Category Archives: School

Shane attends The Cyzner Institute – Day School & Therapeutic Center. The Cyzner Institute is a school designed to help children build key developmental skills which set the foundation of learning.

I’ve Lost Myself

I feel like I’ve lost myself. My purpose. My what. My why. I don’t know the exact moment it happened, but it’s been slowly vanishing over the past year. Life has a way of reminding you that you’re not in control no matter how much you think you are. You’re not. But, kudos if you’ve read enough Anthony Robbins books to make you think you are.

I lost a friend to suicide in November. I haven’t really dealt with it or written about it in detail. I knew she was suicidal, but was so wrapped up in my own struggles that I couldn’t stop her or help her. We had lunch together and less than ten days later, she was gone. She wouldn’t accept a cat as a gift (my attempt as lessening her loneliness) because she “didn’t want it to starve” when she died. She had recently moved and wouldn’t let me help her unpack her boxes because she wanted it to “be easy for people to get her things together” after she died. She had dealt with debilitating depression for years and had sunken every dime she had into getting treatment. She could no longer work and was running out of money. She was alone. She was in pain. Her heart broken beyond mending. But, that day at lunch? She was smiling. She was sad, but she was smiling. I can only imagine it’s because she knew her pain would be over soon. She made a plan and stuck with it.

Part of me is envious of her courage. She was tired and knew she couldn’t continue living the way she was. That control thing I mentioned? SHE was in control. She’s at peace now, free of the horrendous visions of abuse she endured as a child and continued in her adult life. Part of me is really mad at her for selfish reasons. Did she think about what it would do to her friends (who shared depression and mental illness)? Did she care? She didn’t owe us anything, but still I wonder. I don’t know how she killed herself, but I imagine she overdosed and drifted off to sleep. I don’t know how long it took before someone found her. I hope she wasn’t alone for long. I imagine her beautiful blonde hair being coiffed perfectly and her lipstick applied as precisely as it could be. Did she wear colors other than the black or grey muted tones she usually wore? I’m glad she didn’t take the cat.

I write about this because I am tired and feel like I’ve been treading water for a long time. I feel like I know where she was in her journey. So tired. I struggle to find joy many days. I’ve put so much into getting Shane the help he needs that I’ve let my own needs go. I’ve stopped working out, gained 30 lbs with no desire to do anything about it. My own treatment-resistant depression needs more intensive treatment, but I can’t pursue it because the next step is TMS or experimental ketamine, both of which require a daily time (and significant financial) commitment for six to eight weeks. So, I’ll continue to struggle until Shane is stable and ready for the next step of his journey and we make it back home and to real life. That’s what we do for those we love immensely.

While away at treatment, Shane has grown leaps and bounds in many areas. But, some of the same bad habits continue to rear their ugly head. Aggression, defiance, “I hate you” when things don’t go his way. We moved here thinking it would make his transition from discharge easier. It’s only been a week, but so far, his behavior on the unit after a home visit is reminiscent of when he first got here. I hope it all falls into place as I doubt myself in my desperate attempt to be in control and lining everything up. See? I thought I was in control. I’m not. Neither are you. Remember?

There have been many moments where I’ve wondered if I would make it through the end of the day. I am no longer myself and know that the journey back will not be an easy one. Do I even remember who I was? Was that person so great, after all? Do I want to be her again (whomever “she” was)? I’ve made many mistakes in the past. I do have regrets (those who say they don’t are full of it). I didn’t do enough to help Pam feel loved and needed among many others. But maybe those mistakes have put me in the right direction of where I’m meant to go. I will die trying to do everything I can to help Shane and our family.

Finding yourself is not an easy journey. I don’t suppose it should be. I’ve been trying to find my purpose my entire life. I find it briefly then it slips away. I don’t suppose that should be easy, either, in an ever-changing world. I’ll delve into volunteering at Shane’s new school and being an advocate for kids who have no one to speak for them. Or, find a new job or a meaningful charity. Or yoga. Or tennis. Or, maybe start running again.

But, my why? I guess that’s easy. It’s seeing my monkey boy successfully finding his place in the world and going to school like a “real boy.” It’s seeing all of the adventures my beautiful daughter and John experience during their time as traveling nurses. It’s being here to give to and receive the unconditional love my dear sweet husband has to offer (even though our cramped quarters are testing our patience). See? The why is easy.

