The Princess Program Foundation

Sharing again to help us get to CureFest 🙏🏻

🎗️💜🎗️💜🎗️💜 Drum roll please..

Who are we taking to Curefest this year? The snow QUEEN herself. Shell be traveling a long way from Arendelle to get to Washington DC.

Curefest is a national event in Washington DC every September in which nonprofits and families come together to advocate for more funding for Childhood Cancer. It’s a weekend long event filled with tabling, performances, and even a shoe memorial for the angels.

But, we need your help to get there. We have so many options to help in our bio and also listed below. Thank you so much for helping us make magic!

Venmo: ThePrincessProgram-Foundation
PayPal: [email protected]
Cashapp: $theprincessprogram
Kindest link in bi0

Throwback to when Elsa visited Princess Gabby. Keeping her family in our hearts today ❤️

Available NOW!

Childhood Cancer Awareness T shirts! If you order now they’ll be here in time for September.

Available for a limited time while supplies last.

https://www.jammavinylanddesign.com/theprincessprogram

2 years ago we brought magic to Curefest with Team Jocelyn (Princess Jocelyn’s family)

You can help us get to Curefest this year to continue to make a difference for kids and families by visiting the link below or using any of our other donation platforms. Thank you for all your help and continued support 💛

https://kindest.com/866568-help-us-bring-magic-to-curefest-2024

It's that time of the year...Curefest for Childhood Cancer 2024 is right around the corner!

We are asking for your help to get there and provide a magical experience to the children and families there.

Every year we attend and rally to the capitol, meet with fighters, survivors, and siblings. As well as, honor the angel children at the shoe memorial. But, we can't do it without your help so please consider donating so we can make Curefest 2024 in Washington DC as magical as ever.

Donation options:
https://kindest.com/866568-help-us-bring-magic-to-curefest-2024

Paypal: [email protected]
Cashapp:$theprincessprogram
Venmo: ThePrincessProgram-Foundation

We have an update regarding our Kentucky trip.

Cheyennes family has asked to cancel the trip to spend time as a family without interruptions. We admire and understand their decision. Due to this we decided to take all donations made for Cheyennes trip and donate directly to the family. Her mom’s cash app is in the screenshot if you would like to send any extra to help the family at this time.

Thank you for always supporting our wish trips and for making a difference for these families.

We’re almost halfway to our goal! Keep sharing please 🙏🏻

We haven’t done this in quite a long time, but our magic team has been called upon to make a wish come true.

Meet 5 year old DIPG warrior Cheyenne. Cheyenne is fighting a terminal cancer in children. She loves Elsa. Everything Frozen is her favorite. As many songs and characters have helped get her through her treatments.

We’d love your help and support to make her wish of meeting Elsa in person come true. Our team would have to fly to Kentucky to make this happen. Anything helps.

Can you help us make this 5 year old cancer warrior’s wish of meeting Elsa in person come true? Thank you for making these wish trips possible 🩷

Link to donate

https://kindest.com/811318-cheyennes-wish

Other ways to donate

Venmo: ThePrincessProgram-Foundation
Cashapp: $theprincessprogram
PayPal: [email protected].

Please share! We’re up to $400 so far! Thank you so much to everyone who’s donated. Let’s make this little girls wish come true 🩷

We haven’t done this in quite a long time, but our magic team has been called upon to make a wish come true.

Meet 5 year old DIPG warrior Cheyenne. Cheyenne is fighting a terminal cancer in children. She loves Elsa. Everything Frozen is her favorite. As many songs and characters have helped get her through her treatments.

We’d love your help and support to make her wish of meeting Elsa in person come true. Our team would have to fly to Kentucky to make this happen. Anything helps.

Can you help us make this 5 year old cancer warrior’s wish of meeting Elsa in person come true? Thank you for making these wish trips possible 🩷

Link to donate

https://kindest.com/811318-cheyennes-wish

Other ways to donate

Venmo: ThePrincessProgram-Foundation
Cashapp: $theprincessprogram
PayPal: [email protected].

We haven’t done this in quite a long time, but our magic team has been called upon to make a wish come true.

Meet 5 year old DIPG warrior Cheyenne. Cheyenne is fighting a terminal cancer in children. She loves Elsa. Everything Frozen is her favorite. As many songs and characters have helped get her through her treatments.

We’d love your help and support to make her wish of meeting Elsa in person come true. Our team would have to fly to Kentucky to make this happen. Anything helps.

Can you help us make this 5 year old cancer warrior’s wish of meeting Elsa in person come true? Thank you for making these wish trips possible 🩷

Link to donate

https://kindest.com/811318-cheyennes-wish

Other ways to donate

Venmo: ThePrincessProgram-Foundation
Cashapp: $theprincessprogram
PayPal: [email protected].

Visited one of our favorite places today Boston Children’s Hospital! The snow princess sang and talked with so many kiddos that needed a little magic.

Thanks for letting us brighten up the day of your patients!

Today we visited with kiddos at an outpatient clinic of Spaulding Rehab Hospital during their annual Easter egg hunt. They were so adorable and we are grateful to the organization who hosted.

