Thank You

Whether you are visiting our page because you’re a family member, friend or random internet browser, thank you for visiting. The posts contained in this site are designed to inform our family, friends and others on the Spina Bifida journey about our experiences. We invite you to learn more about our family, then travel along our road using the links at the bottom left – you can see our most recent posts, a calendar of posts, and an archive of each month’s posts (it all started in September 2012). We try to keep this updated as regularly as life allows, and as changes necessitate. Visit again soon, join us on Facebook, or subscribe to our posts using the email box on the bottom right. Thank you for your support in this adventure!

29 thoughts on “Thank You

  1. “the adventures of colten robert” .. sounds like a kids book/movie! love you both and i can’t wait to meet my nephew!

  2. Hundreds upon hundreds of prayers are being sent to the Richard/Kate family. All of you are surrounded by love and support.

  3. Although I know your religious views, mine tells me that this little boy couldn’t have been blessed with two more capable and loving parents in this world. It might not be the adventure you would have wanted but you and Richard will make it the adventure of a lifetime. Love you guys!

  4. Hi Katie and Richard,

    I have learned of your recent diagnosis from our good friend Brock as well as my sister Robyn. I just wanted to let you know that you are not alone on this journey. My husband and I remember all too well being in your shoes just two short years ago. The first few days/weeks were the hardest. I also had my first son naturally, but in a hospital setting so I remember writing to our natural birth instructor and needing to mourn the fact that I was not going to be in control of our birth story. I also remember searching for hours online for stories and families that had traveled this road before us so that I could see stories of kids and families who were living with SB, rather than googling it (because that can be a little scary). I will tell you that although this diagnosis turned our world upside down, the minute I met Grayden it all changed. Grayden is the light of our lives and he has changed us in ways that I could not have predicted. I want you to know that both Austin and I are here for you. If you ever want to connect please feel free to e-mail me or find me on facebook. I am part of an amazing support group here in Grand Rapids and now consider some of these women some of my very best friends, thanks to Grayden!

  5. Dear Richard and Katie:

    I am so sorry to hear that you and little Colten have so many challenges ahead. I can tell that you are very brave, hopeful, and faithfilled. Know that you are all in my prayers and that my prayer partners have started to intercede as well.

    God bless you and give you strenght for the journey.

    Love,

    Cousin Connie

Comments are closed.