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28 Comments

Reply Kelley Arnold
9:50 PM on October 2, 2017 
I found myself reading this touching story and for some reason was pulled to look deeper into the lie of this adorable little boy. I soon found the reason this story drew me in. We share the same birthday! Stay strong
Reply Valerie
6:05 PM on September 22, 2015 
I am so happy to hear of Nick's progress! I think of your family often and say a prayer for all of you during these early stages in a life long journey. Havelock was Nick's neighbor in the NICU. Havelock is also doing well. He was discharged the end of August and is growing like crazy! In a sort of odd irony, while in the NICU they discovered a stenosis in his heart so we will have some follow up work to do in a few months. I hope Nick continues to grow and thrive- and congratulations on no more feeding tube! I look forward to reading of his progress. -Valerie (and husband, Dave)
Reply Susan Brown
11:42 AM on September 19, 2015 

Praying with you and for you every day! 

Reply David
7:44 PM on September 17, 2015 

Beautiful family-I'm enamored at your bravery. May God bless you and keep you. David

Reply Alex Kwilinski
4:06 PM on May 1, 2015 

Keep it up! I'm proud of you guys. Keeping you in my prayers.

Reply Ray Deats
12:53 PM on May 1, 2015 

I appreciate what you're doing here about heart defects! <3

Reply Robert Barr
12:33 PM on May 1, 2015 

I may not have any money to give the foundation, but I give my full support to it.

Reply Josh Lawrence
12:10 PM on May 1, 2015 

Hold onto hope, you guys!

Reply Luke Wenclasky
11:41 AM on May 1, 2015 

Let's get this charity famous! I love what's going on here.

Reply Johnathan Stolcenburg
11:39 AM on May 1, 2015 

I really love what you have done despite the fact you yourselves are affected by this through Nicholas. I hope you continue to help more people, "One Heartbeat at a time".

Reply Madison Shenefield
11:30 AM on May 1, 2015 

I'm glad I found this foundation, and I'm really happy with everything you're doing here. Stay strong. <3

Reply Zack Remo
11:28 AM on May 1, 2015 

We're all hoping for Nicholas to recover from all of this when he is born.

Reply Kyle
11:19 AM on May 1, 2015 

Hope everything goes well with Nicholas.

Reply Demon Danderberg
11:14 AM on May 1, 2015 

Sending love for anyone affected by heterotaxy syndrome. <3

Reply Brianna Ross
11:12 AM on May 1, 2015 

Hope for Nicholas, and hope for him to get over the worst! <3

Reply Joel Meyers
11:10 AM on May 1, 2015 

I give my heart to Nicholas and anyone else suffering from Heterotaxy syndrome. 

Reply Sebastian Brattain
11:07 AM on May 1, 2015 

Sending prayers up for Nicholas. Best wishes.

Reply Kennedy Mason
11:05 AM on May 1, 2015 

Here's to hoping this foundation goes viral

Reply Anthony Lang
10:45 AM on May 1, 2015 

Sending out hope to all of you.

Reply Anthony Ulberg
10:44 AM on May 1, 2015 

Best wishes to the Viner family

Reply Ethan Grant
10:43 AM on May 1, 2015 

Best of luck to the entire Viner family.  <3


Reply Gene Osytek
10:34 AM on May 1, 2015 

Matthew 8:3 "Jesus reached out his hand and touched the man and said, “I will. Be healed!” And immediately the man was healed from his disease." I pray that you will do great for people who suffer from this!

Reply Matthew Martell
4:42 PM on April 30, 2015 

have a nice day

Reply Aimee
10:55 AM on April 30, 2015 

In the face of adversity, the Viner family is shining by creating a non-profit to support other families who have or will walk the same path.  Keeping you all in my prayers. 

Reply Lizzie
10:19 AM on April 30, 2015 
Sending love to the whole Viner family. What you guys are doing here is truly amazing. XOXO
Reply Preston
9:56 PM on April 29, 2015 

<3

Reply Erin
11:08 PM on April 28, 2015 

Thanks for spreading the word.  It's a great cause.  Love you all so very much!  ;)

Reply Danielle Viner-Regner
6:06 PM on April 28, 2015 
This is a great cause and your dedication to this cause will hopefully make many differences in many lives to come.

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