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4 Women With Parkinson’s Share What They Wish They Knew When They Were First Diagnosed

Photo credit: Hearst Owned
Photo credit: Hearst Owned

From Good Housekeeping

While Parkinson’s disease affects men twice more often than women—Michael J. Foxx has been one of the most famous to be afflicted by it—data shows that women experience a faster progression of the disease and a higher mortality rate.

With symptoms like tremors, rigid muscles, slowed movements, and speech changes, a Parkinson’s diagnosis can wreak havoc on the body. These four women, who have been living with Parkinson’s for up to two decades, open up about what they wish they knew when they were first diagnosed, including how important it is to have a rock solid support network.

“You can live a great life with Parkinson’s, but you have to accept help along the way.”

Photo credit: Hearst Owned
Photo credit: Hearst Owned

After Kelly Weinschreider, 47, of Chicago, Illinois, was diagnosed with Parkinson’s disease at just 29 years old, she was prescribed several medications that lessened her symptoms. Since she felt fine, it made it easier for her to ignore what was going on, especially since she didn’t tell many people about it. “I didn’t want people to feel sorry for me, or for my diagnosis to change my relationships, personally or professionally, ” she said.

That denial—plus side effects from the medicine and the disease’s progression—forced her to leave her job as a quality manager 10 years later. “I should have been seeing a behavioral health specialist to understand how Parkinson’s affected me and how to accept it,” she says. “Instead, I took my medications sporadically. I mismanaged time and commitments, and I had trouble performing my job and, ultimately, spun out. I wish I would have been more forthcoming with family and friends as to how the disease was affecting me.”

After living with the condition for 18 years, Weinschreider came to terms with her diagnosis. She also realized it truly takes a village to live life with Parkinson’s to its fullest and started to communicate with friends and family when she needed help. “You need the support of family and friends, the care of multiple specialists, and the foresight to plan for the future. You can live a great life with Parkinson’s, but you have to accept help along the way,” Weinschreider says.

“I wish I hadn’t dismissed early symptoms.”

Photo credit: Hearst Owned
Photo credit: Hearst Owned

Denise Coley, 68, of Morgan Hill, California was diagnosed with Parkinson’s two years ago, after months of having trouble balancing and experiencing insomnia and mood changes—all things she thought were unrelated to each other, not signs of a slow degenerative disease. “It wasn’t until the motor symptoms appeared, like the tremors, that I realized what was going on was a bigger issue than I originally thought,” Coley says.

In hindsight, Coley wishes she had responded differently, and run to the doctor first thing. “If I had realized sooner,” she says, “I would have spent more quality time with family. I would have looked into what changes in my life and home were needed earlier in order to manage a long-term degenerative disease, both from a legal perspective and in terms of my future care.” If you think there is even the smallest chance you might be dealing with Parkinson’s, see a doctor as soon as you can—don’t wait, she adds.

“I wish I knew how vital stress management is to slowing the progression of Parkinson’s.”

Photo credit: Hearst Owned
Photo credit: Hearst Owned

Lisa Cone, 57, of Wheat Ridge, Colorado, first experienced Parkinson’s symptoms 12 years ago. Her neurologist later explained that the tremors, insomnia, and intense pain that came with her diagnosis issues could be linked to stress; in fact, research shows that stressful life events may increase the risk of the disease and result in more severe symptoms.

While Cone doesn’t believe stress was the root cause of her Parkinson’s, she’s a firm believer that stress management and listening to your body is vital to one’s wellbeing. “I also wish I’d known I’d have to make difficult life-changing decisions like leaving a high pressure job and a bad marriage in order to reduce my stress—but these changes are worth it,” Cone says.

“I wish I knew that depression can very much be a part of Parkinson’s.”

Photo credit: Hearst Owned
Photo credit: Hearst Owned

Lou Eisenbrandt, 73, of Overland Park, Kansas was 55 when she was diagnosed with Parkinson’s after dealing with symptoms like a tremor, stiff muscles, and difficulty walking. She was diagnosed with depression shortly after that. “My depression set in a few days after my Parkison’s diagnosis. I was caught off guard—I would cry without knowing why, I had trouble concentrating, and I was dealing with fatigue and anxiety, all of which I’d never experienced before,” Eisenbrandt says.

Her neurologist prescribed an antidepressant, and she also learned holistic ways to minimize her depressive episodes. In addition to doing a bit of exercise each day to keep up her spirits, Eisenbrandt keeps busy with projects that she enjoys, like gardening and cooking. “I also journal and write regularly, sometimes just a line or two about a positive happening during the day,” she says. “Meditation as well as spending time with friends and grandchildren are beneficial for warding off depression, too.”

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