Our Groundbreaking Non-invasive Approach to CRPS

by Dr. Katinka van der Merwe of The Spero Clinic and author of “Putting Out the Fire: New Hope for RSD/CRPS.”

I set out on a journey eight years ago that made treating the nervous systems of those suffering from CRPS (Complex Regional Pain Syndrome) not only a part of my life as a chiropractic physician, but my passion and my mission. My first CRPS patient was a man named Carlos, who suffered from full body CRPS. This case revealed to me how complicated but also rewarding treating patients who suffer from CRPS can be. I have kept in touch with Carlos through the years, and I’m delighted to say that as of today, Carlos is still in remission. In the past eight years, as my patients have shared their results, patients have come to me from all over the USA as well as Australia, Canada, Europe and South America.

The first question patients usually is “is your system like ____“  (fill in the blank). Is your healing system like Calmare? Is your system like Ketamine? Is it like Mirror Therapy? The simple answer to this question is that my system I have designed is not like any other system. Since I treated Carlos, I have developed a simple formula I use in the ongoing development of my treatment. I can sum it up in the following way:

My soul purpose in treating the human body is to remove anything that may interfere in the nervous system’s ability to heal the body from within. Any treatment that has shown marked (and I do mean marked) success in this department is worth a second look. To this end, I have always maintained that one of the most powerful tools any doctor can arm themselves with is an open mind. When we are closed to new ideas, we are closed to growth.

Through the years, I have adopted systems and discarded systems. This has never once meant that anything I used didn’t work, it just meant that it didn’t work consistently. Of course, there is no medical treatment that I am aware of that is universally successful. After all, I am treating the marvelous human body, not a predictable machine. However, if I find a promising treatment, I examine it, test it against our old treatments and if it works better than my old way, I replace it. In this way, the model I used eight years ago is very different from the one I use now.

That brings me to the next question. What exactly do we do? I will attempt to explain as briefly as possible. The treatment approach I have designed is deeply rooted in my basic philosophy as a chiropractor. Chiropractors are known by the public to “pop” backs and necks, because they hurt. However, what the public generally does not understand is that our healing art stems from the belief that the body is a self-healing organism, capable of surviving and healing even catastrophic injuries.

Most accepted treatments for CRPS are rooted in pain control. While the need for these are obvious, they also do not offer long term solutions. When the drug or chemical compound’s effect runs out, the pain returns. Spinal Cord Stimulators is a notable exception to this rule. However, in my experience, Spinal Cord Stimulators, even when successful, merely take the edge off the pain. Neridronic acid is a new treatment currently making its way to the US. We know for certain that it may have severe side effects and does change the structure of the bones permanently. In addition, it does not work for everyone, although it has proven to work miraculously well for some. No long- term studies have been done on this treatment. Of course, the same may be said for our system. The difference, however, is that I require that none of my treatments alter the normal function the human body, but only enhance its function.

Our system consists of what I call “punches”. The first “punch” is using a technique that I have personally developed to decrease pressure on the Vagus nerve. The Vagus nerve is one of the twelve cranial nerves that generally control senses like smell, balance, taste and sight. The Vagus nerve is the 10th cranial nerve and it is vastly important. It controls inflammation of the body (including nerves), GI function and immune function, to name a few. The autonomic nervous system (the automatic nervous system) is divided into two parts: Sympathetic (fight or flight) and Parasympathetic (rest and digest). The Vagus nerve contains parasympathetic fibers. In my experience, virtually 100% of CRPS patients suffer from malfunction of the Vagus nerve to at least some degree, with sympathetic dominance of their autonomic nervous system, rather than a balance between Sympathetic/Parasympathetic.

This, of course, explains why so many patients CRPS patients suffer from symptoms associated with cranial nerve dysfunction, such as sensitivity to light and sound. Also, it explains the very common failure of the digestive tract in CRPS patients, generally a symptom that is regarded as a separate diagnosis in the medical community, requiring a separate treatment.

