Skip to main content
HCONRES 179 109th Congress House Health Access to health care Blood diseases Bone diseases Economics and Public Finance Federal aid to research Health counseling Health education Health surveys Medical research Medical tests Nonprofit organizations Quality of care Science, Technology, Communications Social Welfare

Expressing the sense of the Congress regarding bone marrow failure diseases.

Introduced: June 16, 2005 See on congress.gov
 Everywhere this bill has been 3 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Jul 1, 2005
Referred to the Subcommittee on Health.
Jun 16, 2005
Referred to the House Committee on Energy and Commerce.
Jun 16, 2005
Introduced in House
 Plain-English summary Congressional Research Service

Expresses the sense of Congress that: (1) individuals diagnosed with bone marrow failure diseases and their families should have access to a variety of treatment and counseling options; and (2) such families should be linked to support networks and counseling information serviced provided by nonprofit organizations like the Aplastic Anemia & MDS International Foundation.

Calls for the federal government to: (1) raise awareness about the importance of early detection of and proper treatment for such diseases; (2) provide adequate funding for research on such diseases; (3) engage in such public health initiatives as surveillance, education, and awareness of such diseases; and (4) continue to consider ways to improve health care services for such diseases.

What's happening now July 1, 2005

Referred to the Subcommittee on Health.

 Committees of jurisdiction 2