Jasmin was diagnosed with Fibrodysplasia Ossificans Progressiva, a rare genetic disorder, in January of 1999. The disorder turns muscles, tendons and other connective tissue to bone. Jasmin's mobility and immune system have become compromised, making it necessary for her to be schooled at home. This decreases the risk of infection and further illness.

Despite Jasmin's limitations, she manages to run her greeting card company , Jasmin Ariel Creations (www.jasminariel.com), to raise awareness about FOP on the internet.

Jasmin became inactive with Hugs and Hope January, 2009. We wish her well!

For email and snail mail addresses, personal web site URL, medical fund information, and a current list of interests and hobbies, visit our "Kids List" page.

For CURRENT UPDATES visit our updates page.