2018 is here. A new year is a wonderful opportunity to start fresh and set new personal goals. This year, we did the hard work for you and listed four attainable New Year’s resolutions we know you can achieve this year.
For the newly diagnosed person with Parkinson’s
The Edmond J. Safra National Parkinson’s Wellness Initiative extends Parkinson’s care beyond the walls of the clinic. It uses a unique, medical-community partnership approach – pairing a Jewish Community Center (JCC) with a Parkinson’s Foundation Center of Excellence – to create inclusive, welcoming community hubs for people affected by Parkinson’s around the country. This video highlights how deeply impactful the program is for people with Parkinson’s and their care partners.
My Parkinson’s spouse has many physicians, as PD has taken its toll on so much of his body. I go to most his medical appointments as I am his constant observer, and I am the one fighting for his health. I have decided to write about having a voice when speaking with physicians as I find this extremely important, not only for me to be aware, but most importantly for him to get the best care as possible.
This quick starter guide for families and caregivers is from Honor. Every person with Parkinson’s disease (PD) is unique — and so is every caregiver. With the right preparation, planning and support, you can do this!
My big sister, Janet Reno, died on November 7, 2016. She lived with Parkinson's disease for 21 ½ years. I have walked that road by her side, but we have not walked that road alone.
It takes a village.
Everyone’s Parkinson's journey is different. Since it is age related, most people die of something else. There is no point dwelling on the last chapter if you are not going to get there.