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Savvy mom of two on the autistic spectrum. Writing about special education, advocacy and community support for parents of children with special needs.
Tuesday, October 21, 2014
Taciturn Tuesday - Biological Basis for Sensory Processing Disorder
Thursday, October 16, 2014
Tranquil Thursday: Yoga for Kids on the Spectrum
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and also check this video:
Wednesday, October 15, 2014
The Short List Social Story: How to Write a Better Social Story
We have had to use several social stories for various activities with Sensi. The scariest for me was this emergency situation.
Recently we had to do a blood draw and needed a social story. The first time we went in it was a failure. We had just finished up with our well checkup and the doctor needed Sensi to give some blood to check her levels for iron and vitamin D.
We went down to the lab, signed in, drank some water and waited. I explained to the phlebotomists that day that Sensi has autism and they need to explain everything to her so she understands what they are doing so she doesn't feel afraid. They had trouble finding a vein to use and then after prodding and tapping her arms for about 5 minutes they called in another technician. The new tech was irritated that Sensi had taken off the rubber band while we waited for her. She also instructed yet another technician to hold Sensi's other arm. She put the needle in without any warning aside from all the instructions to the other techs, and Sensi pulled away from the pain. She said very irately "She backed off the needle!" I just replied that we are done for the day and we'll come back another time, and asked if Sensi could get her lolly. They were surprised and I think a little relieved to not have to hold down a kid to get a blood draw. We left before there were any bad situations to undo and gave it another try another day.
I googled social story blood draw and came up with this: oneplaceforspecialneeds.com/main/library_blood_test It has lots of information about the environment and interesting pictures.
But upon discussing it with Sensi's speech therapist we decided that there were too many steps and too much information to address the issue at hand. She reduced the process down to 8 short steps, and practiced with her the day before the next try. We practiced again that night, and I reminded her and showed her the steps before we went into the clinic.
1.Sit in chair with hot pack on arm
2.Rubber band will squeeze around my arm
3.Put arm flat
4.The Nurse will tap,tap,tap, flick, poke.
5.They will stick the needle in, hold still. It will hurt a little bit.
6.(Pop sound effect) they will pull the syringe out
7.(Pop sound effect) they will pull the needle out
8.(Smack sound effect) Put a band-aid on.
The nurse has the blood, I am all done helping the doctor.
The most important thing I learned this time around is to be prepared with a social story for the medical staff. When we arrived I showed the short list social story to the phlebotomists, and explained that Sensi has autism and we worked out a story with her teachers. They all read the list and followed the script closely. I saw they made sure to check it a couple of times.
Since Sensi knew the steps and the medical staff knew the script everyone was comfortable with what was going on and it made everything go smoothly and quickly. I was relieved it went so well, and I think everyone else was too.
Resources:
Sarah H, SPL
http://www.oneplaceforspecialneeds.com/main/library_blood_test.html
Recently we had to do a blood draw and needed a social story. The first time we went in it was a failure. We had just finished up with our well checkup and the doctor needed Sensi to give some blood to check her levels for iron and vitamin D.
| image via: http://www.bestalliedhealthprograms.com/wp-content/uploads/2012/07/phlebotomist-job-description.jpg |
We went down to the lab, signed in, drank some water and waited. I explained to the phlebotomists that day that Sensi has autism and they need to explain everything to her so she understands what they are doing so she doesn't feel afraid. They had trouble finding a vein to use and then after prodding and tapping her arms for about 5 minutes they called in another technician. The new tech was irritated that Sensi had taken off the rubber band while we waited for her. She also instructed yet another technician to hold Sensi's other arm. She put the needle in without any warning aside from all the instructions to the other techs, and Sensi pulled away from the pain. She said very irately "She backed off the needle!" I just replied that we are done for the day and we'll come back another time, and asked if Sensi could get her lolly. They were surprised and I think a little relieved to not have to hold down a kid to get a blood draw. We left before there were any bad situations to undo and gave it another try another day.
