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The Annual Walk for Scleroderma in Manitoba is held each year during June Scleroderma Awareness Month to raise awareness of this disease, and to raise funds for patient support and research into better understanding
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The Scleroderma Society of Canada is a non-profit organization dedicated to supporting individuals affected by scleroderma, raising awareness about the disease, and funding research to improve treatments and outcomes.
Individuals and organizations involved in conducting activities related to scleroderma in Canada may be required to file documentation with the Scleroderma Society of Canada, especially those seeking funding or support.
To fill out forms related to the Scleroderma Society of Canada, individuals should obtain the appropriate forms from the society's website or office, complete them with accurate information regarding their activities, and submit them as per the guidelines provided.
The purpose of the Scleroderma Society of Canada is to provide support and resources for individuals with scleroderma, raise public awareness, advocate for patients' rights, and fund research initiatives to advance treatment and understanding of the disease.
Information to be reported typically includes details about the activities undertaken, funding needs, research purposes, outcomes achieved, and any challenges faced in addressing scleroderma.
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