Comments on: November 29, 2007 http://localhost/2007/11/30/november-29-2007/ Reflections on Living at the End of Life - MDS and Leukemia Sat, 09 Oct 2010 13:56:10 +0000 hourly 1 https://wordpress.org/?v=4.2.28 By: Paul Kasten http://localhost/2007/11/30/november-29-2007/comment-page-1/#comment-49698 Fri, 30 Nov 2007 20:22:34 +0000 http://www.connieore.com/2007/11/30/november-29-2007/#comment-49698 Dear Connie:
I have been reading your musings here for almost 2 years with interest and great concern; I have not posted any comments until now.
First of all, let me say that I’m glad you enjoyed “Frau…” at Lyric; Jim and I are supposed to see it on the 16th of December. While I love Strauss, “Frau” has never been something I’ve wanted to experience; it’s nice to know that perhaps all the shouting is about something, after all.
Now, the reason for this posting: I’d like to remind you about the wonderful Holiday gatherings you and Charles hosted almost 30 years ago, in the late 70’s. It was SO incredibly kind of you both to open your home to organ students for events of that sort. Your house was a beautiful world away from the college, and being invited into it tremendously influenced my life…you were responsible for helping me form my own ideas about home; a place that should be filled with art, music, beautiful things and good companions (4-legged, winged, etc, as well as human….)
Please believe me when I say that I will never forget your kindness; I remember those parties every Advent as I prepare for the Holidays. In a way, your Holiday gatherings were a perfect summation of the meaning of Advent: you gave a taste of the way life ought to be to all in attendance. We all pray every Sunday for the coming of the reign of God, and yet we often fail to recognize it (until much later) when it touches our lives. Like Moses, we’re not allowed to see the face of God, but we DO know where God has been.
You are in my thoughts and prayers…….Paul

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By: Janna http://localhost/2007/11/30/november-29-2007/comment-page-1/#comment-49680 Fri, 30 Nov 2007 16:30:40 +0000 http://www.connieore.com/2007/11/30/november-29-2007/#comment-49680 Dear Mom,

At first, we read on the internet that people with your type of MDS have an average expectation of 4 months after diagnosis. (I remember that day of discovery, and talking about it with Heidi on my cell phone. I was parked in my car, eyes leaking, and when we finally hung up I got out of the car, the cell phone tumbled from my pocket and I slammed the car door right on it, smashing it spectacularly. Not completely “accidental”, I suspect.) Well, here we are, 22 months later, and you are walking Alphie and giggling at operas.

Early on I expected the doctors to give us a road-map, telling us how long until we reached each landmark, what it would look like at that place, and when the Exit was. I sympathize with those doctors as I think back at it – imagine seeing all that expectation and knowing: there is no map!

So onward, mapless, we go. And in the meanwhile, a blue-jay sounds like a red tailed hawk? The sun shines bright here today, the leafless trees dance in the breeze like sculptures against the blue sky, my parrot is sitting contentedly with me in the sun, and my mother is miraculously alive and once again buying underwear for my husband for christmas. My heart feels warm and soft, my eyes start to leak, and I say: Thanks Be To God!

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By: Sheila http://localhost/2007/11/30/november-29-2007/comment-page-1/#comment-49671 Fri, 30 Nov 2007 14:40:15 +0000 http://www.connieore.com/2007/11/30/november-29-2007/#comment-49671 Hi Connie, Miracles happen. They are now and will be in the future happening for you. Your doctor’s conferece may bring back new medications to try with new hopes.
Your trip to Chicago sounds so exciting. You must have had a wonderful time and wonderful memories.
I wait for the time when I will feel like beening in public. My counts have got to chance before that happens. And so does my weakness.
Hang in there as you always do. No one gives me as much support with words and from the heart as you do.
Prayers for you. Your Holidays will be the best ever.
I’m always thinking of you. Sheila

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