Potty training with Brycen...just not happening anytime soon! We spoke with the U of I doctors about it last summer and we agree that it is impossible to potty train a child that can't effectively communicate when they have to go. Whether that communication is verbal or sign language, Brycen is not even close to being ready for that...and we are just fine with that. There are so many more important things in his life we want to work on with him that potty training has taken a backseat to those.
Now, after saying all of that...we are very happy to share that he is starting to recognize when he needs to be changed! He has had control over his bodily functions for some time now as he usually refuses to have a BM when we are away from the house and he can stay dry for hours at a time which is why we have the issues with flooding out in the middle of the night when he wakes up. Many people have mentioned to me about cutting back him fluids in the evening, but that is not possible. The only fluid he has after 5:30/6pm is the 6 or so ounces of juice that needs to be mixed with his Melatonin each night. He caught on way too fast to the crushed pills in pudding and yogurt, so we had no choice but to go to the liquid form which can easily be hidden in his juice with his bedtime snack. That is a whole different battle for us...so I'm going back to the fact he is recognizing when he needs to be changed.
If he has a BM, we usually know the signs...but if we don't notice, he will refuse to sit down, will stop playing, and sometimes go back to his room and point at the changing table. If we ask him if he has a "poopy diaper," he immediately begins walking back to his room and waits for us. If he doesn't have one, he will yell "uhuh" at us (which means "no") when asked, and he is ALWAYS RIGHT! This may not be a big deal to many parents out there, but to us it is HUGE! First of all, he is recognizing his bodily functions, and second of all, he is communicating effectively with us when we ask him the question about his diaper!
Sorry if this is too much info for some people...I gave fair warning in the title! But it's a part of parenting and someday if you have yet to experience it, you will also experience pleasure in knowing your child is taking steps to independence, saving you money, and a ton of garbage each week!
"When one door of happiness closes, another opens;
but often we look so long at the closed door that we do not see the one which has opened for us."
Helen Keller
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Autism and Our Family
"Autism"----It's one word that can change the life of a child and family in so many ways. Autism Spectrum Disorders are being diagnosed at a rate of 1 in 68 children currently. If you do not already know someone that has been diagnosed, the statistics say it won't be long before you do.
Our son developed typically until around the time he turned 2 years old. We heard words...we saw him play with other kids...we watched as he played with his toys appropriately...we made eye contact with him...overall we understood his wants and needs. In a matter of a few months, that was all taken away from him. He began lining up toys, lost all of his words and signs except for one word "ball", ignored other kids, could not sleep through the night, lost eye contact and the ability to follow directions, and he had no way of letting us know what he wanted or how he felt. It was heartbreaking to see something happening to our child that we couldn't stop!
Brycen began receiving home therapy 1-2 times per month for about 6 months before we realized it wasn't just developmental delays. We knew it was Autism...we just didn't want to say it outloud to anyone. He was officially diagnosed with Autism (classic form and regressive), as well as Mental Retardation in August 2009 by the University of Iowa Hospitals and Clinics.
We continue to learn as we make our way through this journey with Brycen and we will continue to share this journey with you on this blog! The blog has been a great therapy for us to be able to vent our frustrations and struggles with accepting that we have a child with special needs, while sharing how blessed we are to have a child teach us what life truly means. It has also been a great way to inform others of his progress and changes over the last couple of years.
Thank you for your support of Brycen and our family! We hope you are able to learn something through this blog no matter if you are a parent of a child with special needs or a neurotypical child, a teacher or therapist, a family member, or just someone that is interested in the journey that a family goes on as they learn their child is battling a life-long disorder.
Our son developed typically until around the time he turned 2 years old. We heard words...we saw him play with other kids...we watched as he played with his toys appropriately...we made eye contact with him...overall we understood his wants and needs. In a matter of a few months, that was all taken away from him. He began lining up toys, lost all of his words and signs except for one word "ball", ignored other kids, could not sleep through the night, lost eye contact and the ability to follow directions, and he had no way of letting us know what he wanted or how he felt. It was heartbreaking to see something happening to our child that we couldn't stop!
Brycen began receiving home therapy 1-2 times per month for about 6 months before we realized it wasn't just developmental delays. We knew it was Autism...we just didn't want to say it outloud to anyone. He was officially diagnosed with Autism (classic form and regressive), as well as Mental Retardation in August 2009 by the University of Iowa Hospitals and Clinics.
We continue to learn as we make our way through this journey with Brycen and we will continue to share this journey with you on this blog! The blog has been a great therapy for us to be able to vent our frustrations and struggles with accepting that we have a child with special needs, while sharing how blessed we are to have a child teach us what life truly means. It has also been a great way to inform others of his progress and changes over the last couple of years.
Thank you for your support of Brycen and our family! We hope you are able to learn something through this blog no matter if you are a parent of a child with special needs or a neurotypical child, a teacher or therapist, a family member, or just someone that is interested in the journey that a family goes on as they learn their child is battling a life-long disorder.
Awesome!!! Definitely a step!
ReplyDeleteThose are steps in the right direction - if only you could get him showing you the changing table first right!?!? :) Someday we'll get there undoubtedly - may just be a while.
ReplyDeleteAngie
Hi Timmer family,
ReplyDeleteJason and I would like to contribute money to the Autism walk. I have a 10 year old nephew with Autism, so it would be in honor of Brycen and Samuel.
Can you please send the link to mittsknits@yahoo.com ?
Thanks!~ Monica Mitts
This is a huge deal! Wow! I love your updates. Hugs to all of you.
ReplyDelete