Search results for #raredisease
Thank you, Eddie, for supporting Kaleidoscope #RareDisease Stories! Have you gotten your copy? Send a pic to [email protected]. Not yet? Now's the time! Kaleidoscope #RareDisease Stories is available on Amazon. ~🦋 a.co/d/1qhe4Je #KaleidoscopeRare #ZebraStrong🦓
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14 miles in total, walking and running, today including parkrun 👊🏻 🙌🏻 Just over 28,000 steps! I’m definitely not moving for the rest of this afternoon/evening. #happysaturday #positivity #raredisease #justkeepgoing #NHS1000miles
It is not uncommon for families of children with medical complexity to experience a shift in their circle of friends. #MedicalComplexity #RareDisease #Caregivers #SupportCircle
ASHEVILLE: We hope to see you TODAY for our social meetup! Do you know anyone in the area? Reach out to us to help get them connected and we will see you there! buff.ly/4a62xAr 💙💜 #HDreach #ReachForHope #ReachingForHope #curehd #curejhd #raredisease
The Faces of Congenital Diaphragmatic Hernia cdhi.org #CDH #CDHAwareness #NotJustAHole #CongenitalDiaphragmaticHernia #CDHAwarenessMonth #April19 #CDHCharity #PediatricSurgery #GlobalSurgery #RareDisease #PatientAdvocacy #Donate
Because it can take years for the cholestanol buildup to cause problems, symptoms may vary and show up at different times in a person’s life. #CTX #CTXAlliance #ULF #CerebrotendinousXanthomatosis #Leukodystrophy #RareDisease
Thank you to these 5 biotech and pharmaceutical leaders for joining our Industry Advisory Board! As we work to advance promising treatments to clinical trials, their collective expertise is invaluable. 🤝 Meet all our advisors: kabukisyndromefoundation.org/about-ksf/whos… #kabukisyndrome #raredisease
ഇന്ത്യയില് ആദ്യമായാണ് ഒരു സംസ്ഥാനത്ത് അപൂര്വ രോഗത്തിനുള്ള മരുന്നുകള് സര്ക്കാര് തലത്തില് സൗജന്യമായി നല്കാനാരംഭിച്ചത്...#RareDisease #FreeMedicine #SpinalMascularAtrophy manoramaonline.com/health/health-…
We are based in #Wales with a #Global following #FindYourPower #Ataxia awareness project powered by ataxia-and-me.org Check our #QR code and #SocialMedia channels to find out more. #StrongerTogether #RareDisease #Neurology #Health
3 weeks to go 😊 @SclerodermaRF Family Day Saturday 18th May 2024, The Atrium, @RoyalFreeNHS FREE to attend accessible to all #SclerodermaFreeWorld #RaynaudsFreeWorld #Research #Scleroderma #SystemicSclerosis #Raynauds #Autoimmune #RareDisease #NoCure #UnknownCause #LifeChanging
@Jane_L_Edwards You are in the best hands. The team at Addenbrookes have saved my sight and my life over the past 3 years. #vasculitis #GPA #raredisease
HAE S.A wishes all South Africans a happy Freedom Day 🇿🇦 💜💚💙 #haesouthafrica #hae #hereditaryangioedema #hereditaryangioedemaawareness #togetherwecan #rarediseasessa #raredisease #careforrare #haesa
Early detection improves lives – get tested now! alpha1europe.org/about-the-dise… #unitedforalpha1 #EuropeanAlpha1AwarenessDay #alpha1awareness #AATD #alpha1antritrypsindeficiency #raredisease #alpha1testing #earlydetection #alpha1diagnosis
One drop of blood is all it takes – get tested now! alpha1europe.org/about-the-dise… #unitedforalpha1 #EuropeanAlpha1AwarenessDay #alpha1awareness #AATD #alpha1antritrypsindeficiency #raredisease #alpha1testing #earlydetection #alpha1diagnosis
Pleased to be a new member of @CMTUnitedKdom Providing support and raising awareness for the debilitating inherited neurological #CharcotMarieTooth disease - The most common #RareDisease you've never heard of? Factsheet: cmt.org.uk/wp-content/upl…
2 of my friends shaved their heads in support of my cancer journey. #malignantphyllodestumor #phyllodestumor #rarecancer #raredisease #metastatic #stage4
Dr. Caramelo @raredisease
122 Followers 0 Following
RareDisease @NadirHastalik
965 Followers 78 Following 28 Subat 2019 Dunya #NadirHastalik Gunu Nadir Hastalik Toplulugu #TurkeyRareDisease Amacimiz #NadirHastalik farkindaligi olusturmak. #RareDisease
Rare Disease Day @rarediseaseCH
167 Followers 2 Following Am Sonntag, den 28. Februar 2010 findet in Basel und Zürich der TAG DER SELTENEN KRANKHEITEN statt.
