The publication is reproduced in full below:
STATEMENTS ON INTRODUCED BILLS AND JOINT RESOLUTIONS
By Mr. THUNE (for himself, Mr. Barrasso, Mr. Braun, Mr. Cramer,
Mr. Crapo, Mr. Hawley, Mr. Hoeven, Mrs. Hyde-Smith, Mr. Inhofe,
Mr. Lankford, Ms. Lummis, Mr. Moran, Mr. Risch, Mr. Rounds, Mr.
Rubio, Mr. Scott of South Carolina, Mr. Sullivan, Mr. Wicker, and Mr. Cruz):
S. 3412. A bill to prohibit the use of Federal funds to enforce the rule submitted by the Department of Health and Human Services relating to COVID-19 vaccine and mask requirements for Head Start programs; to the Committee on Health, Education, Labor, and Pensions.
Mr. THUNE. Mr. President, I ask unanimous consent that the text of the bill be printed in the Record.
There being no objection, the text of the bill was ordered to be printed in the Record, as follows:
S. 3412
Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled,
SECTION 1. SHORT TITLE.
This Act may be cited as the ``Preventing Mandates on Toddlers Act''.
SEC. 2. PROHIBITION ON FUNDING THE HHS RULE ON HEAD START
COVID VACCINE AND MASK REQUIREMENTS.
Notwithstanding any other law, no funds appropriated or otherwise made available to the Department of Health and Human Services shall be obligated or expended to--
(1) implement or enforce the rule submitted by the Department of Health and Human Services relating to ``Vaccine and Mask Requirements To Mitigate the Spread of COVID-19 in Head Start Programs'' (86 Fed. Reg. 68052 (November 30, 2021)); or
(2) promulgate, implement, or enforce any rule, regulation, or other agency statement, that is substantially similar to the rule described in paragraph (1).
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By Mr. KAINE (for himself, Mrs. Feinstein, and Mr. Padilla):
S. 3422. A bill to establish a grant program to support schools of medicine and schools of osteopathic medicine in underserved areas; to the Committee on Health, Education, Labor, and Pensions.
Mr. KAINE. Mr. President, communities of color and those living in rural and underserved areas face significant barriers to healthcare, including physician shortages that have only been exacerbated during the COVID-19 pandemic. Unfortunately, in many communities of color and rural areas, there are few pathways to enter the medical profession. While medical school enrollment is up by 30 percent, the number of students from rural areas entering medical school declined by 28 percent between 2002 and 2017, with only 4.3 percent of all incoming medical students coming from rural areas in 2017. Similarly, Black, Hispanic/Latino, and Native American students face several barriers to matriculate and graduate from medical school, and there is significant underrepresentation of these students at all U.S. medical schools with the exception of historically Black medical schools. These medical schools represent 2.6 percent of all medical schools but 15 percent of Black medical students, indicating the important role that these institutions play in increasing the diversity of the physician workforce. Health outcomes for patients of color improve when they receive care from doctors of their own racial or ethnic background, and the shortage of providers of color exacerbates the barriers to care that these communities experience. The COVID-19 pandemic worsened long standing health inequities, and it is critical that we expand the diversity of our physician workforce to tackle these rampant disparities and the systemic biases within our health care system.
This is why I am introducing the Expanding Medical Education Act, which aims to tackle the lack of representation of rural students, underserved students, and students of color in the physician pipeline by encouraging the recruitment, enrollment, and retention of students from disadvantaged backgrounds. The bill would provide grants through the Health Resources and Services Administration, HRSA, to colleges and universities to establish or expand allopathic or osteopathic medical schools in underserved areas or at minority-serving institutions, including historically Black colleges and universities, HBCUs. These grants can be used for planning and construction of a medical school in an areas in which no other school is based; hiring diverse faculty and staff; recruitment, enrollment, and retention of students; and other purposes to ensure increased representation of rural students, underserved students, and students of color in our physician workforce.
