By Guest Blogger, Phil Ash, GRIN2B Foundation Board Member

Hello again! This is Phil Ash, teacher, father, Board Member of GRIN2B Foundation, and host of Celebrating Rare: The GRIN2B Podcast. Here is the second part of our 2-part episode of Celebrating Rare, featuring GRIN2B parents Brittaney and Mike Crider. The first part discussed Brittaney and Mike’s seven year old daughter Natalie, her personality and the family’s journey to a GRIN2B diagnosis for her. Now, in the second part of the episode, Brittaney and Mike discuss how they both discovered and created their new “normal” for Natalie, her younger brother Mikie and themselves. It was a wonderful discussion with two amazing people, and I hope you find it interesting and motivating.

 

If you have comments or suggestions for future topics, or are interested in being a guest on future episodes, please send an email to phil.ash@grin2b.com or send a tweet to @grin2bsyndrome, using the hashtag, #CelebratingRare. My goal is to continue having parents as guests on the program as well as medical researchers. If you’d like to be a guest or have suggestions for future guests, reach out!

To further protect myself from any unintended mistakes, each episode will have the following written disclaimer when you click on the link:

 

PODCAST Disclaimer: While I make every effort to broadcast correct information, I am still learning. I make every effort to double check my facts, but realize that medicine is a constantly changing science and art. I am simply sharing my views and personal experiences as a GRIN2B parent. I am not a medical professional. I welcome any comments, suggestions, or correction of errors. This entire disclaimer also applies to any guests or contributors to the podcast. Under no circumstances shall Phillip Ash, GRIN2B Foundation, any guests or contributors to the podcast, or any employees, associates, or affiliates of GRIN2B Foundation be responsible for damages arising from use of the podcast.