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#Nurown Lucha mundial contra la ELA - No podemos esperar @US_FDA @EMA_News - Sign the Petition! chng.it/VDbYxxS5 via @Change
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Eliana Goncalves
40.8K posts
Eliana Goncalves
@AlsChange
We need to accelerate the processes related treatments for ALS - Amyotrophic Lateral Sclerosis: Nurown cuATSM. https://t.co/7DlNP3WKjs?amp=1
Portugal Katılım Ekim 2019
2.2K Takip Edilen890 Takipçiler
Eliana Goncalves retweetledi
“It’s a horrible disease, but we’re creating awareness and we’re gonna get a cure one day…”
After courageously going public with his ALS diagnosis, @Senators assistant coach Bob Jones sat down with @SNChrisSimpson to share his story.
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Eliana Goncalves retweetledi
Tres personas enfermas de ELA mueren al día mientras la #LeyELA está paralizada en el Congreso. Nos hemos aliado con @pons_sabate para que el Gobierno se ponga las pilas y aplique la ley. Para más información mira la nota de prensa: pressroom.citizengo.com/2022/06/21/jor…
#DiaMundialELA
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Eliana Goncalves retweetledi
Amazing effort & love this pic @myoddballs !
Thank you to everyone who has bought tartan undies - you're helping to make a huge difference 💛💙
OddBalls@myoddballs
Today is #globalmndawarenessday! We’re delighted support and raise awareness of the brilliant @MNDoddie5 Foundation, through the sale of our underwear in Doddie’s signature tartan. 💙💛 So far we've raised a total of £44,500. Thank you to everyone who’s helped us reach this! 😍
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Eliana Goncalves retweetledi
Today is Global ALS Awareness Day. ALS is a neurological disease that affects up to 30,000 people in the United States
We are committed to revolutionizing the treatment for people living with neurodegenerative diseases like #ALS. #ALSMNDWithoutBorders @ALSMNDAlliance #MND $CLNN
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Eliana Goncalves retweetledi
Another important milestone on the road to treatments and cures!
Huge thank you to the ALS champions in appropriations who helped make this happen: @KenCalvert, @BettyMcCollum04, @TomColeOK04, @RepMikeQuigley, @RepKayGranger and @rosadelauro!
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Eliana Goncalves retweetledi
Eliana Goncalves retweetledi
Please do all you can to raise awareness of MND, today is #globalmndawarenessday , we won’t rest until MND is treatable and ultimately curable.
MND Association@mndassoc
It's #GlobalMNDAwarenessDay - a day to raise awareness of motor neurone disease around the world. • 6 people will be diagnosed today • 6 people will die today • It has NO cure Please retweet our graphic highlighting the key facts. More people need to know 💙 thank you! #MND
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Eliana Goncalves retweetledi
It’s #GlobalMNDAwarenessDay just taking a moment to remember all those who fought and lost their battle with #mnd it’s just another day but it’s also a day nearer to the @mndassoc aim of a world free from mnd
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Eliana Goncalves retweetledi
This #GlobalMNDAwarenessDay we're proud to share that a £4.25 million grant has been awarded to MND researchers 🔬
My Name'5 Doddie Foundation helped to fund the research grant which aims to make MND treatable within years, not decades.
More info: myname5doddie.co.uk/whats-on/artic…
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Eliana Goncalves retweetledi
It's #GlobalMNDAwarenessDay - a day to raise awareness of motor neurone disease around the world.
• 6 people will be diagnosed today
• 6 people will die today
• It has NO cure
Please retweet our graphic highlighting the key facts. More people need to know 💙 thank you! #MND
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Eliana Goncalves retweetledi
Eliana Goncalves retweetledi
El 21 de junio se celebra el día internacional de la #esclerosislateralamiotrófica o #ELA, una enfermedad del sistema nervioso central, caracterizada x degeneración progresiva de neuronas motoras causando una debilidad muscular y parálisis en el organismo
somosdisca.es/dia-internacio…
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Eliana Goncalves retweetledi
El centro de salud 'San Hilario' de #DosHermanas, @AGSSurSevilla, se suma a la visualización de la #ELA con una mesa informativa, la implicación de profesionales y la colaboración de familiares de pacientes.
#DiaMundialELA
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Eliana Goncalves retweetledi
On #GlobalMNDAwarenessDay, we’re sharing portraits of people living with motor neurone disease #MND, by celebrity photographer @CannonPictures.
We’re delighted our Patron @Rob7Burrow wanted to virtually open the exhibition! @leedsrhinos
📸 artsteps.com/view/62a85c0a8…
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Eliana Goncalves retweetledi
This is my 9,000 tweet or reply. That means 2 things:
First, my wife is right about me tweeting a lot.
Second, despite its best efforts, ALS has not killed me yet which makes me truly lucky.
Not today ALS. Not today.
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Eliana Goncalves retweetledi
Now, this is a publication of persistence, not giving up..
NurOwn is moving forward to the finish line.
Especially for patients who are considered to be in the later stages for other clinical trials, who do not have any other choice, this is a very very good news I think
Jill Brattain@MommaJillB
BrainStorm Cell Therapeutics Announces peer reviewed publication of NurOwn's® Phase 3 Study for ALS in Muscle and Nerve ir.brainstorm-cell.com/2021-12-13-Bra…
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Eliana Goncalves retweetledi
A significantly greater proportion of ALS patients with less severe disease responded to the cell-based therapy NurOwn than to a placebo. buff.ly/30zHPdO
#ALS #ALSNewsToday #amyotrophiclateralsclerosis #livingwithALS #ALScommunity #ALSadvocacy #healALS #DisabilityTwitter
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Eliana Goncalves retweetledi
Eliana Goncalves retweetledi
Started the year w our #DrugsinBodies campaign to get the #ACTforALS passed & to get #NurOwn approved.
Data in @MuscleNerve proves NurOwn is clinically meaningful for ALSFRS-R scores 26+.
@FDACBER give the community a holiday blessing by asking @BrainstormCell to submit a BLA.
Lisa's Legacy for ALS@LisaLegacy4ALS
What a week for #ALS — the #ACTforALS passing right after the long-awaited publication of #NurOwn data. Now it’s time for Act 2: What’s next for @US_FDA? Will you exercise regulatory flexibility? What’s next for NurOwn BLA filing? @BrainstormCell The community can’t wait!
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