Dr Chris Steele, MBE talks about Low Dose Naltrexone, LDN

Since there is no incentives for pharmaceutical companies to fund trials, why not go to the people who would save billions if this drug is proven to work: the insurance companies in the U.S. The approved drugs for M.S. in America are very expensive.. which the bulk of which is paid for by insurance companies. Wouldn't they have a financial incentive to fund such a trial?

For all those wishing to acquire LDN, go to the website in the video and send us a request via the request form and we will assist. Also, if you are a UK citizen, do sign the petition too, available via the ldnnow website also.

well done Dr Chris for bringing attention to this issue, have signed the petiition

I also have had MS for almost 21 years, I want to start taking LDN, please let me know where or what I need to d0o to begin.
thank you
Joanne

Do I need to get LDN from my doctor?
please let me know what I need to do to begin.
Thank you

I have been on LDN for 7 months for MS and it is helping me better than anything else I've tried. It should be the FIRST thing offered by doctors. Thank you Dr. Chris Steel.

Thank you Dr. Steele for sharing your knowledge of and belief in LDN. I have used LDN for MS four years this month with NO disease progression, nearly complete symptom relief, no side effects, and low in cost. I know of no other medication that can truthfully make such a claim nor one which can restore quality of life as LDN has for me and many thousands of others. God Bless all of you who persist in promoting the recognition, trial, and use of this most beneficial life saving medication.

Thank you Dr Chris Steele. A doctor of humanity. God Bless You!

Thank you Dr Chris for being a shephard not a sheep. Also Great work Jayne and Andrew for having the belief in LDN to start the petition. Surely everyone should be entitled to this safe, effective drug.