Tag Archives: neuromodulation

Home / Posts tagged "neuromodulation"

Richdeep, Sandra & Jon

Early experiences with Spinal Cord Stimulation for Spinal Cord Injuries

Meet Richdeep, Sandra and Jon who participated in a panel discussion about their experiences as clinical trial participants using spinal cord stimulation for the treatment of spinal cord injuries. The discussion is moderated by Barry Munro with the Canadian Spinal Research Organization and John Chernesky with the Praxis Institute. Topics explored include participant expectations, benefits of involvement, and challenges to participate.

Learn more about neurotechnologies for spinal cord injury with our neurotech directory.

Jessica G.

How closed-loop spinal cord stimulation gave her a new outlook

Watch this exclusive video interview.

Learn more about neurotechnologies for pain management with our neurotech directory.

Jon L.

Deep Brain Stimulation for symptoms of Parkinson’s disease

Jon
Parkinson's disease
Deep Brain Stimulation

This story is a combination of immediate impact and slow progression of Parkinson’s Disease, a degenerative brain disorder, and how one man changed his cards to gain a better quality of life.

As a cardiac anesthesiologist, Jon was living his dream. He had a great job, a wonderful wife and two beautiful daughters. Although there was stress related to his job and long hours, he truly enjoyed his work. A strange symptom surfaced that sparked Jon to seek medical assistance. He was pouring a Coke into a glass and observed his pinky finger quivering. That was it, a tremor. That tremor motivated Jon to seek the advice of a neurologist. Without any hesitation, the neurologist diagnosed Jon with Parkinson’s Disease. He was 38 years old. After receiving the news, there was a sense of relief. He was relieved to have a name associated with the strange symptoms he was experiencing. Now that he had a diagnosis, he educated himself about the disease and ways to manage the symptoms.

The initial symptoms of Parkinson’s Disease can be very subtle and often do not surface until the symptoms reach an escalated level. People can have Parkinson’s Disease all their lives but they do not receive a diagnosis until a larger amount of neurons in the brain begin to be impacted. At that point, the outward symptoms begin the surface.

Accepting his diagnosis, Jon began to educate himself about the disease and inventory his options. Being an anesthesiologist helped with his quest.  One of his options for the treatment of Parkinson’s Disease is a medical device called Deep Brain Stimulation (DBS). Several times in the past, Jon had been the anesthesiologist during surgeries to implant deep brain stimulators. Even with this knowledge, Jon took the medical advice and began the typical pharmaceutical regime of taking a myriad of medications.

As Jon began to do his research about DBS, he watched video after video on the internet about success stories of people who received a DBS system. Not all of the videos were about success stories. Jon watched one video about a man for whom the DBS was not successful and he had the device removed. In his research, Jon educated himself about the system, how it works, the surgical procedure, the complication rates and spoke with other doctors regarding the DBS technology. He approached his neurologist with an inquiry as to whether he would be a candidate for the technology. Once Jon asked, his neurologist agreed that he would be good candidate.

As he became more resistant to the medications, his symptoms began to impact every aspect of his life. He was no longer able to work much less perform basic activities of daily living. For Jon, DBS was an option he couldn’t deny. “Once I get my wires, I’ll be able to function.”

The day that the system was activated was a vivid day for him. His appointment was for one o’clock in the afternoon. That morning, he could not take any of his medications and his body reacted to the lack of medications. His symptoms were severe as Jon’s body became stiffer and stiffer. To one point, he could hardly move. He went to the hospital early with the escort of his parents.  His doctor came into the waiting room and said, ‘Come with me.’ It was time to activate the system; one side of the electrode at a time.  His doctor activated one side and immediately the stiffness in Jon’s muscles melted away. The DBS system gave him new freedom of movement that was strangled by Parkinson’s Disease.

This short story is an adaptation of Jon’s full story featured in the book Bionic Pioneers.

There are many symptoms associated with Parkinson’s disease. There’s an array of options includes those of neurotechnologies like DBS, robotic therapy, peripheral nerve stimulation, and more. Learn about neurotechnologies for Parkinson’s disease with our neurotech directory

Patrick S.

Wellness & Cranial Stimulation

The feeling that you have exhausted all of your options. Have you ever felt this way? For many people who know that feeling, the search for alternatives almost becomes a life pursuit. This is a common feature among people who use alternative therapies. For Patrick, he went down a similar path. Medically discharged from his career as a medic in the military, Patrick found himself retired at a relatively young age. While in the process of building his house, he started to get panic attacks. Clinically, it could be classified as anxiety, depression, or even PTSD but for Patrick is was impacting his daily life. 

