Casey's Cure

01/25/2024

Support ! Join us on Feb 24 for the first annual event!!

01/25/2024

Think life can get you down? Not today MD- not today…

01/01/2024

Wishing everyone a happy and healthy New Year!

Here’s my wish: to Cure Casey’s Mouse! Let’s make 2024 the year we cure HMERF!

12/29/2023

Last day to order a zip up hoodie to support The Mouse research is 12/30!

We’re $40k short and every donation helps!!

Please support the next phase of research that cures HMERF Muscular Dystrophy!💕

Buy Cure The Mouse! merchandise that supports Foundation for Caseys Cure Inc.. Featuring Deep Heather Zip Up Hoodies, professionally printed in the USA.

11/28/2023

Please save my Ci-Ci- We need your help to pay for the 2024 research that will test 2,500-3,000 drugs on replicas of Casey's muted cells. Please... help her live so I can spend more time with her...

This aggressive goal of raising $40,000 by the end of the year is because we … Casey Duffield needs your support for Please give us more time with my grandma

11/24/2023

Wishing all families a safe and Happy Thanksgiving! Despite the world’s turmoil, we have much to be grateful for. We send wishes out to our community and our service members here and abroad that guard us and give us the liberties we can sometimes take for granted. God’s speed to all 💕

11/23/2023

Happy Thanksgiving to you all!!

11/20/2023

Putting out gratitude for Será Será Photo & Design ‘s kind words for Casey 💕 Looking forward to the upcoming /upsdating photo shoot!

11/12/2023

Happy Diwali to you celebrating this day of joy! Please post pictures of your Diwali designs. ⬇️ I miss seeing them!! 💕

11/10/2023

Thank you to ALL who have served. Because of your sacrifice, we are able to live in a democratic republic, something my father reminded our family on a regular basis. Thank you … from the very bottom of my heart ❤️. Casey’s father served his country proudly in the US Airforce as the man who transcribed Russia’s first space shot. And he died from the same disease that Casey suffers from. On behalf of her father on this , please give to the research that will cure his debilitating disease that Casey carries. ↙️⬇️↘️.

11/02/2023

PROTECT RARE ACT! Congress needs to act fast and pass the Act because people with rare diseases don’t have time to wait. Please help the rare disease community!

Thank you and . Share your story with Congress Senator Jon Ossoff Senator Reverend Raphael Warnock Twin Cedars Youth and Family Services, Inc. Junior Service League of LaGrange, Georgia

Taylor Swift La Grange Noon Lions Club Team Golden, Coldwell Banker Spinks Brown Durand Wellington Subdivision LaGrange Art Museum Wellington Subdivision https://www.votervoice.net/HaystackProject/Campaigns/108649/Respond

10/17/2023

Had the greatest surprise to run into fellow partner , , at National Organization for Rare Disorders, Inc. (NORD) convention in DC where we are fighting for rare disease research including and ! Follow me for more information. Rotary Club of LaGrange, Georgia