Tuesday, June 18, 2019
OT 640 Debriefing
Here's the link to my debriefing for OT 640! I had a great experience and can't wait to hear everyone's stories when we get back from break. Have a great summer!
Wednesday, June 13, 2018
Neuro Note 4
On May 30th, our class had the opportunity to watch the Memphis Rollin' Grizzlies play wheelchair basketball during one of their practices. This was one of my favorite experiences in OT school so far. It was really interesting to learn about the sport. For instance, they follow what they call "modified NCAA rules". So that means, they follow the college basketball rules with some adjustments. Traveling is only called if they player is holding the ball for more than two pushes and charging is only called if the team member runs into someone without the intention of getting the basketball. Getting to see it first hand is an experience I will never forget. I expected them to be rough out there, but they exceeded my expectations. Also, the athleticism required for this sport is astounding. Never would I ever be able to compete at the level that they do.
I can see myself using this knowledge gained in my future practice. I think finding a group like this in the community that continues the competitive spirit of basketball while still having fun is something that a lot of people can benefit from. Especially someone at a young age with a new SCI. Showing them that sports aren't out of the question can be a big morale boost for an athletic individual. It's a way to get them connected back into the community, give them that support system of individuals that are going through similar things, and provide that team morale to let them know they are not alone in this. As we know, attitude has a lot to do with success and progress so giving a client the tools to improve their outlook could not only help their mental status but physical growth as well.
If anyone is interested in seeing the best wheelchair basketball team this side of the Mississippi, their practices are open to the public and they would love some people to cheer them on. They practice every Monday and Wednesday from 6-8 at the Glenview Community Center in Memphis, TN.
If you aren't in the area, but still want to show support, you can donate at their website http://www.rollingrizzlies.org/. They use the funding to buy new chairs, for travel expenses, and they have a goal of starting a youth league.
I can see myself using this knowledge gained in my future practice. I think finding a group like this in the community that continues the competitive spirit of basketball while still having fun is something that a lot of people can benefit from. Especially someone at a young age with a new SCI. Showing them that sports aren't out of the question can be a big morale boost for an athletic individual. It's a way to get them connected back into the community, give them that support system of individuals that are going through similar things, and provide that team morale to let them know they are not alone in this. As we know, attitude has a lot to do with success and progress so giving a client the tools to improve their outlook could not only help their mental status but physical growth as well.
If anyone is interested in seeing the best wheelchair basketball team this side of the Mississippi, their practices are open to the public and they would love some people to cheer them on. They practice every Monday and Wednesday from 6-8 at the Glenview Community Center in Memphis, TN.
If you aren't in the area, but still want to show support, you can donate at their website http://www.rollingrizzlies.org/. They use the funding to buy new chairs, for travel expenses, and they have a goal of starting a youth league.
Monday, June 4, 2018
Media Project
Throughout this project, I gained a lot of knowledge and surprised myself with what I already knew. One of the most useful things I learned is that an activity can help a client in numerous ways. At first, I was focusing on Dennis' left neglect. I though the plant hanger would be useful to work on using that left hand because it's pretty difficult to tie a knot with only one hand. This activity would encourage him to use both hands. But then as I started thinking deeper, not only was this activity client-centered, but it was working on many other things that could be potential barriers in the future. It worked on spatial relation, finger flexion and extension, left/right discrimination, and even could work on his shoulder ROM by having him hang the planter in different areas of his rehab room. I was very happy with the outcome and feel like this would be an effective intervention for Dennis.
When I first started thinking of the assignment, I was stuck because I felt like I didn't really know the best intervention to work on a lot of his barriers. I was stuck in an EBP mindset and even did some research to see what was best for left neglect and didn't come up with anything too useful to me from an OT standpoint. I was trying to bring in that previous knowledge to make sure his intervention was effective but realized down the road that I was thinking too much into it. Once I started breaking down and individualizing his barriers, the hanging planter began to fit into place as the perfect client-centered intervention for Dennis. I now know that a big part of our job is to make sure the client is working towards his goals, finding his "clinical carrot", and doing all this in a creative, client centered manner.
