as anyone had any experience with this

April 30, 2008

this was sent to me by a distant cousin I have never met. But

certainly sounds interesting. I have had neusosarc since 2003 and

now am in wheelchair and have severe double vision.

THIS IS OUR FAMILY---PLEASE READ

Over four years have passed already since Joy was diagnosed with MS.

I

remember Dot and Charlie Schauss (her grandparents) were up here

visiting

and how devastated they were because Joy could not see or walk well

enough

to be able to do such a simple task as go to the store with them -

something

she had always done from the time she was a little girl. Dot (about

78

years old!) grabbed her out of the car and literally carried her as

best

she could, into the store. Joy was hanging on to her " gram " and

doing her best to use her failing legs.

Joy was always so full of life, but her immune system was compromised

when

the MS attacked. The areas she was hit the hardest were her eyes

(optic

neuritis in both eyes) and her legs. She always kept very positive

mentally

though - I believe more for our sake than for hers. " Don't worry!!

I'm

fine!! " she would tell us all the time. But we knew she wasn't. We

started looking into schools for the blind and were trying to decide

on

what kind of wheel chair would work best for her. She was self

injecting

the

junk that her well-meaning neurologist prescribed, but she just kept

deteriorating. We did get a second opinion, diagnosis and prognosis -

all

concurring.

An answer to prayer came by the way of our Luke talking about

" alternative

therapies " that we immediately started to investigate. After

filtering

through all the snake oil, we were led (Divinely) to a Manhattan

neurologist

who wrote about his success in MS and other auto-immune patients

using

LDN.

We immediately made an appointment and got the prescription. Only by

our

Fathers grace and to His glory, Joy's sight was fully restored and

her

legs returned to normal.

She is again full of life and harassing her friends and relatives -

especially her poor old dad! ;-)

We went back to her original neurologist showing him the great

results

and

hoping he may be able to help his other patients with LDN, but of

course

he

was more than just resistant and tried to discourage Joy from taking

LDN. I

brought this information to a friend and co-worker of mine who

happened

to

be the doctor heading our research department. " Forget it - Big

Pharm is

making too much money on existing therapies - they'll never fund any

research " .

Since this " miracle " drug does not offer the pharmaceutical companies

any

financial gain (it's a very old patent) there is no aggressive

clinical

testing being done. There are many people whose lives have been

changed,

like Joy, by using LDN.

We are hoping to motivate the medical community to put aside their

financial

motives and get back to patient care via this petition. I'm asking

you

to sign this petition to help us reach our goal of 20,000

signatures. I

care deeply about this cause, and I hope you will support our

efforts.

Please pass this on to other " email buddies " . Thanks! - Tony and

Barbara

You can view this petition at:

http://www.thepetitionsite.com/1/sign-support-the-campaign-for-

research-trials-in-low-dose-naltrexone-for-multiple-scierosis

April 30, 2008