I met Steph Courdin in the summer of 2015 at an Ice Bucket
Challenge to raise awareness and funds for ALS. I was dressed as “Super Carpe
Diem Woman,” a goofy super-hero who’s ‘power’ is to live life fully. Steph, a
photographer, was taking pictures of the event with a very fancy looking
camera. He was smiling as though he
didn’t have a care in the world. The fact that Steph was in a wheelchair was my
only clue that he might have ALS himself.
Though it’s easy to ‘live life fully’ when you have a fully functional body, I believe the real super-heroes are people like Steph who set that example, despite an ALS diagnosis. Steph doesn’t let the disease stop him from hitting the trails, traveling, and most recently, “rolling” his daughter down the aisle on her wedding day, via a standing wheelchair.
Though it’s easy to ‘live life fully’ when you have a fully functional body, I believe the real super-heroes are people like Steph who set that example, despite an ALS diagnosis. Steph doesn’t let the disease stop him from hitting the trails, traveling, and most recently, “rolling” his daughter down the aisle on her wedding day, via a standing wheelchair.
ALS, a fatal, degenerative disease, also known as Lou
Gehrig’s Disease, gained national attention during the Summer 2014 Ice Bucket
Challenge mania. Until then, it was a comparatively unknown disease with little
progress made towards a cure. It’s encouraging that the money raised from the
ice bucket challenges are making a difference, but the cure won’t come
overnight. In the meantime, Steph had an idea to help.
In 2015, Steph, in addition to living a full and active
family life, created the non-profit ALS Never Surrender Foundation aimed at
helping with research and ultimately finding a cure for ALS. Having a background and experience
with data analytics, Steph had the idea of creating a mobile application that
would collect data pertinent for ALS patients. By monitoring the progression of
patients as well as their treatments, researchers and doctors can gain valuable
knowledge and feedback about treatments that will slow or even stop the
progression of symptoms.
Steph shared his idea with some contacts in San Diego and in
the Fall of 2016, the designs and use-cases became a reality with the
availability of a beta version of the ALS iNVOLVE application. In January of 2017,
students from Georgia Southern University pitched in to finish the first
version.
To help fund this massive undertaking, Steph initiated ‘Art4the Cure’ – a group of 42 artists from
9 countries and 14 states who have donated art to help raise money for the
cause. Additionally, Steph started a ‘Faces of ALS’ portrait series to feature
and highlight others who are surviving and thriving despite ALS.
Steph’s courage, determination, and will to ‘never
surrender’ are an inspiration. For those of us who are healthy, we are reminded
not to take that health for granted. And for those who do have ALS, Steph is a
reminder that living fully is always possible. He’s a leader who is not going
to let ALS stop him from living his dreams and finding innovative ways to move
the world closer to a cure for ALS. He is, in short, the super-hero who shows
us all how to live life to the fullest.
Please help Steph and ALSNeverSurrender launch this life-saving
application by donating at http://alsneversurrender.org/donate. If you have ALS or know someone who does, get involved by using a beta version of the application.
1 comment:
My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Tree of Life Health clinic. It has made a tremendous difference for me (Visit w w w. treeoflifeherbalclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
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