Posts filed as My Remarkable Mom

This morning a gathering of Tech Plan employees, friends, and family participated in the Dallas-area MDA Stride & Ride charity walk. Sporting their “Glenna’s Warriors” baseball jerseys, this group walked to raise money for MDA & ALS research and to

For Christmas this year I updated a cookbook my Mom put together back in the dot-matrix printer days. She titled it, WHEN MOM COOKED. This cookbook contains 65 recipes my Mom cooked when her family was young. All the recipes

Approximately 30,000 people worldwide suffer from ALS (Amyotrophic Lateral Sclerosis), better known as Lou Gehrig’s disease. Each year, about 6,000 people are diagnosed with ALS. Once diagnosed, almost 50% of all ALS sufferers die within two-years and within five-years, nearly

For my Mom’s funeral, I updated an earlier video by including photos to accompany the words in the poem my Father wrote for her. This poem, THE SUMMER OF ’62, was featured in the inside-front panel of the Funeral Program

*** Non-Marketing Related Post *** Many of you will remember that my Mother is living with ALS. The disease continues to creep along and when I tell others about how my Mom is doing I usually say something like, “Everything

As the son of Glenna Moore, I am so proud to share the results of a fundraising activity which raised $16,000 to support the Muscular Dystrophy Association (MDA). Last Saturday, a team comprised of Tech Plan employees joined together to

I’ve done some housekeeping as it relates to the mini-documentaries I’m creating which share family stories as told by my Mother. The mini-documentaries now have a semi-permanent home on offshoot blog from Brand Autopsy. You can access the As Told

** If needed, click here for the backstory.** The ALS disease is progressing as expected with my Mother. Which means … each day Glenna Moore finds doing everyday activities like talking, writing, and swallowing a little more difficult to do.