Brushing teeth has been an ongoing battle in our house. Easton and Christian usually do pretty good with it, but Charlie wants nothing to do with it. He hates the taste of any toothpaste (trust me, we've tried no less than 8 different types of toothpaste) and he doesn't like how the toothbrush feels on his teeth and gums.
Our most recent visit to the dentist was pretty eventful as well. Everything went fine until Charlie witness Christian getting x-rays done on his teeth. While Christian had no issue with it and showed no signs of trauma from it, Charlie was NOT going to do that. When it came time for him to hop into the chair, he ran. He ran out of the room, into the hall and hid behind some toy machines. It took a lot of coaxing from mom to get him out from behind there and into the chair. Sunny did a beautiful "lap" and laid half her body on his legs to help assure him he'd be ok. Charlie was adamant that he was not going to have x-rays done and was NOT going to let the hygienist look inside his mouth, let alone let her clean his teeth! Oh boy. In the end, the dentist was able to clean a few teeth without toothpaste. The dentist also suggested using a mild mouthwash with him if he was not willing to brush.
So, that's what we've been doing the last couple months. It's hit or miss if he'll actually use it. A couple nights ago when we were getting ready for bed I was trying to convince Charlie to use the mouthwash. Many times I have to do it with him to get him to participate. I reminded him that he needs to take care of his teeth or they would all rot and he wouldn't have any teeth left. Here's where the conversation went:
Charlie: I don't want my teeth to fall out!
Mom: Ok, then we need to do your mouthwash every day. Let's get in there and do it before bed.
Charlie: Wait, if my teeth fall out, I'd just get fake teeth.
Mom: Probably not, fake teeth are expensive, I'm not sure we could afford them
Charlie: Ok, I'll just have no teeth. What would I eat?
Mom: You'd have to eat all soft food
Charlie: OH! So I could eat ice cream for every meal?
Mom: Nope, you'd have to eat mashed potatoes forever.
Charlie: (a look of astonishment on his face). Fine. Let's do the mouthwash.
He still hates it. But it's better than nothing!
Sunny, on the other hand, has no trouble keeping her teeth nice and clean!
Tuesday, June 26, 2018
Sunday, June 10, 2018
To the Parents of Children with Autism
We write this blog and share our story, not to get sympathy from others, but to educate others on what Autism is, how different it can look from one person to the next and to offer support to others who are walking the same road. We don't write it to complain about our life, but to celebrate life and our son's.
The support for others is a big reason why we do this. To all the Autism moms and dads out there. We see you, we know your struggles and we stand beside you.
To all the moms out there who juggle your family's chaotic schedule- sports schedules to social schedules, from work to school schedules to therapy schedules just to ensure your child has the therapy support they need to help them to develop the much needed skills they need to make it in this world.....I see you.
To all the parents out there that are functioning on very little sleep every day of their lives because your child with Autism has never slept through the night, I feel your exhaustion. I've been there myself. The nights seem so terribly long when you're awake for most of it and it's hard to see the light at the end of the tunnel. Keep your chin up and raise your coffee cup to others who are in your shoes. Please know you're not alone.
To all the dads out there who find it hard to connect with their sons because they don't seem to be able to connect to much of anything in this world, because their interests don't make much sense and you're not sure how to relate to them. I see you. Keep trying and don't give up on them. Your actions make an impact on them more than you know.
To the mom who feel trapped in her own home because it's incredibly difficult to take your child out of the house to do activities- because the meltdowns, the sensory overload, the stares from strangers (and sometimes rude comments) and the aftermath of any outing can be too much to handle. I see you. I feel you. I don't judge. Because we, too, have been in that position and it can be lonely.
To the parents who haven't had a date night in who knows how long- because the stress of finding a sitter who knows how to handle your child's behaviors and quirks isn't easy, because you don't trust easily and because sometimes the aftermath of being gone isn't worth the few hours you have to yourself. I see you. I am you.
To the moms who struggle at meal time- because your child has food aversions, selective palate, won't try new foods or massive sensory issues and doesn't like how food feels in their mouth. I see the stress you go through to find foods or to even get your child to eat. I know the worry you feel when your child has barely eaten anything all day. We walk that road too and it's hard worrying if your child is gaining enough weight or getting the right nutrition.
To the parents who had planned your day/evening one way, but then have to adjust according to your child's meltdowns/stress/anxiety. It can seem like a never-ending battle, one that never is in your favor. I feel your stress. I know the let down of plans never going as planned. And it's ok to feel let down. I don't mean let down by your kid, but being let down that this is not the life you envisioned.
