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RE: Re:LDN Short story book

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Yes he did speak at last year’s LDN Conference (I’ve watched the

video) – good stuff, and I am excited and pleased to see that he will be speaking

at the First European LDN Conference in Glasgow.

Best,

Jayne

Please sign the petition to the UK Govt to fund trials for LDN

http://petitions.number10.gov.uk/LowDNaltrexone/

From: low dose naltrexone

[mailto:low dose naltrexone ] On Behalf Of foxhillers@...

Sent: 18 March 2009 17:10

low dose naltrexone

Subject: [low dose naltrexone] Re:LDN Short story book

Thank

you for the comprehensive update, Aletha.

Do

you remember how, after I edited your wonderful welcome letter several years

ago, we talked about doing a website focused on testimony (stories) indexed

on specific health issues? I looked at that provisional site just

last week. :) Like old times......

Meanwhile,

please know that my recent LDN research has identified yet another book that

you can add to your list. " Google LDN " by ph Wouk. I

think he even spoke at the LDN Conference in 2008. He deals with MS.

mjh

LDN Short story book

Posted

by: " Aletha Wittmann " Aletha@...

wittmann.aletha

Tue

Mar 17, 2009 10:26 pm (PDT)

Hi

MJH,

I am officially collecting the stories, my friend Debra is helping me edit and

work with the stories (with full permission from the writers on the final

drafts), Bradley will be doing the publishing end, Cris, and many

others have been instrumental in helping to collect stories etc. And this is

really everyone's book in the LDN community, because it is everyone's stories.

So I feel much more comfortable saying " we " .

LDN would not be where it is without everyone coming together on the internet,

in chat rooms and by approaching people and sharing their experiences and

stories. I started my husband on LDN because I found stories from 60 people on

a web page describing how LDN gave them their lives back. Common sense told me

that this many people could not be wrong. Many of us would not have ventured

out and pursued this avenue if we had not heard the stories and experiences

from those that came before us. And we know without this drug being essentially

people powered or people driven, it may never have caught the attention of so

many doctors, pharmacists and researchers. It would not be where it is today

without these stories.

I feel it is very important to get these stories documented and in a book form

that people can get off of the shelves. It can be so helpful for those

suffering from an ailment to be able to relate to what someone else has been

through and what things have helped them. These stories can also highlight the

difficulties that patients go through when the want to try something that might

be best for their own bodies. I can't tell you how many excuses doctors have

given for why they can't prescribe LDN to people. They usually don't mind

writing a script for expensive toxic medications, but lord have mercy if they

were to prescribe this $1/a day non-toxic med that has been approved by the FDA

at 50mg, and can potentially be more effective than most drugs currently being

used for auto-immune diseases (this of course is my opinion).

At this time we have the following books available that are specific to LDN:

Bradley's book " Up the Creek with a Paddle " http://www.marybradleybooks.com/

which gives one woman's amazing journey with LDN and the many people she has

helped through her advocacy of LDN.

SammyJo and Elaine's 's book " The Promise Of Low Dose Naltrexone

Therapy " http://www.ldners.org/

a reference for researchers, practitioners and patients who want to understand

the therapeutic potential of LDN.

Cris Kerr's free e-book publication " Those who suffer much, know

much " http://casehealth.com.au/case/about.html

features 29 case studies of people using LDN for auto-immune diseases and

cancer.

I believe that the LDN Short Story book would be an important addition in

telling the LDN story and getting it in publication will help people to feel it

is more " real " holding a bound book in their hands.

Kindest of regards

Aletha

Great

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