“SOLD: Jeep Painting to Benefit Dove House Children’s Advocacy Center”
Jeep Painting is SOLD benefiting Dove House Children’s Advocacy Center
Jeep Painting is SOLD benefiting Dove House Children’s Advocacy Center
The Association of Shoulder and Elbow Surgeons (ASES) Gala in Singer Island, FL, was an unforgettable evening of art and impact! Michael Israel took the stage and blew the audience away with his signature live-action painting performance. From the very first brushstroke, the room was buzzing with excitement as Michael brought his incredible creations to life right before everyone’s eyes.
His electrifying show not only wowed the crowd but also made a huge difference, raising just under $25,000 in support of ASES and their ongoing mission to advance shoulder and elbow care through education and research. Every moment of Michael’s performance kept the audience on the edge of their seats, with his stunning artwork generating both admiration and generous bids during the auction.
The energy, enthusiasm, and generosity of the attendees made this an extraordinary night, and thanks to Michael’s captivating show, the ASES Gala was a tremendous success!
The Peterson Health Foundation Gala in Kerrville, TX, was nothing short of spectacular, and Michael Israel’s performance stole the show! With his high-energy, live-action painting, Michael mesmerized the audience, bringing art to life in a way that left everyone speechless. His stunning creations didn’t just wow the crowd—they made a huge impact, raising just under $40,000 for Peterson Health Foundation!
From the moment Michael took the stage, the energy in the room was electric. With every brushstroke, the audience was on the edge of their seats, watching in awe as his masterpieces came together in real-time. By the end of the evening, not only had Michael delivered a show that people will be talking about for years, but he also helped raise vital funds to support healthcare initiatives in the Kerrville community.
It was an unforgettable night of art, generosity, and inspiration, all in the name of a great cause!
Many thanks to Niessa, Kasy, Leah, Jordan, and Celeste (and any other awesome nurses & staff I’ve failed to mention) for the incredible care you showed Josh, Carolina, and I during our stay with you all for labor, delivery, and recovery. We were so pleased with our choice of PRMC and those who served us on such an important and special day as we welcomed our daughter Carolina into this world. Thank you again for being so trustworthy, and for making us feel so at ease and well cared for!
Sarah
Getting ready for performance on FOX to promote an appearance for the Payton Wright Foundation gala.

In early 2006, three-year-old Payton Wright began complaining of a pain in her knee. Thinking that it was nothing more than growing pains, her parents, Holly and Patrick, took her to the doctor, who told them the pain would probably go away on its own. When it persisted, the Wrights were told that it was probably juvenile arthritis or perhaps diskitis.

After a few weeks with no improvement, Dr. Bob Morelli, the ER doctor at All Children’s Hospital in St. Petersburg, FL ordered an MRI. On May 17, 2006, just weeks after her 4th birthday, Payton was diagnosed with cancer when the MRI revealed a tumor on her spine and pelvis. Always concerned for others, Payton looked at her worried father as she was wheeled into her first surgery and said, “Don’t worry, Dad. It’s gonna be a good day.” Payton fought her entire battle with the attitude that every day was going to be a good one.
The doctors determined that Payton had Medulloepithelioma, a very rare form of brain cancer, and one for which there was no treatment protocol and very little hope for recovery. First at All Children’s and later at Duke University Medical Center in Durham, NC, doctors pieced together Payton’s treatment, which included intense rounds of chemotherapy and radiation.

In August of 2006, Payton was paralyzed from the waist down due to the tumor’s compression of her spine. She received as much radiation as a human body can tolerate, but the tumor continued to grow. Payton continued to fight, and she was able to graduate with her preschool class in May of 2007. However, the cancer continued to spread, and on May 29, 2007, Payton passed away at the age of 5.
Patrick and Holly Wright saw how courageously their daughter fought, and they promised her that they would never stop fighting. The Payton Wright Foundation was created both in Payton’s memory and with her fighting spirit so that children with brain cancer will know that “it’s gonna be a good day!”
Members of the Wright family kept a blog during Payton’s Journey. You can read all of the posts here:
Payton’s Journey – The blog Payton’s mom kept during her treatment and after her death.