This assignment is definitely going to impact the way I view interventions in upcoming fieldwork. We really focused on the client-centered part of intervention for this project and I believe that's because that is what distinguishes a good OT from a great OT. In fieldwork, I'm going to be looking out for that. Even as an OT myself, this project has made sure I never forget the importance of client-centered activities in our profession.
Thursday, May 24, 2018
Neuro Note 3
In the article, OT's Role in Helping Kids Understand Dementia, Mandy Chamberlain talks about Kathryn Harrison, an author of a children's book that helps children understand Alzheimer's and dementia. I was intrigued by this article because I had a great grandmother with Alzheimer's who passed away when I was only 5 and thinking back on my faint memories of her, I now understand the difficulties she was going through with Alzheimer's. I think it's important for there to be a children's resources like this for parents to turn to when their own parent is diagnosed with a form of dementia. If you think about the population of people older than 60, the likelihood of them having a young grandchild is probably pretty high. Having a children's book that explains this complicated disorder in a way that children can understand is not only further educating the family, but can help the client's relationship with their young grandchildren, which is something many people find meaningful.
I love how Kathryn Harrison explains from a personal standpoint how her kids were involved in her mothers life, even when she was in a nursing home. It really shows how health care professionals can impact not only the client, but their family as well. The nurses would teach her children (I'm sure with supervision) how to work the bed and explained what they were doing when taking vitals. This not only could potentially grow a health care professional out of those children but made the client feel included and that her family truly understood her situation.
This was a great article for people that have a parent with a form of dementia and young children as well; as described in the article, the "sandwich generation". I would love to read the book and see how it bridges the gap between young children and their grandparents with dementia.
Reference
Chamberlain, M. (2016, April 15). OT's role in helping kids understand dementia. Retrieved from https://www.seniorsflourish.com/kidsanddementia/
I love how Kathryn Harrison explains from a personal standpoint how her kids were involved in her mothers life, even when she was in a nursing home. It really shows how health care professionals can impact not only the client, but their family as well. The nurses would teach her children (I'm sure with supervision) how to work the bed and explained what they were doing when taking vitals. This not only could potentially grow a health care professional out of those children but made the client feel included and that her family truly understood her situation.
This was a great article for people that have a parent with a form of dementia and young children as well; as described in the article, the "sandwich generation". I would love to read the book and see how it bridges the gap between young children and their grandparents with dementia.
Reference
Chamberlain, M. (2016, April 15). OT's role in helping kids understand dementia. Retrieved from https://www.seniorsflourish.com/kidsanddementia/
Sunday, April 22, 2018
Inside the O'Briens
Inside the O'Brens by Lisa Genova gives in inside look at a family that recently discovered they carry the HD gene. Joe O'Brien lived his whole life thinking his mother died at a young age, in a state hospital due to 'being a drunk'. It's not until he gets the Huntington's diagnosis at age 44 that he realizes he was wrong. Genova does a great job educating the reader on the effects of Huntington's and what it does to a family. I even learned a couple things about the disease that I never thought of before reading, such as there is a grey area in genetic testing where they have enough CAG repeats that they could get Huntington's. Also, I learned that as the disease progresses, people actually lose weight due to excessive chorea. I never thought fidgeting could take up enough calories to have an effect like that. My favorite thing about this book was that Genova gave the perspective of Joe, as well as, Katie, his youngest daughter. With hearing Joe's thoughts, the reader gets a first hand experience of the social hardship of having the disease, the difficulty with symptoms and proprioception, and how the public reacts to Joe and how that effects him. With Katie, the reader sees the family side of HD. They get to see the difficulty behind the decision for genetic testing, the constant fear in every little clumsy thing they do, and what it's like to watch a loved one struggle with a disease that you could potentially get one day. Throughout the book, you find out that two of the siblings tested gene positive for HD but you never find out if Katie, one of the characters we grow to love, is positive or negative. I think this is for a reason. Katie represents a family coming to terms with the disease. It's not about being gene positive or negative, it's about learning to live your life to the fullest, no matter the circumstances and not letting HD define who you are or who you are going to be in life.
