LDN Video Interviews and Presentations

Johnny - US: Chronic Fatigue Syndrome (CFS/ME) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Johnny has suffered from ME for nine years; since the age of 21. He rates his overall quality of life at 3 before taking Low Dose Naltrexone. Since taking it that's gone up to around 6. Though he still has several health issues it's made a huge difference.

He suffered from insomnia, swollen glands, sore throats, headaches, joint pain, overwhelming fatigue, which is probably the most common, symptom, sleeping a number of hours and not feeling refreshed, memory loss, brain fog, feeling disorientated at times, not retaining information, forgetting what he was talking about halfway through a sentence.  He also had IBS after the ME, so he had bowel issues. 

He has been taking Low Dose Naltrexone (LDN) for seven months and the severity and frequency of those conditions has decreased slightly. It's the only thing that has relieved anything other than overall health, eg diet and supplements.

This is just a summary. To hear the full story simply click on the link.

John from the United States takes Low Dose Naltrexone (LDN) for Crohn's disease.

"I was diagnosed with Crohn's when I was 19 years old. I'm 55 now. When I was about 17 years ago I had a resection done.

During the time before the resection there were times when I felt great and then there were times when I had major flare-ups where I was cramping in excruciating pain with diarrhoea, vomiting and always promising that I'll be better.

I walked around with a perforated intestine for three months and I was down to 127 pounds.

 I was in the hospital for 20 days and at that point, I came to the conclusion that I just have to come up with a plan so I started reading everything.

I finally accepted my disease and I embraced it. My life really changed a lot. I made sure that I ate what I was supposed to eat.  I had acupuncture four to six times a year. I took vitamins. I stayed away from beef and dairy.

I was only on two milligrams of prednisone every day and I was fine until my doctor told me that I had strictures and on top of that I had active crump, even though I was pretty much pain-free.

And I just freaked out because, at that point, my mom was dying of cancer. And so anything that had cancer written into it just about a death sentence for me.

So I started searching out any avenue for alternatives.

One day when I was looking for more answers, all of a sudden Low Dose Naltrexone (LDN) came up and Crystal gave me the name  an LDN doctor in my area, and she put me on a very strict diet along with some anti-inflammatory supplements like curcumin and EPA and DHA and stuff like that. On top of that, I take three milligrams of LDN, and my C reactive protein level went from a an 8 to 0.19 in two months.

The biggest thing that's really helped me with Low Dose Naltrexone (LDN) is my mental health.

One thing that I learned is that you have to accept and embrace your disease and  to search out all the answers. And I'll be honest with you. Traditional medicine is going to send you towards trying to beat it into submission whereas LDN is going to love your body and it's going to help you heal your own.

You're going to have to take on traditional medicine and you're going to have to go against your doctor. Unless you're willing to go with your traditional doctor, but there's a lot of side effects. You can't stay on that poison forever. Sooner or later, you've been happy to get off of it, and you'd have to come my way sooner or later".

Summary of John's interview. Please listen to the video for the full story.

John - US: Manic Depression, Pain (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

John from the United States who takes LDN for manic depression and first heard of LDN in April 2013.

His dear friend who was an osteopathic physician, and had severe mania and depression for a period of over eight years. She recommended LDN, because LDN he. He was experiencing a lot of anxiety and was very uptight, unable to relax was not sleeping well.

Since starting LDN he's had no pain in his body body at all, anywhere, no headaches, which he used to get all the time, and now sleeps very deeply. He felt very relaxes and finds LDN amazing!

Before LDN his quality of life was struggling to be 3 out of 10 and he said it's now 25 in just 6 months.

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. 

John (2) - England: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

John from England takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS), he was diagnosed in 1987 at the age of 38.

He was healthy and working at the time as a police officer and played squash and went swimming with his children and did other activities with them. He suffered from Optic Neuritis and wasn’t unti 1998 that he started having spasms on his right side.

When the neurologist told him he had MS it was like, he took a sledgehammer to his head, he first thought was, “Oh my kids. Oh my God” MS affects the whole family 

He managed to obtain a private prescription about 2 years ago and improvements have been in the bladder and his advice to other people with MS is LDN is a Life-changer give it a go. 

