Re: Hostile Take over time.

[Guest guest]

sickness and disease are HUGE MONEY MAKERS. We have to take care of our health and get the word out to as many as we can.

[low dose naltrexone] Hostile Take over time.

Hello everyone,I have rrms for 3 years now and been on LDN for 10 months and I have been relapse free since being on LDN and I am 99% symptom free.I have been following the disscussion of how the ms society does and knows very little for us who have ms. I agree 100% and feel something must be done. They continue to stick their head in the ground about LDN, CCSVI and diet and anything that might help us besides letting us inject our bodys with harmful expensive drugs that make us sicker than better.Now the question of the day is. How do we the sick people take control of the ms society and run it for the patients and not for the big pharma companies? They have our money and are filling their pockets and the pockets of big pharma.We need to get LDN trials and CCSVI testing available and need it done NOW. We should not have to go to Poland or elesewhere to have CCSVI done or fight with our doctors to get on LDN. Two very important things for people with ms.We elect the idiots in Ottawa and Washington and every other capitol and they do very little for us. How do we make people stand up and take notice that we are not going away and we demand LDN trials and CCSVI testing and treatment in Canada and the USA for ms.Lets here what everyone has to think.Sorry for the rant but I am pissed off and I think we all are at how we are being treated.

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[Guest guest]

As a person who will no longer donate to the MS Society, I do understand a part

of the problem. They can support only those proposals sent to them. As far as I

can see, nobody has proposed a trial that is in the realm that they can support

financially. It is hard to bitch about being turned down if we have never asked,

right? I might be wrong in this and they have refused funding to a valid test,

but I have not heard about that. If we want the MS Society to support testing

for LDN, we have to send them a test in the proper format.

Is there a way to do this? Can we do some brain storming on it? Then if they

turn it down, we can raise heck over that too. " Any publicity is good

publicity. "

Francie

http://www.LDN-for-MS.com

> I have been following the disscussion of how the ms society does and knows

very little for us who have ms. I agree 100% and feel something must be done.

They continue to stick their head in the ground about LDN, CCSVI and diet and

anything that might help us besides letting us inject our bodys with harmful

expensive drugs that make us sicker than better.

>

> Now the question of the day is. How do we the sick people take control of the

ms society and run it for the patients and not for the big pharma companies?

They have our money and are filling their pockets and the pockets of big pharma.

>

> We need to get LDN trials and CCSVI testing available and need it done NOW. We

should not have to go to Poland or elesewhere to have CCSVI done or fight with

our doctors to get on LDN. Two very important things for people with ms.

>

[Guest guest]

i think you are wrong and they were asked many times