Name: Joe O’Brien Date:
04/22/2018
Occupational Profile
Client Report
|
Reason the client is
seeking OT services and concerns related to engagement in occupations (may
include the client’s general health status)
|
Joe is seeking OT for relief of symptoms of Huntington’s
disease. He is noticing an increase in chorea, causing weight loss, beginning
to experience some muscle weakness in his jaw with slurred speech, and
difficulty controlling mood.
|
||||||||||||
Occupations in which the
client is successful and barriers or potential barriers to his/her success in
those occupations (p. S5)
|
The client is independent when it comes to feeding and is
drinking from a straw. He’s noticed barriers when it comes to some ADL such
as self-dressing and has adjusted his wardrobe to sweatpants and t-shirts to
accommodate. He is also worried about his anger outbursts that cause
destruction of their home.
|
|||||||||||||
Personal interests and
values (p. S7)
|
Joe has been a Boston police officer for 25 years and
takes pride in his independence and strength. He is a huge Boston sports fan,
“Go Sox” and avid Irish Catholic. He values his relationship with his family,
his friendship with Tommy and Donny, and providing for Rosie, now and in the
future.
|
|||||||||||||
The client’s occupational
history/life experiences
|
Joe lives on the first-floor of his family’s three-story townhome
in Charlestown, MA. He lives with his wife of 26 years, Rosie, and his
youngest son, Patrick. His oldest son, JJ, and his wife live in the apartment
above them and his two daughters live in the apartment above them. They all
get together and have a family supper every Sunday.
Hx: Diagnosed at age 44 with HD, mother died of HD. Two of
four of his kids have been confirmed HD positive. Currently prescribed a
neuroleptic for temper flare-ups by Dr. Hagler
|
|||||||||||||
Performance patterns
(routines, habits, & rituals) – what are the client’s patterns of
engagement in occupations and how have they changed over time? What are the
client’s daily life roles? Note patterns that support and hinder occupational
performance. (p. S8)
|
Travis describes his current roles as husband, father, and
friend.
Since diagnosis, has a
habit of using holy water to make the sign of the cross when entering and
leaving his house to cleanse him of his sins.
|
|||||||||||||
Context
|
Aspects of the client’s environments or contexts, as
viewed by the client (p. S28)
|
Supports to
Occupational Engagement:
|
Barriers to
Occupational Engagement:
|
|||||||||||
Physical
|
No physical supports
|
Chorea affecting performance in ADLs
|
||||||||||||
Social
|
Strong family support system, Rosie is understanding of
outbursts and has friends at work looking out for him.
|
Being described as drunk or on drugs in public by people
that don’t know of his HD diagnosis
|
||||||||||||
Cultural
|
Expected to be sufficient in work activities and provide
for his family. Strong Irish Catholic family
|
Was forced to recently quit his job at Boston PD and is
only receiving 30% pension to support his family
|
||||||||||||
Personal
|
High school education, graduated police academy at age 19,
middle SES
|
Still young at 44 but experiencing difficulties in ADLs
that wouldn’t typically be experienced at this age. Difficulty coming to
terms with it affects of HD
|
||||||||||||
Temporal
|
In his later stage of life with 4 grown children and 1
newborn grandchild
|
Has been given the “10-20” years to live post diagnosis
|
||||||||||||
Virtual
|
Has a cell phone to text and call friends and family
|
No virtual barriers
|
||||||||||||
Client Goals
|
Client’s priorities and
desired target outcomes (consider
occupational performance – improvement and enhancement, prevention,
participation, role competence, health & wellness, quality of life,
well-being, and/or occupational justice) (p. S34)
|
Joe’s number one goal is slowing the progression of his
chorea. He values his independence and wants to prolong time without a walker
or wheelchair. He also wants to be able to tell his kids and wife that he
loves them in the later progression of the disease so working on mouth and
jaw muscle strength is also on his list of goals. He is also dealing with
lots of guilt associated with not knowing his mother died of HD and passing
it on to his children without knowledge so some coping skills and stress
management would be beneficial to Joe.
