Re: Fw: from kellie dominey in sydney Australia- lLDN petition in Ireland

[Guest guest]

Let's see if we can get at least some of the doctor's who are willing to prescribe LDN to at least release their names and whereabouts - even if they don't have time to respond to individual e-mails. That way new doctors looking at the problem for the first time will get at least some indication of LDN's acceptance and use by the medical community itself. I am sure there must be some doctors that are willing to stand up for what they believe to be a proper and safe use of a drug that offers potential relief to people all over the world??? Even if it is not going to make some big drug company rich!

Tom from Edmonton

----- Original Message -----

From: hellkell1@...

kim

Sent: Saturday, May 01, 2004 4:04 PM

Subject: [low dose naltrexone] Fw: from kellie dominey in sydney Australia- lLDN petition in Ireland

----- Original Message ----- From: hellkell1@...

elsegood@...

Sent: Sunday, May 02, 2004 7:41 AM

Subject: from kellie dominey in sydney Australia- lLDN petition in Ireland

Hey and others petitioning - great to see worldwide push for LDN.

I am a very rare person who got script for LDN in Australia by my local GP( very modern young forward thinking Dr. (a woman) who said it cant hurt you especially at such a low dose) and realises we have got nothing to lose here - having MS.

I came in armed with my facts off LDN site

low dose naltrexone -to convince to write script.

I am sorry I cannot give you her name as I was asked to keep it quiet( she is a very busy Dr and has full patient schedule as is- and didn't want a 1000 MSers at door of surgery - badgering for script - it has to be called in here - Govt. authority needed -so also they would focus on her if she started writing tons of naltrexone scripts.(our regulations tight here)

It is ONLY AUTHORISED FOR ALCOHOL ABUSE OR HEROIN WITHDRAWAL-IN AUSTRALIA LEGALLY ONLY !

and I can only get the 50mg naltrexone and chop up the tablets(not easy-small oblong tabs-1/4 of a 1/4 tablet to get about 3 mg.

This is the only way as of course-no trial done here for its use for MS-it would take years in the way our system is set up here-and actually I was lucky in the sense I used to have an alcohol problem-(2 years clean and sober) now...so my script would not have been questioned.

Most Dr's here say NO (most never even heard it being used for MS or other auto-immune diseases)- I believe -not willing till trial done for use in MS... are they going to consider prescribing....bit of legal fear here? .(trials are expensive and involved to set up - no funding available too - same old excuse)

My MS Unit at Royal Prince Alfred Hospital (RPA) in Sydney neurologist(MS researcher) Dr. Barnett said NO to - but asked me to send him any trial details on LDN I could find if there had been one...of course there hasn't been one done officially.

I mailed him through post - at his request - oodles of testimonials of LDN users around the world from my LDN group as noted above- on the positives they have found since starting LDN and said HERES YOUR TRIAL-A HUMAN TRIAL IN PROGRESS! - and I shall be seeing him at RPA on Wed May 12 - as I want to get his interest - and will be going for the jugular on this!!!!! lol! - to start LDN trial in Australia...

We can make a difference each and everyone of us...I support you totally with your petition - and Godspeed a trial soon!

cheers - sending healing light to you all..(.gotta love da Irish!)

love

Kellie Dominey (Irish descent Aussie - from Manly Beach Sydney NSW) - email hellkell1@... (I check daily)