| image via: http://inspirably.com/uploads/user/27189-another-day-another-try.png |
I googled social story blood draw and came up with this: oneplaceforspecialneeds.com/main/library_blood_test It has lots of information about the environment and interesting pictures.
| image via; http://www.oneplaceforspecialneeds.com/images/content/blood_draw3_med.jpg |
But upon discussing it with Sensi's speech therapist we decided that there were too many steps and too much information to address the issue at hand. She reduced the process down to 8 short steps, and practiced with her the day before the next try. We practiced again that night, and I reminded her and showed her the steps before we went into the clinic.
| image via: http://brandimpact.files.wordpress.com/2012/07/id-10043426.jpg?w=250&h=250 |
Blood Draw Short List Social Story
1.Sit in chair with hot pack on arm
2.Rubber band will squeeze around my arm
3.Put arm flat
4.The Nurse will tap,tap,tap, flick, poke.
5.They will stick the needle in, hold still. It will hurt a little bit.
6.(Pop sound effect) they will pull the syringe out
7.(Pop sound effect) they will pull the needle out
8.(Smack sound effect) Put a band-aid on.
The nurse has the blood, I am all done helping the doctor.
| image via: http://www.learnblooddraw.com/wp-content/uploads/2014/04/Phlebotomist-At-Work-199x300.jpg |
The most important thing I learned this time around is to be prepared with a social story for the medical staff. When we arrived I showed the short list social story to the phlebotomists, and explained that Sensi has autism and we worked out a story with her teachers. They all read the list and followed the script closely. I saw they made sure to check it a couple of times.
Since Sensi knew the steps and the medical staff knew the script everyone was comfortable with what was going on and it made everything go smoothly and quickly. I was relieved it went so well, and I think everyone else was too.
Resources:
Sarah H, SPL
http://www.oneplaceforspecialneeds.com/main/library_blood_test.html
Tuesday, October 14, 2014
Taciturn Tuesday: Myths about Sensory Integration Disorder
Thursday, October 9, 2014
Tuesday, October 7, 2014
Taciturn Tuesday: Social Story for a Medical Test
Thursday, October 2, 2014
Tranquil Thursday: MSN Yoga Videos
Tuesday, September 30, 2014
Taciturn Tuesday: Asperger Experts
Thursday, September 18, 2014
Tranquil Thursday: MyFreeYoga
| image via: http://media-cache-ak0.pinimg.com/736x/0c/1a/53/0c1a5390b42574393ef6312f2412898a.jpg myfreeyoga.com |
Wednesday, September 17, 2014
Special Education Parent Skill Set
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Sitting in the waiting room at one of my kids' therapy appointments, I met a mom who is just starting her special education journey. Our conversation made me realize that being a special education parent you evolve a certain skill set. With practice you get good at some things that may not come naturally to you and are not taught. Most of us learn this by trial and error.
| image via: http://studyhungary.dev.xtremedia.hu/upload/images/comm.jpg |
Communication - Once you are a special needs parent it is important to communicate what your child needs and to advocate for them. You are going to have to communicate with lots of different professionals. Make sure you understand what they are telling you and ask lots of questions. Also make sure they understand what you are telling them. I send a getting to know you letter to my children's educators every year. This year I also discovered it was helpful to share that information with the transportation staff too.
| image via: http://www.theopennotebook.com/wp-content/uploads/2011/10/ask-215x300.jpg |
Ask for what you need - If your child needs something, the sad truth is you are going to have to ask for it. There may be offers for help here and there but if your child or family needs something from a school district, or the local government you most certainly have to ask. The honest truth is that's how they keep their costs down. They sometimes can't help you UNTIL you ask, so ask.
| image via: http://tweakyourbiz.com/management/files/shutterstock_187332701.jpg |
Hold the professionals accountable- If you don't understand what is going on with your child at school ask for some explanation. Once your child is labeled and designated special needs you get either an IEP or a 504. As a parent of a child with an IEP you can call a meeting to discuss their services at any time of year. If the school district withholds information or services, remind them of your rights. Wrightslaw.com is a great resource for what you can legally advocate for and what you should expect from the professionals serving your child.