Please play the video to watch the whole story.

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

John - England: Chronic Fatigue Syndrome (CFS/ME) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

John from England takes Low Dose Naltrexone (LDN) for his Chronic Fatigue Syndrome (ME/CFS). During the years 1981-82 he had a muscle virus, where he had to deal with the aftermath. During this time he was 31 years old, still teaching judo, so he was an incredibly fit, strong and active person.

His symptoms included, trouble walking, he was tired all the time and found concentrating difficult. He even had a headache from October to July the following year. After his first consultation, it took the doctor some time to be able to prescribe the LDN medication to John. Initial symptoms with the new medication included insomnia, although he no longer had brain fog and his ability to concentrate went up, and he has now been on LDN since January of 2010. He quotes it has been excellent.

John quotes that if other people would like to try LDN for themselves, they have to be brave, the reason being that you have got to stop the pain killers and opiates. But, do give it a serious try.

To view the full interview, watch the video attached. Thank you

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

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

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

John began to notice symptoms in 2004 when he began to stumble regularly while walking. Over the following months this progressed until he had multiple seizures, leading to his diagnosis of Multiple Sclerosis (MS).

He didn’t find any solution for six years, meaning he could no longer run nor take part in golf anymore due to his lack of energy and increased fatigue. John’s discovery of Low Dose Naltrexone (LDN) changed his life, as he is now able to walk properly again and get back to playing golf and doing the things he enjoys.

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

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

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

John started to notice issues with his health when he began stumbling while walking due to a developing pain in his left leg, eventually leaving him in a wheelchair.

While his wife worked as a waitress at the local restaurant, John began to research his own treatments which was when he came across Low Dose Naltrexone (LDN), learning about how successful it can be in combating Multiple Sclerosis (MS) patients.

He says he can now control his bladder and his overall energy levels have improved. John recommends LDN to anyone who’s interested, saying “there are only benefits to be had”.

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

Joanna - England: Chronic Fatigue Syndrome (CFS/ME) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Joanna was 14 when she first started noticing Chronic Fatigue Syndome (ME) symptoms. At first she had acute pancreatitis which was caused by gallstones, further leading to infections. As well as this, normal symptoms included muscle pain and pains in her eyes which only got worse over time. 

Unfortunately, the NHS gave little help or understanding over Joanna’s difficulties with her disease. All that they offered was referral to a support group. Later on Joanna heard about a clinic based in Liverpool, where she told her GP that she was referring. Joanna heard about Low Dose Naltrexone (LDN) through a friend who was using LDN treatment himself. Which resulted in him having much success and recommended that Joanna would look into it. 

Using a private doctor, blood tests resulted in Joanna having the LDN medication, which she agreed to and was on it for 6 months with this private clinic in Liverpool. Due to circumstances, Joanna had to go back to the NHS where it took her countless attempts for the NHS to oblige for the LDN medication prescription.

As she knows of, Joanna did not have any side effects, it took two months for her to notice improvements which resulted in more energy and bad fatigue, which she then rated her quality of life a 6/10.

Summary of Joanna’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: ME, Chronic Fatigue Syndrome, acute pancreatitis, gallstones, infections, muscle, pains, NHS, Low Dose Naltrexone, LDN, quality of life, fatigue, energy

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

Joan from the United States shares her LDN  story for multiple sclerosis. She first got symptoms back in 1985 when she was 30. She got double vision and originally the doctor thought she had a brain tumour, but it turned out to be MS. She also experienced bladder issues. She first heard about LDN through Facebook and Yahoo. The only side effect she experienced was sleeplessness for only a couple of weeks. She didn’t get the effects that everyone else got on LDN but she still recommends people take it. She just didn't have time to constantly take it.

To hear the full story please click the video.

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

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

Jim from England takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS), where he was diagnosed in 1978 at 33 years old. 

Symptoms at first included confusion with body temperature and feeling cold. And even did not experience any initial side effects when he first started Low Dose Naltrexone (LDN). James does in fact recommend people to try LDN, quoting that it has not done any harm and to try and continue with it.

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