TRPM3 Foundation (@trpm3foundation) 's Twitter Profile
TRPM3 Foundation

@trpm3foundation

Patient advocacy and support for those affected by #TRPM3 #ionchannel related disorders. #RareDiseases linktr.ee/trpm3foundation

ID: 1633918055108554753

linkhttp://www.trpm3.org calendar_today09-03-2023 19:50:09

46 Tweet

52 Followers

186 Following

Rare Diseases Clinical Research Network (@rarediseasesnet) 's Twitter Profile Photo

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: rarediseasesnetwork.org/research-groups #RareDiseaseDay #RDDNIH #RDCRN20

Rare Disease Day (@rarediseaseday) 's Twitter Profile Photo

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

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
Beacon for Rare Diseases (@rarebeacon) 's Twitter Profile Photo

⏰ Just one day to go until #RareDiseaseDay 2024! #DidYouKnow there are 6000+ known rare diseases? Visit rarediseaseday.org for key statistics on rare conditions. 🦓 #ShareYourColours

⏰ Just one day to go until #RareDiseaseDay 2024!

#DidYouKnow there are 6000+ known rare diseases? 

Visit rarediseaseday.org for key statistics on rare conditions. 🦓

#ShareYourColours
National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

We can't wait to see landmarks like the Eiffel Tower, Empire State Building, Benjamin Franklin Bridge and more #LightUpForRare tomorrow! Share your photos of landmarks illuminated for #RareDiseaseDay & see how else you can get involved in the celebration: bit.ly/2BrULms

We can't wait to see landmarks like the Eiffel Tower, Empire State Building, Benjamin Franklin Bridge and more #LightUpForRare tomorrow! Share your photos of landmarks illuminated for #RareDiseaseDay & see how else you can get involved in the celebration: bit.ly/2BrULms
National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

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! energycommerce.house.gov

National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

Mark your calendars for #RareDiseaseDay on Feb. 27–28! NCATS & U.S. FDA are teaming up for a two-day, hybrid #RDDatFDANIH event! RSVP now to listen and engage with panel discussions, #RareDiseases stories, and more: go.nih.gov/CaSKChZ #FDA #NIH

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

<a href="/ncats_nih_gov/">NCATS</a> &amp; <a href="/US_FDA/">U.S. FDA</a> are teaming up for a two-day, hybrid #RDDatFDANIH event! RSVP now to listen and engage with panel discussions, #RareDiseases stories, and more: go.nih.gov/CaSKChZ 

#FDA #NIH
YingYin (@ying__yin) 's Twitter Profile Photo

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:doi.org/10.1038/s41594… Duke Department of Biochemistry

National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

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: rarediseases.org/campaign/relief #Palisades #DisasterRelief

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: rarediseases.org/campaign/relief

#Palisades #DisasterRelief
National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

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: bit.ly/40lU35Z We’d love to see you wearing it—don’t forget to tag us!

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: bit.ly/40lU35Z

We’d love to see you wearing it—don’t forget to tag us!
National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

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: bit.ly/41ytHhR

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: bit.ly/41ytHhR
Rare Disease Day (@rarediseaseday) 's Twitter Profile Photo

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: rarediseaseday.org

National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

Another great slide from Cleveland Clinic'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

Another great slide from <a href="/ClevelandClinic/">Cleveland Clinic</a>'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
TRPM3 Foundation (@trpm3foundation) 's Twitter Profile Photo

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: trpm3.org/donate #RareDiseaseDay #TRPM3 #TogetherForRare #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:
trpm3.org/donate

#RareDiseaseDay #TRPM3 #TogetherForRare #TRPM3Foundation
Tibor Rohacs (@rohacstibor) 's Twitter Profile Photo

TRPA1 and TRPM3 ion channels in central terminals of sensory neurons facilitate synaptic activity in the spinal dorsal horn physoc.onlinelibrary.wiley.com/doi/10.1113/JP…

VJ Neurology (@vjneurology) 's Twitter Profile Photo

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 American Academy of Neurology #Headache #Neurology

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 <a href="/AANMember/">American Academy of Neurology</a> #Headache #Neurology
National Organization for Rare Disorders (NORD) (@rarediseases) 's Twitter Profile Photo

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

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
TRPM3 Foundation (@trpm3foundation) 's Twitter Profile Photo

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: trpm3.org/donate #TRPM3 #GivingTuesday #RareDisease