David Ali
@davidiali
MND advocate and supporter and working towards a world free from ALS/MND. Views/RT my own
ID: 2945932298
28-12-2014 06:25:05
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World Health Organization (WHO)
@who
We are the #UnitedNations’ health agency - #HealthForAll. Always check our latest tweets for updated advice/information Support WHO: oneworldhealthforall.org
ALS Advocacy
@alsadvocacy
ALS = Lou Gehrig's Disease Thought it had been cured by now? Still no known cause. Still no cure. Still no treatment. Still quickly fatal. Still outrageous.
LifeArc
@lifearc1
Medical research non-profit transforming promising life science ideas into medical breakthroughs that change patients’ lives.
Susan Baker
@ksalsfighter
KS farm girl passionate about promoting awareness about Familial FTD ALS
Ed Slater
@edslater
ALS/MND is living with me. Former Rugby Player for Gloucester and Leicester. Charlton Ath fan. No particular order 🙂 #KeepMovingForward
MND Australia
@mndaustralia
Care, advocacy and research in support of those living with motor neurone disease (MND).
ALS Uncensored 🏴☠️
@scottsfight
Scott Craig. ALS Uncensored podcast. Digital Artist. AI Student. Typing with my eyes. Living Impossible! #ALSUncensored #ALS #EyeGazeArtist #AI #IWriteALS
Jayne Halhead
@jaynes__world
In memory of my Dad, a burly #Lancashire dairy farmer, I'm raising awareness of motor neuron disease.... #MND #MoreNeedsDoing! Championing #Lancashire🌹
Richard Cave 🇺🇦
@speedoftrust27
Speech and Language Therapist. UCL post-doc GDI Hub Research Fellow, MND Association. RCSLT advisor for voice banking & MND ALS Alliance professional award 2022
Tammy Moore
@temeritytm
Digging in. ALS Canada CEO. Finding adventure and appreciation in the everyday - seize the day because life is too damn short. Be bold.
Professor Matthew C. Kiernan AM Nerve Centrals
@nervecentrals
CEO & Executive Director @Neuraustralia Scientia Professor of Neuroscience @UNSW. Neurologist @SEastSydHealth. President @brainfoundoz Editor Emeritus @JNNP_BMJ
Sunny Brous
@sunnystrongals
I have ALS but it does not have me. No apologies, no excuses, no regrets, just me.
James Vickers
@jamescvickers
Neuroscientist + Director of the Wicking Dementia Centre
Guðjón Sigurðsson
@gaui_mnd
ALS Society of BC
@als_bc
To cure ALS through funding research, while advocating for and supporting people living with ALS.
David Setters
@dsetters
Got slowly progressing MND. Luckier than most so have to make extra days count. I intend to! Making memories with family. Campaign, raise awareness & funds.
Palliative Care Australia
@pall_care_aus
PCA is the national peak body for palliative care, representing all those who work towards high-quality palliative care for all Australians.
Fleur Garton
@fleurryg
Scott Sullivan MND Reseach Fellow, University of Queensland; passionate about the genetics of neurodegenerative & neuromuscular disease
Sammy J
@sammyjcomedian
Comedian. Writer. Composer. Nerd.
wayne thomas
@nwaynet
ALS Warrior! World Trvlr - 38 countries, Joanna.Foodie.Xmas.Fur kids:Callie & Skye. FCPHR, CMC, MBA, Sr. Leader. LIVING LIFE NOT WAITING TO DIE.🇨🇦🇺🇸🥂🍽
Nick Goldup
@nickgoldup1
Chair and Chief Operating Officer of the Wheelchair Alliance CIC
Tamara Oudyn
@tamaraoudyn
Presenter: @ABCMelbourne. Podcaster: The Good Divorce, Life Matters. Voice trainer. Choir leader. Freakishly good at self-administering eye drops.
Rare Diseases Clinical Research Network
@rarediseasesnet
NIH-funded network fostering collaborative research among 20 teams of researchers, patients, and clinicians, each focused on a group of rare diseases.
MND Scotland
@mndscotland
Making time count for people with motor neuron disease (MND).
Debbie Redfern 💙🧡
@debschebs
Assistant Director of Quality Improvement at Bolton NHS Foundation Trust- fundraising for Redfern’s Fightback Fund for MND Association 💙🧡 views my own
Asoc. ELA Argentina
@asociacionelaar
Centro de afectados por la Esclerosis Lateral Amiotrófica.
MND Association
@mndassoc
Our vision is a 🌎 free from 𝐦𝐨𝐭𝐨𝐫 𝐧𝐞𝐮𝐫𝐨𝐧𝐞 𝐝𝐢𝐬𝐞𝐚𝐬𝐞 #MND
Mick Geary
@mickgeary
Brian Dickie
@drbriandickie
Chief Scientist @ MND Association
ALS/MND Alliance
@alsmndalliance
A World Free of #ALS #MND
Andrea Pauls Backman (she/her)
@andreabackman05
Follow me at AndreaALSstrategy.bsky.social. Passionate about people w ALS/MND & fighting for cures.
Andrew Corbett
@agcorbett1000
Pharma Medical Advisor
Team Gleason
@teamgleason
Nonprofit founded by former New Orleans Saints player, @SteveGleason, after his diagnosis with Amyotrophic Lateral Sclerosis (ALS) in 2011. NO WHITE FLAGS
ALS News today
@alsnewstoday
We are dedicated to sharing the latest news, research, and ALS patient perspectives.
MNDA Soton & Winch
@mndasoton
Southampton & Winchester Group of the Motor Neurone Disease Association. Championing the amazing work of our volunteers. #MND
Lee Millard
@onein300
1/300 is the lifetime risk of developing #ALS #MND. My living with Motor Neurone Disease blog.
