LDN

[michaela13]

When is the research on low dose nalproxen going to be available to the public? If this drug is as good as people say, then everyone who is suffering with these horrible illnesses should be able to easily get it. Anyone have ideas how we can make it public knowledge?

[Norton1]

Michaela13

Although there are 'success' stories of people reversing Parkinson's symptoms when taking LDN and long may they continue, not everybody who has tried it has experienced similar or even any improvement. LDN works for some PwP just as Sinemet does, but not all.

I think anybody who has 'Parkinson's and visits the various forums such as this one, will sooner or later come across LDN.

Norton1

[ancee]

what is considered a low dose of naproxen?

[FMundo]

I would say that research on LDN will not occur as there is "no money in it." Big Pharma has no interest, as Naltrexone is FDA approved and is no longer patentable.

Research scientists have no interest as fame and fortune won't come their way either. I've been taking LDN for a year and a half and even though I have the "faster" version of PD, PIGD (Posture Instability Gate Disorder as opposed to the Tremor at Rest version) and I am "late onset"... the progression of symptoms has stopped and there are no side effects (other than waking up briefly at 2:00 a.m.) And the cost of LDN is $25 a month.