Hello. My name is Sarah and I was diagnosed with Parkinson’s at the age of 39 years old. It was the biggest shock of my life and I still have days when I can’t believe it has happened to me. My husband and myself realised we needed to start a network, as we found there wasn’t much support for us when I was first diagnosed.  It been going since December 2011 and it’s been amazing to see it grow. My goals are to help find that CURE, offer help & support to fellow Parkies, plus try and raise as much money and awareness of Young Onset Parkinson’s. 

My name is Sue and I was diagnosed in March 2013. I heard about SLYPN through my consultant and it has helped me over time because I feel that I’m not alone…. I was introduced to Pauline when I first joined and the two of us are now good friends. I am also in touch with Sarah and Susan – Susan and I have very similar symptoms. I know that by being part of this close network, there is always support. There are also many social gatherings and fund raising events. Please feel free to contact me, I look forward to speaking or meeting you very soon.

I have known Sarah since our boys started at our local pre-school nursery.  We have always spoken about social media and the importance of it for SLYPN and now I am part of the team! I’ve lived in the Wimbledon area since my son was born so it’s great to become more involved in the community. I work with technology every day as I work part time for a digital magazine, so social media is core to what I do for my job. I hope to meet lots of followers in person over the next few months at the various events that I will be tweeting about!