Avalynn's Hope Foundation

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Avalynn's Hope Foundation Helping Families of Medically Fragile & Disabled Children
Get the Support & Resources They Need All of us have an Avalynn in our lives.

Avalynn’s Hope Foundation was created in memory of Avalynn Wallace, daughter of Nicole and Louie Wallace, to provide support and resources for families with medically fragile and disabled children. Avalynn was diagnosed with AML leukemia in December 2016, at the age of four. For the next three years, she went through grueling treatment to overcome the cancer; in October 2019, at the age of seven, Avalynn lost the battle and was called to Heaven. Avalynn was a beautiful soul who captured the hearts of thousands in her community and beyond with her joyful nature, infectious laugh, and wisdom years beyond her age. To continue her legacy, Nicole and Louie founded Avalynn’s Hope Foundation an independent 501(3) organization endeavoring to help families who are experiencing medical tragedies their lives and need friendship, support, and help. What We Do
Avalynn’s Hope has three primary objectives:

- Recreation: To provide a recreational park and playground (Avie’s Place) that’s accessible to children and adults of all capabilities and physical impairments, as well as resources for foundations that offer recreational activities for families of medically fragile and disabled children.

- Resources: To provide resources and guidance for families of medically fragile and disabled children, including help navigating the medical system, financial assistance, family support,

- Support: To provide funding and advocacy for cancer and disabilities research, as well as establish partnerships with like-minded nonprofit organizations. They may be your child, your niece or nephew, or even the child of a friend or co-worker. Together we can make a difference in the lives of medically fragile and disabled children and their families. Visit www.avalynnshope.org

Some parts of childhood cancer and illnesses are hard to witness. So much more happens out of sight, the sleepless night...
22/10/2026

Some parts of childhood cancer and illnesses are hard to witness. So much more happens out of sight, the sleepless nights, the waiting, the fear that follows a family home.

When it feels easier to look away, please lean in. Check on them. Bring a meal. Keep showing up, even when treatment stretches on and the updates grow quiet.

You don’t have to know the perfect thing to say to help a family feel less alone.

Take a minute right now and message a family you know right now who is needing you to lean in.

The truth is, we didn’t know how either.We didn’t choose the diagnosis, the hospital stays, or the fear. We love our chi...
20/10/2026

The truth is, we didn’t know how either.

We didn’t choose the diagnosis, the hospital stays, or the fear. We love our child, and we keep showing up, even when we’re exhausted, scared, and unsure of what comes next.

If you’re parenting a child with cancer, you don’t have to feel strong every day. You deserve support, too.

Reach out, we would love to support you.

I didn’t know how much I would miss the things I used to complain about.The constant “mom, mom, mom.” Figuring out what ...
19/10/2026

I didn’t know how much I would miss the things I used to complain about.

The constant “mom, mom, mom.” Figuring out what to make for dinner. Three girls arguing. Brushing tangled hair. Being woken up in the middle of the night.

I loved our life. I just didn’t understand how much of it I was counting on being there tomorrow.

A skinned knee that only needed a Band-Aid. Friends stopping by without having to ask if anyone had been sick. All five of us eating dinner at home. Sleeping in my own bed.

Those things felt ordinary then. Now I know how much they held.

I’m not sharing this to make another mom feel guilty for being tired or needing a break. I was tired. Those days were hard, too.

I just wish I could go back for a little while. Hear the noise. Brush her hair. Make the dinner we could all eat together.

And stay a little longer in a moment I didn’t know I would miss so much.

You can ask them to explain it again. You can cry. You can need help and still be the parent your child needs.Those firs...
16/10/2026

You can ask them to explain it again. You can cry. You can need help and still be the parent your child needs.

Those first days can feel like learning a new language while your mind is still trying to understand the diagnosis.

We want you to know: you don’t have to learn everything today. Start with your next question. Let someone bring dinner. Hold your child’s hand and read their favorite story.

Your child is still your child. And you’re still a family, even in a hospital room.

Save these reminders, or send them to a parent facing those first overwhelming days.

You get so used to the next thing.The next round. The next medication change. The next scan. Watching the numbers. Watch...
15/10/2026

You get so used to the next thing.

The next round. The next medication change. The next scan. Watching the numbers. Watching their breathing. Long nights, hair loss, good days that give you hope, and hard days that leave you holding your breath again.

Then something changes, and the survival mode you’ve been living in doesn’t know how to stop.

For some families, it’s after hearing “remission.” There is relief and joy, and still fear. You want to exhale, but part of you is already waiting for the next scan.

For others, it’s after the funeral. Everyone goes home, and you’re left with the quiet where caring for your child used to fill every hour. You still wake up ready to do something for them.

These are different kinds of pain. Each deserves room, care, and time.

You don’t have to know how to live in this part yet. You can be grateful and afraid. You can laugh and still be grieving. You can have a good day and need help getting through tomorrow.

Learning to breathe again takes time. And you deserve support long after the hospital doors close.

Put a 💛 in the comments if you’re learning how to breathe again.

Childhood cancer should make us uncomfortable. And that feeling can move us to care for the families living through it.B...
14/10/2026

Childhood cancer should make us uncomfortable. And that feeling can move us to care for the families living through it.

