Kidney Advocate, 50 year PKD Patient, Streamyard Broadcaster, Prolific Poster, Please no Crypto, Investing and Sexual DMs. Views are my own
Dad of two, Professor of Biology @UMass, rare disease researcher and advocate, SPINES @MBL director, and runner. I use zebrafish to study the genetic control of locomotion and epilepsy genes. 🧪🧬🧠
Democratic candidate for Congress in Florida's 11th congressional district covering The Villages to Disney World
Rare Disease Advocate and MLD Mom
BarbieforCongress.com
features editor @endpts.com / fall 2021 fellow
@ksjatmit.bsky.social
Writing (and editing) stories on rare disease medicine, diagnostics and China
Reach out privately on Signal: jaredwhitlock.73
Retired RN ER Trauma 🚫Maga Former Republican 🚫DMs Activist Reproductive Healthcare, All Women, LGBTQ+, Indigenous Latino rights, Black rights, All people are equal. I have MDA5 Dermatomyositis, a rare autoimmune Disease #Myositis
#TheResistence
Assoc. Prof. Interested in CRISPR, Zebrafish, Disease Modeling, Rare Diseases, and Neurodevelopmental Disorders. The opinions expressed here are my own.
Associate Professor. UW Center for Rare Disease Research, @MyGene2, Deputy Editor of @HGGAdvances. #raredisease genetics. CovidWA data
Just a dad of a disabled son, a deceased son and an amazing daughter with a rare disease. #DoBetter
RDND Lab at King’s College London led by Cristina Dias. Clinical Geneticist and Rare Disease researcher. Rare Conditions, neurodevelopmental disorders of chromatin regulation and chromatin remodeller-TF interactions.
https://tinyurl.com/rdndkcl
The FTD Disorders Registry is a powerful tool in the movement to create therapies and find a cure for frontotemporal degeneration. Numbers have power. Join the Registry. Advance the science. #EndFTD www.ftdregistry.org
AFTD envisions a world with compassionate care, effective support, and a future free of Frontotemporal Degeneration (FTD). #EndFTD
https://www.theaftd.org/
Associate Professor, Northeastern University School of Law
www.davidasimon.us
Co-Director, Amy J. Reed Collaborative for Medical Device Safety
https://www.safemedicaldevices.org/
Researcher, the CLASSICA Project
https://classicaproject.eu/team/
Research, news, and commentary from Nature, the international science journal. For daily science news, get Nature Briefing: https://go.nature.com/get-Nature-Briefing
Facts & strategy, in an authoritarian takeover.
Rightwing billionaires want to privatize NIH and use it to control universities.
We work to cure diseases like cancer.
Pers views. #science #medicine
Author of EMPIRE OF EXILES and RELICS OF RUIN (Orbit, out 4/24)| Brimstone Angels Saga | Dungeon Scrawlers DM and Concentration Check host | STXBP1 mom | co-host of Writing About Dragons and Shit | she/her
🧠 🧬 Neuroscientist. Looking for new medicines for #CDKL5, #SCN1A, #SHANK3, #DHPS and other neurological #RareDiseases with #epilepsy
Seattle-based game marketing goon at Pokémon. Formerly Capcom & Six Foot. I also love writing, photography, and world travel. All views and opinions are both my own and likely based on a Simpsons quote.
doing my best over here.
mom, daughter, sister, advocate. progressive.
prefers weirdos over normies.
needs a vacation.
TSF is a global nonprofit organization dedicated to raising awareness of rare neuroimmune conditions, building community, supporting research, advocating on behalf of patients. www.sumairafoundation.org
Clinical geneticist and rare disease researcher at the Broad Institute and Boston Children's Hospital
Mom, wife, rare disease patient. Systemic Mastocytosis. Treading water till I find the right Dr.🦋🦓💙
Rare disease and cancer analysis models for sequencing data. Scientist at PacBio. Art school survivor. Views my own.
Professor of Respiratory Science University of Cambridge. Lung doctor. Fellow St Catharine’s College. Cell biology. Pleural medicine. Rare disease. Genetics.
Lab webpage = https://www.cimr.cam.ac.uk/staff/professor-stefan-marciniak
official Bluesky account (check username👆)
Bugs, feature requests, feedback: support@bsky.app
