LDN Video Interviews and Presentations

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

Marjorie from Scotland shares their multiple sclerosis (MS) and low dose naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Marjorie began to notice symptoms of MS)in the mid-nineties but was not officially diagnosed with MS until 1999. At the time she was experiencing severe numbness on one side of her body, stretching from her shoulder to her foot, as well as low energy levels and cognitive processes.

It wasn’t until April 2010 that she was able to get a prescription for LDN. Nevertheless, within a few months of starting on LDN she knew she was improving: she began to regain more feeling in her arm and leg as well as her fatigue becoming less prominent.

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

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

Marie from Sweden shares their multiple sclerosis (MS) and low dose naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Marie was diagnosed with MS in 2005 and was 45 years old at the time. Her first sign of MS was when she began to struggle with seeing out of her left eye. Her symptoms progressed to the point where could no longer speak, only being able to mutter the words yes or no.

Within weeks of starting LDN, Marie was able to see clearly again and communicate freely. She thoroughly recommends LDN, saying that it “LDN is the best thing I have ever done”.

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

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

Maria from Canada was diagnosed with idiopathic uveitis in 2006, and the following year suffered a vertigo attack. She had many falls due to dizziness, sometimes hitting her head and also experienced extreme fatigue, headaches, piercing ear ache, hand numbness and insomnia. 

In 2008, Marias GP told her she had multiple sclerosis (MS). The following year she was prescribed Copaxone as a daily injection, however after two and a half years of using the injections, she ran out of places to inject due to hard lumps all over. After returning back to the GP, she was given Avonex, which resulted in flu-like symptoms for six months.

After asking about low dose naltrexone (LDN), she was told there was not enough research behind it so she was not given a prescription. 

Maria sourced a GP in Canada  who was open to LDN, and has been taking it for almost a year. She started to feel a new burning sensation down the middle of her left leg, however this went away after a few months. Maria was able to sleep without pills, and cut out all other medication besides LDN and one other. She is able to walk straight without the use of her cane and experiences fewer leg spasms. Her quality of life has drastically improved and she “would like a lot of people to know about  Low Dose Naltrexone (LDN)”

To view the whole interview, watch the video.

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

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

Margaret, previously  from England but now from Spain, was diagnosed with multiple sclerosis (MS) in 2008. She has had MS ever since she was near 20 years old, and is now 60. 

Margaret broke her back in a horse riding accident when problems started happening. When she was about 40 her leg started going numb, and once investigated, they found a crushed fracture in her back.

At this time, after countless operations on her back, Margaret started using a walking stick as she kept losing her balance. Her neurologist then diagnosed her with MS. 

Her MS symptoms included eyesight problems, she could no longer play sport, as well as being constantly tired. Then she started having swallowing difficulty. This is when she started noticing numbness in her legs.

Margaret could not manage to get a prescription for LDN in Spain, it was not an accepted protocol. So therefore she had to find her own chemist to prescribe it to her.

After the first week, she noticed she could taste and smell better, her urge to go to the toilet was slowing down, and even though she was still sleeping during the day, this was no longer as much, and she would feel fantastic after. Now Margaret has been on LDN for ten months, and recommends people to try it.

Please watch the video to view the whole interview. Thank you

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

Malcolm from the United States, takes Low Dose Naltrexone (LDN) for multiple sclerosis (MS). He was diagnosed around 1991, in his early thirties. Now 53. 

Before his diagnosis, Malcolm was involved in sports. He worked for a large corporation in sales and marketing, as well as having a child.  

At first his optic neuritis, which was treated with steroids, did not affect his life too much but stopped him with the sports. Malcolm did not know about LDN until around 2003, 2004,where he learnt about it over the internet. 

His doctor recommended Low Dose Naltrexone (LDN) to Malcolm, after finding out that his old medication - Tysabri - was extremely dangerous, causing sometimes death and brain diseases. 

