Jack Hagman | Prayers for Baby Jack
Donation protected
This little cutie is baby Jack. Together with his parents, Nicole and Luke, and big sister, Charlie, we want to share Jack's unfolding story with you...
For his 8 months of life, Jack has struggled with feedings, gaining weight, and staying healthy.
After a disheartening number of attempts, and to no avail, his parents tried to get answers from doctors as to why Jack couldn't seem to thrive. Near the end of July, Jack was finally referred to a specialist who determined he has Esophageal Achalasia; a rare disorder that makes it difficult for food and water to pass into the stomach.
On Monday, August 5th, Jack was transferred via ambulance to a different hospital three and a half hours away from home where pediatric specialists are better equipped to provide the care he needs.
Jack's lead doctor has assembled a team of specialists and hospitalists, who are collaborating on exams, tests, and procedures to find the answers needed to help him.
During initial exams and tests they found that the wrong nasogastric tube (NG) was used, and that not only does Jack have Esophageal Achalasia, but he also has motility dysfunctions in his esophagus.
Jack is now being fed and having medications administered solely through his new NG. This will continue to be a very slow and steady progress, as doctors believe Jack has never had a full tummy. A majority of his feedings was either coughed up, or was pooling into the back of his throat and spilling into his lungs.
Nicole and Luke are amazing parents who have fought tirelessly for their sweet Jack, and are so thankful to finally be receiving answers.
With trust in the doctors and an understanding of what's to come, they are ready to learn everything they need to know to care for Jack. Tomorrow they will start being taught the Bolus feeding method; where they'll be using a syringe to deliver formula and medications through a feeding tube.
Jack will continue to be fed via tube for at least a month, with the possibility of a more permanent gastrointestinal tube (G-Tube) replacing his current NG tube within the next three to five days.
As the teams of doctors perform more exams and tests to learn more about Jack's unique circumstances, we know this for certain: his journey toward healing is going to be a long and often times difficult one, with expenses adding up by the minute.
In addition to the cost of special equipment necessary for Jack's care, hospital expenses, and extended hotel stays for supporting family members; the Hagman family will also face the financial burden of a reduced income.
It has been advised for Nicole to utilize the FMLA for at least one month, considering the around-the-clock care that will be required for baby Jack to thrive, and to allow her the time at home to help their family transition through these imperative weeks.
As a family that is so giving and generous to others, we invite you to join us in financially supporting this incredible family in their time of need.
And we kindly ask for prayers for baby Jack, his parents, Luke & Nicole, big sister, Charlie, and the professionals who will be helping Jack get back home soon!
Blessings to you!
#prayersforbabyjack
For his 8 months of life, Jack has struggled with feedings, gaining weight, and staying healthy.
After a disheartening number of attempts, and to no avail, his parents tried to get answers from doctors as to why Jack couldn't seem to thrive. Near the end of July, Jack was finally referred to a specialist who determined he has Esophageal Achalasia; a rare disorder that makes it difficult for food and water to pass into the stomach.
On Monday, August 5th, Jack was transferred via ambulance to a different hospital three and a half hours away from home where pediatric specialists are better equipped to provide the care he needs.
Jack's lead doctor has assembled a team of specialists and hospitalists, who are collaborating on exams, tests, and procedures to find the answers needed to help him.
During initial exams and tests they found that the wrong nasogastric tube (NG) was used, and that not only does Jack have Esophageal Achalasia, but he also has motility dysfunctions in his esophagus.
Jack is now being fed and having medications administered solely through his new NG. This will continue to be a very slow and steady progress, as doctors believe Jack has never had a full tummy. A majority of his feedings was either coughed up, or was pooling into the back of his throat and spilling into his lungs.
Nicole and Luke are amazing parents who have fought tirelessly for their sweet Jack, and are so thankful to finally be receiving answers.
With trust in the doctors and an understanding of what's to come, they are ready to learn everything they need to know to care for Jack. Tomorrow they will start being taught the Bolus feeding method; where they'll be using a syringe to deliver formula and medications through a feeding tube.
Jack will continue to be fed via tube for at least a month, with the possibility of a more permanent gastrointestinal tube (G-Tube) replacing his current NG tube within the next three to five days.
As the teams of doctors perform more exams and tests to learn more about Jack's unique circumstances, we know this for certain: his journey toward healing is going to be a long and often times difficult one, with expenses adding up by the minute.
In addition to the cost of special equipment necessary for Jack's care, hospital expenses, and extended hotel stays for supporting family members; the Hagman family will also face the financial burden of a reduced income.
It has been advised for Nicole to utilize the FMLA for at least one month, considering the around-the-clock care that will be required for baby Jack to thrive, and to allow her the time at home to help their family transition through these imperative weeks.
As a family that is so giving and generous to others, we invite you to join us in financially supporting this incredible family in their time of need.
And we kindly ask for prayers for baby Jack, his parents, Luke & Nicole, big sister, Charlie, and the professionals who will be helping Jack get back home soon!
Blessings to you!
#prayersforbabyjack
Co-organizers (4)
Kelsey Rae
Organizer
Fargo, ND
Lucas Hagman
Beneficiary
Jamie Fuglestad
Co-organizer
Sarah Card
Co-organizer
Stacy Larson Gray
Co-organizer