RareMD Inc
RareMDx™️, is a diagnostic algorithm with 4043 distinct Rare Diseases and 7693 symptoms that have a relevance weight to each RD. Selected symptoms create an instant differential diagnosis of ≤ 10 RD ranked by probability. RareLook™ is its layman's version.
@altnps.bsky.social
The official "Resistance" team of U.S. National Park Service. Our website: www.ourparks.org
@adamkinzinger.bsky.social
Former US Congressman, Proud RINO, husband, and military man. Fighting the MAGA brain worms daily! Adamkinzinger.komi.io Adamkinzinger.substack.com
@scottgottliebmd.bsky.social
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.
@georgetakei.bsky.social
I’ve boldly gone into the clear blue yonder. Follow for more recipes and tips.
@camrare.bsky.social
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
@cuimcglomcenter.bsky.social
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.
@stacyhurt.bsky.social
Chief Patient Officer 🫶 Cancer survivor, Rare disease mom/caregiver, Advocate for the unseen/unheard in healthcare 📣 Opinions are my own
@laurendwyer.bsky.social
Chicago-ish. Rare disease advocate. Metabolic dietitian. Nephrology medical science liaison -Travere.
@jessicakain.bsky.social
genetics PhD candidate 👩🏻💻🔬 Stanford, CA 📍🌲 metabolomics & multi-omics for rare disease 🧫🧬🥼
@philbscfc.bsky.social
Music lover, rare disease warrior and hater of injustice. #FBPE #Acromegaly #AcroStrong 💪
@crystalline-entity.bsky.social
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.
@melondc.bsky.social
Living, working, and doing OK with rare disease. Support all cats. Please #MaskUp indoors and save disabled and elderly lives. We are all related. Freelancer & online retail side-gigger. Jewelry Store: https://bsky.app/profile/cutedotjewelry.bsky.social
@etfalchemy.bsky.social
Quant, diver, endurance junkie, rare neurogenetic disease dad (HPRT1). Leadville Trail Run survivor. Tweets are not endorsements or investment advice.
@profnickwebb.bsky.social
Paediatric nephrologist VP Medical Affairs / Clinical Development at Sobi Basel 🇨🇭 Anti-complement therapy for rare kidney disease 🏃 and ⛷️and COYS
@iamchronic.bsky.social
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.
@tinyhands.bsky.social
💙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
@stern-sydney.bsky.social
Scientist-Patient-Advocate👩🏻🔬 improving rare disease treatments 🦓🦓🦓 | check out http://TGCTSupport.org | views and opinions are entirely my own. #MedSky #ScienceSky
@caitlinray.bsky.social
rhetoric and composition, focusing on disability/rhetoric/rare disease. Now in public health. Rare disease patient and advocate. Grant/scientific writer. In Omaha!
@chloereuter.bsky.social
Genetic Counselor, Clinical Assistant Professor @ Stanford Medicine cardiovascular genetics | rare disease | all things genomics and multiomics | she/her | views my own
@maryoverfield.bsky.social
Rare disease advocate Long-suffering 7️⃣6️⃣ers fan Rochester, NY
@purplemamabear.bsky.social
Patient advocate, advocate for healthcare reform, wife/mom of those w #rarediseases, rare disease legislative advocate, interested in systems, sociology, psychology. Enjoy hiking & kayaking. Love 💕 people, books, traveling & laughing.
@allyann.bsky.social
Living with & advocating for ME, POTS & FM, ex-IT. Homebound & at times bedridden. News and Recipe junkie. Living in Millowl, home of the Bunurong people, Victoria, Australia
@sumonkyawmyint1.bsky.social
population health, scientist, feminist, living with rare disease, disability and chronic illnesses, NDIS, lover of books & science, all posts are personal
@taratisch.bsky.social
Artist🎨, Rare Disease Warrior, Patient Advocate, Wife, Bonus Mom, Gramma, Finder of 🍀
@pedlungdoc.bsky.social
Pediatric pulmonologist, sickle cell and rare lung disease researcher at Johns Hopkins, mom, gardener. Chair of ATS Pediatric Advocacy Subcommittee.
@elizbach.bsky.social
Labor/Ethics Lawyer, Grieving Mom, Rare Disease Advocate, Anti-Elitist, Documentary Junkie, Bi-Pedal Carbon-Based Life form, Roughly Symmetrical.