Over the course of four years, he tried various pharmaceutical treatments for either anxiety or depression. He tried traditional therapies with his psychiatrist, but nothing seemed to work. He even tried ECT sessions without success. “It was just day after day after day. It is doesn’t seem to stop.” Feeling like he had tried all of his clinical options, he started to look for other lifestyle modalities in the field of wellness. Diet and meditation seemed to help but they just didn’t get him to a sense of balance. “I just ran out of ideas,” he expressed about his search for balance and away from the roller coaster of anxiety and depression.

He was on Facebook one day and saw an advertisement for a device that uses pulsed electromagnetic field therapy (PEMF). Patrick swore he would never buy anything on Facebook, but he felt compelled to click on this advertisement. PEMF is a therapy that has long had different forms over the decades but its history dates back to ancient eastern medicine in the use of magnetic fields. The technology used today takes the form of a home-use device that is non-invasive and worn as a headset. Patrick was not convinced this type of therapy could help him but he decided to learn more about PEMF.

To him, science is important so he looked into the scientific research on PEMF. He found nothing that raised the red flags about the therapy. With claims that it could help him with sleep, relaxation, and meditation, there was some potential with this therapy. He even discussed it with his psychiatrist. She was aware of PEMF and encouraged him to try it. As a device that can be purchased on-line, he was skeptical but the vendor offered a 60-day money-back guarantee and they accepted Paypal. He bought it.

Within 5 days, he saw results. He uses the device to help him with meditation. It seems to help him focus. After more use, Patrick started to see a change in his sleep patterns. Before using PEMF, he was a restless sleeper and would typically get three hours of sleep per night. Now, he is enjoying a full 8 hours per night. Today, he uses it twice per day along with meditation. He feels like he has some normalcy back in his life. For others in a similar situation, Patrick advises to “Do the research and find a good doctor who can help guide you.”

To learn more about neurotech devices and treatments related to wellness and human performance, visit our free directory.

Ray D.

Post-traumatic Stress (PTSD) & Chronic Pain

This veteran’s name and photo have been masked to protect his identity.

All too often neurological conditions are complex and there are combined conditions to treat for one person. This is a story of a veteran living with PTSD and chronic pain.

High altitude is high adrenaline for Ray, a retired Marine serving from 1997 to 2003 with two years in Iraq then Marine reserves until 2012. He was conducting reconnaissance missions that logged more than 300 jumps from airplanes at a high altitude. From that flight level, your thoughts revolve around the oxygen that you need at the time but not the real toll that jump is taking to your body upon landings. With over 560 parachute landings under his belt, Ray’s back and legs were damaged in the process. When he returned from the combat zone, he knew that he had mental health issues but pushed them aside for work. He found himself drinking and isolating himself and then turning to suicide to ease the pain. He was diagnosed with spinal disc damage and as a result lives with severe chronic pain.


It was not until 2009 did he finally seek help. The DAV (Disabled American Veterans) assisted him with his paperwork. When he finally received help, he was diagnosed with PTSD. He finds his network of fellow veterans helps him with his PTSD and he also volunteers for the veterans crisis line. In 2012, two major events happened in his life. His wife signed him up for the VA wheelchair games and after doing so she passed away. Still grieving from the loss of his wife, he attended the VA wheelchair games any way. He found that attending those games was the greatest gift his deceased wife could give him. He recognized that he is not alone and there are other veterans living with PTSD. Adaptive sports and, even more so, the competition helped him turn his life around. 


But even with adaptive sports, work, and volunteer duties, Ray still deals with chronic pain on a daily basis. He finds in the evenings when things settle from the day, he slips into symptoms of PTSD and he focuses on his pain. Both make it difficult for him to sleep. He tried many different treatments but just dealt with the pain. This scenario frequently happens with people living with multiple complex conditions. Treating clinicians tend to focus on one area rather than looking at how the various conditions can mask or magnify other conditions. In Ray’s case, he tries to live with the pain while addressing the symptoms of PTSD.


A novel neuromodulation device was introduced to him as a non-invasive high-frequency surface stimulation device. He agreed to try it for three months to see how it works. After one week, his response was “this thing is amazing.” With 6 slipped disks in his back, his pain ranges from his legs, back and arms. He wears the device for 4 hours per day which happens to be the life of its rechargeable battery.  “It feels like a vibration on the skin, like a deep massage,” Ray explains. The small adhesive patch with a smartwatch size processor is a wearable that recently came onto the market with FDA clearance. Ray wears it all day and can’t tell that he is wearing it. On first use, he feels pain relief within 10-15 minutes of turning the device on with a residual effect for about 24 hours. He feels like his pain levels have dropped by 20% within just one week of use. The device connects to a smartphone app allowing Ray to control the device including the levels of current going into his body with a range of 0 to 100 milliamps. He has tried TENS units before but this is nothing like a TENS. “There are no wires and it’s comfortable like a massage.”  Even his mother noticed a difference in Ray, she mentioned to him that he has been able to focus more than before. With his pain reduced, Ray’s mind can now concentrate on other things other than his pain.