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@msnewstoday.bsky.socialOct 1, 2026, 5:38 PM

Take a closer look: https://bit.ly/4iZNzUa

The FDA agreed to speed its review of a Roche drug the developer says could be the first oral high-efficacy therapy approved for two MS types.

#MultipleSclerosis #MS #MultipleSclerosisNewsToday #Bionews

@mgnews.bsky.socialOct 1, 2026, 5:38 PM

Discover more: https://bit.ly/4xU2AKQ

Columnist Sarah Bendiff can sense a myashtenia gravis flare-up before one happens and knows that living with the disease means being prepared.

#MyastheniaGravis #RareDisease #MG #MyastheniaGravisNews #Bionews

@alsnewstoday.bsky.socialOct 1, 2026, 5:37 PM

Discover more: https://bit.ly/4jtayXO

Advocates are cheering as legislation to renew the ACT for ALS headed to President Trump's desk days before the program is set to expire.

#ALS #ALSNewsToday #Bionews #ALSCommunity

@mgnews.bsky.socialOct 1, 2026, 5:31 PM

A small adjustment in your plans can be an act of courage: https://bit.ly/4oXeFeg

#MyastheniaGravis #MyastheniaGravisNews #Bionews #ChronicIllnessCommunity 

@mgnews.bsky.socialOct 1, 2026, 4:02 PM

Fatigue with myasthenia gravis can affect much more than how much someone sleeps.

Connect with others who understand life with MG in the MG News Forums: https://bit.ly/47db7xP

#MyastheniaGravis #ChronicIllness #MGCommunity #MyastheniaGravisNews #Bionews

@alsnewstoday.bsky.socialOct 1, 2026, 4:02 PM

Kiersten, who lives with Friedreich’s ataxia (FA), speaks to that unseen exhaustion and why understanding from others can matter.

Join the ALS News Today Forums to connect with others affected by ALS: https://bit.ly/47daX9H

#ALS #ChronicIllness #ALSCommunity #ALSNewsToday #Bionews

@angioedemanews.bsky.socialOct 1, 2026, 3:45 PM

Discover more: https://bit.ly/3W0Sfzn

Hereditary angioedema should be considered in children with recurrent severe abdominal pain and vomiting, the case of a young boy shows.

#Angioedema #RareDisease #HAE #AngioedemaNews #Bionews

@msnewstoday.bsky.socialOct 1, 2026, 3:44 PM

Get the scoop: https://bit.ly/4yqdlpj

An estimated 3.1 million people worldwide are now living with MS, up from about 2.8 million in 2020 and 1.8 million in 2013, a report shows.

#MultipleSclerosis #MS #MultipleSclerosisNewsToday #Bionews

@mgnews.bsky.socialOct 1, 2026, 3:43 PM

Take a closer look: https://bit.ly/4hVRGQ2

Cemdisiran lowered hospitalization rates and reduced the number of myasthenic crises for gMG patients, a global clinical trial showed.

#MyastheniaGravis #RareDisease #MG #MyastheniaGravisNews #Bionews

@alsnewstoday.bsky.socialOct 1, 2026, 3:43 PM

Explore the details: https://bit.ly/4hTaM9r

A walk past fruit trees reminds columnist Kristin Neva of her father, and she thinks about what will remind her children of their dad.

#ALS #ALSNewsToday #Bionews #ALSCommunity

@angioedemanews.bsky.socialSep 30, 2026, 11:31 PM

Discover how to navigate intimacy and angioedema: https://bit.ly/43DYuLc

Your condition doesn’t define your worth—take charge of your sexual and emotional well-being, one step at a time. 

#Angioedema #SexualHealth #ChronicIllness #PatientSupport #RareDisease #AngioedemaNews #Bionews

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@mgnews.bsky.socialSep 30, 2026, 10:03 PM

'Fine' isn't enough: https://bit.ly/4va2L4t

#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport 

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@mgnews.bsky.socialSep 30, 2026, 9:31 PM

A quiet breath for the relief that comes with finally being believed: https://bit.ly/48gxROw

#MyastheniaGravis
#MGCommunity #MyastheniaGravisNews #Bionews #AdvocacyHealthcare

@mgnews.bsky.socialSep 30, 2026, 7:31 PM

A quiet moment of validation for symptoms others can’t see: https://bit.ly/4oEZy9s

#MyastheniaGravis
#MGCommunity #MyastheniaGravisNews #Bionews #MGTreatment

@angioedemanews.bsky.socialSep 30, 2026, 6:46 PM

Gene therapy could transform HAE treatment: https://bit.ly/4mxg8aV

#GeneTherapy #HAETreatment #InnovationInMedicine #RareDiseaseTreatment #MedicalAdvances #AngioedemaNews #Bionews

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@msnewstoday.bsky.socialSep 30, 2026, 5:38 PM

Get the scoop: https://bit.ly/4hlq3jd

Having MS results in columnist Desiree Lama waging a sometimes silent battle against pain, but she's learning to listen to her body's cues.

#MultipleSclerosis #MS #MultipleSclerosisNewsToday #Bionews

@mgnews.bsky.socialSep 30, 2026, 5:38 PM

Get the scoop: https://bit.ly/3Ttxdsz

Trying to get an Ultomiris infusion reminds columnist Mark Harrington how navigating MG can leave him feeling stressed out and worn down.

#MyastheniaGravis #RareDisease #MG #MyastheniaGravisNews #Bionews

@mgnews.bsky.socialSep 30, 2026, 5:31 PM

A little space to acknowledge how unpredictable MG weakness can be🫶: https://bit.ly/4rj7kXu

#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport #InvisibleIllness #ChronicIllnessWarrior #MGJourney #MGWarrior #ChronicIllness

@msnewstoday.bsky.socialSep 30, 2026, 3:44 PM

Take a closer look: https://bit.ly/4rCpkgW

Experimental therapy kamuvudine-9 (K-9), derived from antiviral drugs, restored lost mobility and vision in a preclinical MS study.

#MultipleSclerosis #MS #MultipleSclerosisNewsToday #Bionews

@mgnews.bsky.socialSep 30, 2026, 3:44 PM

Take a closer look: https://bit.ly/4yhNP5A

The experimental CAR T-cell therapy miv-cel led to sustained disease control for people with generalized myasthenia gravis in a recent trial.

#MyastheniaGravis #RareDisease #MG #MyastheniaGravisNews #Bionews

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