CLINICAL UTILITY OF A NOVEL SENSORIMOTOR APPROACH FOR A PATIENT PRESENTING WITH IDIOPATHIC NEUROLOGICAL SYMPTOMS: A CASE STUDY

Abstract

Event Abstract Back to Event CLINICAL UTILITY OF A NOVEL SENSORIMOTOR APPROACH FOR A PATIENT PRESENTING WITH IDIOPATHIC NEUROLOGICAL SYMPTOMS: A CASE STUDY Edythe Heus1* and Alexander Kalinkos2 1 Neuro Think Tank, United States 2 Neuro Think Tank, United States Movement and other neurodegenerative disorders can encompass a wide variety of disease entities, many of which are difficult to diagnose. Here we present a 50 year old female, with idiopathic, progressive neurological symptoms including ataxia, idiopathic dyskinesia, dysphonia, dysarthria and dysphagia. MRI showed a nonspecific, small, right paraventricular hyperintensity. PET scan showed mild decreased activity in cerebellum and temporal lobes. Patient was unresponsive to conventional drug therapy (clonazepam), neuropsychiatry and lifestyle changes. Patient was only able to work limited hours, with assistive equipment from home, and any excessive stimuli would trigger physical collapse. Patient participated in an inexpensive, novel sensorimotor approach comprising of specific patterns of movement on equipment that enhances sensory feedback and is unstable by design. The instability and sensorimotor stimulation was speculated to increase cerebellar functioning, neuroplasticity and cognitive function. 3, 20 minute sessions over 5 weeks were increased to an hour, 2 times weekly as her condition improved, for 14 months with noticeable improvement upon commencement. At week 56, patient’s neurologist noted a 90% improvement. Progress was steady during treatment, with gradual recovery of activities of daily living (ADLs). After 16 months of treatment, patient returned to work, without the use of assistive equipment, and ADLs were within normal limits. Excessive stimulation combined with weariness can trigger dyskinesia but is less severe and easily managed. Given the degree of improvement with this patient, we believe that a larger study is warranted to determine if this outcome is repeatable in other cases of idiopathic, progressive neurological dysfunction. Keywords: Ataxia, idiopathic dyskinesia, Dysphonia, Dysarthria, dysphagia, sensorimotor, Neurodegenerative disorders Conference: International Symposium on Clinical Neuroscience: TBI and Neurodegeneration, Orlando, Florida, United States, 10 Dec - 14 Dec, 2015. Presentation Type: Poster Presentation Topic: Case Study Reports Citation: Heus E and Kalinkos A (2015). CLINICAL UTILITY OF A NOVEL SENSORIMOTOR APPROACH FOR A PATIENT PRESENTING WITH IDIOPATHIC NEUROLOGICAL SYMPTOMS: A CASE STUDY. Front. Neurol. Conference Abstract: International Symposium on Clinical Neuroscience: TBI and Neurodegeneration. doi: 10.3389/conf.fneur.2015.58.00032 Copyright: The abstracts in this collection have not been subject to any Frontiers peer review or checks, and are not endorsed by Frontiers. They are made available through the Frontiers publishing platform as a service to conference organizers and presenters. The copyright in the individual abstracts is owned by the author of each abstract or his/her employer unless otherwise stated. Each abstract, as well as the collection of abstracts, are published under a Creative Commons CC-BY 4.0 (attribution) licence (https://creativecommons.org/licenses/by/4.0/) and may thus be reproduced, translated, adapted and be the subject of derivative works provided the authors and Frontiers are attributed. For Frontiers’ terms and conditions please see https://www.frontiersin.org/legal/terms-and-conditions. Received: 31 Oct 2015; Published Online: 02 Nov 2015. * Correspondence: Dr. Edythe Heus, Neuro Think Tank, Kenmore, United States, dredythe@revinmo.com Login Required This action requires you to be registered with Frontiers and logged in. To register or login click here. Abstract Info Abstract The Authors in Frontiers Edythe Heus Alexander Kalinkos Google Edythe Heus Alexander Kalinkos Google Scholar Edythe Heus Alexander Kalinkos PubMed Edythe Heus Alexander Kalinkos Related Article in Frontiers Google Scholar PubMed Abstract Close Back to top Javascript is disabled. Please enable Javascript in your browser settings in order to see all the content on this page.