Our Mission
Our Commitment
At HAE Nepal, we strive to enhance the lives of those affected by hereditary angioedema through education, advocacy, and support. Together, we create a community that fosters understanding and hope.
Who We Are
HAE Nepal is dedicated to enhancing the lives of those affected by hereditary angioedema (HAE). As part of the global HAE International network, we raise awareness, facilitate timely diagnoses, and advocate for access to life-saving treatments. Our compassionate community of patients and caregivers works tirelessly to ensure that every individual suffering from HAE receives the support and resources they need.
4300+ Happy Customer
Our community members express gratitude for the support and resources that HAE Nepal provides on their journey with HAE.
20+ Awards Won
HAE Nepal has received accolades for its outstanding contributions to patient advocacy and awareness efforts within the HAE community.
40 Years of Experience
With extensive experience in HAE advocacy, HAE Nepal has been a trusted resource for patients and caregivers for several years.
At HAE Nepal, we believe in creating a united front against HAE. Together, we share our stories, support one another, and push for better treatments and awareness.
Anu Sharma, Founder
Founder
At HAE Nepal, we strive to enhance the lives of those affected by hereditary angioedema through education, advocacy, and support. Together, we create a community that fosters understanding and hope.
Patient Advocacy
We champion the needs of HAE patients, ensuring their voices are heard in the development of healthcare policies and treatment access.
Education and Awareness
Through informative resources and outreach programs, we raise awareness about HAE, helping patients and caregivers recognize symptoms and seek timely diagnosis.
Global Community
As part of a worldwide network, we connect families and individuals affected by HAE, fostering a sense of belonging and shared experience.
Join us in making a difference for those affected by hereditary angioedema. Your support is essential.