Transcript
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Hello everyone and welcome to today's episode of On the Spectrum with Sonia.
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We have a very special guest today joining us Nikki Shipp.
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She is the podcast owner of Pieces for my Puzzle podcast, which I had the lovely privilege of being a guest on, which I had the lovely privilege of being a guest on.
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On the Spectrum with Sonia is a podcast designed to discuss autism spectrum, mental health challenges and anybody who's overcome any challenge.
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That is inspirational and leaves people feeling filled with hope, connection, love, support and empowered.
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So today, let's please join me in welcoming Nikki to our show.
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Nikki welcome.
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Thank you so much for coming on here this morning.
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Hi Sonia, Thank you so much for having me.
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I'm very excited to be here today.
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I'm excited to have you.
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So tell us a little bit about yourself and how autism got introduced into your life years ago because I was introduced with about autism, I should say because my son was diagnosed at the age of three, just after the age of three.
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So I didn't know much about autism prior to that.
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I'd always heard about you know, quote unquote autism, but I didn't really know what it was and so I didn't.
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You know, jason wasson was my first biological child and I didn't necessarily know or understand that maybe developmentally he was behind in certain areas.
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So, um, I noticed he wasn't speaking much and that was the biggest thing for me.
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Um, so we did have a wonderful pediatrician that um, one day, at one of his wellness exams, saw Drayson stemming, flapping his hands, and so she referred us to a developmental pediatrician and we were very fortunate and blessed as well to have another wonderful physician with us to help us with Drayson's care.
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But basically we found out that Drayson had autism at the age of three.
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But basically we found out that Drayson was had autism at the age of three and that put my husband and I both in kind of a tailspin, I think, you know, it's really common for a lot of families to feel that way, when you receive a diagnosis and you know nothing about it and you're not sure what to do and you know they hand you this list of things to do and say, okay, you know, come back in six months and let us know how you're doing, kind of thing.
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So that's, that's how we got thrown into the world of autism and and it was.
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It was a little daunting at first.
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You know, our developmental pediatrician was fantastic, is fantastic, but she just was also very real.
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Like he might speak, he might not ever speak, he might call you mom, he might not call you mom, and that was really devastating for me personally.
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So I had a little bit of a grieving period, and when I say grieving, not because I lost all hope or anything, it's just the idea of what I thought my son could become or the picture that the expectation I almost put in my head was there.
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I had to completely dispel myself from that and to realize that he just learns differently, he might communicate differently.
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Everything that I thought was going to be quote unquote normal was now not going to be normal.
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So after my grieving period of that and kind of letting go, I really delved into what type of care he would need, what type of resources I could find I kind of became that squeaky wheel of a mom and you know, excuse me asked a ton of questions, wasn't afraid to ask questions.
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I probably got a bad rap at some places because I was almost maybe probably too intrusive, to be honest with you, but I wanted to get that care for my son and um, and so we were very lucky.
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We put him into preschool, um at the age of three and a half and um his preschool teacher had a master's with special needs, in special needs education with an emphasis in autism.
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So she was a great mentor to me and taught me quite a few things about, in terms of educationally, what I could do for Drayson and questions I could ask.
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So I was very fortunate to come across that it still didn't inhibit moving like later on.
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It didn't inhibit some of the problems that we had at his school.
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But it was very, very difficult in the beginning for us to even find services and I think it took me almost a full year to qualify him, have him become eligible for services and then to find the care providers to provide care for him.
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So, fast forward, a year later, we finally got things implemented for him.
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We started to see progress.
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I was happy to announce.
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About six months after his diagnosis, he called me mom for the first time.
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So I knew, I knew in that moment that he was capable.
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The first time I ever heard him call me mom and um.
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And that's actually a really fabulous story, because I was headed to his daycare to pick him up and I didn't realize that, I didn't realize that my own child was calling my name.
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I heard some kid in the background yelling mom and I thought it was some other kid, you know like, where's this kid's mom?
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And I realized it was him.
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He saw me walk past the room and he was coming after me and I remember feeling very hopeful, like I realized in that moment oh my gosh, he's, he is capable and he's going to be able to do these things.
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So that's where my moment of belief started for Jason, about six months after his diagnosis.
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That's when I really started to understand that he was capable.
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I just had to find a different way to expose him so that it worked with his learning capabilities, so that he could then, you know, have a voice or try to communicate in some fashion, even if it wasn't going to be vocal.