The what? I have to learn to trust that I am where I’m supposed to be and what I’m supposed to be. Maybe I’m not lost. Maybe this is the new me…who has some work to do on finding joy in all that surrounds me. It’s there. I just have to open my eyes and heart to see it. As Kristen Bell says, choose happiness over suffering. Easier said than done, but I’m trying. Namaste, bitches.

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Through the Darkness

As I prepare to head to Shane’s school to participate in a promotional video about the difference they’ve made in our boy’s life, I can’t help but think of this song. Through the darkness and good times, they’ve not given up on him. They’ve invested time in getting to know him. They don’t take his refusal to do work for his lack of ability to do work. They didn’t take his poor test scores as his “normal” and repeated the tests realizing that the vast differences in results was an indication of deeper issues. Not all kids learn the same way and they’ve taken on the challenge of having to be creative to find what works for him. All of the kids there march to the beat of their own drum. They’ve not been given the same opportunities typical kids who make the honor roll have been given. Many are bruised and broken…the staff at Ki Charter gets that. Often those who are hurting the most lash out at others the hardest. The staff is there because they want to be there and they want to make a difference in the short time they have the kids in their care hoping that their short influence will ignite a love of learning and find confidence in the kids. Lord knows there are much easier teaching positions they could choose. But, at Ki, they have the opportunity to be a catalyst for great things.

They know Shane has a great heart deep down and is a kind and loving little soul and don’t take his tantrums or lashing out as “mean.” I wonder if they’ve ever had the chance to hear his deep belly laugh or to hear his incredibly creative stories. I wonder if they know he’s one of the sweetest boys they’ll ever meet. I wonder if they know how thankful I am that they are including him with the other kids with support as needed instead of insisting on division and one-on-one. 

I listened to this song everyday when we were trying to conceive a second child over a span of seven years. After multiple miscarriages and failed IVF attempts, we decided to give up in July of 2005. Shane came into our lives in a way I never thought he would in December of 2005. The universe had a different plan for us…for Shane. The world thought I had it all, but I was waiting for you.

Where it was dark now there’s light
Where there was pain now there’s joy
Where there was weakness, I found my strength
All in the eyes of a boy

There’s a Place for Us

While at San Marcos, Shane has been enrolled in Ki Charter Academy, a public charter school on the grounds of the treatment center. It’s a totally separate entity of San Marcos Treatment Center. All kids enrolled in the treatment center attend Ki Charter, but not all kids there are from the treatment center. School has been a huge issue and challenge for Shane and we were worried about how he would handle the academic setting surrounded by peers.

When Shane was as young as two, we couldn’t even leave him at the Y long enough to work out without them calling us to come get him. Every daycare decided that he “wasn’t a good fit” for their program. Once it was time for him to start kindergarten, we enrolled him into the public school and within a few weeks, he’d been suspended several times for throwing erasers, knocking over a chair, pushing a kid, etc. The public school refused to accept the diagnoses and testing we had from doctors and insisted on doing their own evaluations before making any changes or accommodations. Each time they called me to pick him up, I went and scooped him up in tears (both of us). We decided to pull him out when we found Cyzner Institute which was a small private school that provided ABA therapy and a small teacher to student ratio. Even in a class with 6-8 kids, Shane wasn’t successful and instead of leaving him in the classroom to help him build social skills, they insisted on one-on-one instruction. No one would give him a chance. So, Shane’s entire academics have always been one-on-one which is why we were so anxious about him starting at Ki Charter Academy. But, we were hopeful.

As soon as it was obvious that he was struggling behaviorally and academically in a somewhat traditional classroom setting, I discussed having Shane tested for special education services and began wondering what else could be done to help him. With Ki Charter, I got immediate cooperation. They tested him over a period of a couple of months, repeating some tests multiple times because the results were so drastically different each time. They didn’t accept his refusal to perform particular tasks as his inability to learn. They were diligent and took a genuine interest in trying to figure out what makes him tick.

