LDN Video Interviews and Presentations

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.

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

Huw from Wales started noticing symptoms for Multiple Sclerosis around the year 2000. She felt both muscle and mental fatigue, and had problems walking and sleeping. 

Huw had heard of LDN through a friend, and obtained the medication through a private prescription around three years ago. Initially, after upping the dosage to 4mg per day, she began to have “strange dreams.” Huw has noticed improvements mentally, as she's now able to help her son with his business, including accounting.

When asked what she would say to those contemplating LDN, she urged they try it so long as they follow the advice, and gradually introduce the dosage.

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.

Holly Warner, LDN Radio Show 04 Oct 2017 (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Holly Warner shares her Low Dose Naltrexone (LDN) experience on the LDN Radio Show with Linda Elsegood.

Holly Warner is a Board Certified Holistic Health Practitioner who has her own clinic in Ottawa, Canada. She deals with hormone imbalance, thyroid issues, gut health, adrenal dysfunction, metabolic syndrome, and most autoimmune diseases. 

Her fascination with medicine began at an early stage. In her late teens she was focussed on cancer preservation but kept on getting drawn towards thyroid issues. Her experience as director of a medical facility for a number of years has added to her a great depth of knowledge in the pharmaceutical sector.

Warner specializes in clinical Nutritional Therapy. Her clinic does Skype appointments in Canada and the USA. She prescribes LDN and explains how it moderates and balances our autoimmune system and reduces the bad antibodies.

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

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

Hillary from Waales takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS). She was first diagnosed in 1990 at the young age of 31. 

Before her diagnosis, she was an active person, she had an 18 month old baby and happily married. 

Symptoms included, tingling in fingers which then became numbness and spread to her hands, for a two year period. 

She found LDN through a friend who was already taking the medication. Hillary’s GP was incredibly supportive and completed research into what LDN was, they thankfully prescribed it to her. Hillary had no initial side effects, and noticed positive experiences with LDN after 6 months. 

Hillary recommends people to try Low Dose Naltrexone (LDN), there is nothing to lose and more to gain she quotes.

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

Helen - Scotland: CFS/ME (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Helen from Scotland, was diagnosed with Chronic Fatigue Syndrome at the age of 26, shortly after the birth of her daughter. Within the first couple weeks, she felt acutely unwell and experienced muscle spasms and twitching. Not only was it physical, it was also mental fatigue being experienced “all the time”, leaving Helen unable to function. 

The doctors didn't say much, as tests came back normal. The only abnormality was her Thyroid’s function. Eventually, she went to hospital for further testing, where they noticed her spleen was enlarged. Helen was not offered treatment, and she was diagnosed with CFS/ME. She relied heavily on her husband and family to help her. 

Every time Helen visited her GP, she was always told that there was nothing that can be done. 

Helen found out about LDN, after seeing it on the news in Scotland. She visited her GP in England and mentioned LDN, however they showed no interest. 

She has been on LDN for over two years, showing no initial side effects. However, when dosage is increased she felt “quite fuzzy,” so dropped it back down again. Smaller increases were used and the symptom disappeared.

LDN has helped Helen immensely, as she now suffers no symptoms of CFS/ME at all and would recommend gaining knowledge of the medication, via research and speaking to their GP or others who have used it.

Please watch the video to view the whole interview.

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