Today, on the front page of our newspaper, is a story "When Care Can't Wait-But It Does".
My husband and I read the entire article.
Right now, for what it is worth, this article is the #2 most popular on the Press Connects website. #1 most popular article is one about a man who died in a car crash.
It's about time this issue gains front-page status. This is hidden to a lot of people, but isn't going to be hidden for many people longer, especially as the parents of those "one in every 150" children age...as do these children, once they are adults.
It is going to be very visible.
Bil is just in the "front" of this problem. Soon, his 80ish year old mother is no longer going to be able to care for him. It may be tomorrow, it may be 5 years from now, but it is going to happen.
And, some years ago, she gave up the opportunity for Bil to be in a good placement, because she didn't want to have him leave her house. Now, with increasing disabilities, she finds that Bil can only help her so much. I really don't know what she was expecting. But what is done is done.
We were recently told by the supervisor of service coordination at the agency where Bil receives service coordination that the group homes in downstate NY are closing. And, because my mother in law rejected this placement, he was taken off a group home list. (he is still on another list, NYS Cares).
Bil is in what is called the '2nd tier' of NYS Cares. First tier are individuals who are a danger to themselves or others, or who are in imminent danger of being homeless. Bil right now is not in this situation, but could be at any time. 2nd tier, where he is, is for individuals whose caretakers are aging and might soon be too infirm to care for them.
I want to make it clear that my mother in law cares for Bil by choice. And, because I am not a mother in this situation, perhaps I can not totally understand how she thinks. But it is a matter of frustration, and it is starting up again.
We are going to see Bil and my mother in law sometime in August, and I wonder if this is going to come up. All the interested parties seem to be tap dancing around this-and I have expressed my frustration before.
But with these budget cuts, we have to be active advocates. We can't sit back anymore.
An autistic brother in law entering his senior years. His elderly mother. Our family. This blog chronicles the struggles and joys - and, yes, rants, of life.
Sunday, July 31, 2011
Saturday, July 30, 2011
Summer Reading Autism List
It is interesting that "teen with autism" seems to have become a sub-genre of young adult literature. It doesn't take much guessing to figure out why - with 1 in every 166 births resulting in a child on the spectrum, this becomes a very natural trend.
Here are a couple of books I found out about recently that have teens or adults with autism/Asperger Syndrome as the main characters. Do I plan to read them? Yes, if I can fit them into my summer schedule.
1. House Rules by Jodi Picoult. This won't be the first "autism mystery" book I've read. A couple of years ago I devoured "The Curious Incident of the Dog in the Night-Time" by Joe Haddon. I enjoyed that book very much: the teenage narrator's thought processes were quite believable and a twist in the middle of the book only added to the suspense. It wasn't a book about autism; it was a book that happened to feature a teen with autism as its main character. (note, the book itself does not identify the narrator as someone on the spectrum, but to me it is pretty obvious.)
I read some of the reviews of House Rules on amazon.com and the only thing that concerned me is that a reviewer with Asperger Syndrome thought it did not ring true, that it was more a work of someone who did a lot of research but hadn't really been exposed to people on the spectrum.
I've counted myself fortunate in knowing several people on the spectrum, including a very good friend of my son. And, people on the spectrum can vary quite widely. So I'll have to read and judge for myself.
2. "Marcelo in the Real World" by Francisco X. Stork. This was recommended by the reviewer in #1 above.
Some of the plot of this book seems a bit strange but sometimes those kinds of books are the most rewarding. Other than that, I didn't read the other reviews. This one will be a "surprise me!" book.
If I do read any of them, I'll let you know what I felt about them.
Here are a couple of books I found out about recently that have teens or adults with autism/Asperger Syndrome as the main characters. Do I plan to read them? Yes, if I can fit them into my summer schedule.
1. House Rules by Jodi Picoult. This won't be the first "autism mystery" book I've read. A couple of years ago I devoured "The Curious Incident of the Dog in the Night-Time" by Joe Haddon. I enjoyed that book very much: the teenage narrator's thought processes were quite believable and a twist in the middle of the book only added to the suspense. It wasn't a book about autism; it was a book that happened to feature a teen with autism as its main character. (note, the book itself does not identify the narrator as someone on the spectrum, but to me it is pretty obvious.)
I read some of the reviews of House Rules on amazon.com and the only thing that concerned me is that a reviewer with Asperger Syndrome thought it did not ring true, that it was more a work of someone who did a lot of research but hadn't really been exposed to people on the spectrum.
I've counted myself fortunate in knowing several people on the spectrum, including a very good friend of my son. And, people on the spectrum can vary quite widely. So I'll have to read and judge for myself.
2. "Marcelo in the Real World" by Francisco X. Stork. This was recommended by the reviewer in #1 above.
Some of the plot of this book seems a bit strange but sometimes those kinds of books are the most rewarding. Other than that, I didn't read the other reviews. This one will be a "surprise me!" book.
If I do read any of them, I'll let you know what I felt about them.
Friday, July 29, 2011
A Woman with Breast Cancer - and Autism
I sometimes dread the time that Bil will become seriously ill. You have to know that day will come one day. How will doctors be able to communicate with him? How will we?
One effect autism has on a person is that is makes it very difficult for that person to communicate with others. And it is so difficult to know what that person understands, and doesn't.
Thanks to a blogger with autism who has been blogging about her experiences, readers are going to experience, second hand, how a woman with autism copes with a diagnosis of breast cancer. I need to pay special attention to this.
