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Autism- oh the places you will go!


 All I can say is that I've missed everyone!
 



I am back. Who knows for how long, or how much, but for today, I'm back. I've missed everyone, and I promise I have read all of your wonderful comments, and I appreciate every one of them.

This has been one long and ridiculous rollercoaster ride this year. Right now I'm not sure if we're on our way up or down. Maybe we're on the part that just spirals. Who knows. I would really like to just stop and get off and take a breather.

I don't even know where to start up again. Let's see...we've all been sick multiple times this year, the most recent being me this past weekend. It was pretty bad. I'm wondering if it was food poisoning actually. Fever of 102, vomiting, diahrrea, chills, cramps, etc. I know what you're thinking...yummy, right? I'm still not quite right, and not eating real food just yet. Then there's the fact that my son has put my neck out of place twice this year. Again- no fun. I'll go into detail about it another time. Oh, and by the way, we were denied crisis by the judge. Also, we went into an incredible amount of debt over the last several months to replace flooring and furniture in the house, as well as to paint the entire interior. Disaster. All of it. The furniture was purchased in January...we are still missing pieces that went on "backorder" right after we purchased it. We had a leak with our air handler, and it ruined 1/2 of our laminate flooring, so we are walking on concrete in our family room for now. Loni has managed to bust a hole in the wall in the same spot 5 more times after it has been repaired each time. I finally told the person fixing it to just leave it alone. Then I was told that my washer was leaking. So, with hardly any money left, I went out and bought a brand new set on my credit card. As it was being delivered, I found out it wasn't the old washer that was the problem, it was my connections. It's a long story, but it was too late to turn back at that point. My oldest son fell skateboarding and busted his lip open and broke his two front teeth. I had one of my group members completely bash me in an email to me, my friends, my family, and part of the school system...that was fun. She apparently thought a prayer request was too much. There is oh-so-much-more, but I think I've given you an idea of why I've been a schmuck and haven't blogged in a while.

I will make an honest effort to write more. I promise!!

Thanks for being so understanding!!
~Leslie

P.S. We were in the paper today...here's the article (with my son's name changed to "Loni"):

Wait Is All Many Disabled Can Do

When "Loni" gets upset he bangs his head on the nearest surface available - the tile floor, the counter, his mother.

A 5-inch-by-5-inch hole in the kitchen of his family's Spring Hill home is proof of the 5-year-old autistic boy's condition. So are two neck injuries his mom endured. And the now-repaired family-room window through which he once thrust his head.

"Loni", who doesn't speak, is one of 14,528 disabled Floridians on a six-year waiting list for funds to help pay for therapy, job coaches, home nurses, even dental treatment. Their disabilities range from mental retardation and autism to spina bifida and cerebral palsy.

Another 6,095 are waiting for increased Medicaid assistance through a program called Home and Community-Based Waiver.

Among those waiting is Christopher Morris, a 9-year-old mentally retarded and mentally ill Largo boy whose grandmother gave up her pets last week to keep them safe after his return home. Reports about his case in the St. Petersburg Times spurred the state to provide him temporary crisis funding through June.

But as the waiting list for people like Christopher nears an all-time high, state lawmakers are debating whether to limit how much can be spent on 30,000 disabled people statewide.

Hardly mentioned is what it would take to care for people like "Loni" who are on the waiting list and get nothing.

His family has been waiting three years.

"I feel desperate," said Loni's mother, Leslie, 30, who also has a 4-year-old autistic daughter and a 13-year-old son. "I know how precious every month is that ticks away that he doesn't get the help.

"It's setting his pattern for life more and more."

Lawmakers are considering various plans to limit spending because of a $153-million deficit at the Agency for Persons With Disabilities.

Some lawmakers said they have no choice but to control spending because of the deficit and the escalating expenses for those receiving services.

In 2006 the cost of services increased 12 percent over 2005.

"We are basically balancing the budget on the backs of the people they serve," said state Rep. Loranne Ausley, D-Tallahassee. "It's not their fault that the agency was mismanaged."

One House proposal would cut two-thirds of services to some people and place a cap on what they receive annually at $14,000.

Last year, the average waiver was $30,589, but hundreds of severely disabled people receive more than $100,000 in services.

