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Whether you are newly diagnosed, well-versed in Parkinson's, or a care partner, finding the right support group can make a significant difference. Social activities provide a valuable network, combat feelings of loneliness, and connect you to new information. Being diagnosed as young onset, poses its own challenges in finding people a group of people that look like you.

Your NDIS plan is built around your goals and support needs and funding is divided into Core, Capital and Capacity Building budgets. Core funding is generally the most flexible. Capacity Building funding can support your allied health therapies (e.g. AEP, APD, Speech Pathology, Physiotherapy, OT, podiatry, psychology, social worker). Plan management offers flexibility while reducing administrative burden, but you have the option of self-management.

Parkinson’s can affect intimacy, sexuality and relationships in physical, emotional and practical ways. Sexual difficulties are common, but they are not experienced by everyone. Many people continue to have satisfying intimate relationships after diagnosis. Communication is one of the most important factors in maintaining intimacy and connection. Intimacy involves more than sexual activity. Touch, affection, companionship, emotional connection and shared experiences all contribute to healthy relationships. Professional support is available if Parkinson’s affects your sexual wellbeing, confidence or relationship.