MND Research Australia
@mnd_ria
Motor Neurone Disease Research Australia has built & sustained MND research nationally for 40 yrs. MNDRA is the research arm of MND Australia.
Mary Kay Turner
@marykayturner1
Government Affairs | Health Policy| Mom| Dog Lover | Oregon Ducks Fan| Traveler| Defender of Biopharma | Innovation Matters | ALS Advocate| Opinions Are My Own
Ammar Al-Chalabi
@ammaralchalabi
Professor of Neurology and Complex Disease Genetics, King's College London Co-Director UK MND Research Institute MND ALS Specialist. @ammaralchalabi.bsky.social
Brian Wallach
@bsw5020
Dad, husband, activist, entrepreneur, unlikely movie star, living with ALS, a currently fatal disease.
Jean C9orf72
@jeanc9orf72
C9orf72 gene carrier - advocate and leader for our community. Founding Chair, Genetic ALS & FTD: End the Legacy @end_the_legacy
David Taylor
@vpresearch_als
ALS Canada VP, Research. Passionate ALS research nerd since 2001. Science brain, advocate heart. Opinions are my own. he/him
I AM ALS
@iamalsorg
I AM ALS is a patient-led movement revolutionizing how to end disease with our sights set squarely on ALS.
My Name'5 Doddie Foundation
@mndoddie5
Registered charity, established by Doddie Weir & friends to fund vital research into motor neuron disease (MND) & support those living with MND.
MND-SMART
@mndsmart
Innovative UK MND clinical trial from Euan MacDonald Centre for MND research at @EdinburghUni. Designed alongside people with MND. Searching for new treatments.
MND Research
@mndresearch
We fund cutting-edge #MND #ALS research in the UK and worldwide. 🔬 Join us at the largest international conference dedicated to ALS/MND #alsmndsymp
ALS CURE Project
@alscureproject
The purpose of the ALS CURE Project is to provide laser focused leadership and sponsor scientific research leading to a cure for ALS (aka. Lou Gehrig’s Disease)
ALS Action Canada
@alsaction
We're Canada's first and only ALS patient-led nonprofit organization fighting to #EndALS forever. Join us! Charitable organization BN: 791367204 RR 0001
ALS ONE
@alsone_official
Our world leaders in ALS research & care have united 2 advance critical research towards a cure while improving the qual of life of individuals living w/ALS now
Racing for ALS
@racing_als
An amazing group racing to make a difference... Praying for a cure!! 501c3 - Over $1.85 Million donated!! Info & Merch via our website.
EverythingALS
@everything_als
We are a patient-focused non-profit bringing technological innovations and data science to support efforts, from care to cure, for people with ALS.
ALSUntangled
@alsuntangled
Every day more deaths and tortuous suffering. It’s time to stop clowning around with ALS research and those whose lives depend on it. #dyingwaiting
Thanuja Dharmadasa
@dharmadasa_t
Neurologist, ALS/MND clinician researcher, music lover
Kos Samaras
@kossamaras
Director at RedBridge Group Australia. Endurance athlete. Religion: Stoicism. Research posted - paid by and for RedBridge.
Brandon @ Crucible Of Thought
@crucibleofthght
If we let it, this season can be a refining, a crucible experience, where the dross burns away and only pure gold remains. Blog at crucibleofthought.com
Your ALS Guide
@youralsguide
A user-friendly website where people living with ALS, caregivers, and professionals can find educational guides, expert video clips, resources, and more...
Me v MND
@me_v_mnd
The #MND #ALS related account of @edcooke. Living with MND since 2023. Trustee of @mndassoc. Views own.
EUpALS
@eupals
European organization for professionals and people with ALS
Rebecca San Gil
@rebecca_sanglia
MND researcher_CRISPR enthusiast_Early Career Postdoc
newsGP
@newsgpau
As the RACGP’s news hub, we report on all the latest general practice developments as they happen. newsGP does not chase clicks, it deals in facts.
Wheel 4 MND
@wheel4mnd
We are raising funds for MND after a work mate passed away from MND. To donate head to chuffed.org/project/wheel4… our email address is [email protected]
Evy Reviers
@evyreviers
CEO & Chairwoman ALS Liga Belgium, proud mom together with my partner Wim "daddy" of our beautiful daughter Skye! We are over flowing with happiness! 👨👩👧
Racing for MNDi
@racingformndi
We’re here to supercharge the search for a cure for MND with a laser focus on targeted genetic research. 🚀🔎 📈
Dr Sina Shadfar
@sina_shadfar
Neurobiologist/ Neuropharmacologist/MQCRF Postdoctoral Research Fellow at @AtkinMNDlab, @MND_mq with prime focus on MND and neurodegenerative disease
Steve Vucic
@stevevucic
StampOutMND
@stampoutmnd
Solo Charity Fundraiser For The Motor Neurone Disease Association since 2015, Check out FB for more detailed posts.
Jorge C. Abdalla Jr.
@jorgeabdallajr
Fundador e Presidente do Conselho de Administração da Associação Pró-Cura da ELA e Presidente da UNELA “Founder and Chairman of ALS Pro-Cure Association” Brasil
Associazione conSLAncio Onlus
@conslancioonlus
Patient led Italian #ALS Association 🇮🇹🌎 Founded by Andrea Zicchieri | Member @ALSMNDAlliance @EUpALS | EU ALS Coalition | @CoalizioneSLA
Darryl Borsato
@borsatodarryl
ALS Fighter, proud husband and SOD-1 Mutant #FuckALS #WorldStrongestALSPatient ALS Action Canada board member / ALS Society of BC Advocacy Committee member