Persistence - Sometimes you will have to ask more than once, or someone will have a bad attitude when you deal with them, and you need to devise a work around. You will have to continue to advocate for your child even in the face of an adversarial attitude and ignorance. Keep trying and keep looking for a solution or resolution. Resources are limited and sometimes they count on you giving up. Don't give up.
Problem solving- I have been a noodler since I was a kid, so problems solving and puzzling out solutions is a natural state for me. Sometimes the problems are bigger than your abilities or experience. Look for solutions in other places if you are not getting what you need from your local school district. Ask for help from local advocacy agencies like your local autism society or your local version of PACER. I home schooled my son with K-12.com last year when his transition to middle school failed. I also pulled my daughter from the school district when they targeted her autism program for elimination. Even though her school placement last year was far from ideal, it positioned us to be one of the first families to attend the new autism school in the special education district that serves the northern suburbs of our area.
| image via: http://media-cache-ak0.pinimg.com/736x/89/ec/eb/89eceb77fa0f69aa49fa8aa4775a09e2.jpg |
Pick your battles/Know when to cut your losses-If the school district has decided that all special education students belong in the general student population no matter what their needs, there isn't much you can do about it besides a lawsuit. That takes time, (which you don't have since your child's development is at stake,) and money. You may be able to win a legal battle, but sometimes its just best to look for your solution somewhere else. I am not saying not to go through the steps of advocacy. Talk to your school board, the special education department, even your local newspaper. But sometimes you cannot change the tide and you need to devote your energies elsewhere.
| image via: http://lisbethcalandrino.com/wp-content/uploads/2012/10/networking1.jpg |
Networking - Look for other parents either online or in your school district. Having a special needs child can be isolating. There usually aren't enough of us concentrated into our neighborhoods and with enough free time to form a local support group. You may be lucky and get someone from the school district to host a monthly support meeting. You should look to see if there is a special education advisory council in your school district and join. This is where you will get the information of what the school district plans are for special education in the coming months or years.
The online special needs community is there for you 24/7 or at least as often as some of us can get to a computer. There are Facebook pages and groups, as well as lots of blogs to follow (Snagglebox has been one of my favorites.) You may be overwhelmed by all the information available about your child's diagnosis at first, but with time you will find your trusted information sources. The Thinking Person's Guide to Autism, Autism with a side of Fries, and Shut Up About Your Perfect Kid are some examples of my favorite special needs communities online.
Tuesday, September 16, 2014
Taciturn Tuesday: Sensory Triggers
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Thursday, September 11, 2014
Tranquil Thursday: Autumn Roses
Tuesday, November 5, 2013
Taciturn Tuesday: Hiatus
| image via: http://www.publiusnm.com/2012/11/publiusnm-on-hiatus/ |
Thank you to all who have visited and commented here. I have started home schooling my oldest with K-12.com, and have found I don't have the time to attend to a blog regularly. Sensi is doing well in her new school at a neighboring district. I will still keep my pages on Facebook and Pinterest, and will share any tidbits I find there. I expect to return to blogging when my son, Random goes back to a brick and mortar school. Again, thank you for your interest and support.
Thursday, October 31, 2013
Thursday, October 17, 2013
Tranquil Thursday: Small Blue Dot
Tuesday, October 15, 2013
Thursday, October 10, 2013
Wednesday, October 9, 2013
Bullying in Schools: Elementary to Middle School, Our Experience
| image via: http://www.startribune.com/local/stpaul/184573741.html |
Bullying in middle school starts
in the first week of classes, when students are establishing their
status and friendships. They may try bullying a student to impress
others or just to make themselves feel better.
The teachers and administration need
to be proactive in this issue. To announce their expectations for the
students' behavior as much as they emphasize the expectations for
homework.
When bullying occurs, teach the whole
class what the expectations are, again. Bullying is not acceptable,
the parents of the bully should also be taught what the expectations
of behavior are for their children.
Peer mediation fails at all grade
levels as it gives the bully a platform to intimidate again.
