Traveling with Parkinson’s disease is predictably unpredictable
Planning a vacation or any type of trip can be exciting; it’s fun to have the calendar full of events. Our family has been fortunate to have traveled to many parts of the world.
The Bright Side — Jamie Askari
Jamie E. Askari is from Cleveland, Ohio, and serves as the managing director of Premier Health Advocates, LLC, a small medical advocacy organization. Her husband Arman was diagnosed with young-onset Parkinson’s disease in 2009, at age 38. Jamie and Arman have three grown children: Lexy, who is an attorney; Mandy, who is a dietitian; and Jake, who is an undergraduate student studying finance. She has named her column “The Bright Side” (actually, her husband named it!) because of their positive attitude regarding Parkinson’s and all other things in their life.
Featured Post
Let’s celebrate the family caregivers in our lives
It’s been such a warm fall season here in Ohio that it’s hard to believe that Thanksgiving is quickly approaching. Not only do we celebrate Thanksgiving in November, but it’s also National Family Caregivers…
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Botox for Parkinson’s disease symptoms? It’s not just for wrinkles.
If you thought Botox (onabotulinumtoxinA) was only used to reduce wrinkles and fine lines caused by aging, think again! It’s also used to treat many types of medical conditions, including the…
Just because someone carries it well doesn’t mean their load isn’t heavy
I’m not typically a private person by nature. But for nearly 15 years, I’ve worked hard to hide my heavy load, to keep it tucked away from the world. Some days, this load weighs…
The perks — and we found some! — of living with Parkinson’s disease
My family always looks for the good in every situation. We try to find the humor and the positive in times that can be hard. It’s our way of looking on the bright…
The long journey to my husband’s deep brain stimulation surgery
When I look back on our journey with deep brain stimulation (DBS), I wish I’d documented our experience on paper rather than the bits and pieces of memory my brain struggles to recall.
It’s not how much you do, but how much love you put in the doing
When dealing with a disease like Parkinson’s, eventually a caregiver will be needed. I suppose the politically correct term for this person is now “care partner,” at least in some circles. The…
To reveal or not to reveal a diagnosis of Parkinson’s disease?
Opening up about a diagnosis of Parkinson’s disease is a personal and complicated decision. While some share the diagnosis immediately with friends, family, and colleagues, it’s common for people with Parkinson’s to…
What happens when the caregiver needs care?
So what exactly happens when a full-time caregiver gets sick? Needs to take a well-needed day off? Can’t perform the necessary tasks of caregiving? As full-time caregivers, some crazy questions run through our…
Parkinson’s fatigue makes my husband’s days difficult
One of the most challenging nonmotor symptoms of Parkinson’s disease is fatigue. When I think about the word, a poor night’s sleep comes to mind, resulting in a day of being tired…
The freedom to choose our attitude: That has made all the difference
“Everything can be taken from a man but one thing: the last of the human freedoms — to choose one’s attitude in any given set of circumstances, to choose one’s own way.” — Victor…
How Parkinson’s disease has shaped our oldest daughter’s life
The name Alexa is of Greek origin and means “helper” or “defender of humankind.” Back in 1996, when my husband, Arman, and I were deciding on a name for our first child, we had…
Becoming an expert on my husband’s early-onset Parkinson’s
When my husband, Arman, was diagnosed in 2009 with early-onset Parkinson’s disease at the age of 38, I learned everything I could about it. I purchased every book I could get…
