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Old 03-10-2008, 11:10 PM #21
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Joelle - How nice of you to think of us and give us an update during this most difficult time. Thank you so much. I've been keeping you, your mom and family in my thoughts and prayers.



Quote:
Originally Posted by joellelee2000 View Post
Sorry for being such a downer. I will try to cheer up but it seems like that would just take too much effort right now.

Oh my gosh, with everything you have going on, don't even give that a second thought. We're here for you, no matter what.

Sending lots of love your way.
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Old 03-11-2008, 04:59 PM #22
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Sorry I am so late welcoming you back! It's been one of those weeks, but not anything like you are dealing with!

Everyone's given you good advice already, so mine is just ditto on what they said. Rest, regroup, do your Ty infusion, and relax.

I read your other thread too and I have no advice. Cancer is different with everyone, just like MS. I am hoping that the radiation and chemo will shrink the tumor and ease the discomfort your Mom is going through right now.

I went through it with my Dad and it just whittles you down to a nub when you are trying to care for a parent as well as dealing with your own chronic disease.

Let us know how it goes, ok?
__________________
I know the sound the river makes, by dawn, by night, by day. But can it stay me through tomorrows that find me far away?


.
I have this mental picture in my mind of you all, shaking bones and bells and charms, muttering prayers and voodoo curses, dancing around in a circle of salt, with leetle glasses and tiny bottles of cheer in the middle...myyyyyy friends!

diagnosed 09/03/2004
scheduled to start Tysabri 03/05
Tysabri withdrawn from market 02/28/05
Copaxone 05/05-12/06
Tysabri returned to market 06/05/06
Found a new neuro 04/07
Tysabri 05/25/07-present
Medical Marijuana legally 12/03/09
.

Negative for JC virus antibodies!
.

I'm doing alright and making good grades,
The future's so bright, I gotta wear shades!
.
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