The attitude we experienced of the middle school
staff, specifically, the social worker, towards verbal bullying is
weak and ineffective. It was stated to me that “well, at least
he's not in danger of getting stabbed or shot, the kids are just
using words...” Word will and can drive a student to suicide as discussed in several articles in Psychology Today :
and also here:
The school districts policy toward bullying is intentionally vague:
The District cannot monitor the activities of students at all times or eliminate all bullying. However, to the extent such conduct affects the educational environment of the school district and the rights and welfare of its students and is within the control of the school district in its normal operations, it is the District’s intent to:
• Prevent bullying by teaching and modeling positive behavior, and
• Investigate, respond to, remediate, and discipline bullying behavior that has not been successfully prevented.
The District cannot monitor the activities of students at all times or eliminate all bullying. However, to the extent such conduct affects the educational environment of the school district and the rights and welfare of its students and is within the control of the school district in its normal operations, it is the District’s intent to:
• Prevent bullying by teaching and modeling positive behavior, and
• Investigate, respond to, remediate, and discipline bullying behavior that has not been successfully prevented.
| image via: http://threatormenace.com/2012/06/14/exclusion-the-ties-that-bind-us/ |
The social worker's solution was to
observe the classes for the bullying behavior. What bully is going to
engage in that behavior with an extra set of adult eyes watching? The
result was she and other adults saw no peer interaction with my
child. So basically, if they are not bullying him they will ignore
him and exclude him.
I find the lack of a coherent bullying policy negligent on the part of the school district. I have been aware of the need of a policy for student behavior since my child was in the first grade. We moved schools in 3rd grade because of the ham-fisted way our neighborhood elementary school handled the situation. It was so bad that I began to feel bullied by the principle. I was called and yelled at by the principal. I was told not to talk to the other children without the consent of the parents when all I had done is model for my son (who was yelling at his bully,) to state calmly to the bully what behavior was bothering him. The end result was I was informed that bullying can go two ways and my child and I were part of the problem.
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| image via: http://katyshamitz.blogspot.com/2011_07_01_archive.html |
I find the lack of a coherent bullying policy negligent on the part of the school district. I have been aware of the need of a policy for student behavior since my child was in the first grade. We moved schools in 3rd grade because of the ham-fisted way our neighborhood elementary school handled the situation. It was so bad that I began to feel bullied by the principle. I was called and yelled at by the principal. I was told not to talk to the other children without the consent of the parents when all I had done is model for my son (who was yelling at his bully,) to state calmly to the bully what behavior was bothering him. The end result was I was informed that bullying can go two ways and my child and I were part of the problem.
This was not the case. My child was
systematically bullied by the other child multiple times and the
school had been made aware of the problem previously. This was the
second year that my child had been bullied in their school. Rather
than beat my head against a wall constructed by an insensitive,
ignorant administration at the school, I moved my son to a different
school within the district. We still had some trouble with
bullies, but it was dealt with in a explicit and efficient manner and
it was made clear to the student and parents what was acceptable
behavior. I have had to use moving schools as a strategy twice now in
his school career to deal with bullying, and he is only in 6th
grade.
| image via: http://murray.spps.org/aboutus |
I have instructed my child that for the
remainder of the time he is in school, if he is bullied he
is to walk away from the bully. He is to tell the teacher he is
being bullied and wants to go to the office, once there he is to tell
the staff that he is being bullied and he wants to go home, and I
will come and pick him up. This not only makes the teachers aware of
what is happening in their classrooms it makes the school
administration aware of it too. A bonus is it tracks the class it
occurred in and my child doesn't have to endure an entire day of
being bullied.
resources: Saint Paul Public Schools Policy 505.00
Adopted: 8/21/2012, page 84/164
SPPS_POLICY_MANUAL_REV._2008-ALL.pdf
resources: Saint Paul Public Schools Policy 505.00
Adopted: 8/21/2012, page 84/164
SPPS_POLICY_MANUAL_REV._2008-ALL.pdf
Tuesday, October 8, 2013
Taciturn Tuesday - Thoughts on Neurodiversity
Thursday, October 3, 2013
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