Discover more: https://bit.ly/3VnJC1G
A study found 55 DNA methylation regions differed in pediatric MS, with Epstein-Barr virus infection emerging as the top-ranked pathway.

Discover more: https://bit.ly/3VnJC1G
A study found 55 DNA methylation regions differed in pediatric MS, with Epstein-Barr virus infection emerging as the top-ranked pathway.
Explore the details: https://bit.ly/4iVGUdG
Voice Back, an AI app, helps people with ALS and other causes of speech loss communicate using a voice that sounds like their own.
Find practical steps and resources to take action after a hereditary angioedema diagnosis: https://bit.ly/3FD176u
#HAEJourney #PatientEmpowerment #RareDiseaseSupport #TakeAction #HealthResources #AngioedemaNews #Bionews
How knowledgeable do you consider yourself about MG? https://bit.ly/47tSNRN
#MyastheniaGravisNews #Bionews #MGStrong #MGSupport #MGJourney #MGWarrior
A moment of validation: MG is real, heavy, and you’re doing your best: https://bit.ly/4rkfT4v
#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport #InvisibleIllness #ChronicIllnessAwareness #MGJourney #MGWarrior #MGCrisis #Thymoma
A single treatment that could end HAE attacks for good: https://bit.ly/3FHecMk
Gene therapy research is bringing us closer to that reality.
#HAE #HereditaryAngioedema #GeneTherapy #CRISPR #RareDisease #AngioedemaNews #Bionews
Leave a 🏥 if you've had a thymectomy: https://bit.ly/3JUv3gA
#MyastheniaGravis
#MGCommunity #MyastheniaGravisNews #Bionews #Thymectomy
Over 16 years of living with ALS, Dagmar Munn says she has changed the way she responds when her body does not move the way she expects: https://bit.ly/4e39UN4
Sarah spent years defining womanhood for herself. Then myasthenia gravis began changing what her body could do: https://bit.ly/4rB9X8A
#MyastheniaGravis #WomenWithMG #ChronicIllness #MyastheniaGravisNews #Bionews
Take a closer look: https://bit.ly/3Tx5ZBg
Higher blood levels of a marker of nerve damage are associated with lower daily activity in people with progressive forms of MS, per a study.
Discover more: https://bit.ly/4xOMWjW
For columnist Shawna Barnes, myasthenia gravis (MG) disease progression is like waking up every day in a body that feels less like your own.
#MyastheniaGravis #RareDisease #MG #MyastheniaGravisNews #Bionews
Explore the details: https://bit.ly/4hAsKMH
A progressive decline in lung function is unavoidable in ALS, but there are steps that patients can take to improve breathing issues.
Stay up to date on promising experimental treatments and clinical trials for hereditary angioedema: https://bit.ly/43PupIn
#ClinicalTrials #ExperimentalTherapies #HAEResearch #RareDiseaseResearch #FutureOfMedicine #AngioedemaNews #Bionews
A soft moment for muscles that need longer to recover today: https://bit.ly/4i0ssOL
#MyastheniaGravis
#MGCommunity #MyastheniaGravisNews #Bionews #MGTreatment
A kinder voice toward yourself matters when your body can’t keep up: https://bit.ly/4oWi1Ou
#MyastheniaGravis #MyastheniaGravisNews #Bionews #MGRelapse
Your mental health matters: https://bit.ly/4jEt387
Self-care, mindfulness, support groups, and therapy can all help you cope 💙
#HereditaryAngioedema #HAEAwareness #MentalHealthMatters #ChronicIllness #RareDisease #PatientSupport #AngioedemaNewsToday #Bionews
Stop comparing your MS journey here: https://bit.ly/4ga7bRV
#MSAwareness #ThisIsMS #MSLife #MSCommunity #MSSupport #MSFighter #MSNewsToday #Bionews
A calm pause belongs to you today: https://bit.ly/4rp5Gnw
#MyastheniaGravis #MyastheniaGravisNews #Bionews
Connect with support: https://bit.ly/4nfP1Bx
#HAE #SupportGroups #Community #AngioedemaNews #Bionews