Halloween is just around the corner. Stores have had costumes stocked for a few weeks now. With school back in session students will be discussing which characters they will be wearing as a costume or if you are The Sewing Mom you are making costumes.
I have one article on my site for Halloween, which I did three years ago. I want to have more options available for readers to gain insights into the Halloween Experience for the child on the autism spectrum.
My 12 and 13 year old do not participate in Halloween. Their Elementary Schools had parades. I would pick up Matthew early and he would wear regular clothes to school. Now that he is in Middle School I am not sure what the procedure is for this Holiday in terms of wearing the uniform to school or allowing a costume. Nicholas is homeschooled with California Virtual Academy so he will be home.
I am looking for input from families that have had past experiences with their child on the autism spectrum by wearing a costume to school, participating in a party at class or elsewhere, and also those that have parties in their home and take their kids out for trick or treating.
If you have blogged about it and interested in sharing your link please post it in the comments. If you want to create a blog post please let me know your website address so I can follow when it gets posted. If you are planning already for this year you can also comment here about the preparations and let me know if this is something I can include in my article.
As an example I can just say that a Mom in NY to a 4 year old boy did this and that. If you want me to link to your blog please indicate that as well. I would like to have an article helping new families gain insights from other families on what type of costumes kids can handle, how long they last outside doing the visiting of homes, what about barking dogs, diet issues for treats and parties and sensory issues with the costumes and makeup, etc. If there is a certain book, CD or DVD you have used to help prepare for Halloween, please share. I have reviewed a few Winnie the Pooh ones and curious to know if any exist specifically for those on the autism spectrum.
I am looking forward to hearing from other autism families on their experiences sine we just bypass the Holiday and wait for November to show up. If you have any recipes or blog post on gluten casein free treats please share those here.
Saturday, September 6, 2008
PE Activities for Homeschoolers
My 13 year old son who is high functioning on the autism spectrum is in seventh grade. We are utilizing California Virtual Academy, known as CAVA and utilizes K12 curriculum. This is our second year with CAVA. Prior to this Nicholas was in Elementary School in general education with just RSP consult with teacher.
We are doing CAVA for the Middle School years since it is our hope that he will get accepted into The Los Angeles Zoo High School Magnet, although it is College Prep. He wants to work at the Zoo and looking forward to reaching the age you are allowed to volunteer.
This year we will be visiting the Zoo on a monthly basis. I hope to get him a nice camera to take photos like animal photographers do out in the wild. He also likes to visit animal sanctuary websites and Humane society sites. His two main interests are Dinosuars and Cats - big and little cats. He did a report last year on Jaguars that he is very proud of.
The focus of this post is on PE Activities. CAVA has a form parents need to fill out and turn in each quarter, know as the Physical Education Activity Log. Students are required to complete an average of twenty (20) minutes each day. The teaching adult is responsible for completing and submitting the log.
These are activities that are structured, organized and supervised, like participating in an athletic class, dance class or sports team. Activities like bicycling, hiking, jogging or calisthenics are listed as examples.
We have an Exercise Bike from Sears that Nicholas started using last year, but with the September heat here in Los Angeles that is not comfortable. There is also yard work that is done once a week using the Craftsman Reel Mower. I cannot get him motivated to go down to the lake for a few laps, which is what we did last year on the way back from dropping Matthew off at school.
This year the bus picks up Matthew so we can go before 7:30 AM, but many bring their dogs and he is afraid of many of them. There is also a stench down there from the trash and the birds, etc. I had to put my membership with 24 Hour Fitness on hold due to the cost not within my budget at this time.
He is not interested in sports at all. I thought maybe some sort of DVD showing kids exercising might be good to alternate between the bike, outside and walking. I am looking for feedback from other homeschooling families on how they incorporate PE into their daily routine. Also ideas from other autism families on what types of exercise their young teenagers participate in, sports and extra curricular activities.
I would like to do an article on my autism site on the topic of PE and sports. It is a topic I have little experience with my boys and would like links to reviews on DVDs for all age groups and posts from blogs on this topic to include for resources within the article.
At summer camp this year Matthew's class went to the high school and ran around the track. The teacher mentioned to me how fast he was and wanted to know if I was looking into Special Olympics. Than the other day at school Matthew's assistant took pictures of him on the track and said he was really good and mentioned Special Olympics.
Nicholas has a friend from summer camp who swims and is in Special Olympics. Anyone who has a kid in the Special Olympics and has written about the experience is welcome to send me or post the link so I can add that to my article. I was already looking into the Parks and Recreation Services here in Los Angeles. Matthew already has a long day with bus time, so I need to see about weekend offerings in the area. We would probably need someone to assist and that would be through the Regional Center, but with California in a Budget Crisis and funding non existent that is highly unlikely.
