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.
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Welcome to the National Parkinson Foundation's blog, where you can keep up-to-date on the latest research, read about what's hot in the Parkinson's community, learn caregiving tips and more.
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.
“Sexual health is the fundamental right of each person to enjoy and control his/her sexual and reproductive behavior in accordance with social and personal ethics,” states the World Health Organization, 2004. The Tel Aviv movement disorders center, a Parkinson’s Foundation Center of Excellence believes in helping their patients with Parkinson’s disease (PD) in all facets of life, including sexual health.
Three out of four people with Parkinson's disease (PD) do not get their medications on time when hospitalized, according to a National Parkinson Foundation (NPF) research study. As a result, 61 percent of those patients develop serious complications. In 2011, the Struthers Parkinson's Center, a Parkinson's Foundation Center of Excellence, decided to change these statistics.
Over the past two decades, deep brain stimulation (DBS) therapy for patients with Parkinson’s disease (PD) has been extremely successful. It has been estimated that DBS has meaningfully helped tens of thousands of patients worldwide, improving tremor, dyskinesia, on-off fluctuations and several other Parkinson’s symptoms. DBS has however, fallen short in addressing disease progression issues including walking, talking and thinking.
Something resonated with me on my recent visit to the Beth Israel Deaconess Medical Center, a Parkinson’s Foundation Center of Excellence (COE). As I listened to the Parkinson’s patients and caregivers panel, I was impressed to learn that everyone unanimously agreed on the vital importance of team care. From the movement disorder specialist to the nurse, everyone kept referring to “our” care plan. It was working.
Learning how to take care of yourself early in your journey as a Parkinson’s disease (PD) caregiver is more important than you might think. If you’re feeling exhausted, overwhelmed, too stressed to think clearly, then you can’t be at your best, as a person or caregiver.
2017 is here! Every New Year is a chance for a fresh start. Use our 5 simple tips to craft a resolution that can stand the test of time. Not the type to make resolutions? Scroll down to see our list of already-written Parkinson’s-related resolutions that may just help make life a little better for 2017.