Several times a year the International Brain Research Foundation (IBRF) team visits Ryan at our home. We use the IBRF protocol (among others) as part of Ryan’s treatment and recovery. On Monday, October 15, the team is doing a complete assessment. The doctors and technicians will come right to our home with all their equipment.
Fallacy: Whatever Doesn’t Kill Me…
There are few, and maybe no other, expressions I despise more than “Whatever doesn’t kill me, makes me stronger.. I see it all the time on FaceBook and Twitter; usually just this vague statement, and nothing more. Each time I do it stirs my outrage. I must do everything I can not to write back. […]
Guest Post: Another Refuses to Sit Quietly
Today’s insightful post is done by Elana Canetti, a graduate student in Psychology at American University; author of the blog Flying Off the Handle. I just stumbled across this website, and your son’s story, from a blog that I follow. I am only a year older than your son, and it breaks my heart to […]
How You Can Help. It’s Not All About the Money.
Note: If this looks familiar, this is a slight modification of a post I put out last month. Over the past several days many new readers have found our website. I don’t want to miss the opportunity to share the ways you can keep Ryan and his story relevant. You should know, this is both uncomfortable […]
Team Diviney Rallies: Anti-Parole Petition Over 15,000!
This is probably my twentieth attempt at finding the right words to just begin writing. Each time I start it’s quickly followed by backspacing over everything and trying again. Truth is, I won’t find the words that can even come close to surround the support shown to Ryan (and my family) yesterday from long-time followers and […]