Keep Misty Dancing

Our beloved Misty Owens needs your help.

In September 2021, Misty was diagnosed with sporadic Amyotrophic Lateral Sclerosis (ALS).

It will come as no surprise to you that Misty has faced this devastating diagnosis with her unparalleled tenacity and signature firecracker spirit. Misty’s determination and creativity has allowed her to continue teaching dance full-time at the University of Texas at Dallas and at her family dance studio, all while remaining committed to her true passion—sharing the joys and benefits of dance with people living with Parkinson’s.

Despite Misty’s internal strength and courage, she has experienced many changes in the last year and a half, including diminished physical function and a waning ability to communicate vocally, which directly impacts her independence and autonomy. A power wheelchair is a necessity and around-the-clock care is a must.

As Misty's reality of living with ALS continues to evolve and advance, the costs of her treatment and care—vital to sustain her quality of life and extend her life expectancy—will continue to rise. Estimates on annual healthcare costs range from $16,000 to $200,000 and can vary depending on the stage of the illness, increasing as the disease progresses.

As a founding teacher of the Dance for PD program, Misty has been a champion for the global Parkinson’s community for more than two decades. For me personally, in the twelve years I’ve been a part of the program, Misty has been my irreverent cheerleader. Thank you for joining me cheering Misty on and easing the significant financial burden of ALS treatment. Contributions of all sizes are welcome and will be used for Misty’s ongoing and emerging care needs.

In Misty’s words, “remember our circle doesn’t end.”