TRPM3 Foundation

Patient advocacy and support for those affected by #TRPM3 #ionchannel related disorders. #RareDiseases

[TRPM3 Foundation @trpm3foundation]

TRPM3 Foundation is officially a 501(c)(3) charity! We are asking for your support to make a difference in the lives of those living with or impacted by TRPM3! Donate today! #RareDisease #trpm3

https://t.co/sdgletYG1g

[TRPM3 Foundation @trpm3foundation]

In 2019, we had 1 paper and 0 connections.
In 2025, we have a Foundation, a Community, and Hope. But we still need a Cure.
Today is Giving Day! We are small, but we are fighting for a big future for our kids.
Donate here: https://t.co/sdgletY8bI
#TRPM3 #GivingTuesday #RareDisease

[Tibor Rohacs @RohacsTibor]

TRPA1 and TRPM3 ion channels in central terminals of sensory neurons facilitate synaptic activity in the spinal dorsal horn https://t.co/FQWttCmanX

[VJ Neurology @VJNeurology]

Today kicks off with an interview from Volkan Granit on a first-in-human trial of BHV-2100, a first-in-class TRPM3 antagonist, for the treatment of pain and #migraine.

#AANAM @AANMember #Headache #Neurology

[National Organization for Rare Disorders (NORD) @RareDiseases]

The 40 NORD® #RareDisease Centers of Excellence have united in calling for the reinstatement of the Advisory Committee on Heritable Disorders in Newborns and Children. #NORD and our network are committed to working with leaders to protect newborns from preventable death and suffering through life-saving #NewbornScreening. This work must continue.

[TRPM3 Foundation @trpm3foundation]

Today, on Rare Disease Day 2025, we stand in solidarity with the 300 million people worldwide living with a rare disease.
Donate to the TRPM3 Foundation:
https://t.co/gwflI5x5X2

#RareDiseaseDay #TRPM3 #TogetherForRare #TRPM3Foundation

[Rare Disease Day @rarediseaseday]

How will you you support on Rare Disease Day this year? 💜🌍
Sharing a personal story, joining an event, or simply starting a conversation, every action is a step closer to equity for the 300 million people living with rare diseases.
Find out more: https://t.co/AUKfGZJLJB

[National Organization for Rare Disorders (NORD) @RareDiseases]

Rare patients and families cannot afford delays or obstacles to receiving quality healthcare. Take action NOW and urge Congress to prioritize several pieces of lifesaving rare disease legislation this #RareDiseaseDay.

All it takes is one minute: https://t.co/VEDU9pPwzJ

[National Organization for Rare Disorders (NORD) @RareDiseases]

Another great slide from @ClevelandClinic's #RareDiseaseDay event:

Imagine a classroom of 30 kids — one or more of them, on average, has a #genetic disorder. This results in differences that are visible or invisible, life-threatening or simply unique. So many possibilities that having one of them isn't exactly rare!

#ChildrensHealth #Pediatrics

[National Organization for Rare Disorders (NORD) @RareDiseases]

It's that time of year! Show your support for #RareDiseaseDay on February 28 and make a difference for the 1 in 10 Americans living with a #RareDisease by purchasing NORD's #ShowYourStripes gear: https://t.co/ZUArkk4GFD

We’d love to see you wearing it—don’t forget to tag us!

[TRPM3 Foundation @trpm3foundation]

@ying__yin @dukebiochem Wonderful work! This is extremely important to those of us impacted by TRPM3-related dysfunction.

[YingYin @ying__yin]

New study out! We reveal binding sites for the neurosteroid PregS, agonist CIM0216, & anticonvulsant primidone in TRPM3. Insights into neurosteroid recognition, agonist synergy, inhibition, & disease mutation effects on TRPM3 gating. Read more:https://t.co/axXkipuZ9O @dukebiochem

[Membrane Protein PDB @MemProtPDB]

Molecular basis of neurosteroid and anticonvulsant regulation of TRPM3 | Nat Struct Mol Biol

https://t.co/VUKQmjnd60

[National Organization for Rare Disorders (NORD) @RareDiseases]

1 in 10 Californians has a #RareDisease. The #LAFires have added more hardship for many in our community. Your donation to NORD’s Natural Disaster Emergency Relief Fund can help with home repairs, lodging and more. Give here: https://t.co/3MiqfOwcls

#Palisades #DisasterRelief

[National Organization for Rare Disorders (NORD) @RareDiseases]

Mark your calendars for #RareDiseaseDay on Feb. 27–28!

@ncats_nih_gov & @US_FDA are teaming up for a two-day, hybrid #RDDatFDANIH event! RSVP now to listen and engage with panel discussions, #RareDiseases stories, and more: https://t.co/Qmc5Pvy5VN

#FDA #NIH

[TRPM3 Foundation @trpm3foundation]

@Chemist_Payne Beyond exciting for those of us impacted by TRPM3-related neurodevelopmental disorders!

[National Organization for Rare Disorders (NORD) @RareDiseases]

The #RAREAct is a critical piece of legislation being heard in today's #RareDiseaseDay hearing. It would protect a key drug development incentive established by the life-changing Orphan Drug Act. Tune in to the hearing here! https://t.co/hgnMUYbEDA

[TRPM3 Foundation @trpm3foundation]

#RareDiseaseDay #TRPM3 #ShowYourStripes @RareDiseases

[Rare Diseases Clinical Research Network @rarediseasesnet]

We study over 180 #RareDiseases at more than 380 active clinical sites—both in the United States and internationally—and partner with over 160 patient advocacy groups.

Learn more about the diseases we study: https://t.co/BQJ8FuGHpT

#RareDiseaseDay #RDDNIH #RDCRN20

[Rare Disease Day @rarediseaseday]

Tomorrow is #RareDiseaseDay! Join the Global Chain of Lights! 🌍

The rare disease community will unite to spread solidarity with monuments, offices, schools, and homes lighting up in the Rare Disease Day colours!

Don't miss out on Feb 29, 7 PM local time!

#LightUpForRare