Scene: A Saturday afternoon in a sunny living room. A woman sits on the couch working on her laptop. Her husband comes into the room, yawns and tells her that he’s just woken up from a nap. It’s already his second one of the day and he jokes that he’s becoming like a newborn who needs to sleep every three hours.
The scene seems light at first, but as the couple talks, there are clues that something is going on with the husband beyond just normal weekend siesta. In the next scene, in fact, the couple finds out that the husband is experiencing early symptoms of Parkinson’s disease.
The skit is part of a health education project created by AshaUSA, a Minnesota-based nonprofit organization that provides culturally specific programs to South Asian communities. Since 2000, the South Asian population in the state has more than doubled, with about 70% of South Asian Minnesotans being first generation immigrants. With the growth in numbers has come more support needs and AshaUSA works to address the specific health, family, and youth development challenges faced by South Asians in Minnesota.
One of the areas the organization focuses on is educating community members about health and wellness topics that are seen as “taboo” in some South Asian cultures. In 2023, the AshaUSA team decided to focus on bringing awareness to and breaking down stigmas associated with Parkinson’s Disease. Parkinson’s is a progressive nervous system disorder that causes tremors, stiffness, and slow movement.
Kamala Puram, AshaUSA founder and Board Chair, shared, “There is limited knowledge about this disease in our community and most of them do not know how to react or support the person who is recently diagnosed with Parkinson’s. As a result, people try to hide and not seek help from friends and family. When the community understands the issues, they will be in a better position to provide the needed support for these individuals.”
Structural barriers also prove challenging. “Even getting a Parkinson’s diagnosis is difficult,” Kamala said. “There is a shortage of neurologists, so people wait a long time to be seen.” She has personal experience navigating the disease with a loved one–her husband was diagnosed with Parkinson’s in 2002.
While some organizations might have designed a pamphlet or organized a community event to raise awareness, Kamala and the AshaUSA team decided to create a skit about a family dealing with a new Parkinson’s diagnosis. “People remember more when we share the information as a story instead of a presentation,” Kamala said. They envisioned that the skit would include South Asian community members as actors and culturally specific details that would help the audience connect with the story.
The AshaUSA team had one problem: No one knew how to write the script for a play.
Kamala’s friend Lakshmi Reddy suggested that she post their request for support on Taproot to find with a volunteer who could write a script for the skit. Lakshmi founded a nonprofit called New Creation International that regularly uses Taproot volunteers to help further their mission. Lakshmi had always been pleased with the quality of work done by Taproot’s skilled volunteers, so Kamala decided to submit a request of her own.
As it turned out, the volunteer who offered their service for the project came with an impressive resume. Fred Raker is a freelance copywriter working primarily in marketing and advertising. Early in his career, Fred was a television comedy writer in Hollywood, penning jokes for Johnny Carson and Larry David. He has also written plays, screenplays, and other types of scripts for more than 40 years.
Fred began his skilled volunteer journey with Taproot in 2008. He was experiencing a period of unemployment and needed something to keep him busy. “Meeting new people and getting involved in a worthy project was the perfect thing to do. Interestingly, after I did the Taproot project, I started getting more freelance work. (There’s a moral in there somewhere.)”
Fred applied for the AshaUSA project on Taproot Plus because he knew his scriptwriting skills could be a great fit, but he was drawn to the subject for personal reasons as well: both Fred’s father and father-in-law battled Parkinson’s disease.
Kamala and Fred worked closely together to determine the best direction for the skit to take. “Kamala was very clear on what information needed to come out,” Fred remembered. “She wanted the script to be both informative and creative and she gave me the freedom to do that.”
Kamala and her team recruited volunteers from the community to play the four acting roles the script called for: the husband and wife, a neurologist, and the husband’s “commuting buddy.” The actors rehearsed their parts and eventually filmed each scene of the skit. The result is a series of vignettes that run the gamut from funny to emotional to educational.
“Someone is diagnosed with Parkinson’s disease once every 7 minutes. Often, people do not know how to react or support a loved one when they find out that they have the disease. The skit will help people understand what the person diagnosed with Parkinson’s may be going through and how to support them,” Kamala said.
AshaUSA now has all the pieces to make a knockout public health advocacy piece. But there’s still one final step—they need a volunteer to put it all together.
Kamala recently listed a project on Taproot Plus to find a skilled volunteer to help turn the scenes into a final video. Each scene is recorded and voiceover narration and graphics are ready to go. They just lack the tools and expertise to edit them all together into one final, shareable piece.
The AshaUSA team intends to upload the final video to their YouTube channel and distribute it through social media. They also hope to perform the skit live on stage in the future. Kamala, who is on the board of the American Parkinson’s Disease Association, plans to share it with that network, too. If it goes well, they have also discussed using the same model to create skits to educate the community about other diseases like Alzheimer’s and cancer.
“We are so grateful to Fred for his help in putting together the script and bringing his expertise to this project. I was really impressed with his ability to incorporate humor into this serious subject. We’re also thankful to Taproot for connecting us. The process was so easy and smooth,” Kamala said. “I look forward to raising awareness about Parkinson’s and hopefully creating a supportive environment where the families who are impacted by the disease don’t feel isolated and lonely.”