LDN Video Interviews and Presentations

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

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

Jay first experienced symptoms of Multiple Sclerosis (MS) around 2010, when he suddenly had a muscle spasm in his left arm when he was sat down one evening. Shortly after, his vision became blurred and Jay began to suffer from brain fog.

He said “It (MS) made the task of bringing up two children even harder than it already is. The fatigue limited my ability to continue my full time job. Everything was not easy.

My quality of life has soared since starting on Low Dose Naltrexone (LDN). The brain fog is gone, I no longer have muscle spasms and have much more energy than before.

You’ve obviously got to research to check if LDN is going to help you out, but in most cases it will. It’s certainly worth a try.”

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

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. 

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. 

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

Ina from Scotland shares her Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Ina was diagnosed with Multiple Sclerosis in 2002 yet she was suffering from the symptoms for a while beforehand. Around ten years prior to her diagnosis she had great pain in her left leg, which eventually led to her being unable to walk and put into a wheelchair.

Ina heard about Low Dose Naltrexone (LDN) through a friend of a friend and never looked back. She experienced vivid dreams at the beginning but slowly after began to regain feeling in her legs which completely improved her quality of life.

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

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

Ian from England was diagnosed with Multiple Sclerosis (MS) in 1999. He experienced symptoms prior to the diagnosis, such as lack of balance, resulting in difficulty walking and feelings of weakness. 

Ian heard about Low Dose Naltrexone (LDN) through a friend who already took the medication, and was privately prescribed it around six years ago. He noticed it helped his bladder stiffness, as well as his ability to walk. To those thinking of taking Low Dose Naltrexone (LDN), Ian recommends they “try it for a couple months as it affects everybody differently.”

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.