Gray Colored Glasses blog offers a lens into the everyday challenges of life with a medically-complex child.
These posts are for everyone, for people who relate to our story, and perhaps especially for those who don’t: for grandparents, teachers, doctors, and parents of neurotypical kids who make up our communities of support but rarely get a glimpse behind the curtain of our day to day life. We hope they serve not only to raise awareness but also to generate compassion and understanding for children and families impacted by PANS and other rare and little-known diagnoses.
Hopefully, sharing our story will encourage others living with PANS and other challenges to share their stories, as well. If you’d like to do so on my blog, please submit your story for consideration.
Even before we learned Isaac’s diagnosis, we knew his gross and fine motor skills were delayed. But I clearly remember thinking, surely speech would be…
The first days, weeks, and months after we received Isaac’s genetic diagnosis were full of challenges, none more important than learning how to accept this…
This post continues the story of our concerns about Isaac’s unexplained developmental delays and our search for answers. For more backstory, see my previous posts,…