raredisease_cbi @raredisease_cbi
146 Followers 16 Following 5th Annual Rare Disease Leadership Summit -- July 13-14, 2010
Rare Disease India @raredisease_in
591 Followers 213 Following 70 million Indians suffer from #RareDiseases. #Genomics offers them a new #hope.
NCL_RareDisease @NCL_RareDisease
600 Followers 912 Following @UniofNewcastle Centre of Excellence for Rare Disease works with @NewcastleHosps @NHIPartners & more, to constitute a 'Newcastle RD' community(Tweets V.Hedley)
RareConnect @RareConnect
19K Followers 5K Following 🌐Connecting #raredisease patients globally at https://t.co/v6rTTK0X6I. 💻Website help at @RareConnectSup.
Rare2Aware @Rare2Aware
4K Followers 350 Following #RareDisease awareness initiative by Takeda. For an audience outside the US and the UK. Contact us via DM. Community guidelines: https://t.co/HOHonTBQ9i
Rare Disease UK @rarediseaseuk
22K Followers 2K Following National campaign run by @GeneticAll_UK to improve the lives of those affected by rare conditions and all who support them. #RareDisease.
Carrie Ostrea, MBA @RareDiseaseAdv
1K Followers 111 Following Little Miss Hannah's Mom #RareMom. Providing education & mentoring to #raredisease advocates. Comments and opinions are my own.
Special Needs Jungle @SpcialNdsJungle
40K Followers 10K Following #SEND news, views, resources. Parent-led SEND influencers #FixSEND #Health #Disability #mentalhealth #autism #RareDisease #adhd Led by @TaniaLT @RenataBplus3
한국희귀질환재.. @raredisease_
262 Followers 348 Following 한국희귀질환재단은 뜻있는 시민과 지자체, 기업, 단체 등의 후원과 참여로 이루어지는 순수공익재단으로써 희귀질환 치료를 위한 사회적 여건 개선을 통해서 환자와 가족들의 삶의 질 향상에 힘쓰고 있습니다.
Urddad-Foundation @RarediseaseNI
52 Followers 608 Following My name is Cavan Hoey I have two Rare Diseases called XLP,and HLH I live in Bodmim Cornwall I am raiseing awearness of Ultra Rare Diseases
RareDisease_Mie @RareDisease_Mie
471 Followers 613 Following 一人でも多くの方々に「稀少難病」を知っていただきたいです。NPO法人三重難病連加盟団体 （三重県難病相談支援センター事業受託団体 前三難連理事 稀少難病の会みえ会長 RDDJAPAN MIE主催 桑名市民活動団体)
Rare Diseases India @rarediseasesind
4K Followers 259 Following A public awareness initiative by Sanofi (Specialty Care) India on #RareDisease issues. For India residents only. #EveryLifeIsPrecious https://t.co/YH80r3SUFk
Tasha 💫 @feelinfroggy181
29K Followers 2K Following Mom to a real life superhero ❤ #raredisease #egids #mito #chd #masto #eds #pots PettyBettyCrocker 🥧 on hiatus $bradensmom14 💜 Raccoonteur🦝 NBA Addict🏀
Kevin E FitzGerald @IPFAdvocate
17K Followers 13K Following Pulmonary Fibrosis (IPF) Patient Advocate - Raising Awareness of #IPF #PulmonaryFibrosis #RareDisease #CureIPF #IPFAdvocate • Inspirational Speaker • Ambassador
Michele Rhee @michelerhee
2K Followers 317 Following #RareDisease & #AYACSM / #AYA Cancer #PatientAdvocate| Board of @CostsOfCare | Overall enthusiastic person! | Tweets are my own.
