Thursday, March 15, 2007

ASTAR

I feel it's fair to say I've weathered a few storms in my life. I know, it’s all part of the plan. But for me, nothing has been more difficult than the challenges of mothering a child with special needs.

The journey has been much too long and detailed to recount here. My insecurities and heartaches have caused me to refrain from sharing details of our experiences and I have therefore spent a lot of time feeling very alone. As I grow in my acceptance of this challenge, I am becoming more prone to sharing the happenings, heartaches and blessings of this journey.

I’m quite sure if I had the skills and the time, I could write a book. It wouldn't be a short story, but one with many chapters. There would be a chapter on the early years of Caleb's life, one for his medical history and the countless specialists he has seen. There could be one devoted to his diagnosis of Auditory Processing Disorder and speech deficits. I could write a chapter for each year of his schooling beginning with preschool. I'm not sure I could fit my emotional heartache into just one chapter, so that might take two. I'd have to mention the times I've felt judged and offended by other parents, professionals, friends and even family. I would also have to include my growth toward acceptance of our reality and how becoming an advocate for our son became a full-time job. I’d make note of the times I felt my faith was tested, when the dark days wouldn’t cease and tears flowed freely. The book would include a chapter on his failings, his unique challenges but more importantly his successes and accomplishments. There would be more than a few sentences devoted to pointing out what a truly amazing boy I’ve been blessed to raise!

Today, we added a new chapter to this book. This chapter is far from being finished but it is, nevertheless, a new chapter. Caleb had an appointment with Dr. Gary Stobbe, a neurologist that runs a clinic called ASTAR. ASTAR is an acronym for Autism Spectrum Treatment and Research. After a 90 minute visit, he confirmed what I feel I have known for quite some time, that Caleb meets the criteria for Asperger’s Syndrome. Asperger’s is a mild or high-functioning form of autism. He feels that Caleb has a great prognosis for leading a successful and happy life. Caleb’s IQ has not been assessed but based on the information he does have, the doctor feels that he most likely has a high IQ which will also make dealing with his challenges easier. He also pointed out that even though Caleb’s interests are narrow, like most autistic children, his interest in sports is a functional one, one that can provide him many opportunities in his life. Even if he doesn’t have the skills to be a player, Dr. Stobbe said his memory would make for an amazing statistician! He praised us for the work we’ve done with Caleb, giving us a glowing report card. I left feeling very validated.

Caleb’s book has many unwritten chapters, but I would certainly be remiss if I did not include a chapter on the blessings we’ve received by having him be a part of our family. He is a good boy that has taught me so much! I have learned lessons that I’m sure could not have come any other way. Everything is more exciting when Caleb is around! I love my boy more than any words could ever express. And though there will be more hard times and many hurdles to climb, I’ll be by his side fighting the fight! I feel strongly that I am the best mom for Caleb and it’s with great humility that I thank my Heavenly Father for giving me the privilege of raising this special boy!

12 comments:

Camille said...

Tara, I think you are an AMAZING mom and all of your children are SO lucky to have you and Jon as parents. I look forward to reading your book someday!

Jay said...

I love Caleb and all of you. My life has been blessed by Caleb. You and Jon are amazing parents.

Emily said...

Trials are never easy, but it's true we come out of them stronger. Your last paragraph says it all. (((hugs)))

Anonymous said...

You write as well as you live your challenges. I'm so glad you are able to share with us your feelings. We love Caleb and appreciate his talents as we do you and your talents which are many. With much love,

jenny said...

Tara, I must say you have a great attitude which goes ALONG way. No trials are easy, hang in there!! Big hugs from our neck of the country.

Anonymous said...

You had me in tears thinking how special Caleb is. I love that boy dearly and wish I could spend more time with you all. You and Jon are such great parents and I admire the way you raise your children. Thanks for being a great example. Love you all.

Lucy said...

I feel silly making a "comment" about such a big thing. I wish I could hug you...and Caleb...and let you both know and feel how much I love you both.

Thank you for trusting us to know about how you feel and what is going on with Caleb. It must be hard to make him and you vulnerable like that. I hope I never do anything to violate that trust.

Erin said...

We love and appreciate Caleb no matter what kind of label they put on him. I think back on all the wonderful times I've had with him...starting from a very young age and I feel so blessed to have such a smart and caring nephew. He has taught me a lot too and I know his life will be a success.

As we begin our journey, we only hope to be as good of parents as you two.

Bridget said...

Thank you for sharing your feeling with us. I am so impressed. Even though I don't "know" you, I can tell you are an amazing mother. You are doing wonderful things for your son. Don't ever doubt yourself! :)

Heather said...

Tara, I feel so sad that I had no idea what you've gone through the last 9 years. I will be praying for you and for Caleb. You are right when you say you are the best mom for Caleb...GOd did not make a mistake when He gave Caleb to you...he chose you and Jon for the job. May he bless you in all your attempts to do the right thing for your family and for Caleb. I miss you my friend and am excited about reconnecting. God Bless. Heather

mom and dad said...

Dearest Tara and Jon,
How we love and admire you and the way you have met your chllenges. You are an example to all of us. Little Caleb is a dear boy and we always have known that, but,now we can appropriately assist in making him and all of you more comfortable during our visits. Everyone has a little rain fall in their lives but when it is a cloud burst, the only thing I have ever been able to do is just eat "chocolate chip cookies". Love and Hugs to you and please come and see us in Orem.
love, Shauna and family

Anonymous said...

Dearest Tara and Jon,
How we love and admire you and the way you have met your chllenges. You are an example to all of us. Little Caleb is a dear boy and we always have known that,but,now we can appropriately assist in making him and all of you more comfortable during our visits. Everyone has a little rain fall in their lives but when it is a "cloud burst", the only thing I have ever been able to do is just eat "chocolate chip cookies". Love and Hugs to you and please come and see us in Orem.
love, Shauna and family