This course involved collaborating with a quartet that met every week with the end goal being to serve and learn with a certain population in our community. This quartet included two students, including myself, as well as a person with a neurodegenerative disease (PwNDD)  and their care partner. My quartet specifically was made of myself, another student, a female with alhziemers, and her husband who was her care partner. Every week, my student partner and I would meet online to have a coaching session with a certified art therapist. She would check in with us and give us different ideas of what activities to do with our quartet. At the end of every week we would hold an hour long online session, with our quartet, consisting of different art, music, and mindfulness activities. Some of our favorite activities as a group included a clapping circle, tapping to the beat of songs, “rose, bud, thorn”, drawing to songs, mountain meditation, and dancing together. The couple that my partner and I worked with loved to dance, so at the celebration meeting we had during the last week of classes, we led a dance for the other quartets to follow (see picture to the left). Throughout this seminar, I learned how to properly interact with people who have neurodegenerative disorders and their care partners. I learned how much the illness impacts both of them and how these short activities help to decrease some stress in their lives. Before this class, I knew about alzheimerz's and how it impacts the brain but I had never actually interacted with people who are directly impacted by it. I also learned how to get out of my comfort zone since singing and dancing isn't something I’m comfortable with but it's something I was willing to do to bring happiness to my quartet. Now that the course is completed, I have a different perspective on PwNDDs and the life of care partners. I feel like most of the time when I hear that someone was diagnosed with a disease, I begin to think about how they might be affected physically and mentally but now I have learned to think about the care partner or family members as well and how they might be impacted.