Your support makes a difference and stays local! 100% of your donations through events like our annual #VegasCares5K go toward programs and services such as our popular medical and therapy equipment program. Through it, we provide mobility and therapeutic tools which are often not covered by insurance to qualifying families who apply.
As a sponsor or donor, your generosity empowers us to provide Vegas-area kids living with rare diseases the resources they need to live richer, fuller lives. Donate today and help us create brighter futures at littlemisshannah.org.
#TheLittleMissHannahFoundation #GivingBack #MakingADifference
It's #RareDiseaseDay!
Today, we celebrate the millions around the world living with rare diseases. You inspire us with your strength, determination, and incredible spirit!
Our Little Miss Hannah families help to raise rare disease awareness year-round by sharing their stories and showing support for each other in our amazing tight-knit community. ✨
Today’s the day to spread the word about what it means to be rare. Happy Rare Disease Day!
Live in Southern Nevada, or know a child with a rare disease who does? Join our rare family at littlemisshannah.org.
#RareDisease #CelebratingRare #TogetherWeCan
#TheLittleMissHannahFoundation
Tomorrow is #RareDiseaseDay, a day bringing attention and awareness to the millions around the world affected by rare diseases. When navigating a rare disease journey, community is critical. Rare mom Heidi explains how she was able to make new friends and build relationships through her connection with Little Miss Hannah, and how it helped her find the confidence to approach other parents in similar situations to offer support.
We're so grateful for the incredible rare disease community that surrounds us here in Southern Nevada. You inspire us every day! Join our Little Miss Hannah family at littlemisshannah.org. ✨ #RareDisease #CommunityMatters #TogetherWeAreStronger #thelittlemisshannahfoundation
We are so energized from spending time with our Little Miss Hannah family Saturday at the 8th annual #VegasCares5K. Our Executive Director Jenny Krshul, a rare mom herself, speaks about the indescribable feeling of togetherness when rare families unite. Rare disease can be a lonely journey, and we’re here to help. We welcome all families in Southern Nevada whose children are living with rare and medically complex conditions. Join us and become a part of our joyful, supportive, and inclusive family at littlemisshannah.org. #raredisease #rarediseaseday #littlemisshannah #vegascaresaboutrare
Our executive director, Jenny Krshul, extends our heartfelt thanks for the amazing turnout at this year’s Tee Up Fore Rare charity golf tournament. The event raised $15,000 that will go directly to help children with rare, life-limiting, and complex medical diagnoses in the Southern Nevada area. Golfers, sponsors, and volunteers, you made a difference in the lives of many families this weekend, and for that, we are sincerely grateful. We hope to see you again next year! #teeupforerare #teeupforerare2023 #lmhfoundation
And they’re off! A huge thank you to all of our wonderful golfers who came out to support us today at Tee Up FORE Rare. We couldn’t do this without you! ⛳️❤️ #teeupforerare #lmhfoundation
Little Miss Hannah Foundation - August 2023 Equipment Distribution
We were so excited to meet new families and greet old friends at our equipment distribution event this past Sunday! Families picked up new Special Tomato US chairs, a WonderFold wagon, a Burley Biketrailer, and more!
Funded by the generosity of our donors, our grants program enables us to deliver this vital equipment at no cost to families across Southern Nevada. To learn more about our mission to improve the quality of life for children diagnosed with rare, life-limiting, and complex medical conditions in Southern Nevada, visit littlemisshannah.org. #lmhfoundation
Tilton's Therapy for Tots, Las Vegas - Vegas Cares About Rare Kids 5K
Little Miss Hannah Kids - Halloween 2019
We love seeing all of our local Little Miss Hannah kids in their Halloween costumes! Our Little Miss Hannah family is growing <3
College scholarship applications due 11/15 for siblings affected by childhood rare disease!
2018 Vegas Cares About Rare Kids 5K
Want to see how much fun we had at this year's Vegas Cares About Rare Kids 5K? Special thank you to Z Squared Multimedia Productions for creating this fantastic video!
Be sure to join us for our 2019 event by clicking "going" or "interested" here:
https://www.facebook.com/events/203752180285548/
Thank you Vegas Golden Knights from the Little Miss Hannah Foundation
Special thank you to the Vegas Golden Knights for our Little Miss Hannah night! Our families had an amazing time and we had the opportunity to share our organization with our community!
Little Miss Hannah Foundation on CBS 8 News with Kirsten Joyce
Thank you 8 News Now and Kirsten Joyce for having Robert Ostrea, Nick Krshul, and Bradley on your show last week. We appreciate all of the support you continue to show our organization and special kids like Bradley with rare and medically complex conditions!
Thank you to our incredible volunteers who came out today to create special gifts for our VIP kids for our Vegas rare 5K next weekend!
2018 Vegas Cares About Rare Kids 5K (1)
Register today for Early Bird pricing on our 2018 Vegas Cares About Rare Kids 5K! If you have any questions, message us :)
www.VegasCaresAboutRare.org
Noah gets his new stroller!
Meet Noah, one of our adorable LMHF kids. He was so excited to get this stroller today that he couldn't stop smiling, which put a huge smile on our faces! His smile and his family's heart is why we love being able to provide medical and therapy equipment to families who need it. We hope that he and his family had a great time strolling and spending time together today.
2017 Vegas Cares About Rare Kids 5K
Thank you to everyone who came out to our Vegas Cares About Rare Kids 5K for World Rare Disease Day in February 2017! We hope you enjoy this video recap - and we can't wait to do it again in 2018!
www.VegasCaresAboutRare.org
Little Miss Hannah's dad speaking to 400+ rare disease advocates at the Rare Disease Legislative Advocates annual legislative training conference. Robert Ostrea
Vegas Cares About Rare Kids 5K 1 M
Vegas Cares About Rare Kids 5K was a huge success! We had over 500 people come to our event including 388 registered runners and walkers. This BEYOND exceeding our expectations when we first decided to put this together. Special thank you to our sponsors, our volunteers, Celesta Davis (our amazing MC), our Little Miss Hannah families, the Vegas community and friends from Missouri, Arizona, Illinois, California, and Canada.
The response to today's event and the enthusiasm from those who who were there was us was so overwhelmingly uplifting and humbling. Thank you for all of you who braved the cold weather to help create an experience that we will never, ever forget.
Photos and pictures will be coming over the next few weeks!! But for now, I wanted to share this little snippet of our 5K start (can't wait to share the VIP rare kids start).