Our rural communities and communities of color face significant challenges accessing healthcare. It is time our physician workforce reflected these communities. We need to diversify our physician pipeline and change the disparity in representation, and this bill will help get us there. I am proud to reintroduce this important legislation to help us get one step closer to ensuring communities across Virginia and the Nation have access to the medical professionals they need. I hope the Senate passes this legislation quickly.
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By Ms. COLLINS (for herself and Mr. Lujan):
S. 3427. A bill to authorize the Secretary of Health and Human Services to establish a Neuroscience Center of Excellence; to the Committee on Health, Education, Labor, and Pensions.
Ms. COLLINS. Mr. President I rise today with my colleague, Senator Ben Ray Lujan, to introduce the Neuroscience Center of Excellence Act of 2021, legislation that would establish a Neuroscience Center of Excellence at the Food and Drug Administration, FDA. This program would be modeled after FDA's Oncology Center or Excellence, which was authorized through the 2lst Century Cures Act. Building off that successful and bipartisan model, I hope we can make critical advances for those living with neurological diseases.
In July, FDA's Director of the Center for Drug Evaluation and Research testified that neuroscience is an area of medicine where there is tremendous unmet need, and neurodegenerative diseases are particularly challenging from both a research and a drug development perspective. I have seen this firsthand as founder and cochairman of the Senate Alzheimer's Disease Caucus. I have vigorously advocated for record funding increases to support additional NIH research over the past 25 years. Over the past year, many have noted the success of Operation Warp Speed and wondered why we can't achieve the same rapid progress in other health conditions.
The Neuroscience Center of Excellence would encompass more than 20 neurological diseases, including conditions that are very rare. For example, Huntington's disease is an inherited disease characterized by the progressive loss of brain and muscle function. It has sometimes been described as having ALS, Parkinson's, and Alzheimer's simultaneously. It is an autosomal dominant condition, so families with a history of Huntington's disease can see it appear in every generation. In Maine, Nancy Patterson has seen Huntington's disease in four generations of family. In addition, I lost a friend and coworker in former Senator Bill Cohen's office to this devastating disease. Sadly, there is no cure.
Through our bill, this new Neuroscience Center of Excellence would establish several programs aimed at supporting innovation. The first is to identify some of the current and emerging regulatory science and public policy challenges associated with developing medical products for neuroscience diseases and disorders through a series of public meetings and guidances. The Center of Excellence would also establish a program to facilitate both the collection and the systematic use of patient experience data in the development of medical products for neuroscience diseases and disorders.
Another component of the Center's work would be around using digital technologies, an area of much promise. In 2018, the National Academies of Medicine Forum on Neuroscience and Nervous System Disorders hosted a workshop on using mobile technology to advance research and treatment of central nervous system disorders. As Dr. William Marks, head of clinical neurology at Verily Life Sciences, observed, the current state of assessing brain disorders is ``exquisitely crude'' and there is a large unmet need for better measures of disease burden that are objective, quantitative, more frequently measured, and in the context of normal life.
Finally, the center would help promote inclusion of traditionally underrepresented populations in the research and development of medical products for neuroscience diseases and disorders through public meetings and industry guidance. Senator Lujan and I have worked together on this issue before as part of our Equity in Neuroscience and Alzheimer's Clinical Trials Act of 2021. Whether the barrier to participation is a distrust of the medical community or logistics concerns like time and travel, we need to overcome those hurdles in order to ensure the best possible science.
Researchers from the University of South Florida looked at the nine most prevalent and costly diagnosed neurological disorders and found the annual cost totaled nearly $800 billion. We desperately need to change this trajectory and renew our focus on these critical unmet needs. I urge my colleagues to support this important legislation.
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SOURCE: Congressional Record Vol. 167, No. 217
The Congressional Record is a unique source of public documentation. It started in 1873, documenting nearly all the major and minor policies being discussed and debated.
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