Why You Should Get Your Child Diagnosed Even If You’re Scared

May 14

It’s funny because I wrote this post last June. I can’t believe it’s been in my drafts folder for almost an entire year. I suppose there was a part of me that was hesitant because I feared that my choice to share this was a bit short-sighted in that I never got permission from my child to share it.

I’ve been battling with myself. I see value in sharing it because I would have appreciated reading a mother’s perspective during these dark times, yet I played out a number of “what if” moments in my mind… What if they got it wrong? What if I make it worse for someone? What if he hates me later on because some cruel classmate stumbles upon my post 10 years from now and reads it and teases my kid? What if people judge him? What if people judge me for oversharing? What if my family thinks I’m stupid for putting it all out there on the internet for EVERYONE to read and judge? <<< I told you there are a lot of “what if’s”…

At the end of the day, I’ve decided to publish the post because it was really what I was feeling, and we are at such a good place these days that I want people to know that there are still good days. In fact, there are more good days than sucky, awful ones at the moment. Isn’t that inspiring? Anyway, here it is… enjoy!

I’m a parent of three awesome kids, two boys + one girl. They’re each so different. They have their own personalities, their own strengths, their own weaknesses, what makes them happy/excited/laugh, what makes them sad/scared/cry. 

One thing that is constant for all of them is how much I love being their mom. So when one skips crawling and wants to start walking, we celebrate. When one gets potty trained before turning two, we celebrate. When one jumps off the diving board with no fear, we celebrate. 

But what happens when doctors say your baby breathes more than he has to? What happens when he doesn’t start walking until after he’s one? What happens when he’s not talking when he’s supposed to? <— They’re all pretty scary stuff that make you worry. And honestly, parenthood wouldn’t be as fun or crazy if all children were the same. 

 Information I've gathered from the autism speaks website . Information I’ve gathered from the autism speaks website .

The Autism Spectrum is a scary thought. In fact, it was my greatest fear when I had my first son. (I don’t know why. I didn’t fear cancer or something terminal, but I was deathly afraid of this). I’ve read so many articles and blog posts from people who document their lives with someone on the spectrum. It doesn’t matter what you read, or whether the author’s situation is mild or severe, because at the beginning, you’re certain that your situation is the worst case scenario.

I can only speak for myself, so for me, the scariest part was uncertainty of progress. My brain would go as far into the future as I could and think of everything wonderful my child wouldn’t be able to do, all the things we would miss out on. It wasn’t until a friend from high school, whom I had run into for the first time in 17 years, said something to me. When you’re in the situation and waiting to see progress,  or even a diagnosis, you can’t help but wonder, “Why my kid? Why is this happening? Why can’t everything just be normal?” She told me she did the same thing, and her husband said, “F— it! This is OUR normal.” 

He was right, because what is normal anyway? One of my kids loves apples over cookies. That’s our normal. One of my kids, I swear, said “hi” at four months old. That’s our normal. One of my kids goes to speech therapy, and that’s our normal. One of my kids made me have a meltdown at Wal-Mart because I was that crazy mom who couldn’t control her kid in the store, and that’s our normal. I love them all the same. 

Here is my advice, and the advice I have heard so many times: 

