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Friday, July 8, 2011

A few words about Y@P


Once diagnosed, I headed for the computer, where I found solace and company in chat rooms. There I met people with this 'disease' in common with me.
But I wanted to meet people in person; local people.
The first people I met, were Leonie and Bron. (Bron has since passed on.) It was great to talk about Parkinson's with others who had it and understood.
Ross Collins invited me to his group, where I met the Brocchis, loyal Y@P friends to this day, and Liz and Mark.
I decided that I was too young to go to the local support groups.
So I started up my own.
With the support of Parkinson's Victoria, I arranged for a group of us to meet at a Richmond pub.
Y@P - Young@Park, is for Young Onset who also are not ready for local, older groups. We have guest speakers. Our issues differ; many still work and have kids at home.
The group has grown over the years, with about 40 turning up to our informal gatherings.

2 comments:

  1. My father was diagnosed with Parkinson's disease at 57.his symptoms were shuffling of feet,slurred speech, low volume speech, degradation of hand writing, horrible driving skills, right arm held at 45 degree angle, things were tough for me, but now he finally free from the disease with the help of total cure from ULTIMATE LIFE CLINIC, he now walks properly and all symptoms has reversed, he had trouble with balance especially at night, getting into the shower and exiting it is difficult,getting into bed is also another thing he finds impossible.we had to find a better solution for his condition which has really helped him a lot,the biggest helped we had was ultimate life clinic they walked us through the proper steps,i recommended this www.ultimatelifeclinic.com to anyone who needs there help.

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