@clinicianinmotion: When should you start medication for Parkinson’s? 💊 This is one of the questions I see asked again and again — and honestly, it’s something I’ve had to navigate myself. There’s a common fear that starting levodopa too early means you’ll “use it up” or develop complications sooner. The evidence doesn’t support that. The LEAP trial and its 5-year follow-up found no significant difference in disease progression or prevalence of motor complications between people who started low-dose levodopa earlier and those who started 40 weeks later. So for me, the bigger question is: What are your symptoms stopping you from doing? Work? Exercise? Hobbies? Walking? Sleeping? Or simply feeling like yourself? I personally started medication last month following discussion with my Parkinson’s team. The aim was to see whether it could reduce my tone and tremor, improve the brain fog I was experiencing, and help me get more from my rehabilitation. So far… it seems to be doing exactly that. Medication isn’t the whole treatment plan. For me, it’s another tool alongside exercise, strength training, cardiovascular fitness, sleep, nutrition and managing stress. There isn’t one universal “right time” to start. It’s an individual decision made with your Parkinson’s team — based on your symptoms, your goals and your life. And remember: a scan doesn’t tell you when you should start treatment. This is my experience and interpretation of the evidence, not medical advice. Always discuss medication decisions with your Parkinson’s team. #Parkinsons #YoungOnsetParkinsons #Levodopa #ParkinsonsAwareness #ExerciseForParkinsons

ClinicianInMotion
ClinicianInMotion
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Tuesday 18 August 2026 10:01:59 GMT
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melliissssah
melliissah~dancing•in•the•rain :
I agree 💯. Medication gave me back the ability to move, and I am much more active and feel so much better today, 8 years post diagnosis, than I did 10 years ago.
2026-08-18 13:25:18
1
juneursini2
June :
Been on low dose meds 1x per day for 6 months now. Sleep with great lucid dreams.
2026-08-19 01:34:55
1
claire.harrison.p
Claire Harrison Poole :
Do Parkinson’s make pain worse
2026-08-18 18:11:04
1
maisondesdelices22
maisondesdelices22 :
Great advice. I chose not to start meds yet as my symptoms aren’t affecting my daily life too much right now 😁
2026-08-18 16:30:35
1
clairegroves04
Claire Groves :
My dad has Parkinson’s and he only has a Parkinson’s nurse to contact. Obviously we can take him to the doctors if he needs it but does anyone have any advice where else we can get support we are based in Colchester
2026-08-18 16:40:15
1
abdulwadudlouws
Opa Abdul :
Brain fog, I hear that a lot: what's the definition of it?
2026-08-18 14:28:45
1
elizabethggallegos
Elizabeth G. Gallego :
What about the diskensia😭
2026-08-20 09:46:01
0
albiragazzi
Fez :
Forty Weeks Is Too Little time to see any difference
2026-08-18 12:58:02
0
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