Michele Stellato

Communicator. A fan of kindness and living in the moment. ALS advocate.

[Michele Stellato @shellymckenna]

@BurningBrule @Yankees @SlangsOnSports Thank you so much!

[Michele Stellato @shellymckenna]

What. A. Day. Thank you @Yankees and @SlangsOnSports

[New York Yankees @Yankees]

Today, the Yankees honored native New Yorker & beloved baseball statistical analyst Sarah Langs, who was diagnosed with ALS in 2022. Thank you to @SlangsOnSports & @HerALSStory for joining us today!

“Langs Stars” can be purchased by visiting https://t.co/APBOLXmdOP with 100% of the profits going to @ProjectALSorg 💙

[Michele Stellato @shellymckenna]

Just pre-ordered my shirt!

[Project ALS @ProjectALSorg]

Don't miss out on this @RotoWear t-shirt created to support @SlangsOnSports who always reminds us, baseball is the best. This initiative has raised over $57,000 for our cutting-edge ALS research!

Pre-order your Baseball is the Best t-shirt today: https://t.co/sCiWEq6kwK

[Michele Stellato @shellymckenna]

Register now to join the discussion

[Sunny Brous @sunnystrongals]

TOMORROW! Our grand finale of #fightalsfilmfest we get to meet Shelly and Charlie from #matterofminddoc
Be there: https://t.co/HfDpUut5l2 #alsawarenessmonth

[BrainStorm @BrainstormCell]

Join us for our final #ALSFilmFest for #ALSAwarenessMonth on 5/28 @ 5:30 PST/8:30 EST for Matter of Mind: My ALS. In this intimate exploration, three people with ALS, bravely face different paths as they live with this progressively debilitating illness. #MatterofMindPBS

[Michele Stellato @shellymckenna]

@limpbroozkit Yesss!!

[Michele Stellato @shellymckenna]

Thank you! It’s an honor to represent this community 💜

[Lisa's Legacy for ALS @LisaLegacy4ALS]

Both tears and inspiration. Thank you @shellymckenna @pfreelon and Charlie Wren for sharing your stories. We are in awe of your courage and determination. #EndALS #TeamALS
👀📺Matter of Mind: My ALS https://t.co/8lsHyNVFKw

[Michele Stellato @shellymckenna]

@SethPoling10 @HerALSStory Thank you @SethPoling10 it was an honor representing @HerALSStory and the #ALS community.

[Her ALS Story @HerALSStory]

YOU ARE INVITED: This #ALSawarenessMonth, please join us in participating in the #FightALSFilmFest, where each week you will have the opportunity to view a film and join a conversation about the realities of #ALS. Register here for the month-long event: https://t.co/kblqAaBDJh

[Michele Stellato @shellymckenna]

And I’ll be 35 in a week! A donation to @HerALSStory would be greatly appreciated

[Angelina Fanous @NotSoVanilla]

i turn 38 in a week! buy me a drink with a donation to @HerALSStory warrior weekend! due to the high costs of als, we're aiming to make it free for all members & their caregivers. anything you can give (even a rt) is much appreciated! https://t.co/UHbTHltTiL

[Michele Stellato @shellymckenna]

This is unacceptable

[Shah Minokadeh, M.D. @MinoShah]

I was diagnosed by Dr. Robert Miller at CPMC. He was among the top ALS neurologists.

It was incredible to me that a "top doctor" in ALS didn't have ANY answers to my questions. Only riluzole.

What to eat? Should I exercise? Off-label Treatments? Etc.

I was sent home to die.

[Brian Wallach @bsw5020]

In exactly one week @US_FDA and @BrainstormCell will meet to discuss NurOwn.

The ask from the ALS community is simple: Give NurOwn an Advisory Committee Meeting like every other treatment.

It’s time to let the science speak for itself.

[Her ALS Story @HerALSStory]

Limited edition HOPE bracelet now available!! When you order using this link @littlewordsproj will donate 25% of proceeds directly to Her ALS Story 💙

https://t.co/eiBD2m9rIA

[Project ALS @ProjectALSorg]

To say last week’s fall gala was a success would be a massive understatement. Not only did we raise close to $1 million for cutting-edge ALS research, the outpouring of support from everyone involved was truly heartwarming. We couldn’t do what we do without YOU.

[Michele Stellato @shellymckenna]

This makes me so 🤬Do better @Delta

[Sunny Brous @sunnystrongals]

This is my friend @Kate4218 and this is right before @Delta SCREWED her over! She was connecting through @JFKairport and waiting on her wheelchair to go to the next gate when the gate agent informed her that since she wasn’t at the departure gate 45 minutes early her seats were

[Project ALS @ProjectALSorg]

If you look up “strength” in the dictionary, we’re pretty sure you’ll find a photo of Desi Kessler. ⭐ @HerALSStory #EndALS #ALS

[Michele Stellato @shellymckenna]

@RepMikeQuigley Thank you for fighting for us @RepMikeQuigley !!! You’ve given us hope.

[Michele Stellato @shellymckenna]

👏👏👏

[AZ Latina ☮️🌊🟦 @aVoice4ALS]

🎉BREAKING NEWS:
@BrainstormCell announces it will file a BLA seeking FDA approval of #NurOwn for #ALS.

⬇️See Press Release for other promising news!
https://t.co/xTzpqMIZF1

#NurOwnWorks #neurology #neurologists #motorneuron #musculardystrophy #MND
#MedTwitter #NeuroTwitter

[AZ Latina ☮️🌊🟦 @aVoice4ALS]

5 yrs ago, the beautiful @shellymckenna spent her day on the beach exchanging vows with the love of her life. Today, she is fighting #ALS.

@BrainstormCell #FileTheBLA for #NurOwn so 34 yr old Shelley has a chance to spend many more days at the beach.

@DrCaliff_FDA @FDACBER

[Her ALS Story @HerALSStory]

For the next 3 days, 20% of all sales will go directly to Her ALS Story when you shop at https://t.co/pjkGZbk2Ov with the code GIVEBACK-CGOSH

It's the perfect opportunity to treat yourself or your friends to fabulous new jewelry at the same time as you support the lovelyladies