A Lasting Mark
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Luke was diagnosed with Linear Scleroderma in 2013. His goal is to spread awareness and raise funds His disease has presented in his right upper extremity.
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
01/01/2026
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 ...
07/18/2025
Time well spent in Utah for A Lasting Mark and the Medolla family 🩵
Last pic 🥰
07/12/2025
Family Summit in Utah 🩵
06/03/2025
June is National Scleroderma Awareness Month! Click the link below to learn more about scleroderma, Luke’s story, our foundation and how to donate 💙
www.alastingmark.com
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
12/02/2024
Thank you to everyone that participated in our Black Friday raffle!! We truly appreciate all of the support. Happy Shopping Lori!! 💙
11/30/2024
THANK YOU to all of our sponsors, players & volunteers for supporting our Jayhawk Cup event. Because of each and every one of you we are raising awareness and funds towards helping those affected with pediatric scleroderma.
With much appreciation and gratitude ~ Luke, Marybeth, Michael and the Medolla Family
A Lasting Mark 💙
www.alastingmark.com
11/29/2024
The winner of our 2024 3rd annual Jayhawk Cup is the class of 2020!!! Congratulations!!
11/29/2024
We’re ready for our 3rd annual Jayhawk cup! ⚽️💙
11/28/2024
Happy Thanksgiving!!
We are so thankful for all of our sponsors who helped make tomorrow’s Jayhawk Cup event possible. We’re looking forward to a great day of soccer but today we wish all of you and your families a wonderful Thanksgiving!
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Jericho, NY