Reminder - if you have any input to add about PE activities for homeschoolers or specifically for a kid (tween, teenager) on the autism spectrum, please leave a comment with details, link to post, blog, etc. I am working on an article and will include your link and also feedback for Special Olympics would be helpful as well.
We are doing CAVA for the Middle School years since it is our hope that he will get accepted into The Los Angeles Zoo High School Magnet, although it is College Prep. He wants to work at the Zoo and looking forward to reaching the age you are allowed to volunteer.
This year we will be visiting the Zoo on a monthly basis. I hope to get him a nice camera to take photos like animal photographers do out in the wild. He also likes to visit animal sanctuary websites and Humane society sites. His two main interests are Dinosuars and Cats - big and little cats. He did a report last year on Jaguars that he is very proud of.
The focus of this post is on PE Activities. CAVA has a form parents need to fill out and turn in each quarter, know as the Physical Education Activity Log. Students are required to complete an average of twenty (20) minutes each day. The teaching adult is responsible for completing and submitting the log.
These are activities that are structured, organized and supervised, like participating in an athletic class, dance class or sports team. Activities like bicycling, hiking, jogging or calisthenics are listed as examples.
We have an Exercise Bike from Sears that Nicholas started using last year, but with the September heat here in Los Angeles that is not comfortable. There is also yard work that is done once a week using the Craftsman Reel Mower. I cannot get him motivated to go down to the lake for a few laps, which is what we did last year on the way back from dropping Matthew off at school.
This year the bus picks up Matthew so we can go before 7:30 AM, but many bring their dogs and he is afraid of many of them. There is also a stench down there from the trash and the birds, etc. I had to put my membership with 24 Hour Fitness on hold due to the cost not within my budget at this time.
He is not interested in sports at all. I thought maybe some sort of DVD showing kids exercising might be good to alternate between the bike, outside and walking. I am looking for feedback from other homeschooling families on how they incorporate PE into their daily routine. Also ideas from other autism families on what types of exercise their young teenagers participate in, sports and extra curricular activities.
I would like to do an article on my autism site on the topic of PE and sports. It is a topic I have little experience with my boys and would like links to reviews on DVDs for all age groups and posts from blogs on this topic to include for resources within the article.
At summer camp this year Matthew's class went to the high school and ran around the track. The teacher mentioned to me how fast he was and wanted to know if I was looking into Special Olympics. Than the other day at school Matthew's assistant took pictures of him on the track and said he was really good and mentioned Special Olympics.
Nicholas has a friend from summer camp who swims and is in Special Olympics. Anyone who has a kid in the Special Olympics and has written about the experience is welcome to send me or post the link so I can add that to my article. I was already looking into the Parks and Recreation Services here in Los Angeles. Matthew already has a long day with bus time, so I need to see about weekend offerings in the area. We would probably need someone to assist and that would be through the Regional Center, but with California in a Budget Crisis and funding non existent that is highly unlikely.
Reminder - if you have any input to add about PE activities for homeschoolers or specifically for a kid (tween, teenager) on the autism spectrum, please leave a comment with details, link to post, blog, etc. I am working on an article and will include your link and also feedback for Special Olympics would be helpful as well.
Thursday, September 4, 2008
Housing Options for Autism Families
I enjoy watching House Hunters on HGTV, which airs nightly at 10 PM. Sometimes my 13 year old son Nicholas catches the show as well. We have dreams of moving out of this duplex house we have now rented for over ten years. I regularly peruse Cragislist, Westside Rentals and Mobile Home Village to check new listings.
We cannot live in an apartment or condo. That would mean four neighbors to deal with and having to endure listening to Matthew running across the rooms, banging walls and screaming. Amenities like pool, fireplace, deck, patio and french doors would have to be avoided.
I need to have parking, tired of the street hassles for a space near the house. An on-site laundry room or at least a hook-up would be necessary. Trying to deal with laundry during school holiday times and vacations are not easy. Due to my skin issues with my severe eczema it is essential that I get a dishwasher. Also the bathroom must have a window and fan vent. This will help when giving Matthew baths and starting the toilet training.
We also need a fenced yard and preferably central air conditioning. For many years now I have paid a rental fee to my landlord for the stove and refrigerator, probably paying for appliances two times during this period. I would like a shower that has the sliding door and a garbage disposal for the kitchen sink.
The neighbors next door have their grown sons living theere for many years. It is like a pot festival coming through my windows. Today when the bus arrived my front yard was a stench bucket from them. Earlier in the day our kitchen had smells from the other neighbor. My son Nicholas had problems with his eyes and throat.
I am tired of living at this dump, but there are not many options for us. I also want to try to buy a mobile home by the time I am 50, which is under two years. It is a long term goal that most likely will not get met, but a dream nonetheless.
Nicholas has a dream of living in his own apartment with his cat Junior and another companion animal. He wants to drive a truck and not get married or have kids. I am trying to teach him about finances and what a struggle it is to pay bills and have anything left over.
