INAD Warriors INC. @INADwarrior
Our mission is to raise awareness in the global community about infantile neuroaxonal dystrophy (INAD). Join us in this mission! #INADWarriors inadwarriors.org Indiana, USA Joined August 2024-
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INAD Warriors exists to bring hope where there once was none — supporting families, raising awareness and funding research for a treatment and cure. Today, we rest in faith and trust God with the work still ahead. 🤍 #SundayFaith #INADWarriors #TogetherWeFight
INAD Warriors is more than a nonprofit. It’s a family! A place where faith, advocacy, research and love come together. This Sunday, we thank God for every warrior walking this journey with us. 🤍 #INADWarriors #TogetherWeFight #FaithInAction #SundayGratitude
From our warrior families to yours—Happy Thanksgiving! 💛 Today we celebrate love, togetherness and the little moments that mean everything. Thank you for being part of our journey. #INADWarriors #ThankfulHeart #TogetherWeFight
As this season continues, we’re reminded that gratitude grows when it’s shared. We’re especially thankful for the moments of connection—every message, every fundraiser, every brave story—that brings our INAD Warriors community even closer. #INADWarriors #TogetherWeFight
INAD is caused by changes in a gene called PLA2G6. This gene normally helps keep nerve cells healthy. Because INAD damages this nerve cell, children slowly lose skills they once had. #inadwarriors #raredisease #TogetherWeFight #faithcanmovemountains
It’s Thankful Thursday, and today our hearts are overflowing with gratitude for the incredible INAD Warriors community; families, friends & supporters who stand beside us in this fight every single day. Your love gives strength. Your support gives hope. What are you thankful for?
All INAD Warriors & their families face challenges that most could never imagine. INAD is rare, relentless & has no cure. Yet through every setback, our faith remains. Our mission is to find a cure. Faith is powerful. Love is unbreakable. When we stand together; #TogetherWeFight
Infantile Neuroaxonal Dystrophy (INAD): Ultra-rare genetic disorder that affects the brain & nervous system •Fewer than 200 known cases •Leads to loss of movement, speech & motor skills #inadwarriors #rarediseaseawareness #TogetherWeFight #faithcanmovemountains
Let’s recognize a few incredible children— all diagnosed with INAD, which slowly takes away a child’s abilities but never their spirit. They remind us why we fight 💫 Mila - left: 3 years old Warner - middle: 5 years old Sage - right: 5.5 years old #INADWarriors #togetherwefight
As this year comes to a close, we celebrate all the progress we made raising awareness and fundraising for research for INAD. Together we fight. Here’s to a happy - healthy - 2025 to all our supporters. inadwarriors.org/donate/
Thank you! prlog.org/13048726-inad-…
Celebrating the launch of the new FDA Rare Disease Innovation Hub to enhance and advance outcomes - including children with INAD. fda.gov/news-events/fd…
Had a wonderful evening at the “Gatsby Style” INAD Gala! Not only is it an amazing event for a great cause - but an opportunity to spend time with close friends and colleagues! 💙@BiggerstaffIN @MsvlCIA @caseygibson37 @MrsvlPioneers @INADwarrior
Big Night planned at the historic Columbia Club downtown Indy! All sold out but you can still support our mission - follow our story / donate online inadwarriors.org
2nd Annual Blue Ties & Diamonds Gala Silent Auction open & bidding here: qtego.us/qlink/inadwarr… *𝗔𝘂𝗰𝘁𝗶𝗼𝗻 𝗰𝗹𝗼𝘀𝗲 𝗔𝘂𝗴 𝟮𝟰𝘁𝗵 𝗮𝘁 𝘁𝗵𝗲 𝗚𝗮𝗹𝗮. 𝗗𝗼 𝗡𝗢𝗧 𝗻𝗲𝗲𝗱 𝘁𝗼 𝗯𝗲 𝗽𝗿𝗲𝘀𝗲𝗻𝘁 𝘁𝗼 𝘄𝗶𝗻.*
Partnership with @nbia_disorders results in Grant Award prlog.org/13030240-inad-…
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