Because behind a diagnosis is a parent trying to listen to the doctor while wondering how long they can afford to miss work. A sibling missing their family. A child who still wants to play, see their friends, and sleep in their own bed.

The needs reach far beyond the hospital room. And when you’re overwhelmed, even knowing what to ask for can feel impossible.

At Avalynn’s Hope Foundation, we help families find a place to start. Through financial grants, help navigating applications and resources, and connections to emotional and grief support, we work to ease some of what families are carrying.

We can’t take away every hard part. But we can help a family find answers, access support, and take the next step with someone beside them.

Share this post. A family you know may need help they don’t yet know exists.

Over Avalynn’s sickness and death there have been many days, this is definitely one.The day I watched my baby need help ...
13/10/2026

Over Avalynn’s sickness and death there have been many days, this is definitely one.

The day I watched my baby need help doing something we so often take for granted, breathing. I didn’t actually die. But there was a before that day, and there has been an after.

It’s hard to explain what it feels like to be grateful for the help keeping your child alive and heartbroken that she needs it. To want to be close, to want to fix it, to know that loving her with everything you have still can’t make this part easier.

This photo holds a moment. I carry so much more of that day.

And through all the fear, she was still my Avalynn. My baby. The one I just wanted to hold.

Our favorite Gigi turned 90 last week. 🥳This photo was the last birthday Avalynn spent giving Gigi a hug, Avie passed aw...
08/10/2026

Our favorite Gigi turned 90 last week. 🥳

This photo was the last birthday Avalynn spent giving Gigi a hug, Avie passed away 6 days later.
Gigi has been part of our lives since the mid 1990’s and we are grateful for every day we get to spend with her.

Thank you Gigi for being the best to my kiddos and to us. Dee Hutcheson Kirk
We love you!

This girl, she had all the faces.What she was thinking, how she felt, what she liked and didn’t like all showed on her f...
07/10/2026

This girl, she had all the faces.
What she was thinking, how she felt, what she liked and didn’t like all showed on her face.

Enjoy the many faces of Avalynn.
She was spunky, kind, sassy, loving, spicy, funny, joyful and sometimes hangry.

Sitting here on the eve of the 7th anniversary of my daughter’s death, I remember that night so clearly.Death was encroa...
06/10/2026

Sitting here on the eve of the 7th anniversary of my daughter’s death, I remember that night so clearly.

Death was encroaching, and we knew it. The signs were all over her. We knew that at any moment she could take her last breath.

I left UC Davis that night to go be with my other two girls at the Ronald McDonald House, leaving Louie at the hospital with Avalynn. I remember thinking she might take her last breath that night.

And if I’m completely truthful, part of me secretly hoped she would.

Not because I wanted her to die. I desperately wanted my daughter to live.

But watching your child suffocating on her own body’s fluid, unable to speak, unable to tell you what she needs, brings a desperation I don’t know how to explain unless you’ve lived it.

I wanted life and death in the same breath.

I was begging God to heal her while also begging Him to take the pain away.

Those two prayers collided inside of me, and I didn’t know what to do with either of them.

We had watched our daughter suffer for so long, and now everything was coming to a screeching halt. We knew we were getting incredibly close to saying goodbye forever.

Tomorrow marks a threshold I’ve thought about for a long time.

Seven years here.
Seven years gone.

Avalynn lived seven years on this earth, and tomorrow she will have been gone from it for seven years.

I’d be lying if I said it wasn’t affecting me tonight.

This week has been filled with Avalynn’s Hope Foundation, walking alongside a sick friend, and standing beside friends who lost their son in a horrific accident.

Today, I sat beside those friends in a courtroom as they once again had to tell the story of their son’s death and wait to hear what consequences would come from the life that was taken.

And now tonight, I sit here on the eve of the day we lost our own daughter.

Maybe that’s why everything feels a little closer to the surface tonight.

Sometimes I look at what Avalynn’s Hope has become and realize that it looks like so many different things.

Sometimes it’s financial help.

Sometimes it’s holding someone’s hand.

Sometimes it’s talking with a social worker or helping a family navigate a hospital.

Sometimes it’s going to doctor’s appointments.

Sometimes it’s sitting beside someone who just received news they never wanted to hear.

And sometimes it’s helping a family plan a funeral for a child they never imagined they would have to bury.

We put ourselves out there to stand beside people who are hurting, overwhelmed, scared, or simply need someone in their corner. And sometimes that means putting our own pain aside for a moment to carry some of the weight of the person standing next to us.

Most days are good.

And then there are days like today when it hits differently.

The weight of what we carry reminds me of where we came from and who we have become in the middle of all of this.

Tomorrow, October 6th, as we remember Avalynn and mark seven years without her, I’m asking you to consider giving to Avalynn’s Hope Foundation in her memory.

Your donations allow us to keep walking alongside families just like ours. Families sitting beside hospital beds. Families trying to understand diagnoses. Families struggling financially because everything in their lives suddenly stopped. Families preparing for outcomes no parent should ever have to prepare for.

No amount is too small.

Every gift helps us keep showing up.

Thank you for loving our family, remembering our girl, and continuing to believe in what has grown from the most painful chapter of our lives.

Seven years here. Seven years gone.

We miss you, Avalynn Hope.

And we will keep showing up for families in your name.

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