@sung-yun-pai.bsky.social
Physician-scientist, blood and marrow transplanter, gene therapist, immunology and rare disease enthusiast—views are mine not my employer’s
@elizabethmarie.bsky.social
MD/PhD student @Penn, interested in genetics, rare disease, pediatrics and oncology 🇨🇺🦓🧬🌈
@maureenforryso.bsky.social
Proud member of team #dotnews and #bostonirish. Marketing & Sales Pro | Disability Advocate | Rare Disease Mom | Poodle Enthusiast | Co-publisher Boston Irish Mag. Originally from Dorchester, currently in Newton MA. www.dotnews.com
@rarediseasectn.bsky.social
HRB-funded clinical trial network aiming to increase the quantity and quality of rare disease clinical trials in Ireland, keeping the patient voice at our core.
@marvandijk.bsky.social
Spinale Musculaire Atrofie (SMA) Rare disease 👩🦼 Getrouwd - Zorg -PGB - Lezen - Katers Teddy en Casper - Metal - Verjaardag 8 september 1952
@drmelissageraghty.bsky.social
🦋 CEO of Phoenix Rising with Dr. G 🦋 Clinical Health Psychologist (Complex Medical, Rare Disease, Eating Disorders) 🦋 Medical Gaslighting Sensitivity Trainer 🦋 Keynote Speaker 🦋 #IamRare 🦓 ♿ www.phoenixrisingwithdrg.com
@speccymcspec.bsky.social
Enthusiastic and exhausted. Read, hang out at the seaside. Live with ME. Volunteer in health. Ramble about rare disease & rant about politics. Belfast & Donegal. Unimpressed by royalty. She/ her
@melanie448.bsky.social
Democracy Defender. Fighting For Freedom. Human Rights For All. Spanish Instructor. Family. Friends. Married To My Favorite Person. Rare Disease Advocate. Ally. Animal Lover. 🇺🇸🏳️🌈🏳️⚧️🇺🇦💙🦋🌊🫶✌🏻
@drjennylord.bsky.social
Lecturer in Systems Biology at the University of Sheffield. Interested in bioinformatics, RNA, splicing, big data, rare disease diagnostics and neuroscience. Also dogs.
@drtishawang.bsky.social
Senior executive clinical vice chair at UCLA DOM. Pulm/cc. Advocate for women in medicine, medical educators, and the rare lung disease community.
@andiskilton.bsky.social
I support capacity and capability building for societal impact and participatory research practices | Chair of trustees for a rare disease charity | Cat daddy | LGBTQIA+ | he/him
@slappadabass06.bsky.social
Woke and proud! Partner, rare disease advocate, dog dad, musician, gamer, blue speck in SWMO. #xbox #nintendoswitch #Ibanezbass #Traceelliot #feoldstrombone 🚫MAGA/CRYPTO/AI/CULT spam
@tamaraciocci.bsky.social
Former editor and writer at BV Media. Free Lance artist, designer and rare disease advocate. Lost father to gun violence.
@dannygale.bsky.social
Nephrologist @RoyalFreeNHS and rare disease researcher @UCL using genomics to understand kidney disease. @RenalRaDaR director. https://www.ucl.ac.uk/medicine/research/genetics-and-genomics
@gc4gc.bsky.social
rare disease neurogeneticist | epilepsy | epigenetics | iPSCs | mentor & genetics MedEd | here for the science, lab fun & occasionally my tiny hooman https://sites.northwestern.edu/carvilllab/
@wywywa.bsky.social
UBC bioinformatics researcher focused on gene regulation and rare disease diagnosis
@heatherhg.bsky.social
Scientist. Engineer. Mom. Wife. Lover of macrophages. #EoE and rare eosinophilic disease daughter, patient, and mom. Finding a love of eosinophils. Trying to help kids with cancer, running a lab at #UW and #SeattleChildrens: Editlabs.org . Views are my own
@melissajhogan.substack.com
Attorney • Advocate • Author, “Afraid of the Doctor” • Parenting a son with rare disease/special needs • Grieving the loss of another son • I #amwriting about the intersection of the law, faith, and abuse at melissajhogan.substack.com
@sabucha.bsky.social
Genetic Counselor. Swiftie. Cat Lady. Ally. Traveler. VW Beetle owner. 36. Views are my own.
@alextremophile.bsky.social
Postdoctoral Bioinformaticial in the Computational Rare Disease Genomics group (Nicky Whiffin). univ. Oxford 🧬💻 Loves Evolution, regulation, cheese and cats. She/Her