You’re Not Alone.
Bridging the gap between empowered patient and
compassionate providers and providing Lipedema Support and Resources.
17 Million American Women
Live with Lipedema
Why Lipedema Navigator Exists
1 in 10 Women go undiagnosed.
Only 5% get the help they need.
Diagnosis Gap
Studies indicate that only about 5% of patients are diagnosed by their general practitioner, meaning 95% often have to find answers themselves.
Overlooked Symptoms
Key indicators include disproportionate fat accumulation, pain, tenderness, easy bruising, and a "cuff" of fat stopping at the ankles.
Living Undiagnosed
Individuals suffer in silence and experience years of progressive pain, decreased mobility, and emotional distress.
What is Lipedema?
Lipedema is NOT Lymphedema.
Lipedema is a chronic, often inherited disorder characterized by the symmetrical, abnormal buildup of fat tissue, typically in the legs, hips, and buttocks—and sometimes arms—while sparing the hands and feet. It largely affects women and is triggered by hormonal changes (puberty, pregnancy, menopause), causing pain, tenderness, and easy bruising.Â
11%
of the adult female population is effected.
100
Percent of patients experienced chronic pain and easy bruising.
64%
of women with Lipedema experience depression or anxiety.
13
The average age of symptom onset, yet diagnosis often occurs around age 48.
"I waited months
in the dark. Lipedema Navigator was there after I reached out to give me answers."
Maya, 65
Every Woman
Deserves To Feel
Supported
We Connect Providers With Patients and Resources.