What a wonderful month of global support we have felt as we’ve led towards today, Rare Disease Day!
The Lead Up
Throughout this month Tallulah’s uncle’s company Core4 Property Services has been doubling donations to help #CureSPG56!
This was beyond brilliant and such a fantastic way to raise awareness and love for Our Moon’s Mission: Genetic Cures for Kids in the lead up to #RareDiseaseDay2022!
Thank you so much to every beating heart at Core4
We are so exhilarated by this incredible initiative. With socially responsible corporations like Core4 behind us, this #moonshot has wings to fly!
Rare Disease Day Arrives
As the Earth spun and the sun wrapped its warmth around the globe, #RareDiseaseDay rainbows shone all over our planet!
What a journey this has been for a new foundation pushing its first campaign, Our Moon’s Mission: to cure SPG56.
We rallied Tallulah’s Army on social media to join us to fly the rainbow stripes for Rare Disease Day. And Tallulah’s Army responded with gusto!
As the momentum grew, we shouted out proud to our international community, and the official Show Your Stripes website also posted our digital, local and international event on its official events page! We were stoked!
Show Your Rainbow Stripes for Our Moon’s Mission! – Rare Disease Day 2022
Now today, as the 28th of February rolls across the planet, we’ve just watched 24 hours of celebrations unfold.
We know, because of floods in Australia right now, there have been some cancellations so people can stay safe. But rest assured there are more rainbow celebrations to come as the rain settles and the rainbow gatherings regroup.
As co-founders of GC4K, Chris and I were absolutely overjoyed to experience this monumental level of support. It’s your energy and joy that propels us forward with our mission; thank you so very, very much.
We will keep your images in our ‘Highlights’ on our Instagram page, should you ever want to check them out again.
Together, we are raising a vibration of inclusion, awareness, and empathy for those living with a #raredisease. And you are helping us with Our Moon’s Mission: Genetic Cures for Kids. You are wonderful.
