

Ted Wilton
Forum Replies Created
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Ted Wilton
MemberJune 27, 2025 at 3:00 pm in reply to: What was your first Parkinson’s sign or symptom, and how did you respond to it?For quite some time my family marveled at stories about my dreams, but no one connected the to me having Parkinsons (our son is a critical care paramedic, and three of our four daughters are nurses). One day one of our daughters (she has Parkinsons and is not a nurse) observed me walking down the street, and I was not swinging my arms. At that time, I was also having difficulties sleeping and our daughter wondered if I had Parkinsons (my father also had it). My wife made a comment to our family doctor about my strange gait and my dreams, and he made a preliminary diagnosis. So, a daughter (not a nurse) who has Parkinsons, and a strange gait were the were the keys to my diagnosis.
Ted Wilton
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I do not like the term “Parkie”. It seems to convey a light-hearted reflection on Parkinson’s Disease, and from my experiences, Parkinson’s is not a lot of fun.
Ted Wilton
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Ted Wilton
MemberJuly 28, 2023 at 12:12 pm in reply to: Which Parkinson’s symptom bothers you the most?Dizzy spells [perhaps caused by low blood pressure] and the so-called “goofy head” are most annoying to me, as both have hindered my mobility on uneven surfaces [I am a geologist, and this has essentially eliminated all of my field work now. As time advances these two symptoms seem to be getting routine, especially for the first few hours after I get up in the morning.
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After I take my Sinemet along with a single Colace tablet in the morning, I take a single cap full of MiraLAX (actually the Costco version, which is less expensive than the MiraLAX brand) in a large cup of coffee. This seems to work almost all of the time and is generally effective in keeping me regular. I used to travel extensively with my job, and that always upset my system, even when I was able to use my regular routine, and it took a few days to get “back on schedule” once I returned home.
Constipation showed up several years before I was diagnosed with PD, and the routine of daily MiraLAX was endorsed by a doctor when I had my most recent colonoscopy (about two years prior to the PD diagnosis). My neurologist has supported my use of MiraLAX, and suggested taking a double dose if problems become more frequent, but I have not had to resort to this increase.
TED
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Ted Wilton
MemberSeptember 15, 2022 at 2:34 pm in reply to: What are your thoughts about Deep Brain Stimulation?Our youngest daughter, who is 37, had the surgery earlier this year, and it turned her life around, essentially it has been a miracle for her. So many of her symptoms are no longer active, and the reduction in her medications has been significant.
I had been skeptical of its benefits, but in her case I was wrong. My PD is less pronounced than hers was, but if I ever get to that point, I will reconsider my earlier objections to it.