Columns

Note: This column describes the author’s own experiences with deep brain stimulation. Not everyone will have the same response to treatment. Consult your doctor before starting or stopping a therapy. When I was diagnosed with Parkinson’s disease in 2015, I thought deep brain stimulation (DBS) was a last…

Hope can be found in unexpected places. When you’re lucky enough to find it, grab it, hold onto it, and allow it to fill your life. One of the highlights of attending the 6th World Parkinson Congress, held in early July in Barcelona, Spain, was watching the opening ceremony…

Drooling is embarrassing. I’ve caught myself spacing out with a trickle of saliva slipping out of my lips before. I can’t help but peer around the room to see if anyone noticed. I know I’m not the only one who has experienced this. My dad recently explained to me that…

When I was diagnosed with Parkinson’s disease in 2015, I was alone. I had an appointment with the neurologist, and I never even considered bringing somebody. My husband, John, was working as a vendor at a farmers market, so I drove straight there after the appointment. He was busy…

I recently discussed the importance of creating a solid care team to treat Parkinson’s. Expanding on that, I thought it’d be helpful to discuss a vital part of our current care plan: physical and occupational therapy. Before the pandemic, my husband, Arman, began working with a…

When I’m not busy writing my weekly column for Parkinson’s News Today, I’m the managing director of a small medical advocacy organization in Cleveland. In this role, I’ve learned much about our ever-changing healthcare system and the importance of having a dedicated team to manage all aspects…

Planning for travel is essential, and my recent trip to Spain for the 6th World Parkinson Congress (WPC) posed a question: While the host city, Barcelona, had planned for me and others with Parkinson’s through the World Parkinson Coalition’s Parkinson’s Ready program, would I be able…