|
||||||||||||
Friday, April 20, 2018
Neuro Note: Alix Reese
In an article entitled, Alix Reese: "I'm Still Myself", a young woman, Alix, is interviewed about her life after her spinal cord injury. Alix was giving her friend a ride home in Columbus, OH when she was caught in the crossfire of a street shooting. The bullet went through the back of her neck, damaging part of her spinal cord and leaving her paralyzed from the shoulders down. She uses a suck and blow device to control her motorized wheelchair and is on a ventilator but she's not letting that slow her down.
The one thing that stood out to me in this article was her attitude about her situation especially considering it was completely out of her control. She wasn't being reckless or doing something risky, she was doing a favor for her friend and her life was completely altered due to it. But rather than have resentment, she has a positive outlook and hasn't let the incident change who she is. She still loves science fiction movies and novels and is still planning on fulfilling her goal of becoming a teacher.
My clinical take away from this article is the importance of attitude when it comes to life altering diagnoses. Although she's 31 and living in a nursing facility with people over twice her age, she knows that she still has a ton to accomplish in life. The day she was shot, she was looking into going back to school to be a teacher or speaker and she still has that plan in mind today. I think that is a big part of ones attitude if they can still picture themselves accomplishing the goals they had set before the injury. That's something we as OTs can work on with them to do. Find their passion or goals they had pre-injury and find a way to incorporate that into their therapy and lives.
References
Oliphint, J. (2016, May 27). People: Alix Reese: "I'm still myself". Retrieved from http://www.columbusalive.com/content/stories/2016/05/26/people-alix-reese-im-still-myself.html
The one thing that stood out to me in this article was her attitude about her situation especially considering it was completely out of her control. She wasn't being reckless or doing something risky, she was doing a favor for her friend and her life was completely altered due to it. But rather than have resentment, she has a positive outlook and hasn't let the incident change who she is. She still loves science fiction movies and novels and is still planning on fulfilling her goal of becoming a teacher.
My clinical take away from this article is the importance of attitude when it comes to life altering diagnoses. Although she's 31 and living in a nursing facility with people over twice her age, she knows that she still has a ton to accomplish in life. The day she was shot, she was looking into going back to school to be a teacher or speaker and she still has that plan in mind today. I think that is a big part of ones attitude if they can still picture themselves accomplishing the goals they had set before the injury. That's something we as OTs can work on with them to do. Find their passion or goals they had pre-injury and find a way to incorporate that into their therapy and lives.
References
Oliphint, J. (2016, May 27). People: Alix Reese: "I'm still myself". Retrieved from http://www.columbusalive.com/content/stories/2016/05/26/people-alix-reese-im-still-myself.html
Friday, April 6, 2018
Neuro Note: Ray's ALS Journey
Ray is a nurse, husband, dad, bicycle enthusiast who was recently diagnosed with ALS. He has a blog, full of humor and sarcasm that is dedicated to telling his story. This particular article I read was entitled One Year. It describes his first year post diagnosis. He talks about his family life, what it was like to tell everyone that he had ALS, and the changes he experienced in the first year.
A couple things I noticed when reading is that Ray is using humor to make his situation better. Immediately, I go into an OT mindset and think if that's the reason he is still doing so well. Seeing the funny side of things, keeping a positive mindset, and having a supportive family all could have impacted his ability to stay strong through this progressive disease. I also noticed that he has had to make some drastic life changes since his diagnosis. Ray is the epitome of an outdoorsman. He used to love mountain climbing and would ride his bike daily. These are both important occupations for Ray that he has come to terms with not being able to do like he used to. One of his bucket list items was to bike from coast to coast. One cool thing that people following the blog have done is kept track of how many miles they've biked in order for Ray to "bike across the country". They've accumulated 42,000 miles so far!
