Monday, April 23, 2018

Thank You, Kindergarten

In less than thirty days our kindergarten year will be over. I say our because this has been a team effort.

We are a few weeks away from summer and E2 is almost a first grader. I could cry, actually I am crying, just typing those words. I cannot believe kindergarten is over. I cannot believe E2 not only survived kindergarten, but rocked it.

Let's be honest, I was not expecting E2 to rock it. Hell, if I am being real fucking honest, I figured she would be homeschooled by Halloween. The hubs and I were prepared for public school not to work out. I was petrified to send E2 to school. E2, however, was ready, willing, and excited to go to big kid school like her sister.

Being my controlling self, I met with the principal and explained all of E2's struggles and cried while she assured me there was an amazing teacher for my daughter. Our teacher letter arrived in August and the name on that letter forever changed the course of E2's life.

Meet the teacher happened and because I cannot help myself, I followed up with an email. You see, I am that mom. I am that mom every day, but for E2, I am that mom, every day, hour, minute, second, of her life. In that email I explained E2 the best I could. I was overwhelming, crazy, overbearing, and basically said "Yep. I am THAT mom and I am saying sorry for all I will do before we even have day one." While not my proudest moment, it was a necessary one. You see, when your kid has special needs there is no off button. There is no wait and see. There is no let things happen and see where we are at Halloween. There is now. And now cannot wait.

My email was received with grace and a tad confusion, but within a few days our kindergarten teacher began to see examples of the struggles I had described. Emails were exchanged and conferences were had and trust was formed. This phenomenal woman knew E2 as well as I did....some days I felt like she knew her better.

Our kindergarten teacher, yes OUR.
Sure, she spends her day teaching E2, but she has taught me so much more. It's true what the poem says- everything you need to learn, you learn in kindergarten.

I have learned that advocating for your child is necessary and if done properly, you will find a fierce advocate in your teacher. I have learned that honesty is the best policy. I have learned to appreciate the smallest of gestures. I have learned to celebrate every victory no matter how big or small. I have learned that crying in a parent teacher conference is a-o-k. The tears are not a sign of weakness, but validation of what you've been thinking all along. I have learned to listen, to truly listen to someone who has been there. I have learned to trust my instinct. I have learned that a label will never define E2, for greatness is always within arm's reach. I have learned to trust. I have learned letting E2 fall in order to teach her how to get back up is exactly what she needed. I have learned what an amazing, dedicated, hard working person our kindergarten teacher truly is.

While I cried through my Kindergarten lessons, E2 soared. She became a new version of herself. From day one to now, I have watched her go from a baby lamb trying to walk to running with grace like a cheetah in the wild. E2 has learned to make friends, share, problem solve, speak up for herself, engage with others, resolve conflict, ask for help. She has gained independence, become more generous and thoughtful, and learned how to be a part of a community. She grew. She went from little E2 to big kid. She learned what you are supposed to learn in kindergarten - E2 learned how to be successful without her mom in her corner.

And did she succeed? She did indeed. Mid way through this year we received E2's Cerebral Palsy diagnosis and with a hug our teacher let me know the only thing that changed is now we know why E2 struggles. Knowing why didn't change our expectations and it didn't change our teacher's expectations. Striving to be better is what life is all about. Being pushed (gently) to be better is how we grow as people. E2 has been pushed and pushed and pushed. And when I didn't think she could do anything more, she and our teacher proved me wrong. From mathematics to writing to learning to read, my daughter has done the impossible. E2 has become a successful student.

Our kindergarten teacher knows I think she hung the moon, but I have never really been able to express fully how she has changed our lives. Each day as summer draws near, I get a little twinge in my stomach. I know E2 is ready to move on, but when I look back on the year she has had I cannot begin to think how we will all say good bye. First grade is only a hallway over, but light years away from our comfort zone.

And just like last summer, E2 is excited and ready to go to first grade. She is ready to tackle new challenges while I sit here crying, anticipating what I will say in my "Yep. I am THAT mom" email.

To our kindergarten teacher, THANK YOU. Thank you for seeing past the toothless smile, the happy green eyes, and her big Texas bow. Thank you for seeing a clean slate and drawing the first steps in what will prove to be a bright future.

