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Chronic Pain Recovery with PEMF

BY PAT BOUTELL

Struck by a car

Pat Boutell describes how PEMF helped her recover from chronic pain following being struck by a car.
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In 1985 I was a pedestrian hit by a car. The bumper hit my knee, which severed the Anterior and Posterior Cruciate and Medial Collateral Ligaments. The surgeons only found the MCL to reattach. I had a compound fracture of the Tibia, and as I landed sitting up, a fractured Coccyx and compressed spine – I lost 2 inches in height. My more “minor” injuries were extensive soft tissue damage to my neck and hand.
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Because of the extensive injuries to my leg, I’ve had a muscle rotation, a muscle flap of the Soleus, three skin grafts, and both knees replaced in my 25 surgeries. I don’t remember not being in pain, but I worked to reduce my painkillers for my health’s sake.
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Every night I do my back exercises before bed and take two painkillers. Then, after 2 hours of sleep, I’d wake up, do more back exercises, and take more meds for pain. After about 2 hours, I’d be able to fall asleep again but would wake up again, needing more exercise.
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PEMF Treatment for Chronic Pain
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I began PEMF treatments in August 2014 at Roadway to Wellness, which exclusively uses Curatronic equipment. I was not expecting fast results, so I have been pleasantly surprised that I am sleeping much better and am in far less pain. I have reduced my meds from 2 painkillers twice a night to 2 twice weekly. I no longer have to do an hour’s worth of back exercises in the middle of the night, but less than 10 minutes. As a result, I have more energy and feel more alert.
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With my recovery, my husband and I have had the wonderful opportunity to travel the Mediterranean. Here we are depicted in front of a statue of King David in Israel.
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I am very grateful for the treatments and so impressed by Curatronic that I purchased an XPSE home unit from Pemf-Tech Inc. I don’t want to ever be without PEMF!
Pat Bouttell

XPSE Systems for Pain

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Curatron products have been approved by health authorities as medical therapy for human applications in the European Community and are certified as medical devices according to the Medical Device Directive. The products are manufactured according to ISO 13485 for Good Manufacturing Practice. In North America the Curatron devices have not been evaluated by the FDA and the products do not claim to diagnose, treat, cure, or prevent any medical condition. The information provided on this website is not medical advice and readers are encouraged to obtain the help, services and recommendations of doctors and other licensed medical practitioners. By continuing to use this website you agree to our privacy policy.

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