The Rafting Trip
Good Clean Fun

Past Perfect, Future Tense.

Class of 89 By Cathy Jameson

I’m in denial that this year is almost over.  Autumn has already slipped through my front yard as I send my sweater- adorned children outside for longer playtime.  The kids are able to make their way to the back yard for some adventures while I stay inside to work with Ronan on some of his ABA-VB goals.  He and I can do this since he’s quickly learned how to function better with these skills.  It helps that the baby, who is looking more like a toddler getting up on her two feet, can play with the big kids’ toys.  It keeps her happy and occupied while I conduct these therapy sessions with Ronan.  

I home school my typical kids and am proud of how quickly they understand and accomplish the school work I set before them.  My oldest is getting to be a grade ahead of herself while my five-year old son is able to do math computations in his head.  We started our school year in the summer when it was still oppressively hot. It was planned this way since we always run into a medical crisis or two with Ronan mid-winter.  The one to two weeks it takes for him to recover stops our entire family’s schedules in their tracks.  I needed to get a good month of school work under our belts before the changing weather brought those pesky seasonal viruses our way. 

Fortunately so far, we haven’t had any crazy illnesses as we start the final quarter of this already-busy year.  With Halloween approaching and talk of our Christmas holiday planning already underway, I sit in awe at how time is quickly going by the older I get.  A week goes by in the blink of an eye.  Weekends are over before I know it.  By the time I flip a calendar page, half the year is gone!  I’ve always heard time goes by faster as you age but I never knew how fast.  I was reminded of how quickly a couple of decades go by when I prepared to travel to my twentieth high school reunion this summer.  

I long for some of the days of my youth that are mere memories now. Oh to be carefree and to think only about me again!  It was a treat to reconnect with classmates the closer the reunion date came.  The committee set up a website for all of us to share our information so we could see who we are now, where we’ve been, what we’ve done and if we were going to make it to the weekend-long events in July.  You bet I was.  I loved high school! I did well academically and athletically, was friends with everyone and I was just happy to be alive. I moved out of state as soon as I graduated and wanted to go back to the little town in Texas that helped shape my early adult years.  I had been able to stay in touch with some friends, but not too many as we all became busy with our professional and personal lives.  The rush of memories and the chance to make new ones this reunion weekend made me giddy like the teenager I used to be.

A few weeks before my trip though, I got really nervous. As much as I still felt a part of the class of ’89, I knew I’d be bringing some emotional stuff to the reunion.  I hadn’t seen some of my classmates since the 10-year reunion. Others, I hadn’t seen since graduation night June 1989—we’ve all changed, grown up, moved on and turned into real live adults.  Many of us are parents, but I hadn’t heard if any of them had special needs kids like mine.  I wanted this weekend to be fun and a break from the daily stress I live while being Mom of the Century to five young children. 

I joke with my sister that I use one of the social networking sites to go back to my past since I’m afraid of my future.  The older my son Ronan gets, the more scared of the world and our future I become.  Many of us from high school were able to reconnect via the internet as we planned our big get together.  I learned that the guys who were the loudest and most attention-getting were now Dads.  Oh, how proud I was of each of them.  They grew up! The girls in my class—holy hot stuff, they are gorgeous women!  They were successful business women or Super Moms like me.  Even so, I had the tiniest anxiety of how out of place I may feel when I finally get to see them all, be in the same room with them and do what people do at reunions—talk and visit and share and enjoy.

I joked with my best friend Shannon, who accompanied me to the outings since my husband stayed home to watch our kids, “Maybe they won’t recognize me…”  As we walked into the bar Friday night for the first get together, we both heard the loudest, “CATHY!  We’re so glad you made it!”  Since I had traveled half-way across the country to be with these people for just a few short hours, I was overwhelmingly humbled and felt welcomed back into the days of my youth with the 80s music blaring in the background. 

Rounds of hugs and “OHMYGOSH you look fantastic!” echoed over and over again.  Chit chat, engaging conversations, sharing of pictures and success stories were seen and snapped on digital cameras.  Shannon and I made our way through the small groups catching up with these kids I used to idolize and hang out with.  It felt surreal but had that right-at-home feeling too. 

