Robert Weygand on Health Care

Voted NO on Prescription Drug Coverage under Medicare.

HR 4680, the Medicare Rx 2000 Act, would institute a new program to provide voluntary prescription drug coverage for Medicare beneficiaries through subsidies to private plans. The program would cost an estimated $40 billion over five years and would go into effect in fiscal 2003. Reference: Bill sponsored by Thomas, R-CA; Bill HR 4680 ; vote number 2000-357 on Jun 28, 2000

Voted YES on banning physician-assisted suicide.

Vote on HR 2260, the Pain Relief Promotion Act of 1999, would ban the use of drugs for physician-assisted suicide. The bill would not allow doctors to give lethal prescriptions to terminally ill patients, and instead promotes "palliative care," or aggressive pain relief techniques. Reference: Bill sponsored by Hyde, R-IL; Bill HR 2260 ; vote number 1999-544 on Oct 27, 1999

Voted NO on establishing tax-exempt Medical Savings Accounts.

The bill allows all taxpayers to create a tax-exempt account for paying medical expenses called a Medical Savings Account [MSA]. Also, the measure would allow the full cost of health care premiums to be taken as a tax deduction for the self-employed and taxpayers who are paying for their own insurance. The bill would also allow the establishment of "HealthMarts," regional groups of insurers, health care providers and employers who could work together to develop packages for uninsured employees. Another provision of the bill would establish "association health plan," in which organizations could combine resources to purchase health insurance at better rates than they could separately. Reference: Bill sponsored by Talent, R-MO; Bill HR 2990 ; vote number 1999-485 on Oct 6, 1999

Collect data on birth defects and present to the public.

Weygand sponsored the Birth Defects Prevention Act

collect and analyze, and make available data on the causes of birth defects and on the incidence and prevalence of such defects;
operate regional centers for the conduct of applied epidemiological research on the prevention of such defects;
provide information and education to the public on the prevention of such defects;
collect and analyze data by gender and by racial and ethnic group9/6/2004
collect such data from birth and death certificates, hospital records, and such other sources; and
(3) encourage States to establish or improve programs for the collection and analysis of epidemiological data on birth defects and to make the data available.

Corresponding House bill is H.R.1114. Became Public Law No: 105-168. Source: Bill sponsored by 35 Senators and 164 Reps 97-S419 on Mar 11, 1997

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