Today's Guest Post is by fellow autism mama and writer, Renee from "It's 5 O'Clock Somewhere". With a blog name like that...how could we not relate to one another? Renee also runs a Facebook Community of the same name. Please drop by and check out her blog and join her on Facebook.
![]() |
Renee & Her Family |
They say opposites attract, don’t they? I’ve heard that all my life. I always thought there was some truth to that but it wasn’t until I met my husband that it really, really rang true.
When we got together our obvious physical and personality contrasts are what people noticed and would comment on often. He’s above average in height and I am the size of your average 4th grader. He rarely talks and I’m a chatterbox. He prefers solitude to any kind of social interaction while compared to him I am a social butterfly. He has no filter to speak of and since I am super sensitive, I try to think before I speak so feelings aren’t hurt. Oh, and there’s one other that’s worth mentioning: my husband has Aspergers, and I do not.
Okay, those are just a few of the differences between my spouse and I, but at this point anyone reading this can grasp the idea that we’re not exactly alike. It wasn’t until we were married for a couple years that I really began to see how wide the gaps were. It was rather like pulling back the layers of an onion; with each layer I realized there were even fewer similarities than I thought.
Not surprisingly we’ve had a rocky road over the years. It hasn’t been all bad but it’s been a struggle at times to keep it together. After five years of marriage we decided to try to have a baby. I thought he had grown up enough at that point to be the father I knew he could be and it was time. We were blessed with a gorgeous little boy in August 2002 and settled into family life with the child we both adored. When our son was just shy of turning three he was diagnosed with autism which naturally rocked our world and forced us to reconsider whether the second child we were thinking of was a good idea. Mutually we decided that we should just focus on the child we have and do all we can to get him the help he needs. To anyone on the outside we seemed like we were a united front in that goal and for a while we were.
Shortly after our son was diagnosed my husband began to suspect that he himself was on the spectrum as well. He didn’t want to see a doctor and get a formal diagnosis so he took a series of online tests that made it very clear that he was indeed an Aspie, as they’re commonly referred to. It was shortly after that that anything autism related began to fall on my shoulders. He no longer wanted to be as involved as he had been in our child’s treatments. I began to think that my husband felt like he had caused our son’s condition and that thought made him withdraw from being a part of our son’s therapies. We discussed that and I told him truthfully that I didn’t blame him or any one thing for causing our child’s autism but there was a backing away on his part that was very noticeable and upsetting to me.
When he told me that he was on the spectrum I did a ton of research on the subject. I read books and articles about being an NT (neurotypical in clinical terms) married to someone with autism. Suddenly little quirks of his began to make sense to me. What seemed to be such cold insensitivity before began to bother me less. I’m a sensitive person so I cannot say that each comment that he said rolled off of me. I tried to see it from the standpoint that he was unaware how his words or actions (or in many cases inactions) affected me. I started to understand why he’d forgo going anywhere with us unless it was a special occasion he couldn’t get out of, such as a major holiday or wedding. He’d never offer up a reason when I would ask him why sitting home was more appealing than getting out, and I started to realize it was just easier and definitely more comfortable for him just to not go.
Now, let me say this: coming to the realization of those things doesn’t put an end to them bothering me. I just found myself working harder to try to understand where he’s coming from. He still says insensitive things without thinking, isn’t able to recognize human emotions (i.e when I am pissed off or hurt) unless I tell him, and is extremely difficult to drag out of the house unless necessary. It’s very frustrating most of the time, so I vent. I vent to him and to those I trust, and I try to deal with it in whatever way gets me through it. I tell him exactly how I feel and how it often feels as if I am raising two special-needs kids instead of just one. He’s unflinchingly honest with his feelings, so I am the same way with him. When he chooses to stay home instead of going out with us, I try to make the best of it and enjoy my time out with our son as my date. The questions and comments still annoy me, but at this point I am so used to it and the people who invite us to functions are used to seeing us show up as a twosome instead of our whole family.
