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Familiar faces.


Bradley Shane Woodard, 2, looks ready for anything! Bradley has Down syndrome and underwent heart surgery at 6 months of age to correct an atrioventricular canal defect. Bradley attends preschool and receives physical, occupational, and speech therapies. According to his parents, Abbie and Shane, he is a "people person" and touches the lives of everyone he meets. The family make their home in Tallahassee, FL.



Victoria Solorzano, 4 years old on April 1, is sitting pretty! Victoria was born with arthrogryposis, a congenital disorder affecting the limbs, and cannot walk or move her arms. She is in pre-K and according to her mom, Christina, is very bright. She loves playing with her little brother, Daniel, 18 months, and she also enjoys swinging, splashing her feet in her baby pool, and painting (she paints with the paint brush in her mouth). The children live with their mom and dad, Douglas, in Miami-Dade, FL.



Daniel Patrick Holm, 2, looks like one happy guy! Daniel has Down syndrome and, according to his parents, Joe and Mary, is a pioneer at his daycare center. He was the first baby with a disability to attend the center, and because of the positive experience his caregivers are having, two other infants with Down syndrome are attending as well. His mom says, "Everyone remarks about what a cute boy he is, and his father and I couldn't agree more!" Daniel and his parents live in Omaha, NE.



Devin Wackter (left), and Grace Walline, both 1, are best friends! Both girls have Down syndrome and attend the Lee Ann Britian Development Center. Devin likes to play with her dog, make music, and sing. She lives with her mom and dad, Carla and Pat, in Shawnee Mission, KS. Grace, who is adopted, loves playing the drums and emptying mom's tupperware drawer! Grace has four brothers: Jordan, 13; Kyle, 10; Grant, 8 (who also has Down syndrome); and Berkley, 5. The children live with their mom and dad, Melissa and Tim in Overland Park, KS.



Devon Victor, 5, smiles for the camera. Devon has full trisomy 13 with translocation 5 and 13. His parents, Penny and Joe, were told that Devon would not be able to sit up, crawl, walk, talk, or grow properly. Penny says that instead, he has done all of these things! Devon attends a multi-varied exceptionalities kindergarten at Starke Elementary School in DeLand, FL, and loves learning. He also enjoys Barney, Pooh Bear, food, and Stuart Little. He has an older brother, Nicholas, 10. The family live in DeLand, FL.



Jonathan Hunter Carrington, 3, stands tall with the help of his nurse, Dennis Rushing. Jonathan had a reaction to the hepatitis B vaccine, experienced brain death three times, and now has spastic quadriplegic cerebral palsy, cortical blindness, and a severe seizure disorder. Dennis helps Jonathan with daily therapy and care. Jonathan enjoys rocking, being tickled, and has started to enjoy toys. Jonathan's parents, Tammy and Fred, say he is very proud of himself when he can stand and hold his head up. Jonathan is, according to his mom, "a true blessing--our miracle boy." He and his parents live in Diboll, TX.

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Publication:The Exceptional Parent
Geographic Code:1USA
Date:Apr 1, 2001
Previous Article:Behavior problems in children with epilepsy: what is the link? (Medical Research Update).
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