Easter Seals Disability Services

Megan Jennings

At the age of eighteen months, Megan was diagnosed with Juvenile Progressive Spinal Muscular Atrophy (SMA). SMA is a genetic neuromuscular disorder that gradually weakens the muscles of the arms and legs.  She has never walked independently and has used power mobility since the age of six. She receives physical and occupational therapy as treatment for her condition. Due to the significant physical challenges she encounters, Megan needs personal care assistance twenty-four hours a day, along with much specialized equipment.
Megan feels that although her life is consistently challenging, she lives it to the fullest by excelling in numerous curricular and extracurricular activities. She graduated first in her class from Brookland -Cayce High School.
During her spare time, Megan enjoys reading, writing and advocating for individuals with disabilities. She also hopes to become a foster parent one day.   She will begin her freshman year at Presbyterian College in the fall as an English major.  She hopes to become an English professor.