It would be nice someday to share a house with another autism family and have the street or community consist of families with kids who have special needs. Safety for everyone and living where neighbors know what your life is like and can offer support in many ways.
We cannot live in an apartment or condo. That would mean four neighbors to deal with and having to endure listening to Matthew running across the rooms, banging walls and screaming. Amenities like pool, fireplace, deck, patio and french doors would have to be avoided.
I need to have parking, tired of the street hassles for a space near the house. An on-site laundry room or at least a hook-up would be necessary. Trying to deal with laundry during school holiday times and vacations are not easy. Due to my skin issues with my severe eczema it is essential that I get a dishwasher. Also the bathroom must have a window and fan vent. This will help when giving Matthew baths and starting the toilet training.
We also need a fenced yard and preferably central air conditioning. For many years now I have paid a rental fee to my landlord for the stove and refrigerator, probably paying for appliances two times during this period. I would like a shower that has the sliding door and a garbage disposal for the kitchen sink.
The neighbors next door have their grown sons living theere for many years. It is like a pot festival coming through my windows. Today when the bus arrived my front yard was a stench bucket from them. Earlier in the day our kitchen had smells from the other neighbor. My son Nicholas had problems with his eyes and throat.
I am tired of living at this dump, but there are not many options for us. I also want to try to buy a mobile home by the time I am 50, which is under two years. It is a long term goal that most likely will not get met, but a dream nonetheless.
Nicholas has a dream of living in his own apartment with his cat Junior and another companion animal. He wants to drive a truck and not get married or have kids. I am trying to teach him about finances and what a struggle it is to pay bills and have anything left over.
It would be nice someday to share a house with another autism family and have the street or community consist of families with kids who have special needs. Safety for everyone and living where neighbors know what your life is like and can offer support in many ways.
Labels:
autism,
autism families,
autistic,
behavior,
housing,
issues,
loud,
moving,
neighborhoods,
sensory
Tuesday, September 2, 2008
The To Do List Begins
My nonverbal son Matthew starts school tomorrow. Once he graduated Elementary School in June there was six weeks of summer day camp. After that commenced we had almost four weeks of down time at home.
While autism camp was in session I was able to do laundry and grocery shopping, but during this break Matthew had to accompany me everywhere I went. Several times this meant enduring an attack from behind if I took too long making a choice in an aisle. Waiting too long at the Pharmacy Counter produced similar results. Errands worked best if we went directly to the coloring book section so he could pick one out. But then he wanted to get home so he could color.
I have now compiled my To Do list of errands and things I can do that will go smoother and faster.
Get the car washed
Go to laundromat
Grocery Shopping
Take Nicholas for a haircut
Clothes Shopping
Go to the library
Take Nicholas Bowling
See a Movie with Nicholas
Visit the Zoo with Nicholas
Take Nicholas to Community Day
Paint over the fingerprints on the walls
Take Nick to Dentist for fillings/root canal
Find an Ortho for consult for Nick - needs braces
Find an Eye Dr for me - need exam, new glasses, no vision Ins
Follow up with Dentist for me - need new Dentures, no dental Ins
Take the cat to Vet - flea bath, trim nails
Get back to 24 hour fitness for daily workouts
Start swim lessons for Nicholas
Practice riding a bike - in neighbor's driveway with their bike
Take Nicholas to get hearing and vision test
At home we will no longer have to walk around the kitchen holding our food and plates away from his fingers. Glasses of milk will no longer get dipped by his fingers. The ice cream container will not get squeezed. I will not have to trip over the vacuum cord because he is playing with it while I try to maneuver it away from his grip.
I might not have to lock the bathroom door or see his feet under the door way banging on the door. My face will not be mashed against his while I sit at the computer. Constant running through the hallway and banging the walls will not occur constantly. I am sure there is more that I will be aware of tomorrow and as the quiet days arrive.
I hope to get a lot accomplished during the day so that I can attend to his needs once he gets off the bus. Transitions for the whole family - earlier dinner time and sooner to bed for everyone.
Cheers to a new day.
While autism camp was in session I was able to do laundry and grocery shopping, but during this break Matthew had to accompany me everywhere I went. Several times this meant enduring an attack from behind if I took too long making a choice in an aisle. Waiting too long at the Pharmacy Counter produced similar results. Errands worked best if we went directly to the coloring book section so he could pick one out. But then he wanted to get home so he could color.
I have now compiled my To Do list of errands and things I can do that will go smoother and faster.
