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Director, Mary Clark, M.D.
Mary is a pediatric orthopedic surgeon, with a particular interest in children [and adults] with congenital or acquired limb differences. "A professional" on the I-CAN list for about 8 or 9 years, she has attended two of the summer gatherings [Memphis and New Orleans], and looks forward to more.

Her professional training began at Yale Medical School, then surgery and orthopedic surgery residencies at the University of Pittsburgh. Part of that residency included 3 months at the Rancho Los Amigos Hospital in Downey, California--an orthopedic rehabilitation hospital. After residency, she stayed on the faculty at Pitt, and helped establish an amputee clinic at the Children's Hospital there [and a few years later, an amputee camp that's still going, 28 years later]. Over the years her practice has taken her to several other places, but she has always kept amputees and their families a part of her work. 

She is a co-author, with Dr. Hugh Watts, of Who Is Amelia?: Caring for Children with Limb Difference (1998).

An excerpt from In Motion

 
Director, Joyce Wheeler

Joyce has been an active member of I-CAN since 1997, about a year after the birth of her first child, Kayla.  Kayla was born missing both legs at the hip, right arm above the elbow and left arm/hand differences.  Their family has attended all but one of the annual meetings since she signed on and hosted the Seattle meeting in 2003. 

Joyce’s professional background is in accounting but she chose to cease working outside of the home shortly after the birth of her second child in 2000.  Since then she has chosen to volunteer at her children’s schools, is the Assistant Leader/Treasurer for Kayla’s Brownie Girl Scout Troop, and was Special Needs Coordinator for the Saint Edwards State Park Playground project in 2003.  She hosted the Seattle 2003 meeting with great enthusiasm and is helping to co-host the 2005 San Diego meeting.

Joyce’s hobbies and interests include gardening, reading and various craft activities.
Director, Lisa Swanzy

Lisa Swanzy is a Disability Specialist at Auburn University.  She has a bachelor's degree in General Rehabilitation Services and a master's degree in Vocational Testing and Counseling.

Lisa was born with bilateral above elbow limb differences (BAE).  She does have an elbow joint in her left arm; however, it is fused. The fusion was from birth rather than being a surgical one.  She also has bilateral proximal femoral focal deficiency (PFFD) resulting in a height of 3 feet, 10 inches. 

Lisa has been an I-CAN mentor almost from the beginning.  She wanted to be a mentor because she wanted parents and kids to be able to ask questions, express true feelings e. g. anger, bewilderment, etc. to people who had “been there, done that.”  

Growing up, Lisa’s parents treated her just like her brother (who has no disability).  She had chores to do, had to do all of her homework at the same time her classmates did, etc. 

She was fitted with her first arm at 18 months old.  At about 25 years old, she decided to stop wearing her arms ALL the time.   She now wears them about 15 to 30 minutes at most each day depending on what she need to do. 

Lisa's Profile 

 
 
 
Director, Jeff Brantly

 

 

 

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