My IzzyB
November 23, 2011 by Heather Somaini
Filed under Family, Heather Somaini, Same Sex Parent
By: Heather Somaini
Everyone writes about being thankful, grateful around this time of year and I won’t be any exception. It’s just too easy and feels like the right thing to do.
It’s been a rough twelve months. Not the kind of rough when you’re diagnosed with cancer or your world gets turned upside down because someone close to you dies. It wasn’t the earth shattering kind. It was just the normal, life comes at you from lots of angles kind of rough.
In early December last year we started to get a sprinkling that would soon become a full blown hurricane. The teachers at our pre-school let us know that they were going to make some adjustments to our daughter’s schedule to see if it would smooth out some recently noticed issues. At first it just seemed that she was quiet and maybe had a fiery personality but it was quickly turning into more than that. Soon she was refusing to speak and having full blown temper tantrums at school which could lead to hitting her brother, screaming, throwing things, and a quirky habit of stripping all of her clothes off. We didn’t understand why it was happening at school and not at home.
Soon one meeting at the school turned into many. There was a lot of pressure to have her tested for a “processing issue” – whatever that was. It was an incredibly difficult time and nothing seemed to get easier. If anything, things just got worse. Soon our entire family felt as if it was being torn apart at the seams. Free was desperate to protect his sister at school and wouldn’t leave her side, Tere and I had already been struggling to keep us together through this life-altering experience of parenting and now we felt completely at odds with the school that had come to mean so much to us.
Against many people’s advice but bowing to the pressure we felt we were under, we had Izzy observed and the result wasn’t what we had hoped. The therapist said something was definitely wrong although she had no idea what it really was. At this early stage, she said it could be a number of things that none of us had any control over. The next step was to have her tested for language and speech but we had to wait a couple of months until she turned four. In the meantime, we re-arranged our schedules, created new house rules and began to focus on Izzy. When she was finally tested, she scored lower than she should in a few areas and twice a week speech therapy was recommended. We worked closely with the school to find any area that we could help Izzy understand her world better. Soon progress was noticeable. So much so that the teachers asked if we could have her observed again. Sure enough, the therapist said that massive, beautiful improvement had taken place but we were still a long ways away from where she should be.
In the past year, Izzy has worked diligently at everything we have all asked her to do. Her language skills were recently re-tested and she is exactly where she should be. Her graduation ceremony from speech therapy was last week. We all had cupcakes and she received a certificate. Her speech therapist adored her and I think actually had to sneak away into her office as we left to have a good cry. We’re not completely out of the woods and will probably have to re-visit different therapists from time to time as Izzy grows and grapples with new concepts and challenges, but she’s on the right path.
I am grateful for my daughter. She is beautiful and delightful and perfect. She shows me every day that we are who we are and sometimes you can’t rush what will be. I’m confident that she will struggle through life in a myriad of ways but then so did I and I think I’m the better for it. Izzy taught me early that she is unique and can’t fit into any mold that was predetermined for her. Any attempt to lead her down a path other than hers would be futile. Izzy makes me stop and realize that life without her would be meaningless.
What are you thankful for?
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I am glad Izzy is doing so well. Also, glad you got right on it. I am thankful for my family with all it’s dysfunction. I love them to death and can definitely see my genes and how they affected future generations for the good and bad. A lovely story about your adorable Izzy and the conscientiousness of you and Tere.
Thanks Madge! Have a great Thanksgiving surrounded by your family.
Beautiful tribute to your beautiful daughter. Your positive attitude is very inspiring!
Thanks Megan! My attitude hasn’t always felt so positive but I guess it’s a process…like everything in life I’m finding out.
Amazing story Heather… always appreciate the posture with which you engage life. So glad to hear that Izzy is doing well.
There’s definitely a lot to be thankful for.
THIS is why you and Tere are Izzy’s mother:
“Izzy taught me early that she is unique and can’t fit into any mold that was predetermined for her.”
We went through somewhat of a like ordeal with Cole’s “pre-school” when he was 3 (they had him observed without our knowledge): Cole is not a cookie-cutter child, he will never be, and his father and I do not expect this of our son. We’ve taught the public school system many things, and I think they realize they will not break us.
Much Peace to your family this Thanksgiving,
D
I am just thankful for all of my beautiful kids, all of you.
Love dad
Heather…. I am so glad Izzy does not fit a predetermined mold and that you recognize that…. NO child should ever be “put” into a “mold”…..and teachers should never expect any child to fit in one!!! Every child is unique and special in their own way and that is the way it should be!! Kudos to Izzy for staying focussed and showing everyone that it is now her time to shine!!!!
We need to thank our children everyday for being who they are!!!
Wonderful tribute to your daughter! I also have a little one who breaks all the molds. My Nicholas is a unique little boy who has always done things at his own pace. I have imagined every possible thing in the world that could be wrong with him. He didn’t sit up or walk on time, so I assumed he had some horrible muscle disease. He did not talk on time, so assumed he had some sort of cognitive defficiency. He used to be meticulous about things being in straight lines–meticulous to the point of being obsessed–so I assumed he was going to be autistic. I have feared the worst for him his entire life. In reality, there is nothing at all wrong with Nicholas. He is just a little boy who does things at his own pace and lives life on his own terms. Nothing at all wrong with that!