Wednesday, November 13, 2019

OT 533 SIM


Over all, I think the SIM encounter went well. I was very prepared and I feel like I communicated the information well to the client. I was very conscious of my body language and made sure that I thought through every word I said to ensure that my intentions were clear. If given the opportunity to do the SIM lab over, I think I would give the client more opportunities to speak. While I think my communication was effective, it was kind of like a one-sided conversation. I did stop a few times and ask if she had any questions, but I think I could have been more intentional with my pauses. I think a lot of it had to do with the amount of information I had to present in such a short period of time. I was very focused of hitting all the points mentioned in the rubric.

An OT student can communicate an attitude of caring by using active listening skills and proper body positioning. Positioning yourself beside your client, especially in an emotional situation like today, levels the playing field in a sense. It shows the client that we are in this together and that you are in their side. Active listening communicates to the client that their feelings are valid and important. It shows that you are hearing what they are saying and that what they are saying matters.

This encounter, for me, has just reiterated the fact that we are there to serve our clients. Our clients should be our center focus at all times. You have to be able to see things from their perspective. Another thing that I took away from this encounter is that we have to be able to accommodate all moods and situations. As OTs it is so important for us to be adaptable, to be able to roll with the punches. Situations may not always be ideal and there will be times that the unexpected happens, but even when the environment is less than ideal, we must maintain calm, cool, and client-centered.

Wednesday, August 28, 2019

Neuro Note 4


For Neuro Note 4, I chose to watch Beth Malones Ted Talk, How My Dads Dementia Changed my Idea of Death (and Life). I chose this Ted Talk because we recently covered this topic in my Neurological Aspects of Occupational Therapy class. This topic is also close to my heart because my grandfather has early/middle stage Dementia due to Parkinsons disease. I thought this video would be interesting when I read the title, but what I did not know is how much I would actually relate to what Beth Malone had to say.
Beth starts off this TED Talk with a statement that can only be described as morbid. She says, I am going to kill my dad. To someone who has never witnessed the reality of this condition, this seems unthinkable, but to someone watching this condition take hold of their loved one, it may seem like the only practical way out.  Beth Malone's father was diagnosed with Frontotemporal lobe Dementia at the age of 65.  In her talk, Beth describes the harsh realities of Dementia. Having to move her father from his house to a nursing home, watching his personality change, and watching his physical and mental states decline, these things not only take a toll on the individual diagnosed, but on the loved ones that care for them.
While my grandfathers case of dementia is quite different to that of Beths dad, I can relate, in a sense, to her thought process. It is unbelievably hard to watch someone that you have seen as a strong caretaker, slowly turn into someone who is fragile and needs to be taken care of. Like I said previously, not only does this condition affect the client, but it affects the family as well.
Another thing that Beth talks about in this video is the importance of death preparation and education. Death is not necessarily a fun topic, but it is something that needs to be talked about. In the video, Beth talks about how her family discusses her fathers death frequently after his diagnoses. She also mentions how her family was not prepared, and how she wished they had talked about death when everyone was healthy. This is just another reason why educating and preparing the family and caregivers is so important.
From an Occupational therapy perspective, I think this is why it is not only important to take care of your client, but  also to take care of their family as well. While we need to educate our clients and make sure adaptive equipment and other resources are available, we also need to be sure that the caretakers and family are educated on the condition. When a client is diagnosed with a condition of this nature, it is so important that their loved ones be prepared for what the condition looks like and what the future of the client may hold.
In the case of my grandfather, I am so thankful that he has made his final wishes known. He is currently in the middle stages of Parkinson's disease, but has made sure he has everything written down and in order before his condition progresses, even down to the songs he wants to be played at his service. My grandfather was a medical doctor who practiced general medicine in our little community for 50+ years. When he realized he had Parkinsons disease, he made sure that everyone in our family knew what the future held and was prepared for it. I believe that because of this, it has made his diagnoses just a little bit easier to cope with, especially for my grandmother and his children.
Overall, I think this TED Talk did a great job of explaining the harsh realities of dementia and what families dealing with this diagnosis may go through.  Beth Malone did a great job sharing her story and relating it back to a topic that is so important, death education and preperation. I would recommend this video to all future OT practitioners. This video is a great example of how important it is to empathetic towards our clients and their families, as well as how important client/caregiver education is.  Diagnoses such as Dementia are hard for everyone, especially the client and their families. This is why it is so important that we as practitioners do everything we can to help them process it and prepare for the future.

