J. Magill-evans et al., Are families with adolescents and young adults with cerebral palsy the same as other families?, DEVELOP MED, 43(7), 2001, pp. 466-472
This study compared adolescents with cerebral palsy (CP) and their families
to adolescents without physical disabilities and their families as the chi
ld enters and leaves adolescence (age ranges 13 to 15 years and 19 to 23 ye
ars). Families of 90 individuals with CP (42 females, 48 males) and 75 indi
viduals without physical disabilities (34 females, 41 males) participated.
They completed the Family Assessment Device, Life Situation Survey, Multidi
mensional Scale of Perceived Social Support, and Future Questionnaire, Ther
e were few differences in family functioning, life satisfaction, or perceiv
ed social support between the groups. Expectations of young adults with CP
and parents of both adolescents and young adults regarding future independe
nce and success were lower than the expectations of the control group. Whil
e the group results emphasize similarities between families during the two
stages of adolescence, individual families and individual family members re
port specific challenges.