National Bleeding Disorders Foundation
@nbd_foundation
Dedicated to finding better treatments/cures for inheritable blood/bleeding disorders & preventing complications via education, advocacy, research. #WeAreNBDF
ID: 39823988
https://bleeding.org/ 13-05-2009 20:18:00
23,23K Tweet
7,7K Followers
1,1K Following
Dr. Jason Vassy
@jasonvassy
Primary care physician and genomic medicine researcher @VABostonHC | Assoc Prof @HarvardMed | @BrighamWomens | @Genomes2People
Gerry Smith
@gerryfsmith
Biotech reporter for @business. Views are my own. Tips: [email protected]
ISTH
@isth
Plan to learn the latest science and network with global leaders at the #ISTH2025 Congress in Washington, D.C. Early registration ends April 22: isth2025.org
The Plasma Professor
@petermjaworski
Ethicist. Canadian. Faculty, @MSBGU. I mostly research and tweet about paid plasma. Projects: donationethics.com and plasmaforall.org
Vincent Rajkumar
@vincentrk
Editor-in-Chief, Blood Cancer Journal; Oncologist; Chair, Board of Directors @IMFmyeloma; Cancer Research; Opinions solely personal views bit.ly/3f4TnJl
Jared S. Hopkins
@jaredshopkins
Pharma for @WSJ but I also once interviewed John Oates. [email protected] jaredshopkins.com
HRSA
@hrsagov
The official government account of the Health Resources and Services Administration, an agency of @HHSgov. Authentication: hhs.gov/web/social-med…
Arturo LoAIza-Bonilla, MD MSEd
@drbonillaonc
Co-founder @MassiveBio | Systemwide Hem/Onc Chief at @mystlukes | Using #tech #AI & #genomics to fight cancer at global scale 🌎 🚀 🧬 🖥️ - My Opinion
Michael Makris
@profmakris
Emeritus Professor of Haemostasis and Thrombosis in Sheffield, UK. I tweet about thrombosis, hemophilia, COVID-19, medicine, NHS & AI. Opinions are my own.
ASH
@ash_hematology
The American Society of Hematology (ASH) is the world's largest professional society concerned with the causes and treatments of blood disorders.
WFH
@wfhemophilia
The World Federation of Hemophilia improves and sustains care for people with inherited bleeding disorders around the world.
National Library of Medicine
@nlm_nih
Official account of the National Library of Medicine at @NIH. Serving scientists & society. More at @MedlinePlus and @NCBI. Privacy: go.usa.gov/x6k7C
Patrick James Lynch
@pjlynch
Founder & CEO, BelieveLimited.com, filmmaker & rare disease advocate
Haemophilia Society
@haemosocuk
We are a community that makes each other feel stronger every day. Membership is completely free and everyone affected by a bleeding disorder is welcome.
Mark Hobraczk
@mhobraczk
Ai Arthritis Director Public Policy. Soccer dad and patient with ankylosing spondylitis. Wendish. Opinions my own.
Clive Smith
@clive_smith_
President of The Haemophilia Society, World Federation of Hemophilia Youth Chair, Criminal Barrister & Lecturer
Megan Ranney MD MPH 🌻
@meganranney
I fix problems and promote health 🔸️Dean @YaleSPH🔸️ER doc 🔸️ Cofounder @researchaffirm #ThisIsOurLane🔸️press inquiries [email protected]
Jeff Zwicker, MD
@jzbos
Blood, clotting, Red Sox, repeat. Chief of Hematology Service at Memorial Sloan Kettering Cancer Center #MSKCC
Irene Benedicto
@irenebenedicto
Staff writer @elperiodico ~I covered Putin @BuzzFeedNews, Obama @EFEnoticias & the AI bubble @Forbes/ Bylines @nytimes @washingtonpost/ Berkeley alumna @ucbsoj
Cesar A. Garrido
@cesargarridod
World Federation of Hemophilia PRESIDENT
haemnet
@haemnet
Undertaking in-depth mixed methods research into the lived experience of people affected by bleeding disorders
Anita Brikman
@anitabrikman
President & CEO, Plasma Protein Therapeutics Association (PPTA Global) @plasmaproteins @pptaeurope
Elizabeth Fernandez
@efernandezucsf
UCSF PIO, former journalist
U.S. Surgeon General
@surgeon_general
Official X account for the U.S. Surgeon General. Tweets before 01/20/25 are from prior federal officials. Privacy: hhs.gov/privacy.html
Amy Dockser Marcus
@amydmarcus
Health and science reporter for The Wall Street Journal, author of We the Scientists (2023) @riverheadbooks
Marie Eales
@mariethenurse
Paediatric Haemophilia ANP, Oxford. Always hoping to make life easier for my patients and families...
