The LDN for MS Research Fund

[Guest guest]

Hi group,

Not sure if you all saw this very important information that was posted here

and on the www.ldninfo.org site. It is the LDN for MS Research Fund and what

they are trying to do is get 100 people to donate $200.00 per person to

raise $20,000.00 to begin the long awaited trials on LDN and MS. I know that

we have all been trying to get this done and someone has finally gotten it

all together so that it can be accomplished. I know that Aegis polled the

group a few months back to see who might be willing and many of you said

that yes, you indeed would be willing to help. I will be sending my check in

on Monday morning and I hope that others will " put their money where their

mouths are " so to speak. Come on guys...this is way too important an

opportunity to pass up. I realize that everyone cannot afford $200.00 but I

suspect that whatever you can afford would be greatly appreciated. We might

just need more then 100 people but by God..it is doable. My thanks to Art

Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for making the

first move to make this a reality. We have waited so long and it's time that

we all got into that mindset that it ain't gonna happen on it's own. JoyceF

[Guest guest]

Hi Joyce,

I will be mailing in $400. Monday. Thanks for letting me know.

Aletha

[low dose naltrexone] The LDN for MS Research Fund

> Hi group,

> Not sure if you all saw this very important information that was posted

> here

> and on the www.ldninfo.org site. It is the LDN for MS Research Fund and

> what

> they are trying to do is get 100 people to donate $200.00 per person to

> raise $20,000.00 to begin the long awaited trials on LDN and MS. I know

> that

> we have all been trying to get this done and someone has finally gotten it

> all together so that it can be accomplished. I know that Aegis polled the

> group a few months back to see who might be willing and many of you said

> that yes, you indeed would be willing to help. I will be sending my check

> in

> on Monday morning and I hope that others will " put their money where their

> mouths are " so to speak. Come on guys...this is way too important an

> opportunity to pass up. I realize that everyone cannot afford $200.00 but

> I

> suspect that whatever you can afford would be greatly appreciated. We

> might

> just need more then 100 people but by God..it is doable. My thanks to Art

> Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for making the

> first move to make this a reality. We have waited so long and it's time

> that

> we all got into that mindset that it ain't gonna happen on it's own.

> JoyceF

>

>

>

>

>

>

>

[Guest guest]

I cant do that much money all at once, but i can send 20.00 now and more later. i need an address to send it to though. Thanks Aletha Wittmann <Aletha@...> wrote:

Hi Joyce,I will be mailing in $400. Monday. Thanks for letting me know.Aletha [low dose naltrexone] The LDN for MS Research Fund> Hi group,> Not sure if you all saw this very important information that was posted > here> and on the www.ldninfo.org site. It is the LDN for MS Research Fund and > what> they are trying to do is get 100 people to donate $200.00 per person to> raise $20,000.00 to begin the long awaited trials on LDN and MS. I know > that> we have all been trying to get this done and someone has finally gotten it> all together so that it can be accomplished. I know that Aegis polled

the> group a few months back to see who might be willing and many of you said> that yes, you indeed would be willing to help. I will be sending my check > in> on Monday morning and I hope that others will "put their money where their> mouths are" so to speak. Come on guys...this is way too important an> opportunity to pass up. I realize that everyone cannot afford $200.00 but > I> suspect that whatever you can afford would be greatly appreciated. We > might> just need more then 100 people but by God..it is doable. My thanks to Art> Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for making the> first move to make this a reality. We have waited so long and it's time > that> we all got into that mindset that it ain't gonna happen on it's own. > JoyceF>>>>>>>

Links>>>>>>>

Start your day with - make it your home page

[Guest guest]

The address to send in your check is

Accelerated Cure Project

300 Fifth Avenue

Waltham, MA 02451

I would think any amount would help out.

