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My letter to the MS Society

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I am quite disappointed in your article lambasting the use of Low Dose

Naltrexone. It is becoming quite clear to me that this society holds no

regard for the well being of MS patients and we shall become quite a bit

more vocal about how we all feel regarding this. I think that you

underestimate the power of a few thousand people that feel that they are

being wronged. Believe me, we shall not take this laying down. I have been

on this therapy for 2 years now and know that it is working to halt any

further progress of my MS. Can you see how we, as MS patients, feel that you

are not working in our best interests. We will do whatever it takes to bring

this to light because believe me, the thousands of us that have discovered

this therapy are not going to give it up in exchange for any of those very

expensive worthless injectables. It is becoming quite clear to us that this

is all a money game. We have way too much at stake here to not fight for

what we believe is right.

JoyceF

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