Sprinkled Bliss

12/24/2025

And that’s a wrap for 2025 cookies!

200+ mini Christmas cookies baked with lots of yummy goodness!

Thank you all for your support this year!

Merry Christmas and Happy Nee Year!!

07/19/2025

Book Release Cookies!

My friend wrote a book and asked me to do cookies for her release party! So honored to be apart of her special day!

Check out her book, Shattered Bonds!

https://britneyfarr.com/books/

07/16/2025

Summer calls for a crab boil! Why not have some crab cookies for dessert?! 🦀

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06/03/2025

SB will be celebrating 5 years in September, I thought it might be time for a little branding update! Sprinkled Bliss with extra sprinkles! Same great taste, same handcrafted designs!

05/31/2025

Congratulations Grant & Alaina!

Loved making these Colorado themed wedding cookies for a couple I will share an anniversary with! 5/31 is a great day to get married!

03/24/2025

Happy Birthday Evan!

01/18/2025

It’s 14 degrees out and snowing but I’d rather be in Hawaii with these Hawaiian themed birthday cookies. I might be obsessed that I have to post close ups!

01/13/2025

Happy 6th Birthday Baylee!

Last cookies I was able to make for her was her third birthday! It felt so good to be back in my creative space making her special “Hawaii Girl” cookies!

09/09/2024

It’s that time of year again!

My family and I are walking and rolling for Cure SMA!

Paisley Ashlynn Brooks was born on March 31st, 2020. Three days after she was born she was diagnosed with SMA through Colorado's Newborn Screening.

After further blood tests her doctors diagnosed her with SMA Type 2. She started treatment at 28 days old. She had 7 doses of Spinraza (lumbar punctures) before switching to Zolgensma. In September of 2021 Paisley was treated with Zolgensma, a gene therapy. In just 6 months post dosing and just shy of her 2nd Birthday, Paisley started walking! A true miracle!

Paisley shines brightly with everything she does in life. Please support us by donating or joining us for CureSMA's Walk and Roll.

Spinal muscular atrophy (SMA) is a disease that robs people of their physical strength, significantly impacting an individual’s ability to walk, swallow, or breathe. It affects one in 11,000 births in the United States, and one in 50 people is a genetic carrier. There is no cure yet, but there is great reason for hope. And that is why I am fundraising for the Cure SMA Walk-n-Roll!

Research funded by Cure SMA is driving therapies that are changing the course of SMA. Together, we have the power to meet the ever-changing needs of all people with SMA and build a stronger future for generations to come.

Support me by making a tax-deductible gift or registering to walk or roll with me today! Together we are stronger and can make a difference.

Thank you!

https://walk-curesma.donordrive.com/participant/RobertKillingbeck

Cure SMA leads the way to a world without spinal muscular atrophy (SMA), the number one genetic cause of death for infants. We fund and direct comprehensive research that drives breakthroughs in treatment and care, and we provide individuals with SMA and their families the support they need for toda...

03/23/2024

A little Star Wars mixed with EDM

Happy Birthday Evan!!!

08/29/2023

Auntie’s littlest (not so little) dude started kindergarten today! So I’m true cool Auntie fashion I had to send him (and his brother) with some delicious back to school cookies!