Team Cure ALS Foundation/Support Mike Lopez

01/20/2026

●(Monday, January 19th)●

Happy Monday January 19th!
#19 Forever in Our 💕

Pictured: Michael & his dad doing what they loved. Watching a good game of football! OSAA Football Championship game. 🏈

01/13/2026

❤ 🕯🕊13 years ago (January 12, 2013) we all celebrated a courageous warriors life well lived. It was a glorious day to celebrate Michael's legacy & honor his courageous 17 1/2 year fight with ALS/Lou Gehrigs Disease.
❤Michael touched many, many lives in his lifetime. It was very evident the impact he had when 800+ people were in attendance for his memorial service on Jan. 12, 2013.....I certainly know I will never be able to brag about having that many loving supportive friends & family give me a final goodbye.
🔹️Michael left a lasting legacy.

📽 Here is a video link of Michael's Memorial Service in full length, feel free to watch:
https://vimeo.com/57326971
(Thank You Dirk Knudsen)

THANK YOU to all the friend's & family near & far that supported & helped Michael & my Lopez family on this ALS journey and beyond. We are FOREVER GRATEFUL.
❤🕯🕊🙏🏽

12/26/2025

New drug may slow progression of ALS in small group of patients:

A new drug may slow progression of -- and even reverse -- symptoms of a rare form of amyotrophic lateral sclerosis, or ALS, a new study published Monday finds.

12/19/2025

🎄❤️ Happy December 19th!
#19 Forever in our hearts, today and always.
This time of year is always a struggle missing our loved ones. Michael LOVED this time of year like a little kid! 🎄🎅❤️
📷 : Michael with his niece's.

12/12/2025

☆Today We Celebrate #19 ♡☆
Happy Heavenly Birthday Michael! 🎁🎈🎂
Forever in Our Hearts♡ #19

11/20/2025

☆Happy Wednesday, November 19th!

Remembering Michael today, #19.
Forever in Our Hearts 💕 Always Near, Never Far. ♡😇
☆☆☆☆☆☆☆☆☆☆

11/17/2025

is on Brilliant Minds NEXT MONDAY 11/24 at 10pm EST/9pm CST!

Don’t miss it—tune into next Monday!

11/02/2025

November is National Caregivers Month, and Team Gleason knows the importance of respite and ease of burden for those who dedicate their time to caring for someone living with ALS. We see you, we appreciate you, and we're working hard to provide innovative solutions that make your days easier 💙

ALSCaregivers.org is hosting a free “Caring for the Caregiver” Virtual Workshop on Tue Nov 18 7pm cst. and we hope you'll join!

Topics Include:
🔹Keeping the Caregiver Healthy
🔹Don’t Fight the Battle Alone
🔹The Empowered Caregiver

Current or former ALS Caregivers share insights on equipment and best practices to keep the caregiver mentally, physically, and emotionally healthy. Tips on leveraging others for assistance and making the most of together time. Sponsored by ALSCaregivers LLC.

Reservations are required before Thur Nov 9th. As a Caregiver of someone living with ALS, emerge from this workshop empowered and encouraged.

Register here: https://loom.ly/tpgeDfg

10/20/2025

Eric Dane has joined the NBC medical drama “Brilliant Minds” as a guest star. He will play a heroic firefighter who struggles to share his ALS diagnosis with his family.

https://variety.com/2025/tv/news/eric-dane-als-patient-brilliant-minds-1236557223/

10/16/2025

10/14/2025

Our current policy unintentionally excludes the spouses of Veterans who die from ALS from receiving compensation benefits. Justice for ALS Veterans would change that, providing relief to thousands of families nationwide!

SUPPORT Justice for Vets TODAY @ bit.ly/justice4Vets

09/30/2025