LDN Video Interviews and Presentations

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

Dee is from England and has multiple sclerosis (MS) since she was about 27. She developed a mild attack of optic neuritis just after her now 15 year old son was born in 2000, that went away on its own. She also recalls not being able to walk properly, feeling like she had 2 bands around the legs at the top. About 2 years later, after a stressful period in her life, she had a second attack of optic neuritis and it was severe. After MRI scans and various tests, a neurologist told her she had a benign form of MS based on what she was seeing at the time. Dee felt frustrated and alone in dealing with her MS. Her best comfort came from other MS patients receiving oxygen therapy.

But she overdid it and got burnt out, perhaps got a bit of virus, and her MS flared up for 2 weeks. Her legs started to drag, particularly her left leg. She tried steroid treatments. She also was diagnosed with an underactive thyroid. Dee read in a New Pathways book about LDN, and finally started LDN in 2008. She noted improvements in energy and feeling more fulfilled from doing positive things she couldn’t before. Her left leg is her worst problem, and has a foot drop. She started 1.5 mg of LDN and only noted some apprehension from weird dreams; and seeing strange patterns when she closed her eyes. Currently she varies between 2.5 mg and 3.0 mg LDN depending on her need, but cannot tolerate 3.0 mg for long because of nausea. Dee feels LDN has made a big difference in the quality of her life.

Looking back, Dee wishes she had started LDN earlier.  She advises not ignoring it or giving up; but recommends others to give it a go as there  is more to gain and nothing to lose. She tries to share her knowledge of LDN with other patients. Her best friend has MS, couldn’t walk far, and was dragging a leg behind her. She started LDN and was completely changed for the better. Dee is 100% behind LDN.

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

Keywords: LDN, low dose naltrexone, multiple sclerosis, MS, foot drop

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

Debbie Judd, ARNP - US: 30 June 2017 LDN Radio Show (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Debbie Judd shares her Low Dose Naltrexone (LDN) experience on the LDN Radio Show with Linda Elsegood.

Debbie Judd is a nurse practitioner in Spokane, Washington, USA. She worked in surgery for 15 years and realized many patients could have avoided these operations with preventative medicine, so she turned to functional medicine. 

She and her husband operate their own naturopathic clinic where they do extensive testing and questionnaires to evaluate and treat their patients. They have utilised Low Dose Naltrexone (LDN) for a host of conditions including cancer and many autoimmune problems. 

She stresses the importance of diet and exercise in maximizing optimum health. Debbie enthusiastically shares some success stories of patients treated with LDN.

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

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

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

Debbie first noticed her Multiple Sclerosis (MS) symptoms during her mid-twenties when she used to have very bad flu symptoms. However, it wasn’t until 10 years ago that her symptoms worsened and she began to lose control of her hands and ability to balance.

Debbie had to pester multiple neurologists before managing to obtain a prescription for Low Dose Naltrexone (LDN), yet her persistence paid off in the end. After finding her optimal dose, LDN has drastically improved her focus and general stamina, making daily activities easier to complete.

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

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

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

Deanna first began to notice her Multiple Sclerosis (MS) symptoms prior to the birth of her second child. She had been misdiagnosed on multiple occasions meaning she never received the right treatment to treat her correctly.

She was originally a certified nurse assistant, but as her symptoms worsened and fatigue began to settle in, her hours at work were reduced until within a matter of weeks she could no longer muster the energy needed to treat others.

However, Deana came across Low Dose Naltrexone (LDN) when one of her colleagues recommended it to her, and now she is almost back to full fitness. She goes to the gym three times a week and says she doesn’t even remember that she’s got an autoimmune disease.

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

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

Dawn from England shares their Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story with Linda Elsegood.

Dawn began to suffer from Multiple Sclerosis (MS) symptoms around 8 years ago when she experienced numbness in her muscles. However, it wasn't until she experienced a severe attack 2 years later which prompted her to search for solutions.

Her vision also began to deteriorate yet she thankfully found Low Dose Naltrexone (LDN) swiftly meaning her symptoms didn’t progress too much further.

“My mobility is back to 100%. There’s nothing I can’t do now and my energy levels are so much better.”

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

David - US: Trigeminal Neuralgia, Ganglionopathy (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

David shares his Trigeminal Neuralgia and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.

David’s pain caused by Trigeminal Neuralgia gradually developed from the top of his neck throughout his whole back. Trigeminal neuralgia is a chronic pain condition that affects the trigeminal nerve, which carries sensation from your face to your brain. 

David noticed that even a mild stimulation of his face, such as from brushing his teeth triggered excruciating pain. Desperate for finding a solution, David came across Low Dose Naltrexone (LDN) which has helped him “get his life back”, hailing it as the “greatest drug of the 20th century”.

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

David (3) - US: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

David from the United States shares his Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story with Linda Elsegood.

David was hospitalised when he was only 19 years old having experienced serious Multiple Sclerosis Symptoms (MS), including an inability to walk properly due to a severe loss of balance.

This prompted David to conduct his own research while his condition deteriorated to the point of him being dissabled. Fortunately David came across Low Dose Naltrexone (LDN) online and the rest is history.

“I can now feel 75% of my body again. It feels weird to walk but LDN’s given me that back and that’s amazing.”

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

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

David from the United States shares their Multiple Sclerosis (MS) and Low Dose Naltrexone (LDN) story with Linda Elsegood.

David first noticed something wrong with him around 30 years ago when a carton of orange juice fell out of his hand in the supermarket. Despite being only 34, his symptoms progressively became worse, developing a limp in his right leg and losing almost total control of his hands.

David received multiple treatments that had little effect on improving his Multiple Sclerosis (MS) until he found Low Dose Naltrexone (LDN) online. Ever since he has had great success: less muscle spasms, regain of muscle control and better sleep.

David is a strong advocate for LDN and recommends it to all who have been diagnosed with MS and those who are yet to try it.

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

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

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

David first noticed symptoms of his Chronic Fatigue Syndrome (CFS/ME) in the spring of 2000 upon returning from a trip to the West Coast. For the next 6 months David suffered from a drop in his overall energy levels and was unable to exercise regularly anymore.

David thankfully had prior knowledge of Low Dose Naltrexone (LDN) and sought it out from his local pharmacy. Within three weeks of starting on LDN he was already beginning to feel much better and was able to return to regular running.

David strongly recommends that people research LDN and learn about its benefits so that if you know someone, or even if you yourself, is diagnosed with an autoimmune disease you can tackle the issue swiftly.

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

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

David from Spain shares his LDN story for multiple sclerosis.

It was 11 years ago when he started having symptoms. He was losing feeling in his legs so he looked up different therapies and medicines and he found out about LDN.

LDN helped him get his quality of life back. He can swim, walk and run now. He can also do daily task much easier.

To listen to the full interview play the video.

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