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Pediatrician In Congress Tells RFK Jr.: I Will Blame You For All Vaccine-Preventable Deaths

Pediatrician In Congress Tells RFK Jr.: I Will Blame You For All Vaccine-Preventable Deaths

Yahoo6 hours ago

WASHINGTON – Rep. Kim Schrier (D-Wash.) on Tuesday tore into Health and Human Services Secretary Robert F. Kennedy, Jr. for his decades of lies about the safety and effectiveness of vaccines, saying she will blame him every time someone dies from a vaccine-preventable disease on his watch.
'You have lied to the American people,' Schrier, who is a pediatrician, charged as Kennedy sat silently before a House committee. 'You have lied to parents about vaccines for 20 years.'
'And I also want to be clear that I will lay all responsibility for every death from a vaccine-preventable illness at your feet,' she said.
Here is a clip of their exchange.
Kennedy, who has a long history of peddling dangerous misinformation about vaccines, was testifying before the House panel about his agency's budget request when Schrier began describing what happens when unvaccinated babies and children get sick with things like measles, bacterial meningitis or whooping cough.
'Have you ever treated measles?' she asked.
Kennedy replied, 'No.'
'Well, I have. Let me tell you how miserable it is,' said the Democratic congresswoman. 'These kids have high fevers, struggling to breathe and they are crying. They suffer. The great news is there's a vaccine to prevent it.'
Schrier went on, describing babies in the emergency room 'so sick,' 'floppy' and with high fevers because they have bacterial meningitis. She recalled treating one baby who came down with whooping cough, who was weeks old and had 'stopped breathing and turned blue.'
'Let me tell you how scared those parents were,' she said to Kennedy. 'I've treated a bunch of older kids with it. They cough so hard they vomit. They run out of air. They break ribs. If you don't catch it before two weeks, antibiotics don't even work.'
'You know what's great? There's a vaccine that prevents this,' Schrier said. 'Of course, here's the thing: Vaccines only work if you actually give them. And we know your record on this.'
Kennedy's record includes pushing the debunked claim that vaccines cause autism. He's floated bizarre conspiracy theories about COVID-19 being 'ethnically targeted' to spare Jewish and Chinese people. He's referenced the Holocaust when talking about vaccines and public health mandates.
As HHS secretary, he has said that getting vaccinated is a personal choice instead of citing science-based evidence that vaccines are safe, effective and strongly recommended. He's called for cutting billions in funding for a program that provides vaccines to children in low-income families, and he directed the Centers for Disease Control and Prevention to no longer recommend COVID vaccine boosters for children and pregnant women.
We believe Sen. Cassidy more than we trust you when it comes to vaccinations.Rep. Kim Schrier (D-Wash.)
During Tuesday's hearing, Schrier also accused Kennedy of pulling a fast one on Sen. Bill Cassidy (R-La.), who only voted to confirm Kennedy to his current post because he said he got assurances that the HHS secretary wouldn't make changes to the Advisory Committee on Immunization Practices, a panel of medical and public health experts that provides recommendations on vaccine guidance for various diseases.
Kennedy fired all 17 members of that panel earlier this month, saying in a statement that the move was about 'prioritizing the restoration of public trust above any specific pro- or anti-vaccine agenda' with a plan to replace the panelists. His actions inevitably mean that, going forward, HHS's guidance on vaccine safety will be rooted in misinformation and views from outside the scientific community, one vaccine policy expert told HuffPost.
'Did you lie to Sen. Cassidy when you told him you would not change this panel of experts?' she asked.
'I never made that agreement,' Kennedy replied.
After some back and forth, Schrier said she simply doesn't believe him.
'I just want to tell you that for most of us sitting here right now, we believe Sen. Cassidy more than we trust you when it comes to vaccinations,' she said.

