Re: 's Low Dose Naltrexone Journal: Month One

[Guest guest]

Hi Cat,

I'm presently working on this year's free LDN book, and I'd love to include

your story as a case study, so that every time the book is passed on,

someone new will learn of LDN through your eyes, and from your experiences.

Through the book, the value of your contribution will grow every time the

book is freely shared-forward.

To protect privacy, no identifying details are requested during the

creation of a case study.

Thanks to all who continue to share their experiences here to help others.

Together we can create a more enduring record of each unique journey,

Cris

**RIP 'Case Health - Health Success Stories' website May 2001 to May

2009.**

**Cris Kerr remains an advocate for the value of patient testimony.**

(1) If you'd like a copy of the free LDN book, email Cris at casehealth @

optusnet.com.au (remove spaces first).

(2) If you're just beginning your journey, please keep a diary record.

" The good we secure for ourselves is precarious and uncertain

until it is secured for all of us and incorporated into our common life. "

Jane Addams

8b. Re: 's Low Dose Naltrexone Journal: Month One

Posted by: " cat.mosley " cat.mosley@... cat.mosley

Date: Wed May 13, 2009 11:07 am ((PDT))

Ive been on LDN for about two weeks and I am thrilled. I no longer wake

up with that awful pain in my legs and feeling like the tin man. I know

exactly what you mean when you say you're having bouts of total

normalcy. It's amazing, I, too, had forgotten how wonderful " normal "

is.

I stopped the CRABs about six months ago, (I was diagnosed in 1991) I

simply hit a wall and could not bear the thought of one more needle or

days of flu like symptoms or welts all over my body, I just couldn't do

it. Now I feel like I've been given my life back and want to tell the

world!

The tradgedy is that the medical community, to a large extent, is

withholding information and more impoortantly, prescriptions for LDN

because the double blind, triple placebo trials have not been done.

They seem to be woefully uninformed as well. To my way of thinking that

is the arrogance of health. They can afford to wait for a day, a month,

a year.... I and my sister and my fellow MS sufferers can't.

I've told everyone and anyone who will listen about this wonderful

" find " that's been around for 20 plus years. Oh well, I am determined

to not live in the past but to enjoy my new found freedom and live life

the best way I can.

My very best wishes for your success with this wonderful drug, may it

restore good health and good thinking!

Namaste,

cat