Part of Steven Goldenthal’s job is to get people connected. He wants to know how they feel, gets to know their medical history, what medications they take and if they are happy with their Parkinson’s disease (PD) care.
National Parkinson Foundation's blog
Safinamide (Xadago) was approved by the Food and Drug Administration (FDA) for treatment of Parkinson’s disease (PD) medication fluctuations. Safinamide is a pill that when absorbed in the bloodstream travels to the brain and affects dopaminergic and non-dopaminergic systems.
In Mood: A Mind's Guide to Parkinson’s, the newest educational book from the Parkinson’s Foundation, we explore mood changes associated with Parkinson’s disease (PD), why people with Parkinson’s might experience these changes and how to treat and cope with them.
Miriam* stopped using her cane. It was beat up, falling apart and wasn’t helping her manage her Parkinson’s disease (PD) symptoms. Medicare told her she had to wait to qualify for a new one.
Learning to take the best care of yourself is caregiver job #1. When you’re a Parkinson’s disease (PD) caregiver, life seems like an endless list of things to do with never enough time to do them. Every day can feel like it goes by in 10 minutes — and lasts two weeks.
Do you ever walk into a room and forget why? Incredibly, there is an easy way to help jog your memory: try closing your eyes. Your brain is a mysterious organ that researchers are still working to better understand.
One of the powerful concepts to emerge in healthcare over the past decade is health confidence. Health confidence is the confidence that you can control and manage most of your health problems, according to Dartmouth College health policy professor John Wasson. People with high health confidence are significantly less likely to be hospitalized long-term, fear their medication or feel like they were harmed by their disease versus similar people with low confidence.
Dr. Danny Bega’s favorite part of conducting the first-ever Parkinson’s disease (PD) improvisation comedy clinical research study is when participants told him how good it felt to make people laugh again.
Hope is something that is critical for everyone living with Parkinson’s disease. Hope for improvement in symptoms. Hope for a better life. Hope for a treatment that may one day arrest disease progression or even deliver a cure. We should embrace hope, but we should also protect everyone living with Parkinson’s disease and their family members from emotionally as well as financially draining opportunities which may overpromise and under-deliver.