Donna Williams, a talented artist in her late 40's (who also happens to have autism) from Australia, was recently diagnosed with breast cancer.
One of the special things about Ms. Williams is her ability to communicate. It is much more highly developed than the ability of Bil, or, for that matter, a lot of people with autism. That is what makes reading Ms. Williams blog so special.
She has written several posts over the last several days about her experiences. She has chosen to make them public. I can only wish her the best.
To me it is even more amazing that one of Donna's recent posts is "How Do I Talk to Someone with Cancer?" This comes from her experience when she revealed her diagnosis to others. (Warning - the post contains language some may consider inappropriate).
It doesn't solve the problem of how to communicate with Bil but perhaps reading Ms. William's experience, I will gain some insight for Bil.
One effect autism has on a person is that is makes it very difficult for that person to communicate with others. And it is so difficult to know what that person understands, and doesn't.
Thanks to a blogger with autism who has been blogging about her experiences, readers are going to experience, second hand, how a woman with autism copes with a diagnosis of breast cancer. I need to pay special attention to this.
Donna Williams, a talented artist in her late 40's (who also happens to have autism) from Australia, was recently diagnosed with breast cancer.
One of the special things about Ms. Williams is her ability to communicate. It is much more highly developed than the ability of Bil, or, for that matter, a lot of people with autism. That is what makes reading Ms. Williams blog so special.
She has written several posts over the last several days about her experiences. She has chosen to make them public. I can only wish her the best.
To me it is even more amazing that one of Donna's recent posts is "How Do I Talk to Someone with Cancer?" This comes from her experience when she revealed her diagnosis to others. (Warning - the post contains language some may consider inappropriate).
It doesn't solve the problem of how to communicate with Bil but perhaps reading Ms. William's experience, I will gain some insight for Bil.
Thursday, July 28, 2011
Golden Alerts
Kudos to Andrew Cuomo, the governor of NY, for signing into law a new alert system to alert the public when adults with cognitive impairments go missing or run away. (this is a special problem for people with autism, also.).
I don't like to take political positions but I will mention that people I know of "both sides of the aisle" like Andrew Cuomo very much.
Let's hope he continues benefiting those in our community who struggle with taking care of loved ones with developmental difficulties.
I don't like to take political positions but I will mention that people I know of "both sides of the aisle" like Andrew Cuomo very much.
Let's hope he continues benefiting those in our community who struggle with taking care of loved ones with developmental difficulties.
Tuesday, July 26, 2011
Vacation's Over
Both Bil and we have been on vacation - not together.
It's been nice but it's time to return to reality.
When we returned home, we found a phone message from Bil's new Medicaid Service Coordinator. So trying to get ahold of her is going to be the first order of business.
We have found out a couple of details of the wonderful post-budget cut world for the developmentally disabled, and although we're told Bil won't be affected, I don't believe it.
More details as soon as we know more.
It's been nice but it's time to return to reality.
When we returned home, we found a phone message from Bil's new Medicaid Service Coordinator. So trying to get ahold of her is going to be the first order of business.
We have found out a couple of details of the wonderful post-budget cut world for the developmentally disabled, and although we're told Bil won't be affected, I don't believe it.
More details as soon as we know more.
Sunday, July 24, 2011
Summertime - and the Worry's Not Easy
Summertime is always a challenge for Bil.
He has asthma. And very fortunately, he has an air conditioner in his room.
Before the modern medicines, Bil sometimes had breathing issues in the summertime. Now, with the extremely hot weather we've had in the Northeast, this has become a concern again. He won't exercise (he is afraid of an asthma attack) and, shall we say this delicately, his weight is catching up with him. So he is basically a prisoner in his room. He used to be pretty content in his room, but more and more he seems to want to come out. But with the hot weather, there aren't many places he can go.
Weather is supposed to moderate after today-let's hope so.
He has asthma. And very fortunately, he has an air conditioner in his room.
Before the modern medicines, Bil sometimes had breathing issues in the summertime. Now, with the extremely hot weather we've had in the Northeast, this has become a concern again. He won't exercise (he is afraid of an asthma attack) and, shall we say this delicately, his weight is catching up with him. So he is basically a prisoner in his room. He used to be pretty content in his room, but more and more he seems to want to come out. But with the hot weather, there aren't many places he can go.
Weather is supposed to moderate after today-let's hope so.
Saturday, July 16, 2011
Still Nothing
Right now things have been quiet on the "Bil" front. He's on vacation from work, and we are having no success getting call backs from his new Medicaid Service Coordinator.
Because of things happening in our personal life, we haven't been able to do an every day call thing, like we will have to do. This is one of the prime lessons of advocacy, that you have to keep (in a nice way) persisting. You can't call and then wait and wait and wait. You just have to keep callling until someone answsers the phone.
This is one of the hardest things about advocacy-being persistent.
I realize I haven't been posting very much recently. This will hopefully come to an end in August, when I hope to be posting more.
Because of things happening in our personal life, we haven't been able to do an every day call thing, like we will have to do. This is one of the prime lessons of advocacy, that you have to keep (in a nice way) persisting. You can't call and then wait and wait and wait. You just have to keep callling until someone answsers the phone.
This is one of the hardest things about advocacy-being persistent.
I realize I haven't been posting very much recently. This will hopefully come to an end in August, when I hope to be posting more.
Subscribe to:
Posts (Atom)