LDN Video Interviews and Presentations

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

Shana from the United States was diagnosed with Multiple Sclerosis in 2007. She experienced body pain, blurred vision, fatigue and migraines. 

Shana has been taking Low Dose Naltrexone (LDN) for around a year and a half now, and found out about it through a friend who had spoken to practitioners in San Diego who recommended she tried the medication. It took a month after speaking to her GP about LDN to be prescribed it. Shana noticed within a day of taking LDN, that the pain had gone away. And after a longer period of time, her concentration has improved alongside her ability to walk. However, Shana did experience loss of appetite and struggled to sleep for the first few nights on this medication due to the large dosage size. 

When asked what she would say to those contemplating taking LDN, she replied with “definitely try it” and urged that even if it's difficult to get a prescription for it, to keep trying.

For the entire interview, watch the video.

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

Shaianne from Canada was diagnosed with Multiple Sclerosis (MS) at the age of 28, six years ago. She first started feeling symptoms in her early twenties, which included weak legs, hip pain, balance issues and dizziness. Seven years after these symptoms showed up, Shaianne was diagnosed with MS. She chose to be put on Copaxone, however, she found out she had a severe allergic reaction and had to stop taking it. She then started to research medication and found Low Dose Naltrexone (LDN). Shaianne was prescribed LDN by her GP after showing him all the research she had found. After taking the medication, she noticed instant improvements with no side effects. The next morning she had no stiffness or fatigue, and in the past three years, has experienced no MS symptoms. 

Shaianne prompts people to do research and to take Low Dose Naltrexone (LDN) information in to show your GP before trying it. “It's worth the push for anyone to try.”

For the entire interview, watch the video.

Any questions or comments you may have, please Contact Us. 

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

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

Sarah first noticed her Multiple Sclerosis (MS) symptoms in early 1990, yet they developed “overnight” for her. She woke up one morning and couldn’t lift her own leg off the ground, she was admitted to hospital for a week but was offered no medication.

Over this period of time Sarah has had to learn to use her left-hand more as her right hand became more numb. Low Dose Naltrexone (LDN) was the first medication she has used to treat her MS.

She says that she heard about LDN through her MS society and the strong reviews she heard were enough to convince her to try LDN and have great success.

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

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

Sarah first noticed her Multiple Sclerosis (MS) symptoms in early 1990, yet they developed “overnight” for her. She woke up one morning and couldn’t lift her own leg off the ground, she was admitted to hospital for a week but was offered no medication.

Over this period of time Sarah has had to learn to use her left-hand more as her right hand became more numb. Low Dose Naltrexone (LDN) was the first medication she has used to treat her MS.

She says that she heard about LDN through her MS society and the strong reviews she heard were enough to convince her to try LDN and have great success.

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

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

Sarah from England was diagnosed with Multiple Sclerosis (MS) in 1995 after an MRI scan due to optic neuritis in her right eye and a tingling sensation in her right cheek.

Sarah’s brain doesn't use her right eye on a day to day basis, and describes it as “looking through fog when vision kicks in.” 

In 2002 after more testing, she was told she didn't actually have MS by a neurologist. However, in May 2010, Sarah felt a strange sensation and numbness in her fingers and feet, and pain in her neck that was so bad she could barely move it. She was re-diagnosed with MS in June of the same year after various tests such as an MRI. 

After speaking to her GP about Low Dose Naltrexone (LDN), she was refused prescribal, so sourced an online doctor which gave her the prescription. Sarah noticed her fatigue had eased after around two weeks on the medication. She had an operation in August whilst still on LDN, and shortly after, practically all symptoms had gone. She still experiences light numbness occasionally, but overall her quality of life is much better.

For the entire Low Dose Naltrexone (LDN) interview, watch the video.

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

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

Sara from England takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS).

In 1990, my symptoms started just literally overnight. I got up one morning, and my left leg couldn't lift up the ground. And then I went to the doctors who arranged very quickly within a week to get me into Liverpool hospital for tests.

I had pain across into my shoulder every now and again, not very often.

I was diagnosed with MS and I was not offered anything. I stayed in the hospital for the week. They basically always said they couldn't offer me anything.

Low Dose Naltrexone (LDN) definitely gave me back mobility. I'm having some really, really good days. I go to the gym. I've been taking LDN for two years.