Get the car washed
Go to laundromat
Grocery Shopping
Take Nicholas for a haircut
Clothes Shopping
Go to the library
Take Nicholas Bowling
See a Movie with Nicholas
Visit the Zoo with Nicholas
Take Nicholas to Community Day
Paint over the fingerprints on the walls
Take Nick to Dentist for fillings/root canal
Find an Ortho for consult for Nick - needs braces
Find an Eye Dr for me - need exam, new glasses, no vision Ins
Follow up with Dentist for me - need new Dentures, no dental Ins
Take the cat to Vet - flea bath, trim nails
Get back to 24 hour fitness for daily workouts
Start swim lessons for Nicholas
Practice riding a bike - in neighbor's driveway with their bike
Take Nicholas to get hearing and vision test
At home we will no longer have to walk around the kitchen holding our food and plates away from his fingers. Glasses of milk will no longer get dipped by his fingers. The ice cream container will not get squeezed. I will not have to trip over the vacuum cord because he is playing with it while I try to maneuver it away from his grip.
I might not have to lock the bathroom door or see his feet under the door way banging on the door. My face will not be mashed against his while I sit at the computer. Constant running through the hallway and banging the walls will not occur constantly. I am sure there is more that I will be aware of tomorrow and as the quiet days arrive.
I hope to get a lot accomplished during the day so that I can attend to his needs once he gets off the bus. Transitions for the whole family - earlier dinner time and sooner to bed for everyone.
Cheers to a new day.
Labels:
autism,
behavior,
dentist,
errands,
middle school,
nonverbal,
sensory,
to do list
Saturday, August 30, 2008
Seeking Toy Reviews for Kids on the Autism Spectrum
I am hoping to find some families that have a child on the autism spectrum that can share a review on a toy, game, sensory item or something similar. If you are not already an Amazon Associate, I suggest Signing Up for their affiliate program.
The reviews I am requesting are for the Autism Spectrum Disorders site at BellaOnline. September is just about here and traffic pick up at this time for families looking for holiday gifts for their children on the Autism Spectrum.
I am a single parent to two boys on opposite ends of the spectrum, ages 12 and 13. I am interested in getting some reviews from families who have girls and also younger children so there is something recommended on the site for all ages. This call also goes out to those with children who have the diagnosis of PDD-NOS or Asperger Syndrome.
I have been writing at BellaOnline since June of 2005. There is a 400 word minimum for articles. This should be no problem. My articles average 1000+ words. You will need to sign a Guest Contributor Agreement. This is what an article consists of:
Title - under 50 characters
Article Author - you would be listed here as guest author
Date - the article stays in archives and under subject header (toys, music, etc)
Article description - this is 300 characters
Keywords - under 300 characters
Text - 400 word minimum
Subject - I will help with this
Three links - these would be other articles on my site linked at bottom
You can do a sentence or two bio that can be placed at the bottom of the article and include your personal site or blog. Give me your amazon ID and the item on amazon you are reviewing and I will add that to the article. While the article is on the site you will get the amazon associate credit. Articles are never deleted so the article could be at the site for several years. I can help you with the title, description and key words as well.
Here are some examples of mine:
Crayola Folding Table Top Art Easel
This example has more than one product being reviewed, which is also a possiility should guest contributor have a few items and want to combine into one article. An affiliate link for each item can be placed in the article.
Leap Frog Phonics for the low functioning child
Matching and Sorting Activities for the child on the autism spectrum
Movies for children
Music and Software Reviews
I am looking for families that use toys in their home. This is not for those who own companies to market their products. The site gets 55,000 page views a month. This will be an opportunity for sharing about your family, making some amazon affiliate money and linking to your site. There is no compensation, writing at BellaOnline is a volunteer gig.
A newsletter goes out each week so the article will be linked there. Currently there are 1100 subscribers. An article can be clicked to Digg or Del.icio.us. There is a section where visitors can email an article to a friend, bringing more readers to your article.
BellaOnline does not have a comment section, but there are is a forum for the autism spectrum disorders site. I can start a thread there linking your article and can be a place for discussion of the article.
Here is what a Guest Author article looks like, note the top with the name and bottom with contact info.
Please leave a comment if you are interested and let me know the age, sex and toys or related items you can write on. Remember to check out the guest contributor agreeement as well.
The reviews I am requesting are for the Autism Spectrum Disorders site at BellaOnline. September is just about here and traffic pick up at this time for families looking for holiday gifts for their children on the Autism Spectrum.
I am a single parent to two boys on opposite ends of the spectrum, ages 12 and 13. I am interested in getting some reviews from families who have girls and also younger children so there is something recommended on the site for all ages. This call also goes out to those with children who have the diagnosis of PDD-NOS or Asperger Syndrome.
I have been writing at BellaOnline since June of 2005. There is a 400 word minimum for articles. This should be no problem. My articles average 1000+ words. You will need to sign a Guest Contributor Agreement. This is what an article consists of:
Title - under 50 characters
Article Author - you would be listed here as guest author
Date - the article stays in archives and under subject header (toys, music, etc)
Article description - this is 300 characters
Keywords - under 300 characters
Text - 400 word minimum
Subject - I will help with this
Three links - these would be other articles on my site linked at bottom
You can do a sentence or two bio that can be placed at the bottom of the article and include your personal site or blog. Give me your amazon ID and the item on amazon you are reviewing and I will add that to the article. While the article is on the site you will get the amazon associate credit. Articles are never deleted so the article could be at the site for several years. I can help you with the title, description and key words as well.
