Helpful Web Sites
Each of the links below will take you to a Web site to which our Privacy Policy does not apply. You are
solely responsible for your interactions with such Web sites.
The following Web sites are neither owned by nor controlled by Pfizer. Pfizer is
not responsible for the content or services on these sites.
Pulmonary Hypertension Association (PHA)
The mission of PHA is to seek a cure, to promote awareness and advocacy among the
PAH community, and to provide hope, support, and education. The organization sponsors
scientific research and helps patients learn about new treatments and ways to cope
with PAH.
801 Roeder Road, Suite 400
Silver Spring, MD 20910
800-748-7274 (Toll-free patient-to-patient helpline)
301-565-3004 (Administration)
E-mail: pha@phassociation.org
http://www.phassociation.org
Pulmonary Hypertension: The Complete Resource
This is an Internet resource for PAH-related information for patients, caregivers,
and medical professionals. The site offers chat rooms, patient diaries, news and
events, an online store, and links to other resources.
http://www.phcentral.org/
National Institutes of Health (NIH) Office of Rare Diseases
NIH’s Office of Rare Diseases Web site has a little information about pulmonary
hypertension (PH) and offers a database of current PH clinical trials. The National
Heart, Lung, and Blood Institute (NHLBI), which is part of NIH, sponsors and conducts
research and training related to PH. The NHLBI site offers patient education as
well as information about clinical trials and lifestyle.
National Institutes of Health Office of Rare Diseases
http://rarediseases.info.nih.gov
National Heart, Lung, and Blood Institute
http://www.nhlbi.nih.gov/index.htm
National Organization for Rare Disorders, Inc. (NORD)
NORD is a nonprofit federation of voluntary health organizations that helps people
with rare diseases such as PH by supporting education, advocacy, and research.
National Institutes of Health Office of Rare Diseases
PO Box 1968
Danbury, CT 06813-1968
800-999-6673
203-797-9590
http://www.rarediseases.org
National Registry for Familial Primary Pulmonary Hypertension (FPPH)
Funded by NIH, this genetic research program is designed to collect information
from families with hereditary PH, with the goal of learning the cause of the disease
and developing new treatments. By identifying genes associated with PH, the aim
is to find ways to modify the course of the disease and to learn about the relationship
between PH and environmental factors. If you have more than one family member with
PH, you are encouraged to enroll in the program. Confidentiality is protected.
800-288-0378
http://www.mc.vanderbilt.edu/root/vumc.php?site=vupphstudy
American Lung Association®
The American Lung Association is the oldest voluntary health organization in the
United States, with a national office and constituent and affiliate associations
around the country. Founded in 1904 to fight tuberculosis, the American Lung Association
today fights lung disease in all its forms, with special emphasis on asthma, tobacco
control, and environmental health. The site offers news and information about lung
diseases, treatment, support, advocacy, and environmental issues that affect public
health.
61 Broadway, 6th Floor
New York, NY 10006
212-315-8700.
http://www.lungusa.org/
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