It’s not all bad, this being married to an Aspie business. For one thing, since they’re pretty much incapable of being phony in any way, you always know where you stand with them. They don’t just say things because it’s the polite or socially acceptable thing to do. When they do or say something nice, you know it’s genuine and not just an empty compliment that people sometimes feel they have to. That’s something I appreciate about him and always tell him so. Another benefit is that since he’s very focused on details, he often is able to see things that I don’t, especially with respect to our child. Our son has a more classic form of autism but my husband can often understand why he’s upset and heading towards a meltdown, whereas I am not always able to. He is, in a sense, the autism whisperer in this household.
Every marriage or long-term relationship has its challenges to face. I’ve heard of situations that make our differences seem like nothing. He is who he is and I am who I am: the same person who went into this marriage with the best intentions and the highest of hopes. It takes work like everything else in life but there are times, not all the time, mind you – that it is worth it.
Adelaide Dupont · 285 weeks ago
And for those of us who knew and appreciated these points in high school to a greater or lesser extent - always good to have a refresher and feel them through the current and future generations who we survived to be able to see.
I especially appreciated points 5, 7 and 10.
And young women not settling or settling down yet is a good thing.
"It's never too late to live our dreams" - but it may be too early for some of them!
And 8 of course.
nicole · 243 weeks ago
Risa · 230 weeks ago
LAH · 221 weeks ago
Maira L. Coral · 216 weeks ago
I was looking for information for my Multi-Genre Disability Research Project from my Early Childhood Special Education class on the web, when suddenly I came across your blog. I started reading this out of curiosity and I want to tell you that as you said yourself, you will not be Amanda Gorman, but you managed to make me shed some tears, perhaps because I felt totally identified with your words, especially in the part that you speak of your son. My son also has Asperger's syndrome, he is 19 years old and he is in the second semester of College. Also like yours, he takes classes from home, likewise my eldest daughter is also taking college classes from her room. At the same time, that I work as a preschool teacher from my kitchen through a computer, my husband sleeps in the room during the day because he works at night. Also in the afternoons I myself take virtual school classes. I am a 51-year-old Latin woman who began to learn the English language as adult, so maybe you find some deficiencies in my writing, however, I was very moved by how proud you express yourself about your son. Referent your mother, I liked the humorous tone that you give when your talk about her, so I did not want to miss this opportunity and stopped my assignments for a moment to let you know that your words do make a difference, since they reach the heart of at least those who have opportunity to read you. I want confess you that is the most long I have written to someone I don't know, because your words inspired me, thank you...
Gavin Bollard · 209 weeks ago
Thanks for this post. I've been very distracted of late and so this was how I found out about our friend Kate. Kate's struggles were very real but they were so constant and so wide-ranging that it was difficult for people around her to address them. I think it's going to take a while longer for me to process all this.
I learned so much from Kate because she was always quick to point out the many injustices in the world. In her glory days, she was very much a crusader and she cared for everyone. Over the years, as her situation took its toll, I came to realise that it was the fact that she couldn't be put in a single specific category, that made the system fail her. She needed help that they weren't set up to provide.
She needed more care and she needed to be less alone. I'm so sorry that this has happened.
For a long while we were corresponding almost every day but a couple of months ago, I realised that she had become so stressed that nearly every interaction I had with her was starting to trigger her. I backed away to give her a bit more space. She only had a little time that she could stand to be online and there were too many things that she wanted to do in that time. I thought that by taking a step back, she could reach out to more people who might be geographically closer and able to assist.
Kate was a beautiful soul and she will be sorely missed by all of us.
diyalabs6192603 11p · 192 weeks ago
Robots for kids
Robotic Online Classes
Robotics School Projects
Programming Courses Malaysia
Coding courses
Coding Academy
coding robots for kids
Coding classes for kids
Coding For Kids
Spoil your cat · 122 weeks ago
Many of these living arrangement aren't good, and many of the people who run those places really don't have the residents' best interest at heart. Those places are like old age homes and foster homes, where you sometimes hear horror stories. They're hard to trust. But then there are good ones, of course.
The best thing for an autistic adult is either to go on living at home or working and renting an apartment and living independently, but that isn't always an option.
Duncan · 112 weeks ago