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Re: Re: Urgent: pl. bombard the networks..

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HI THERE..IM IN A CHAIR.HOW LONG DID YOU DO LDN BEFORE YOU WERE WALKING.HOW LONG WERE YOU IN CHAIR. THANKS KENT

[low dose naltrexone] Re: Urgent: pl. bombard the networks..

I was out of town and came in late on this, might as well pound them right up to the last minute!Here's mine:Dear Dr. Zwibel,I suffered for 9 years with MS and only got worse on Copaxone, Avonex and Novantrone. Then I stopped all the MS drugs 1.5 years ago and started Low Dose Naltrexone, and have improved continuously. Went from wheelchair to walking 1 mile. The Univ. of Milan is beginning a 24 mo full trial to investigate the effect of LDN on MS. Can you address when and who may do this research in the US, and if not, why? The NMSS updated their position in April, saying this deserves investigation. What is the next step?--- In low dose naltrexone , "aegis_on_ms" http://www.nationalpatientforum.com/MS/MS_Home.htmThe best way is to address your queries by name to the differentpanelists. The chances are that each panelist will receive a list ofquestions..with some luck they might choose to investigate further.At the very least you would have educated them. Choose one of themany themes..Give specifics: Link Low dose naltrexone (spell it out) and one ofthe following..-e.g. ask if they have heard of the NY conference- low dose naltrexone is oral therapy-Hypothesis by Agrawal YP: based on science- Stick with MS..its a MS panel-have they seen the LDN survey at Accelerated Cure (previouslyBoston Cure)-Survey at Remedy find- Ongoing MS trials in germany, italyThis is a golden opportunity..our success will be measured bygetting the word LDN uttered on CNN.Pl. post this mail on other boards..with the linkAegis

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