Thursday, February 23, 2006

Beyond Rudy: Athena Senior Inspires

Beyond Rudy: Athena Senior Inspires

A truly wonderful and inspiring story to start your day! Way to go, Jason McElwain!

"Once the severe autistic child can break through, they can live in this world. Just like anyone else," Deb McElwain said.

Video: J-Mac's hoop dream come true from CNN.

http://www.cnn.com/video/partners/clickability/index.html?url=/video/sports/2006/02/23/catalana.ny.rochesters.rudy.wham

You'll have to watch a short ad first, but it is WELL worth it!



Tuesday, February 21, 2006

A-CHAMP.org - KEEPING MERCURY OUT OF VACCINATIONS --Rep. Dan Burton

A-CHAMP.org - KEEPING MERCURY OUT OF VACCINATIONS --Rep. Dan Burton:

"KEEPING MERCURY OUT OF VACCINATIONS --Rep. Dan Burton speech on Floor of House of Representatives - February 16, 2006"


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Action Alert
KEEPING MERCURY OUT OF VACCINATIONS --Rep. Dan Burton Speech on Floor of House of Representatives - February 16, 2006


KEEPING MERCURY OUT OF VACCINATIONS
(House of Representatives - February 16, 2006) [Page: H357] GPO's PDF

The SPEAKER pro tempore. Under a previous order of the House, the gentleman from Indiana (Mr. Burton) is recognized for 5 minutes.

I think that it is good that they are telling the American people that. But [Page: H358] GPO's PDF at the same time that that is going on, our health agencies are allowing mercury to be put into almost every vaccine an adult gets and many of the vaccines that children get.

The interesting thing about it is that it has never been tested. You might say it was tested back in 1929, because they said they tested it on 27 people that had meningitis. All of them died from meningitis, but none of them died from the mercury they were being injected with. But they died anyhow from the meningitis. There wasn't enough time to find out about the neurological problems that might ensue because they were having mercury injected into their bodies.

We have gone from where 1 in 10,000 children were found to be autistic to one in 166. It is an absolute epidemic. We have also seen a tremendous increase in people that have Alzheimer's and other neurological diseases. Yet we continue to allow our health agencies to allow the pharmaceutical industry to put mercury into the vaccines going into every single human being into this country, and in particular our military personnel overseas.

It does cause severe neurological problems when it is given over a long period of time. Your brain accumulates this mercury. It doesn't chelate out of the body in a very efficient way. So if you get 10 shots, that mercury stays and keeps building up, and it gets worse and worse as time goes by. The health agencies know this is a problem, and yet we continue to allow mercury to be put into these vaccines.

It can be done. This Thimerosal is supposedly a preservative. If we go to single shot vials, which don't cost much more than the multi-shot vials being used, you can take the mercury out of them because you don't need that preservative in there, you don't need that kind of purifying agent, if you will, in that vaccine.



Thursday, February 16, 2006

Finding Sense in a Senseless World

A Charlotte Observer editorial entitled "Hoodwinked!" comments that NC Governor Easley has told the the state auditor that some $200 million now being spent to reduce class sizes in lower grades and help at-risk pre-kindergartners will go back to the general fund and be replaced by lottery proceeds. Lottery proceeds that don't even exist yet.

This is counter to what the public was led to believe: That lottery funds would ADD TO, and not REPLACE current spending on schools. The Observer reports that State Auditor Les Merritt states "There is a pretty big disconnect, I do believe, between what is the public perception and what the actual legislation allows about the uses of lottery revenue," he said.

It took years for the state of North Carolina to pass the controversial lottery, amid opposition blaming lotteries for possible gambling addictions and citing the fact that some poorer families will be using grocery money to excessively purchase lottery tickets. If so, poor children will suffer.

But what gets me in this case is that the programs being de-funded are programs for our children, including at-risk programs such as the early intervention program that my son Alec has attended in the public schools for nearly two years. These programs are a source of hope for at-risk kids, and an opportunity for them to become active members of society as they grow. It seems NC is trading the future (our children's future and our future) something else in this deceptive move. Not real classy, Governor Easley.

The entire lottery start-up in NC has been a walk through the dirt. Initial effort to prevent TV commercials teaching kids how much fun it is to gamble have been whittled away leaving the door open to TV lottery ads "blanketing" the state. Was that necessary?

The Charlotte Observer reports that: "Alicia Hansen, a lottery expert at the Tax Foundation, warned that lottery revenue isn't always used as promised: 'Money ostensibly raised for education can be spent on other things -- even in states where there is a `lockbox' protecting lottery revenue. Legislators can shuffle funds and allocate less money to education than they otherwise would, knowing lottery funds will make up the difference.' "

I'm not writing this to oppose lotteries. I'm writing because I think parents need to raise their voices now to protect current and future funding for education. If we don't, we know we can't trust the NC government to protect our kids, based on their actions to date.



