Defeat ALS: Happy New Year 2013!!

Tuesday, January 1, 2013

Happy New Year 2013!!

I've been writing in a notebook for about a year, capturing random thoughts around ALS, Bill's life, our adventures with ALS and a little about my post-ALS journey. One of my resolutions for the new year is to write regularly. My intent is to have this resolution last longer than most!

May 2013 support your resolutions and bring all that you hope for!!

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Dedicated to the ones we love....

This BLOG is dedicated to my late husband Bill Lichtig, who lost his battle with familial ALS on Aug. 10, 2005, and the many patients, families, caregivers and friends that I am privileged to know. This site is a collection of my personal reflections on living with ALS, Advocacy for ALS and tools to help get the job done. And...more importantly...learning to enjoy the journey.

There are so many sites/links with technical and diagnostic information regarding ALS (aka Lou Gehrig's disease). This is NOT one of them! Please feel free to comment and let me know how you like/use the posts. If you like the work, please subscribe through the link below or via Networked BLOGS on Facebook.

Please note: DFTALS is a collection of my thoughts, personal opinions and experiences as a wife and primary caregiver for my husband Bill, an ALS patient. Whatever you read here is based on our personal experience. It should not in ANY way be considered medical advice. Please use common sense and check with a medical professional if you have any questions or concerns about anything you read here. You are responsible for you own actions.

Enjoy! Kathie

"Never underestimate the power of a small group of dedicated people to change the world. Indeed, it's all that ever have." Margaret Mead