Thanks for letting us make magic with you!

Princess hugs on the last day of Chemo.
She did it ! 🔔 ✨♥️

Thank you for letting us be part of this special day!

Obsessed 😍😍

Thank you Jamma Vinyl and Design for these amazing designs.

Get these designs and many more from now until March 1st.

www.jammavinylanddesign.com/theprincessprogram

Meet our Fairygodfamily! 💜
(Also known as our executive board)

Alyssa Banks: CEO and Founder

Marisa Blass: Director of volunteer programming

William Moskaluk: Associate Director of volunteer programming

Samaya Joshi: Director of diversity services

Molly Gibson: Director of performance

John Yanen: marketing consultant (treasurer)

Lauren Bolkovatz: Secretary of Communications

Are you ready for some new merch?

Support the princess program by wearing one of our latest designs.

Our merchandise collection includes some themed shirts, magic of course, and CHD awareness for the month of February. This specific set of designs will only be available until March 1st.

We hope you love it!

Shop here: www.jammavinylanddesign.com/theprincessprogram

Check out the latest news article about The Princess Program by Bold Journey.

A news article based out of California, sat down with our founder Alyssa, to discuss our nonprofit work, granting Lunas wish in California, and the latest going on for The Princess Program.

Read it here 🩷✨: https://boldjourney.com/news/meet-alyssa-banks/

Princess Jocelyn 🦋🤍

12•3•17-9•28•21

We’re remembering someone very dear to our hearts today.

Jocelyn enriched our lives with her sweet little smile and the way she loved her Disney characters (especially Minnie).

Our favorite day was playing with Joce in the park. It was her first time ever meeting Minnie and she ran over to her yelling “Hi Minnie Hi”. When it was time to go home, we can still hear her little voice saying “I’ll miss you so much”. Sweet Joce, we miss you so much.

Her impact touched millions of hearts. Including the hearts of her princesses and her Minnie. We were honored to play a small part in her story. Her legacy.

Jocelyn who is forever 3, changed the lives of so many people that knew her and even those she never met.

We will never forget her. Hope we’re making you proud up there 🪽🩷

Have you signed up for a virtual magic mirror visit yet? 🖥️✨

Our fall schedule is filling up fast and we’d love to zoom with your little fighter. Siblings are welcome to join in the fun too!

Link in bio to set up your zoom call today and experience the magic!

Curefest Day 3- the final day of events 🤍

Today we had a shoe memorial ceremony for all of the angels lost to childhood cancer. We honored two little girls that had a huge impact on us this year. The Ice Queen met both of them during a time they needed her most.

Today we honored them and every single child of the 1800 that pass away each year from childhood cancer.

That’s a wrap for Curefest 2023.

Thank you to the wonderful mommas who allowed us to also love their babies.

See you next year 🎗️

🦄🦄

Curefest Days 1-2 🎗️💜

Curefest is a national childhood cancer awareness event in Washington DC

We are honored to be here to raise awareness for every single child still fighting, who won their fight, and the angels that inspire and guide us.

The first day of events consisted of networking with other nonprofits and families. We also paid tribute to two angels: Savanna and Luna. Whose moms are both here advocating with us. What an incredible community to be part of.

The second day of events included a special breakfast for DIPG/DMG cancer awareness. Next, we advocated for more funding for Childhood Cancer by making posters of who we are fighting for.

Next up: tonight’s show and the shoe memorial tomorrow

Thank you to everyone who continues to support our organization to make these trips possible 💛🎗️

Curefest 2023 we are ready for ya!

If you’re at Curefest come stop by our table and say hi 🩵

SWIFTIESSSS only a few hours left to enter our Swifties for a cure raffle giveaway 🚨🚨

The Princess Program Foundation and Jocelyn's Legacy Foundation have teamed up to bring you this one of a kind Swiftie raffle!

ONE winner takes all:
- 2 ERAS TOUR MOVIE TICKETS : to the theater of your choice (or a $50 movie gift card! The choice is yours.)
- Taylor's Version Crewneck Merch Shirt
- Taylor Swift Water Tumblr & Tote Bag
- Friendship Bracelet Bundle
- Official Eras Tour Movie T-shirt
- Eras Tour T-shirt
- Swiftie Sticker Bundle Pack
- Speak Now Taylor's Version Vinyl

**See images of prizes on the website**

Run, don't walk to get your raffle tickets today! Time is running out!! Ticket prices start as low as $10 for 2 tickets!

The link can be found in our bio and at http://jocelynslegacy.org/taylorswift

All proceeds will benefit both nonprofit organizations that focus their missions on helping bring smiles to children battling cancer.

Sale ends
09.20.2023 @ 11:59pm MST.

SWIFTIES For a Cure | Jocelyn's Legacy The Princess Program Foundation and Jocelyn's Legacy Foundation have teamed up to bring you this one of a kind Swiftie raffle!

We leave for curefest in 2 days!

We aren’t even close to our fundraising goal right now and really need your help!

