The official "Resistance" team of U.S. National Park Service. Our website: www.ourparks.org
Stupid dumbass baby idiot esjesjesj or eeesssjjj on Twitter
Former US Congressman, Proud RINO, husband, and military man. Fighting the MAGA brain worms daily!
Adamkinzinger.komi.io
Adamkinzinger.substack.com
Senior Fellow at the American Enterprise Institute. Partner, New Enterprise Associates. Contributor CNBC. 23rd Commissioner of the U.S. FDA. Public boards: Pfizer, Illumina, TempusAI.
I’ve boldly gone into the clear blue yonder. Follow for more recipes and tips.
Making rare disease an everyday conversation.
CamRARE is a charity empowering rare disease communities & fostering cross-sector collaboration to improve outcomes for those affected.
#RareDisease
Local | National | Global www.camraredisease.org
Created in 2000 as the first glomerular disease center in the United States, we are dedicated to the care of people with rare diseases of the glomerulus.
Chief Patient Officer 🫶 Cancer survivor, Rare disease mom/caregiver, Advocate for the unseen/unheard in healthcare 📣 Opinions are my own
Chicago-ish. Rare disease advocate. Metabolic dietitian. Nephrology medical science liaison -Travere.
genetics PhD candidate 👩🏻💻🔬 Stanford, CA 📍🌲
metabolomics & multi-omics for rare disease 🧫🧬🥼
Music lover, rare disease warrior and hater of injustice.
#FBPE #Acromegaly
#AcroStrong 💪
Running a Structural Biology and Protein Production group at a Boston biotech. Previously worked in rare disease, but focusing on drug discovery in precision oncology the last few years. Crystallography with a splash of CryoEM and NMR. Opinions are my own.
Living, working, doing OK w/chronic illness. Please #MaskUp indoors and save disabled and elderly lives. We are all related.
MUTUAL AID Amazon List for DC here>>>
https://www.amazon.com/hz/wishlist/ls/1JS9LWXP66CIC/ref=nav_wishlist_lists_2
Quant, diver, endurance junkie, rare neurogenetic disease dad (HPRT1). Leadville Trail Run survivor. Tweets are not endorsements or investment advice.
Paediatric nephrologist
VP Medical Affairs / Clinical Development at Sobi Basel 🇨🇭
Anti-complement therapy for rare kidney disease
🏃 and ⛷️and COYS
Chronic: pain, illness, rare disease, lichen nerd, & ND.
I write, read, garden, and do my best to support my friends & community. Equity & Disability Justice are priorities.
💙Professor, Ally, Mom of daughter w/rare neuromuscular disease (SMARD), Disability Advocate, Married, Liberal, National Parks fan, and Etsy shop with handmade GOP VOODOO dolls. Part of profits goes to DEMS! Started in 2016. https://etsy.me/2CeAZIl
Scientist-Patient-Advocate👩🏻🔬 improving rare disease treatments 🦓🦓🦓 | check out http://TGCTSupport.org | views and opinions are entirely my own. #MedSky #ScienceSky
rhetoric and composition, focusing on disability/rhetoric/rare disease. Now in public health. Rare disease patient and advocate. Grant/scientific writer. In Omaha!
Genetic Counselor, Clinical Assistant Professor @ Stanford Medicine
cardiovascular genetics | rare disease | all things genomics and multiomics | she/her | views my own
