June is Hereditary Hemorrhagic Telangiectasia (HHT) Awareness Month

The Pulmonary Hypertension Association and Cure HHT are partnering to learn more about the pulmonary arterial hypertension (PAH) and HHT community. Please share your experience and help us raise awareness about the risks associated with PAH + HHT.

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* 1. Have you been diagnosed with PH and HHT

Yes

No

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* 2. Do you currently have recurring nosebleeds?

Yes

No

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* 3. Does anyone in your family have recurring nosebleeds?

Yes

No

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* 4. If appropriate, may PHA send you additional information about PH and HHT?

Yes

No

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* 5. Contact Information (optional)

Name

Address

Address 2

City/Town

State/Province

ZIP/Postal Code

Country

Email Address

Phone Number

100% of survey complete.