yoni יוני @Primary_Immune
41K Followers 27K Following Human being. Jew. Israeli. Primary Immunodeficiency patient. הודו לה׳ כי טוב כי לעולם חסדו #Immunology #raredisease #ISRAEL
Henna Tyynismaa @HTyynismaa
910 Followers 190 Following Professor / Vice Dean of Research, Faculty of Medicine @helsinkiuni #mitochondria #proteostasis #stemcells #motorneurons #raredisease
RareDisease_HU @RareDisease_HU
29 Followers 0 Following A community for people affected by rare diseases. Learn, share, and connect with peers and healthcare professionals.
ra🐾 @___raredisease
19 Followers 43 Following
Sickle cell disease @Sicklecell_RM
801 Followers 357 Following Page no longer active. Follow @RaremarkHealth for #SickleCell Our vision is to shape a world where all rare conditions are understood and treated. #RareDisease
NORD @RareDiseases
41K Followers 3K Following National Organization for Rare Disorders (#NORD) is the voice of the #RareDisease community. Official US sponsor of #RareDiseaseDay.
Rare Disease Advisor @RareDisease_Adv
5K Followers 1K Following Trusted knowledge base of practical information and resources focused on treating and diagnosing #RareDisease.
Liz Worthey @lizworthey
6K Followers 2K Following #AssociateProf #CompBio #Omics #WomenInScience #PrecisionMedicine #RareDisease #ME/CFS #hEDS #UndiagnosedDisease #SciFiNerd #Mama #Scottish #Texan
Boston Biotechs @BostonBioTechs
2K Followers 160 Following Simplifying #ClinicalResearch. #ClinicalStrategy and #CostEffective #TrialDesign specialists. #RareDisease and #OrphanIndication experts.
Elijah's Hope @ElijahsHopeCIC
1K Followers 941 Following Aiming to help people with #genetic condition, Apert syndrome and other #disability #raredisease Find our RareConnect community: https://t.co/OgRBk6051H
Yann Le Cam @yann_eurordis
1K Followers 263 Following CEO @eurordis, #raredisease #patient advocate. Member of @rarediseasesint council. Tweets are my own.
Scott Pearl @scottpearlmktg
4K Followers 2K Following Executive Director | CEO. Top 50 Influential #CMO & #Marketing Leader. #Tech. #Nonprofit. #Healthcare. #Startup Mentor. #RareDisease Advocate. Tweets mine.
Victoria Warren @vwarrenmedia
8K Followers 2K Following News reporter turned healthcare storyteller. #RareDisease and #FoodAllergy advocate and coffee addict! @DanaFarber #7News alum. Tweets are my own.
Ana @Ana4raredisease
18 Followers 64 Following Yes, I am a that mom who stalks her daughter on social media.
Stanford CUD @stanford_CUD
425 Followers 139 Following Stanford Center for Undiagnosed Diseases. Hospital affiliate of the Undiagnosed Diseases Network @UDNconnect. #raredisease #science #genetics #genomics
The DECIPHER Project @deciphergenomic
2K Followers 107 Following Enabling #matchmaking and interpretation of phenotype-linked pathogenic genetic variation in patients with #raredisease by effective #datasharing.
Cambridge Rare Diseas.. @camraredisease
8K Followers 7K Following Improving #RareDisease lives. Creators of #RAREfest, #RAREsummit, Companies Forum & #UniqueFeetCam https://t.co/bWJ8DVF9iw
Ben's Friends @bensfriends
4K Followers 2K Following #BensFriends is a network of #patientcommunities for people with #raredisease and #chronicillness. 501c3 Nonprofit: https://t.co/X2Pip2rsIz
Barby Ingle Official @BarbyIngle
20K Followers 8K Following #AZ State Rep Candidate #LD7 |#PCRC D5, | #IAm #Writer #RareDisease #ChronicPain, #UniversalPetite, Creator of #NERVEmber
Youlianwang @YLW_raredisease
1 Followers 15 Following Youlianwang website is a mutual aid public welfare platform spontaneously created by rare disease patients and volunteers.
Heather Corini (forme.. @hcorini
2K Followers 1K Following artist | attorney | #catlady | Disney AP | #ePatient #patientadvocate for #raredisease #dermatomyositis #SJIA #stillsdisease #juvenilearthritis #IVIG + she/her
Santhera @Santhera
791 Followers 233 Following #Santhera is passionate about improving the lives of patients suffering from a rare disease. #Duchenne #DMD #neuromuscular #theirfutureourfocus #raredisease
Stephanie Fischer @RarePOV
7K Followers 6K Following #Raredisease patient advocate & #stroke survivor.🦓 Member of @PARareDisease. Opinions are my own.
