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.
Blog Introduction Text
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.
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.
As winter melts into spring, you may be realizing that your exercise routine suffered through the cold season. You probably already know that exercise is a vital component to maintaining balance, mobility and daily living activities for people with Parkinson’s disease (PD).
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.
“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.