How could I not talk about my son who rules and runs my life now?  Ronan has created a new person in me.  I stand on a perpetual (and thanks to the Internet, virtual) soap box.  I used to be so quiet, so silly and so go-with-the-flow, hang out in the back of the crowd and don’t you dare call attention to me even when I just ran a race and won a medal.  That’s the me some of these people will remember.  How they react to who I am now and the cause I champion (i.e., fighting those damn vaccines) made me nervous. 

It’s only slowly, as I came to grips of who this child of mine was over the last few years, that I’ve had to change and become a very informed person, the kind that sounds like an annoying reference book focusing on topics that others take as a given and even for granted.  Ronan has shaped so many parts of the new me.  Did I want to bring that up at a reunion?  There would be plenty of time for us late thirty-somethings to talk at the events…did I want to talk about Ronan, vaccines, autism, the law or just keep quiet about what’s happened to me and my son and pretend things were just peachy after all these years? 

Turns out, I didn’t have to.  People came to me.

My brother’s best friend in high school came up to me with open arms.  Damien had me roaring laughing many, many times in class at school and at track meets.  His newest baby was born not even a week before my return to Texas—I was so proud of him, a new Dad again.  I wondered if he knew anything about vaccines though.  We hugged and smiled, not knowing where to start since we had so much to share with many years of separation between the last reunion.  He came right out and said, “Cat, what’s this autism stuff you write about?”  Boom.  That could be a conversation make-or-break question.  “Are you just compassionate for the cause or is it more?” he went on to ask.  

I took a deep breath and explained what we’d discovered with Ronan’s medical issues, how I had started to look for a connection, any connection, and what had been revealed when we connected the dots.  How I’d walked into doctor’s offices and marched right out not letting their arrogance or attitude stop my quest for answers.  How I didn’t just stop searching for Ronan but continue to read and now write as much as I can so other families can avoid unnecessary damage and pain to their children.  Damien nodded his head, shared some stories of his own family’s experiences and offered another hug of ‘hang in there, sister, I get it and I believe it.’  Yea, me!  Yea, Damien!

Not having more than a second to catch my breath, another guy friend yells out over the music, “Yeah, Cat!  Don’t stop writing what you’re writing about. I know exactly what you’re saying and it’s true!”  Rick?!  What?  You read my posts? You know this stuff I speak of?  Really?  Tell me more.  Another conversation, another believer, another hug.  Thank you, Rick.

Shannon and I made the rounds, catching up with old friends and life-long friends even though distance is between us.  Both of us could not believe how old we were to have an event like this to go to but were forced to believe it since we were so tired and not feeling like the spring chickens we used to be back in the day. 

After a full day traveling to the reunion, we had to call it a night and started our goodbyes.  I missed seeing some classmates but knew Saturday night was another chance to catch up with everyone again.  I left the bar with a little more confidence.  I thought it might be okay to be that 1-in-150 parent (which is now 1 in 91).  I was representing the autism community!  I could do this thing with people I knew and loved from so long ago.  As much as I hated being that one person, I would stand up and let Ronan’s story be a reminder of how one decision can change a life forever.

Saturday night’s dinner was fantastic. I was leaving Sunday to head back home so this was the last chance to see everyone, to have some fun, full of laughing and catching up.  I was again nervous since it was a dress-up thing.   There’s just no time for that stuff at home.  Shannon was my date again as we headed into town.  At the awards portion of the dinner, I laughed so hard at the comments from the emcees. We got to hear some under-the-microphone comments from the guys you may consider the class clowns. Oh, the memories of how they carried on. Some things don’t change which is good. I needed the belly laughs to really remind myself that as hard as life gets, laughing can be a cure. 

After the formal sit-down, it was time to mingle. There were so many people I hadn’t gotten to see Friday night and Saturday night was quickly coming to an end. There was one person in particular I wanted to say hello too. He was one of the guys in school you could hear before you could see.  He was one of the ones I was so happy to read about on our class reunion website.  He had become a Dad and ‘grew up.’  I darted over to Marc before he got up to talk to people. I felt silly going up to him to say, “Wow, you did it!  You grew up!  Look at you!”  I was really proud of him though. Something drew me to him and I needed to say thanks for all those laughs in high school, God love you and continued good luck to you and your beautiful family. 

