1. The needs of people with Parkinson's and their families.
2. Member's Survey.
3. Quality of life.
4. Children with parents with Parkinson's.
5. A psychological group approach.
6. Support networks.
7. Communicating with Parkinsonians.
8. Referral Criteria for speech and language problems.
9. A targeted physiotherapy service.
10. The use of video recording in assessment.
11. Parkinson's disease and driving.
12. The new community care.
13. Action research in a time of change.