LDN Video Interviews and Presentations

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

Jill from England was diagnosed with Multiple Sclerosis in 1996. Her symptoms included fatigue, lack of motivation, numbness in the legs and blocked vision in her left eye. She mentioned LDN to a urologist, however he dismissed it. She started taking Low Dose Naltrexone (LDN) last August as symptoms were getting harder to manage, after conducting her own research. 

Within two weeks Jill had noticed a relief in the fatigue, and also her quality of life had improved. She recommends people try it, as you won't be any worse off, and may find enormous improvements.

To view the whole interview, watch the video 

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

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

Jessica is from the United States and since 1996 has had Multiple Sclerosis (MS). During this time, she had Optic Neuritis where she encountered balance issues, bumping into walls and tripping. In the month of November, she had her first MRI which confirmed she had multiple sclerosis (MS). Jessica was suggested that she take medication, but declined as she wanted to handle it herself. This is where she decided to try acupuncture, homeopathy, chiropractic, body work methods and more. 

Low Dose Naltrexone (LDN) was the first medication she agreed to; before trying these medications, her symptoms were: double optic neuritis in both eyes, loss of hearing in the right ear, numbing of hands, itchy face, partial sleep. Furthermore, this wasn’t the end, her right side of her face went palsy, as well as vertigo which caused bed ridden. Although these symptoms were very on and off. 

Jessica heard about LDN through alternative therapies in New York. Her primary care physician would not prescribe it to her, which she then switched doctor who heard about amazing results the LDN medication had given other patients.

Luckily, she was given the approval of the Low Dose Naltrexone medication, the effects were vivid dreams for roughly 2-3 days. But symptoms were also abated due to Jessica being pregnant with her second child. 

Now, Jessica has been on LDN medication for three years, there has been no lesions, no exacerbations, and feels more positive that her disease is now stabilised.

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

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

Key words: LDN, Low Dose Naltrexone, Multiple Sclerosis, MS, Acupuncture, homeopathy, chiropractic, double optic neuritis, hearing,  numbing, sleep, symptoms, medication

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

Jennifer from Canada shares her Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) Story on the LDN Radio Show with Linda Elsegood

Jennifer was officially diagnosed in 2000 with Multiple Sclerosis (MS), but had suffered from a  litany of symptoms prior to her diagnosis. These included blurred vision, which she noticed when mowing the lawn one day and she couldn't see the bottom of the garden and bladder problems. Jennifer had also been suffering from fatigue since she was a child.

Jennifer had also tried multiple other medications that had little to no benefit on improving her health before she found Low Dose Naltrexone (LDN). 

“I noticed improvements in my health almost immediately. The muscle spasms in my legs stopped allowing me to walk again properly, and also the spasms in my bladder which were causing me to use the bathroom so frequently and have restless nights.

I would like to say that if you’re thinking about trying LDN, then give it a shot. It’s really not that expensive. Just start low and go slow, work your way into it.”

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

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

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

Jennie was diagnosed with Multiple Sclerosis (MS) at the age of twenty. She began with simple flu-like symptoms at first, but then began to notice that her balance was off; she couldn’t walk far without stumbling. 

Within five months of discovering and starting on Low Dose Naltrexone (LDN), Jennie noticed considerable improvements in her health almost instantly: she could stand up properly, she could walk further distances and her bladder was under greater control.

“I also no longer need my afternoon naps, which was another bonus. Overall, my quality of life has just increased tenfold.

I understand that LDN can affect everyone differently but, certainly from my experience, it can dramatically improve your health and enjoyment of life.”

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

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

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

Jeanette’s first suspicion that something was wrong with her health was in 1998 when she woke up one morning and could barely see nor do anything other than go to a local optician. She was not officially diagnosed with Multiple Sclerosis (MS) for another 2 years.

After the initial relief of recognising the issue, Jeanette’s problems grew as fatigue began to settle in. She had a large relapse following the death of her mother, leading to great stress. However, finding Low Dose Naltrexone (LDN) helped her to recover and boost her health.