To the moms who struggle to balance time with your neuro-typical kids. Boy, do I know the tight rope you walk. I know the worry you carry on how Autism affects their lives, your worry that they aren't getting quality time with you or any time at all. I know the concern all to well, that your other children will come to resent the sibling with Autism because of all the struggles you all deal with on a daily basis. I have those same worries too. But think of all that they are learning. Think of the compassion and patience they see every day and learn to do that with others. Think of the lessons of accepting differences among people and that it's ok to be different- to not fit in a mold the world thinks everyone should fit into.
To all the moms who have ASD kiddos with major meltdowns who can be aggressive. We know these aren't tantrums. We call them meltdowns for a reason. I know the hits you take-literally, the kicks, the punches and toys being thrown at you. I know mama, it can be hard. Those bruises and scratches hurt. And I know it's hard to see your baby struggle with feelings they don't understand or know how to deal with. I know those big feelings are difficult to deal with. But you're doing a good job, mama. Keep up the amazing work you do with your baby.
To all the parents out there who have yet to hear your child speak a word, my heart goes out to you. Having a non-verbal child has got to be one of the hardest parts of this journey, never hearing your child's voice, never hearing them call you mom or dad.
To all you Autism parents out there, I'm here to tell you that you are nothing short of amazing. You are the strongest people I know. We were given these children for a reason, sometimes big reasons beyond our understanding. I'm here to tell you, that even though this road seems lonely most days, please know you are not alone. The rest of us Autism parents know what you're going through, the heartache, the struggles each day and the BIG wins your kids have when they reach a goal or have a breakthrough. These children were given to you. YOU are their parent for a reason. Keep on rockin' each day and never give up on them, no matter how bleak the day has been. I see you. I am you.
The support for others is a big reason why we do this. To all the Autism moms and dads out there. We see you, we know your struggles and we stand beside you.
To all the moms out there who juggle your family's chaotic schedule- sports schedules to social schedules, from work to school schedules to therapy schedules just to ensure your child has the therapy support they need to help them to develop the much needed skills they need to make it in this world.....I see you.
To all the parents out there that are functioning on very little sleep every day of their lives because your child with Autism has never slept through the night, I feel your exhaustion. I've been there myself. The nights seem so terribly long when you're awake for most of it and it's hard to see the light at the end of the tunnel. Keep your chin up and raise your coffee cup to others who are in your shoes. Please know you're not alone.
To all the dads out there who find it hard to connect with their sons because they don't seem to be able to connect to much of anything in this world, because their interests don't make much sense and you're not sure how to relate to them. I see you. Keep trying and don't give up on them. Your actions make an impact on them more than you know.
To the mom who feel trapped in her own home because it's incredibly difficult to take your child out of the house to do activities- because the meltdowns, the sensory overload, the stares from strangers (and sometimes rude comments) and the aftermath of any outing can be too much to handle. I see you. I feel you. I don't judge. Because we, too, have been in that position and it can be lonely.
To the parents who haven't had a date night in who knows how long- because the stress of finding a sitter who knows how to handle your child's behaviors and quirks isn't easy, because you don't trust easily and because sometimes the aftermath of being gone isn't worth the few hours you have to yourself. I see you. I am you.
To the moms who struggle at meal time- because your child has food aversions, selective palate, won't try new foods or massive sensory issues and doesn't like how food feels in their mouth. I see the stress you go through to find foods or to even get your child to eat. I know the worry you feel when your child has barely eaten anything all day. We walk that road too and it's hard worrying if your child is gaining enough weight or getting the right nutrition.
To the parents who had planned your day/evening one way, but then have to adjust according to your child's meltdowns/stress/anxiety. It can seem like a never-ending battle, one that never is in your favor. I feel your stress. I know the let down of plans never going as planned. And it's ok to feel let down. I don't mean let down by your kid, but being let down that this is not the life you envisioned.
To the moms who struggle to balance time with your neuro-typical kids. Boy, do I know the tight rope you walk. I know the worry you carry on how Autism affects their lives, your worry that they aren't getting quality time with you or any time at all. I know the concern all to well, that your other children will come to resent the sibling with Autism because of all the struggles you all deal with on a daily basis. I have those same worries too. But think of all that they are learning. Think of the compassion and patience they see every day and learn to do that with others. Think of the lessons of accepting differences among people and that it's ok to be different- to not fit in a mold the world thinks everyone should fit into.
