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Category | H |
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Domain name | haea.org |
DNS servers | ns-143.awsdns-17.com,ns-680.awsdns-21.net,ns-1514.awsdns-61.org |
IP | 34.202.217.172 |
Country by IP | US |
Web server type | Nginx |
Hostname | ec2-34-202-217-172.compute-1.amazonaws.com |
Alexa traffic rank | 920505 |
Majestic traffic rank | 743705 |
Welcome to the US Hereditary Angioedema Association, a non-profit advocacy organization serving people with Hereditary Angioedema (HAE) and their caregivers. HAE is a very rare and potentially life-threatening genetic condition involving swelling of various parts of the body, hands, feet, or face. Our association is a community of people ... Visit website
The HAEA is an advocacy and research organization committed to actively engaging our community in a wide variety of grassroots activities that promote HAE education and awareness. We provide personalized services to address the unique needs of people with HAE and their families, which includes helping them secure access to and reimbursement for ... Visit website
HAEA Compassion Fund - offers financial assistance for patients in need who must travel to see an HAE medical specialist. HAE Research - supports expert researchers in their efforts to solve the remaining scientific mysteries of HAE through the US HAEA Angioedema Center at UCSD. Stand up strong for HAE by registering for the HAE IN-MOTION ... Visit website
The US Hereditary Angioedema Association (HAEA) celebrated the Year of the HAEA Youth in 2016! As part of this celebration, the HAEA provided the Brady Club for our youngest patients. To keep current on all that the HAEA is working on to benefit our … Visit website
User login example. Enter your email to receive a login url. Receive Login URL Visit website
September 2021 Newsletter Topics include: The 2021 US HAEA Virtual Summit Series programs are now available for on demand streaming! , The US HAEA Sponsors Ground-breaking Research Study on Quality of Life for People with HAE, Save the Date! 2021 HAEA Virtual Capitol Hill Day Friday, October 15, 2021 - 1:00 PM ET, HAEA Webinar Brief: ... Visit website
? Participate in the HAEA VIRTUAL SUPPORT GROUP MEETINGS! Whether you are an HAE patient or caregiver, you may find it helpful to turn to others outside your immediate circle for support. For more information, contact Troyce Venturella at troyce@haea.org or (866) 798-5598. Visit website
HAE is an inherited condition, and each baby born to a parent with HAE has a 50 percent chance of inheriting the disease. You may wish to speak to a genetic counselor if you have specific questions about HAE as an inherited condition. Visit website
The HAEA Research Fund, which supports a variety of research initiatives including the HAEA Scientific Registry. Please donate using the form below, or you may also mail a check or money order to: US HAEA – Donation. 10560 Main Street, Suite PS40. Fairfax City, VA 22030. *We are a 501 (c) (3) non-profit organization that takes pride in ... Visit website
The HAEA is pleased to invite our HAEA friends to a Virtual Meet & Greet on Tuesday, April 19th, 2021 at 6:30 PM MT. This Meet & Greet will provide an overview of the great programs the HAEA offers as well as an opportunity to connect with people with HAE as well as caregivers in your area from the comfort and safety of your home.. Chat with local HAE families! Visit website