Spina Bifida of Surry Foundation

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Spina Bifida of Surry Foundation

Welcome! We are here to support the individuals and families who are impacted by Spina Bifida!

10/26/2026

🎉🎉 GO AHEAD AND MARK YOUR CALENDARS!! BINGO NIGHT IS COMING! 🎉🎉

Y’all know we’re getting ready for another BIG night of BINGO, baskets, prizes, and lots of fun! 🥳🩵 We’ve been working hard behind the scenes, and we can’t wait to see everybody come out and support the Spina Bifida of Surry Foundation!

📅 Saturday, November 14, 2026
📍 Faith Baptist Church
⏰ Doors open at 3:30 PM | Bingo starts at 4:00 PM

🎟️ $30 per bingo pack
🎁 We’ll have 20 amazing gift baskets up for grabs, plus a coverall prize!

There will be plenty of chances to win, so bring your family, grab your friends, and come ready for a fun afternoon!
The best part?

Every bit of support helps us continue serving local families affected by spina bifida and hydrocephalus. From helping families through medical challenges to making special memories for our kids, this is about so much more than bingo. 💙

We’re praying for a great turnout, and we’d LOVE to fill the room! 🙌

👇 HELP US SPREAD THE WORD! Share this post, tag your bingo crew, and tell us who you’re bringing!

Also let us know you are coming by clicking GOING on our bingo event page.

NOVEMBER 14TH — FAITH BAPTIST CHURCH — BE THERE! 🩵🎉

https://facebook.com/events/s/spina-bifida-of-surry-foundati/2110560659811417/?

10/19/2026

💙 Spina Bifida Awareness Month 💙

From the very beginning, Nate has wanted the Spina Bifida of Surry Foundation to be centered around God. This foundation is about more than raising awareness or providing resources. It is about serving others, loving families, sharing hope, and giving God the glory in all we do.

Living with Spina Bifida and Hydrocephalus has brought challenges, but through every season, Nate knows that God is faithful. His heart is for this foundation to be a reflection of that faith and a reminder that even in the hardest moments, we can keep our eyes on the Lord.

Every family we meet, every event we hold, every resource we provide, and every life we have the opportunity to touch is a chance to show God's love. We don't want the recognition for what we do. We want our actions to point people to Him, because all the good we are able to do is an opportunity to serve Him and bring Him glory.

As we recognize Spina Bifida Awareness Month, our prayer is that God continues to lead this foundation, guide our decisions, strengthen the families we serve, and use us for His purpose.

Our mission is to serve with love, lead with faith, share hope, and give God the glory in everything we do. 💙🙏

“Whether therefore ye eat, or drink, or whatsoever ye do, do all to the glory of God.” — 1 Corinthians 10:31 (KJV)

May everything we do through the Spina Bifida of Surry Foundation always point back to Him.
All the glory belongs to God. 💙

10/12/2026

💙 Spina Bifida Awareness Day 12💙

This year, we put up a sign in our yard to help spread awareness about Spina Bifida and share what our foundation does for families right here in our community!
🍂 If you’re coming to Mount Airy to enjoy the beautiful fall leaves, keep an eye out for our sign located right off the Main Street area! We hope it catches your eye and helps more people learn about our mission.

Sometimes, something as simple as a sign can start a conversation, introduce someone to a cause they may not know much about, or remind a family that they aren’t alone. That’s what it’s all about! 💙

If you spot our sign while enjoying the fall season, let us know in the comments! Also you can take a picture at it!
Support – Awareness – Hope

10/08/2026

💙💛 DAY 8 — THE PEOPLE BEHIND THE MISSION 💛💙

A foundation is never built by one person alone. It takes a community of people who are willing to show up, lend a hand, give their time, and help make a difference.

Today, we want to take a moment to recognize some of the amazing people who have volunteered and helped support the Spina Bifida of Surry Foundation throughout the years.
Whether they helped at an event, helped get events ready, served food, set up, cleaned up, donated their time, helped a family, or simply stepped in wherever they were needed — we are grateful.

