Solid Biosciences @Solid_Bio
Solid’s mandate is to improve the lives of patients living with devastating neuromuscular and cardiac diseases. #TogetherWeAreSolid solidbio.com Boston, MA Joined October 2016-
Tweets665
-
Followers2K
-
Following205
-
Likes335
Next week, we're attending the 2026 Friedreich's Ataxia Symposium hosted by Friedreich's Ataxia Research Alliance (FARA) and the Friedreich’s Ataxia Center of Excellence at Children’s Hospital of Philadelphia. Matt Harmelink, Neuromuscular Therapeutic Area Head, will join the FA Drug Development Pipeline Panel Discussion to speak about our work in FA and our Phase 1b FALCON clinical trial. Stop by our exhibit table if you're attending, or register to join the panel virtually: curefa.org/get-involved/e… #FACommunity #RareDisease
We recently joined @defeatduchenne's 2026 Family Forum, which focused on fostering education and connection for individuals and families living with Duchenne. We're proud to support initiatives that empower families with knowledge, foster connections and dialogue, and build community. #Duchenne #RareDisease
We're committed to shaping the future of gene therapy. POLARIS-101™, our proprietary next-generation, muscle-tropic capsid, has potential to transform the safe, efficient and scalable delivery of genetic medicines across neuromuscular and cardiac diseases. With our #SolidInside approach, we're building a suite of technologies available for partnership and out-licensing to help developers accelerate innovation. Learn more below or on our website: solidbio.com/partners/
At the Annual World Muscle Society Congress, we're presenting six posters across our neuromuscular portfolio highlighting our work in Duchenne, Friedreich's ataxia and our proprietary POLARIS-101™ capsid, which is designed to enable safe and effective gene therapy delivery and has shown encouraging clinical signals in #Duchenne. We look forward to connecting with leading global experts to advance scientific progress in rare neuromuscular diseases. #WMS2026 #SolidInside
We look forward to attending the Annual Neuromuscular Study Group Scientific Meeting, where we'll share two posters highlighting our work in #Duchenne, including our POLARIS-101™ capsid and our Phase 1/2 INSPIRE DUCHENNE study. We value opportunities to engage with researchers, clinicians and advocates working to shape the future of patient care. #SolidInside #RareDisease
In honor of #WorldDuchenneAwarenessDay, we joined @JettFoundation at the Gals for Cal women's triathlon, coming together with the community to raise awareness, recognize progress and advance a future that is #StrongerThanDuchenne. Every day, we're proud to support greater access to care, continued research and inclusive experiences for individuals living with Duchenne. #WDAD2026
$SLDB: Today, our CEO Bo Cumbo will participate in a fireside chat at the @HCWCO 28th Annual Global Investment Conference. Join us live or watch the replay here: investors.solidbio.com/news-and-event…
$SLDB: This week, our CEO Bo Cumbo and CMO Gabriel Brooks will participate in fireside chats at the @Official_Cantor Global Healthcare Conference and the @Citi Biopharma Back to School Summit. Tune in live or watch the replay here: investors.solidbio.com/news-and-event…
Today on #WorldDuchenneAwarenessDay, we reflect on the profound impact that access to care, resources, scientific breakthroughs and opportunities can have for individuals and families affected by #Duchenne. We remain committed to advancing research and innovation, working alongside the Duchenne community in pursuit of meaningful progress. #WDAD2026 #RareDisease
Improving access for individuals living with Duchenne is about more than healthcare. It's about creating opportunities to fully participate in their communities and engage in activities they love. As we approach #WorldDuchenneAwarenessDay, we reflect on the importance of expanding access, and we stand with the Duchenne community in raising awareness, driving innovation and removing barriers. Read more from Annie Ganot, Solid Co-Founder, SVP Patient Advocacy and Duchenne mom. #WDAD2026 #RareDisease
$SLDB: We're looking forward to attending several investor conferences this month, where members of management will join fireside chats to discuss Solid's strategy and recent progress. Read more: investors.solidbio.com/news-releases/…
