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Fighting an Invisable Monster

A blog about my family's experience with ALS. Lou Gehrigs Disease. My attempt at gaining awareness for Amyotrophic Lateral Sclerosis.

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Fighting an Invisable Monster | cure4als.blogspot.com Reviews
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A blog about my family's experience with ALS. Lou Gehrigs Disease. My attempt at gaining awareness for Amyotrophic Lateral Sclerosis.
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Fighting an Invisable Monster | cure4als.blogspot.com Reviews

https://cure4als.blogspot.com

A blog about my family's experience with ALS. Lou Gehrigs Disease. My attempt at gaining awareness for Amyotrophic Lateral Sclerosis.

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cure4als.blogspot.com cure4als.blogspot.com
1

Fighting an Invisable Monster: One Year

http://cure4als.blogspot.com/2014/06/one-year.html

Saturday, June 28, 2014. One year- many meanings behind those two words. It's been a year since I put my story out there. A year that has brought me new friends from the ALS community. A year that I finally feel like my voice is being heard. A year that I finally feel I am making a difference! Before I knew it, my cousin had started calling buddies and seeing if they would fish such a tournament. Lo and behold. within 2 hours, we had ourselves the beginnings of a fishing tournament! Which leads me to thi...

2

Fighting an Invisable Monster: Round Fourteen: Exhaustion

http://cure4als.blogspot.com/2013/07/the-beginning-of-august-2005-arrived.html

Monday, July 15, 2013. Subscribe to: Post Comments (Atom). Mid Fight Report: Blog Blunders. Round Thirteen: Why I Fight. Round Twelve: The Damage. Mid-fight Report: ALS News. Round Eleven: Bait and Switch. Mid-Fight Report: ALS News. Round Ten: A New Reality. Round Nine: Heartbreak pt 2. Mid-fight Report: ALS News. View my complete profile. Awesome Inc. theme. Powered by Blogger.

3

Fighting an Invisable Monster: August 2013

http://cure4als.blogspot.com/2013_08_01_archive.html

Wednesday, August 7, 2013. I will never get to see that. Stupid, stupid monster! I hate you. as God as my witness, I will work tirelessly to eradicate you. So one day, someone's daughter won't be sitting in front of a screen, tears running down their face, wishing that their parents were still around! Subscribe to: Posts (Atom). View my complete profile. Awesome Inc. theme. Powered by Blogger.

4

Fighting an Invisable Monster: June 2014

http://cure4als.blogspot.com/2014_06_01_archive.html

Saturday, June 28, 2014. One year- many meanings behind those two words. It's been a year since I put my story out there. A year that has brought me new friends from the ALS community. A year that I finally feel like my voice is being heard. A year that I finally feel I am making a difference! Before I knew it, my cousin had started calling buddies and seeing if they would fish such a tournament. Lo and behold. within 2 hours, we had ourselves the beginnings of a fishing tournament! Which leads me to thi...

5

Fighting an Invisable Monster: June 2013

http://cure4als.blogspot.com/2013_06_01_archive.html

Friday, June 28, 2013. Round Eight: Heartbreak pt 1. It's taken me longer to write this post. Writing these memories means that I am reliving them in my head. My mind is back in the moment and this chapter is hard to relive. My head was in a tornado that night. Even now as I prepare to delve back into the darkness of that night. my heart is racing. With a deep breath and tissue at hand. my mind travels back. It was then I could hear him sobbing and calling my name. "Whats going on? And I ran out. June be...

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Connecting with Other PALS | The Team Gleason Experiment

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The Team Gleason Experiment. Awesome Ain't Easy. Where in the World is Team Gleason? Kids for Team Gleason! Tatts for Team Gleason! FUNdraisers for Team Gleason! Connecting with Other PALS. Racing for Team Gleason. Connecting with Other PALS. Siobhan Rock, Ottawa Canada. Http:/ www.alsbeaware.com/. Http:/ reallyalsreally.wordpress.com/2012/10/02/tim-the-possible-vs-andre-the-giant-in-a-hospital-bed-grudge-match-you-dont-want-to-miss-this/. Http:/ reallyalsreally.wordpress.com/. Chrystie Lose, aka Sam.

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Fighting an Invisable Monster

Saturday, June 28, 2014. One year- many meanings behind those two words. It's been a year since I put my story out there. A year that has brought me new friends from the ALS community. A year that I finally feel like my voice is being heard. A year that I finally feel I am making a difference! Before I knew it, my cousin had started calling buddies and seeing if they would fish such a tournament. Lo and behold. within 2 hours, we had ourselves the beginnings of a fishing tournament! Which leads me to thi...

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