Yesterday, we had our first IEP meeting. I’ve heard horror stories from parents about their IEP meetings. Scott and I sat at the table and listened to the results and their interpretations of Shane. Most of what they said was no surprise. But, some things were amazing. They agreed that he needs extra support in various subjects and that it would be put into place immediately. They talked about how creative, funny and curious he is. It’s no surprise that he struggles with peer interaction. He’s never experienced it. I braced myself waiting to hear the “your kid needs one-on-one” instruction. They said the opposite. They want him to remain in class with peers. Such a pleasant surprise. They believe in him and are giving him a chance to find success. We spent the next few minutes after the call in silence and tears wondering why we didn’t fight harder for Shane at other places once again placing blame squarely on our shoulders.

We anticipate our insurance running out for the treatment center toward the end of March. Because Ki Charter has put so much care into helping Shane learn to navigate “real school” with peers, we want him to finish out the school year there. It would be virtually impossible to expect Shane to come back to South Carolina and be successful with only a couple of months left in the school year.

On March 1, we’ll be packing up Memphis and Tux and heading to San Marcos planning to stay through the middle of July. That will give Shane the opportunity to continue at Ki Charter learning to interact appropriately with peers in an academic setting under a staff trained in special education and undoubtedly passionate about their work. The last day of school is June 1, but Shane has been granted permission to continue for six more weeks in their summer program. It is our hope that he will also be able to successfully join some summer camps like “real” kids (his words).

I’m excited about our little place on the river in San Marcos. Tears dry faster in the sun. I may not ever want to leave. I can easily say that the last year has been the most challenging year of our lives. But, at this moment, I can finally breathe knowing that for right now, for Shane, there’s a place for us.

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#noalternateroute

As we continue to pack and get ready to leave for Texas, my heart continues to break. So many conflicting emotions. I don’t even know which way to go. I suspect I will run on autopilot for the next week for the most part. I have no clue what to do or how to do this, but I know that we have each other. There’s no manual for autism. There’s no manual for having to take your child 1200 miles away to get them the help they desperately need and deserve. There’s no manual for healing hearts that have been broken so many times pieces are missing. Yet, we carry on. Desperate for hope. Desperate for help. Desperate for peace. Desperate for change. We owe that much to him. We owe that much to ourselves and our family.

“Roads may be sometimes rough. But, with you, no matter how rough the road is, I’ll take no alternate route. Because together we can make it through. No matter how tough the going, I’ll keep on going. Because with you, my loves, the journey will never be boring.”-T.O.Y.

#neverthelesstheypersisted #autismawareness #searchingforpeace

#1 and #2

This blog has been swirling around in my head for days and days. So, here goes nothing.

The past few months have demanded big decisions. Life changing ones. The ones that could scar a kid forever if you make the wrong one…as if having me for a mother isn’t scarring enough. 😀

Our daughter will be entering her junior year at Western Carolina. She got into the Nursing Program which is highly competitive and selective. She’s a great student and her hard work paid off. Our big decision…on-campus or off-campus. She suckered me in joining the off-campus camp which meant I kicked it into high gear to convince the dads. We found an awesome place midway between Western Carolina and Asheville. Her clinicals will be in Cullowhee, Waynesville and Asheville. We picked up the keys and began moving in this past weekend. Next week, she goes for good. She’ll continue to work in that area after she graduates and hopes to attend graduate school there to become a Nurse Anesthetist. I know it’s the best thing for her but that doesn’t make it any easier to accept the fact that she’s on to her own life now. For real this time. My role is different and ever-changing. I guess I was still in denial up to this point. I’m so proud of her but it breaks my heart at the same time. In my mind, she’s still the adorable little girl with the big hair bow and the impish grin. So, there you go. Life decision #1. Next Thursday will be one of the most difficult days of the last 20 years of being a mom…right up there with seeing her walk into the school with a backpack bigger than her as she turns to wave goodbye. Seeing her back out of the driveway for the first time as a driver alone as she waves goodbye. Seeing her close the door to apartment #9 as she waves goodbye.

As Jess moves on to the next phase of her life, so does Shane. I cannot begin to tell you how proud we are of the little man he’s become. I honestly don’t know if the winds have changed because of the outstanding therapy he’s received from those who love him as though he is their own, because of maturity, because we’ve figured out how to roll with it or a combination of it all. In any case, I am thankful to the moon and back for the good karma that’s come our way. He’s incredibly sweet, funny, loving, smart and determined. Last week, one of his teachers told me that she loves working with him because he’s like a little adult with a wicked sense of humor trapped in an 8 year old’s body. That’s a great description. We have deep conversations about things from adoption to compassion to time travel to being an alien and more. He leads the conversations and takes great delight in sharing his insights with us. Sometimes when we’re tucking him into bed, he’ll say, “Will you stay here so we can have a conversation?” And, we do. About everything and about nothing.