Ahead of #WorldDuchenneAwarenessDay on September 7, we're joining the global Duchenne community in recognizing this year's theme, "Access Changes Lives." Access is a fundamental driver of better outcomes for individuals living with #Duchenne. This year's theme focuses on removing barriers to knowledge, research and support, helping people make informed decisions and creating opportunities to live full lives. Learn more from @worldduchenne: worldduchenne.org/world-duchenne… #WDAD2026 #RareDisease
Recently, we joined @PPDCRO at their GMP Lab in Middleton, WI, for a discussion with patient advocates in the #FriedreichsAtaxia (FA) community. This panel featured firsthand perspectives from those impacted by FA and insights into our work in FA, fostering a deeper understanding of the patient and caregiver experience. We're proud to be part of important conversations that strengthen collaboration and advance our shared goal of improving outcomes for people in need. Thank you to Sam, Aiden and Rachel for sharing your stories! #FACommunity #RareDisease
Solid Biosciences today announced our financial results for the second quarter of 2026, along with business and pipeline updates. Read the full release: investors.solidbio.com/news-releases/… #SolidBiosciences $SLDB
This weekend, #TeamSolid had a great time at the fourth annual rideATAXIA Hometown Boston bike ride, hosted by Friedreich's Ataxia Research Alliance (FARA). We're proud to join FARA and the local Boston community in advancing Friedreich's ataxia (FA) research. #FriedreichsAtaxia #FACommunity
Duchenne UK @DuchenneUK
5K Followers 891 Following Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
AnnemiekeAartsma-Rus @oligogirl
3K Followers 450 Following Translating science from bench to bedside and from jargon to lay language
Terri Ellsworth @TerriEllsworth
2K Followers 2K Following Duchenne Advocate/Rare Disease Activist Mom, Designing Mom-Creating awareness & advocating for approval of safe & effective drugs. Words are always my own.
Matthew S. Alexander @Matt_Muscle_Guy
6K Followers 4K Following Geneticist, Skeletal Muscle, Drug development, Gene therapies. Non-coding RNA, and Zebrafish Aficionado. All tweets are my own. Instagram @thealexanderlab
Edgewise Therapeutics @EdgewiseTx
550 Followers 52 Following Biopharmaceutical company focused on therapeutics for cardiovascular diseases.
CureDuchenne @CureDuchenne
6K Followers 604 Following We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.
World Duchenne Organi... @worldduchenne
3K Followers 952 Following Global organization to find a cure and viable treatment for those lives affected by dystrophinopathies: Duchenne and Becker Muscular Dystrophy. RT ≠ endorsement
TREAT-NMD® @TREAT_NMD
4K Followers 530 Following Advancing diagnosis, care and treatment for those living with neuromuscular diseases around the world.
Joining Jack @alljoinjack
56K Followers 2K Following We are joining Jack in the fight to find a cure for duchenne muscular dystrophy. Will you?
Dwi U. Kemaladewi @DKemaladewi
1K Followers 2K Following 👩🏻🔬Principal Investigator @US_FDA | Therapeutics Genetics in Rare Diseases 💪🧠🧬🐀💉 | 🔋 by ☕ & 😍 | HopOnHopOff 🇮🇩🇳🇱🇨🇦🇺🇸➡️🚀🌜
Alliance for Regenera... @alliancerm
8K Followers 2K Following ARM champions the benefits of engineered cell therapies and genetic medicines for patients, healthcare systems, and society.
Duchenne Data Foundat... @DuchenneDF
786 Followers 422 Following Bringing data to life to improve the world of dystrophinopathies
CheckRare @CheckRare
3K Followers 2K Following Leading publisher and learning platform focused on rare diseases. Rare Diseases Are Our Focus, Expertise, and Passion.
Virginia Arechavala @VArechavala
2K Followers 2K Following Scientist and mum. @ikerbasque Professor @biocrucesHR Interested in #RNAtherapy for #neuromuscular disorders. De Bilbao de toda la vida and adopted Londoner.
Ryan Flinn @RS_Flinn
4K Followers 8K Following Freelance journalist & comms strategist, focused on healthcare, biotech, AI. Ex-Bloomberg, J&J.
Centre for Muscle Res... @UniMelbCMR
3K Followers 1K Following Advancing muscle biology and its importance in health and disease. #myotwitter #sarcopenia #myology #skeletalmuscle #musculoskeletal #neuromuscular #cachexia
Beacon for Rare Disea... @RareBeacon
12K Followers 10K Following Beacon is a UK-based charity that is building a united rare disease community with patient groups at its heart. Previously known as Findacure.
