When people change meds, take out ,put in, higher dose, lower dose etc etc. Now and then people will state wow what a difference and wow what an impact please what am I missing.
I am 51 diagnosed 5 years still working just about for 25 hours a week get very weary and stiff first think on getting up could sleep for england but generally I keep going because I push myself currently my cocktail is the follwing
I found myself being increasingly rooted to the spot, falling, and then along came sinemet, 62.5m, which loosened my limbs, freed my feet and I was walking briskly again. My facial expression has become a look, as opposed to a glare, and yes, night time activity has improved because my body movement has. Tiredness is still a factor but not on the same scale as before, my timing when playing my guitar or keyboard is almost back.
Hi ....thank you for your comment and I can understand your 'wow' from what you have said.
I live in the UK and see my neurologist every 6 months and my PD nurse in between these times do you think this close monitoring has an impact I think it may.
Are you in UK ? I find it quite startling the efforts other people have to go to for meds and the cost.
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