The other punches to my system is like a tool bag full of different tools. Most patients will require a customized approach, based on their unique circumstances. Please note that in my experience, our system is like a cookie recipe. You cannot pick and choose individual ingredients and expect the same outcome as when all the treatments are used together. Synergy is vastly important, where one punch is exponentially more powerful when part of my system. Following is a brief mention of each tool:

  • Detoxification (based on patient tolerance)
  • A functional blood analysis. Our doctor who specializes in this specifically looks for signs of a viral and/or bacterial infection. For example, patients who suffer from CRPS often will also suffer from a chronic Epstein Barr Viral (EBV) infection, making long- term healing unlikely unless the infection is addressed. Chronic bacterial bladder infections will also impede healing, and are often overlooked. Blood is not drawn unless the patient is considered stabilized, as a needle prick may spread CRPS in unstable cases.
  • Magnetic Resonance Therapy is used to calm the nervous system and decrease pain, in order to “set the table” and prepare the body to accept other therapies.
  • Emotional healing therapies. I have a doctor on our team who specializes in neutralizing the effect of emotional stress on the Central Nervous System. In addition, I host The Lightning Process, a patented training course presented by a certified provider from Oregon right in our clinic about once every two months. In our experience, most CRPS patients suffer from severe PTSD and fear, as they no longer trust their bodies to naturally be healthy. This course provides our patients with powerful tools to influence their lives and their health.
  • Neuromuscular Re-education, FDA approved for relaxation of muscle spasms, prevention of muscle atrophy, muscle re-education and increasing range of motion. The patient is connected to a machine that uses Direct Current (patented in a way to not cause the nervous system to “guard”) while put through specific rehabilitative exercises. This process is overseen by an experienced and dedicated therapist, familiar with your case. You will grow very close to your therapist and the day you graduate, they will be right by your side to watch you ring the bell (more about that later).
  • Sound wave technology is used to break up adhesions and scar tissue, both of which may impede healing to the body as a whole.

I like to refer to our clinic as the “anti-clinic”. What does this mean? Most clinics are quiet environments where patients do not interact much with each other. In our clinic, I encourage and promote bonding among our patients. I have found that when patients can encourage each other in a “buddy like” system, it is a central part to patient’s recovery. I have a tradition where new patients meet outgoing patients to discuss the treatments, what to expect, and provide encouragement made possible because of their own progress. We encourage hugs, laughter, and humor all around.

My staff was handpicked from all walks of life. Some were waiters, some were patients, and some worked with world class athletes. In my experience, the most important quality a staff member can possess is empathy and compassion for those who suffer. Virtually everything else can be taught. While we all wear scrubs, it is not unusual to spot piercings, tattoos and pink hair among our staff. We definitely focus on the things that matter most and don’t waste our time on the little things that don’t.

Does our system work for everybody? As with every treatment, my system is not universally successful. It is my strong position that we do not treat specific conditions, but bring healing to the central nervous system. In addition to CRPS, many of my patient suffer from other conditions like Ehlers Danlos Syndrome (EDS) and Postural Orthostatic Tachycardia Syndrome (POTS). The body knows how to heal from the inside out, sometimes it just needs a tour guide. If you look at my clinic’s Facebook page, you will see many videos of people “ringing the bell”. This is a tradition where my patients and staff gather when a patient graduates to their satisfaction. In most cases, that means that my patients are leaving my clinic pain- free. Of course, not everybody rings the bell. However, if you look at the many success stories you will understand that my approach should be more widely accepted as a whole, as an alternative to the philosophy that the body should be healed from the outside.

Why is my system not more widely accepted? My system is a complicated one, fueled by years of experience and trial and error. I am fully aware that it is an effective one that should be widely available across the world. While this is my ultimate goal, it will take years to get there. As we take the first steps in this direction, for now, patients have to travel to us from distant states and countries.

Another common question is: “I have had CRPS for longer than a year. Is there still hope for me?” Yes! In my experience, time passed has no effect on the effectiveness of my treatment.