THANK YOU





Sunday, April 8, 2018

Time Marches On

It's April?!!

How in the hell did I miss an entire month and not blog one time...where was I? What the hell have I been doing since February?? At first, I was going to say I have no idea, but that is so not true. I know where I have been, I know what I have been doing, and I know I am literally emotionally exhausted from fighting the good fight.

March was a month dedicated to E2. Just ask her big sister - she will let you know how she was ignored and then she will let you know I told her to build a bridge and get over it. Funny how the month leading to Autism Awareness was all about E2 and getting her the proper help. I fought for E2 all of March. Different fights, different people, different days, but I had my fierce lion mom hat on for way too many days.

March literally marched across my face and caused me to learn more lessons of being a special needs mama- the first being fight until you've made the difference you need to make.

April is Autism Awareness month and while E2 does not have Autism, she does qualify as a special needs child therefore making me a special needs mama. This month is dedicated to the children, the parents, the village of therapists helping these children. This month you can read a tremendous amount of positive blog posts about how their special needs kiddo adds so much to their life and they really wouldn't a change a thing. You will find less heart wrenching, truths about the daily life of being a special needs parent. I have watched a few vlogs and cried because those truths, that honesty, that rawness of real life is what speaks to me. Autistic or not, I share many of the same hopes, dreams, and reality.

While I agree that E2 is a beautiful gift from G-d and her ability to overcome any obstacle is inspiring, the daily ins and outs of parenting a special needs child is not filled with sunshine and rainbows. The daily is filled with anxiety, frustration, and a fierce love that keeps you fighting for a child that cannot fight for themselves.

Daily thoughts that cross my special needs parent brain:

Will my daughter be able to live alone?
Will she continue to have friends or will they tire of her?
At what grade will it all come crashing down because there is no doubting it will.
Will we have to send her to a special school?
If we cannot afford a special school, is home school the answer?
How long will she need speech therapy?
How long will she need occupational therapy?
When will the children in her class notice she is different?
Will she get invited to the slumber parties?
Would she able to handle herself if she got lost?
Does she know what to do in an emergency?
How do I explain to people what motor planning is?
Will we always spend a ridiculous amount of money on therapies?
Why am I still fighting insurance companies?
Why is that people don't like to discuss the struggles?
How come everyone thinks because she is so cute, it will all be alright? Pretty don't pay the rent.
Will she go to college?
Will her rate of progression continue at this pace leaving her a little behind or will the rate of progression slow down causing a further delay?
Will everything be a struggle?
Will she ever get tired of fighting for the simplest of lessons?
For how long will my oldest resent the attention she gets?
Will my daughters ever truly be close or will the disability stand in their way?
How many more times do I have to explain that she is in fact a special needs kid?
Is it wrong to wish she was typical? (No. It's human nature)
How many more stares will we get when she melts down in public because she spilled something?
How many more head tilts and so sorry will we get when people find out she has CP?
How many more times will I hear I played alone?
How many more times will I struggle to hear about her day because of her language delay?
How often will I truly know the realness of her day?
When will I, as her parent, let go of my fears and let her navigate her own life?
Will I always run interference?
Will I always have to fight?
Will I constantly live a life waiting for the next shoe to drop?
Will I always being holding my breath?
Will I always have to call or email teachers and/or coaches to prepare them?
Will she always be immature and seem younger than she really is?
When will people stop thinking I am special for doing what's necessary?
When will people understand that raising a neuro-typical child cannot be compared to a child that is not?
Who will fight for her when I am gone?

Will her smile continue to melt my heart and forget all these worries even for just a moment?

No one likes to hear the above questions, but that is the damn reality. Just this morning E2 spilled a drink and cried like she broke her arm. She froze in her wetness and cleaning up her own mess was a struggle. While the tears and snot poured down her face, E1 rolled her eyes and walked out of the room mumbling.  That is our daily life. People say I don't know how you do it and while I understand the rhetorical question, the reality is I don't have a choice. She is my daughter and I would do anything for her (and for her sister).

Our daily life is balancing tough love and understanding for both girls while simultaneously teaching E1 that they will never be parented the same. And that different parenting is not favoritism, it is necessary.