Laura McLinn @LauraMclinn
939 Followers 2K Following Founding President, Best Day Ever Foundation. Passion for helping patients access treatments. Duchenne mama bear.
Patient Worthy @PatientWorthy
8K Followers 7K Following We're a resource for engaging, informative content and rare patient news, well done.
Keep Pace for Duchenn... @KeepPaceDMD
1 Followers 26 Following Parent-led Duchenne advocacy. Pushing for an FDA as fast & smart as AI-era science. Advancing gene & cell therapies with rigor & urgency. Not medical advice.
Manoj Kamble, PhD @biosciencenut
48 Followers 372 Following Manager, Cell and Gene Therapy, Intas Pharmaceutical, Ahmedabad.
Daniel Shteinbuk @DanielShteinbuk
678 Followers 7K Following
Elliot Favus @efavus
346 Followers 6K Following
Roma Dominique @RomaDominique1
0 Followers 19 Following
Chameleoninja @Flyonthewallfpv
17 Followers 37 Following
Mike Burns @mburns7
266 Followers 359 Following Defend it and they will come. CISSP. CEH. @Mandiant Blueteam.
Sia @enosiaa
38 Followers 374 Following
RarasNoInvisibles @NoInvisibles
55K Followers 7K Following Hablamos de salud, enfermedades raras, inclusion social y biomedicina. Escribe @Sombradoble Mas Información: [email protected]
Biotech Bob @biotech_ecosyst
14 Followers 578 Following
Jadsuper @JadSuper123
295 Followers 1K Following Forget about the web3 posts, still a believer though. Moving over to Media buying for dental, orthodontic and fertility clinics.
Genewriter-001 @001Genewriter
15 Followers 248 Following
QUAN CHAO @QUANCHACDZW
36 Followers 191 Following
gamze kulak @gamzeekulak
66 Followers 104 Following
Lorenzo @Lorenzo178051
12 Followers 10 Following
michael.stuber@twolab... @mstu48469
3 Followers 180 Following
Sevtap Demir @sevtap_dem34830
2 Followers 8 Following
Lucas Felipe @paimcer
8 Followers 71 Following
Mary Reyes @MaryReyes212121
0 Followers 28 Following
Ryan Akram Mohammed @RyanJourneyDMD
282 Followers 2K Following Ryan, 7 | DMD Warrior 💙 Still Walking. Still Smiling. Still Hoping. 🇾🇪 Yemeni | Born in Saudi Arabia 🇸🇦 #DMD #Duchenne #RareDisease
KırmızıBeyaz @__krmzbyz__
437 Followers 428 Following hûvâllahûllezi lâ ilâhe illâ hû 🇹🇷 ރ Dalgalan sen de şafaklar gibi ey şanlı hilal! Olsun artık dökülen kanlarımın hepsi helal. #DmdİçinYeniDoganTaraması
PharmaKonsult @PharmaKonAdvise
7 Followers 121 Following Advisor on corporate culture and launch excellence for rare disease Neurology and Endocrinology. Help biotech companies make commercial decisions.
TMM The Music Makers @tmmwemakemusic
22 Followers 77 Following Music makers × AI dream shapers. Beats, visuals, code & culture collide. Turning sound into vision and vision into vibe. Future audio-visual art.
M On The World @M_On_The_World
68 Followers 3K Following
BlueDog @BlueDog98515
5 Followers 166 Following
Dinesh @hornsunglory
34 Followers 45 Following
Bio Man @BioMan14896
342 Followers 8K Following Biotech ecosystem — particular focus on cancer/oncology
Beverley Engler @BeverleyEn43264
2 Followers 71 Following
米国株バイオセ... @namekuji526
1 Followers 43 Following 米国株ウォッチャー。バイオセクターにある希少疾患、難病開発を手掛ける企業の取組をつぶやきます。投稿の推定重要度は上市の可能性、開発市場における希少性などを踏まえた個人の見解です。地道な研究活動の成果である治療薬が、速やかに患者のもとへ届くことも期待しています。
Hyperbolic Discounter @HyperbolicDisco
2K Followers 3K Following Amateur dog walker, and investor. Caveat emptor, caveat venditor. Contra mundum. There is no rescue party.
