Sitosterolemia Foundation

Our Story

Cyndi Jones, president of the Sitosterolemia Foundation, shares her family's journey with sitosterolemia, a rare sterol disease affecting her sons. After years of struggling to understand their high cholesterol levels, they discovered the condition through research and collaboration with medical professionals. This personal experience motivated Cyndi to advocate for awareness, support, and research for families dealing with sitosterolemia.

Impact

The Sitosterolemia Foundation is dedicated to enhancing the quality of life for individuals affected by sitosterolemia through support, research funding, and awareness-raising efforts.

Why Donate?

Donating to the Sitosterolemia Foundation helps support families affected by this rare condition, fund critical research, and raise awareness among healthcare professionals, ultimately leading to better diagnosis and treatment options.

Get Involved

Your contribution can make a significant difference. Support the Sitosterolemia Foundation today by donating cryptocurrency or cash. Together, we can improve lives and foster hope for families affected by sitosterolemia.