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What is HHT? Capital Research Program Medical Professionals Members Print

August 31, 2005: New HHT Treatment Center Opens in England, The Hull Royal Infirmary

August 28, 2005: Board Members for 2005 are announced: SMAB Board and HHT Board

August 23,2005: HHT Foundation Announces 2005 Research Grant Award

August 19, 2005: The Summer 2005 newsletter for members is available.

July 27, 2005: HHT Foundation announces a Patient Mini-Conference in Portlandt, Oregon - October 1, 2005!

April 14, 2005: Are you a SHOPPER? Help the HHT Foundation raise money by being a SHOPPER

February 18, 2005: We are very excited to report that S.306, the Genetic Information Nondiscrimination Act 2005 (GINA), just passed in the Senate by a vote of 98-0!

January 27, 2005: HHT Foundation has announced the 2005 request for proposal (RFP) for the following topic: “HHT: Mechanisms of Disease” .

January 24, 2005: Medical Professionals: Sixth HHT Scientific Conference in Lyon.

November 28, 2004: Dr. Shapshay is conducting a study on the effect of estrogen and intensity of nosebleeds.

November2, 2004: Dr. Deborah Proctor at Yale University has received a grant to study HHT and GI bleeding in women. Volunteers are still needed.


Do you want to help or donate to the HHT Foundation?

Click the link below for ideas on how to fund raise.
click here.

Mission Statement
The HHT Foundation was formed in 1990 to aid and support persons with Hereditary Hemorrhagic Telangiectasia (HHT) also known as Osler-Weber-Rendu Syndrome; to provide patients, families and doctors with educational information; to foster an exchange of information about the diagnosis and treatment of HHT between patients, physicians, researchers, genetic counselors, charitable organizations, government agencies, industry, academic institutions and the general public; to raise funds for genetic and clinical research and for sponsoring special scholarships for studies pertaining to HHT.

What is this about?
This website is operated by the Hereditary Hemorrhagic Telangiectasia Foundation International, Incorporated. HHT Foundation International is a worldwide, non-profit organization whose purpose is to support patients and families and educate medical professionals. This site is dedicated to the individuals and medical professionals who encounter the daily challenges of managing Hereditary Hemorrhagic Telangiectasia (HHT) also known as Osler-Weber-Rendu Syndrome. HHT is a genetic disorder, which affects blood vessels. This disorder is worldwide affecting males and females of all races and ethnic groups. Up to 1/3 of HHT patients can have multiple organ involvement, which can be disabling and or life threatening. HHT can be treated successfully if correctly diagnosed.

We hope that the information provided on this website is informative and helpful. We encourage visitors to become a member of the Foundation in order to stay fully aware of advances made in research, treatment and education. If you are a member of the HHT Foundation and request a password and still are unable to successfully enter the new website, assume that the Foundation does not have your e-mail address. Please either e-mail your correct address to us or call us at the 800 number below. We will then enter your information into our database and you can then log in within a few hours and request a password which then will enable you to enter the site.

If you have any comments or questions about the site, please email us at hhtinfo@hht.org.

HHT Foundation International, Inc.,
P.O. Box 329
Monkton, MD 21111
1-800-448-6389
410-357-9932
FAX: 410-357-9931
hhtinfo@hht.org

" To wrest from nature the secrets which have perplexed philosophers in all ages, to track to their sources the causes of disease, to correlate the vast stores of knowledge, that they may be quickly available for the prevention and cure of disease-these are our ambitions,"
-- Sir William Osler

© 2004, The Hereditary Hemorrhagic Telangiectasia Foundation, Privacy Statement

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