Some babies with ARTHROGRYPOSIS don't make it - My Arthrogryposis DAY 14

[@lornagee3510]

Oh boy that was a hard watch, thank you both for sharing your story. Nana I love you guys

[@ruthe.chidley6979]

What beautiful loving parents for their amazing daughter, Olivia! Love and prayers for Robert and Michelle! ❤️🙏

[@paulamcgehee6066]

1:30% 2.Arthrogryposis.Multiplex Congentic

[@chrissywelch918]

That was a beautiful but sad story, we need to treasure 😢❤every moment in our child's lifè💙

[@TheJamesrennicker]

It was hard for me to click the like on this one. I wish KZbin had more supportive options like FB for reactions. 😭 Even though it's sad, it is an important part of Arthrogryposis that people should be made aware of.

[@unicorn063]

If tears could happen they did so sad how severe AMC can take a baby,child people have to be so strong and loving and brave God bless all the families of AMCers this is why it’s so important to support such condition for all these people . Just reach out and help .

[@chrisbergstrom2749]

🥺😢

[@AMCPrincessAna]

*DAY FOURTEEN - This is the video you will_ comment on for the scavenger hunt/giveaway! Please comment in your own separate comment below (do not hit reply to THIS comment).* Here are the 3 questions for DAY 14 : 1) What percent of babies born with AMC will die in the newborn period? 2) Misha is the adult AMCer who helps raise awareness for Arthrogryposis on social media and she is the one who captured this interview with Robert and Michelle. What is the (exact) name of Misha's KZbin channel? 3) Provide the link here where others can go to purchase our LIMITED EDITION "blue for amc" awareness shirt.

[@cstark0824]

Question 1. 30% Question 2. AMCSI AMC Support Question 3. www.amcprincessana.com