LDN Video Interviews and Presentations

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

When Wendy first started her Low Dose Naltrexone (LDN) journey, initial side effects included vivid dreaming and on some days, very tired.

Wendy rated her quality of life a four to five out of ten before Low Dose Naltrexone (LDN) , and now a lot higher due to her feeling as if she can do anything. 

Wendy recommends people to go for LDN, saying that you will feel better from it, so is definitely worth some research to try it,

Please watch the video to view the full interview. Thank You.

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

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

Vivien from England shares her Chronic Fatigue Syndrome (CFS/ME) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Vivien had been living with Multiple Sclerosis (MS) since 1992 but in 2009 she was rushed into hospital and put onto a ventilator following issues with breathing, which led to her second diagnosis of Chronic Fatigue Syndrome (CFS/ME).

After researching for alternative treatments herself, Vivien was able to get a prescription of Low Dose Naltrexone (LDN) from a private clinic and hasn’t looked back since. She no longer needs a walking stick and feels full of energy.

She recommends LDN to all those who are curious, praising the many benefits it has to offer.

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

Viv - Scotland: Hashimoto's Thyroiditis (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Viv from Scotland shares their Hashimoto’s and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Viv first noticed an odd symptom in late 2012 when she had a strange rash on her wrist. It disappeared after a few antihistamines, but returned later on all over Viv’s body and this recurred multiple times, leading to multiple visits to the hospital. 

Viv was then later diagnosed at 37 years old with Hashimoto’s. The symptoms were never properly under control from any treatment until Viv found Low Dose Naltrexone (LDN).

She said “I suffered zero side effects when I initially started LDN, and still have zero now. Within a couple days I began to feel better. No more rashes at all.

If you’ve been diagnosed with Hashimoto’s, I thoroughly recommend you go and speak to your doctor about LDN. You’ll find that this drug is nothing short of a miracle.”

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

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

Vicky from the United States was diagnosed with Multiple Sclerosis(MS) in 1997 after starting to experience symptoms the previous year, such as weakness, fatigue and hand and walking problems, as well as cognitive issues. After diagnosis, the symptoms had worsened to excruciating pain, she became sensitive to heat and cold. Vicky also lost muscle control, meaning walking was difficult, including problems swallowing.

Vicky heard about Low Dose Naltrexone (LDN) from her husband due to him researching forums and websites for her. However when she brought it up to her GP, she was instantly shut down due to it not being FDA approved. So she called up a different GP, and was eventually written up a prescription.

Since being on LDN, Vicky has stated that all of her symptoms have gone and her quality of life has drastically improved, claiming that “days are not long enough.”

When asked what she would say to those contemplating Low Dose Naltrexone (LDN), she was enthusiastic in saying for them to give it a try, emphasising the fact they have nothing to lose. 

This is a summary, to hear the whole interview click the video link.

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

Vera - US: Dermatomyositis, Microscopic Colitis (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Vera takes low dose naltrexone (LDN) primarily for dermatomyositis which appeared at 30 years old after her first child was born; and secondarily for microscopic colitis, which appeared after her second child was born. She rated her quality of life at 5.

Once on LDN she noted improved mood and energy, and by the third week she noted the rash started calming down, as well as her colitis. Now she rates her quality of life at a 9 or 10.

Listen to the video for the full story.

Any questions or comments you may have, please contact us at contact@ldnresearchtrust.org. I look forward to hearing from you. Thank you for joining us today.

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

Valerie from Wales has fibromyalgia (FM), where she first started noticing symptoms in 2006. Symptoms included stomach problems, headaches, forgetfulness, tingling feet and fingers, as well as aches and pains, particularly in her shoulder.

She was diagnosed in 2009 at the age of 65/66, very abruptly by her doctor.

Her doctor would not prescribe the Low Dose Naltrexone (LDN) to her, that is when she came to our website for help on how to receive it. 

Valerie recalls that the medication was not instant, but she does feel a lot better, she still does have aches and pains, but on a whole it is much better.

She rated her quality of life before her medication a 5 out of 10, and now an 8 or 9, which is a great improvement.

Valerie recommends people to try it, It doesn't have any side effects as far as she is concerned anyway and there is no reason why you shouldn't at least try it.

Please watch the video to view the whole interview.

Any questions or comments you may have, please contact

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

Valarie from the United States shares her Chronic Fatigue Syndrome (CFS/ME) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

Valarie grew up knowing she has issues with her health but her symptoms were exacerbated when she joined a health club and tried to exercise more regularly. This worsened to the point where one day she could no longer get up out of bed.

After doing some research, Valarie found Low Dose Naltrexone (LDN) on Facebook and learnt of its many benefits for patients diagnosed with Chronic Fatigue Syndrome (CFS/ME).

“LDN has made me so much less anxious and stressed. I feel better about myself. I’m a very strong supporter of LDN and it’s definitely worth trying.

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

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

Val from England has multiple sclerosis (MS), where she was diagnosed in 1993. Before her diagnosis she used to play squash and badminton, as well as working as a secretary. After her diagnosis, she gave up living, her job, where she then had to depend on my husband and family. Symptoms included losing the ability to walk, her eyesight went at times, meaning she went blind many times, leg spasms were also included in her symptoms. 

Val has now been taking Low Dose Naltrexone (LDN) since 2010. Now she doesn't have as many spasms, eyes are completely better, and she doesn't become as tired. Although she does use a wheelchair outside. 

Val rated her quality of life between a 1-2 before her experience with Low Dose Naltrexone (LDN), and now after, a 9-10. 

Val recommends LDN to anyone, she can now enjoy life and play with her children!

Please listen to the video to view the whole story. 

Any questions or comments you may have, email us at contact@ldnresearchtrust.org

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

Trisha from England was diagnosed with Multiple Sclerosis in December 1983. Her symptoms consisted of balance and core issues as well as problems with her feet resulting in the need for a wheelchair.

Trisha heard of Low Dose Naltrexone (LDN) by reading articles in magazines about medication that could help her, and after showing the research she had accumulated to her GP, she was prescribed it in 2010. Within a few months Trisha had noticed improvements in the muscular toning of her core, had more control of her own body, including the ability to sit, and also her speech.

When asked what she would say to those contemplating trying LDN, Trisha replied with “try it and see if it helps. Don’t expect massive improvements, just be realistic.”

For the entire interview, watch the video.

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

Trish from the United States was diagnosed with Multiple Sclerosis after starting to notice symptoms from the age of around 40. Her symptoms included fatigue, feeling heavy limbs, weakness in her left leg and twitching in her eyes and ears.

In 2010, after experiencing further symptoms such as chest pain, nausea and dizziness, Trish was diagnosed with MS after a series of tests in November. She started taking Copaxone injections prior to Low Dose Naltrexone (LDN), and did not like the side effects.

After taking LDN for the first time in January 2011, Trish was unable to sleep well. However, by changing the time she took the medication(changing from night, to morning) her sleep improved. She feels much healthier, more energetic and eating better after starting on LDN. Trish has also said her anxiety and ability to walk has improved, alongside her bladder problems.

When asked what she would say to those thinking about trying Low Dose Naltrexone (LDN), Trish said she “highly recommends it”. Also, that there is nothing to lose, but a lot to gain.

For the entire interview, watch the video.

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