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HR 1849 114th Congress House Health Advisory bodies Cardiovascular and respiratory health Health care costs and insurance Health facilities and institutions Health information and medical records Health programs administration and funding Hereditary and development disorders Medical research Medical tests and diagnostic methods Medicare Research administration and funding

Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2015

Introduced: April 16, 2015 See on congress.gov
 Everywhere this bill has been 4 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Apr 29, 2015
Referred to the Subcommittee on Health.
Apr 17, 2015
Referred to the Subcommittee on Health.
Apr 16, 2015
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
Apr 16, 2015
Introduced in House
 Plain-English summary Congressional Research Service

Hereditary Hemorrhagic Telangiectasia Diagnosis and Treatment Act of 2015

Amends the Public Health Service Act to require the Department of Health and Human Services (HHS) to establish and implement a hereditary hemorrhagic telangiectasia (HHT, a genetic vascular bleeding disorder that causes abnormalities of the blood vessels) initiative to improve early detection, screening, and treatment of people who suffer from HHT, focusing on advancing HHT research and increasing physician and public awareness of HHT.

Directs HHS to establish the HHT Coordinating Committee to develop and coordinate implementation of a plan to advance research and understanding of HHT, including by conducting or supporting research at the National Institutes of Health (NIH) and making recommendations regarding NIH research grants relating to HHT.

Requires the Centers for Disease Control and Prevention to carry out activities with respect to HHT, including conducting surveillance and establishing an HHT resource center to provide comprehensive education on and disseminate information about HHT to health professionals, patients, industry, and the public.

Requires the Centers for Medicare & Medicaid Services to award grants for HHT research, including an analysis of health care expenditures associated with untreated HHT and costs associated with preventable medical events among Medicare beneficiaries with HHT.

What's happening now April 29, 2015

Referred to the Subcommittee on Health.

 Committees of jurisdiction 4