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How was I going to get him to communicate more with us.
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So in the beginning things were great.
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We had a lot of supportive educators.
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It wasn't until he was in second or third grade we really kind of started having problems, which, educationally, sometimes that's a pivotal point in curriculum, right they kind of start laying on a little bit more heavier curriculum with the kids and that's when we really started having problems.
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Was was first, second, third grade.
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We really started seeing that the support wasn't what we thought it was going to be.
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And and also the when I say support, I'm not just talking about educationally supporting a child, I'm talking about the social, emotional component.
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Sure, and you know, and before we go more into that, I was just, I would like to hear from you just the fact that you were at one point told right, yes, yes, your kid might not ever speak to you, he may never call you mom, you may never ever say I love you, or anything like that.
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Right To finally hear you be getting called mom.
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Six, months after the diagnosis just walk me through what.
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What did that feel like for you Like?
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walk me through what was going on.
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Oh my gosh, I you know I had so many waves of emotion.
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First of all, I cried hysterically.
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I got in the car and I called my husband because I couldn't even believe that he called me mom.
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And it was so, it was so innocent.
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I was walking past the room to go get, to go pick them up and I didn't realize they'd moved into a different room.
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So he saw me walk across the window.
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The lady, the aid, was trying to tell him to stop and he ended up grabbing her by the hand and dragging this woman out of the doorway into the hallway to get my attention and I could hear this mom, mom, mama, mama.
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And I'm like somebody find that kid's mom.
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And I turned around like what is the problem?
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And I was like literally mid-sentence in my you know, like what is going on kind of thing is what I was saying.
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And I turned around and it was him.
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I immediately got teary-eyed.
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I looked at the aid and I said I'm so sorry.
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And she kind of looked at me like and I literally said to her I said he's never called me mom before.
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Oh, my God.
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So she started to break out into tears.
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I got into the car.
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I was hysterically crying.
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My husband thought I got into a car accident.
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I was crying so bad.
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And um, and I remember getting home and hugging Dresen and telling him that I loved hearing him call me mom.
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I told him.
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I said I love hearing your voice.
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I said I love hearing your voice.
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I said, son, I am, I love that you called me mom.
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Thank you.
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I wanted him to know that.
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I wanted him to also feel encouraged to continue to speak Right.
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So I wanted him to know how much I loved hearing his voice.
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I felt a sense of guilt for a moment too, because I didn't recognize his voice.
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So when I realized it was my son, I also almost felt a moment of guilt because I didn't even realize it was him.
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And after that, everything else, everything else that we've been through, that's been extremely difficult.
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I always go back and remind myself of that moment, always.
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And it's so.
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You know, this makes me want to cry, actually, because it's so emotional.
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Like I could feel the emotion.
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I feel like I was just there with you.
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I feel like you know what I was in that hallway with you, as you were sharing that.
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I feel like, oh my goodness, and just I can only imagine just the shock and just the you know the, the pride you must have felt in it, and just the shock and just the you know the, the pride you must've felt in it, and just the idea, just that whole idea of, oh my gosh, you know, he's defied the odds, despite what the doctor said, he might not ever speak to me.
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Oh my gosh, he's speaking to me finally, yay.
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Yeah, and I think that that was my I always call it my moment of belief.
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That was my moment of belief and I think that every parent has that with their child and it was the choice of what do I do with that.
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I wanted to keep going.
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I was like let's do this, like I want to explore this now because I'm seeing that he's capable.
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And if I had just gone into that state of, well, she said he may or may not.
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I guess he's not going to and I settled for that.
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Then where would he be today, right, right?
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So so we're going to be fast forwarding.
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Now he's in first, second, third, we're in early elementary school.
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Now you had started to say that the emotional and social support wasn't what you thought it would be Right, it was very antithetical to what you had experienced in the preschool years.
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Yes, yes, what changed?
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Well, we had moved to a different school.
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That had changed.
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We had moved out of where we currently were living and into a different school district.
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And here in the state of Arizona you can't.
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There's no boundary exemption.
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If you have a special needs child who has an IEP, you have to stay within the district of where that IEP goes to.
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So we knew we wouldn't be able to commute him to the school that where he was currently existing, where he was currently existing.
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We had heard great things about the school.
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We vetted the area we were moving to.
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I did my research, I did my homework.
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Like on paper it all looked fantastic.
