The problem we solve: Children with cerebral palsy (CP) commonly have feeding disorders and swallowing problems (dysphagia) that in many instances place them at risk for aspiration with oral feeding, with potential pulmonary consequences. They also commonly have reduced nutritional status and prolonged stressful mealtimes. The specific nature and severity of the swallowing problems may differ, at least to some degree, in relation to sensorimotor impairment, gross and fine motor limitations, and cognitive/communication deficits. Furthermore, caregivers can be expensive, and the patient may be upset at having limited autonomy.
About our solution: The goal is to invent a device that will allow a Cerebral Palsy patient to eat independently. Through the device, autonomy is returned to the user, and confidence is boosted. It would also have the additional long term benefit of reducing muscle tension and potentially gaining strength through repeated low frequency vibrations. These vibrations would occur on specific points of the jaw, therefore reducing spasticity and dysphagia. Parents and caregivers benefit because as a patient progresses, raising a child with Cerebral Palsy becomes less labor intensive.The more physical challenges a child can overcome or adapt to, the less hands-on assistance is required of the parents. Furthermore, our device is set apart from the competition because it allows the patient to recuperate strength over time by solving the problem from within, instead of just utilizing a common utensil lift/feeding device.Progress to date:
We are currently designing the prototype, which includes an Arduino, EMG sensors/electrodes, and a headstrap for the patient to comfortably wear the device. The traction that we have received so far has been positive. Furthermore, we have received a NSF I-Corps grant for customer discovery funds.
There is an estimated 764,000 individuals in the US with cerebral palsy, so this product has a significant market size. This product could be expanded to other conditions that involve oral impairment or other feeding difficulties (Parkinson’s comes to mind); however, the main focus is on cerebral palsy for the time being.
Creator: Kaila Trawitzki
Location: New Jersey
Bio: I am a fourth year Electrical and Computer Engineering Tech student at the New Jersey Institute of Technology in the Albert Dorman Honors College, with a concentration in Biomedical Technology and Nanotechnology. I currently am the CEO and Co-Founder of a medical assistive technology company, GoodVibe Medical, that focuses on meal assistance for Cerebral Palsy and Parkinson's disease patients using oral vibratory stimulation. I am currently seeking additional seed funding for my startup, and am also open to internship positions for Summer 2018, as my graduation date is currently December 2018.
Title: CEO and Co-Founder
If you or a loved one are affected by Cerebral Palsy, eating independently with ease can seem like a far-fetched dream. Unfortunately, it is a hardship for many patients.
The majority of individuals with Cerebral Palsy, 93%, will experience feeding difficulties. Since Cerebral Palsy results in impairment of muscle groups, facial muscles can be affected. The facial muscles are one of the strongest muscle groups in the body. Impairment hampers a child’s ability to chew, suck, or swallow, thereby creating a high risk for undernourishment, failure to thrive, malnutrition, growth delay, and digestive difficulties. The following conditions are common in those with Cerebral Palsy:
Many do not consider the collateral implications of oral impairment, such as those listed above and more. Furthermore, patients can often face anxiety and depression due to lack of confidence and autonomy. By providing sensory stimulation and repeated motion, excessive muscle tension can be managed, therefore strengthen their individual feeding capabilities. This is especially crucial for children, as this device can greatly improve their home and school life. Additionally, the sooner they begin treatment, the better the outcome will be and the condition will be more manageable.
Finally, imagine the autonomy and freedom you have always wanted!
We will reduce the workload and stress of medical providers by allowing treatment to shift to home-based, outpatient care. This device benefits patients, caregivers, families, doctors, hospitals, and more by returning autonomy to the user and reducing the amount of time spent receiving formal care.
We will allow patients to function more independently and reduce overall pain levels, while preventing potential emergencies (choking, etc.) that typically arise from dysphagia. Furthermore, we are very willing to help your organization gain recognition, publicity, or potential collaboration with the New Jersey Institute of Technology.
Children with cerebral palsy (CP) commonly have feeding disorders and swallowing problems (dysphagia) that in many instances place them at risk for aspiration with oral feeding, with potential pulmonary consequences. kissmanga
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