This school year is a whole new ballgame. Life decision #2. We’ve decided to homeschool him to a degree and enrolled him into the virtual school through the South Carolina public school system. We’ll have a therapist come to the house for several hours everyday to work with him on academics and helping him manage a new situation and all that comes with it. Transition has proven to be tough in the past. But, it is time for the next step. Big decision for us. Do we rock the boat or not? What if it’s the wrong decision for him and/or the family? Even with having to spend so much time learning to manage his behavior and anxiety, he remarkably is on grade level in everything. He’s smart as a whip and a beautiful person inside and out.

As we set up his new school room, we’ve allowed him to play a part in planning. We’ve picked out the new furniture, school supplies and décor together. We decided to go with a world traveler theme. He wants “to be like Charles and go everywhere in the world.” So, we found a giant wall mural of a map and bought green pins to mark every place we’ve been together as a family which is a decent number of places in his 8 short years of life. As we were going through postcards of some of the places we’ve been, I told him we would use a special colored pin to mark the one place he wants to go most of all. His response? “I wanna go WAY WAY back, Mommy. I wanna be a time traveler.” Where the hell do I put the pin for that one?

In the words of George McFly, “Like I’ve always told you, you put your mind to it, you can accomplish anything.”

The Power of Therapy…and Love

Every time I come to this blog and see that it’s been so long since I’ve written anything, it says several things to me. It could be that I’ve been so far into the depths of despair (read: self-pity) that I couldn’t see the light, it could mean that I’ve been lazy (highly possible) or it could mean that I’ve been basking in the light.

This time last year was incredibly challenging for Shane. We were still dealing with massive meltdowns and major defiance. I’m not talking temper tantrums like most parents of typical children experience. I’m talking holes in the wall, name calling, etc…Verucca Salt on steroids. It’s not pretty. And, although it has little to do with parenting skills and a lot to do with PDD-NOS and ADHD, it just feels like the lack of parenting skills is what’s put you in that place to begin with. It’s not. I’m slowly getting that. The behavior at school was extreme. Sure, some of the incidents were funny looking back like the time he pulled the fire alarm and the fire department came. Then, there was the time he pulled the fire extinguisher off the wall and attempted to activate it. Not funny were the broken window, the hitting, kicking and name calling. Everyone was struggling but the one struggling the most was Shane…and believe me when I say that few things are as painful as watching your kid in a downward spiral and there isn’t a damn thing you can do about it other than what you’re doing. I cried daily…most days more than once and many times cried myself to sleep waking with my eyes glued shut (not pretty, trust me). I wasn’t crying so much for me…but for him.

Although I’m an atheist, I’m convinced there are angels on Earth. Virtual strangers who are put here to add beauty to us all. Cyzner Institute is full of them. But, there’s one in particular who has made a difference. He came to us in the form of a big teddy bear of a guy in argyle sweater vests, nice shoes, a shiny head and talent beyond belief. He was such a stark contrast to the rest of the staff that I wondered how he would fit in much like my little monkey boy. Dr. Lisa and the staff introduced him to Shane and he accepted the challenge for one-on-one therapy with him. And, his name happens to be Shane, too…Mr. Shane. From the moment I met him, I felt a sense of relief. I don’t know why. Maybe his aura looked yellow to me. But, from the beginning I knew that he “got” Shane, understood and appreciated him. I could tell that he loved him right away. And, I could tell that it was his mission to see Shane succeed. He once told me that he’s Shane’s conscience…the angel on one shoulder, devil on the other. So, it’s with that angel that we’ve seen the power of therapy and love. He has embraced the wonderful things about Shane and somehow managed to handle the challenges with poise and grace. But, most importantly to teach Shane to handle the challenges on his own giving him strength, control and independence. He is the Creative Director at Cyzner and is an incredibly talented singer, dancer, musician, artist. He sees Shane’s creativity and imagination and figured out how to use it and nurse it to help Shane succeed.  It doesn’t hurt that he likes Rocky Horror Picture Show and has the sense of humor that matches our family. Although he spends a lot of time with Shane, I can also see the impact he’s had on other kids there. Priceless!