Here are some examples of mine:
Crayola Folding Table Top Art Easel
This example has more than one product being reviewed, which is also a possiility should guest contributor have a few items and want to combine into one article. An affiliate link for each item can be placed in the article.
Leap Frog Phonics for the low functioning child
Matching and Sorting Activities for the child on the autism spectrum
Movies for children
Music and Software Reviews
I am looking for families that use toys in their home. This is not for those who own companies to market their products. The site gets 55,000 page views a month. This will be an opportunity for sharing about your family, making some amazon affiliate money and linking to your site. There is no compensation, writing at BellaOnline is a volunteer gig.
A newsletter goes out each week so the article will be linked there. Currently there are 1100 subscribers. An article can be clicked to Digg or Del.icio.us. There is a section where visitors can email an article to a friend, bringing more readers to your article.
BellaOnline does not have a comment section, but there are is a forum for the autism spectrum disorders site. I can start a thread there linking your article and can be a place for discussion of the article.
Here is what a Guest Author article looks like, note the top with the name and bottom with contact info.
Please leave a comment if you are interested and let me know the age, sex and toys or related items you can write on. Remember to check out the guest contributor agreeement as well.
Friday, August 29, 2008
Questions for Middle School
I visited the Middle School the other day with my nonverbal son on the autism spectrum along with his male aide. I had the enrollment papers mailed to me to expedite this procedure and be prepared for the visit with my list of questions.
The person at the Attendance Office noticed my two page typed out document entitled Questions for Mioddle School, mentioning how organized I was. After we left that office we were directed to the Counselor's office. Once they realized my son has an IEP we were sent to the Bridge Coordinator. This is the person I will be in contact regarding IEP issues.
I had both IEPs for their office. The triennial in May with the due process IEP naming their school in June. The aide learned of a meeting taking place the day prior to school starting next week. We had a tour of the school, seeing the lunch area, gym building, classroom from outside and restroom facility close by. We finished at the Main office giving them the aides information.
This is the list of questions I asked the Bridge Coordinator:
Teacher name –
# of kids in class –
# of adults in class
Name and ext # for SLP, Adapt PE and OT
Name of Bridge Coordinator
Do they go to library and computer room – how often, where is it
Time for PE, how often, how long
Do you need extra sneakers for PE
Do you need socks for PE or keep same ones on?
Do socks have to be all white?
What is lockdown policy
What is discipline of special ed students policy
When and where is assembly
Phone in classroom
Bathroom in classroom
Lockers in classroom
Daily communication notebook
Where is the bus location
Where does toileting for those with diapers on take place
What is policy when aide on break and lunch
What is policy when aide is out sick for bus
How often is art, music and science – in separate rooms
Which subjects are with general ed classes
Class schedule
Field trips – how often and where in the past
I have previously written two articles at my site that are checklists for visiting classrooms.
Classroom Visitation Checklist - this is for the younger years, including preschool
Visiting Middle School Autism Classes - this is the list I had when I visited some other schools during Spring Break.
The person at the Attendance Office noticed my two page typed out document entitled Questions for Mioddle School, mentioning how organized I was. After we left that office we were directed to the Counselor's office. Once they realized my son has an IEP we were sent to the Bridge Coordinator. This is the person I will be in contact regarding IEP issues.
I had both IEPs for their office. The triennial in May with the due process IEP naming their school in June. The aide learned of a meeting taking place the day prior to school starting next week. We had a tour of the school, seeing the lunch area, gym building, classroom from outside and restroom facility close by. We finished at the Main office giving them the aides information.
This is the list of questions I asked the Bridge Coordinator:
Teacher name –
# of kids in class –
# of adults in class
Name and ext # for SLP, Adapt PE and OT
Name of Bridge Coordinator
Do they go to library and computer room – how often, where is it
Time for PE, how often, how long
Do you need extra sneakers for PE
Do you need socks for PE or keep same ones on?
Do socks have to be all white?
What is lockdown policy
What is discipline of special ed students policy
When and where is assembly
Phone in classroom
Bathroom in classroom
Lockers in classroom
Daily communication notebook
Where is the bus location
Where does toileting for those with diapers on take place
What is policy when aide on break and lunch
What is policy when aide is out sick for bus
How often is art, music and science – in separate rooms
Which subjects are with general ed classes
Class schedule
Field trips – how often and where in the past
I have previously written two articles at my site that are checklists for visiting classrooms.
Classroom Visitation Checklist - this is for the younger years, including preschool
Visiting Middle School Autism Classes - this is the list I had when I visited some other schools during Spring Break.
