A Lasting Mark

A Lasting Mark

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Luke was diagnosed with Linear Scleroderma in May 2013, at the age of 13. Now all of his fingers, his wrist and his elbow have showed decreased mobility and function. In addition, he has discoloration and hardening of the skin in his lower and upper arm. The discoloration is a permanent mark to remind Luke of his diagnosis. Being diagnosed with a chronic disease has been life changing to Luke and

A Lasting Mark - Advocating for Linear Scleroderma 12/02/2025

is a global generosity Movement unleashing the power of people and organizations to transform their communities and the world on December 2, 2025 & every day.
Whether it’s making someone smile, helping out a neighbor or stranger or giving to those who need our help. Every act of generosity counts and everyone has something to give.
This , help A Lasting Mark fulfill its mission to increase awareness about scleroderma and other autoimmune disease that affect children. Our goal is to raise money for research, treatments and eventually a cure. We want to improve the day to day lives of those children who are affected and provide emotional support for them and their families.
To find out more about A Lasting Mark and how to donate please visit our website

A Lasting Mark - Advocating for Linear Scleroderma Leave Your MarkExtend a Hand for Something Positive.   Donate Now   Watch our TV Commercial Leaving our Mark in Salt Lake City 2025   The Pediatric Scleroderma conference was combined with the Juvenile Arthritis Summit this year. We had a wonderful time in Salt Lake City connecting with families ...

07/12/2025

Family Summit in Utah 🩵

01/01/2025

Happy, Healthy New Year!!!

12/03/2024

is a global generosity Movement unleashing the power of people and organizations to transform their communities and the world on December 3, 2024 and every day.
Whether it’s making someone smile, helping out a neighbor or stranger or giving to those who need our help. Every act of generosity counts and everyone has something to give.
This , help A Lasting Mark fulfill its mission to increase awareness about scleroderma and other autoimmune disease that affect children. Our goal is to raise money for research, treatments and eventually a cure. We want to improve the day to day lives of those children who are affected and provide emotional support for them and their families.
To find out more about A Lasting Mark and how to donate please visit our website www.alastingmark.com

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