I knew about LDN through someone that I know in the MS Society.

My GP got permission to give me a prescription, I didn't have any side effects when I started taking LDN. After a few months I realized LDN was helping me.

I definitely would recommend LDN I definitely think it's worth a try. Nobody says it's a miracle.

I think I'm just starting to really see noticeable benefits now.

We've had some people that have said similar to yourself that they haven't noticed any improvements at all until about 15, 18 months, which is quite amazing.

They hadn't progressed any further progressive disease. That's good news in itself. Some people respond quicker than others.

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

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

Sandra from the United States takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS).  

Sandra was diagnosed in June of 2004 at the age of 42. Symptoms included extreme fatigue, blurred vision and vertigo, severe muscle cramps, spasms in legs and feet, and numbness in hands. These symptoms impacted Sandra’s life a lot, she was unable to drive to grad school and relied a lot on her partner. Also, in 2010, she even had to stop working due to lack of rest and severe bladder symptoms.

After doing research on Low Dose Naltrexone (LDN), Sandra found research groups on Facebook and spoke to her primary care physician where they decided to prescribe it for her.

Sandra experienced no initial side effects with the LDN medication, and after her first night of taking it, she slept through the entire night. After increasing her dosage, she also noticed a reduction in her fatigue levels. Overall, her quality of life is a lot better because of LDN, she feels as though she is not a prisoner in her own home, and she can now go places and not have to worry.

Sandra definitely recommends people to try the LDN, she quotes how there is nothing to lose, and quite a lot to gain.

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

Sam - United Kingdom: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Sam from the UK shares her story about Multiple Sclerosis diagnosed in 2009 and her eventual journey to finding Low Dose Naltrexone (LDN).  From symptoms that caused Sam to lay in bed thinking that if she didn’t wake up in a morning that would be okay to her now being absolutely fine and normal her LDN story, like so many others, is remarkable.  Sam had the usual difficulties getting a doctor to prescribe Low Dose Naltrexone but with determination, she eventually got her prescription and is grateful every day that she did.

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

Sally from England who takes Low Dose Naltrexone medication (LDN) for multiple sclerosis (MS). She was first diagnosed in 2001, but thinks she had constant symptoms within about three years of that.2004. 

Sally first started off having foot drop. This affected her life and her hobby of rding horses. Also, Sally feels that her knee operation did not help with her MS at all, and within five years was in a wheelchair. Sally rated her quality of life a 4/10 before the medication. She heard about the medication from the central health clinic in Glasgow. Within a week of trying Naltrexone (LDN), she says it was “absolutely brilliant”, and is the only medication that has helped her with her MS diagnosis.

Now, Sally rates her quality of life a ⅞ out of 10.

Sally would 100% recommend LDN to others, and has spoken to others with Multiple Sclerosis about it.

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

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

Rosie from England takes Low Dose Naltrexone (LDN) for Multiple Sclerosis (MS). She was diagnosed in 2005 at the age of 25. Symptoms included visual impairment, tingly fingers and numb feet. This then deteriorated to Rosie not being able to feel her fingers and legs. After having tests, she was then diagnosed with Multiple Sclerosis (MS). Even a few months later, Rosie could barely walk when coming home from her honeymoon. She described it as having the flu over and over again.

After two pregnancies, and still dealing with ongoing symptoms, Rosie learnt about LDN from her mum, she tried it eight months into her pregnancy, there were no complications and has been taking LDN since.

Rosie definitely recommends LDN to other people, she had no introductory side effects and has the medication on a private prescription. 

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

Rosanna - Northern Ireland: Multiple Sclerosis (MS) (LDN, low dose naltrexone) from LDN Research Trust on Vimeo.

Rosanna from Northern Ireland takes Low Dose Naltrexone (LDN) medication for Multiple Sclerosis, where she was diagnosed 3 years ago at the age of 60, she went blind in one eye, falling against walls and sickness problems. Rosanna rated her quality of life a 4 out of 10 before her LDN medication, and now a 7 out of 10.

She heard about the LDN medication through her Dentist, she successfully managed to receive a prescription from her Neurologist, and has now been successfully taking it for a year and a half.

Rosanna started to feel benefits of LDN within  the first month and recommends other people to try it, or even look into it.

Please watch the video for the full interview. Thank you 

Any questions or comments you may have, please Contact Us.