Chad's Story

Video of Chad growing up 

About Parnell, Chad's Canine

CCI Training Video

Video of Chad & Parnell

What is Coffin-Lowry Syndrome?

Newspaper Article 

 

We were told that Chad had Coffin-Lowry Syndrome when he was only 3 months old.  I remember the doctor paused for a long time.  When he spoke, he said our little boy would be severely mentally retarded, that he might never walk or talk.  Although his voice was steady as he spoke, there were tears in his eyes.  As first-time parents, we were completely unprepared for this news.  I remember being brave until we got home.  Then we just held Chad, cried, and told him how much we loved him.

My head was filled with images I had already dreamed for my son's future.  I went through the list of events that would never happen as I had imagined them--my son's first steps & words, his first day of school, high school graduation, college, marriage, children of his own.  The simplest expectations for a parent to have was now shattered.

As time passed and with God's & my family's help I realized that those were all my dreams, not Chad's.  Chad has his own set of dreams.  They may not be like those of other children, but they are his dreams, just the same.  Therefore, I was very determined to allow Chad's dreams to succeed by not letting others put limits on my son's abilities.  I wanted to give him every opportunity possible to learn and to be loved.

As you can see from viewing the Video of Chad growing up, Chad's family (The Wards, Chandlers,  Pattersons, Ledbetters, & Seeholzers) wanted to give Chad the world.  Chad goes wherever we go!  We take him to Church, on vacations; to basketball & baseball games; & musicals.  We taught him how to walk & talk, play basketball, swim all by himself, & even with the guidance of his cousins he jet skis & tubes behind our boat.  God has blessed Chad with very loving & supporting families.

But, Chad was still missing one very important piece in his life- A Good Friend.  Chad hasn't been invited to a birthday party other then his family members.  He's never been invited to another child's house to play or have a sleep over.  Actually, we've never heard a knock at our door from a neighborhood child wanting to play with Chad.  When we are out in public I estimate about 1 out of every 30 people who notices Chad will actually acknowledge him with a smile or say "Hello".  That's before Canine Companions For Independence (CCI) came in to play & before Parnell became apart of our family.   Now in public, more people come up to Chad and Parnell and greet them both.  Our Goal is to teach others that Chad & others people with all different types of disabilities, have thoughts, feelings, and long to be excepted just like you.  Therefore, Please don't ignore people who are different than you.  Learn to look them in the eyes. smile, and say "hello".  They might not react like you expect, but your act of kindness will touch their hearts forever.

How I learned about Canine Companions For Independence is a story in itself.  The short version is that I learned about CCI when I was in High School in the early 1980's.  My parents received some information about CCI in the mail and gave it to me thinking I would be interested in helping out this worthwhile charity.  I agreed with them and have been giving cash donations to CCI ever since.  WOW! I never thought the past could or would ever come back to help. 

Then one day, in 1998, as I was sending in my donation to CCI, l thought what better friend could Chad have then a dog.  So I called CCI to see if they could help us.  I filled out a lot of paper work; made it through a telephone interview; then a 4 hour personal interview at CCI North Central Center with the trainers, Chad, & myself; then we were accepted as a candidate and placed on the CCI Team Training waiting list in 2002. We were finally given an invitation & completed Team Training in November 2005.  Seven Years later, Chad brought home his dog & now his best friend.  Parnell has been Chad's S.O.U.L. (Source of Unconditional Love) ever since!

Chad is 15 years old now & we are very thankful that he is able to do much more than we were told to expect when he was diagnosed.  He can talk in 3 to 5 word sentences.  He can walk short distances and he is the most lovable child you would ever want to meet.  God has truly blessed us!

Written by:  Nancy Ward-Patterson (Chad's Mother)