If you've been reading while I was away...you know that I had a fabulous trip! For 5 days I was able to forget who I am, what I do, and just be. I am a woman -an adult who can laugh with her friends and family. Free like a bird -I came and went taking full advantage of my independence. I spa'd, danced, laughed, dined, cocktailed and chatted with old friends and siblings. It was great -until I got to the airport to come back home when I get one of those infamous phone calls.
Yes -that's right. The shit hit the fan on my very last day. My mom calls to ask me a question about medication. She also fills me in on the days events. "We had the opportunity to walk in your shoes today. We now know what you go through."
This time, my husband was there to field the phone call from school, "You need to come and pick up your son. We can't put him on the bus because he is seeking attention by making suicidal threats." Aspergers dad -was in the middle of carpooling Blue and his friends when he gets the call. He had to drop them off and go over to the high school to retrieve an angry, unhappy Aspergers teen.
After a conversation with the school Psych -Red apologized for making those statements. He says he was just angry and didn't know what else to say to express his anger. There is a wall full of positive statements written and posted all over the walls to remind him of all of the good things in his life. The staff is trying their best to be supportive.
By the time they get home...he goes back to the negative script, "Ms. so and so is just mean! No one cares about me! The work is just too hard! The classes are too loud. I hate the cafeteria. Maybe I should go to the hospital. I have no other choice."
The following morning I call his Psychiatrist's office to fill her in on the days events. She wants to see him. Instead of me falling back into bed because I am jet-lagged, I get myself together to take him to see her. She almost hospitalized him based on his statements. He talked his way out of it. Assured her that he just needed to rest at home and wait for the tweak in his medication to kick in. He promised that if he had any more serious bouts with anger he would be willing to go to the hospital. She gave him a mental health day off from school and sent us on our way with a medication adjustment.
It just doesn't seem right that a kid should have so many different meds on board just to make it through the day at school. At the same time, we can't have him exploding all over the place, making threats and creating havoc at school and at home making himself and everyone around him miserable. The whole situation is just screwed!
It's a really difficult decision to give your kid medication, but when he's full of anxiety, depression, anger and heavy moods you feel helpless. I feel inclined to take the advice of the professionals who are close to the situation and have all of the facts to help them make an informed decision on how to proceed. I just wish their was a better way -you know, like a miracle.
If you have any thoughts or feelings about your child, Aspergers and medication...I would love to hear your feedback.

Yes -that's right. The shit hit the fan on my very last day. My mom calls to ask me a question about medication. She also fills me in on the days events. "We had the opportunity to walk in your shoes today. We now know what you go through."
This time, my husband was there to field the phone call from school, "You need to come and pick up your son. We can't put him on the bus because he is seeking attention by making suicidal threats." Aspergers dad -was in the middle of carpooling Blue and his friends when he gets the call. He had to drop them off and go over to the high school to retrieve an angry, unhappy Aspergers teen.
After a conversation with the school Psych -Red apologized for making those statements. He says he was just angry and didn't know what else to say to express his anger. There is a wall full of positive statements written and posted all over the walls to remind him of all of the good things in his life. The staff is trying their best to be supportive.
By the time they get home...he goes back to the negative script, "Ms. so and so is just mean! No one cares about me! The work is just too hard! The classes are too loud. I hate the cafeteria. Maybe I should go to the hospital. I have no other choice."
The following morning I call his Psychiatrist's office to fill her in on the days events. She wants to see him. Instead of me falling back into bed because I am jet-lagged, I get myself together to take him to see her. She almost hospitalized him based on his statements. He talked his way out of it. Assured her that he just needed to rest at home and wait for the tweak in his medication to kick in. He promised that if he had any more serious bouts with anger he would be willing to go to the hospital. She gave him a mental health day off from school and sent us on our way with a medication adjustment.
It just doesn't seem right that a kid should have so many different meds on board just to make it through the day at school. At the same time, we can't have him exploding all over the place, making threats and creating havoc at school and at home making himself and everyone around him miserable. The whole situation is just screwed!
It's a really difficult decision to give your kid medication, but when he's full of anxiety, depression, anger and heavy moods you feel helpless. I feel inclined to take the advice of the professionals who are close to the situation and have all of the facts to help them make an informed decision on how to proceed. I just wish their was a better way -you know, like a miracle.
If you have any thoughts or feelings about your child, Aspergers and medication...I would love to hear your feedback.

Adelaide Dupont · 285 weeks ago
And for those of us who knew and appreciated these points in high school to a greater or lesser extent - always good to have a refresher and feel them through the current and future generations who we survived to be able to see.
I especially appreciated points 5, 7 and 10.
And young women not settling or settling down yet is a good thing.
"It's never too late to live our dreams" - but it may be too early for some of them!
And 8 of course.
nicole · 243 weeks ago
Risa · 230 weeks ago
LAH · 221 weeks ago
Maira L. Coral · 216 weeks ago
I was looking for information for my Multi-Genre Disability Research Project from my Early Childhood Special Education class on the web, when suddenly I came across your blog. I started reading this out of curiosity and I want to tell you that as you said yourself, you will not be Amanda Gorman, but you managed to make me shed some tears, perhaps because I felt totally identified with your words, especially in the part that you speak of your son. My son also has Asperger's syndrome, he is 19 years old and he is in the second semester of College. Also like yours, he takes classes from home, likewise my eldest daughter is also taking college classes from her room. At the same time, that I work as a preschool teacher from my kitchen through a computer, my husband sleeps in the room during the day because he works at night. Also in the afternoons I myself take virtual school classes. I am a 51-year-old Latin woman who began to learn the English language as adult, so maybe you find some deficiencies in my writing, however, I was very moved by how proud you express yourself about your son. Referent your mother, I liked the humorous tone that you give when your talk about her, so I did not want to miss this opportunity and stopped my assignments for a moment to let you know that your words do make a difference, since they reach the heart of at least those who have opportunity to read you. I want confess you that is the most long I have written to someone I don't know, because your words inspired me, thank you...
Gavin Bollard · 209 weeks ago
Thanks for this post. I've been very distracted of late and so this was how I found out about our friend Kate. Kate's struggles were very real but they were so constant and so wide-ranging that it was difficult for people around her to address them. I think it's going to take a while longer for me to process all this.
I learned so much from Kate because she was always quick to point out the many injustices in the world. In her glory days, she was very much a crusader and she cared for everyone. Over the years, as her situation took its toll, I came to realise that it was the fact that she couldn't be put in a single specific category, that made the system fail her. She needed help that they weren't set up to provide.
She needed more care and she needed to be less alone. I'm so sorry that this has happened.
For a long while we were corresponding almost every day but a couple of months ago, I realised that she had become so stressed that nearly every interaction I had with her was starting to trigger her. I backed away to give her a bit more space. She only had a little time that she could stand to be online and there were too many things that she wanted to do in that time. I thought that by taking a step back, she could reach out to more people who might be geographically closer and able to assist.
Kate was a beautiful soul and she will be sorely missed by all of us.
diyalabs6192603 11p · 192 weeks ago
Robots for kids
Robotic Online Classes
Robotics School Projects
Programming Courses Malaysia
Coding courses
Coding Academy
coding robots for kids
Coding classes for kids
Coding For Kids
Spoil your cat · 122 weeks ago
Many of these living arrangement aren't good, and many of the people who run those places really don't have the residents' best interest at heart. Those places are like old age homes and foster homes, where you sometimes hear horror stories. They're hard to trust. But then there are good ones, of course.
The best thing for an autistic adult is either to go on living at home or working and renting an apartment and living independently, but that isn't always an option.
Duncan · 112 weeks ago