Six Unspectacular Quirks
I was tagged for this meme by Mama Mara. The rules are stated below:
1. Link the person who tagged you.
2. Mention the rules on your blog.
3. Tell about 6 unspectacular quirks you possess.
4. Tag 6 following bloggers by linking them.
5. Leave a comment on each of the tagged blogger’s blogs letting them know they’ve been tagged.
My six quirks:
1. I cannot use a sheet of notebook paper if it has been torn. I have to throw it out in the recycle bin. Also when I remove a sheet from a notebook I have to stand over paperbag for recycling and use a scissor to cut it evenly to remove those ridges. I am happy to report that my 13 year old son on the spectrum does the same thing. We are neat with our papers.
2. I take this a bit further with paper towels and will not use one if I tear it unevenly. I use paper towels to blow my nose, so when the paper towel is torn I will wipe down the sink or stove before tossing it so it got used.
3. I have this fascination with candles. At family dinners and holidays I would sit there and fling my finger back and forth through the candle. I think the last time I did this was when living in NJ and I was showing my nine year old cousin. His mother did not think it was something I should be showing her child. Since it is just me and my two sons on the autism spectrum, ages 12 and 13 there have not been any dinners with candles, so this quirk of mine stays with me.
4. I never have a utensil out when the toaster is plugged in. I had a fascination with this as a child and avoid temptation for me or either of my kids by never having them on the counter at the same time.
5. I must have all hangers facing the same way. This includes the clothing as well. Recently when watching one of the home selling shows on HGTV they told the lady to do this since her closet had a variety of hangers and they were all in different directions. So this is another efficient and neat quirk to have.
6. I always have to have the emergency brake on. This is just in case the car rolls down the hill on the street. I think this does damage to my brakes so I am weaning myself off of this quirk. I even wrote an article awhile ago called Keeping Compulsions in Check, which mentions some of these as well.
Next I need to tag six people to follow suit and post about their quirks.
teen autism
three channels
Autism Insights
Crazy Jugs
Life With Autism
Composter Mom
1. Link the person who tagged you.
2. Mention the rules on your blog.
3. Tell about 6 unspectacular quirks you possess.
4. Tag 6 following bloggers by linking them.
5. Leave a comment on each of the tagged blogger’s blogs letting them know they’ve been tagged.
My six quirks:
1. I cannot use a sheet of notebook paper if it has been torn. I have to throw it out in the recycle bin. Also when I remove a sheet from a notebook I have to stand over paperbag for recycling and use a scissor to cut it evenly to remove those ridges. I am happy to report that my 13 year old son on the spectrum does the same thing. We are neat with our papers.
2. I take this a bit further with paper towels and will not use one if I tear it unevenly. I use paper towels to blow my nose, so when the paper towel is torn I will wipe down the sink or stove before tossing it so it got used.
3. I have this fascination with candles. At family dinners and holidays I would sit there and fling my finger back and forth through the candle. I think the last time I did this was when living in NJ and I was showing my nine year old cousin. His mother did not think it was something I should be showing her child. Since it is just me and my two sons on the autism spectrum, ages 12 and 13 there have not been any dinners with candles, so this quirk of mine stays with me.
4. I never have a utensil out when the toaster is plugged in. I had a fascination with this as a child and avoid temptation for me or either of my kids by never having them on the counter at the same time.
5. I must have all hangers facing the same way. This includes the clothing as well. Recently when watching one of the home selling shows on HGTV they told the lady to do this since her closet had a variety of hangers and they were all in different directions. So this is another efficient and neat quirk to have.
6. I always have to have the emergency brake on. This is just in case the car rolls down the hill on the street. I think this does damage to my brakes so I am weaning myself off of this quirk. I even wrote an article awhile ago called Keeping Compulsions in Check, which mentions some of these as well.
Next I need to tag six people to follow suit and post about their quirks.
teen autism
three channels
Autism Insights
Crazy Jugs
Life With Autism
Composter Mom
Labels:
autismfamily,
bloggers,
mamamara,
meme,
quirks,
unspectacular
Twitter Tag
I practically start each day checking out Twitter and end the night or early morning hours by refreshing the page one more time as I pass the computer on my way to bed. So when I came across this twitter tag at Swept Away where I was dropping an Entrecard and seeing twitter caught my eye.
{start copy here}
Rules:
+ Answer all the questions.
+ Add your twitter username to the list and leave a comment on this post so I can add you on the master list.
+ Tag other twitter users you know.
