Shopping Cart
Your Cart is Empty
There was an error with PayPalClick here to try again
CelebrateThank you for your business!You should be receiving an order confirmation from Paypal shortly.Exit Shopping Cart

Mission 22q

Tell Your Story

Tell Your Story Post New Entry

view:  full / summary

Nebraska families work to shed light on 22Q disorder

Posted by Anne Stalker on 22 October, 2013 at 15:00 Comments comments (0)

Brody Schuster's medical problems kept piling up, and so did his parents' concerns.

As a baby, Brody scooted on his bottom and never crawled. His size was normal at birth, but his growth soon began to lag severely. Time passed, and Brody struggled with speech. Then, a physician discovered Brody's hearing loss.

There were too many challenges. His parents knew something was seriously awry.


Click to read the full story on

Jeff's Story

Posted by Anne Stalker on 4 August, 2010 at 10:15 Comments comments (0)
My son, Jeff was born on November 23, 1992 and we immediately knew he had a cleft of the soft palate and low calcium levels. We were told that nothing else was wrong with our son. We took him home on Thanksgiving Day that year and he immediately began having feeding problems. We struggled with these feeding problems for a few months even though we were constantly taking him to see the pediatrician. We finally ended up at Children's Hospital in Omaha, NE, because Jeff was failing to thrive. We began feeding Jeff through an NG tube and hoped that our struggles were over. They were not. The feeding issues improved, but his constant infections and croupy cough continued to worsen. It wasn't until Jeff was six years old that everything fell into place. The doctor that had been treating Jeff for asthma knew that there was something else wrong with Jeff and sent us to see a pulmonologist in Omaha. After a chest x-ray and many other tests, it was discovered that Jeff had a right sided aortic arch and vascular ring (which is a ring of vessels tightly surrounding Jeff's trachea and esophagus). At that point the 22q FISH test was ordered and came back positive. The diagnosis explained everything that had been wrong with Jeff over the years: feeding difficulties, immune system deficiency, breathing difficulties and croupy cough! A month later Jeff had surgery to separate the vascular ring and things began to improve. We thought that Jeff's aorta would always compress his trachea and esophagus, but a recent study showed that it's nice and straight now.. He's an awesome young man who has made our lives amazing. Jeff also has developmental disabilities and still lives at home. He is working hard on his living skills with his staff and hopes to move out in the near future. We will be his guardians until we're gone and then his sister Michelle will take over. When he moves out he will still have staff that will help him with cooking, cleaning, grocery shopping and things like that. He also suffers from severe anxiety which we hope to get under control soon to enable him to live on his own .