In 2014, I wrote the following email to a woman at the Tourette Association of America.
To Whom It May Concern,
First, though I am writing this letter to you today, I would ask that you do not share the following story publicly. At least for the time being.
Last week, I wrote a friend of mine – a renowned storyteller and videographer – with the idea that my wife Jeanette and I have been considering:
sharing our son’s story.
And, inevitably, our story. As parents, painful as it is to admit, we didn’t do this right. You’ll see what I mean in the ensuing pages.
In conclusion to this story, I have attached a brief write up as penned by Nolan, detailing his experience. The combination of our narratives should give you a clear picture of what the past few years have been like.
We haven’t shared this story with anyone. Given Nolan’s current acting and modeling career, we’ve been cautious. We don’t want to ruin his shot at growth within the industry he loves. How, then, can we share our experience in such a way that it doesn’t come across as crippling, but rather: empowering? At this point in our journey, it is finally becoming the latter, but the road has been long and lonely. Only a few people know about what I’m here to share, which I would assume is similar to many of the stories you hear.
Read more at www.CraigBrain.com