
Samantha Quinones
STUDENT
Samantha’s mom describes her as an extremely loving, chatty social butterfly! However, when taking a look at all the obstacles she’s overcome, it is clear that Samantha is an all-around inspiration.She credits her scoliosis journey with helping her build the characteristics that have molded her into, what we can only recognize as, a real-life superhero.
Health struggles have always been prevalent in her life. Samantha was diagnosed with Development Delay, Intellectual Delay, and Abnormality of the white matter of her brain at the age of two years old. Throughout the years Samantha has had many doctors, tests, and therapies. At the age of 9, scoliosis with a 25 degree curvature was added to her list of challenges. She began with bracing, however, a year after the diagnosis, Samantha’s gait pattern started to change. Her family traveled throughout a few states to discuss her specific scoliosis options. The hardest obstacle as a parent was hearing and seeing that your child needs surgery. After making the difficult decision to move forward with surgery, Samantha has been thrilled with the outcome. Samantha is taller, more confident, comfortable, in less pain, and happy that her clothes fit better!
“She has the potential to make great progress and her Spinal fusion has also contributed to the endeavors. We are forever grateful.” Samantha’s Mom
Her family has instilled a positive outlook in Samantha’s character that has proven to be unshakable. They credit this characteristic for helping her through her scoliosis journey. Though she now uses a wheelchair and walker for mobility, Samantha continues to participate in activities that all young kids love. She particularly likes to paint, draw, and play computer games. She recently discovered dance videos on TikTok that have not only been fun to watch, but have also turned into another form of physical therapy. Her favorite is the Piper Rockelle Squad!
By sharing her story, Samantha hopes to help others see that living a happy and joyful life is possible regardless of physical limitations, and that they are not alone in this journey. Samantha’s Mom leaves us with advice for anyone newly diagnosed:
