Katelyn loves to talk about school and gabs non-stop at home. I shot this video of her last night since she was in a talkative mood. Unfortunately, she is overly sensitive to the sound of Ashley's voice, so she gets a little upset at the end and asks for her comfort activity: A hug from Mommy.
Showing posts with label sensory. Show all posts
Showing posts with label sensory. Show all posts
Monday, October 26, 2009
Wednesday, April 22, 2009
Sensory Overload...
When we first started to suspect that Katelyn had autism, we didn't really think that she had sensory issues. However, all of a sudden it has become very apparent that she definitely has a lot of sensory needs. She becomes overstimulated and will get herself all worked up and then crash hard. She will go from being hyper, laughing and talking a mile a minute, and then all of a sudden she will start crying out of nowhere.
It is very common for kids (and adults) with autism to have difficulty regulating their sensory needs and emotions. A lot of these sensory issues can come about due to environmental factors, such as loud noise or bright lights, but the cause is not always obvious. We are still trying to figure out the triggers for some of Katelyn's behaviors and sensory needs.
There are many ways in which to help a person with autism regulate themselves. For instance, sometimes deep pressure helps, which is the case for Katelyn. She likes hard squeezes and squishes, and to be thrown into the couch or covered in pillows and blankets. For this reason, we have implemented a weighted vest, which helps her to remain calm and focused. We have also ordered a weighted blanket, which is supposed to help with this as well. Katelyn also craves activities such as swinging, jumping on the mini trampoline, bouncing on a large exercise ball, and playing with Play-Doh and beans.
Last Thursday, I began implementing a brushing program to help with Katelyn's sensory regulation. It involves brushing her arms, back, and legs every 2 hours with a special brush, and then following this with joint compressions. So far, it seems to be working wonders! Last week, she was having frequent meltdowns and was unable to focus on her therapy, but this week, she has been doing great! She is sitting at the table and attending once again and is remaining much calmer throughout the day. I also believe that it could have to do with the fact that she is now getting used to her much more demanding schedule.
With autism comes many challenges, only one of which is sensory needs, but by educating ourselves and being willing to try new and different methods, we will find what works for Katelyn.
It is very common for kids (and adults) with autism to have difficulty regulating their sensory needs and emotions. A lot of these sensory issues can come about due to environmental factors, such as loud noise or bright lights, but the cause is not always obvious. We are still trying to figure out the triggers for some of Katelyn's behaviors and sensory needs.
There are many ways in which to help a person with autism regulate themselves. For instance, sometimes deep pressure helps, which is the case for Katelyn. She likes hard squeezes and squishes, and to be thrown into the couch or covered in pillows and blankets. For this reason, we have implemented a weighted vest, which helps her to remain calm and focused. We have also ordered a weighted blanket, which is supposed to help with this as well. Katelyn also craves activities such as swinging, jumping on the mini trampoline, bouncing on a large exercise ball, and playing with Play-Doh and beans.
Last Thursday, I began implementing a brushing program to help with Katelyn's sensory regulation. It involves brushing her arms, back, and legs every 2 hours with a special brush, and then following this with joint compressions. So far, it seems to be working wonders! Last week, she was having frequent meltdowns and was unable to focus on her therapy, but this week, she has been doing great! She is sitting at the table and attending once again and is remaining much calmer throughout the day. I also believe that it could have to do with the fact that she is now getting used to her much more demanding schedule.
With autism comes many challenges, only one of which is sensory needs, but by educating ourselves and being willing to try new and different methods, we will find what works for Katelyn.
Sunday, April 12, 2009
How I feel about the "cure" and Jenny McCarthy...
Last night, Kevin and I watched the interview with Jenny McCarthy and Jim Carrey on Larry King Live. Here is my personal opinion on the autism "cure" and Jenny McCarthy's efforts in the "war on autism."
I do not believe that we can "cure" our children (nor would I actually want to), but that we can "recover" our children and help them be able to function as close to NT as possible.
I personally am not looking for a "cure" for Katelyn. I believe that our ASD children can teach us so much about acceptance and love and seeing the world in a whole new way, and I am grateful that Katelyn has come into my life. I love all of her little quirks and obsessions and things that make her HER, but of course I also wish for ways to help her with sensory issues, social skills, and aggression. So I would definitely welcome something that would help her "recover" from the things that will be roadblocks in her life, but would I want her "cured" -- never. To me, autism is a large part of who she is and I love her just the way she is.
I also agree with Temple Grandin that if we "cure" autism, the world would actually suffer because there would no longer be social misfits with brilliant minds inventing all of the wonderful things like the internet, etc. Everyone would be too busy socializing
But I respect those parents who are desperately looking for a cure for their child. All of us have different experiences with our ASD kids and only we as their parents know what it is like to raise them.
As far as Jenny, I read her book, Louder Than Words, when I was waiting to get Katelyn diagnosed. I really enjoyed her book and it gave me hope in a time of worry and confusion. I do think that it is great that she and Jim Carrey are on a mission to educate people about autism, and that they are fighting the battle, but I do believe that she is a little overboard and one-sided. I do wish that she would be more careful and more open-minded about the fact that not every child can be "cured" or "recovered" in the ways that her son has been. She needs to be looking out for the needs of EVERY child with autism.
Here is PART 1 of the Larry King interview with Jenny and Jim:
If you would like to watch the rest of the interview, click the links below:
PART 2
PART 3
PART 4
PART 5
If you would prefer to read the transcript from the show,CLICK HERE.
Glossary: NT = neurotypical or "normal", ASD = autism spectrum disorder
I do not believe that we can "cure" our children (nor would I actually want to), but that we can "recover" our children and help them be able to function as close to NT as possible.
I personally am not looking for a "cure" for Katelyn. I believe that our ASD children can teach us so much about acceptance and love and seeing the world in a whole new way, and I am grateful that Katelyn has come into my life. I love all of her little quirks and obsessions and things that make her HER, but of course I also wish for ways to help her with sensory issues, social skills, and aggression. So I would definitely welcome something that would help her "recover" from the things that will be roadblocks in her life, but would I want her "cured" -- never. To me, autism is a large part of who she is and I love her just the way she is.
I also agree with Temple Grandin that if we "cure" autism, the world would actually suffer because there would no longer be social misfits with brilliant minds inventing all of the wonderful things like the internet, etc. Everyone would be too busy socializing
But I respect those parents who are desperately looking for a cure for their child. All of us have different experiences with our ASD kids and only we as their parents know what it is like to raise them.
As far as Jenny, I read her book, Louder Than Words, when I was waiting to get Katelyn diagnosed. I really enjoyed her book and it gave me hope in a time of worry and confusion. I do think that it is great that she and Jim Carrey are on a mission to educate people about autism, and that they are fighting the battle, but I do believe that she is a little overboard and one-sided. I do wish that she would be more careful and more open-minded about the fact that not every child can be "cured" or "recovered" in the ways that her son has been. She needs to be looking out for the needs of EVERY child with autism.
Here is PART 1 of the Larry King interview with Jenny and Jim:
If you would like to watch the rest of the interview, click the links below:
PART 2
PART 3
PART 4
PART 5
If you would prefer to read the transcript from the show,CLICK HERE.
Glossary: NT = neurotypical or "normal", ASD = autism spectrum disorder
Friday, March 6, 2009
Caught in the Net (Swing, that is)...
When we first showed Katelyn the net swing, she was afraid of it and wanted nothing to do with it. Then a few days later, she asked for it out of the blue. We quickly hooked it up, not wanting to miss the golden opportunity to have her try it out. Just like I had expected, once she tried it, she loved it!!! Now she requests the net swing even more than her "baby swing" (that is what she calls the toddler swing).
The net swing is perfect for her because she can either sit up or lie down in it like a hammock. She also loves to snuggle with Giraffe while relaxing in the net swing. It seems to calm her down, which is a huge plus because she has been extra "stimmy" lately. Now when she feels the need to swing, she will go and grab either the net swing or the "baby swing" and drag it over. It is so nice to be able to provide her with one of her favorite activities while also serving her sensory needs.
Here are some pictures of Katelyn and Giraffe enjoying the net swing:
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