Little Baby Face Foundation

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Little Baby Face Foundation http://www.littlebabyface.org At Little Baby Face Foundation our mission is to transform the lives of children born with facial deformities.

10/15/2026

Every child’s care journey can look different.

For families of children with facial differences, having coordinated support can make each stage easier to understand and navigate. 🌟

Read the full blog to learn more:

10/13/2026

During Hispanic Heritage Month, we’re grateful to celebrate wonderful families like Edelman’s and the trust they place in us. ❤️

At LBFF, we never want language to stand in the way of a family feeling welcomed, heard, and supported.

Know a family who may need our help? Share our mission or encourage them to apply.

10/08/2026

A little reminder for today: being yourself is always worth celebrating. ✨

Every child deserves to feel proud of exactly who they are. 💛

10/05/2026

One of the biggest questions families ask us is: What happens after I apply? The answer starts with an individual review.

After a family completes our confidential online application, our medical team reviews the child’s information to determine whether LBFF may be able to provide care. Families do not have to decide eligibility themselves. That’s what the review process is for.

Our new blog walks through the process so you can better understand what to expect. Read more on our website. https://www.littlebabyface.org/how-lbff-reviews-applications-for-complex-facial-birth-conditions/

09/25/2026

Breathing and feeding are part of everyday life. For some children with facial differences, like cleft palate, nasal clefts, and nasal atresia, those everyday functions may also bring challenges.

That can leave parents with important questions about what their child is experiencing and what comes next.

Our newest blog explains how certain facial differences may affect breathing and feeding, while offering supportive information for families looking to learn more.

Read the blog: https://www.littlebabyface.org/help-baby-cleft-lip/

09/22/2026

Clefts, nasal clefts, and nasal atresia can sound similar, but each can affect a child in different ways.

Our newest parent guide explains these facial differences in plain language and explores how they may affect everyday functions.

Our goal is to give families a clearer understanding of what these terms mean and help them feel more informed as they consider next steps.

Read the full guide on our website today: https://www.littlebabyface.org/blog-2/

09/19/2026

Wondering whether Little Baby Face Foundation may be able to help your child?

You don’t have to figure out eligibility on your own. The first step is to complete our confidential online application. Our medical team will review your child’s information and determine whether LBFF may be able to provide care.

If a child is accepted for care, we provide no-cost treatment and help cover critical expenses associated with that care.

Take the first step today. 💙 Apply here: https://www.littlebabyface.org/apply/

09/17/2026

We have a sweet update to share about Ivy 💛

This little sweetheart recently traveled from Virginia to New York with her mom and dad, Tiffany and Matt, for surgery. Her visit also came right around her 3rd birthday, so there was a little celebrating to do! 🎂

To make the occasion even sweeter, Ivy received a Build-A-Bear during her visit with Dr. Romo. Her new friend was made with love by employees at Apollo Global Management during an event organized with former LBFF board member Alexa Rauch. 🧸

We’re so grateful to Alexa and everyone at Apollo for adding some extra joy to Ivy’s birthday visit. Wishing this sweet girl a very happy 3rd birthday! 💛

09/15/2026

If your baby was born with microtia, the first few months may come with questions you never expected to be asking.

Where do we start?
Who should we talk to?
Do we need to have everything figured out now?

You don’t need to have every answer today.
Start with the information you already have, keep track of the questions that come up, and take things one step at a time.

Learn more about how LBFF may be able to help children with facial differences, including microtia.

Our surgeons donate something incredibly valuable: their time and expertise.But providing no-cost care still comes with ...
09/12/2026

Our surgeons donate something incredibly valuable: their time and expertise.

But providing no-cost care still comes with critical expenses.

Donor support helps us cover costs such as specialized tools, anesthesia, travel, and lodging when a child is accepted for care.

That means your gift helps turn donated medical expertise into care a family can actually access. Every gift helps us continue transforming the lives and faces of children born with facial differences.

💙 Donate today: https://www.littlebabyface.org/donate/

Address

135 E 74th Street
New York, NY
10021

Telephone

+12123335233

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