LDN Video Interviews and Presentations

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. 

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.

Janice - US: Rheumatoid Arthritis (RA) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Janice is from the United States, and has rheumatoid arthritis (RA) since age 53, about 7 years prior to this interview.  It started as pain in the arch of her feet and toes; X-rays were negative.

After 30 months of various unsuccessful therapies, her doctor measured and found a very high rheumatoid factor. Her rheumatologist was not able to find a medication to help her symptoms.

Janice Googled alternative treatments for RA and quickly found low dose naltrexone (LDN). At the time she had a lot of pain, inflammation, swelling in all her joints, and general fatigue. She was using ibuprofen 800 mg twice a day.

She found a doctor to prescribe LDN, and after 4 days did not need to take any ibuprofen. Her pain and fatigue were quickly eased; and over the next several months the swelling and inflammation left her joints. She now feels 95% back to normal, and has a fully active life. Her local physician was amazed with her recovery, and now prescribes LDN for other patients as well. Janice serves as a resource for her physician’s other patients, to talk about how well LDN has worked for her.

If others are contemplating trying LDN, Janice encourages them to try it because it has minimal side effects, and has the opportunity to restore quality of life.

Summary of Janice's interview, please listen to the video for the full story.

Keywords: LDN, low dose naltrexone, rheumatoid arthritis, RA, pain

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

Janet - US: Fibromyalgia (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Janet from Georgia takes LDN for Fibromyalgia, and has been having problems for just over four years, which is when she began to notice it. Symptoms included severe aches and pain in muscles, extreme fatigue and trouble concentrating. 

Janet heard about the Low Dose Naltrexone (LDN) medication through researching for a company she was working with at the time. She saw how well results were and that was her initial thought, to try it for herself. She stopped all of her other medications, and went to her neurologist who agreed to prescribe it. 

Janet did not have any initial side effects when she first started the LDN medication.

Janet has now been on the LDN medication for 8 months, she quoted that before, she did not have any quality of life at all, she was miserable, and her work hours dropped to below half. Now, after the medication, she feels fantastic. , she has managed to get her license back also. Although her symptoms are not completely gone, she says they are a lot more manageable, and she is back to working her full hours.

Janet fully recommends LDN to other people, and quotes that there is no choice about it. She says it is also the best thing to exist.

Please watch the video to view the whole interview.

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

Jane - Scotland: Ovarian Cancer (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Jane from Edinburgh takes Low Dose Naltrexone (LDN) for ovarian cancer. 

Jane's stomach started to swell up, making her look 9 months pregnant in 10 days, she was admitted to hospital where she was told she had a bad diet, but after being readmitted the following week, they took 13 litres of fluid from her stomach, where scans then showed she had ovarian cancer. 

After 6 weeks she started chemotherapy, where she had a bad reaction to the initial dosages. After finishing chemo in July, she started taking Low Dose Naltrexone (LDN), at first she started to have disturbed nights, but now taking it in the morning, she had no bad effects, her mood has improved and will continue taking it where she will continue a follow up next year.

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

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.