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Description:- The RNS® System is designed to prevent partial onset seizures at their source. Contact NeuroPace, Inc by calling 1 (866) 726.3876.
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-- Safety Information Physicians Next Gen RNS System Clinical Evidence RNS Tablet Webinars Scientific Meetings Case Studies Resources MRI Safety MRI for Patients MRI for Clinicians PDMS Home The RNS System How It Works FAQ How it’s Different Hear from Patients Patient Stories Share Your RNS Story Epilepsy Insights Company About Us Careers In The News Press Releases Contact Us Find a Center Get Connected Community Chat Talk to a Patient Educator Get Resources Home The RNS System How It Works FAQ How it’s Different Hear from Patients Patient Stories Share Your RNS Story Epilepsy Insights Company About Us Careers In The News Press Releases Contact Us Find a Center Get Connected Community Chat Talk to a Patient Educator Get Resources Press enter to begin your search Learn how NeuroPace is supporting our patients during the COVID-19 pandemic . Seizures start in your brain. That's where they should stop. Seizures start in your brain. That’s where they should stop. Seizures start in your brain. That's where they should stop. The RNS System is personalized to your unique seizures Learn More How it Works The RNS System is personalized to your unique seizures Learn More How it Works Could the RNS System be Right for You? Answer a few questions to find out Start Now Could the RNS System Be Right for You? Answer a few questions to find out Start Now How the RNS System Works Monitors your brain activity 24 hours a day Recognizes & Responds to your unique brain patterns to stop seizures Records brain activity for your doctors to review Monitors your brain activity 24 hours a day Recognizes & Responds to your unique brain patterns to stop seizures Records brain activity for your doctors to review Proven Seizure Control that is Safe and Effective Sustained Seizure Reduction that Improves Over Time 1 Personalized to your unique seizure patterns No chronic stimulation side effects 2 Life with the RNS System “I truly feel a sense of independence and excitement each day, like I have a new lease on life.” – Richard SEE MORE PATIENT STORIES Michael McKenna, MSW Received the RNS System in 2008 Emily Pidgeon, LMSW Received the RNS System in 2014 Have questions or ready to take the next step? Our patient educators can help. Connect Have questions or ready to take the next step? Our patient educators can help. Connect Michael McKenna, MSW Received the RNS System in 2008 Emily Pidgeon, LMSW Received the RNS System in 2014 1. Nair, et al. Presented at American Epilepsy Society, 2018 2. Heck, CN, et al, Epilepsia, 2014 455 N. Bernardo Avenue Mountain View, CA 94043 24-hr Support Line 1 (866) 726.3876 About Us Legal Careers Contact Safety Information Patient Resources Professional Resources Privacy Policy © 2020 NeuroPace, Inc. × Kimberly’s Story My name is Kimberly. I was born and raised in Norwalk, Connecticut. My whole life, I’ve enjoyed helping others and have been volunteering in the community since middle school. In college at Elon University, I majored in psychology, minored in human services, and began assisting English Language Learners, at a local elementary school, through my honor society. That experience sparked my love of teaching and convinced me to pursue a career in education. From 2006 to 2008, I studied for a Masters of Education (M.Ed.). Upon graduating Loyola University in Maryland, I moved to Spokane, Washington and began teaching second grade. In August 2010, I found a way to combine two of my main passions, travel and education, through a position teaching English to college students in Nanjing, China. Within a few weeks of moving, I began having a constant sense of unease and discomfort. At first, I thought this was culture shock, so I tried to power through, but it quickly became worse. Thinking that exercise might help, I joined a gym. During my third week abroad, I was on a run, and a metallic taste filled my mouth while my smell became overwhelming. I suddenly envisioned myself on a surgical table with a physician hovering over me. He was about to begin a tonsillectomy, which I had had years earlier. Through mental confusion, I was able to stumble to a floor mat. This was my first seizure; the beginning of temporal lobe epilepsy. Unfortunately, my health declined rapidly. I started experiencing seizures on a daily basis. Many were focal awareness based as, my right side would go numb, my face would begin twitching, my throat would close up, and I would often lose my breath. Others involved focal impaired awareness where I passed out. My colleagues took me to local doctors, and I was given medication for Generalized Anxiety Disorder. However, my symptoms worsened, and I started experiencing uncontrollable emotional swings ranging from joy to depression, fear to outrage. By January, life was a struggle, as I felt like I was literally losing my mind. In February 2011, I returned to the States. I was full of fear, sleep was challenging, and I suffered from 30 to 60 seizures per day. Amongst them, I had auras with visual hallucinations of strangers meeting inside my head, while bugs flooded throughout my body. In addition to generalized anxiety disorder, I was given medications for epilepsy, depression, Bipolar Disorder and PTSD. It was May of 2012, when I finally received the diagnosis of Autoimmune Limbic Encephalitis (AE). Essentially, my immune system was attacking my brain and causing inflammation. Under the care of Dr. Souhel Najjar, I began a two-year course of intravenous immunoglobulin (IVIg) that helped me begin to regain my sanity. Unfortunately, my cognition remained low and the daily seizures continued. However, I refused to let epilepsy control my life. I was living in San Francisco and enrolled in a Teaching English to Speakers of Other Languages Certification program at UC Berkeley Extension, while volunteering with the National Alliance on Mental Illness (NAMI) and the Asian Art Museum. In October 2014, after beginning a new anti-epileptic medication, I lost consciousness, fell and fractured my skull. Although the head injury was traumatic, as my sense of smell has been gone since, it brought me to USCF Medical Center, where I came under the care of neurologist Dr. Jeffrey Gelfand and epileptologist Dr. Paul Garcia. I continued struggling and, in December 2015, Dr. Najjar and Dr. Garcia, independently suggested that I was a candidate for brain surgery. Without question, I agreed to move forward. The surgery would take place at UCSF under the care of surgeon Dr. Edward Chang. Interestingly, my pre-surgical MRI showed issues within the left insula, an area that hadn’t been a focus, so the doctors implanted 130 intracranial electrodes to pinpoint the origins of my seizures. Based on the results of testing, I had an eight-hour surgery, in March 2016, to remove the majority of my left amygdala and hippocampus, along with an area of my left insula. When I woke up from surgery, I felt like my true self – a happy, positive person, with a middle ground. Although I was still having seizures, I was determined to give back to the community, and started volunteering at UCSF Benioff Children’s Hospital, along with the Epilepsy Foundation of Northern California (EFNC). Unfortunately, the seizure activity progressively worsened as it became linked to panic attacks and uncontrollable anxiety for hours each day. In March, my doctors conducted an EEG which showed that my seizures were originating within the remaining part of my left insula and spreading to different areas of my brain. We discussed a second surgery but my doctors were concerned that resection, beyond the insula, could cause permanent language impairment. The RNS System became an option. When I learned how it would continuously be working with my brain to monitor and respond to seizure activity, within the inoperable area, I immediately agreed and was eager to proceed. May 19th, 2017, I underwent my second brain surgery at UCSF. This time, I was awake for four and a half hours out of...
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