30/08/2026
, 🦁✨ Our latest Rare Warriors adventure! ✨🦁
What a lovely morning we had on our latest field trip to Lioness Aerial Fitness , followed by a very important stop at McDonald's for a little treat! 🍟❤️
Big smiles, lots of fun, plenty of laughter and, most importantly, families spending time together. 🥰
And honestly… this is what it’s all about. ❤️
Living with rare disease can mean a life filled with uncertainty. Tests, scans, hospital appointments, specialists, therapies, referrals, waiting lists and constantly having to learn and navigate your child’s care through a system that can often feel incredibly difficult and exhausting.
Behind every rare diagnosis is a family learning to live with uncertainty while fighting for the best possible care, opportunities and quality of life for their child. Sometimes parents become their child’s biggest advocate, researcher, coordinator and voice — all while simply trying to be a parent. 💜
That’s why, at Rare Warriors Wexford, we want to create something different too.
We want our families to have opportunities to just be families.
To have fun.
To make memories.
To try new things.
To enjoy little treats.
To see their children smile.
And to spend time with other families who get it without having to explain every part of their journey. ❤️
We work hard to organise fun, accessible and inclusive activities for our rare families because connection matters. Knowing you’re not alone matters.
Rare disease can sometimes feel isolating, but together we can create a community where families feel supported, understood and included. 💜
A huge thank you to Lioness Aerial Fitness for helping us create such a brilliant morning, and of course to McDonald’s for the very important post-activity treats! 😋🍟
Another morning of memories made, friendships strengthened and big rare smiles all around. 🥰
This is Rare Warriors Wexford.
Supporting rare families, creating connections and making memories along the way. 💜