Sitting back now and thinking about it all, I think I haven’t blogged in so long because I’ve been basking in the light. I realize there’s still plenty of tunnel left but Shane is off of all medication for ADHD and is only on a low dose of medication for seizures and migraines and Omega supplements. Doctor’s visits are nearly null. Any meltdowns or “issues” are over in minutes and are manageable. We can see ALL the beauty in our boy…he’s compassionate, loving, caring, empathetic with everyone around him, helpful, sweet as molasses, has an infectious laugh, sloppy kisses and a wicked sense of humor (he still gives anaconda hugs to strangers which is a little scary but there are worse things). I will be honest with you and say that there are times when I still feel sad for the challenges in his life and ours…but the joy in our lives far outweighs the sadness. Keep flying, monkey! Mommy, Daddy, Mr. Shane and all the angels are behind you…and are as proud as proud can be.

Check out https://www.facebook.com/ShaneElks?fref=ts

Hello, Old Friend…

Wow! I use blogging/sharing as therapy. Since I haven’t done it since January, that might explain my need for, well, therapy! In the online sense (and real life, too), my absence means that I’m caught dead square in the middle of a massive shit storm and am living in survival mode. There is a popular saying…what doesn’t kill us makes us stronger. Well, I can honestly say that I’m already fairly strong so the universe can stop trying to kill me now. No matter how many times I feel like the universe is giving me a big “*$%^ YOU,” I have to keep marching. I guess when things are out of your hands, you have no option other than to put on your big girl panties and keep moving forward.

The past six months or so have been a huge struggle for Shane and our family. Just when we feel like he’s making huge strides in many areas, there are others that creep up and send him tumbling backwards. As a mom, nothing breaks your heart more than seeing your kid be unsuccessful in simple things most parents take for granted like playing with the neighbor’s kids, going to the mall, going to Times Square specifically to go to Toys R Us and not being able to go to the third floor where all the super heroes are because he’s deathly afraid of glass floors, high ceilings, stairs and escalators. Talk about feeling totally defeated for a little boy to talk about something so much and be so excited then not be able to do it. I would probably throw myself on the floor and kick and scream, too.

We’re in the process of building a stronger support team than we’ve had in the past to help Shane navigate the world. We’ve added a developmental pediatrician (priceless), a developmental neurologist (pure craziness…think Dr. House with a great bedside manner), a pediatric psychiatrist and a vision therapist (new and yet to be determined). We have a referral to a new pediatric neurologist and an appointment with a geneticist in November…all in an effort to do everything we can. With a well-integrated, invested team in place, I feel more hopeful about the future than ever and am excited to hear their recommendations and plans moving forward. I don’t know how to express my gratitude to each and every one of them for taking the time to get to know and love Shane and being able to see him for the loving, sweet, thoughtful, funny little man he is. The staff at Cyzner has be invaluable and I am so thankful for their guidance, patience and dedication to Shane and our family.

One thing I’ve learned in the last seven years is that sometimes you blame yourself for everything. At least, I do. What could I have done differently? Did I do something wrong? I’ve cried a lot and taken a lot of time to reflect on life…what could’ve been, what is. There is something I know and I’m taking the risk of ticking off a lot of people, but I’m going to say it, anyway. I have friends who have children with special needs of varying degrees and we’ve discussed it so I’m not alone when I say this. When navigating the slippery slope we’re climbing, we often encounter people who might offer “help.” There are two things that, as a mom of a child with special needs, I do not want to hear. Please do not say that God gives “special children to special people.” I am no more “special” than my neighbor, friends or family. What kind of god would create “special” children who have to struggle daily with any disability? Or anyone else who suffers with pain or illness? Not a very nice one. I understand that there are many religious philosophies and I get that some people have to believe that there’s more to life than this, that there’s a better life beyond this one and will believe regardless of anyone says. They have to believe for various reasons…afraid of death, fear of having no purpose, not believing in yourself and your own strength. Do what you need to do to feel better, but please don’t tell me you’ll pray for me. Because you know what? It’s easy to go to bed at night, clasp your hands, say a prayer (for those in need and your favorite football team), then get a peaceful night’s sleep. But, one pair of working hands does more good than a million clasped in prayer.

