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Terry E. (Mojoy the Clown): Morphea Profunda Linear Scleroderma
I volunteer as Mojoy the Clown.

Gold Dahlia for Terry by Sherrill Knaggs, ISN Artist I am a forty-seven year old woman and was diagnosed with this disease on September 13, 2004.

I am a hard worker. I have worked many jobs. The last three years I have been a caregiver for Alzheimer patients. And this past year I started working as an Activity Director at an adult care facility. I also work as a professional clown on the side, volunteering my time. That is when I started having trouble.

My right lower leg started to swell and the ankle grew big. It hurt all the time. But stubborn as I am I did not have it checked until my current boss told me to go to the doctor, so I did. Then it started.

I had my primary care doctor stumped so he sent me to a rheumatologist. He was stumped and then sent me to a specialist in San Francisco, Dr. Kari Connelly, who looked at me and immediately diagnosed me wit morphea profunda linear scleroderma. By that time my whole right leg was affected and I was in a lot of pain. I have started a lot of medications such as prednisone and methotrexate and Folic Acid, but they are still not helping the pain and muscle spasms.

Now it has moved to the other leg and also, my eyes have been giving me problems. So now I have gone to an eye doctor and he thinks it is also part of the disease. I am still in limbo with that and the doctors are working on figuring it out, all who are wonderful and curious at the same time.

I am on medical leave from my job, which is the hardest thing at this time. But I have many people supporting and praying for me and my spirits are staying lifted. This causes me to help others and encourage them. I will fight this with all my might and continue to help some way to find a cure.

Thank you for reading my story. All I can say is " Do not give up". There will be a cure. I would be happy to hear from others who need comfort. Bless you all.

To Contact the Author
Terry (Mojoy the Clown)
Email: mojoy4life@tcsn.net
Story edited 10-21-04
Story posted 10--22-04 SLE

ISN Senior Artist: Sherrill Knaggs
Story Editor: Judith Devlin
LINKS
Linear Scleroderma
Morphea Profunda
Types of Scleroderma
ISN Artist: Sherrill Knaggs (In Loving Memory)
Sherrill Knaggs Sherrill Knaggs, ISN Artist, created the digital photo to illustrate the story on this page. Sherrill lived in New Zealand. Her story was featured in ISN's book, Voices of Scleroderma Volume 2.
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
Maria T: Daughter of Deceased Scleroderma Patient (Italy) He, upon looking at my mom's face and hands diagnosed her with sclerodermia, in fact he took care of her until the end...
(Italiano) Maria T: Figlia di una Paziente Defunta di Sclerodemia (Italia) Lui, come vide a mia madre disse "tu hai la sclerodermia", guardandole le mani e la faccia...
(Update) Dee B: Limited Scleroderma/CREST Syndrome (South Africa) There is so much I want to add to my original letter after reading more of other peoples stories. I am certainly not getting better but wish I was...
Tessa: Morphea The nurse just told me that I have morphea and knew nothing about it and she told me to look online for information...
More New Stories: August-November 2009
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