Friday, April 23, 2010
LOGAN'S RUN
Jackie (my 72 year old neighbor) pops into my apartment to ask me if I need anything from outside.
I'm sitting on the couch with cushions piled under me so I can stand up again. I'm reading threads on "Patient's Like Me" my ALS user's site. Jackie stands before me, animated and energized; like she came in to do a monologue. She tells me she had a dream about her father. He winked at her.
"He's trying to tell me something, but WHAT?! I just don't know. And Charlie, he looked so young!"
(pause)
"Do you know that everyone on the other side is thirty."
This I find hysterical. I laugh so hard I cover my mouth so I won't drool.
"WHAT?!!! It's true. Haven't you heard that before? I'm not making this stuff up.
In the next world everyone is thirty!"
"Jackie, what happens if you die at twelve?"
This quiets Jackie, but only for a moment.
"Charlie! I don't know. You'll have to read the book. Sylvia Brown. Have you read her?"
"No."
"You want me to get her book out of the library? I'm going to get you that book Charlie. Sylvia Brown! She could really be important for you."
Wednesday, April 21, 2010
LUCY

I sit in the lobby of my apartment building because it's too cold to go outside.
I spread out on a low, round sofa and watch the tenants coming home from work.
I read about Stem Cells.
I find human biology fascinating but as I read, I'm alarmed at how little we know.
(We don't really understand how RNA directs DNA (I guess).
I've never paid attention to medical research.
I'd vaguely heard of the Genome project and Stem Cell treatment.
I assumed we were living in the age of "The Jetsons".
We're not.
There is much to be learned. And what occurred to me after getting through a third "Stem Cells for Dummies" is that in seventy-five years, we'll have it all figured out. People won't die from disease. In a hundred years, people will be appalled that people died from cancer or ALS. Stem cells and gene therapy will change everything.
(The Bush Administration greatly slowed the progress for stem cell research. People will die because of Bush's religious convictions. I'm not interested in politicizing - but I despise Bush for halting stem cell research because he cozied up to Billy Graham.
* (I just read in "Stem Cells for Dummies" that Billy Graham has Parkinson's, another fatal neurological disease).
* (Bush didn't stop stem cell research. He actually allowed it to begin. But only with existing stem cells.
Most of these stem cells were ineffectual, too sick or too old? He also greatly restricted federal funding for research. Obama, overturned this in March of 2009.
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After reading for a couple of hours, I try to stand up, but I can't. I can't get up from the lobby sofa. I can't find the strength.
Spiro (my doorman) has taken me on as his responsibility. Spiro is a miracle of human energy. (The New York Times should do a profile on him). He stands by the sofa waiting to assist, my walker at the ready, but no matter how hard I try, I cannot stand up.
Spiro places the palm of his hand on my heart and says with his crazy Albanian accent,
"It's okay."
I shake my head in disbelief.
"No, it's good! Take your time. I'm here. No worries from me."
And I can't help but grin. How is it that I can't get up from this sofa, but last week I could?
It's like some kind of gag. I'm Lucy in the freezer.
After much effort, my upper arms throbbing from overuse, I stand up.
Tuesday, April 20, 2010
BLUE

Sunday, April 18, 2010
STEM CELLS
Saturday, April 17, 2010
WATER WORLD
Friday, April 16, 2010
UNDER WATER

Thursday, April 15, 2010
KEEP IT SIMPLE

Tuesday, April 13, 2010
TONY JUDT
As many of you know, I am afflicted with amyotrophic lateral sclerosis (ALS)-better known as Lou Gehrig's disease. For the past year now I have been wheelchair-bound and dependent on a breathing apparatus. This has not prevented me from working, but the disease is progressive and deadly-and there is no known cure.
ALS is a degenerative neuromuscular disorder of the motor neurons: it is related to Parkinson's and Alzheimer's, as well as lesser-known neurological disorders. A cure for it will almost certainly come from research in the field of cell genetics-whether via stem cell research or molecular biology. But the science is complicated and expensive. In order to attract funding we need to draw the widest possible attention to this deadly disease and its impact.
I am writing to you today about Move for ALS. My former student and young friend Saul Goldberg is planning to cycle with Augustin Quancard from Seattle to New York City to draw attention to ALS and to raise money for Project A.L.S ., which supports scientific research seeking a cure to this disease. I am very enthusiastic about Move for ALS, both because I keenly second its objectives and because I am hugely impressed by the professionalism and seriousness of the two young men involved. They have established a substantial campaign Web site (www.moveforals.com) that has already attracted the attention and backing of Web and print media, as well as the support of professional medical organizations.
I am fully supporting this venture and urge you to join me. If you access the Web site you will see how easy it is to make a donation to the cause, with attractive gifts on offer to substantial donors. Or you could simply send a check with clear reference to Move for ALS to: Project A.L.S ., 3960 Broadway, Suite 420, New York, NY 10032, USA. I would be grateful and take it as a sign of support if you would be good enough to forward this letter to any interested parties. If you have direct access to media or Web outlets (e.g., blogs) where you could give further publicity to our campaign, this would be especially helpful to us. Saul is making a huge personal contribution to the challenge posed by this catastrophic disease: please do anything you can to support him.
Tony Judt
New York City
Thursday, April 8, 2010
Monday, April 5, 2010
EASTER SUNDAY







