Caring for Caleb
On Monday July 13th, 2015 Caleb Olson was welcomed into this world! He looked perfect, 10 fingers, 10 toes...
This beautiful baby boy has been diagnosed with Di George Syndrome, a rare disorder caused by a defect in the 22nd chromosome, resulting in the poor development of several body systems. Caleb struggles with two heart defects, kidney & bladder issues, a rear cleft pallet & not knowing how to swallow, digestive complications, hypoparathyroidism, breathing problems, little to no muscle tone, delayed motor function, and an immunity disorder leaving him unguarded from any sickness in the environment surrounding him.
Since his birth, Caleb has been admitted to the hospital countless times due to his body's inability to ward off sickness and his failure to thrive (couldn’t take in, keep down, or absorb the calories necessary to grow and gain weight). To date, he has already had his first surgery (placement of a G-tube for feeding) and will need future surgeries due to the improper function of his heart and other vital organs. Although, with so much discomfort the last seven months, there is still one person who can always cheer him up and keep him smiling; his amazing big sister Evelyn (3 1/2yrs old).
To accommodate the numerous appointments, hospital stays, and limit Caleb’s exposure to germs/viruses warranted by Caleb's condition, his mom Anna was forced to quit her job. On a single income provided by Luke's career, the Olson family can no longer stay ahead of the mounting bills. They have been denied for Badger Care Coverage, denied for disability, and denied social security benefits. They are constantly faced with sizeable insurance copays, declined insurance claims for appointments/procedures, lengthy hospital stays, and astronomical prescription costs.
To be able to provide the Olson family with the financial means necessary to give baby Caleb the life he deserves, we respectfully request your assistance in the form of a donation.