We know that the disconnects b/t stakeholder groups when it comes to collaboration hinders #raredisease progress for the whole community. That’s why we’ve created #ResourceRare, a multi-functional platform designed to foster collaboration across disease groups. DM for an invite.
Don’t miss this informative panel as we discuss #sharenting with @RareRevolutionM. Where is the line between sharing about your child’s #raredisease diagnosis to raise awareness and invading their privacy? Join us as we look for the line and address what to do when it’s crossed.
Join us at the 4th annual #RareFair, the original virtual event for the #raredisease community. Don’t miss this encore panel of #raredads like @malezebra20202 as they discuss rare fatherhood. #rarefair2022#rareunited
Fantastic to see over 30 organisations working together for change. Making sure health services are equal for all communities. Kerry discussing these barriers at #24HoursOfRare hosted by @MyCityMed
TODAY at 4pm🔔
Naomi Litchfield of @bionicalemas is hosting a panel at the #24HoursofRareEvent!
Naomi will be discussing: What are the #Ethical Preapproval Considerations for #Rare#PatientGroups?
Register for FREE now!
👉https://t.co/llBtGZuRCo
Dr. Veeral Shah of @CincyChildrens speaking on developments in pediatric neuro ophthalmology and advice for med students. “You never stop learning because life never stops teaching.” #24hoursofrare
Tomorrow 9am=my session on "Collaborative Physician & Patient Relationships in the Treatment of Pain"...
Unless u didn't like it, then that was someone else in it 🤣
Huge thanks 2 @MyCityMed 4 hosting #24hoursofrare & providing such diverse programming 4 the #RareDisease comm.