Guest guest Posted December 1, 2010 Report Share Posted December 1, 2010 Hello all, My parents and I are having a meeting tomorrow with my brother's psychologist and the psychologist from his day program, who met and us for the first time today. Initially, the meeting tomorrow was to include others from 's day program, but the program psychologist arranged it for him and us to go to the medical facility where goes for medical and psychological, to meet with 's psychologist. The purpose of this meeting is to discuss how we can help with his agoraphobia/anxiety. has not left the house in two weeks and has not gone to his program in 3 months. The program psychologist called and invited himself to come to the house today to meet . To say that today's visit with him was a huge disappointment, is an understatement. He started the meeting by saying that dementia is a possibility. When we told him that 's cognitive functioning has not changed and there is no memory problem, he went on to tell us that he didn't agree with the agoraphobia diagnosis. He criticized 's new psychologist at the medical center, he criticized 's psychiatrist, and even criticized the psychologist had 3 years ago at the medical center. Then he said that if does not like coming to the program then maybe he should drop out. My mother became furious and told him that he should " abandon that thought. " This is doubly incredible since my mother and our entire family have been actively helping the progran for over 20 years, including donating time and money and getting large grants from a trust managed by the last company I was with. He told us that we should offer to serve 's meals in the bedroom, to get him to go upstairs and if that works, to offer to only take him out for lunch/dinner and not serve him in the house. We said we would be open to that, but feel that he needs someone to come to the house to work with him. He said that we would not be able to get this service, that no one provides it and that Medicaid would not pay for it. I mentioned that we had learned of an agency that is providing this service, with money from grants, and that we placed on the 6 month waiting list, but it is critical that we need help now. I also mentioned our support group and that one of the parents was able to get help at home for her son. He said that the family should be able to work with . We did not tell him this, but my parents are in their seventies and I have taken a sabbatical from work to spend time helping them out. We are more than happy to do our share, but we cannot do it alone. I would appreciate any advice that any of you could provide in terms of the meeting tomorrow. Many thanks, Irene sister to , mosaic DS, ASD, 40+ Quote Link to comment Share on other sites More sharing options...
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