The cuts are painful, said state Sen. Nan Rich, D-Sunrise, vice chairwoman of the Health and Human Services Appropriations Committee.

"We want to make sure everybody who needs services gets them," she said. "We also want to make sure people are not getting more services than what their needs are."

Growing cost

Rich said one reason the waiting list is so long is the growing cost of services. If spending is capped, she said, the money could be stretched to reach more people.

Advocates for the disabled are alarmed.

"It basically takes us back to the old days of institutions," said Sue Buchholtz, chief executive officer of the Pinellas Association for Retarded Children, which operates group homes and provides other services to about 700 disabled people in the Tampa Bay area.

Families and advocates believe many disabled people will withdraw from the community because they'll no longer be able to afford the aides who help them live and work independently.

"We're going to put people in crisis," said Debra Dowds, executive director of the Florida Developmental Disabilities Council. "We recognize there needs to be some changes. The problem is the level they've done is way too severe."

Dowds also fears the cuts will pit families on the waiver and those on the wait list against each other. "We need to be funding people on the wait list," Dowds said, "but not at the expense of people currently receiving services."

The waiver program, which receives state and federal funding, was designed to keep the disabled out of costly institutions that isolate them from society.

But funding has always run short. So many wait.

The waiting list has been the subject of several federal suits.

When Jeb Bush became governor in 1999 he vowed to eliminate a decades-old waiting list of 10,000. But as the old list dissolved, a new one grew. By 2002, the new list had 6,000 names.

"We were catching up, but we were not keeping up," said the agency's regional director in Tampa, Carl Littlefield.

The Agency for Persons With Disabilities had a record waiting list in November 2004 of 15,500.

Even though lawmakers added $350-million since 2001, Rich said, it was not enough.

No new approvals

In January the state stopped approving new people for the waiver, though it continues to add names to the waiting list. Each month it approves funding for a few people in crisis, like Christopher Morris. But families worry about those who get nothing.

"No individual should sit at home watching TV all day," said Palm Harbor's Ann Millan, 67, whose daughter, Robin, 36, has autism. "That's what would happen."

Robin Millan, a Publix cashier, has received the Medicaid waiver since 2000. It helps pay for her language therapy and provides someone to help her pay bills, buy groceries and clean the condominium where she lives alone.

Annemarie Prater, 29, of Spring Hill wishes lawmakers could see the needs in person.

"If these people in Tallahassee would just have one hour in our life, they'd probably cry all the way home," Prater said.

Last month, she and her husband received crisis funding for their autistic son, Kevin, 9, after she nearly wrecked her car on U.S. 19 when he unbuckled himself.

He has been on the waiting list since 1999. And even though her son is getting crisis help, she said she still has to find people willing to work with her son: someone to help him with his behavior problems, someone to go with her during doctor's appointments, someone able to drive to her rural home and accept the waiver's low pay rates. "My goal for him is to be able to function a little bit," Prater said. "My son didn't ask to be this way.

"The way it's going, it's like they wait for your child to be totally out of control before they step in."

Times researchers Angie Drobnic-Holan and Caryn Baird contributed to this report. Melanie Ave can be reached at 727 893-8813 or mave@sptimes.com.

Medicaid waiver

Purpose: to keep the developmentally disabled out of institutions.Receiving the waiver: 25,293. Overall, 31,388 receive various waiver services.

Waiting: 14,528 people who receive no services and 6,095 who seek additional services.

Who: people with developmental disabilities including mental retardation, autism and cerebral palsy. About 70 percent of those waiting are mentally retarded.

Average wait length: six years.

Funding: state and federal.

Services: 33 categories including job coaches, therapists, in-home nurses, transportation, respite care.

Amount available: unlimited.

Average waiver last year: $30,589.

Source: Agency for Persons With Disabilities.

Posted by autismmom at 1:26 PM - 19 Comments   Add a Comment  
 

 Autism Every Day
 

 
This is the most accurate, honest explanation of what parents of autism go through that I have ever seen. To watch it, click on the link below, then scroll down and click on "high", "medium", or "low", depending on your connection speed. My ADHD hubby actually watched the whole thing...we were both saying "Wow!" at the end of it...and kind of shaking our heads that just 13 minutes could capture so much of what we deal with.
 
