LDN Video Interviews and Presentations

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

Denise from the United States shares her Low Dose Naltrexone story for multiple sclerosis. 

She was diagnosed with a cat scan first and then an MRI that was around 10 years ago. She was on Copaxone at the time. The meds at first weren’t working out, she was allergic to them. Her quality of life was around a 1 at the time. She started researching looking for different ways to treat MS and she found through a FaceBook group LOW DOSE NALTREXONE. 

After three years of not being on any kind of meds, a doctor finally prescribes it to her. She had mild side effects of gastro problems.

She started seeing major improvements including sleeping better and 75% of the pain went away. Her quality of life increased from a 1/10 to 8/10.

To hear the full summary of Denise experience please listen to the full video.

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

Delores from the United States takes LDN medication for multiple sclerosis. 

Delores first started noticing Multiple Sclerosis symptoms after an endoscopic vein laser therapy to help with the varicose veins that she has. Right after the procedure she developed bad foot drop, where she was tripping over her feet, which resulted to not being able to keep up her fitness regime with running. 

After a year, a Neurologist approved an MRI scan where Delores was diagnosed with Multiple Sclerosis (MS); where she has lesions in the brain, cervical spine, and thoracic spine. 

After finding the Low Dose Naltrexone medication in books and online she began to try it. Where it has now made her feel stronger and able to walk better.

Delores heard about the LDN medication roughly a month and a half after her diagnosis. She found it very hard to obtain a prescription, despite having a countless amount of doctors. This resulted into a holistic doctor giving her a prescription for LDN, during her trialling of different dosages, she started to develop headaches, but three months later, this has improved.

LDN has helped Delores with bladder functions, and slightly with her vision. 

Delores recommends others to try LDN, but to test the waters with dosages, after experiencing how quickly her headaches developed and soon went with the Low Dose Naltrexone.
 

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

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

Keywords: multiple sclerosis, endoscopic vein laser therapy, foot drop, MS, lesions, cervical spine, thoracic spine, headaches, Low Dose Naltrexone, LDN

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 - 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 (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 - 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. 

p>

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

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

David first noticed issues with his health a year following his marriage in 1998. It was in fact his brother who pointed out that David may be unwell during a game of football as he kept giving the ball away, something David says he didn’t usually do.

At the time David was 30 years old and as his energy levels decreased, so did his bladder control. As his eye sight also deteriorated, David became motivated to find a solution to the problem which is when he came across Low Dose Naltrexone (LDN).

After finding his optimal dose, David began to reap the benefits of LDN and was able to return to football and travelling with his wife. His life quality before LDN was a 3; now it is a 8/10.

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