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Amendment to the script. I am without a doubt very cynical. However,

along with the CP has come the experience that I can reliably expect

straight talk, advice, insight from any parent (just about) of a special

needs child.

Crosby

>>===== Original Message From ccrosby <ccrosby@...>

>=====

>I appreciate reading the many thoughtful responses on the topic of

having

>a child with a disability, a difference in the family. For me, it is always

a

>mix of feelings. There are the highs and there are the lows and I

struggles

>to stay somewhere in the middle, balanced. Some of what I have to say

>you might not want to put in your book, but I think maybe the feelings are

>realistic.

>

>

>> Deep down I know that I will never

>>get over>the pvl, the cp. When I heard the diagnosis, it felt like

watching

>those planes hitting those towers, one by one. I replayed the words over

>and over again and saw my whole life crumple right in front of me.

>

>Some say it gets easier but at times I just don't believe

>>that. The emotional issues that do not go away entirely. I am

>>lucky because my son Isaiah, (20 months) while he had tremendous

>functional

>>deficits, he is a straightforward baby and easy to take care of, amuse.

He

>>is very adoring and receptive child. He laughs all the time. He eats

salad

>>with blue cheese dressing amongst other things. He makes his share

of

>>noise and has a few words. So I am lucky. I say that because after

>>receiving the devastating spastic quad cp diagnosis (January, 2002) I

>>then very bravely took Isaiah to see a developmental ped. Just so I

could

>hear more bad news. The news was pretty heartbreaking. The doctor

>looked at me and said I'd be lucky if Isaiah

>>ever knew his name. He was wearing a Mickie Mouse tie and his last

>name was Wolf. That goes to show you that doctors who wear Disney

>ties are not necessarily kid-friendly. What he said turned out not at all to

>be true. However I have had enough bad news to rebuild those towers.

It

>all continues to be

>>shocking. I have come to just expect more bad news. That is

>>what the New Years means to me. More bad news. Let's think. What

>little wrapped treasure could it be ? If I am lucky I will be hit by an

>uninsured motorist. The good news is that I am practically

>>rock-proofed, although I have times when I just want to deteriorate - or

>strangle someone.

>>

>>I am surrounded by triggers on a daily basis. For one I have two

>teen-age

>>stepsons. I contribute heavily to their tuitions. My job pays for the

college

>>tuition for one stepson. The other kid goes to a special school out in

>>Idaho (CEDU) for kids with issues. It is an enormous privilege. And

both

>>my stepsons ski, hang gliders, do wilderness camping, roller blade,

play

>guitar and

>>every other cool activity. My husband at one time was a professional

>skier

>>and our house was covered with trophies until recently. He reads

every

>>ski magazine out there. I am not remotely interested in sports. However

it

>>is my dream and continues to be that my son Isaiah would some day

>>ride a bike. Am I a lunatic for having this fantasy ?

>> The dream never entirely fades but it is not in keeping with

>>the reality of the situation. The contrast is so jarring and painful. I

>>recall

>>last summer I took my son to a beach. I remember I felt like we were

>>being stared at. I remember just feeling bad every time I watched

>another

>>child run around with a pail and shovel. I remember feeling like maybe

I

>>was wanting too much. Some days I feel like life is mocking me. With

>>that comes the bunker mentality. Stay at home. To some extent it works.

>>But I am resentful for that too. I feel like my husband is blessed

because

>>his parenting is more balanced. At least he understands and can relish

>>the pleasure of taking his kids camping or coaching Little League. I

feel

>>like I get the short end of the stick. We have been trying to get a stander

>>now for Isaiah for over 5 months. Despite all his apparent

>developmental issues, I just cannot prove medical necessity. I feel like I

>cannot provide him with what he needs. What kind of satisfaction is that

?

>So I

>>have all these rotten feelings.

>

>>

>> Occasionally I get wild bursts of inspiration to act on my rotten

feelings.

>>Recently I curbed the urge to send my obstetrician a nasty nasty

>>Christmas card. The other alternative I considered would be to

>bombard

>>her office with faxes. Or hang out in her waiting room and stuff all the

>>Baby Talk magazines full of the public record of all the malpractice

suits

>>she has been involved in - what you would never know until it happened

>to

>>you. I have even thought of throwing rocks through her living room

>window ! I feel justified. I feel like I was betrayed by this practice that

>I

>placed all my trust

>>in . I will never forget it. So yeah, I feel like I got jipped and it's

>>hard to

>>manage the vengeful urges.

>

>Their offices, where my son was born is not far from where I live. I

>>drive several blocks out of my way so that I never pass this office, this

>>hospital. The contours of the hallways of the NICU, the ritual rinsing

of

>>hands before you enter, the breast pumping room, the beeping

>monitors,

>>are still fresh to me, deeply impressed within the vault of memory. Is

that

>>strange ? Am I nuts?

>>

>>

>>I am now almost two years away from the NICU and no longer such a

>rookie. In the beginning I believed I was going to find the cure for cp on

the

>internet. I surfed the internet relentlessly every night looking for

medical

>definitions, for research, for miracles. I could not believe what I read. I

>never heard of children who don't walk or talk. That is, I feel the ultimate

>cruelty.

>

>What is

>>more cruel for me today are the institutional hurdles.... the insurance

>appeals,

>>not having the stander Isaiah needs so badly, being denied

>hippotherapy by

>>the insurance carrier, then arguing over the IEPs, the IEPS not being

>>carried out, putting him in a day care for special needs kids that won't

>buy

>>him adaptive toys, an adaptive swing, et, and then days where I feel

>swept up in a web of do-gooders. The bureaucracy that serves

>>these children is a killer. Some days I go to bed imagining I am

involved

>>in a Soviet-style conspiracy that is just determined that I am going to

end

>>up cutting my own throat.

>

> I am very cynical. I perceive this life (and most everyone in it) pretty

>pessimistically. Oddly, we can easily sacrifice Lott for racist remarks but

>gladly receive Dr. Frist, the holy white Heal the Party- Senator. It does

>not

>seem to bother anyone that his documented wealth is at 40 million and

>that all his money is stashed away in blind trusts. He is a shareholder in

a

>hospital corporation (an enterprise of his father and brother) that was

>indicted for 1.7 billion dollars for medicare fraud. So he made a fortune

in

>health care fraud ! How sickening is that !

>

>With all the cynicism, I have learned how important it is to keep my

mouth

>shut.

>

> So I smolder and plot and advocate and research, throw rocks and

>rock-proof, and appeal and re-appeal and litigate . I write letters to

>people I don't even know and will probably never actually meet. That's

>what I do.

>

>

> Crosby, Philadelphia

>>

>>

>>

>>

>>

>>

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