Please know that every single patient that recovers should bring you enormous hope. Their bodies are not more special, more magnificent than yours. In my clinic, I refer to “white crow moments”: you only have to see one white crow to know that not all crows are black. No matter what, you have keep your hope alive! This must happen if you are to recover.

Editor’s Note:  The Neurologic Relief Center is a corporate sponsor of RSDSA. Our blog is not intended to provide advice on personal medical matters, or to substitute  for counseling with a physician.

Tracey’s Story

By Tracey Morales for the RSDSA blog.

Hi, my name is Tracey, I’m 48-years-old, married and have two daughters. I’ve had RSD for 21 years.

My RSD story starts in Jan 1998. A toy V-Tech computer fell on my left foot, fracturing two toes and crushing the MT joints (toe knuckles). After two weeks, I knew something was wrong so I saw a podiatrist, who by the 2nd appointment diagnosed me with RSD. He sent me to a vascular surgeon who confirmed the diagnosis. I went through 6 blocks and a 6-day epidural over 6 weeks.  All worked, but wore off within 24 hours or less. But I found the RSD came back fighting, worse after each treatment. My leg was now on fire, but ice cold and so discolored from my groin to my toes. It looked like someone colored my leg with a magic marker. The decision was made to do a sympathectomy, which was done on March 16th, less than 2 months after the initial injury. The morning of my surgery, my big toe was beginning to get gangrene. Well, it worked, I went into remission for four years. I went back to work, got married and had my second daughter. When she was two, she had her tonsils removed and I stayed in the hospital with her. I fell asleep in the bed with her, not realizing that my foot was pressed up against the footboard. I awoke the next morning stood up and it was back, I could not put any weight on my foot at all without excruciating pain. I saw my Dr that week and he confirmed the RSD was back. My only real option was meds because the sympathetic nerve was gone down my left leg. It had started to regrow at the base of my spinal cord a 1/4 of an inch, that very tiny growth was enough for it to come back. The RSD ended up going full-body over the next 5 years, I was bedridden 95% of the time. I tried more blocks, lidocaine infusions over the years, as the nerve grew more, but nothing worked. It continued to get worse.

A friend suggested ketamine infusions with a pain specialist that she worked with, Dr. Robert Schwartzman, who was doing experimental ketamine infusions. I had to wait a year and a half for my appointment. I started the infusions in Jan 2007. I went initially for 10 days, then for 3 days every 2-3 months for booster infusions over a period of 10 years. The first 8 years worked pretty well. During the last two years, it seemed the ketamine had stopped working. My pain went through the roof again and the RSD started to spread to my right leg. My last infusion was in December 2016.

In April 2017, I started using the OSKA Pulse Device and that has brought my pain down to almost nothing. It’s helping with so many different symptoms and I have been able to take back my life and do the things I love to do again. I’m getting better relief from the OSKA than I did from the infusions. My pain was an 8/9/10+ on a bad day, the RSD was starting to spread into my right leg and a good day was a 5/6, with the infusions. My pain today is a 1/2 on a good day, and a 3 on a bad day, which is rare. The weather doesn’t bother me anymore.  I use to get 3-5 migraines every week and I have not had one since I started with OSKA. I also use to get shocking/electrocution type pains down my leg, those have stopped too. I haven’t had a flare in over a year. The swelling and discoloration are also gone. I’m in the process of decreasing my pain patch. I should be totally off it in a few months, then I’ll be off all meds.

I have managed to find some good in the bad and have started drawing Awareness pictures to keep my mind off my pain. That’s led to a Facebook Artwork page and a store on Zazzle where my designs are available on T-shirts, Fleece Blankets, Leggings, Mugs and many other items. I have items for over 40 different illnesses. I have made several donations with my royalties and plan to make more as time goes on.

Below is some information on the OSKA Pulse Device and some pictures of my RSD foot & leg before and after using the OSKA for several months.

