Support Low Dose Naltrexone

[ThePennygirl]

Am so with you! 1st started on LDN and relasped, I felt good, doc put me on Copaxone! none are a cure and effect all of us in some form or another! I feel like the insurance ginny pig! we will still relaspe and have issues! but LDN needs to get the support ! keep up the good words!

[mwwestiii]

Since big pharma will never fund clinical trials for LDN it is now the moral responsibility of the National Multiple Sclerosis Society to take acton. Write an email today to CEO Joyce Nelson at JoyceNelson NMSS organization urging NMSS to fund a clinical trial. They've got plenty of money and it is very clear that LDN just may be more effective in halting or slowing disease progression than any other MS drug available today.