My Nan (on my mums side) suffered from Parkinson’s for 9 years before she unfortunately passed before I was born.

I was diagnosed with Parkinsons in 2020. So far, I have been going ok. My Neurologist helps me review my medication every 6 months. As a result, I have been able to manage my 'down' time. As time goes by however, it is always in the back of your mind when you may not be able to cope normally with everyday life and activities. I have believed that exercise is 'key' and as a result I try to undertake a range of physical activities on a daily basis. Step up for Parkinsons will keep me on track and continue to motivate me to maintain my exercise / physical activities routine, plus provide some funds to help the continued provision of services.

My dad died with PD a few years ago. My sister and I join Step Up each year in his memory

For my continued own fight and advocacy for the rights of others to access the best Care available for their Parkinson’s.

Although Dad now lives away from mum due to Lewy body dementia, she visits him every day and the love and adore each other.

I’m Geoffrey Duong, retired Financial IT forced by Parkinson Disease (PD) I have been living with PD for the last 12 years. In February 2023, I had Deep brain stimulation (DBS) surgery. Prior to DBS, I was taking a tablet every 2 hours to manage my pd symptoms. At the time my Neurologist had suggested to do DBS, I was so worried… Thanks to him for his professionalism, expertise in the field, I was referred to a neurosurgeon who convinced me to go through the successful 6 hrs long surgery. A big thank you all medical staff that helped me pulled through the surgery. Otherwise I would have been bed bound now, I believe. My current activities to help slow down my pd conditions while researchers are working on a treatment are: PD warrior, KOPD, speech therapy, walking in local parks and attend community support activity. Your contribution will be much appreciated And thank you for your continued supports.