Tina from England shares her Multiple Sclerosis (MS) & Low Dose Naltrexone (LDN) Story

Tina from England has Multiple Sclerosis (MS) and will share her story about Low Dose Naltrexone (LDN).

I started having symptoms 23 years ago. I was 29. my right side went numb.

My husband phoned the emergency doctor, and I was taken to the hospital.

I had to wait for about three months to be referred to the hospital. They took me in for a lumbar puncture, and I was still being told that I had not MS. They told me: " We think it's a slight stroke you've had."

Months later, I was diagnosed with MS.

I heard about LDN on the Daily Express, and then you got back in touch with me, and we all started from there.And that was over two years ago,

I'm getting LDN with my GP. When I first started taking Low Dose Naltrexone (LDN)., I didn't have any side effects at all.

Within weeks, I was less fatigued, and I still work full time.

Tina's interview about LDN. Please watch the video for the full story.