I was raised in the south in a Baptist church. I was baptized and wholeheartedly believed what I was taught. With exposure to different people and cultures, I realized that the world was not full of God-fearing Christians and that there were so many different philosophies. I always considered myself to be spiritual but in recent years, I’ve called myself an atheist. But now I know that I’m not an atheist. I’m a humanist. There, I said it…MY NAME IS JANET AND I’M NOT A REPUBLICAN, LIBERAL (that’s pushing it), DEMOCRAT (although I do think donkeys are cute), A CHRISTIAN OR AN ATHEIST. I AM A HUMANIST.

hu·man·ist

/ˈhyumənɪst or  [hyoo-muh-nist or, often, yoo-]/noun

1. a person having a strong interest in or concern for human welfare, values, and dignity.

Stay calm, carry on and listen to this song.

http://www.youtube.com/watch?v=5TQAjXSD1PY

Part of That World

In 1998 when my daughter was gearing up for kindergarten, I set out on a mission to find a good private school for her. The local public school system did not have a stellar record. I quickly realized finding the right school was going to be a task more daunting than I had imagined. There was a waitlist for most kindergarten classes. But, I met a lady in a store one day whose daughter was wearing a shirt from one of the schools I had visited. I asked her how she liked it and she said loved it. I told her about the waitlist. She said, “Don’t worry about it. Put on every piece of jewelry you own and wear your best outfit. Money talks.” So, that’s what I did. Within a week of the meeting with administration, a space magically became available.

When Jess started there, I threw myself in to every fundraiser that the school had. Somehow, I felt like it was my duty. I took on the challenge of chairing their largest fundraiser, a silent auction, for two years running. Each year, we raised anywhere from $25,000-$30,000 with just that one event. They also had a campaign of selling wrapping paper. All of the money was to buy new computers or playground equipment. Being so involved with the school allowed me to meet most of the parents. 99% of them were people I told myself I would never become, but who I was faintly beginning to see in the mirror daily. They seemed to be self-centered parents who thought they were better than everyone else, who only cared about what people saw. And, their kids were unappreciative spoiled brats who had no concept of reality. They wouldn’t be caught dead in something from Old Navy (or God forbid, WALMART) as they might burst into flames. If they didn’t get to play soccer with the big league or lacrosse, they might faint. It seemed that money (or fake money) was no object to them, image was. Those who didn’t bother volunteering were the first to complain and throw rocks at those who were volunteering. The school had about 100 kids enrolled at the time with tuition averaging $15,000. In other words, the school had a truckload of money for that time. Bottom line is that those kids were going to be okay and were going to have a successful school career without a handful of parents busting their ass to bring in more money to buy computers or a new slide. In hindsight, the school could’ve dropped some of their $1.5M to buy a few computers. We eventually left the school after 4 years when I realized that my child needed to be exposed to more diversity and that I no longer wanted to hang with the Biff’s and Buffy’s of the world. It was a world I thought I wanted to be a part of then realized I didn’t fit in, nor would I ever, nor did I even want to.

Fast forward 12 years…Shane’s been at his new school since December. For those who don’t know, it’s a school for children on the spectrum, ADHD and other issues. It’s a full day of ABA therapy, music therapy, art, etc. Because it’s a small school with less than 25 kids, the parents are not that active. They do meet monthly, but it’s more of a meeting to share information and resources. Recently, they put together the spring yard sale so I jumped at the opportunity to volunteer. The money  raised is generally used for computers and other necessities for the kids. I thought it would be a great way to meet the parents and get to know the administrative staff better.

For this story, it’s important to note that the tuition at Cyzner is approximately $27,000 per school year for a full-time student. Throw in another $5,000 for summer camps. In order for a family to afford the tuition, they have to make a considerable amount of money, make huge financial sacrifices or have great insurance benefits (like us). So, I guess for the sake of comparing them to the families at Jessica’s school, they would be the same economically or better. There’s a vast difference between them, though.