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We routinely post information that may be important to investors on our website at In addition, to learn more, please visit us on and follow us on X at @Pfizer and @Pfizer_News, LinkedIn, YouTube and like us on Facebook at Disclosure notice The information contained in this release is as of June 26, 2025. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments. This release contains forward-looking information about HYMPAVZI™ (marstacimab), an anti-tissue factor pathway inhibitor, including its potential benefits and plans to discuss the Phase 3 BASIS data with regulatory authorities with the goal of initiating regulatory filings for HYMPAVZI for the treatment of patients living with hemophilia with inhibitors, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Risks and uncertainties include, among other things, uncertainties regarding the commercial success of HYMPAVZI; the uncertainties inherent in research and development, including the ability to meet anticipated clinical endpoints, commencement and/or completion dates for our clinical trials, regulatory submission dates, regulatory approval dates and/or launch dates, as well as the possibility of unfavorable new clinical data and further analyses of existing clinical data; the risk that clinical trial data are subject to differing interpretations and assessments by regulatory authorities; whether regulatory authorities will be satisfied with the design of and results from our clinical studies; whether and when any applications may be filed with regulatory authorities in particular jurisdictions for HYMPAVZI for any potential indication; whether and when any such applications that may be pending or filed for HYMPAVZI may be approved by regulatory authorities, which will depend on myriad factors, including making a determination as to whether the product's benefits outweigh its known risks and determination of the product's efficacy and, if approved, whether HYMPAVZI will be commercially successful; decisions by regulatory authorities impacting labeling, manufacturing processes, safety and/or other matters that could affect the availability or commercial potential of HYMPAVZI; risks and uncertainties related to issued or future executive orders or other new, or changes in, laws or regulations; uncertainties regarding the impact of COVID-19 on our business, operations and financial results; and competitive developments. A further description of risks and uncertainties can be found in Pfizer's Annual Report on Form 10-K for the fiscal year ended December 31, 2024 and in its subsequent reports on Form 10-Q, including in the sections thereof captioned "Risk Factors" and "Forward-Looking Information and Factors That May Affect Future Results", as well as in its subsequent reports on Form 8-K, all of which are filed with the U.S. Securities and Exchange Commission and available at and 1 Shapiro AD, Ragni MV, Borhany M, et al. Natural history study of factor IX deficiency with focus on treatment and complications (B-Natural). Haemophilia. 2021;27(1):49-59. doi: 10.1111/hae.14139.2 Valentino LA, Ewenstein B, Navickis RJ, Wilkes MM. Central venous access devices in haemophilia. Haemophilia. 2004;10(2):134-46. doi: 10.1046/j.1365-2516.2003.00840.x.3 Nugent D, Kalnins W, Querol F, et al. Haemophilia Experiences, Results and Opportunities (HERO) study: Treatment-related characteristics of the population. Haemophilia. 2015;21(1):e26-38. doi: 10.1111/hae.12545.4 Soucie JM, Symons Jt, Evatt B, Brettler D, Huszti H, Linden J. Home-based factor infusion therapy and hospitalization for bleeding complications among males with haemophilia. Haemophilia. 2001;7(2):198-206. doi: 10.1046/j.1365-2516.2001.00484.x.5 Teiu P, Chan A, Matino D. Molecular Mechanisms of Inhibitor Development in Hemophilia. Mediterr J Hematol Infect Dis. 2020 Jan 1;12(1):e2020001. doi: 10.4084/MJHID.2020.001.6 Centers of Disease Control and Prevention. Testing for Inhibitors and Hemophilia. Accessed May 14, 2025. Available at: World Federation of Hemophilia. World Federation of Hemophilia Global Report on the Annual Global Survey 2022. Meeks S, Batsuli G. Hemophilia and inhibitors: Current treatment options and potential new therapeutic approaches. Hematology Am Soc Hematol Educ Program. 2016 Dec 2;2016(1):657–662. doi:10.1182/asheducation-2016.1.657.9 Srivastava A, Santagostino E, Dougall A, et al. WFH guidelines for the management of hemophilia, 3rd Edition; 2020. Haemophilia. 26(S6), 1–158. Franchini M, Mannucci PM. Past, present and future of hemophilia: A narrative review. Orphanet J Rare Dis. 2012;7:24. Weyand AC, Pipe SW. New therapies for hemophilia. Blood. 2019;133(5):389–398. Walsh CE, Soucie JM, Miller CH. Impact of inhibitors on hemophilia a mortality in the United States. Am. J. Hematol. 2015; 90: 400-405. Category: Medicines View source version on Contacts Media Contact:+1 (212) 733-1226PfizerMediaRelations@ Investor Contact:+1 (212) 733-4848IR@ Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data

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