  • FOLLOW YOUR GUT because she knows her stuff. Seriously.
  • Also, despite my kids’ pediatrician’s advice NOT to research on the internet, I say DO IT. READ AS MUCH AS YOU CAN now, so that you know all of the options, possibilities, and resources available, with the knowledge that the spectrum is vast + wide but getting a medical diagnosis is only way to truly get peace of mind. (I swear!) I only advise you to read as much as you can with the caveat to avoid spiraling down that abyss of negativity. It’s important to know what’s out there, but remember that at the beginning it feels like you have hit rock bottom and that the world is crashing down around you. 
  • FIND YOUR TRIBE + BUILD IT. For me, it’s easier to talk about it, even though I cry, because there’s always someone who knows someone who can help or give advice. You need those people in your life to remind you that you’re doing the right thing. If it weren’t for my friends, none of which have children on the spectrum themselves, but have taught or coached someone on the spectrum, I would have waited. In the process of waiting, I would have done more harm to my child by remaining hesitant. (BTW, you can always email me or give me a call. I will tell you everything I know).
  • REMEMBER THAT YOU ARE YOUR CHILD’S ADVOCATE. No one will advocate for your child better than you will. All the internet research, conversations with other parents, and degrees don’t make you an expert in ASD. Sometimes I think that even the “experts” don’t even know because each child on the spectrum is different. However, you are an expert in your child, so don’t let anyone tell you they know him/her better than you do.
  • KEEP AN OPEN MIND. Your situation is not preventable. You didn’t do anything to cause it. You do, however, have the ability to help your child, so keeping an open mind will allow you to take action for your child’s best interest. There’s no judgment, I promise.
  • EMBRACE IT AS YOUR NORMAL. I tell my husband all the time that my children chose me to be their mom for a reason. And if God blessed me with one who is not like everybody else, it’s because that kid knew what a fighter I was, and I am my child’s best opportunity for a great life. My child knew I would be the conduit to making sure my child does what God intended — and that’s to make a huge splash in this world. I just know it.

The way every child is different, every day is different, but that’s parenthood. There are days that I cry my eyes out, and there are days that I say “It was a good day.” There are days when I want to fire my entire family and escape the madness, but it does get easier. It gets better, I promise! 

So there it is. That’s our story. I have to admit, it’s time-consuming and stressful at times, but the progress we have seen in just a year is amazing. I’m so lucky because it could be a lot worse. We are very lucky that progress is visible in his behavior and communication. We are so lucky that he’s responding well to therapy. We are so lucky to have such a wonderful support system and amazing therapists, case workers and teachers. Thank you for being on the journey with us.

I guess the whole point in my sharing this, and I suppose my “mission” on this “autism journey” is to spread the word that it is okay to be scared, but you cannot let the fear deter you from your path of helping your child and being his/her advocate. Fear is not an option.

  1. Christina

    April 23rd, 2019 at

    Been a blog subscriber for a while, and just stumbled across this in my inbox! I wanted to say thank you for all the mamas out there that this post will help!

    We started early intervention with my oldest right after he turned 1, and my hubby (and everyone around me) pushed back a lot in the beginning when he needed extra therapies and eventually when I said we need to look at this possibly being ASD. He did end up getting diagnosed at 2.5yr, and it honestly helped us have a leg to stand on with insurance & getting therapy costs covered. It also helped because I reached out to TACA to get local resources & get linked up with another ASD mama mentor. Covering my ears, eyes, and heart because I was sad, angry, worried about his future wasn’t going to help him. They need us to love & ADVOCATE for them, to get them the best therapies we can, the best teachers & school resources, maybe explore other options just try something out of the box for them! Happy to share that my son just turned 7, and hasn’t needed therapy for 2.5 years. I’m amazed at the leaps & bounds he made, watching his progress has been one of our greatest joys, because we know how hard he’s worked through it all.

    “Why me?” and “What did I do wrong” are very real (and normal!) feelings…but redirecting that energy to advocating for your child, positivity & celebrating all their small victories will go so incredibly far in helping them! I’m keeping good thoughts for your son & all his continued progress to come!

  2. Jomylene Ruiz

    May 3rd, 2019 at

    Hi Christina! Thank you for commenting. I think you’re just seeing it because I’m transitioning back to wordpress. 🙂 Thank you for your kind words and encouragement. It was extremely difficult for me to share because 1) I don’t want to be known as the mom blogger whose child is on the spectrum; and 2) I didn’t want to necessarily share my child’s story because what if he/she didn’t want the story public on the world wide web? So I figured I would share “my” story having to deal with it as a mom because it is seriously the toughest thing I’ve ever had to deal with. THANK YOU! We have seen huge progress and I’m so grateful for the people who have guided us along the way.

you said:

Leave a Reply

Your email address will not be published. Required fields are marked *