Although I had a preconceived notion of what the parents would be like, I discovered that the moms I met working with the yard sale at Cyzner do not give a rat’s ass about their appearance to the outside world. I saw the staff bending over backwards to help and lead. The parents will do anything to get their kids the help they need to navigate in a world of neuro-typical kids. If that means wearing clothes from Old Navy, so be it. If it means driving an older car, so be it. Skip the baseball, soccer, dance and other afterschool activities. If their kids have major meltdowns in a restaurant, or wear their clothes inside-out (a travesty!), rubber boots with dresses or shorts, they are not embarrassed. They’re just trying to survive.

After thinking about my experiences with the two schools, I’ve come to a couple of conclusions…the private school Jess went to was a world I thought I wanted to be a part of, but never would be accepted no matter what effort I put forth. While I realize that we are very fortunate to have nice things, get to travel to beautiful places and have many priviledges I never dreamed I would have, I hope that we are not viewed as hypocritical. But, I hope that our character, generosity, desire to “pay it forward” speak for us and do not put us in the category of the Biff’s and Buffy’s in the eyes of friends.

The world at Cyzner is one I never wanted to be a part of, but I am. They’ve shown me what’s important in life. It’s not what you have, what it looks like from the outside, how much money’s in the bank, the car you drive, the house, the clothes you wear or who your lunch date at the country club is. It took a hard knock, but now I know. It’s love, kindness, generosity, tolerance. It’s the world I want to be part of. It’s the world I’m in. It’s where I fit. I have been humbled.

Courtesy of: Enlightenment Ain't for Sissies

I’ve Run Out of Ideas

While I usually try to be funny and entertaining, the last couple of weeks have been especially difficult and full of emotions…inadequacy, anger, sadness among them. If you’re looking for a happy blog about rainbows and unicorns, you should stop reading and go elsewhere. Here’s the problem…I am a self-diagnosed perfectionistic control freak with Obsessive Compulsive Disorder, ADD, future member of Overeater’s Anonymous and Lazy Ass Couch Sitter Club. I feel like I’m losing my sense of humor which is probably my strongest coping mechanism. More and more often, I find myself less likely to laugh about things and more likely to cry instead. No clue why (menopause?). I have a birthday coming up which brings me closer to 50 (ouch). I have a daughter who’s is graduating in June and heading to college. I have a little boy who struggles to “make good decisions” at school and at home (no matter how hard he seems to try). Maybe those are reasons. Realizing that things are happening that are beyond my control probably doesn’t help.

My daughter and I are very close. We have a great relationship. One that I wish I had with my mother. Jessica has professed that I’m her best friend (although I think her boyfriend has weasled his way into that spot Smile with tongue out). The realization that she will be leaving home soon is really hitting me hard. It seems like only yesterday that she was dressing up the cat and pushing her around in a stroller or marrying our golden retriever. I’m not ready for the next stage of life and our relationship with her living 3 1/2 hours away. I’d be lying if I said I was ready. I think it’s going to take a long time for me to be ready. I can’t even hear someone ask her about college without welling up in tears (she looks at me everytime waiting for waterworks). But, I know that we have done a good job raising her. She’s a great kid. She’s beautiful inside and out, smart and ambitious. I’m prouder than anybody has a right to be. She’s going to be okay.

Shaney has been struggling at home and at school for a while now. He’s decided that he’s pretty much the “decider” in most things being asked of him. He’s as stubborn as a mule. At school, he sometimes refuses to do his work, stands up in the chairs, turns his desk over, cries, but what gets him into the most trouble there is potty mouth. He insists on yelling out BUTT and STUPID. I’m sure there are others (like the special word he called out when the teacher asked for words beginning with “F”). His teacher came up with the idea of putting tally marks on the white board in class to show him how many times he said inappropriate words to make him more aware. This week, we decided that I would give him two coins each morning. He would be allowed five tallies before having to surrender a coin. If he got into the car at the end of the day and kept one coin, we would do something extra-special. The first day he got in the car with both coins! YAY (computer time)! The second day, two coins! YAY (small toy and DS)! The third day one coin! YEEHAW (computer time and Happy Meal)! The fourth day…no coins! BOO (nothing electronic :/)! No coins would mean that the child stubbornly used ten potty words in a six hour period. To be honest with you, I don’t care if he says BUTT. I’m not particularly fond of STUPID. And STUPID ASS is definitely not cool. But, since there are only three boys in his class who pick up each other’s bad habits and feed off of each other’s energy, I get it.

