Stephenie from Australia shares her Multiple Sclerosis (MS) & Low Dose Naltrexone (LDN) Story

Stephanie from Australia takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS). Stephanie first started noticing symptoms in the year 1997, she had tingling in her legs, funny feelings in her right hand and little finger, as well as massive fatigue.

After CT scans and tests, nothing showed up, so they offered her physiotherapy. After travelling to Australia, she then noticed numbness in her forehead and heavy feet.

After seeing a new GP, they confirmed it was a relapse remitting MS.

Near this time Stephanie also had optic neuritis on the right eye optic neuritis on the left eye and relapses would hit her legs. 

Stephanie found out about Low Dose Naltrexone (LDN) through a meditation and wellbeing group, she then researched online and found the LDN trust website. Stephanie then went to her GP where her doctor agreed to have it prescribed for her. 

Before LDN, Stephanie rated her quality of life a 4 to a 5 out of 10, and now a 9 out of 10 after trying LDN.

Stephanie recommends people to try out the LDN medication, saying how worthwhile it is. Quoting it as harmless, and gives a really great chance at stopping the disease where it is.

This is a summary to listen to the entire interview by click the video link.