Category: Parkinson’s Disease

Up ENDing Parkinsons

The number of exercise programs / options targeting Parkinson’s continues to grow. Recently, “Up ENDing Parkinsons” made its Charlotte debut. This is rock climbing for people with Parkinson’s Disease (PD). You read that right! Well, I assume you read it right. I really have no way of actually knowing what you thought you read.

But, yes! Rock climbing for Parkies! This seemed like the perfect fit for me. I spent a lot of time during my twenties and very late teen years wandering northern Colorado, looking for rock formations to scale. So, about three months ago, I decided to try Up ENDing Parkinson’s.

Charlotte is not exactly known for cliffs, so this is actually an indoor, human-made climbing wall. Several such walls, even. And this is REAL climbing. With ropes and harnesses. I never bothered with such equipment when scrambling up remote rock formations in my foolhardy days of yore. On some of the climbing ‘routes’ they connect your rope to a machine that prevents you from plummeting if/when you lose your grip. On the rest, they connect your rope to a human “belayer” who stays on the ground while you climb. I imagine that if you fall, the belayer would be catapulted into the ceiling, though I haven’t seen that happen (yet).

I was amazed at my lack of energy and my overall weakness. However, I was assured by several people that it’s normal for folks to feel that way in the first session, and that most folks get past that quite quickly. I went back a week later, but actually felt weaker during that second session. I had planned to go again the following week, but decided I needed to use that time to finish plotting my Maryland trip. Then I was in Maryland for about two weeks ago. Then I started having, ummm, issues with the Vyalev pump. I’ll address that in my next post. For now, I continue to believe in Up ENDing Parkinsons, and intend to go back soon.

Parkinson’s Symptom: Excessive Sweating

The only thing I really want to say about this week’s symptom is: Bleah! Seriously, this one’s pretty straightforward, so I don’t have a lot to say about it.

I remember sweating more than usual for a while, early in my Parkinson’s career. It seems to have stopped happening some time ago, but I wasn’t keeping an eye on the sweat, so I couldn’t tell you which drug (or other treatment) fixed it, or when. Or maybe my body has just gotten used to the increased sweating. Should my couch cushions be sopping wet after I lie down for a five-minute nap?


This was the final symptom I wanted to review as part of Thymptom Thurthdayth. If you’d like me to address any other symptoms, let me know in the comments section below. Otherwise, Thymptom Thurthday is out on its ass. I’ll probably replace it with Medication Monday. That should last about a month. By then, I’ll have some more amazing photos to share, as I will soon be trippin’ across Utah.