Friday, February 10, 2006

A new look at autism as Berlin film festival opens - Yahoo! News

A new look at autism as Berlin film festival opens - Yahoo! News

"Snow Cake," which contains both poignant and off-key moments, was directed by Marc Evans and written by first time screen-writer Angela Pell.

Pell was inspired by her own autistic son Johnny, who like Weaver's character in the film loves to eat snow and bounce up and down on a trampoline.

"I wanted to write a film that showed that sometimes living with autism can be harrowing but that actually most of the time it's really good fun," Pell told reporters.



Wednesday, February 08, 2006

Marital Madness

One of the first persons I spoke to when Matt and I first received Alec's diagnosis was another mother of an autistic child. I have never met her personally. In the early days, I was devouring over any book I could find on autism disorders, ABA and biomedical treatments for mercury poisioning. Somehow, I got the phone number of this mother and called to talk. One thing I have to say about this journey is that I have found that there are so many parents who want to share and encourage each other, drawing from their own personal experiences.

This mother, whom honestly I cannot even remember her name, did tell me something that I have not forgotten: She said that I need to expect my marriage to suffer tremendously. I recall thinking, "How can she say that?"

It wasn't long until I learned of a statistic to back up her comment. I'm told that 80% of marriages of parents of ASD kids end up in divorce. What a horrible statistic. In the several years of walking this road with Alec, I've seen that happen to others in support groups I have been in. It saddens me.

Why does it have to be this way? Is there some element of blame that one or both parents put on the other? Is it the stress?

It is true that it takes more time to care for a child with an ASD than it may for a child who is, and I hate terming it like this, "neurotypical". Is that time taken from caring and maintaining the marital bond? How much is too much?

I don't have answers to these questions. I think often of all of the single parents doing this on their own. My heart and hat goes out to them, because it is a lot to carry.

Is communication is the key? When I have been tired and frustrated, I admit there are times I lash out at Matt. But then, I usually end up admitting to him that I am simply tired and that I don't mean to take it out on him...and apologizing. Identifying what is REALLY setting me off is important to me. He's good at communicating his frustrations to me, too. We don't hide things in this house. All of our dirty laundry is usually out on the table in plain view of all.

I'm no marriage counselor. I wish that, in the face of a challenge such as autism, couples would pull together rather than apart. No one could deny that doing so with be better for all, especially for the child. Unfortunately, this is easier said than done, of course.

In my past, I did not have a good relationship with my father. My parents divorced when I was eight, and it was a struggle finding a place with him after that. He married my stepmother, who was diagnosed with multiple sclerosis in later years. He cared for her in extraordinary ways. He never left her side. I admired that in him, but it meant that he had very little time for me. Still, he was happy, and in time, I came to accept that and it was enough to see him happy.

That said, I so incredibly respect fathers who show unconditional love to their kids! I know in my heart that there is no medicine, no treatment, nothing that compares to the love of a father. I am so thankful that Alec and Elise have a father who is there for them.

Matt and I are celebrating our 10 years of marriage this Friday, inspiring this post. When I married him, I had no idea what "for better or worse" would mean. I look at him, and what he does for Alec, Elise and me, and I am amazed. I fall in love with him all over again.

And you know, if this is the "worse" of the "for better or worse", it's really not that bad! I'm finding the laughter that I had lost for the first few years after receiving Alec's diagnosis. It's coming back. Each night, we gather around the television and watch "America's Funniest Home Videos". We laugh and laugh. Alec rolls on the floor in hysterics. He's like me in loving slapstick. There is such joy in the simplest things. But I have to look for these things.

Life gets better. The tides come and go, but life is good, each day of it. Every challenge is really an opportunity. I wish I could always see that, but often, I see it in hindsight.

Sometime, I fail miserable. Sometimes God teaches me to fly over the challenges. In the process, I learn to fly, or in other words, I learn how to handle more than I thought I could. It's all about grace.

Thank you, Matt, for loving me unconditionally. For refusing to see the flaws in myself that I dwell on so often. For every day, every prayer, every tear, and every promise. May God continue to hold us together, so that we never fall apart. I can't take credit for it, you know.

There is a song by Phillips, Craig and Dean that I selected for our first dance together. I think of the lyrics, now, and pray that each married couple reading this will not be another statistic, and be blessed by God's light:

"Shine On Us"
Lord, let Your light, light of Your face
Shine on us
That we may be saved
That we may have life
To shine our way in the darkest night
Let your light shine on us

Lord, let your grace,
Grace from Your hand,
Come over us
That we may be saved
That we may have life
To shine our way in the darkest night
Let Your grace come over us

Lord, let Your love,
Love with no end
Fall on us
That we may be saved,
That we may have life
To shine our way in the darkest night
Let Your love fall on us
Let Your light shine on us