LAZY S 6 EQUINE, LLC
Forest Road 9604F
Come watch us present and participate
for the 7th year in October 2-4, 2020!
Thank you for making this event a HUGE success!!!
Buckles by Monsoon Silver
Strong Supporters and Sponsors
Jackpot Ranch, Camp Verde
Gallery Kitchen & Bath, Nicholas Casler
KP Ventures Well Drilling & Pump
Plowing Ahead Ranch All Natural Beef
Ben & Missy Rolfes
AG Agricultural, Rimrock
Pistol Customs by Ashley Pistol
Jonna Randall, Farm Bureau
Kim & Len Demoney
Total Building Systems
MIke and Kathy Gardner
Andy and Marybeth Groseta
Thank you to all of our silent auction contributors!
Joyce Tanner of Tanner Photography
Join us January 11, 2020 at The Jackpot Ranch in Camp Verde for a benefit for Baby Woodrow Miller.
#10 Team Roping, Breakaway $25, 5-D barrels, open $45, youth $20, pee-wee $10, Barrel fun run $20 for horses who have never competed in any barrel event including gymkhana, this class is for completely novice to barrel horses (judge onsite so please be honest), silent auction and pit bbq beef meal. No Arena or Office Fees.
If you have or know a baby or child, look at them. Now imagine receiving a phone call from your pediatrician stating that your precious innocent love has an extremely rare and fatal genetic disease. The diagnosis is Niemann Pick DiseaseType C (NPC), also referred to as childhood Alzheimer's disease. This means in short, Woodrow is unable to break down complex lipid compounds forcing the lipids to accumulate inside the cells of multiple organs and tissues throughout his tiny body, including his brain. The lipid build up produces an inflammatory response and eventually leads to cell death, affecting all of his body systems. There is no cure.
I am reaching out with an ask of prayers and assistance for Denise and Rickey Miller, and our sweet Woodrow Troy. They are first time parents and have begun an uncertain journey searching for clinical trials and treatments. These trials and treatments have the possibility of slowing the course of NPC's progressive deterioration of the nervous system. This journey includes frequent travel to take Woodrow to the few NPC specialists and geneticists existing in the US. Woodrow is just 1 of approximately 500 diagnosed cases worldwide. Researchers are hopeful that a cure is near and continue to provide clinical trials with positive outcomes for families desperate to provide quality of life for their babies, experience developmental milestones, birthdays, little league, high school graduation, and create memories to cherish for a lifetime.
Denise and Rickey understand that God's plan is not "their" plan, and through their faith are focused on baby Woodrow's health, living in the moment, and accepting the continuous sacrifices that must be made to be able to provide for his needs. This decision may include uprooting their family to be near medical treatment facilities, frequent travel for bi-weekly infusion treatments, monitoring & follow-ups, insurmountable medical expenses continuing to accrue, inability to work, financial burden, emotional turmoil, and so much more to be endured. Yet, this all pales in comparison when the life of our family's precious lil' Woodrow is the focus.
Please consider giving out of love for this new family, anything will help and be greatly appreciated for this long untraveled road ahead. For those of you that are parents or can relate, I too know that there is not any length that I would not go, no stone left unturned, to protect and provide for my children. Please join me in supporting Denise and Rickey and blessing them both with the opportunity to build all the memories they have dreamt of with #WoodrowTroyDoubleToughCowboy.
A Wells Fargo donation account has been set up under "Woodrow Miller", as well as, this gofundme for those able to give.
"Trust in the LORD with all your heart, and lean not on your own understanding; In all your ways acknowledge Him, and He shall direct your paths" Proverbs 3:5-6