I was more surprised when his wife looked at me and said, “Hey, you’re the one that writes about autism stuff, aren’t you?”  Yep, that’s me.  She stood up, hugged me and said thank you. Surprised, I looked at Anne and Marc and knew that they too were 1-in-150.  We talked as much as we could before other friends grabbed us for pictures and to share their stories.  How amazing it was on one hand to feel relieved I wasn’t the only one representing, but saddened that Marc, this former crack-me-up kid who I loved for being so hilarious, goes through some of the same pain I do.  The feeling I had to go up and just say thank you for the memories from high school turned into a different kind of thank you.  I got an renewed instant friendship with 100% belief in the new me I have become.  Wow!

It was a weekend of emotions for me: to leave my busy family and endless duties to peek at my past.  To rekindle friendships and remember forgotten stories, to laugh at our mistakes while making future plans, to be thankful for the simpler times while preparing for real life again.  That weekend was a nice break from reality if just for the 72 hours I got to sneak away. Thank God for Steve who made me go because I wouldn’t stop bugging him about my trying to get back there.  I would of course much rather had him accompany me to the reunion, but he stayed home and kept everyone safe and happy. 

It’s like that cliché about the season of life changing. I definitely feel that the seasons of my life are changing faster than some of my friends with typical children.  We all know it takes a lot of energy and emotion to raise kids.  Add a special needs kid (and a houseful of typical kids) and you’ve got the makings of a mixed-up emotionally and energy-drained tired thirty-something clinging to the past.  It’s not so bad to hold onto some of the memories since the future really is scary.  Thankfully, finding friends from the past to support me in the future is what I got at my reunion.   

I came home to the usual—our family life revolves around Ronan and his needs.  We’re all still here, surviving, learning, living and loving each other the only way we know how.  We deal with the struggles, celebrate the wows, share everything and keep hoping for better and even the best.  It’s the only way we know how to live.  Ronan keeps us going, keeps us on our toes, keeps us hoping for more when he does something amazing.  We wonder how much more of the negatives we can handle.  He’s the stop sign, the yield sign and the welcome-to-my-world sign.  We never expected to live this type of life, it’s certainly not one we signed up for it, but as this season in our life changes again, we’ll bundle up, grab whatever we need to survive it and get there together.

Cathy, a former Lady Greyhound, is mom to five children. She and her husband Steve have turned into advocates for their son and his special need because that’s just how life is.  Cathy manages the Age of Autism FaceBook page.


 

Comments

cathy

From a mom with Typically developing children...you keep me thinking, and questioning the mdical world and it's motives. I will always apreciate your passion to keep all of your friends informed. But what I really appreciate is your non-judgemental, fact-based way of sharing what you know with us!! I love you girlie!
Always
Cathy

Alison Davis

Cathy, your lovely reflection on your reunion experience post-autism reminds me how my children are my teachers. Their struggles engage me to keep growing to meet their challenges. Their bravery keeps giving me courage to do things I have never, ever imagined I could do.

You are my teacher, too; I'm so happy I know you.

Gatogorra

I hated highschool but it sounds like you were in the right place at the right time and were surrounded by some genuinely marvelous people who've grown up so well.

Why does it not surprise me that the quick witted class clown had an effected child? So tragic but at least you were able to reach out to each other and it seems your writing meant a great deal to many.

The title of your piece was brilliant. Thank you as always for your moving thoughts.

Vicky

Thanks, Cathy, for continuing to share your story and stick up for all children who suffer like this. I'm glad to hear Ronan is learning well and his other siblings are doing so too. Say hi to everyone for us.

Blessings,

Vicky

Twyla

Thanks for writing this wonderful story. So glad that you enjoyed your highschool reunion.

Amazing how on a grassroots level attitudes are changing, even though the press and gov't and mainstream medicine remain so entrenched.