Phelan-McDermid Syndr.. @Phelan_McDermid
1K Followers 583 Following Official site of the Phelan-McDermid Syndrome Foundation. We support families and fund research. #PMS #PMSF #raredisease #specialneeds #pmsfad
Healx @healx
3K Followers 634 Following AI-powered and patient-inspired. We accelerate the discovery and development of #raredisease treatments.
The Mast Cell Disease.. @MCDiseasesUnite
2K Followers 340 Following Transforming lives of patients and families while finding a cure for #mastcelldisease since 1995. #Mastocytosis #MCAS #HereditaryAlphaTryptasemia #raredisease
CureGRIN @CureGrin
773 Followers 350 Following CureGRIN is a parent-run foundation committed to improving the lives of people living with GRI disorder. #RareAsOne #GRIdisorder #raredisease
AdvocacyRSS 🇺🇲 @advocacyrss
5K Followers 4K Following Heather #RareDisease Advocate / Writer/ networking / president / Exec Producer #highstrungmovie / #WritingCommunity no DMs unless requested
Mark2Cure @Mark2Cure
2K Followers 1K Following #Citizenscience effort to search #biomedical literature for clues on #raredisease. Join us!
I AM #RareDisease @EDSZEBRA686
152 Followers 526 Following I am a #chronicpainwarrior fighting #EDS #Dysautonomia #Gastroparesis & #Chiari #HealthcareIsAHumanRight and I #believe in #BernieSanders !
IamLongCovid @IamLongCovid
2K Followers 1K Following I am Long Covid! #IamLongCovid Spread the word! Bring attention to those suffering from #LongCovid, #ME #CFS #EDS #MCAS #MECFS #LongHaulers #RareDisease
Girl Gone Blind @Girl_Gone_Blind
3K Followers 2K Following Maria | #Speaker | #Blogger | #Advocate | Fitness Instructor #SanDiego | #Blind | I have Lebers Hereditary Optic Neuropathy #LHON | #RareDisease 👩🏻🦯
penyakitlangkaIND @RarediseaseIND
15 Followers 0 Following
ANAssociation @ANAssociation
1K Followers 576 Following The premier resource for the acoustic neuroma community. #acousticneuroma #raredisease #vestibularschwannoma #braintumor
Balsam 🪷 @DrBalsamAhmad
6K Followers 4K Following Public Health | NHS | Art & Science | #SocialJustice| Mother #RareDisease | #Storyteller | RTs & likes NOT endorsements | views are my own
Taylor Kane @rarelikeher
3K Followers 1K Following Patient engagement consultant, #raredisease advocate, author, speaker, founder @remember_girls, and more!
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.
SanfordCoRDS @SanfordCoRDS
4K Followers 2K Following CoRDS is the world's only cost-free, international #RareDisease #PatientRegistry - Enroll today and share your #data! https://t.co/DOIhiNxbbF
IRDiRC @irdirc
3K Followers 2K Following #IRDiRC is a consortium of #RareDisease #research funding agencies n stakeholders. RTs shares likes ≠ endorsement. Account managed by IRDiRC Scient. Secretariat
FMDAdvocate @FMDAdvocate
1K Followers 833 Following I am a former research nurse & stroke survivor. Now spending my time as an advocate for #raredisease, #FMD , Fibromuscular Dysplasia
Pheo Para Alliance @PheoPara
2K Followers 613 Following Investing in research and supporting #pheochromocytoma and #paraganglioma patients globally. "Stronger United" #NETCancer #RareDisease #pheo #para
Dr. Heather Mefford @hcmefford
3K Followers 948 Following Physician, scientist, mom, wife #genetics #epilepsy #pediatrics #raredisease @StJude @StJudeResearch formerly @UWMedicine
Katie Helbig @katiehelbig
1K Followers 402 Following epilepsy, neurodevelopmental disorders, genetics 🧠 🧬 | #innovation for #RareDisease | champion of red wine and nacho connoisseur | opinions are mine
Jana Javornik @JanaSvenska
5K Followers 4K Following Academic/Policy Adviser | ex- Director-General of Higher Ed | Advocate #LongCovid #raredisease | Policy, Work/ers, EDI, Impact, Sustainability| Ops mine! |
Bertrand Might @bertrandmight
1K Followers 787 Following I'm a little guy. My parents blog about how I'm changing the world, one smile at a time. #NGLY1 #RareDisease #CDG @NGLY1org
Ataxia and Me CIO 118.. @Ataxia_and_Me
4K Followers 3K Following #Ataxia is a #raredisease affecting #Balance #Speech and #Coordination #Patients Helping Patients #MovementDisorder #Health #Medical #pharma
Raredisease Consultin.. @RarediseaseC
1 Followers 0 Following Focused on Regulatory affairs for rare disease consulting and training for industries and professional, who are seeking new role in regulatory industry.
