The Unequal Care at Life's End for Parkinson's Patients

The way people with Parkinson's disease and related disorders (PDRD) are cared for at the end of their lives isn't fair. Men and people of color often end up in hospitals more than others. Yet, they are less likely to get hospice care. This is a big problem, but why it happens is a mystery. Hospice care is supposed to make the end of life more comfortable. It focuses on quality of life, not curing the disease. But not everyone gets this chance. For some, the hospital becomes their final stop. This isn't just about where they spend their last days. It's about how they spend them. Are they in pain? Are they alone? These are tough questions. Think about it. If you or someone you love had Parkinson's, wouldn't you want the best care possible? Wouldn't you want them to be comfortable and surrounded by love? That's what hospice care offers. But for many, this isn't the case. Instead, they face hospitals, treatments, and often, loneliness. Why does this happen? Is it because of where they live? Is it because of their race or gender? Or is it something else entirely? These are important questions. Understanding them could help make end-of-life care fairer. It could help ensure that everyone gets the care they deserve. Parkinson's disease affects millions worldwide. It's a progressive disorder, meaning it gets worse over time. It affects movement, causing tremors, stiffness, and balance issues. But it's not just physical. It can also affect mood and thinking. Living with Parkinson's is tough. Dying with it should be as comfortable as possible. Yet, for many, this isn't the reality. There are many types of Parkinson's disease. Some are genetic, others are not. Some start early, others late in life. But all share one thing in common: they need good end-of-life care. This care should be fair and equal, no matter who you are. Yet, this isn't always the case. Understanding why is the first step to making a change.