v-ATPase Alliance
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vatpasealliance.org
v-ATPase Alliance
@vatpasealliance.org
Empower and unite families affected by v-ATPase genetic disorders
Advance Scientific Research on v-ATPase. Ultimately get a Cure!
🧬 Several ATP6V- genes
On this #WarriorWednesday we pause to honor four extraordinary children whose lives continue to guide and inspire our mission: Avril, Hawke, Remington and Izabella.

🕊️ Forever warriors. Forever remembered. Forever a part of the Alliance 🤍
July 30, 2025 at 7:35 PM
We are halfway there, but need your help!
We're running the #20for20 Campaign, aiming for 20 biosample collections. You might wonder: why aren't 10 enough? Why is 20 the golden number? Let us shed some light on that!
Donate: donorbox.org/20-for-20-78...
July 29, 2025 at 5:16 PM
July 25, 2025 at 10:56 PM
Today is v-ATpase Awareness Day!
v-ATPase it matters! Kids like Lana matter!
Thank you for helping raising Awareness with your own voice in English and Russian. What a mighty warrior!
Comment, Share and Care.
Get involved: vatpasealliance.org/get-involved
July 24, 2025 at 12:36 AM
Today is v-ATPase Awareness Day! We're highlighting the 23 genes of this vital pump. Its malfunction causes severe multi-system disorders & DEEs in kids, but studying it also offers key insights into fighting cancer, neurodegeneration, & promoting healthy aging.

v-ATPase: it matters! #AwarenessDay
July 23, 2025 at 5:19 PM
New Series coming up later this month:
"Roadmap to a Cure: Navigating the Path for v-ATPase-related conditions" and many other rare genetic disorders!

#vATPaseAlliance #RoadmapToACure #RareDiseaseResearch #HopeForACure #BreakthroughsAhead #PatientAdvocacy
June 13, 2025 at 9:59 PM
There's More to the Story is an Educational Program from v-ATPase Alliance a 501(C)(3) Nonprofit commited to bring positive change to those living with ultra rare diseases.
Learn more and support our vision at www.vatpasealliance.org
June 6, 2025 at 2:59 PM
Community Update!

We are thrilled to extend a warm welcome to our first known v-ATPase family from Serbia!
Help us reach more families and potential partners by sharing this post

#vATPaseAlliance #RareDisease #CommunityStrong #Serbia #GlobalReach #WelcomeHome #CareAboutRare
June 6, 2025 at 2:47 PM
Endosome map reveals v-ATPase IS the ultimate connector!

The biological pathways or functions these proteins influence may ultimately have a more significant impact!

Article here: www.nature.com/articles/s41...
June 3, 2025 at 9:31 AM
Understanding the genetic complexity of v-ATPase DEE is crucial for diagnosis and treatment. See the gene comparison table: ATP6V0A1, ATP6V1A, ATP6V0C. #vATPase #Neurology #RareDisease #Diagnosis #GetToKnowMore
April 16, 2025 at 1:13 PM
Disease detectives, assemble! 🔍
The new 💚 "Get to know more about v-ATPase" campaign aims to drive awareness of v-ATPase-related diseases and emphasize that gene testing is essential for accurate diagnosis and effective treatment of v-ATPase-related disorders. Stay tuned!
April 14, 2025 at 4:43 PM
Tomorrow, Feb 27th, we will be at the #Texas Children's Hospital from 9am-4pm CST
Stop by, say hello, and help make a difference! 🙌

#RareDiseaseDay2025 event with #NORD / Center of Excellence at Baylor College of Medicine (BCM) / Baylor St. Luke’s Medical Center (BSLMC) in the Texas Medical Center.
February 26, 2025 at 11:10 PM
Have you ever found yourself staring at a Google search bar, the weight of the world pressing down on your shoulders, desperately trying to decipher how to find the right support for your child?
Try www.librarey.com A collaborative resource for rare diseases. Find support and share knowledge.
February 24, 2025 at 10:46 PM
The RARE Advocacy Exchange kicks off on March 10th at 1 PM EST. A year long virtual patient summit!

🌟 We've already signed up; will you join us?
📌 Register here: globalgenes.org/rare-advocac...
February 6, 2025 at 4:05 PM
Punxsutawney Phil predicts six more weeks of winter ☃️🧣🧤
We’ve got you covered!
With 2 NEW hoodie options to Care About RARE!
Orders close in 3 days: Friday, February 7th!
www.customink.com/fundraising/...
#GroundhogDay #RareDiseaseAwareness #RareDiseaseDay
February 4, 2025 at 11:37 PM
It’s February! 🗓️ You can kick off Rare Disease Day month by framing your profile picture with this custom badge showing your support for the v-ATPase Alliance. Help us raise awareness for rare diseases with this one simple action! ✅
Join Us!! www.canva.com/design/DAGdY...
February 1, 2025 at 2:10 PM
Show your stripes & support v-ATPase research! 🦓 Shirts are available for purchase (proceeds benefit research). Rocking last year's shirt? Donate to v-ATPase Alliance while you #WearYourStripes on Feb 28th! Every bit helps advance research & find treatments. #RareDiseaseDay #CareAboutRare
January 31, 2025 at 9:35 PM
Mark your calendars! 🗓️📣 Rare Disease Awareness Month starts tomorrow, culminating in #RareDiseaseDay on Feb 28th! Join us & 300 million others impacted by rare diseases. We'll share ways to spread awareness, show support, & take action for v-ATPase research & treatments. #CareAboutRare ❤️💛💚💙🔬🤝
January 31, 2025 at 9:31 PM