JMG @JMG_BMJ
2K Followers 1K Following Journal of Medical Genetics - a leading international peer-reviewed journal ➡ Original research in human #Genetics #Research #Genomics #RareDisease #Cancer
Rafael J. Yáñez-Mu�.. @RJYanezMunoz
502 Followers 304 Following @RoyalHolloway Professor; @_BSGCT President. #RareDisease #GeneTherapy #StemCells #GenomeEditing #ATMP #StudentWellbeing. He/him
Sanath Ramesh @sanathkr_
2K Followers 1K Following Father of #RareDisease baby Raghav. Finding cure for GPX4 gene disorder 🧬 ; CEO @OpenTreatments_; Podcast https://t.co/hVuvGUSRtl Start. Pivot. Quit. Repeat
Sandy Smith @sandysmith317
3K Followers 2K Following #RareDisease #SYNGAP1 auntie. Working for a cure with @cureSyngap1. Healthcare IT professional. Micah 6:8 💜#epilepsy💙#autism💚#id
Chloe Reuter @ChloeReuterCGC
912 Followers 914 Following Genetic Counselor | @stanford_CUD @StanfordHCM @UDNConnect | #gcchat #CardioGen #raredisease #undiagnosed | @StanfordMed, @Cornell alum | she/her | views my own
Rachelle Dixon @RachelleM_Dixon
1K Followers 1K Following President/Co-Founder of HSAN1E Society / Rare Disease Advocate / Speaker @hsan1esociety #raredisease #theother50percent
Crinetics Pharmaceuti.. @Crinetics
878 Followers 545 Following Discovering and developing novel therapeutics for #RareEndocrine disorders. #Crinetics #RareDisease #acromegaly #CarcinoidSyndrome
GBS|CIDP Foundation @gbscidp
2K Followers 1K Following To support those affected by GBS|CIDP & variants so each patient obtains an early diagnosis, proper treatment &the opportunity for a full recovery #raredisease
ECD Global Alliance @ECDGA
570 Followers 282 Following The ECD Global Alliance is the only nonprofit worldwide solely dedicated to people living with #ErdheimChester disease #histocytosis #histocyte #raredisease
TheLAMFoundation @LAMFoundation
1K Followers 468 Following Delivering facts about #LAM #RareDisease and The LAM Foundation. We're dedicated to funding research, advocacy and awareness to improve the QoL for all LAM pts.
Jessica Lynn @JessTheWriter33
3K Followers 2K Following #RareDisease and Education Writer | VCU Ram | Traveler | Wino 🍷 | #LGM | Poet | Opinions are my own | Open to freelance opportunities: [email protected]
Adam Johnson - DadVoc.. @RareDiseaseDad
1K Followers 1K Following Dad w/#RareDisease | #Mito Advocate |🎙Host: #ParentsAsRare | Educator | Support | Kindness | Dad Jokes |#MentalHealthMatters | #BoiseState | ⚾️ @Cubs 🏈@49ers
Myositis Support and .. @MyositisSupport
2K Followers 2K Following MSU, patient-led, all-volunteer nonprofit empowering the #Myositis community. Patient support, education, financial assistance, research. #RareDisease
Effie Parks @OnceUponAGene
5K Followers 3K Following Nuclear Advocate | Award Winning Podcaster | Speaker | Captain Connection | #RareDisease #RareMama to my sweet, Ford, who lives with #CTNNB1 🦓
Lauren Perry @LaurenPerry80
2K Followers 2K Following #ColoradoNative☀️⛰️ | #RareDisease Advocate🦓 | #ISFJ✌️| #melomaniac 🎶 | #Xennial💾 | #SYNGAP1🧬 mom | Ops Mgr📃 at #SyngapResearchFund | @cureSYNGAP1💜💙💚
Nancy M. Anderson @nma08244
1K Followers 1K Following Passionate Advocate for #ChildhoodCancer & #RareDisease patients #CompassionateUse #ExpandedAccess #4Nathalie #MedGift 🎗Pass the 🎗#STARAct🎗& 💜#CuresNow💜
Fondation Ipsen - Rar.. @FondationIpsen
550 Followers 393 Following Our mission is to improve #Raredisease diagnosis and patient's day-to-day lives. Discover our program, books, webinars, videos or podcasts.