My clinical takeaway from Ray's story was kind of an "ah-ha" moment for me. In class we always talk about home modifications as if anyone can do them. Well, my "ah-ha" moment is that isn't always the case. Ray lives in a 100 year old house with no bathroom on the bottom floor. He talks about how they had contractors come look but that would be a logistical nightmare with their layout and having to live there during construction. He also mentioned the option of a chair lift for the stairs, but that it was way to expensive for them. Ray and his wife talked about moving, but they raised their kids in that house and didn't want to live anywhere else. So my take away is a pretty important one for OT. For some situations, a textbook answer isn't always the right answer for the family.
I loved learning about Ray and getting a first hand account of his first year being diagnosed with ALS. His thoughts and attitude is something that truly inspired me.
A couple things I noticed when reading is that Ray is using humor to make his situation better. Immediately, I go into an OT mindset and think if that's the reason he is still doing so well. Seeing the funny side of things, keeping a positive mindset, and having a supportive family all could have impacted his ability to stay strong through this progressive disease. I also noticed that he has had to make some drastic life changes since his diagnosis. Ray is the epitome of an outdoorsman. He used to love mountain climbing and would ride his bike daily. These are both important occupations for Ray that he has come to terms with not being able to do like he used to. One of his bucket list items was to bike from coast to coast. One cool thing that people following the blog have done is kept track of how many miles they've biked in order for Ray to "bike across the country". They've accumulated 42,000 miles so far!
My clinical takeaway from Ray's story was kind of an "ah-ha" moment for me. In class we always talk about home modifications as if anyone can do them. Well, my "ah-ha" moment is that isn't always the case. Ray lives in a 100 year old house with no bathroom on the bottom floor. He talks about how they had contractors come look but that would be a logistical nightmare with their layout and having to live there during construction. He also mentioned the option of a chair lift for the stairs, but that it was way to expensive for them. Ray and his wife talked about moving, but they raised their kids in that house and didn't want to live anywhere else. So my take away is a pretty important one for OT. For some situations, a textbook answer isn't always the right answer for the family.
I loved learning about Ray and getting a first hand account of his first year being diagnosed with ALS. His thoughts and attitude is something that truly inspired me.
Thursday, April 5, 2018
Developmental FoR
I found interest in the Developmental Frame of Reference. It encompasses the the sequential aspect of development and how behaviors are influenced through the mastery of previous stages. People develop at different rates but each stage of development can only be achieved once the previous stage is completed. Developmental FoR included 6 adaptive behaviors: sensory integration skills, cognitive skills, dyadic interaction skills, group interaction skills, self-identity skills, and sexual identity skills. This FoR works with clients of all ages from childhood on. According to this theory, functional development would mean completing the stages of development in sequential order. An OT helps intervene with maladaptive behavior and promotes sequential development. In school aged kids, a therapist might observe their social interaction with peers to assess dyadic interaction skills.