Last night when I was trying to tuck Shane into bed, he refused to clear his bed of the mountain of toys, pick a book out for us to read and just stop being a jerk, in general. After I asked several times (okay, told him several times), I got no help. So, I said I could not read a story and sing lullabies if he didn’t get ready. That brought the onslaught of tears and a temper tantrum. Once he settled down, I sat on the bed and said, “I’m sorry you’re sad and upset. I’m trying to help you. What can I do to help?” From this adult trapped in a little boy’s body, I hear, “I DON’T KNOW, JANET! I’VE RUN OUT OF IDEAS!” That made me cry…and laugh, he laughed. Maybe, just maybe, my sense of humor is still here. It might be under a layer or two, but it’s there. I think it’s going to be okay.  I’M going to be okay.

You’re Not My Friend!

When you’re a parent, there are days when there isn’t enough wine, chocolate, beer, Xanax in the house to help you not pull every hair out of your head. Days when no matter how hard you try to be patient, nothing works and you turn into a raging lunatic (well, I do, anyway). Days when I am way too hard on myself for not being the perfect parent (whatever the hell that is) which results in crying and feeling worthless. And, when you have a kid who is defiant and has a difficult time with changes, transition and lack of routine, it makes spring break seem like a vacation to Hell.

Several days this week, Shane has had multiple meltdowns and temper tantrums. Let’s brush your teeth and hair…NO! Time to take your medicine…NO! AND YOU CAN’T MAKE ME! Time for lunch…I DON’T WANT TO EAT. IF I DON’T WANT TO, I DON’T HAVE TO! Let’s go see a movie…I’M NOT GOING TO SEE A MOVIE! We’re going to the museum…I DON’T WANT TO GO TO THE MUSEUM TO SEE THE STARS! Let’s go to Carowinds…I’M NOT RIDING ANYTHING EXCEPT THE SNOOPY MOON, NOT EVEN THE CAROUSEL (he wasn’t lying about that). So, I bargain, praise, bribe, provide positive reinforcement, take away privileges, send him to “the chair” to think while screaming and kicking the wall (him, not me). These are all the methods we’ve been taught to do. And, what’s funny is that Shane’s right. How do you make a six year old get out of “the chair” to finish a task because I’m on a schedule when he’s bound and determined to sit there because it’s not HIS idea to get up? Truth is, I can’t “MAKE HIM IF HE DOESN’T WANT TO.”  And, so it goes…I’M NOT YOU’RE FRIEND! I’M GONNA SAY BAD WORDS! I DON’T WANNA STAY HERE WITH YOU!

This has been the first extended break since Shane started Cyzner Institute in December. When he’s in school, the difference in his behavior is insane. He’s a different child. It’s difficult for me to tell what part is autism and what part is just being a brat at home. Obviously, the routine in the classroom helps him stay in control. This week has made me realize how fortunate we are to have the resources and benefits that are available to us. The fact that he has perfect days when he’s in school let’s me know that the therapy is working. Although we’re working with his teacher, therapists and psychologist to learn ways for us to help him manage his frustrations, this week has taught me that I still have a VERY long way to go with my education. We’re fairly new to the world of autism so are still navigating and finding more information daily to help put it all together. We are a family that’s always been spontaneous…spur of the moment movies, trips, restaurants, amusement parks, etc. I have to come to the realization that as much as I think things can be “normal” (whatever that it is) they’re not going to be. At least, not yet.

When things settle down from each instance of tantrums from a six year old amidst tears and hugs (from me and him), I hear, “I do wanna be your friend, Mommy. I love you. I wanna stay here with you forever and my whole wide life, Momma. You’re my favorite. You’re the best Mommy ever.”

And, at the end of the day when the last line of the lullabies has been sung, I whisper, “Always remember and never forget…” the sweetest, most adorable brown-eyed boy I know chimes in, “that Mommy will always love me, no matter what….even if I’m mean. Right, Momma?” Right, Shaney…no matter what. All is well in the universe. For now, anyway. There’s always tomorrow. Smile

We did figure out a way to ride in the car with the top down this week…put on goggles to block the wind and sun! 🙂