With a disease as rare as HAE, it's not surprising to find many patients feeling depression, fear and anxiety, which can be compounded by a lack of understanding among health professionals and the public. The isolation of such a serious diagnosis can be profound, contributing to the negative emotions the disease can create.
But you can find a lot of information to help you with managing your disease; for example, you can use the Web to learn more about HAE as well as connect with others who are in a similar situation. You can learn from each other, sharing experiences, tips, ideas, and inspiration.
Finding people who understand what you're going through, either as a patient or as a caregiver, can be a validating experience. You'll learn that you're not the only one who feels a certain way about the experience, which can help you feel less alone with hereditary angioedema.
Where to start? HAE Hope offers tips from members of our community, as well as insights from medical experts and others who live with hereditary angioedema. Other venues for connection include (Note: by clicking any of the links below, you will leave HAE Hope):
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