Menzel Fine Art

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Menzel Fine Art

Movement through art My name is Scott Menzel and this why I create:

I want to rock and shock the world with bold visual poetry.

Art is something hard to explain but it exists and has a power. I believe my passion to create is the driving force to move myself through life. It allows me to express how I feel and gives me a sense of accomplishment. It is my method to prove my self worth when things seem over whelming and it helps achieve the peace within myself in a world that can seem complicated. My art signifies my inner f

eelings, struggles, likes and dreams. Each creation is a fragment of this journey of discovery. I create my work digitally which ironically reflects my life which is aided by technology. Technology is the tool that aids my existence and allows me to be myself when my natural tools fail. Creating digitally is just an extension of myself in the creation process. My art is universal in the end result and depends on the final decision of application. From interior design to public showings and private collections my art can be applied everywhere. I do it because it feels right to me and I love seeing how what I create connects with the world. It’s an internal drive fueled by lifes ups and downs in this discovery process. It feeds my desire of not quitting and gives me a focus to point my emotions and desires while facing life’s fears and unanswered questions.

18/04/2023

With a heavy heart, we are sad to announce that Scott died unexpectedly but peacefully Sunday afternoon in his sleep. We know Scott has touched many of you, like he has us - not just with his art but with his character. He never let his disability get him down or hold him back. He will forever be missed.

Scott Edward Menzel, 47, June 26, 1975 - April 14, 2023 of Pella, Wisconsin was born in Shawano, WI to parents Patricia Patti and Arlin Menzel. He lived a rich and inspiring life, including meeting his diagnosis of Spinal Muscular Atrophy SMA type 2 with resilience and persistence. He graduated

12/04/2023

01/04/2023

16/02/2023

I was surprised when I was told about this and actually remember painting it from looking at an old logging photograph. I painted it with watercolors when I could still use them.

“I don’t want people to see me for my disability, but rather for my ability."

Thank you to Kevin and Donna Hutchinson for the gift of this artwork by their friend, Scott Menzel, an artist with a diagnosis of spinal muscular atrophy. This drawing is proudly displayed in the GGC clinic waiting room with a plaque reading...

'This drawing depicting the history of the logging industry is the work of Scott Menzel, an artist and designer from Wisconsin, who has Spinal Muscular Atrophy (SMA). SMA is a genetic condition involving the loss of nerve cells in the spinal cord that affects the nervous system and voluntary muscle movement. Despite limited mobility in his arms and legs, Menzel skillfully draws in pen and ink, paints in watercolor, and creates colorful imagery using computer graphics.'

“I don’t want people to see me for my disability, but rather for my ability. Everyone should believe that nothing is impossible and that everything is just a dream that you can reach and make a reality.” - Scott Menzel

20/12/2022

17/09/2022

I was honored to be part of the first ever fashion show in New York City on Fifth Avenue this week sponsored by Genentech with the help of Open Style Lab and the SMA community.....a show promoting the idea of
making fashion more adaptable ....and Vogue posted a article!
by Genentech
More to come!

Biotechnology company Genentech and Open Style Lab partnered with the spinal muscular atrophy community for this first-of-its-kind runway show.

30/08/2022

- As a published and award-winning digital artist living with spinal muscular atrophy ( ), I’ve long had aspirations of taking my art worldwide while galvanizing change in the public perception of those with disabilities. When I was asked to help and be part of the with , I was honored to say yes. It’s a chance for the SMA community to embody and show off our unique senses of style, beauty, and empowerment.
Double Take is the first fashion show designed by the SMA community and dedicated to everyone with a disability. On September 8, right before New York Fashion Week 2022 ( ), we’ll take to the runway to show the world that fashion can be as accessible as it is striking. Check it out here: https://bit.ly/3CrOnMe

29/08/2022

25/02/2022

Scott was born with a condition called Spinal Muscular Atrophy Type 2.

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#sponsored - As a published and award-winning digital artist living with spinal muscular atrophy (#SMA), I’ve long had aspirations of taking my art worldwide while galvanizing change in the public perception of those with disabilities. When I was asked to help and be part of the #DoubleTakeShow with @Genentech, I was honored to say yes. It’s a chance for the SMA community to embody and show off our unique senses of style, beauty, and empowerment. Double Take is the first fashion show designed by the SMA community and dedicated to everyone with a disability. On September 8, right before New York Fashion Week 2022 (#NYFW), we’ll take to the runway to show the world that fashion can be as accessible as it is striking. Check it out here: https://bit.ly/3CrOnMe

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