Dr Kate Khair PhD
@katekhair
Nurse, researcher, Director of Research @haemnet. Passionate about bleeding disorder care for people globally ....... and 🐘🐘🐘🐘
Laurence Woollard
@thewoollard
Director @PulseInSync | Patient advocacy and policy in rare disease | MSc Health Policy @imperialcollege | Severe haemophilia A
Rachel Aviv
@rachelaviv
staff writer @NewYorker rachel.aviv(at)gmail.com Strangers to Ourselves: tinyurl.com/6fdfe5bs
Matt Delaney
@mattdelaneyny
Government Relations Manager at the National Bleeding Disorders Foundation || patient advocate || former @nysenate || opinions are my own || #GoBills
Aurora Biggers
@aurorabiggers
Union Communications Specialist @OregonAFLCIO | I write stuff; sometimes people read it | former journo, labor columnist @StreetRoots
PhysiciansFoundation
@physiciansfound
The Foundation is a nonprofit that empowers physicians to lead in the delivery of high-quality, cost-efficient healthcare. Likes, Following & RTs ≠ endorsement
Mary Cushman 🫀🧠🩸
@marycushmanmd
Hematologist, University Distinguished Professor & Vice Chair for Emerging Researchers, @UVMDeptMed. Co-Director @UVMHeartBrain. Views mine
Alexandria Phelps
@alex___phelps
EVP @BerlinRosen | fmr @USAID, @Surgeon_General Murthy, @SenGillibrand, @HillaryClinton, @StateDept | @SpelmanCollege alumna
Shematologist, MD
@acweyand
Peds heme onc, mother, dreamer, pacifist, justice seeker. Clueless Mother Theresa. Retweeted by Wonder Woman #CakeForBreakfast HCWvsHunger.org
Brian O Mahony
@brianhemophilia
CEO of Irish Haemophilia Society,former President of WFH and EHC. Supporter of Kerry GAA. Interested in politics,history,advocacy, books. All opinions personal.
EHC_Haemophilia
@ehc_haemophilia
The European Haemophilia Consortium aims to improve the quality of life of people with haemophilia and other rare bleeding disorders throughout Europe.
Haemophilia Journal
@haemophilia_jnl
The official journal of the World Federation of Hemophilia @wfhemophilia, @EAHADnews & @HTRSToday | EiC: @HermansCedric | Social Media Editor: @krumbeve
Len Valentino
@lenvalentino1
Hematologist and Professor
Cathy Harrison 💙
@cathyah1980
Haemophilia ANP. WFH nurses committee Chair. Wife & mum, artist, forever learning. Winner of Nursing Times Nurse of the Year Award 2024. Opinions are mine.
J Roberts
@jonrob08
Classical hematologist; hemostasis/thrombosis, hemophilia, VWD, rare bleeding disorders specialist; severe hemophilia A blood brother🩸, opinions my own
EAHAD
@eahadnews
EAHAD seeks to improve care for people with haemophilia and other bleeding disorders through research, education and multidisciplinary collaboration.
Peter Kouides MD
@pkouides
Prof. of Medicine Univ. Rochester; Medical Director Mary Gooley Hemophilia Center; past prez THSNA;avid cyclist, family enthusiast!
Hemophilia Association Of New York
@hemophiliany
The Hemophilia Association of New York has provided people with bleeding disorders support and aid since 1952.