“My fatigue is much better, I have much more energy and can stay up later which is nice. I can spend more time with my husband and family, it’s all so great.”

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

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

Jean Luc, living in England started noticing symptoms in 1975 with his eyesight, but doctors could not place what the error was. For 10-15 years, symptoms were still regular, with back pain and a common balance problem. As well as tingling hands and fingers.

In 2002, Jean started receiving help from a neurologist, who told him he had Multiple Sclerosis (MS). Jean heard about Low Dose Naltrexone (LDN) after being in an exercise group; Jean loved the LDN medication, finding it “extraordinary!” He recommends Low Dose Naltrexone (LDN) to everyone, and encourages people to try it.  At this time however, Doctors would not prescribe it to Jean, but fortunately his Neurologist agreed to prescribe LDN to him.

During the time Jean was taking his LDN medication, he started having problems with fatigue. But he does feel more logical and focused! 

Before the LDN medication, Jean rated his quality of life between a 1-2 and now a strong 7!

Please watch the video to hear about the full interview!

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

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

Jean from the United States was diagnosed with Multiple Sclerosis in 2000. She experienced dizziness, numbness and vertigo prior to the diagnosis; all of which would come and go after a period of days. Three years before the diagnoses, Jean lost the majority of hearing in her right ear, and almost half in her left.

Jean first came across LDN after searching the web and reading about someone taking it in Florida, and it just so happened that her mother had a place there. So, in 2001 she flew down and saw a GP that prescribed her LDN. Jean felt no initial side effects at all and not long after starting the medication, her vertigo had gone and is now in remission. MRI and other various tests have shown that the majority of Jean’s lesions have also either shrunk or disappeared entirely

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

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

Jean from Scotland shares her daughter Jenny’s story.  Jenny takes Low Dose Naltrexone for Multiple Sclerosis.  Jenny was first diagnosed with MS when she was 23 years old. Under regular health care, Jenny ended up permanently in a wheelchair after eight years. Jean read about Low Dose Naltrexone in a newspaper and started to research, she attended conferences and learned all she could.  Eventually Jean found a doctor who would prescribe Low Dose Naltrexone for her daughter.  Jean explains how her daughter began to get function back with LDN and she would recommend that anybody in their position should try Low Dose Naltrexone.

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

Jazzy from the United States  takes LDN for multiple sclerosis. She first started to notice MS symptoms when she was twelve. She had paralysis on the left side of her face which went away after about a month and it wasn't until she turned 31 that she noticed the left side of her face was numb and didn't know what it was.

She saw a neurologist and he sent her for an MRI and there was plaque build up on the left side of the brain causing  numbness to the right side of the face. And that's when she was diagnosed with MS. 

The bottom of her feet would also sometimes be numb.

She was offered steroids right away but she didn't want to take them.

She began researching healing from MS rather than looking at the negatives. The only thing that really came up in a positive light online was LDN.  Before  starting  Low Dose Naltrexone she had numbness, tingling and was given steroids to alleviate the pain. The numbness and tingling later spread to her spine which scared her so she wanted treatment.  Her quality of life scoring was 4. She was depressed at the prospect of disease progression.

When she began taking LDN she didn't notice any introductory side effects other than finding it hard to sleep on the first night but felt instantly better in the morning; even better than before the MS began and she has taken it since October 2013

She would recommend it to anyone as there are no side effects.

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

Jayne from Canada to share her LDN story she takes for multiple sclerosis. She first got diagnosed back in 2001 she was 41 at the time. She was a very active person before the diagnoses she worked for the workout mags and had a very busy life.

The symptoms she started getting was overtired and she woke up one day and was paralyzed. She started taking LDN for two years now. It only took a month before her energy came back and she was able to get out of the house. Their quality of life increased a lot. She felt like she wasn’t given a death sentence anymore.

To watch the full story please click the link.

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