Liz Burton MOT/S

Since beginning OT school, the field of assistive and adaptive technology, along with the development of numerous creative softwares, has continually amazed me. I am in awe of the ways people work to bring independence and unique opportunities to the lives of individuals with disabilities. There truly is nothing like witnessing someone  use their technology to showcase unique abilities and talent. The Ted  Talk linked below features a young man with Cerebral Palsy who uses technology to create and develop music. https://www.ted.com/talks/tod_machover_dan_ellsey_inventing_instruments_that_unlock_new_music#t-551473 Cerebral Palsy is caused by an abnormality or injury during brain development, and usually occurs in children before birth. CP can affect the whole body, or only partial limbs and can include the following symptoms: High or low muscle tone Spasticity Ataxia, which we have learned in class, means problems with movement and coordination  Rigidity  Involuntary movement 

In order to learn more about the brain and it's role in social isolation, I watched the TedxMidAtlantic Talk with Rachel Wurzman. She focuses on a specific area of the brain, the striatum, which she believes helps us better understand our body's habits and urges when social isolation begins to take its toll on our overall well-being. The striatum is an area of the brain responsible for voluntary movement and control. Studies have shown that the striatum actually contains neurons which are related to our movement and reward, more specifically, our social interaction and the internal reward that comes as a result. Rachel goes on to explain the many different social isolation situations that can severely impact our need for reward such as social media comparison and trouble connecting with others because of physical differences. However, due to current events, my mind couldn't help but relate everything she spoke about with COVID-19 and social distancing. (We will circle ba

One word I can use to summarize the TEDx Talk (TEDxDalhousieU) with Sanford Hare is: GRATITUDE.  Sanford was simply a teenager, entering into his last year of high school when he suddenly woke up one night with a tingling sensation in both his feet and hands. This tingling continued and escalated into severe pain and weakness to the point he couldn’t even lift his hands over his head. Immediately, his parents rushed him to the ER where diagnostic imaging tests such as CT Scans, X-Rays, and a Spinal Tap were used to reveal he had Guillain Barre Syndrome.  Guillain Barre Syndrome is a rare, autoimmune disorder in which the immune system attacks the Peripheral Nervous System, which is responsible for controlling movement and sensation. I was eager to learn more about some of the specifics of this syndrome, so I visited the CDC’s website and examined the risk factors associated with GBS. I learned that only 1 in 100,000 individuals have GBS and that it is more prevalent in men over the