How has having Parkinson’s disease affected your social life? Have you made new friends through online or in-person support groups for people with PD and/or caregivers? Have you enjoyed connecting with people in this forum?
Do you prefer to connect with people in-person or online? For me, it’s a bit of both but everyone is different. What works for you?
For anyone who might be new to the PD community and looking for friends, where would you recommend they start?
Parkinson’s News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website.