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In memory of
Mrs. Pauline Agnes Clark
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Please consider a contribution to Children's Scoliosis Foundation.
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Background
Pauline, had severe Scoliosis and we as a family witnessed what this terrible disease can do to a person’s body. Early detection is critical in helping to combat the progression of Scoliosis and that is why, in lieu of flowers etc. that donations be made to the Children’s Scoliosis Foundation in her honor. In time, we are hoping they can find a cure for this disease but in the meantime perhaps we can help a child get ahead of this disease and live a full happy and healthy life without pain.
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About Children's Scoliosis Foundation
The Children's Scoliosis Foundation is a patient and family led nonprofit that is dedicated to providing support to families, promoting awareness, and advancing the science of scoliosis detection, treatment and prevention.Frequently asked questions
Answered by a team member at Children's Scoliosis Foundation
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How are donations used?
A diagnosis of childhood scoliosis can take an emotional and financial toll on families, especially when they must travel long distances to seek specialized bracing, casting, or surgical treatment. A medical travel grant can help ease the burden on families, while our care packs (featuring Higgy Bears!) help to bring a smile to children who are facing a new and uncertain situation. Through our research and education programs we strive to advance global knowledge about scoliosis detection, causes, treatment, and possible prevention strategies. 100% of your donation will go to our programs, including medical travel grants, care packs, education and research programs.
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In lieu of flowers
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Created with love by
Ian Clark (Pauline's son) and
Caitlin Clark (Pauline's daughter).
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