This year we will be honoring Sweet Savanna. Anything helps 🫶🏻

Donations can be made at

Venmo: ThePrincessProgram-Foundation
Cashapp:$theprincessprogram
PayPal: [email protected].

7 months ago we granted sweet Lunas wish to go to Disney, today she goes in spirit with her momma 💜

Our raffle is still going on!! Only THREE more days to get your hands on some amazing prizes!

SWIFTIESSSS only THREE days left to enter our Swifties for a cure raffle giveaway 🚨🚨

The Princess Program Foundation and Jocelyn's Legacy Foundation have teamed up to bring you this one of a kind Swiftie raffle! 
 
ONE winner takes all:
- 2 ERAS TOUR MOVIE TICKETS : to the theater of your choice (or a $50 movie gift card! The choice is yours.) 
- Taylor's Version Crewneck Merch Shirt 
- Taylor Swift Water Tumblr & Tote Bag
- Friendship Bracelet Bundle
- Official Eras Tour Movie  T-shirt 
- Eras Tour T-shirt 
- Swiftie Sticker Bundle Pack
- Speak Now Taylor's Version Vinyl 

**See images of prizes on the website**
 
Run, don't walk to get your raffle tickets today! Time is running out!! Ticket prices start as low as $10 for 2 tickets!

The link can be found in our bio and at http://jocelynslegacy.org/taylorswift 

All proceeds will benefit both nonprofit organizations that focus their missions on helping bring smiles to children battling cancer.

Sale ends
09.20.2023 @ 11:59pm MST.

Swifties… it’s the 13th of September
LOOK WHAT YOU MADE US DOOOO 🐍🖤

TODAY only for 13 hours on the 13th from 11am PST to 12am PST we are doing a FLASH sale
All raffle ticket amounts will be DOUBLED, meaning if you purchase
2 raffle tickets for $10, you now get 4
13 raffle tickets for $50 you now get 26 and so on..

We know Taylor would approve of us using her lucky number to help out two childhood cancer causes. 🎗️💛

So, GO, RUN, double your chances of winning TODAY only!!
www.jocelynslegacy.org/taylorswift

HAPPY 13th! 🖤

As a reminder the general contest ends 09.20.2023 at 11:59pm MST. Tonight’s double play ends at 12:00am PST.

DROP EVERYTHING NOW ✨✨

The Princess Program Foundation and Jocelyn’s Legacy Foundation have teamed up to bring you this one of a kind Swiftie raffle!

TAYLOR SWIFT FOR A CURE 🎗️💛🎗️💛

PRIZES include:
- 2 ERAS TOUR MOVIE TICKETS : to the theater of your choice (or a $50 movie gift card! The choice is yours.)
- Taylor's Version Crewneck Merch Shirt
- Taylor Swift Water Tumblr & Tote Bag
- Friendship Bracelet Bundle
- Official Eras Tour Movie T-shirt
- Eras Tour T-shirt
- Swiftie Sticker Bundle Pack
- Speak Now Taylor's Version Vinyl

**See images of prizes on the website**

Ain't that the best thing you ever heard?!

Run, don't walk to get your raffle tickets today!

The link can be found at http://jocelynslegacy.org/taylorswift

Ticket Prices:
• 2 tickets for $10
• 7 tickets for $30
• 13 tickets for $50
• 25 tickets for $100

All proceeds will benefit both nonprofit organizations that focus their missions on helping bring smiles to children battling cancer! What better way to win some Taylor Swift merch while helping out a cause! 🤩

**open to all North American Swifties**

Sale ends 09.20.2023 at 11:59pm MST

#1989

Today is the first day of Childhood Cancer Awareness Month.

If you see a child fighting cancer it will change your life forever. They have this spirit that shines light through even in the darkness. But, they go through more than most adults will in their lifetime and if they’re lucky they make it to adulthood. But the 1800 kids that pass away each year is far too many. Even one child is too many. These kids deserve the same future that we are all given. Some of them won’t even see their first day of Kindergarten. Their siblings will grow up taking pictures with their photo frames.

Childhood cancer robs families every single day of normal memories. Please go gold this month for every single fighter, survivor, and child we have lost.

We will be posting all month in hopes to raise awareness for what these kids are going through. We will also be attending a nationwide event in Washington DC to advocate for more funding for research. The link below 👇🏻 is where you can donate to this trip. We need your help to get there.

https://kindest.com/501137-help-us-make-magic-at-curefest-2023-a-national-event-for-childhood-cancer?fbclid=IwAR0HnFT7gtU_l2kMM8s8FnXZtKIlNMBLp9oVsOZWyXPwvODqAvCyNBm_Nmk_aem_ATmxLthLJWRvdvlEjXaAOjrKQu8JrbuL3LDYv3BcPhEZYJlLHN9m6iCTc8HnPuMZ_u8&mibextid=Zxz2cZ

Go gold this month for every single child who deserves a bright future and for the kids that didn’t get one 💔🎗️🤍

Just a handful of the wishes granted thanks to your help! We appreciate you 💜💜

To help with our next trip this September please visit: https://kindest.com/501137-help-us-make-magic-at-curefest-2023-a-national-event-for-childhood-cancer