To all the moms who have ASD kiddos with major meltdowns who can be aggressive. We know these aren't tantrums. We call them meltdowns for a reason. I know the hits you take-literally, the kicks, the punches and toys being thrown at you. I know mama, it can be hard. Those bruises and scratches hurt. And I know it's hard to see your baby struggle with feelings they don't understand or know how to deal with. I know those big feelings are difficult to deal with. But you're doing a good job, mama. Keep up the amazing work you do with your baby.
To all the parents out there who have yet to hear your child speak a word, my heart goes out to you. Having a non-verbal child has got to be one of the hardest parts of this journey, never hearing your child's voice, never hearing them call you mom or dad.
To all you Autism parents out there, I'm here to tell you that you are nothing short of amazing. You are the strongest people I know. We were given these children for a reason, sometimes big reasons beyond our understanding. I'm here to tell you, that even though this road seems lonely most days, please know you are not alone. The rest of us Autism parents know what you're going through, the heartache, the struggles each day and the BIG wins your kids have when they reach a goal or have a breakthrough. These children were given to you. YOU are their parent for a reason. Keep on rockin' each day and never give up on them, no matter how bleak the day has been. I see you. I am you.
Thursday, June 7, 2018
2 Steps Forward, 3 Steps Back
It's always amazing to me how quickly things change with Charlie. Remember my last post? There were so many small victories last week and now this week has been a total 180. We've been expecting it though. Knowing the last days of school are approaching, schedules changing, routines being disrupted...we knew things could get difficult.
A few things are changing and I'm sure that's not helping Charlie's anxiety. On Monday the boys met their nanny for the Summer and spent a few hours with her at our house. She'll do just fine, I know, but they tried to pull a few fast ones on her. She'll be at home with them 3 days/week through the Summer, starting next week.
One of Charlie's therapists is going to be leaving soon. This is one person Charlie has had as a constant over the last couple years and someone he really responds to. Not having her in his normal routine throughout the week will make an impact on him.
He won't have the normal routine of going to school each day. Adjusting to a new Summer schedule can be difficult, we've seen this in years past. The same goes for the Fall when school starts back up again.
The last day of school is tomorrow and the routine at school has been totally turned upside down for the last week or two. Mornings are usually tough for Charlie to get up and get out the door, but for some reason today was a thousand times worse than it normally is. There was screaming, crying, toys and items thrown all around, hitting, kicking, scratching, more screaming and then barricaded himself in his bedroom. I could see through the video camera in the bedroom that he was slowly calming down so I left him to himself for a few minutes while I got Easton and Christian ready for school and out the door. This morning's events, unfortunately, mirrored last nights events where there was another massive meltdown that lasted well over an hour. It took a lot of patience, skill, Sunny intervention, talking and reassuring before he finally came out of his room this morning and even considered going to school. And then a lot more Sunny intervention before I could actually get him to school.....way late.
And now, this is where Sunny has planted herself. She's out. After a morning full of tough work, she's totally out. Looks like a nice option! Work hard, sleep hard. I'm hopeful we'll have a good Summer, no matter how hard things are in the present time.
A few things are changing and I'm sure that's not helping Charlie's anxiety. On Monday the boys met their nanny for the Summer and spent a few hours with her at our house. She'll do just fine, I know, but they tried to pull a few fast ones on her. She'll be at home with them 3 days/week through the Summer, starting next week.
One of Charlie's therapists is going to be leaving soon. This is one person Charlie has had as a constant over the last couple years and someone he really responds to. Not having her in his normal routine throughout the week will make an impact on him.
He won't have the normal routine of going to school each day. Adjusting to a new Summer schedule can be difficult, we've seen this in years past. The same goes for the Fall when school starts back up again.
The last day of school is tomorrow and the routine at school has been totally turned upside down for the last week or two. Mornings are usually tough for Charlie to get up and get out the door, but for some reason today was a thousand times worse than it normally is. There was screaming, crying, toys and items thrown all around, hitting, kicking, scratching, more screaming and then barricaded himself in his bedroom. I could see through the video camera in the bedroom that he was slowly calming down so I left him to himself for a few minutes while I got Easton and Christian ready for school and out the door. This morning's events, unfortunately, mirrored last nights events where there was another massive meltdown that lasted well over an hour. It took a lot of patience, skill, Sunny intervention, talking and reassuring before he finally came out of his room this morning and even considered going to school. And then a lot more Sunny intervention before I could actually get him to school.....way late.
And now, this is where Sunny has planted herself. She's out. After a morning full of tough work, she's totally out. Looks like a nice option! Work hard, sleep hard. I'm hopeful we'll have a good Summer, no matter how hard things are in the present time.
