ALS

[Guest guest]

Hi all, am a grouper watching for a while, am seriously considering ldn

for als, would like to hear from others als users, especially in little

rock area about receptive doctors. thanks

[Guest guest]

Hi ,

By coincidence the Ozpals group (for motor neurone disease sufferers in

Australia and NZ I help moderate) has just received an email from one of

the people on there that I and others convinced to try LDN. It says:

" Have just finished my third week on 4.5Mg Naltrexone and would just

like to thank all the group members who supplied me with information on

this amazing drug!

Just three weeks ago I was beginning to become very distressed as I was

starting to wake up during the night with difficulty breathing, that has

now completly cleared up, as have my mucus and excessive saliva

problems! In addition I have re-gained some movement in my thighs, lower

back and right arm.

Family and friends have remarked that my face seems more animated and my

voice a little stronger. I would urge anyone who has not done so to

check out the LDN website www.low dose naltrexone.org, it is an eyeopener!

I find it astonishing that it is not better publiscised!

Chris. "

I then asked his permission to reproduce it here and he said:

" ,

Thank you, by all means forward it. I should have tempered my

enthusiasm a little, as you say nothing works for everyone. Hard not

to be excited when you have tried so many things over the past 2 1/2

years without effect and then to get such a dramatic result. I feel

confident about my future now.

Cheers,

Chris. "

wrote:

> Hi all, am a grouper watching for a while, am seriously considering ldn

> for als, would like to hear from others als users, especially in little

> rock area about receptive doctors. thanks