MacJ @JRMCAR65
1 Followers 83 Following
Dharmendra C B @DharmendraCB1
39 Followers 97 Following
UF Myology Institute @UFMyology
255 Followers 56 Following The UF Myology Institute brings researchers together in a collaborative effort to further the understanding and treatment of neuromuscular diseases.
Kuppan Subramaniyan @Kupp1000
2 Followers 143 Following
Cody Ryan @CodyRya17639145
44 Followers 706 Following If you help others reach their dreams, they’ll drag you to yours/ It’s important to bring perspective into your life/ journalism/UK student
Byron @TOO_MUCH_T1ME
244 Followers 973 Following
Juan Carlos Correa Ce... @JuanCarlos15750
175 Followers 2K Following
Nick @ashe_op
1 Followers 35 Following
Nancy B @Ratte40755620
22 Followers 1K Following soft as silk, strong as wifi 🧵 mutuals only, i follow back
Onur ERGÜN @Onur02825973
22 Followers 69 Following
Christine Piacentino @chrispiaOTM29
61 Followers 104 Following
Lucas Nivon 🇺🇸 @lucas_nivon
875 Followers 927 Following CEO and Co-Founder at Cyrus Bio. Openfold AI consortium co founder. Computational biologic drug discovery. Auto-immune. New Yorker. Harvard ETH UW trained
Duchenne UK @DuchenneUK
5K Followers 891 Following Duchenne UK has one clear aim – to end Duchenne, a devastating muscle-wasting disease. We are the leading Duchenne muscular dystrophy charity in the UK.
Terri Ellsworth @TerriEllsworth
2K Followers 2K Following Duchenne Advocate/Rare Disease Activist Mom, Designing Mom-Creating awareness & advocating for approval of safe & effective drugs. Words are always my own.
CureDuchenne @CureDuchenne
6K Followers 604 Following We are committed to improving the lives of those affected by Duchenne through accelerating research, improving care and empowering the community.
Muscular Dystrophy UK @MDUK_News
17K Followers 3K Following We connect a community of over 110,000 people living with muscle wasting and weakening conditions. Together we are stronger. Join us. Our #MusclesMatter.
World Duchenne Organi... @worldduchenne
3K Followers 952 Following Global organization to find a cure and viable treatment for those lives affected by dystrophinopathies: Duchenne and Becker Muscular Dystrophy. RT ≠ endorsement
Muscular Dystrophy Ne... @mdnewstoday_
1K Followers 27 Following Your source for Muscular Dystrophy news, support & real stories from the community. Let’s raise Muscular Dystrophy awareness together!🎗️
EURORDIS-Rare Disease... @eurordis
31K Followers 1K Following An alliance of over 1,000 patient organisations working across borders and diseases to improve the lives of all people living with rare diseases.
TREAT-NMD® @TREAT_NMD
4K Followers 530 Following Advancing diagnosis, care and treatment for those living with neuromuscular diseases around the world.
Joining Jack @alljoinjack
56K Followers 2K Following We are joining Jack in the fight to find a cure for duchenne muscular dystrophy. Will you?
MassBio @MassBio
52K Followers 2K Following MassBio is committed to advancing MA's leadership in the life sciences to grow the industry, add value to the healthcare system & improve patient lives.
Alliance for Regenera... @alliancerm
8K Followers 2K Following ARM champions the benefits of engineered cell therapies and genetic medicines for patients, healthcare systems, and society.
Duchenne Data Foundat... @DuchenneDF
786 Followers 422 Following Bringing data to life to improve the world of dystrophinopathies
JWMDRC @jwmdrc
1K Followers 464 Following John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University #dmd #sma #lgmd #fshd #dm1 #gne #col6 #cnm
Muscular Dystrophy Ca... @MD_Canada
5K Followers 1K Following MDC's mission is to help people with neuromuscular disorders live life on their own terms. #WalkRollMDC #MuscularDystrophy FR: @Action_Musclee
Beyond the Diagnosis @BeyondtheDx
8K Followers 5K Following Beyond the Diagnosis unites art and science to raise awareness for children living with life-altering diseases.
CheckRare @CheckRare
3K Followers 2K Following Leading publisher and learning platform focused on rare diseases. Rare Diseases Are Our Focus, Expertise, and Passion.
Cure Rare Disease @CureRareDisease
4K Followers 237 Following 501(c)(3) nonprofit leading a nationwide collaboration of researchers and clinicians in order to develop life-saving therapeutics for rare diseases.
