LDN Video Interviews and Presentations

Jane - England: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jane from England shares her LDN story who has multiple sclerosis.

Jane was diagnosed in 1995. She was experiencing numbness and tingling sensations all over her body. She found LDN on a website and reached out to her doctor to prescribe to her. The only side effect she had was vivid dreams but those went away over time. The LDN as helped her Quality of life. It helped her bladder control, and the numbness hardly comes anymore.

To listen to the full story click the video link.

Any questions or comments you may have, please contact us. I look forward to hearing from you. Thank you for joining us today. 

Jan - US: Chronic Fatigue Syndrome (CFS/ME) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jan from the United States who takes Low Dose Naltrexone (LDN) for Chronic Fatigue Syndrome, Fibromyalgia and sleep issues shares his story.

I have all these diseases since March of 1981. I'm celebrating my 34th anniversary right now. And I have had gotten progressively worse over the years and my pain increased until I was taking the opioid medications and still aren't getting pain control.

So I started taking LDN last July on the advice of my doctor and it has helped tremendously. I had to come off the opioids to start taking LDN 
and that was rough, but it was well worth it because now I take an occasional over the counter pain reliever after eight or nine months that I've been on the LDN. I take ibuprofen and Excedrin.

Before I was taking Low Dose Naltrexone, I spent probably 22 hours a day, either in bed or in my recliner. I was able to do the most minimal self-care. 
My quality of life was a zero when I was bedridden for several years. I'll just get up to go to the bathroom.

LDN has improved my life about 25, 30%. I'm able to do more things in my self-care. I'm a very independent person and not being able to do things for myself was that stressor. And so I'm much happier.

I think definitely people should try LDN. It's not a cure and doesn't expect it to be but it is so worth it. A noticeable improvement in your quality of life and the fact that I'm totally off opioids and the damage they do to your system is well enough reasons for me.

Summary of Jans interview. Please listen to the video for the full story.

Jan - Netherlands: Myasthenia Gravis (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jan from the Netherlands was diagnosed with Myasthenia Gravis(MG) in 2010. He suffered from speaking problems and had severe double vision. Jan was refused an LDN prescription from his neurologist, however found a clinic online so sourced his prescription from there. He noticed his sleep was adversely affected within the first two or three weeks on the medication, then went away.

After just two months on LDN, Jan has noticed drastic improvements in his vision and speaking, however still has a bit of trouble speaking for a long time. Also, noting that his quality of life has improved considerably.

When asked what he would say to those thinking of trying LDN, he said “you have nothing to lose.”

This is a summary to listen to the whole interview please click the video link.

Any questions or comments you may have, please contact us.

Jamie - US: Epstein-Barr Virus, CFS/ME, Fibromyalgia, Resless Leg Syndrome... (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jamie from the United State shares her LDN story which she takes for, the chronic Epstein BARR virus.

She first started getting shooting pains in her arms and legs like she couldn’t move, after doing research she realised what she had.  She found out through a FaceBook group that LDN was a great way to help with ME/CFS.

At first she had weird dreams from LDN but they went away quick. Her life wasn’t the best quality before LDN she could barley get out of the bath, and now she is getting around just fine.

To listen to the full story click the video link.

Any questions or comments you may have, please contact us. I look forward to hearing from you. Thank you for joining us today. 

Jamie - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jamie from the United States takes LDN for multiple sclerosis, where she first started to notice symptoms November of last year, after her second child. That being only 28 years old. 

Before the diagnosis, Jamie started feeling a numb newness which would come appear on her tongue, one time she became extremely, other times she slept for near a week, that being three years ago. Jamie could not walk very well. She was very tired. As well as a numbness in her hand.

After her MRI scan, they could not find anything wrong is where they diagnosed her with Multiple Sclerosis, (MS). After not much support or guidance from her doctors, Jamie started researching, where she then found the Low Dose Naltrexone medication (LDN). After 8 months of research, she found a doctor willing to prescribe her.  

Side effects for Jamie were a; mild relapse, small amounts of numbing, vision problems and confusion.

Now Jamie feels as though she can live again, where she is able to work, take care of her children; but advises people like herself to play around with dosages to see which is best for the individual.

Summary of Jamie’s interview, please listen to the video for the full story.

Any questions or comments you may have, please Contact Us.  We look forward to hearing from you

Keywords: mild relapse, numbing, vision problems, MS, Multiple Sclerosis, Low Dose Naltrexone, tired 

James (2) - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

James was diagnosed with MS at age 39 with vision problems, then brain fog, weakness and fatigue. He had a good relationship with his doctor and tried numerous different remedies without success, then they found LDN. Within a day he began feeling better. He had zero side effects.

His quality of life improved rapidly, from a 3-4/10 to 8-9/10 on LDN for the last 2.5 years. His current MS symptoms include a slight limp, heat intolerance. He is a vocal advocate for LDN.

To listen to the full story click the video link.

Any questions or comments you may have, please contact us. I look forward to hearing from you. Thank you for joining us today.  

James - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

James and the United States Low Dose Naltrexone (LDN) for Multiple Sclerosis. At 40 years old; he was diagnosed 15 years ago, where he lost the vision in his right eye, and after 6 months it was still deteriorating. Eventually James stopped working.
James then found LDN. he considered himself as lucky due to the fact that he noticed a  positive difference. James also knows other people who have tried the Low Dose Naltrexone medication and stated it as “phenomenal.”

Now James has been taking the LDN medication for 5 years, now he can go out more, can continue with the gym and also getting back into biking after having little to no energy before trying his Low Dose Naltrexone medication.

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

James - England: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

James from England shares his Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

At the age of 38, James began to have issues with walking when he noticed his right leg was dragging along the floor in early 2009. Gradually his symptoms worsened, leading to a severe loss of energy.

After finally being diagnosed with Multiple Sclerosis (MS), James researched his own treatments which is when he came across Low Dose Naltrexone (LDN). Over the course of a few months his health has improved and he feels much happier.

This is a summary of James’ interview. Please listen to the rest of James’ story by clicking on the video above.

Jacky - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jackie from the United States who uses LDN for multiple sclerosis to share there story. She started showing symptoms of ms with heat intolerance and fatigue,back problems and pain. She got diagnosed with MS at 32 years old. She are 60 now and had no side effects from the LDN. She didn’t take any other drug before the LDN. There quality of life was about a 5/10 and now it’s a 8/10.

To listen to the full story please click the link above.

Any questions or comments you may have, please contact us. I look forward to hearing from you. 

Jackie - England: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jackie from England who takes LDN for multiple sclerosis shares her story.  She was diagnosed in 1992 after the birth of her second child. She was 27. She had fatigue and optic neuritis. She started on LDN in January in 2011. She experienced no side effects. She still gets dizzy from time to time but her quality of life has increased by a lot.

To listen to her story please watch the video.

Any questions or comments you may have, please contact us. I look forward to hearing from you.