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(Pronounced Sk-AH-L-vihn)
At Scolvin Foundation, we envision a world where every individual living with a chronic illness has access to the resources they need to live a healthy, happy, and fulfilling life, regardless of their background or circumstances.
Inspired by her own battle with lupus, her work supporting people with infectious diseases, and her care for loved ones with autoimmune conditions, our founder aimed to replace uncertainty, stigma, and scarce resources with hope.
Bearing the name of our founder, the Scolvin Foundation began in 2013 with a vision to support individuals through hope and was officially established in 2024 as dedicated stewards of that hope.
The Scolvin Foundation is committed to inspiring individuals and communities affected by lupus, multiple sclerosis, and HIV/AIDS.
Aiming to be a leading charity that supports individuals nationwide and worldwide, it partners with organizations to boost education and awareness, provide scholarships and learning opportunities, and back inclusive research focused on discovering treatments and cures.

To provide hope to individuals diagnosed with LUPUS, MULTIPLE SCLEROSIS, and/or HIV/AIDS through education, research, & illness awareness.
A world where those living with a chronic illness don’t have to choose between surviving and thriving.
I did not die. I lived! And now I’m telling the world what God did. Psalms 118:17
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