Some people may only see the event itself, but behind every event are people working before, during, and after to make it happen.

To everyone who has ever volunteered with us: THANK YOU.

Your time matters.
Your help matters.

And the families we serve matter.
We are so thankful for every person who has been part of this journey.

Support • Awareness • Hope

10/07/2026

💙 Day 6/7 of Spina Bifida Awareness Month 💛

Today, we want to share a little about why our Bingo fundraiser is so important to our foundation.

Bingo is more than just a fun night with our community. It helps provide the funds that allow the Spina Bifida of Surry Foundation to continue supporting individuals and families throughout the year.

Through fundraisers like Bingo, we are able to help with care packages, community events, awareness and education, and helping families when needs arise. And of course we would like to do more each year!

We want our foundation to be there beyond Awareness Month — through the surgeries, appointments, celebrations, challenges, and everyday moments. 💙

🎉 And we need your help!
We are currently looking for 12 baskets to help make our Bingo event possible. We are also looking for:
• Auction items
• Gift cards
• Door prizes
• Donations toward baskets
Donations can be money baskets, TVs, appliances, themed baskets, something fun, or even something handmade. There are so many ways to get creative!

If your family, business, church, organization, or you personally would like to donate, please reach out to us.

Every donation makes a difference!
When you support our Bingo, you're not just supporting one night. You're helping us continue our mission all year long. 💙💛

Thank you to everyone who continues to believe in what we're doing and helps us Move Forward together. 🧡

Also click on the event and let us know you are coming!

https://www.facebook.com/share/19WreT3okv/?mibextid=wwXIfr

10/06/2026

DAY 5 — SPINA BIFIDA AWARENESS MONTH 💙💛

Today’s video is a little different. ❤️
Nate is sharing a little about the Spina Bifida of Surry Foundation and what it means to our family — with a little help from our two girls. 😊

They’re only 3 and 5, so they may not understand everything the foundation does just yet, but they know Dad loves it, they love coming to the events, making special care baskets after a child has surgery, making new friends and they know it’s about helping people. 💙💛

Sometimes awareness starts with something as simple as teaching our kids to love, help, and care for others.

10/03/2026

💙💛 SPINA BIFIDA AWARENESS MONTH — DAY 3 💛💙

Today, we want to share the story of a very special little girl, told by her mama. Her story is a beautiful reminder that Spina Bifida is so much more than a diagnosis.

This sweet girl has also become a special part of Spina Bifida of Surry Foundation. She comes to our events, brings her big personality, and honestly… she’s the star of the show!

⭐️💙 We love getting to watch her grow, smile, play, and be surrounded by a community that understands her journey.

“The month of October is a special month for our family — Spina Bifida Awareness Month — a month that is dedicated to educating and informing others who don’t know what Spina Bifida is.
Spina Bifida is much more than a diagnosis.

Spina Bifida is a happy baby, with more appointments than the typical baby. It’s a surgery where your marriage and faith are tested. It’s a toddler who is learning to walk a little later and with assistance. It’s a young child learning how to navigate life, become independent, a little bit sassy, and who is learning her limits.
Spina Bifida is love, community, patience, understanding, faith and so much more.

If I could look back to four years ago and tell myself one thing, it would be that God’s got this.

Being a parent of a child with any type of disability isn’t for the weak, but I am so blessed to be this sweet girl’s mama. She was picked for me to love and to raise, and for that I am so, so, so thankful.” ❤️

Thank you to this family for allowing us to share their story and giving others a glimpse into their journey.
She is one of the many reasons we do what we do. We want families affected by Spina Bifida to know that they have a community behind them — a place to find encouragement, understanding, friendship, and support.

💙💛 Behind every diagnosis is a child. Behind every child is a family. And every story matters.

10/02/2026

💙 DAY 2 — A MOTHER’S PERSPECTIVE 💙

Today, we want to share something very special with you.

