Caroline

Share This Post

My name is Beth Brownell and this is my daughter, Caroline. She has the GRIN2A mutation.

Caroline was born full-term with hardly any complications during birth. She started showing some health issues shortly after birth including swallowing difficulties and a heart murmur. She has also been diagnosed with Chiari Malformation Type I, Syringomyelia, Ehlers Danlos Syndrome Type III, PFAPA Syndrome, Epilepsy and many other related conditions including an expressive language disorder and an auditory processing disorder. 

Caroline has had two spinal cord surgeries and has been in speech therapy, occupational therapy and physical therapy for most of her life. She was preverbal until she was four years old. 

Caroline is in the third grade and is doing her best with classroom accommodations. She enjoys participating with her Girl Scouts troop, going to the beach, being with her three sisters, and playing with her six dogs. 

Read more posts

CureGRIN Stories

Benjamin

Benjamin Wann was diagnosed with Epilepsy at three years old, after multiple seizure types from myoclonic to tonic clonic lead to status epilepticus.

CureGRIN Stories

Braylon

Braylon is the definition of love! He is 8 years old with GRIN2A and has overcome many obstacles that were put in front of him.