Eliana Goncalves

We need to accelerate the processes related treatments for ALS - Amyotrophic Lateral Sclerosis: Nurown cuATSM.

[Eliana Goncalves @AlsChange]

#Nurown Lucha mundial contra la ELA - No podemos esperar @US_FDA @EMA_News - Sign the Petition! https://t.co/lM83phrhAT via @Change

[Sportsnet @Sportsnet]

“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.

[HazteOir.org @hazteoir]

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: https://t.co/0E7rtidduA

#DiaMundialELA

[My Name'5 Doddie Foundation @MNDoddie5]

Amazing effort & love this pic @myoddballs !

Thank you to everyone who has bought tartan undies - you're helping to make a huge difference 💛💙

[Clene Nanomedicine @CleneNano]

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

[I AM ALS @iamalsorg]

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!

[Julieta @Julieta93787678]

Investigación ¡¡¡YA!!! Cada día, tres personas son diagnosticadas y otras tantas mueren en España a causa de esta dramática enfermedad ¿Cuántas más tienen que dejarnos?

[Nick Goldup @NickGoldup1]

Please do all you can to raise awareness of MND, today is #globalmndawarenessday , we won’t rest until MND is treatable and ultimately curable.

[Richard Shackelford @Shackelford57]

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

[My Name'5 Doddie Foundation @MNDoddie5]

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: https://t.co/AAJtDOGF4R

[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

[Marina Bazan @MarinaBazan7]

21 de Junio
Día mundial de la lucha contra la ELA

[Somosdisc@ @somosdisca]

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

https://t.co/zJCfrFsFUb

[AGS Sur de Sevilla @AGSSurSevilla]

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

[MND Association @mndassoc]

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

📸 https://t.co/mYIifs60xZ

[Brian Wallach @bsw5020]

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.

[Hande Ozdinler @DrOzdinler]

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

[ALS News Today @alsnewstoday]

A significantly greater proportion of ALS patients with less severe disease responded to the cell-based therapy NurOwn than to a placebo. https://t.co/fO8YCmITgo

#ALS #ALSNewsToday #amyotrophiclateralsclerosis #livingwithALS #ALScommunity #ALSadvocacy #healALS #DisabilityTwitter

[Phil Green @pjgreen]

For those arguing why promising #ALS therapies (#NurOwn) should not be approved… We (including you) don’t understand the science well enough to definitively say what works & for whom it will work. Dying people deserve a chance to see if these investigational therapies will help!

[AZ Latina ☮️🌊🟦 @aVoice4ALS]

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.