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You know, initially, in the beginning, kindergarten went well, but it was as he got into first, second and third grade I just started to see some things within the system that that it was just, for lack of better words, a broken system.
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It wasn't just the educational component that I felt like he wasn't being supported on, but the social, emotional component, which is a really big deal for kids.
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You know, sometimes I think that's even a bigger deal than some of the curriculum that we have to that we put our kids through.
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But it changed with the educators and I felt for them in the sense of I could see where their resources were limited.
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There was limitations for these educators, so I could see that frustration for them.
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There was limitations for these educators, so I could see that frustration for them.
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But I also the administration was horrible in delegating the type of care that Drayson really needed under a special needs category.
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But I started noticing things.
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Like you know, we'd make special accommodations for Drayson.
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He had an aide with him all the time, so we were able to get an aide that would sit with him to assist him with tasks and doing things at school.
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I found out that they, you know, in the morning he would walk into the gate and he'd go towards his classroom.
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I thought he was going to stand in line and lo and behold, I found out that they would.
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The aide wouldn't allow him to stand in line and lo and behold, I found out that they would.
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The aid wouldn't allow him to stand in line.
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She was being told to take him to the library and make him sit by himself and I didn't know if there was a behavioral issue going on.
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Was it sensory?
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Was he overwhelmed Like?
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And then I started to notice that he at school pickup.
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They were asking us to go to the front office and not to the school pickup line, and, um, I didn't understand why that was happening either.
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So when I started asking questions, they you know, they sent me an email saying we just feel like it's better for Drayson.
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And so when I I started asking questions well, is there a behavioral issue or is he acting out?
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Because, if so, I want to know so that we can work on that with my home care team, cause I had a, I have a team of home care providers that help us, so I wanted to maybe devise a goal to help with that if that was the case.
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And they said, no, everything's fine, drayson's great.
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We love Drayson.
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He's such a sweet boy.
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And I thought to myself why are they removing him from his peers?
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And you know, they started telling.
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They finally came out that it wasn't for Drayson.
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It was because the, the aid had to clock out by a certain time and it was just easier for them to move him.
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It was just easier for them to take him to the library and sit by himself before he went to the classroom, and so I had to literally advocate for him to be able to stand in line with his peers, because I had to explain to them that the peer modeling watching his peers socialize, observing that, being around, that was important for him because of his social behaviors and not knowing you know, trying to learn how to integrate there was no peer modeling happening.
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They were just putting him into isolation.
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That is so heartbreaking and heart-wrenching.
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It's like it seemed like they didn't really, they were just doing the path of least resistance because they wanted to do things that were convenient for them.
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Notwithstanding the fact that you know and going to your point earlier, you know just the whole social emotional piece of going to school.
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Right, that's huge, because if you're not in a good environment, it doesn't matter how good the education system is.
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If you're not in a good social emotional environment where you can thrive, it only makes the academics that much more difficult and challenging, in my opinion.
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Well, yeah, and I even said to them just because he can't communicate to you how he's feeling right now does not mean that he doesn't communicate to you.
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How he's feeling right now does not mean that he doesn't have a feeling over this.
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You know, you don't.
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You are automatically giving him the belief that he's different from everybody else because you're isolating him and standing 10 minutes in the morning in line with his peers and 10 minutes at the end of the day in line with his peers is 20 minutes a day of peer modeling time times five times a week.
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When you, when you just if you quantify it and that's what I ended up telling the administration when you quantify those minutes of peer modeling that you're taking away from him, you are putting him further and further away from socially trying to integrate with people, right, and that was very upsetting to me.
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I can only imagine the pain that you must have felt, just having to witness everything you know, having to fight with the school system that had no little to no understanding, if any, you know, and even saying little understanding is being generous here, you know, you're having to advocate for your child, who's hurting yeah, because he's being treated like he's some kind of like prisoner for all practical purposes, right, it just seems.
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It's just so heartbreaking, and you know the fact that you're sharing the story.
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I wonder how many more parents share what they had like something similar to what happened to your son.
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What I remember when I told you when I was a guest on your podcast, you know about some of the incidents that I went through and and my parents do listen to my podcast, and so I think when they hear what happened to your son, I think I know, I know they will get a flashback of what they went through with me, even because you know it just.
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It's just the fact that, first and foremost, you know it just shows the power of ignorance.
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Ignorance and power of laziness on top of that, right.