1. Who invited you to join twitter? Lisa Shea
2. How many twitter updates have you made since you signed up? 2,835
3. How many direct messages have you received so far? 220
4. On an average, how many twits do you make a day? 20+
5. How many followers do you have? 461
6. How many are you following? 437
7. Have you ever blocked/denied follow requests? yes, spammers and one recently
8. What did you write in your one line bio? writing on autism and advocating for children to be treated with respect from general public
9. Did you even bother to customize your twitter page? Nope, not interested
10. Do you think twitter is cool or is just a waste of time? cool and neat
Twitters: cherryrose | maileen1| autismfamily | Your Twitter Username
{end copy here}
{start copy here}
Rules:
+ Answer all the questions.
+ Add your twitter username to the list and leave a comment on this post so I can add you on the master list.
+ Tag other twitter users you know.
1. Who invited you to join twitter? Lisa Shea
2. How many twitter updates have you made since you signed up? 2,835
3. How many direct messages have you received so far? 220
4. On an average, how many twits do you make a day? 20+
5. How many followers do you have? 461
6. How many are you following? 437
7. Have you ever blocked/denied follow requests? yes, spammers and one recently
8. What did you write in your one line bio? writing on autism and advocating for children to be treated with respect from general public
9. Did you even bother to customize your twitter page? Nope, not interested
10. Do you think twitter is cool or is just a waste of time? cool and neat
Twitters: cherryrose | maileen1| autismfamily | Your Twitter Username
{end copy here}
Labels:
autismfamily,
BellaOnline,
profile,
tag,
twitter,
updates,
username
Tuesday, August 26, 2008
Preparing for Enrollment in Middle School
My 12 year old nonverbal son Matthew starts sixth grade at a Middle School in September. The homeschool for these grades was not acceptable to me so we had to go to Due Process. This took place at the end of the 2007-2008 school year. My main concern was to get into a school that follows the traditional school calendar of September through June. Los Angeles has year round schools with the offer starting a few days after school let out.
By that time I was already in summer camp mode so I did not get all the pertinent details on the class and school options. Once the six weeks of camp was over we took a week off before I delved into the school information. The school was getting new pavement so for two weeks it was closed and then trying to get anyone to answer in Special Education was not possible.
After several attempts I was able to talk someone in the office into mailing me the enrollment papers instead of having to fill these out with my son and his aide there. This preparation process is very necessary when taking a child on the autism spectrum to their new school for the open enrollment first come first serve four day bonanza. It is one of those times I wished there was special treatment for the special education students. I believe hearing my son screaming in the background with my pleading to make life easier for everyone at the office upon our arrival clinched obtaining these forms in the mail.
The forms were overwhelming, asking the years he attended other schools, what age when he first spoke, sat, crawled, fed himself. They wanted to know the dates of hospitalization and last visit to the Dentist. Other pertinent data like a court order about either parent, which I am bringing since I have sole physical and legal custody with the noncustodial parent on
supervised vistation per a custody evaluation years ago.
I put together a folder for the aide that will be taking the bus with my son. I have copies of both IEPs, a print out of the school calendar, a document I typed up with school name, address, phone number, bus route info, meal times and school hours. I also included the original copy of the document I had provided the Elementary School in using for a communication notebook.
I also taped the school picture of my son on the top of the folder and placed an English and a Spanish autism behavior card inside, as well as one of my business cards. I purchased two books about school buses and want one to be kept at school to help my son learn about the bus and as a reminder. I still need to look through my pecs resources to find a few bus picture cards for the schedule at school and his communication device.
I am hoping to have better communication with the school than with the two previous Elementary Schools. There is still the issue of toilet training at school and finding out if that takes place in the Nurse's office or regular restroom.
I was pleased with the information received from the Bus Supervisor when we talked last week. Hopefully it will be a Safe Bus, as well as a safe campus.
I do not want to overload the aide at the start of the school year, but I really feel two books he needs to peruse and share with the teacher/therapist is the one on the oral-motor program and the strategies at hand laminated bookcards that is portable and has tips on assemblies and fire drills.
I am also planning on going over the Basic Skills Checklist book with the aide to see which ones would be useful to new teacher and therapists.
I have typed out a list of questions for the enrollment tomorrow and what does not get answered will hopefully be addressed at the orientation the following night. I tried several times to schedule a tour and was told to just do it after we enroll. I hope they realize this will not be a quick walk through.
By that time I was already in summer camp mode so I did not get all the pertinent details on the class and school options. Once the six weeks of camp was over we took a week off before I delved into the school information. The school was getting new pavement so for two weeks it was closed and then trying to get anyone to answer in Special Education was not possible.
After several attempts I was able to talk someone in the office into mailing me the enrollment papers instead of having to fill these out with my son and his aide there. This preparation process is very necessary when taking a child on the autism spectrum to their new school for the open enrollment first come first serve four day bonanza. It is one of those times I wished there was special treatment for the special education students. I believe hearing my son screaming in the background with my pleading to make life easier for everyone at the office upon our arrival clinched obtaining these forms in the mail.
