Re: Re: Multiple sclerosis - MS150/Just the facts, ma'am

[Guest guest]

From: Val Hoenecke <valhoenecke@...>Subject: Re: [low dose naltrexone] Re: Multiple sclerosis - MS150/Just the facts, ma'am"art_ldn" <rtee54@...>Date: Thursday, April 1, 2010, 1:29 AM

The MS society of Canada will never get a cent from me or anyone connected to me. They say they represent us and all is well as long as we are sick. If we get well on LDN or CCSVI liberation they won't have a slush fund to play with. I have never been so disappointed in my life. What bothers me the most is they say they represent us msers.

From: art_ldn <rtee54@...>low dose naltrexone Sent: Wed, March 31, 2010 5:31:48 PMSubject: [low dose naltrexone] Re: Multiple sclerosis - MS150/Just the facts, ma'am

The National Multiple Sclerosis Society (NMSS) does not support the use of LDN for MS nor will they properly fund research into its use, in fact they do everything possible to dismiss it. Therefore I give this post two thumbs down. No money from me to them until they recognize LDN for MS.See here how they spend the money. The president of the NY chaptor rakes in over $400,000.00 a year!Charity Navigatorhttp://www.charityn avigator. org/index. cfm?keyword_ list=nmss & Submit2=GO & bay=search. resultsArt-->> Hello,> I'm helping my friend raise awareness about Multiple sclerosis. His name is Yusef and he will be joining the MS150 cause to collect money to help research MS. The pledge amount is low, however he is looking to raise the most amount for this great cause. Kindly, pass the information to your friends to raise awareness or help contribute for this cause. > > For Donations:> https://secure3. convio.net/ nmss/site/ Donation2? idb=228428242 & df_id=27155 & FR_ID=13371 & PROXY_ID= 7958974 & 27155. donation= form1 & PROXY_ TYPE=20 & JServSes sionIdr004= phrmc6xlk1. app323b>

> MS150 Info:> http://www.national mssociety. org/index. aspx> > Thanks,> >

Get the name you've always wanted ! @ymail.com or @rocketmail.com.

[Guest guest]

I agree with Art, and others who have expressed this opinion. Not only do they not support LDN for MS, they also don't acknowledge the benefits of an appropriate diet. I went to a society-sponsored weekend retreat and the organizers had never heard of the Best Bet Diet (or any diet protocol). It was a big deal to get the proper food - to everyone else they served lasagna, lots of pasta and bread, many desserts and candy, etc.

I've stopped taking mailings from them and I also do not go to any of the group meetings that they have locally because of the lack of knowledge on the part of both speakers and patients. On the few occasions I've attended, I nearly wound up lecturing the group on LDN and the Best Bet Diet, and I'm newly diagnosed! I'll stick to this forum, thank you.

IMHO, why would they support a "cure" that didn't generate revenue? It would put them out of business!

From: art_ldn <rtee54@...>low dose naltrexone Sent: Wed, March 31, 2010 7:31:48 PMSubject: [low dose naltrexone] Re: Multiple sclerosis - MS150/Just the facts, ma'am

The National Multiple Sclerosis Society (NMSS) does not support the use of LDN for MS nor will they properly fund research into its use, in fact they do everything possible to dismiss it. Therefore I give this post two thumbs down. No money from me to them until they recognize LDN for MS.See here how they spend the money. The president of the NY chaptor rakes in over $400,000.00 a year!Charity Navigatorhttp://www.charityn avigator. org/index. cfm?keyword_ list=nmss & Submit2=GO & bay=search. resultsArt--