types of Scleroderma
What is Scleroderma Brochure
SCLERO.ORG was the world's leading nonprofit for trustworthy research, support, education and awareness for scleroderma and related illnesses from 1998 to 2021. It was a grassroots movement from the original Scleroderma from A to Z web site, which was founded by Shelley Ensz. We were a 501(c)(3) U.S.-based public charitable foundation. We closed this web site and our nonprofit agency in April 2021.