Three key terms associated with the Developmental FoR:
1) sensory integration skills - ability to receive, select, combine, and coordinate sensory information for functional use
2) dyadic interaction skills - ability to engage in a variety of primary groups
3) self-identity skills - ability to perceive self as an autonomous, holistic, acceptable person who has permanence and continuity over time
Three key terms associated with the Developmental FoR:
1) sensory integration skills - ability to receive, select, combine, and coordinate sensory information for functional use
2) dyadic interaction skills - ability to engage in a variety of primary groups
3) self-identity skills - ability to perceive self as an autonomous, holistic, acceptable person who has permanence and continuity over time
Tuesday, April 3, 2018
Reflection on Health Promotion and Health Literacy
Today in class, we talked about health promotion in the field of OT. Through this lecture, I got a better understanding of our role in a interdisciplinary group. Dr. Flick gave an example about a client she had in acute care in which the dietitian modified her meal plan to a no sodium diet. The dietitians goal was to improve the clients health through food consumed but failed to take into account the ability for the client to continue the diet plan post discharge. That is where the OT steps in. The client had low muscle function in her upper extremity, and typically ate canned vegetables and microwave dinners because they were easy for her to prepare for herself independently. Both of those are high in sodium though, making this new diet difficult to achieve in her home setting. The dietitian and OT worked together to then make a plan that would still promote independence in the client and work with the new diet. I also learned about the importance of health literacy. Making sure a client has a clear understanding of what is going on and what is expected of them is essential to having success in the future. If the client does not understand the purpose behind a task, they're less likely to do it consistently or with purpose. Mutual understanding and building a therapist-client report can help with communication and make the client feel more comfortable when asking questions, and therefore, have a better understanding of their health goal and how to achieve it.
Tuesday, March 27, 2018
OT Observation
When shadowing at an early intervention clinic, one of the OTs I worked with spent a ton of time with Theraputty. Since talking about the importance of using meaningful activities, it makes me question the extent of use for it. But at the same time, at such an early age, are meaningful activities as 'meaningful' to a 2 year old as compared to a school aged child. So from that standpoint, I can see the reasoning behind her actions. Some meaningful activities were used, such as feeding, and play based activities but they weren't the main event. I also shadowed a therapist that worked at a private school in Little Rock for children with special needs and the experience was the complete opposite. His sessions were almost completely full of meaningful activities. We were tying shoes, pouring water from a milk jug into a cup (the clients mom wanted her child to be able to pour himself a glass of milk without spilling it) and working on handwriting. I learned a ton from him including how to give the child an option of what he wants to do. He would write the activities to be accomplished that session down on scraps of paper and let the kid scooter over to the papers an pick one out. I'm glad I got experience with each side of the spectrum and will use it in my future practice.
Monday, March 19, 2018
Reflection on "Au-some Swimmers: The Role of OT in Swim Lessons for Kids with Autism"
This podcast truly helped me understand the importance of seeing an activity through an "OT lens". When I initially thought of swimming, I assumed it would be a predominantly leisure activity. But by looking through the OT lens, there are so many more components of the activity that can be transferred to other tasks or occupations. As Nick Murray explained in the podcast, teaching a child with autism to swim not only teaches them that activity, but works on other skills, such as sequencing, sensory processing, and motor function, that are important for the development of that child.
One example he gave really hit home for me. He told a story about a child with autism who hated getting his head wet. Not only does that make the task at hand, swimming, difficult, but also can make the daily task of showering or washing his hair difficult. By easing him into the idea and allowing him to pour water on the lifeguards head, making the whole experience fun for him, he warmed up to the idea and made progress towards the ultimate goal, submerging underwater and eventually swimming. Not only does this progress show up in the swimming pool, but I can see it transferring into his daily hygiene routine. To me, that's the beauty of our profession. We use meaningful activities to develop skills that will help in future activities and child development.
One example he gave really hit home for me. He told a story about a child with autism who hated getting his head wet. Not only does that make the task at hand, swimming, difficult, but also can make the daily task of showering or washing his hair difficult. By easing him into the idea and allowing him to pour water on the lifeguards head, making the whole experience fun for him, he warmed up to the idea and made progress towards the ultimate goal, submerging underwater and eventually swimming. Not only does this progress show up in the swimming pool, but I can see it transferring into his daily hygiene routine. To me, that's the beauty of our profession. We use meaningful activities to develop skills that will help in future activities and child development.
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Interview Reflection
Overall, I believe the interview went well. I answered the questions professionally and appropriately. I prepared by reading over some of th...
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Throughout this project, I gained a lot of knowledge and surprised myself with what I already knew. One of the most useful things I learned...
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One of the key take aways I got from our driving guest lecturer is that driving is an essential part to someone's independence and they ...