LDN aware

A board to discuss Low Dose Naltrexone (LDN) as a treatment for Multiple Sclerosis

LDN aware

Postby GemLDN » Mon Feb 22, 2010 8:59 am

Hey guys I'd just like to direct you to a new LDN site
We just want as many people as possible to know about the benefits of LDN, we need clinical trials and the more people out there asking for it the more recognition it's going to have.
If anyone wants to contact me my email is lilwhitepoppy@hotmail.co.uk I have had MS for 7 years and been taking LDN for 3 months.
Gemma x
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