Friday, June 1, 2018
Small Strides
There are days that come along where Charlie makes small strides. And sometimes these small strides are things we've been working on for a long time.
Charlie has struggled with major sensory issues since he was a baby. Sensory issues are very common for kiddos with Autism. Certain clothing bothers him, haircuts are a nightmare, loud noises and big crowds overwhelm him, brushing teeth is a struggle and bath time is definitely never easy. He hates the feel of soap or a washcloth on his skin or shampoo in his hair. The essential oil company I work with has recently come out with a baby line of hair/body wash and lotion. This line is specifically formulated for sensitive skin and can be used by anyone, not just babies. The hair/body wash is a foaming wash so when I ordered some we decided to try it with Charlie.
When it comes time for Charlie to get cleaned up, he prefers a bath as he hates how the water feels in the shower hitting his skin. But on this particular evening a couple nights ago, Charlie asked to take a shower. So, in the shower he goes. The next thing he asks for is the new soap. Absolutely buddy, I'll grab the new soap. As I showed him how soft the soap felt on his skin and went to help him clean up he looked at me and said "I can do it, mom." Who is this kid?! Now, not only did he allow the foaming soap on his skin, but there was also no screaming, crying or begging to be done. This is something we've been working on for 6 years! And the lotion....did I mention he also used lotion when he was out of the shower? Yep, he sure did! Lotion with calming essential oils added, followed by a weighted blanket and extra weight and snuggles from his favorite girl.
And today, their school did a Color Run. Charlie has been super anxious about the color run. I think primarily because he didn't know what to expect, but he also didn't want to get color on him. His school counselor had been coaching him as well as us at home. He was told that if he didn't want to get color on him he didn't have to. He was adamant that he was not going to get color on him and the plan was for him and another buddy from school to do the course with his teacher who could be there to help if needed.
Charlie has struggled with major sensory issues since he was a baby. Sensory issues are very common for kiddos with Autism. Certain clothing bothers him, haircuts are a nightmare, loud noises and big crowds overwhelm him, brushing teeth is a struggle and bath time is definitely never easy. He hates the feel of soap or a washcloth on his skin or shampoo in his hair. The essential oil company I work with has recently come out with a baby line of hair/body wash and lotion. This line is specifically formulated for sensitive skin and can be used by anyone, not just babies. The hair/body wash is a foaming wash so when I ordered some we decided to try it with Charlie.
When it comes time for Charlie to get cleaned up, he prefers a bath as he hates how the water feels in the shower hitting his skin. But on this particular evening a couple nights ago, Charlie asked to take a shower. So, in the shower he goes. The next thing he asks for is the new soap. Absolutely buddy, I'll grab the new soap. As I showed him how soft the soap felt on his skin and went to help him clean up he looked at me and said "I can do it, mom." Who is this kid?! Now, not only did he allow the foaming soap on his skin, but there was also no screaming, crying or begging to be done. This is something we've been working on for 6 years! And the lotion....did I mention he also used lotion when he was out of the shower? Yep, he sure did! Lotion with calming essential oils added, followed by a weighted blanket and extra weight and snuggles from his favorite girl.
There are some big transitions going on right now with the end of the school year coming, Summer starting, beginning a nanny 3 days/week and a routine/schedule turned upside down. We're aware of how dysregulated transitions make him so we're trying our hardest to stay ahead of it all. We've had some busy days this last week and more up ahead. Last week we spent a couple hours on Tyler's parent's pontoon. Sunny's 1st boat trip and the boys tried fishing but didn't catch anything this time around.
Charlie's school schedule has been turned upside down this last week as well. He's had several field trips and tons of fun activities out of their normal routine to finish off the year. Sunny and I accompanied Charlie and his class on their field trip to Crayola Experience at the Mall of America this week. Such a fun day and both Sunny and Charlie did amazingly well. Charlie was so excited to be able to spend the whole day with Sunny and made some fun creations at the same time!
A giant light bright board! |
Tyler and I walked over to the school with Sunny just before the run began to watch the boys. The first time the boys came around Easton had a little color on his shirt and Charlie and Christian's shirts were still completely white. We cheered them on. But wouldn't you know....the second time I see Charlie come around and look.....there's some color on his shirt!!
And look at that.....more color the 3rd time around!!! Way to go Charlie!!! Christian was still completely color free, but Easton was drenched in it. They all seemed to have a pretty good time.
We are all looking forward to Summer. The boys are excited to be done with school and our calendar is full of fun activities and trips over the next few months. Look out Summer, the King boys are coming for you!!
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