This video is a really great honest and open account of someone’s experience in taking Levodopa. Well worth viewing for anyone taking the drug or thinking of taking it.
One person’s 10 year journey of taking Le... - Cure Parkinson's
One person’s 10 year journey of taking Levodopa. How the amount has increased, the change in dosing intervals and how they manage it.
Great find! Thanks for sharing. I love her approach and her attitude. I'm going to subscribe to her YouTube channel.
How do you subscribe?
Thanks
On YouTube search for: My Carbidopa/Levodopa Evolution...10 Years w/Parkinson's!
Thank you for sharing this. So interesting and I really think she's got a great attitude. I have subscribed to her YouTube channel. 🙂
Excellent video.
Deals with the need to have:
- a dose that is higher enough for your needs, even if this is above 1000 mg C/L equivalent per day;
- dynamic dosing, taking pills as and when you need them, rather than at fixed times each day;
- for some, dyskinesia may be better than stiffness/slowness.
That's 20 minutes of my life lost watching a wannabe youtuber explaining her drug addiction.Does she work for big pharma?
WOW! I cant help but think that that comment was a bit unfair?
She is a bit light on scientific facts but I kinda appreciate that! Much of the science is hedged about with all sorts of disclaimers about
not everyone.....
you may have the opposite experience..........
there are no standard progressions.............
But I like her style.
The suggestion that she works for big pharma sounds pure tinfoil-helmet conspiracy theory!!
Big pharma comment was tongue in cheek.
She did another YouTube vid gaslighting people who decide to delay taking levodopa. Labelling them all as being levodopa phobes. So, yeah shes very balanced opinions on levodopa ...or maybe not🙄
Gaslighting? Really? Because she’s enthusiastic about a medication that helps her? And referring to the need for levodopa as an addiction is trying to shame people who benefit from it. I sincerely hope you are always able to stay on your high horse and avoid the need for it.
Quite the opposite. I'm happy for people to take levodopa. I use it in small doses myself and will no doubt take more as time goes on. But she referred to people in a previous video as levodopa phobes, which is insulting . And now she seems to be proposing maxing out on it.Perhaps referring to it as an addiction is wrong of me (but possibly not as I'm guessing we'll mostly all end up hooked eventually).
But to those who avoid it and get by through alternative methods, she should leave alone.
It's a documented phenomenon.
nature.com/articles/s41531-....
That isnt it at all. Sinemet is the first drug prescribed for PD. I have often noticed people with kinda obvious signs of PD who say they arent on any medication.
The reason is something to do with an irrational belief that if you can continue to be in denial about having PD, you won't have it.
It is nothing to do with having a phobia about a drug which most of them would never have heard of.
I find this kind of detailed "testimony" very useful, Thanks for sharing!
Rather than just trying to manage the symptoms isn't it better to get to the root causes of why dopamine isn't being generated naturally of what is destroying dopamine? This video doesn't even address the toxic effects of sugar on the body, esp the nerves ( just search for 'sugar toxic' to get a load of results confirming this. youtu.be/OKVi7aClKrA?si=eBE...
Ray Dorsey does good work about avoiding the environmental causes of Parkinson's. Here is another one: healthunlocked.com/cure-par...
However, once Parkinson's developed years later, it is rather late to avoid those causes.
What a perfect 20 minutes to convince any Parkinsonian NOT to start with levodopa! You can see where this is going, as probably within a year she will have had a DBS... 'the next heaven' or whatever.
It was so interesting to listen to your views. I was diagnosed with Parkinson’s 12 years ago and I am on 8x Madopar 25/100 a day. If I take less I become so rigid that I can’t move but I’m now starting to suffer with Bradykinesia on a more uncomfortable level. It can come down to a choice between the two and at least if you’re mobile you can get things done. For my own benefit I have to tweak my medication on a daily basis, it depends on what I am doing and how I’m feeling.
Thank you for sharing, it can’t be easy but you seem to be doing a decent job in managing your symptoms. Good luck in all you do.