You’re here to support someone with HAE. We’re here to support you.
We know that taking care of a loved one with hereditary angioedema (HAE) comes with questions and concerns. Learn what to expect once they start their treatment—and how to help them stay on track.
4000+
ADULTS AND ADOLESCENTS HAVE BEEN PRESCRIBED TAKHZYRO SINCE 2018*
What to expect when your loved one starts TAKHZYRO
Your loved one and their doctor likely chose to help prevent HAE attacks with TAKHZYRO for several reasons. One of those may have had to do with the results of the clinical studies. In those studies, people taking TAKHZYRO had fewer HAE attacks on average, and some even had periods of time with zero attacks.
If you’re caring for a child with HAE, you can find information about HAE in children
You can also explore our pediatric brochure for tips and support on helping your child stay on track with treatment.
Help your loved one start off right
Make sure your loved one remembers why they started taking TAKHZYRO.
Frequently Asked Questions
While we recommend you ask your healthcare team any treatment questions you have, here are some frequently asked questions and answers you may find helpful.
Caregivers have many things they need to pay attention to in the day-to-day lives of their loved ones living with HAE. These can include:
- Any new health issues
- How often they use on-demand medications
- New or existing HAE triggers. These may include stress, exhaustion, hormonal fluctuation, or physical activity
- the location, intensity, and duration of all attacks
- What their attacks were like before preventive treatment and what they’re like now
Your loved one can use the Journey Journal to track these details. As a caregiver, you can help them update this journal and share it with their doctor. This can help everyone see how much progress they’ve made with their treatment goals.