Centre for Muscle Res... @UniMelbCMR
3K Followers 1K Following Advancing muscle biology and its importance in health and disease. #myotwitter #sarcopenia #myology #skeletalmuscle #musculoskeletal #neuromuscular #cachexia
Duchenne Centre NL @duchennecentrum
277 Followers 154 Following Centre of expertise considering care, treatment and research for #Duchenne and #Becker muscular dystrophy.
Gene Therapy Institut... @OSUGeneTherapy
384 Followers 130 Following The Gene Therapy Institute is an interdisciplinary community bringing together world-class faculty with diverse expertise in the area of gene therapy research.
All Wheels Up ♿✈ @allwheelsup
5K Followers 4K Following The only nonprofit crash-testing wheelchairs and tie-downs for air travel safety. #flyinclusive [email protected] | Text FLY to 707070 to donate
Alan Chaulet ♿✈ @AlanChaulet
1K Followers 7K Following @allwheelsup VP and Founding Board Member | @ParentProjectMD PAAC I DMD and Disability Advocate | All Views My Own | Sharing my entrepreneur journey
The Canadian SADS Fou... @CanadianSADS
252 Followers 132 Following Established in 1995, our goal is to provide support and advocacy for patients and families affected by inherited cardiac conditions that can sometimes lead to s
Hearts in Rhythm Orga... @HeartsInRhythm
2K Followers 1K Following HiRO | cardiogenetics experts, researchers, genetic counsellors, nurses & families | improving detection & care of inherited arrhythmias & cardiomyopathies 🇨🇦
Two Disabled Dudes @2DDPodcast
762 Followers 432 Following @kyleabryant and @seanbaumstark have a rare disease. This podcast is all about cultivating the courage to live beyond any circumstance and laugh along the way.
Children's Cardiomyop... @CCFheartkids
1K Followers 660 Following The Children's Cardiomyopathy Foundation (CCF) is a non-profit organization focused on pediatric cardiomyopathy, a chronic disease of the heart muscle.
Mended Hearts @MendedHearts
4K Followers 3K Following Mended Hearts is a international and community-based non-profit organization that offers peer-to-peer support to heart patients and their families.
World Heart Federatio... @worldheartfed
37K Followers 6K Following We connect and inspire the global cardiovascular community to achieve stronger health systems and healthier hearts ❤️
The HCM Academy @theHCMacademy
427 Followers 295 Following A CME-accredited initiative designed to transform the identification, diagnosis, and management of patients with hypertrophic cardiomyopathy
Ataxia Global Initiat... @ataxia_global
633 Followers 138 Following Ataxia Global Initiative is a worldwide platform for clinical research in ataxias.
Heart Valve Society @HeartValveOrg
2K Followers 1K Following The ❤️ Team in Action. Promoting heart valve related research by organizing meetings and maintaining heart valve research networks.
DCMFoundation @DCM_Foundation
247 Followers 476 Following Hope for People with Dilated Cardiomyopathy. If you need support, contact [email protected] or visit our website.
The Children's Heart ... @TheCHF
6K Followers 536 Following Advancing the diagnosis, treatment, and prevention of congenital heart defects (#CHDs) by funding the most promising research.
American Heart Associ... @AmericanHeartMA
3K Followers 1K Following The American Heart Association in Massachusetts. Our Mission: To be a relentless force for a world of longer, healthier lives.
HFSA @HFSA
12K Followers 1K Following HFSA is the first organized effort by heart failure experts to provide a forum for those interested in heart function, heart failure and patient care.
FIA | Inherited Arrhy... @fiacardiac
3K Followers 2K Following We're the Foundation for Inherited Arrhythmias (formerly SADS) 💕🧬 Support, resources, and community below ⬇️
National Ataxia Found... @NAF_Ataxia
3K Followers 654 Following Our mission is to accelerate the development of treatments and a cure while working to improve the lives of those living with Ataxia.
UF Innovate | Acceler... @UFAccelerate
1K Followers 396 Following We inspire entrepreneurs to create, change & cure for a better world.
FA Research Alliance @CureFA_org
3K Followers 588 Following FARA's mission is to marshal and focus the resources and relationships needed to treat & cure Friedreich's ataxia (FA). #CureFA
FierceHealthcare @FierceHealth
60K Followers 3K Following The healthcare industry's trusted source for need-to-know news & analysis. Delivering news, revealing insights straight to your inbox.