The forms were overwhelming, asking the years he attended other schools, what age when he first spoke, sat, crawled, fed himself. They wanted to know the dates of hospitalization and last visit to the Dentist. Other pertinent data like a court order about either parent, which I am bringing since I have sole physical and legal custody with the noncustodial parent on
supervised vistation per a custody evaluation years ago.
I put together a folder for the aide that will be taking the bus with my son. I have copies of both IEPs, a print out of the school calendar, a document I typed up with school name, address, phone number, bus route info, meal times and school hours. I also included the original copy of the document I had provided the Elementary School in using for a communication notebook.
I also taped the school picture of my son on the top of the folder and placed an English and a Spanish autism behavior card inside, as well as one of my business cards. I purchased two books about school buses and want one to be kept at school to help my son learn about the bus and as a reminder. I still need to look through my pecs resources to find a few bus picture cards for the schedule at school and his communication device.
I am hoping to have better communication with the school than with the two previous Elementary Schools. There is still the issue of toilet training at school and finding out if that takes place in the Nurse's office or regular restroom.
I was pleased with the information received from the Bus Supervisor when we talked last week. Hopefully it will be a Safe Bus, as well as a safe campus.
I do not want to overload the aide at the start of the school year, but I really feel two books he needs to peruse and share with the teacher/therapist is the one on the oral-motor program and the strategies at hand laminated bookcards that is portable and has tips on assemblies and fire drills.
I am also planning on going over the Basic Skills Checklist book with the aide to see which ones would be useful to new teacher and therapists.
I have typed out a list of questions for the enrollment tomorrow and what does not get answered will hopefully be addressed at the orientation the following night. I tried several times to schedule a tour and was told to just do it after we enroll. I hope they realize this will not be a quick walk through.
Labels:
autistic,
checklists,
enrollment,
IEP,
middle school,
nonverbal,
preparing for school,
student
Thursday, August 21, 2008
Brilliante Web Award - My first blog award
It was a nice surprise when MT of
The Bon Bon Gazette tagged Autism Family Adventures the Brilliante Weblog Award. Thank you for the recognition. I have been writing online for many years, but just started this blog as a way to communicate with readers since Autism Spectrum Disorders @ BellaOnline.com does not support comments. I was feeling left out of the blog world since I was visiting, reading and commenting on autism related blogs.
The rules for this award are as follows:
1. The winner can put the logo on their blog.
2. Link to the person you received your award from.
3. Nominate at least 7 other blogs.
4. Put links of those blogs on yours.
5. Leave a message on the blogs you’ve nominated.
Here are the lucky seven I have chosen:
1. Coping with Disability - Rudy Sims is known as Rudy 10 on Twitter. He was among the first I met at the site. He has shared interesting articles he reads online and writes from firsthand experience as someone with Cerebral Palsy. He is a master at reading and blogging, plus he resides in my homestate of New Jersey.
2. A Deaf Mom Shares Her World - I have known Karen as Barefooter on Epinions for eight years now. We both started writing reviews in January of 2000. While Karen has not been as active in the past year like I have, we have kept in touch over the years through email communication. I joined Disaboom after reading a blog of Karen's on that site. Karen leads a busy life and has a fun personality. I even learned after all this time why she used the pen name barefooter.
3. Fun Cool Collectibles - Christina runs the company that is known as All Things Character Unique. She is busy getting her site ready for the upcoming holiday season. Great ideas for presents for kids. She is also a whiz on Squidoo with a lens on Autism. I hope to emulate her on that site and learn from her expertise.
4. Laura Loves Art - Laura is always on the move and I like her style. It just so happens we were both born in April of 1960. We are also part of the Adoption Triad in different roles. You have to read about the audition Laura took her cat Oliver to for the Meow Mix Think Like A Cat Game Show, it is a fun excursion. I enjoy following her on Twitter.
5. Do It Myself Blog - Glenda has Cerebral Palsy and is known as the left thumb blogger. She has a book entitled, I'll Do It Myself. Here is the trailer. I plan on getting her book soon. She is very outgoing on Twitter. Make sure to read her Accessibility 100 series, which are free and inexpensive tips for improving accessibility for people with disabilities.
6. Floortime Repository - Alexis and her husband created this ning group. In fact thanks to Alexis I am learning my way around the Ning groups I have since joined. Besides her blog at the site there are her home made videos showing therapy with her son. Very dedicated parents that are in the process of creating another website known as Coolest-Kids-Games. This will be another site to check back for holiday gifts.
7. April Tara - April Tara and I have a few things in common. We are both single mothers working at home, homeschooling and we are members that help out other families on the website Wish Upon A Hero. April Tara has launched a website that is seeking bloggers, But What About The Kids. This is a unique site since it targets custody, co-parenting and court issues. I should share my past experience with supervised visitation.
I enjoy reading these blogs and award this recognition to each of them.
Labels:
autism,
Brilliante Weblog Award,
recognition,
tag
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