Date: Dec 10, 2014
Stories from Mindy, a daughter impacted by her father's disease, and Greg, an individual living with Parkinson's, on how they are utilizing life with Parkinson's as an occasion to rise to.
I'll never forget the day I found out my dad was diagnosed with Parkinson's disease. I couldn't believe it when my mom told us. It was almost an out of body experience; and I'm still amazed by how quickly it changed my perspective on things.
I first thought about his relationship with my children. Would he be around to watch them graduate? Will he feel healthy enough to coach their soccer teams? I then switched my thoughts to my mom and prayed for the strength to be her support system, even before she needs it.
I woke up Monday morning to a slight buzz throughout my body. “Today is the day!” I thought. I rode the BX bus from Boulder to Market Street Station, then took a quick 16th Street Shuttle ride, and walked a block or so to my destination. The buzz was still present as I walked through the door of the Colorado Ballet and read the note saying “Rhythm & Grace meets in Practice Room C.” I was 30 minutes early for the noon class. “Today is the day!” Wow!
This posting is a snippet of the Recently Diagnosed with PD blog, written by Betsy Vierck.
Almost three years ago I was also diagnosed with Parkinson's. Ginny and I became refuges for each other. We have been extremely tight, speaking in a language that non-PDers can never understand.
As I sit here remembering one of the best ski outings I have experienced in recent years, I decided to share my joy with others affected by Parkinson’s disease. The January Parkinson’s Association of the Rockies’ newsletter featured an upcoming Ski Program for people with Parkinson’s sponsored by the Breckenridge Outdoor Education Center (BOEC). ...
Live in the moment
- Learn from the past, plan for tomorrow, but live for today.
- Don’t put off those activities that you have talked about doing “some day”.
- Make time for fun.
Be sure your doctor is a movement disorder specialist/neurologist (MDS).
Even if your doctor is a neurologist, this does not mean that he/she has the experience or education with movement disorders that will enable them to provide the specific care you need.