Posted in Government/Legal Matters Related to Special Needs, Recreation/Leisure and Special Needs

Blog #41~Back to the Future

Blog #40~Back to the Future

Candles blown out, presents opened and heads resting on pillows.  Another birthday week celebrated.  It’s was a big one for Al the 5-0 and Nick now 19 years old.  Only a day apart separates them. On the night of his birthday, Nick had crashed in his room, but he woke up and crawled in the king bed next to me.  I hesitated but pulled the covers up and nestled my cheek next to his.  I should have walked him back to his bed, but I wanted him near me. I needed to feel his warmth and hear his breath against my cheek.

Flashback to 19 years ago, Nick was held in ICU under oxygen and monitored.   I didn’t get to hold him or nurse him that first night.  I barely knew him. Small, helpless, holding on, I had no idea if he would be okay.  I wouldn’t be able to put my arms around him that night and it crushed me.

And so on the evening of his 19th birthday, I took in his breath and felt his limbs stretched long like a mature adult. I gazed at his features, the almond shaped eyes and tiny nose.  Similar they were, as if I could close my eyes and transport myself back to 1994.  And for a moment I did, to the time when I was in fear for my son’s health and whether he would be okay as the two nuns entered my room to hold hands and pray.

Exhale, I am back to the future. Slapped into what I should face.  But I don’t want to.  It’s an ugly web that is snagged with red tape. The maze of bureaucracy is daunting. First it was filing to continue to be Nick’s guardian (yes when he turned 18 we had to file to become his legal guardian since he can’t take care of himself.) Second it was to apply for SSI benefits that he qualifies for. Third, when your child turns 19 then you must contact DHS to have them switched from child Medicare benefits to adult. I only found out about this snafu the night before his 19th birthday, yikes!  I still don’t think I have my mind wrapped around any of this.

And on top of this, Nick is graduating high school in May and moving into a transition program until age 22.  I can’t say that I am ready to face the future after that.  Where will he live? Will he be taken care? Is he going to be safe and happy?  I attended a transition fair last week on the eve of Al’s 50th birthday.  I filled up my goodie bag with flyers, free pens, pads, cinch bags and sage advice. I came home and hit the wall, overwhelmed and that is where I stopped; until tonight.

After dinner out with Nick’s grandparents we came home to celebrate the birthdays. It is cold.  The heater went out sometime over the weekend. We kept our coats on as we gathered around the kitchen island.

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As I lit the candles on the chocolate cake for Nick to blow out, I had a flashback. While we cupped our hands around the steamy cups of coffee I spoke.

“Isn’t this ironic, here we are with no heat in the house.  It is just like when Nick was born and the ice storm had knock out the power. We didn’t know what we were doing while Nick lied there in ICU or whether he was going to be okay.  And poor Hank was so scared of the fireplace; that’s all we had to heat the house.”

Al pointed out something I had forgotten. “Mom you had the oven and heaters blaring on the stove top to keep it warm, remember?”

Oh how we were lost, Nick in ICU…. No power, and a new diagnosis of our son having Down syndrome…There is more to the story….. But you are going to have to wait for the book 🙂

Back to the present, I sit by the fire writing and try to stay warm.  I pictured little Hankie just 19 months old and scared standing at the staricase immobilized, pointing to the fireplace saying, “hot.”

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Birthdays bring a time to pause and reflect back and also look to the future. I don’t have any answers on Nick’s transition plan. In a way like Hank, I have been immobilized. I am trying to push the webs out of my face, and walk through but I feel a push and pull. I need to look to the future for my son.  He is 19 and like his brother Hank who is 20 and a sophomore at NIU, there is a need to let him spread his wings. But Nick knows no fear or evil.  I can’t help but feel like I am the only one who can protect him. That’s what is in my noggin this week. For now I will continue to pray for strength to fight my way out of this tangle.

~Teresa

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Baby nick 🙂

Author:

Teresa is the mother of two boys. Her youngest son, Nick is 23 years old and has special needs including Down syndrome, autism and verbal apraxia. She is a parent advocate, speaker and writer who is currently working on the memoir of raising her son, Nick. You can follow Nick world on our Facebook page and Pinterest @Down Syndrome With A Slice of Autism. Find Nick on Instagram@ #nickdsaustism, Twitter @tjunnerstall.

9 thoughts on “Blog #41~Back to the Future

  1. TJ
    This really touched my heart. I feel the wrenching prospect of the next step in Nick’s world-transitioning. I will be eager to learn what that means for him and you. Blessings to you for your rich sharing.

  2. I remember all of this like it was yesterday. I hung on every word reading today as if I were writing it myself when Nick was born, so surreal, so hard, yet so sweet and precious. This was one of your best “serious” posts yet Big T. I love you Sis !!
    Aunt Whoa

  3. What a recap of emotions and memories T! You will plow right through that web when the time is right! God will lead you!!! Prayers coming from my way….. transition is hard, I hear ya loud and clear! I’m off to unpack some boxes of my own and am sure I’ll find more webs too!

  4. Oh dear friend… Thanks for sharing the tough stuff with me and everyone else. You help me see the future and let me know I’m not alone! What a gift … You… Your writing…Your family.. Our friendship… Our young “men”. 🙂
    Thanks!

  5. Wow! I just started reading your blogs and they are lwonderful and so full of love. Nick is so lucky to have such awesome parents. I barely knew Alan and had never met you when Nick was born, but I still remember my phone conversation with Alan when he called to tell me about Nick just a day or two after he was born. I have thought of that conversation many times over the last 19 years. I tried to comfort Alan at the time and never dreamed that one day you would bring so much joy and comfort into my life. You are an amazing family and I am so blessed to have you in my cheering section. I hope you do write a book some day. It could be a best seller and offer great encouragement to parents of special needs children as well as anyone going through any kind of difficult situation in their life. You go girl!

    1. Thank you Brenda, I am curious as to what Al said to you on the phone after Nick was born. If you get a chance to ellaborate drop me a message on Facebook. It’s been a wild ride and the chapters are all written. I just need to hunker down and finish the book proposal so I can get it out to publishers. Stay tuned and appreciat your kind words and support! 🙂

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