Pauline from England shares her Multiple Sclerosis (MS) & Low Dose Naltrexone (LDN) Story on the LDN Radio Show

Pauline from England takes Low Dose Naltrexone (LDN) for her diagnosis with Multiple Sclerosis (MS). She was diagnosed in 1992 at the age of 43.

Before her diagnosis, Pauline was an active person, but she had optic neuritis twice in her right side where she started to become paralyzed. At first, Pauline’s GP said her problems could be related to a stroke.

Pauline found out about Low Dose Naltrexone (LDN) through a magazine, and managed to receive a prescription in 2006. Thankfully, she managed to receive this from a new GP after her old one refused.

Now, she has been taking it for four and  a half years. Pauline has found her progression slower than she did before LDN, but everyone reacts differently. 

Pauline’s introductory side effects included pain in her legs so they refreshed her dosage to very little. Ater this, she had no pain. 

Pauline will continue taking LDN, and she now gets her prescription from a Neurologist. She recommends people to try the medication, to give it a try and it may do a lot of good. She now thinks more positively and feels better about her diagnosis and being open with it, after LDN.

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