UMass Chan Medical Sc... @UMassChan
15K Followers 4K Following Official X home of UMass Chan Medical School: pioneering education, research and healthcare delivery. See how we are advancing medicine together.
MASS AWIS @MASSAWIS
1K Followers 360 Following The Association for Women in Science Massachusetts Chapter, championing the interests of women in science, technology, engineering and mathematics.
Association for Women... @AWISNational
10K Followers 3K Following For over 50 years, AWIS has advocated for #WomenInScience and #WomenInSTEM thanks to our members, board, donors, and allies. Tweets/RTs ≠ endorsement.
Reuters Science News @ReutersScience
1.3M Followers 18 Following From newly charted astronomical anomalies at the far reaches of the universe to the rise of nanotechnology, nobody covers science like http://t.co/RtkLii8CUo.
Team Joseph @TeamJosephInfo
586 Followers 481 Following Our mission is to fund research to find a cure for Duchenne muscular dystrophy and support families with immediate needs to help care for a child with Duchenne.
Charley's Fund @CharleysFund
900 Followers 220 Following Our goal is to cure Duchenne Muscular Dystrophy in time to save Charley's life and the lives of thousands of boys like him.
Rarity Life @raritylifemag
229 Followers 811 Following A new online publication that offers those affected by rare disease, disability & cancer the opportunity to unify & share our collective experience.
News from Science @NewsfromScience
765K Followers 638 Following The latest stories in science, brought to you by the @ScienceMagazine news team.
Modern Healthcare @modrnhealthcr
147K Followers 401 Following Award-winning healthcare business news, research and opinion | https://t.co/IqTQOt0NUe (RTs are not endorsements)
Oxford-Harrington Rar... @OHRareDisease
1K Followers 887 Following Rare Disease Centre @UniofOxford in partnership with @HarringtonDI_UH @UHhospitals, accelerating cures for rare diseases
Health Affairs @Health_Affairs
163K Followers 4K Following Health Affairs Publishing delivers rigorous, nonpartisan research and analysis to improve health and health care. Follows/Tweets/RTs ≠ endorsements.
Scientific American @sciam
4.2M Followers 789 Following Awesome discoveries. Expert insights. Science that shapes the world.
AllStripes @_allstripes
3K Followers 1K Following Our mission is to unlock new treatments for people affected by rare disease.🚀
Rare Genomics @RareGenomics
9K Followers 3K Following RGI is a non-profit organization that provides research to families in need of diagnosis & treatment for rare genetic diseases.
ThinkGenetic, Inc. @ThinkGenetic
1K Followers 1K Following Finding individuals in need of a diagnosis. Supporting pharma, research institutions, and healthcare systems. #RareDisease #ai
NYT Science @NYTScience
1.1M Followers 443 Following Science, Medicine, Environment, Space & Astronomy. Sign up for the Science Times email, in your inbox every Tuesday: https://t.co/kpdN2C1hDy
MedPage Today @medpagetoday
74K Followers 6K Following Better informed, better care. #MedPageToday Retweets, likes, and comments are not endorsements.
Remember The Girls @remember_girls
2K Followers 761 Following Nonprofit organization aiming to break the stigma facing females impacted by X-linked conditions. #NotJustCarriers
Guardian Science @guardianscience
988K Followers 2K Following This account has been archived. Follow us on https://t.co/d51tzVvasA
New Scientist @newscientist
4.3M Followers 278 Following The best place to find out what’s new in science – and why it matters.
Rare Advocacy Movemen... @RareAdvocacy
3K Followers 1K Following Network of people with #RareDisease #LivedExperiences dedicated to evolving the #LivingRare experience into opportunities for the global community to thrive.
Rare Disease Live @RareDiseaseLive
1K Followers 295 Following RareDiseaseLive is dedicated to empowering the rare disease community through education.
Medscape @Medscape
291K Followers 34K Following Medscape provides breaking medical news and expert perspectives, drug and disease information, and free CME across 30+ medical specialties.
Science News @ScienceNews
5.4M Followers 512 Following Covering the latest news in all fields of science. Publisher @society4science. See also @SN_Explores.








