Craig* is 10 years of age. He likes being out, enjoying walks, going to community clubs, swings, playing catch with a ball, strumming the guitar, with his favourite thing being balloons. He attends Oaklands Special School.
Craig’s diagnosis is global developmental delay, right-sided haemoplegia, hydrocephalus and epilepsy. Craig has limited mobility but recently has made progress managing stairs with support. He uses a wheel chair when outside. Craig is non verbal but has begun to use PECS symbols.
Craig has lived at home since birth where his mother cared for him alone. Craig’s mother has worked hard to maintain him at home. However, in February 2012 Craig’s behaviour changed significantly and he became difficult for his mother to care for i.e. hitting himself and others, biting his hand, not eating, banging his head off the wall and floor. Additional supports were put in but not enough to sustain Craig at home and on the 8th of June Craig moved to Hillview Children’s Unit. He has been at Hillview five nights a week since then, going home to his mother for the other two nights. Craig also continues to attend Seaview Respite Unit, a service which he received prior to the recent difficulties Craig has recently had input from BIBSS and CAMH Learning Disability intensive support team.
On going to Hillview Craig’s distressed behaviour has settled including his eating, which is appropriate again. There were problems with Craig’s sleep pattern with him waking in the night and being distressed but this has lessened significantly. now requires a foster placement where the progress he has made at Hillview can continue.
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*names have been anonymised to protect confidentiality.