Welcome

This blog is about a new walk with my husband Rick & I since he was diagnosed with ALS (Amyotrophic Lateral Sclerosis) or Lou Gehrig's Disease or MND (Motor Neuron Disease) on February 1, 2008.

This blog was started as a way to keep our family and friends and anyone else interested in our battle with ALS updated.
So as you read this blog please keep us in your hearts and prayers.

The blog starts from the most current to the oldest entry. Rick has started to blog now also as of April 1,2008 so this site has become officially "our blog".

My dearest husband Rick passed away on August 13, 2010,
2 1/2 yrs after diagnosis. Now I have to learn how to walk in the courage, strength and bravery that he did in fighting this disease. He promised me he would be waiting for me in eternity on a park bench. Together Forever!

Sunday, July 5, 2009


This past year the Whitemouth School posted some jobs for their students and each student had to apply for a position. Tia and her friend Angela were picked to visit Rick throughout the year.
During the course of their weekly visits the girls learned to play chess, learned some food nutrition and how to count calories for Rick's daily food intake, did some weeding in the flower bed as that was something Rick would have done, ran uptown with Rick to do errands, wiped down his wheelchair, played wii, and had the home care lady, Carol, teach them about range of motion exercises. She had them put on rubber gloves and did the toe wiggling one just to get a feel for the process. They were such great girls!!!