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Well, and it's just, and you know, based on all the conversations you and I have had, sonia, you you'll know as well as I do this.
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What I'm describing right now is just one of several types of incidents that we had to deal with with with Jason.
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I mean even down to the progress reports.
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Like the progress reports I was receiving, they would tell me, oh, you know, he's met 30% of this goal.
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So when I would ask to see the data to understand how they were articulating that he had made progress on 30% of the school, they weren't providing data points to me and I couldn't understand where they were getting his progress.
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And oh, he's not really progressing here.
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But oh my gosh, here he at 60%.
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I'm like okay, but it doesn't seem like he's progressing or advancing.
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So what's going on here?
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And when I started asking questions about that, we kind of entered another stage of um of of a huge debacle, basically that I found out that they were not, basically they were not taking data to support what they were telling me on the progress boards.
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Because when I finally asked for the files, they said we can't give you a file.
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We can't give you a file because there is no data to support there is no data in his file and said over a two-year time span that they had missed 786 service hours because they didn't have data to support any of it.
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So they had been giving me progress reports for two years with no data to support where they were getting those numbers from.
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Wow, that's just flabbergasted yeah it was and that's when I always call it my mama bear internal rage moment really happened and, like you were saying, how many other parents has this happened to?
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We ended up transferring Drayson and finding a school that was much better suited for him.
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Suited for him and, um, and I remember saying, after we went through that whole ordeal with that school, I said to my husband how many other parents and families is this happening to that?
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We cannot.
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You know that that the amount of frustration because it's not just it's not just the logistics that you're putting up with, you're dealing with your own emotions I was, I was pissed, I was upset, I was sad, I was worried for my son, um, my anxiety went through the roof.
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I mean, it was almost like I felt like I was developing a form of PTSD, because every time I would get a progress report or I get a call from the school, I would trigger Sure.
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And so, get a call from the school, I would trigger Sure, and so I think that was the biggest thing for me personally, and that's how I ended up starting the podcast, because I said to my husband how many other families is this happening to?
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This Can't, this can't go on like this and we have to know how to advocate for our children and to be able to speak on their behalf, and that takes a lot of courage and it takes a lot of strength to do that.
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It does, it does and you know it.
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It just makes it so much more arduous when, there, you feel like you're basically traveling in this maze where you're kind of blindfolded, whereas everybody else has these, you know, are fully able to see and hear and everything, but it's like you can't even see well and you're getting at all at all because you're blindfolded and you're just going into hedge after hedge after hedge in a maze, whereas everybody else is finding pathways everybody else has access to, perhaps maybe throw some breadcrumbs, you know, to find their way out.
00:22:14.574 --> 00:22:22.257
It's just so, um, I just can only imagine how lonely this must have felt for you as well.
00:22:22.257 --> 00:22:38.527
You know it just felt, you know, for you to have to go through this, and you know, and I hear you talk about like you know, it just felt, you know, for you to have to go through this, and you know, and I hear you talk about, like you know, of course you know, part of being in special ed is it's for people who have a different way of learning right and they learn differently, right.
00:22:38.548 --> 00:22:41.195
It's not that they're any less intelligent or anything like that.
00:22:41.195 --> 00:22:55.410
And you know there are different types of special ed programs but, um, and you know there are different types of special ed programs but you know the you know.
00:22:55.410 --> 00:22:56.191
So you had certain progress goals.
00:22:56.191 --> 00:22:57.314
You know that was supposed to have been met by the team.
00:22:57.314 --> 00:23:01.002
What were some of the goals that you were hoping to have Drayson achieve with those goals in those meetings?
00:23:03.066 --> 00:23:05.315
You know it's funny because the way that the IEPs here are broken down are.
00:23:05.315 --> 00:23:08.507
You know it's funny because the way that the the IEPs here are broken down, or you know, by category.
00:23:08.507 --> 00:23:21.449
So of course he had, like his reading, his math, his comprehension, um, one of the things that I couldn't understand was the comprehension piece, because he didn't seem like he was still comprehending things very well.
00:23:21.449 --> 00:23:34.396
And, um, at the time and I was very blessed, I had a, I had a team of advocates, I did, I had a company that two women that were very, very pivotal in helping me.
00:23:34.396 --> 00:23:41.578
They were, they were advocates and they helped coach me and and even advocated for me in that room.
00:23:42.226 --> 00:23:48.828
But some of the goals were written as such that we, you know, I kept saying I think there's something more going on with his comprehension.