I recently traveled halfway across the country on brief trip to Texas, too, to see my aging father, aunt & uncle, youngest sister and her family -- and two brothers traveled from the other side of the country to meet me there. A refreshing treat to travel unencumbered by care for anyone else -- much as I would have loved to bring the whole family!

Jessica

In my small office of 12 full-timers, 3 of us have vaccine-injured chidren. One has a 19 year old with ASD who is nonverbal, I have a 4 year old with "classic" autism in recovery, and another woman I just found out has a 7 year old diagnosed with Aspergers. That's 3 out of 12! And that's just the people I know about for certain!

Pretty soon everyone will know someone with a vaccine-injured child, if they don't already.

rileysmom

Cathy, I love to read your writings. When I get on AoA in the am and see you've written something I dive right in. This was a great article too. Through FaceBook I have found 8 other classmates have children on the spectrum...one lady has 2 vaccine injured children and they all say the same thing, I gave birth to a child that was fine, then....a total of 10 children.
My graduating class was 68. That's right 68 and 8 of us have children that are vaccine injured. Not to mention that 3 of us have had cancer. Myself and girlfriend of mine and my friend Jimmy who lost his battle with bone cancer last year. He was 36.
If someone can figure out the math on the 10 in 68 fine but it's still a staggering number coming from one small town in Ohio. We graduated in 1991.
I haven't gone to any class reunions because I was afraid. My own family now rolls their eyes when I walk in a room so I know I'd probably step on toes at a reunion. I don't know though Cathy, reading your story...I might just show up at the next one and step on some toes!!! I'll tell all my fellow classmates that I've reconnected with on FB to join me.
Thank you again sweet!!!

Odysseus

Thanks for sharing Cathy. These personal stories are what make this website so special.

Teresa Conrick

Cathy,

What a great writer you are! Ironically, I was just at my high school reunion last night - not 20th - as that one was 10 years ago so a big YES, that time goes by so fast.

I. too had the same trepidations that you had, though most knew 10 years ago about Megan's autism diagnosis but at that time, it was "idiopathic", that word I loathe.

Last night, I had much more to add and like your old friends, they believed me, too. In fact, most were angry that their TV's and papers are telling them differently and one even said, "I knew that they were lying about this!".

It was better than I could have imagined. Talking about regression and specifically, what that looked like - my precious daughter stopped talking, wouldn't hug, began to have GI pain, had no tolerance to noise, cried all the time, etc - and these people could understand how devastating an autism diagnosis is and that a 1:91 ratio is utterly frightening and unacceptable.

Thanks for sharing our parallel reunions.

Sunny

Cathy, THANK YOU SO MUCH for this post! You put my very complex, mixed-bag of feelings into words---perfectly, and it was such a refreshing read for me! This absolutely could've been my story. I related to every word. Wow. I always run through that nervousness of being "that mom" when we're gearing up for any social situation (that's NOT an autism conference =))---but I always find clear, God-given opportunities to share a little about our lives and our children and our cause. I, too, am a New Me on this journey---someone I never imagined being. But if we can spare one other family from this path by sharing our story, then share it we will. How can we not??? Thank you for what you do. You're a brilliant writer and an AMAZING advocate for our families. God bless you and yours!
Sunny (from Texas)

Lisa Thompson

I attended my 30th high school reunion last November, and I met at least six other classmates with children on the spectrum.

After chatting with one guy and working the fact that I had a child with ASD into the conversation, he quickly confessed that he did as well, and that we were in very good company, while he reeled off the names of classmates who are part of our club.

So, reunions — good times, old friends, catching up, and an unexpected feeling — commiseration. Who would have thought back in 1978 when we graduated that this is what the future held for so many of us?

Julia C.

I recently discovered (through Facebook) that my husband's college roommate and best man at our wedding also has a vaccine injured son. It is nice to have someone you love and respect who understands your cause and will stand by you in your mission, while also being sad that either of you had to walk down that road in the first place.
Eventually things will change. They will have to, since so many will be affected. Famous people, politicians, doctors, and regular people like you and me will know first hand what vaccines have done, and the denials from industry and the government will become weaker in the face of the mountain of evidence that is our children. Our time is coming.

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