Re: New group started - FOR JOE

[Guest guest]

Hi Joe, Glad to see you here at this site. Please forgive me if you've already shared this info somewhere here, but have you been on LDN for 20 years? Is this the first time you've posted here? There are tons of newbies here, but the good 'ol non-newbies are few and far between. I really rely on the tried and true LDNers here for advice and encouragement. I know if I was just now seeking out LDN and I saw your story, I would've RUN to my doc to get the LDN. PLEASE keep posting for all the other new ldners coming on board. It's scary stepping out on your own and success stories like yours, with such passion, will help new ones even all the more. I plan on purchasing your book as well !!Thanks a Bunch,Janet KunselmanRRMS 1994, LDN May '07From: joe wouk <joseph.wouk@...>Subject: [low dose naltrexone] New group started - googleldn/To: low dose naltrexone Date: Tuesday, December 16, 2008, 11:45 PMThis group is dedicated to discussing ways of letting the world knowabout the benefits of LDN.My first effort was to publish the book, Google LDN ! It should beavailable everywhere by the end of January. My website, googleldn.com(formerly sclerotics.wordpress.com) has been up and running since Ibegan writing over 9 months ago. Through the website and now throughthe book I hope to be able to help a lot of people.But this is just the beginning. The time has come to put an end to thevirtual embargo on

LDN information that Big Pharma has managed to pulloff over the last 20 years. We all need to help each other get themessage out...Every person whose life has been helped by LDN should put up awebsite, or at minimum a blog describing their experience. If enoughsites go up, even the most sinister of reverse search engineoptimization will be unable to stop the tide.I'm offering my help and advice to anyone who wants to start a sitebut doesn't know how.I'm offering to come and speak at any venue that invites me and coversmy travel expenses. Don't worry, I'm a good speaker. Ask anyone whoattended the 4th Annual LDN conference.I need help. I need ideas. So do you. Please join Google LDN ! andlet's work together to make the world a safer and healthier place forall of us to live in.This LDN group is in no way meant to compete with the other LDN groupsthat are out there helping

people with practical advice. This group ismeant for ACTIVISTS who care enough to give of their own time andenergy to help the vast numbers of sufferers out there who never evenheard of LDN.Thank you in advance for your contributions, whatever they may be.ph Wouk------------------------------------

[Guest guest]

Thanks for your kind words Janet.

To answer your question, I began LDN in April 2008 and by July ALL my

PRMS symptoms disappeared.

Since then my brain has been rewiring itself around the parts

destroyed by the subcortical dementia before LDN halted it.

I have cut my intake of desoxyn from 5 pills to 2 per day. I hope to

be off them completely in 3-6 months.

You won't be sorry you bought the book, I promise. Any hesitant

patient who reads it will not only want the LDN afterward buy will

have the scientific clout contained in the appendix to FORCE the

physician to prescribe it.

I hope this book is just the first of many. I encourage any of you

out there who can write at all to tell your story. It costs very

little to self publish in this 21st century.

Working together, I hope we will by the end of the year FORCE congress

to change the law so as to never have a travesty like the 20 year

delay of LDN from happening again.

In my book I suggest an idea that will work and that I think Big

Pharma will support.

Don't believe me? Read the last chapter before the appendix that is

up on the previw.

Warmest,

Joe

> From: joe wouk <joseph.wouk@...>

> Subject: [low dose naltrexone] New group started -

googleldn/

> low dose naltrexone

> Date: Tuesday, December 16, 2008, 11:45 PM

>

> This group is dedicated to discussing ways of letting the world know

> about the benefits of LDN.

>

> My first effort was to publish the book, Google LDN ! It should be

> available everywhere by the end of January. My website, googleldn.com

> (formerly sclerotics.wordpress.com) has been up and running since I

> began writing over 9 months ago. Through the website and now through

> the book I hope to be able to help a lot of people.

>

> But this is just the beginning. The time has come to put an end to the

> virtual embargo on LDN information that Big Pharma has managed to pull

> off over the last 20 years. We all need to help each other get the

> message out...

>

> Every person whose life has been helped by LDN should put up a

> website, or at minimum a blog describing their experience. If enough

> sites go up, even the most sinister of reverse search engine

> optimization will be unable to stop the tide.

>

> I'm offering my help and advice to anyone who wants to start a site

> but doesn't know how.

>

> I'm offering to come and speak at any venue that invites me and covers

> my travel expenses. Don't worry, I'm a good speaker. Ask anyone who

> attended the 4th Annual LDN conference.

>

> I need help. I need ideas. So do you. Please join Google LDN ! and

> let's work together to make the world a safer and healthier place for

> all of us to live in.

>

> This LDN group is in no way meant to compete with the other LDN groups

> that are out there helping people with practical advice. This group is

> meant for ACTIVISTS who care enough to give of their own time and

> energy to help the vast numbers of sufferers out there who never even

> heard of LDN.

>

> Thank you in advance for your contributions, whatever they may be.

>

> ph Wouk

>

>

> ------------------------------------

>

>