References:
Malone, B. (n.d.). How My Dad's Dementia Changed My Idea of Death (and Life). Retrieved from https://www.ted.com/talks/beth_malone_how_my_dad_s_dementia_changed_my_idea_of_death_and_life/up-next#t-233447

Monday, August 26, 2019

Media project-Innovators Statement



 For the media project, my assigned material was newspaper and my client's name was Susan. Susan was a 55 year old who was diagnosed with ALS. She had some trouble with fine motor function in her hands and mobility in her upper extremities. When I first read Susans case, I thought, What in the world am I going to do with newspaper? After much thought and consideration, I came up with newspaper flowers. In Susans file, it mentioned that she enjoyed scrapbooking and crafting, so what better way to work on fine motor skills and upper extremity mobility than crafts!
Before this project, I had not given much thought into how everyday materials could be used in Occupational therapy. Of course, I had seen therapists use tin cans and other weighted objects, but newspaper? I had never thought about using something like newspaper to come up with an intervention or activity. After completing this project, I am now aware of how useful everyday objects can be in occupational therapy. Whether you have to come up with an intervention on the fly or the materials you need are not readily available, everyday objects can come in handy.
This assignment has changed the way I think about the materials used in therapy. Before this project, I considered things like weighted cuffs, universal cuffs, and peg boards as occupational therapy materials, but now, I see that almost any material can be used in therapy with a little bit of thought and creativity.
This project also emphasized the importance of client-centeredness. It would have been easy to come up with just any activity that involved a newspaper, but the fact that it needed to incorporate something important to my client really made me think. It also showed me new ways to be client-centered. Say, for instance, that your client can not afford to order equipment from a therapy company. I now feel that I can confidently provide advice on how to use everyday materials to achieve the same goals in a more cost effective manner. 
Overall, I think this project helped make me a better future OT practitioner. It made me think outside the box and pushed me out of my comfort zone. It also taught me to look at things through an OT lens” and emphasized the importance of being client-centere. Even when things may seem challenging, we as OT practitioners have to be adaptable and innovative, doing whatever it takes to meet our clients needs.


Sunday, August 18, 2019

Neuro Note 3


For Neuro Note 3, I chose to watch and read about Alex Coriells Journey with ALS. I chose this topic because it is one we recently covered in class and I was interested in seeing how a younger adult dealt with this diagnoses. Alex Coriell’s wife, Melissa, filmed this video. It shows just how fast this condition progresses and how devastating it is.
Alex Coriell was diagnosed with ALS when he was 29 years old. He was a Husband and a father to 3 young children. The video begins with footage of when he was first diagnosed in January 2013; Alex still had the ability to walk and could use his hands. By September of 2013, he opted to have a feeding tube placed after he lost his ability to swallow. A few months after having the feeding tube placed, Alex lost his ability to walk. Alex decided to start a blog to advocate for and encourage others with ALS. When Alex lost the ability to use his fingers, he continued to blog using his noes to type. When he could no longer use his nose, he used his eyes (via eye gaze).
 Despite the inevitable outcome, Alex never gave up on life. He continued to live his life to the fullest, doing everything he could to stay active and keep moving. Along with blogging, he spoke at public events and advocated for ALS, spreading awareness of the condition.  Alex is quite possibly one of the best examples of strength and perseverance I have ever seen. He never lost his joy. Alex passed away in November of 2015, about 2 years from the time he was diagnosed.
One thing that I noticed about this video is how much adaptive equipment Alex used. It featured clips of him using an eye gaze device, a shower chair, an iPad base that attached to his chair, and even a paintbrush that was attached to a helmet. This video shows so many good examples of different adaptive equipment and tools that may be useful to someone with the same or similar diagnoses.
The video also showed how Alex modified some everyday tasks to fit his level of physical function. When he lost the use of his hands, He was still able to figure out how to shave and brush his teeth on his own. When he could no longer walk or use his arms, he figured out how to play a game with his children using his feet.
Another things that really stuck out to me was the role that spirituality played in how Alex processed and coped with his condition. He was a practicing Christian (as am I) and saw his diagnoses not as a death sentence, but as a way to show Christ to others. I believe that this played a big part in the strength and positivity he displayed throughout the progression of his disease. He continued to stay positive and find joy, even in the hardest circumstances.
There a million things in this video that I could talk about in relation to Occupational therapy. It features so many things that we talk about in our Occupational Therapy classes, ranging from adaptive equipment to spirituality. This video also shows the progression of ALS and the toll it takes on the individual diagnosed as well as the family.  Overall, I would recommend this video to any and all OT students.


References:

Henderson, W. (2018, February 1). Alex Coriell's Journey with ALS. Retrieved August 18, 2019, from https://alsnewstoday.com/2018/02/01/alex-coriells-journey-with-als/?utm_source=ALS News&utm_campaign=856209f0b7-RSS_FRIDAY_EMAIL_CAMPAIGN&utm_medium=email&utm_term=0_0593028b75-856209f0b7-71721017