Be Biopharma
@bebiopharma
Rare & Ready: A Genetic Condition Coalition
@rare_ready
Supported by BioMarin & Ultragenyx, the Coalition educates state policymakers on the impact of conditions. Social media guidelines bit.ly/3AzXLue
Sue T Johnson
@suetjohnson
Blood Bank Educator, Immunohematologist, AABB PEP Ambassador
Eric D. Hargan
@depsechargan
Deputy Secretary of @HHSgov. Husband and father. Regulatory reform enthusiast and proud Illinois native. Privacy: hhs.gov/privacy
USTMA Alliance and Consortium
@ustmaconsortium
The mission the USTMA Consortium is to improve outcomes in through observational studies, clinical trials of novel therapies and translational research.
Institute for Gene Therapies
@gene_therapies
Gene therapy is transforming how we treat diseases. But today’s healthcare system can’t realize its potential. We’re changing that.
Patient-Led Research Collaborative
@patientled
Patient-led research and advocacy for #LongCovid and infection-associated chronic conditions!
Gabrielle Flores
@gabrielleaflo
University of Colorado • Bleeding Disorders Advocate #AllCopaysCount
CIBD HTC
@cibdhtc
Center For Inherited Blood Disorders proudly serves SoCal. We are a safety net clinic specifically for patients with inherited and rare blood disorders.
yannick-robin eike mirko 🇵🇷
@mirkoyannick
multi-disciplinary vejigante | Biawaisa/Yamoká-hu/Maorocoti | rare disease crew
GANSID
@iblooddisorders
Versiti
@versiti
We are Blood Health Innovators who enhance lives through discovery, diagnosis, and treatment. #Versiti #VersitiLife #VersitiScience #VersitiResearch
Hopkins Medical Archives
@jhmedarchives
The Johns Hopkins Alan Mason Chesney Medical Archives. We collect, preserve, and share the history of Johns Hopkins Medicine, Nursing, and Public Health.
Jessica Garcia, MD
@drjessgarcia
#girlmom,#wife,#FirstGen,#26.2|🇲🇽🇺🇸|@UofIllinois|@UICOMPeoria|@MedicalCollege| peds heme, bleeding & clotting doc @UTSW_PedsHemOnc|Asst. Prof| Tweets=own.
Doctor Swathi
@doctorswathi
Jerlym Porter, PhD
@drjsporter
Licensed Psychologist | Sickle Cell Researcher @stjuderesearch | Alum @UVA @FloridaState @VCU @NUFeinbergMed | Tweets are my own.
Priya Parikh
@priyaparikhmd
Pediatric Hematologist/Oncologist. Clinical research/epi, and health equity. Views my own.
Robert Brodsky
@docsdock200
ASH President 2023 @ASH_Hematology. Chief of Hematology Johns Hopkins.
Aaron Cheng, M.D.
@aaronchengmd
Hematology/Oncology Fellow @PennMedicine | @MGHMedicine | @HarvardMed '20 | Interests in hematology, heavy metal, and poetry.
CDC Health Equity
@cdchealthequity
The official Twitter page for CDC’s Office of Health Equity, which aims to achieve health equity for all. Privacy policy: bit.ly/2MhQ6Hp
BCM Department of Medicine
@bcmdeptmedicine
The official Twitter account of @BCMHouston's Department of Medicine, where we advance future medicine, educate future doctors, and provide compassionate care.
From the Labs at Baylor College of Medicine
@bcmfromthelabs
From the Labs at Baylor College of Medicine spotlights the newest and most interesting research information from the bench at the College.
ari parker
@ariparkerjd
All things Medicare. Author of #1 new release "It's Not That Complicated" (read.amazon.com/kp/embed?asin=…)
Haemophilia Nurses' Association UK 🇬🇧
@nurseshna
The HNA is a professional group that represents specialist nurses caring for people with bleeding disorders in the UK.
Jonathan Saltzman
@saltzmanglobe
Report at The Boston Globe; covers biotech; former Spotlight Team member; Bob Dylan fan; swimmer