new LDN Petition

A board to discuss Low Dose Naltrexone (LDN) as a treatment for Multiple Sclerosis

new LDN Petition

Postby LarryLDN » Wed Mar 24, 2004 10:41 am

Passing this along ....


Dear Friends,

I have set up an LDN petition: "Sign & Support the campaign for Research & Trials in
'Low Dose Naltrexone for Multiple Sclerosis'"

I am campaigning for LDN with Lorna from Scotland and Linda from England who's working closely with Dr. Bob Lawrence. And I am from the Republic Ireland. We are trying to reach 100,000 signatures, and we need
YOUR HELP!

Please help by signing this petition to help everyone with Multiple Sclerosis have easy access to Low Dose Naltrexone.

It takes 30 seconds and will really help. Please follow this link:

http://www.thepetitionsite.com/takeaction/110785607

Once you have signed, help even more, by telling your friends and family to sign as well!


Thank you!

Edwina
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Postby BrendaH » Thu Mar 25, 2004 11:25 am

Done! Thanks Larry, for posting this. Hope it helps to get LDN approved quickly.
Brenda H.
Only one thing has to change for us to know happiness in our lives: where we focus our attention. -Greg Anderson
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Postby LarryLDN » Thu Mar 25, 2004 11:33 am

Well... Today WE started something. Don't know what yet, but I've seen many countries signing up and showing in the last 25's that I've seen.

Thanks.

Got a long way to go, but Today, We started Something. This may be just what we need.
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Postby LarryLDN » Sun Jul 30, 2006 5:42 am

Wow, people are still signing this petition!

http://www.larrygc.com/ldnpetition is a shortcut link to it.
-- LarryGC/LarryLDN http://www.larrygc.com/ms
-- My LDN journal http://www.larrygc.com/mystory
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