Malcolm has been taking LDN for nearly three years now, he has noticed that his MS is not progressing, where he seems not to have gotten any worse. Now, Malcolm no longer naps like he used to, when he used to be exhausted all the time. He has no more fatigue and his balance is much better. He even quotes that he ‘will continue taking LDN for as long as he lives.’ So he values it greatly, and recommends to all who are struggling with symptoms such as Multiple Sclerosis. 

Please watch the video to hear the full interview. Thank you

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

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

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

Lynn was diagnosed with multiple sclerosis (MS) in 1995, at the age of 49. Her diagnosis seriously impacted upon her health and overall activity, meaning she could no longer run as frequently as she previously would have liked.

Her dropped foot meant she could not walk properly, yet she came across Low Dose Naltrexone (LDN) which completely revolutionised her health.

In this interview she explains how LDN has changed her life, restored her balance and ability to walk properly and is now able to get back to doing the things she enjoys.

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

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

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

Louise was first diagnosed with Multiple Sclerosis (MS) in January 1995 at the age of 26. Working in her local store, she began to notice a constant sensation of pins and needles in her left leg. Going to see her doctor, she was dismissed and told the problem would disappear eventually.

Her MS returned following the birth of her son, when for about a year afterwards her head would not stop spinning. Determined to find a solution, she began to research alternative treatment plans which is when she came across Low Dose Naltrexone (LDN).

Having obtained LDN from a local chemist as her doctors wouldn’t prescribe it for her, Louise is overjoyed with her progress and is able to spend more time with her son.

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

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

Lorraine from Scotland has multiple sclerosis (MS), where she first started noticing symptoms in February 2000. She developed extreme headaches, and recalls her scalp was sore, as well as bad weakness on her left side and fatigue. A day after an MRI scan she had received her MS diagnosis.

After taking Low Dose Naltrexone (LDN), she now has that “Wow energy”. To Lorraine it was amazing, and it also kept her awake and more active.

Lorraine heard about LDN through a neighbour who knew someone who was suffering with MS, who advised her to try it. Lorraine did have problems trying to convince her GP to prescribe it to her. Within three days, she felt so much better, she even ended up moving back to work full time. Lorraine even experienced no first initial side effects. Her quality of life has improved 100%, now feeling more human. 

Lorraine recommends people to try Low Dose Naltrexone (LDN), quoting that it will not harm you, so there is no loss to give it a go. 

Please watch the video to view the full interview.

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

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

Lorraine from England who takes Low Dose Naltrexone (LDN)  for multiple sclerosis, she was diagnosed at the age of 36, her legs started to behave rather awkwardly, and had some strange sensations in one leg and a strange sensation at the base of her spine. 

When she was diagnosed she was with her husband and was crying saying “tell me whether I've got multiple sclerosis (MS) or not” After the extensive tests she had to ask again. She found out a week later from her doctor who told her she has MS and was told they would  send some brochures. She felt pretty much on her  own. 

The first 10 years were not too bad and then small things started to happen. She was in a lot of pain. It was excruciating. She refused steroids. That was her first attack. For five to six years, nothing really happened. After about ten years,  she had her second relapse, which left her with some disability. She had numbness in her legs, arms and fingers. 

She started Low Dose Naltrexone (LDN)  about 2 years ago with good success and recommended it to everyone.

Play the video to listen to the whole story.

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

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

Lisa from Wales shares her Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story.

Lisa was diagnosed with Multiple Sclerosis (MS) in 2006. However, she had been experiencing a serious numbness in her feet and legs for two or three years prior, which progressed to the point where she couldn’t even feel her legs when walking.

Other symptoms began to develop, including fatigue. She explains how she began to feel tired for no apparent reason, which affected her ability to do her job and spend time with her family. 

After committing to researching alternative treatments, Lisa came across Low Dose Naltrexone (LDN) on the internet. Once she managed to obtain a prescription, she was able to think clearly for the first time in years and spend more time with her children.

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