Hereditary Angio Edema Kenya

We are an advocacy group for patients with hereditary angio edema as well as their caregivers, physicians and researchers. We all come together to create an enabling environment to improve the lives of patients with Hereditary Angio Edema in Kenya

Benefits of joining HAE Kenya

  • Access to appropriate and relevant information
  • Enrolment into the HAE Kenya support group sessions
  • Access to available medication for HAE
  • Access to a HAE Management programme
  • Being part of our advocacy activities and programmes

Sign up and become a member/ Jiandikishe ukuwe mmoja wetu

    Member type

    If you are a patient, please fill in these informations as well:

    HAE type

    View the video:
    My Journey with Hereditary Angioedema; Patricia Karani

    View the video:
    Abled Differently, featuring Rare Disease Day 2017 in Kenya

    View the video:
    HAEi Global Conference Madrid, Spain 2016; Current medical situation in Kenya; Patricia Karani

    Tumia ramani yetu ya maingiliano kupata rasilimali karibu na wewe

    Reach out to Hereditary Angio Edema Association Kenya

    Welcome to HAE Kenya, the Kenyan association for HAE patients and care givers

    Say Hello/ Tusalimie

    Kindly fill in the form to give us any information on your personal story, events happening around you or incase you wish to ask any question or inquire further concerning hereditary angio edema. We will be glad to hear from you.

    (Tafadhali jaza fomu utufikishie ujumbe, upeane hadithi yako, au uulize swali lako hapa. Tunaomba kusikia kutoka kwako) Swahili

    Jaza fomu ya mawasiliano

    Stay tuned

    Be the first to know what’s going on in the world of HAE

    –  Join us today at