The document describes a situation where the author helped a resident with Parkinson's disease eat by singing to her. Singing helped the resident raise her head and straighten her spine to more easily swallow food. The author gained confidence through this interaction and communicating through body language. They learned that adaptive methods like using music can help those with Parkinson's disease live more easily.
The document describes a situation where the author helped a resident with Parkinson's disease eat by singing to her. Singing helped the resident raise her head and straighten her spine to more easily swallow food. The author gained confidence through this interaction and communicating through body language. They learned that adaptive methods like using music can help those with Parkinson's disease live more easily.
The document describes a situation where the author helped a resident with Parkinson's disease eat by singing to her. Singing helped the resident raise her head and straighten her spine to more easily swallow food. The author gained confidence through this interaction and communicating through body language. They learned that adaptive methods like using music can help those with Parkinson's disease live more easily.
residents eat. So at the beginning I fed a person with Parkinson's who has difficulty swallowing and has a very bent position in the wheelchair and this makes it even harder for her to swallow. But one day at lunch when I helped her eat, I thought that if I sing her the Viennese waltz, she will hear sounds and raise her head to look for the sound. That's how it was when I was feeding she, I would start humming and then he would raise her head to look for the sound and that way she would swallow more easily. I'm usually left alone to help a resident to help them eat, so I'm not ashamed to put my idea of singing into practice. That way I also got a smile and the lady eats more easily. I wouldn't have wanted anyone to come at that time because otherwise I don't think I would have hummed anymore. 2. FEELINGS The first time I had to help this lady eat, I was shaking and had a lot of emotions. I thought she would drown, that he wouldn't be able to swallow, that I was giving her too much food in a spoon. Then when I started to help her being alone in the room with her, I was more relaxed and I tried to improve the eating process. I tickled her cheek to open her mouth, I smiled to get her attention and that's how I gained confidence that I can communicate with body language and when I had the idea to sing to her, she was 60% confident that it would work to straighten her spine so she could swallow better. At this moment, I feel that I have confidence in my own strength, but that I need courage to put my therapeutic adaptation ideas under the observation of others. Many times the feeling of not making mistakes overwhelms me. 3.EVALUATION I think that in this situation, I did the right thing because I made the resident raise her head and straighten her spine in order to swallow the food better. I'm glad that she was receptive and responded to the auditory stimulus. I interacted visually and received a response, which is very good. I think that through this experience I gave a good idea to the other girls who are willing to try as well when they help other people to eat. 4.Analysis I think the situation went well because I knew how to stand in front of her, to be in the visual field, because the auditory, visual and tactile functions are still working, so she was capable of receptivity. I think that this situation can be found in many people who have this problem and opening the epiglottis through different tricks like this, can make swallowing easier and at the same time can improve breathing during swallowing, which leads to a much better transit. 5. CONCLUSION From this experience I learned that through careful observation and knowledge of Parkinson's disease you can find adaptive methods to help people with this disease to live more easily. 6. ACTION PLANS if I were in the same situation, I would try to place more visual and auditory stimuli intermittently at the level at which she raises his head. That is, I would place a radio on a higher table or I would place a light painting on the wall at head level and open it when it is time for dinner. In order for these objects to be purchased, I would explain the incident to the occupational therapist and ask her to talk to the owners and explain to them the advantages of having a radio or a light board at the time of feeding.