Posted by autismmom at 10:20 PM - 16 Comments   Add a Comment  
 
 So here's my story!
 

The story on my support group came out in today's paper, so I thought I would put it out there for everyone to see. There are some minor inaccuracies, but nothing major worth noting. There will be 3 more stories, each coming out on Sundays, so I will try to post them as they come out. Feel free to ask questions, or make comments!
 
Thanks,
Leslie
 
Posted by autismmom at 11:34 AM - 6 Comments   Add a Comment  
 

 oops
 

oops...I got cut off in my last blog. All I was going to say was that we are leaving toight to go on our vacation to Indiana, Illinois, and Tennessee. All while I am totally not feeling well (I have a cold). So I will try to blog again as soon as I can, but until then, everyone have a safe and wonderful holiday season!

Take care,
Leslie

Posted by autismmom at 8:55 AM - 8 Comments   Add a Comment  
 
 Hi everyone!!
 

Well, hello there! Sorry it's taken me so long to blog again, but as you all know things have been crazier than the usual craziness here. I'll start with the most important thing: court.

We had our hearing on Wednesday, and I won't know the outcome for a mnth or so. However, last Sunday, Loni yet again did serious damage to our home. This time he put his head through a wall. He was upset that his sister got a drink before he did, so he tried to take it from her. She started crying, which always upsets him, and he banged his head 3 times on the wall and put a nice hole in it. It's probably about 4-5 inches wide. Anyway, then he physically attacked his sister by pulling her hair and banging his head against hers. I was trying to pull him off of her, but wasn't too successful, so I was screaming for my hubby at the same time. He came out and helped, got Loni a drink, and then let him go into his room to calm himself. Knowing the hearing was coming up, as soon as everything was calm, I grabbed my camera and took pictures of the hole and his forehead.

I spoke with the opposing attorney several times before the hearing and she was actually quite helpful. At least as much as she could be, all the while reminding me that she was the attorney for the opposing side. She did give me one bad bit of info though. She said that the only evidence allowed was what had previously been given to the Agency when they made their determination. She informed me that she would object to all new evidence (such as the hole in the wall photos, etc). I decided to bring it anyway, and spent most of Tuesday establishing relevance between the new information and the old, so as to hale it allowed. Turns out I didn't need to. The first thing the judge said when we sat down was that we were starting from scratch, as if no one knew anything about the case at all, and she would only consider the evidence brought to her attention that day!

They only had one witness, and that was the actual person that denied him the services. She explained that the reason for denial was based on the facts that :

1. No one had had to seek emergency medical treatment as a direct result of Loni's behaviors

2. Social services has never been called

3. the POLICE had never been called on him (umm...he's 5?!) and

4. that there was a plethora of services available here in my area.

So my counter argument? I happen t be a good parent, who is completely stressed out because I cannot take my eyes off my son for a second or ER treatment will be needed. I also happen to believe that it won't be too long before ER treatment will be needed if we don't get this help. I refuse to call social services or the police because he is 5, and what would they do? As far as the so-called services available, I have exhausted all posibilities, as few as there are around here, and it turns out that my own support group is the only one!

I had to literally be Loni's lawyer that day, objecting to things, calling witnesses, questioning them, redirecting, etc. It was quite stressful, but I think I did pretty well. As the matter of fact, I think what made the whole thing worth it, was the look my husband gave me when I finally got home that night. He had to leave the courtroom early because Loni was causing such a disturbance, so when I walked in the door, there was a look in his eyes that I have never seen before. It was a look of sheer admiration and I could tell he was so proud of me. Everyone that was a witness said they thought I did a great job, and I felt pretty good about it too. My witnesses were all wonderful, and I was honored that they were there on my behalf.

As for now, I have to get going. There is no school today, so I have t try and keep up with the kids, along with pack

 

Posted by autismmom at 8:52 AM - 3 Comments   Add a Comment  
 
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  About Me
Author: autismmom
From Florida, USA
Age: 31
 
This blog is about...
I have 2 kids on the Autism spectrum, and can never find any paper...so I'm bloggin'!
 
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