orphanwriter @orphanwriter
1K Followers 1K Following Senior Advisor, National Organization for Rare Disorders. Honored to work with amazing #raredisease patients, caregivers, researchers & clinicians.
Hope for Trisomy @HopeforTrisomy
682 Followers 459 Following Helping others make informed decisions by funding research, promoting education, raising awareness, changing lives. #Trisomy13 #Trisomy18 #Trisomy #raredisease
Melissa Haendel @ontowonka
2K Followers 2K Following At the intersection of biology and everything else. #AttributionForAll. #UnitedAgainstHate #raredisease #FactsMatter, also at @[email protected]
CENA Project @CENAProject
2K Followers 2K Following CENA is a PCORI funded project led by Genetic Alliance working with 10 orgs to expand a health data network. #RareDisease #ChronicIllness #Genetic #Research
AtaxiasARG @AtaxiasARG
882 Followers 701 Following 🇦🇷Ataxias Argentina #Ataxia #MovementDisorders #AtaxiaAwareness #Brain #Cerebro #Neurology #Neurologia #raredisease #livingwithataxia #Research 👩🔬👨🔬👨
Kimberly Amelia @fireflyrn84
1K Followers 2K Following RN/full time pt, advocate, #raredisease blog @PatientsLikeMe TOA Alumni @WEGOHealth Patient Leader/Expert #BreakthroughCrew Ambassador #SavvyPatient #pinksocks
BLACKSWAN Foundation @raredisease_act
17 Followers 0 Following
Alice Rathjen @dnatimes
6K Followers 4K Following CEO Founder DNAcompass GIS earth #maps reuse for #genomics #Raredisease #patientadvocacy #spatialgenomics https://t.co/Tzkyh8c3D3 [email protected]
Lisa Weinberger, MAT @LisaWeinberger
741 Followers 484 Following Digital Marketing Professor | Content, SEO for a state university | Owned by @2_boxers_ivy_zo #pemphigus #raredisease #advocate https://t.co/BrNNLIIFhH…
Sarita Edwards @SaritaEdwards
1K Followers 811 Following Rare Mom (#Trisomy 18) | MHA | CEO @everyoneiswe | Podcaster | Global Keynote | Award Winning Advocate | #RareDisease #Equity #MentalHealth #Policy #MeToo
Leah Bush @LeahNBush
543 Followers 505 Following Wife/Mom | CHW | Advocate #RareDisease l Program Director at The Family Place NC l Community Manager #SJIA Parent Network (#CureSJIA) *Opinions are my own
Della Cogar @dc_raredisease
11 Followers 0 Following
Dr. Kathleen Bogart �.. @kathleen_bogart
2K Followers 1K Following Social/health psych prof: #Ableism #DisabilityPride #FacialParalysis #RareDisease. Writer/speaker: @PsychToday @TEDx @ScienceMagazine. Founder: @DARN_Disability
𝕆𝕙 𝕟𝕠, �.. @WallaceUofE
749 Followers 401 Following Politicians/Officials? Love software & IA. FT carer & LOUD Activist 4 #RareDisease patients/carers. https://t.co/oF1E9HTZOD; https://t.co/T7B3Hgecf4. Veteran
Jasmine L. Carter, Ph.. @JasmineLCarter
499 Followers 458 Following Neuroscientist @ODC_UPenn | Previously @FinkLab @ucdavis_neuro @UCDavisStemCell | #raredisease research | wine | doxies | she/her
Ashish Marwaha BMBCh,.. @DrAshM2
2K Followers 2K Following Clinical Medical Geneticist 🇨🇦, immunogenetics, #T1D polygenic risk. #raredisease clinical trials. Tweets=own opinionTrends for United States
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