Before there was a nonprofit…
Before there were awareness events…
Before there were care baskets…
Before there was Spina Bifida of Surry Foundation…

There was a little boy named Nathaniel and a mother learning how to navigate life with a child with Spina Bifida.

Today, we’re sharing a video from Nate’s mom, giving us a mother’s perspective of what it was like to raise a child with Spina Bifida.

The appointments.
The surgeries.
The uncertainty.
The questions.
The challenges.
The victories.
The memories.

And most importantly—the love.
Along with her story, we’re sharing a picture of Nate as a child.

That little boy’s journey is a big part of what eventually inspired the heart behind Spina Bifida of Surry Foundation.

To every mother who has walked this journey:
❤️ We see you.
To every parent who has ever wondered if they were doing enough:
❤️ You are not alone.

And to Nate’s mom:
Thank you for sharing your story and allowing us to see a little more of the journey that helped shape the person and the mission behind this foundation.

🎥 Take a few minutes to listen to her story below.

And remember, this month isn't just about facts and statistics.
It’s about the PEOPLE behind Spina Bifida.
The children.
The adults.
The parents.
The siblings.
The grandparents.
The caregivers.
The families.

Every person has a story.
If you or someone you love has been affected by Spina Bifida or Hydrocephalus, we would love to hear your story too.
📸 Send us a picture.
🎥 Send us a video.
💬 Send us your story.
With your permission, we may share it throughout October to help raise awareness and let another family know they aren't alone.
And if you are a local family looking for encouragement, support, or resources, please reach out to Spina Bifida of Surry Foundation.
We want to be a local resource for our community.

🧡💙 You don't have to walk this journey alone. 💙🧡

10/01/2026

🧡💙 DAY 1 — SPINA BIFIDA AWARENESS MONTH IS HERE! 💙🧡

October is Spina Bifida Awareness Month, and this year we want to make it about something bigger than facts and statistics.
We want to celebrate YOU.
We want to hear from the individuals and families who live this journey every day.

Throughout October, we're going to be sharing:
🧡 Facts & education
💙 Myth vs. fact
🧡 Personal stories
💙 Family experiences
🧡 Resources
💙 Community support
🧡 Care baskets
💙 The people behind our foundation
🧡 What we do locally
💙 And the many different ways people live with Spina Bifida

📸 WE WANT TO SEE YOUR FAMILY!
If you have a loved one with Spina Bifida or Hydrocephalus, send us a picture or short video that you're comfortable sharing.
It could be:
👶 Your child
🧑 Someone growing up with Spina Bifida
❤️ Your spouse
👨‍👩‍👧 Your family
🏆 An accomplishment
😊 A favorite memory
🏥 A medical journey
🎉 A celebration
💙 Or simply a picture that represents your loved one

Have a personal Spina Bifida story you'd like to share?
We'd love to hear it.
Maybe you're a parent who wants to share your child's journey.
Maybe you're an adult living with Spina Bifida.
Maybe you're a sibling, spouse, grandparent or caregiver.
Maybe someone with Spina Bifida has changed your life.
Your story could help another family feel less alone.

📩 Send us your pictures, videos or stories through Facebook Messenger or whatever method we provide for submissions. By sending them, please make sure you have permission from everyone pictured or featured for us to share them publicly.

🧡💙 This month isn't just about raising awareness. It's about putting faces, families and stories behind the diagnosis.
And if you are a local family affected by Spina Bifida or Hydrocephalus and you're looking for support or resources, reach out to Spina Bifida of Surry Foundation.
We want to be a local resource for you.
You don't have to walk this journey alone.

Let's make October a month our community never forgets. 🧡💙

05/20/2026

Spina Bifida of Surry has been blessed and is growing! We are looking for a 6 / 12 trailer so we can travel for more events that will be planned in the future. Does anyone have one or know where I can go to buy one? Thanks!

Shares and comments appreciated!

Address

Mount Airy, NC

Telephone

+13367102861

Website

https://sites.google.com/view/spinabifidaofsurry/home

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