Help Jackson Strong Medical

My name is Jess and I am sweet Jackson’s Gigi. We would appreciate all of love and support to help John, Kaitlyn, and Jackson with all of the upcoming surgeries and trips to Seattle Children’s Hospital that are about to begin on November 27th. 

Jackson was born with a very rare gene mutation, (ACTA1 Nemaline Myopathy) a muscle disease that usually babies don't survive, but Jackson is a fighter.

John and Kaitlyn are currently waiting on a call to get a sleep study done in Seattle. We were told this could be any day. Meaning they would have to pack up and go!

They are excited to finally start getting Jackson seen by specialists in Seattle, as his local doctors are not comfortable to be his primary care of certain specialities. They will be getting set up with cardiology, neurology, pulmonology, cranial, facial, and many more specialists. These trips will be frequent.

Jackson has already had:

Gtube/hernia repair/ double foot surgery. He was born with his hip out of the socket and will have to have hip reconstructive surgery at 1.5 years old. And, possible jaw surgery after their consult with the Specialist in Seattle.

They will need to get a new car seat that will allow Jackson to travel long distances more comfortably with his medical conditions and he does not choke and aspirate while traveling.

I know they would more than appreciate any burden financially that comes with these huge hurdles and be able to solely focus on their beautiful son. Even if you are not able to donate they would appreciate every single prayer. Thank you so much. ❤️

#JacksonStrong