If you, or someone you love, suffers from Parkinson’s disease, then this is going to be one of the most important letters you’ll ever read.
Plus, most of the authoritative answers are written in medical language that you need a medical degree to understand.
You deserve to have all the information you need in one place, written in an easy-to-understand everyday language that won’t confuse you. Why should you be frustrated in your attempt to find relevant and important information?
(As if having Parkinson’s disease or caring for someone with the disease wasn’t challenging enough.)
Hi, my name is Lianna Marie and back in 1991 my mother Val was diagnosed with Parkinson’s Disease. Needless to say, the family was devastated.
We had no idea what Parkinson’s Disease was or what was in store for her, or how it would affect her life. We immediately began to ask questions such as…
Would she still be able to live a "normal" life… to be able to walk or dance or keep on playing the piano? (playing the piano is one of her greatest joys in life)
These were just some of the questions we simply didn’t know the answers to. This led to despair, sadness and a crushing fear of the unknown.
We did some things wrong because we simply didn’t know any better. I really wanted to help my mother. This was an emergency situation for me and sometimes we’re not our best in emergencies.
I checked the bookstores … searched the internet … and spoke to as many people as possible about how they coped with the disease and what worked for them.
I desperately wanted to help my Mom and nothing was too much to do if I thought it would lead to finding some useful information.
It’s taken…