Aletha

[low dose naltrexone] The LDN for MS Research Fund> Hi group,> Not sure if you all saw this very important information that was posted > here> and on the www.ldninfo.org site. It is the LDN for MS Research Fund and > what> they are trying to do is get 100 people to donate $200.00 per person to> raise $20,000.00 to begin the long awaited trials on LDN and MS. I know > that> we have all been trying to get this done and someone has finally gotten it> all together so that it can be accomplished. I know that Aegis polled the> group a few months back to see who might be willing and many of you said> that yes, you indeed would be willing to help. I will be sending my check > in> on Monday morning and I hope that others will "put their money where their> mouths are" so to speak. Come on guys...this is way too important an> opportunity to pass up. I realize that everyone cannot afford $200.00 but > I> suspect that whatever you can afford would be greatly appreciated. We > might> just need more then 100 people but by God..it is doable. My thanks to Art> Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for making the> first move to make this a reality. We have waited so long and it's time > that> we all got into that mindset that it ain't gonna happen on it's own. > JoyceF>>>>>>>

[Guest guest]

Aletha - thank you for your generous contribution!

Joyce, thanks so much for helping get the word out!

http://ldninfo.org/research_funding.htm

SammyJo

--- In low dose naltrexone , " Aletha Wittmann " >

> Hi Joyce,

>

> I will be mailing in $400. Monday. Thanks for letting me know.

>

> Aletha

[Guest guest]

I agree 100% this is way too important to ignore. I sent my $200 in

last week. Hope everyone else will get on the stick and do likewise

or at least send whatever amount they can. Every little bit will

help.

Diane

--- In low dose naltrexone , " Joyce F. " <joyce445@h...>

wrote:

> Hi group,

> Not sure if you all saw this very important information that was

posted here

> and on the www.ldninfo.org site. It is the LDN for MS Research Fund

and what

> they are trying to do is get 100 people to donate $200.00 per

person to

> raise $20,000.00 to begin the long awaited trials on LDN and MS. I

know that

> we have all been trying to get this done and someone has finally

gotten it

> all together so that it can be accomplished. I know that Aegis

polled the

> group a few months back to see who might be willing and many of you

said

> that yes, you indeed would be willing to help. I will be sending my

check in

> on Monday morning and I hope that others will " put their money

where their

> mouths are " so to speak. Come on guys...this is way too important

an

> opportunity to pass up. I realize that everyone cannot afford

$200.00 but I

> suspect that whatever you can afford would be greatly appreciated.

We might

> just need more then 100 people but by God..it is doable. My thanks

to Art

> Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for

making the

> first move to make this a reality. We have waited so long and it's

time that

> we all got into that mindset that it ain't gonna happen on it's

own. JoyceF

[Guest guest]

Is someone on this forum able to keep us posted on how much is being

collected?

So far I only count 4 people from our forum.

Thanks

Aletha

[low dose naltrexone] Re: The LDN for MS Research Fund

>I agree 100% this is way too important to ignore. I sent my $200 in

> last week. Hope everyone else will get on the stick and do likewise

> or at least send whatever amount they can. Every little bit will

> help.

>

> Diane

>

>

>> Hi group,

>> Not sure if you all saw this very important information that was

> posted here

>> and on the www.ldninfo.org site. It is the LDN for MS Research Fund

> and what

>> they are trying to do is get 100 people to donate $200.00 per

> person to

>> raise $20,000.00 to begin the long awaited trials on LDN and MS. I

> know that

>> we have all been trying to get this done and someone has finally

> gotten it

>> all together so that it can be accomplished. I know that Aegis

> polled the

>> group a few months back to see who might be willing and many of you

> said

>> that yes, you indeed would be willing to help. I will be sending my

> check in

>> on Monday morning and I hope that others will " put their money

> where their

>> mouths are " so to speak. Come on guys...this is way too important

> an

>> opportunity to pass up. I realize that everyone cannot afford

> $200.00 but I

>> suspect that whatever you can afford would be greatly appreciated.

> We might

>> just need more then 100 people but by God..it is doable. My thanks

> to Art

>> Mellor, Dr. Yash Agrawal, Rob Lester, and SammyJo Wilkinson for

> making the

>> first move to make this a reality. We have waited so long and it's

> time that

>> we all got into that mindset that it ain't gonna happen on it's

> own. JoyceF

>

>

>

>

>

>

>