00:23:48.828 --> 00:23:54.570
Oh no, he's fine, I'm like, and the advocate said do you know, have you considered he might be dyslexic?
00:23:54.570 --> 00:23:57.808
And the school said oh no, he reads just fine.
00:23:57.808 --> 00:23:59.352
And I said it's not just reading.
00:23:59.352 --> 00:24:04.431
There's more to dyslexia than just being able to verbally read a page.
00:24:04.431 --> 00:24:09.140
He's not answering, he's not seeming to recall immediately.
00:24:09.140 --> 00:24:16.267
So we read a simple paragraph and he couldn't recall who, who in the story and I was like something's going on.
00:24:16.267 --> 00:24:21.224
So we ended up pushing him to have him tested and they didn't want to test him.
00:24:21.224 --> 00:24:22.147
They denied the test.
00:24:22.147 --> 00:24:37.719
So I requested an independent evaluation, which I don't know if a lot of parents know this, but you have the right to requested an independent evaluation, which I don't know if a lot of parents know this, but you have the right to request an independent evaluation If you are not satisfied with the evaluation that the school has done, sure, or if they don't want to.
00:24:37.719 --> 00:24:42.972
So I ended up going straight to district and I requested an independent evaluation.
00:24:43.594 --> 00:24:50.513
And, lo and behold, after his assessments it came back that he not only was dyslexic, but he had dyscalculia and dysgraphia.
00:24:50.513 --> 00:24:54.660
I am not the educator, okay.
00:24:54.660 --> 00:25:01.355
What upset me was that how come nobody was open to the idea of that?
00:25:01.355 --> 00:25:09.057
If you know within your profession what some of these things might look like, I have to.
00:25:09.384 --> 00:25:14.236
That was a level of trust that I had to try to have and I couldn't have it anymore within them.
00:25:14.236 --> 00:25:16.568
Wow, you know.
00:25:16.568 --> 00:25:21.132
So they would tell me oh, you know, he's not doing really well with comprehension, but he's getting there.
00:25:21.132 --> 00:25:22.384
He increased by 10%.
00:25:22.384 --> 00:25:27.031
He wasn't increasing at all, he wasn't advancing at all because they weren't ever assessing it.
00:25:27.031 --> 00:25:33.587
Social emotional goals were written in there and his social emotional goal was really low too.
00:25:33.587 --> 00:25:52.698
Well, when I found out that they were pulling him out of a line and not allowing him to be around his peers, or letting him go doing something else at recess and not kicking him outside with the rest of them right and trying to to put some things in place to allow him to be socially integrated, um, he wasn't hitting the goal on social emotional either.
00:25:53.984 --> 00:26:09.250
Right, you know, and I just feel like that's such a travesty in the field of education that you have these people who are supposed to know a little better and who are supposed to at least you know.
00:26:09.250 --> 00:26:15.891
You know if they're red flags, that you know, maybe there's some things that need to be evaluated.
00:26:15.891 --> 00:26:27.086
If you know a person is having trouble, you know, with reading comprehension, a person we already know is on the autism spectrum, Is there maybe perhaps another contributing problem to this too?
00:26:27.086 --> 00:26:31.573
Because you know it's so?
00:26:31.573 --> 00:26:36.671
It just, it's just a travesty that these, it just seems like those people didn't want to do anything.
00:26:36.671 --> 00:26:39.642
It seems like they they'd rather just sit and be lazy.
00:26:39.642 --> 00:26:41.186
It's, it just seems to me.
00:26:41.186 --> 00:26:42.971
And what you're telling me and I don't.
00:26:43.192 --> 00:26:46.367
I don't necessarily blame the educators, I think what's?
00:26:46.367 --> 00:26:47.885
Because I see both sides of that.
00:26:47.885 --> 00:26:49.510
They are limited in their resources.
00:26:49.510 --> 00:26:53.170
They've got 30 kids in a classroom, they've got, you know, all these things.
00:26:53.170 --> 00:26:56.184
And then they have to deal with also what the administration is telling them.
00:26:56.686 --> 00:27:05.092
And you know, I taught in higher education for a better half of a decade, so I understand the the kind of the behind the scenes dynamic of what happens.
00:27:05.092 --> 00:27:12.569
You know, from a performance standpoint, schools have to produce numbers, they have to produce results, they have to do all this stuff.