Individuals may contact me at [email protected]

INFORMATION ON THE OSKA

Oska Pulse is a small portable PEMF (pulsed electromagnetic frequency) device. It’s the size of a cell phone. It has no wires or electrodes, and can be used anytime anywhere. It charges like a cell phone. It decreases inflammation, increases blood circulation and improves range of motion. It works on a cellular level.

When cells are injured or have degenerated, they lose their electrical potential and are no longer able to exchange ions, causing inflammation and pain.

Oska Pulse uses optimized PEMF to restore the electrical potential cells need to receive nutrients and oxygen, which stimulates cellular regeneration—relieving pain, and activating the body’s natural healing process.

It works great for all types of conditions including RSD/CRPS, POTS, Fibro, Lyme, MS, RA, TMJ, Migraines, Endometriosis and much more. I have a list of 150+ different conditions that PEMF can treat.

The great part is it doesn’t even have to touch your body to work. You can strap it to you, your arm, back, leg etc. Or you can just set it next to you or the affected area. You can put it in your pocket or your purse, on your lap, it will still work. You don’t feel anything, no tingling, no zapping, no vibration, nothing.

There are no side effects that have been reported. If it’s used properly, at least 6-8 times a day consistently, more if you choose to, it should work and give you pain relief. You have to be consistent and patient. Some people see results within 2-4 weeks, others it may take up to 2 months. Everyone is different but once you start to feel results, they only get better with continued use. It’s not a cure, but can reduce the pain so that you can get back to life and doing things you used to do.

The device can be ordered here:

$55 will be automatically taken off at checkout so the cost will be $344 USD. You’ll also get free shipping in US and a 30-day full money back guarantee. If this link is used, the company is willing to give an extension to 60 or 90 days on the guarantee if needed.

Editor’s Note OSKA is a corporate sponsor of RSDSA. Our blog is not intended to provide advice on personal medical matters, or to substitute for counseling with a physician. We asked Ms. Morales to share her story as she been a member of RSDSA’s community for many years and has responded well to this treatment and OSKA does offer a 30-day money back guarantee and they mean it.

 

Jennifer’s Legacy

Written by James W. Broatch, RSDSA’s Executive Vice President, Director

I want to introduce you to a special book which was recently published as a testimony to Jennifer Abramson’s brief but wonderful and impactful life.

Jennifer lived only 31 years. However, her wisdom and can-do spirit live on in JEN’S Gift, a book which is filled with Jen’s poems, insights, and quotes that touched her soul. The posts were uploaded to her Instagram account lovingly titled Goal2Soul (Sending Out Unlimited Love).  Annie Abramson, Jen’s mother writes, this is Jen’s gift to us. Every page reflects the humor, wisdom and feelings we need to help us appreciate our own journey in life… May her gift inspire you and may you too be touched by her love and kindness.”

Jennifer was a beautiful young woman who graduated with a BA in Communications from Rutgers and worked for a publicist until discovering her passion for acting as a corporate host and spokesperson while acting in commercials. But life can change on a dime. Jen developed Lyme disease and was exposed to black toxic mold which entered her body. After years of treatment for Lyme and mold, she developed Complex Regional Pain Syndrome CRPS Type 2.  Rendered homebound with indescribable pain, Jen created her Instagram account posting beautiful, unique photos with insights, quotes, clever humor, and wisdom that will inspire you. Jen passed away in November 2016.

Her Mom took her creation and published it, hence we have Jen’s Gift! It is truly a special read and will touch your heart, a book for all ages.

ALL proceeds from the sale of Jen’s Gift will be gifted to RSDSA, to help promote greater awareness of CRPS, further research, and help find better treatments and a cure.

Diane Martin shared her thoughts after reading JEN’S Gift, “my daughter and I had the honor of knowing Jen. She was such an inspiration to all. Jen’s Gift was an such an amazing inspirational book. Jen had a gift for words. Her book is filled with such beautiful quotes and pictures that went along with them beautifully. Jen was wise way beyond her years. I found myself laughing, crying at times and learned not to take life for granted.”

To purchase your copy, please visit jensgiftbook.com.