Re: Re: Remedyfind Parkinson's LDN

September 2, 2005

Hi Windy,

I understand your frustration about getting the stories out there for LDN

and Parkinson's. Someone has mentioned that Remidyfind.com might start up a

section for LDN. That might be helpful. My husband has been using LDN now

since November for MS and it has been remarkable. I hope it is the same for

Parkinsons.

My best

Aletha

[low dose naltrexone] Remedyfind Parkinson's LDN

>>

>> > Hello, I check on this site almost daily and I don't see many posts

>> > from people with Parkinson's. Briefly, I've been on 4.5mg LDN for the

>> > past 14 months. My main symptom has been uni-lateral tremor which

>> > developed over the past 3-4 years and became progressivly worse. At

>> > first the doc's said it was MS but when I was put on 3x 25/100 Sinemet

>> > and 0.5 Mirapex by 3rd neuro 11 months ago, the tremor went away and

>> > it became apparent that I have Parkinson's. I have over the past

>> > several months cut back on the Sinemet to 1x 25/100 day and I am still

>> > doing well. I appear to be in the Sinemet " honeymoon " , it could last

>> > for 2-5 years before Sinemet begins to not work well. Or, LDN could

>> > keep me where I am now forever. So the problem with LDN and

>> > Sinemet/Parkinson's is; how do you know if LDN stops progression if in

>> > the short to mid term Sinemet has returned you to " normal " ?

>> > I was hopeing that Dr. Bihari could provide more detailed information

>> > on his Parkinson's patients and how he can be almost certain that LDN

>> > has stopped their progression. Maybe in the next LDN webpage monthly

>> > update?

>> > Are there any members here with PD who have been on LDN for any length

>> > of time and have an opinion if LDN is working as claimed?

>> > I would also like to claim to be the first one to post (ashleyk) on

>> > LDN in the Remedyfind Parkinson's (PD new to RF) section. Are there

>> > others who can comment and get the ball rolling on LDN and PD at

>> > Remedyfind?

>> >

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