Embracing Emma

Embracing Emma Sweet Emma was diagnosed with a DIPG brain tumor in October 2020. She passed away in May 2021 The strength on her left side is improving.
(1)

On Sunday, October 18th, Laura and Mark Welp and their 6-year-old twins, Emma and Abby, were having a great weekend. The day was normal until lunchtime when Emma started complaining of a bad headache. It was discovered that she had a brain bleed and was immediately taken by helicopter to the Children's Hospital in Peoria. On Monday afternoon, Emma had surgery to reduce swelling and remove a blood

clot. Sadly, while in surgery, a tumor was discovered on her brain stem, which was sent for biopsy. The biopsy results revealed that the tumor is stage IV DIPG (diffuse intrinsic pontine glioma), which is a type of tumor found in an area of the brainstem known as the pons. At this time there is no cure for this rare cancer and it is inoperable. Emma has had her breathing tube removed, a speech therapist working with her to help her with swallowing food, and a PT to begin working on her right side of her body. She had a visit last weekend from her best friend and twin sister, Abby, and it was a happy reunion. On December 22, 2020 Emma completed six weeks of radiation. May 23, 2021 Emma passed away from DIPG.

Happy 6th birthday in Heaven, sweet Emma💜 Our hearts break that you aren’t celebrating 12 years with your sister. Life i...
06/07/2026

Happy 6th birthday in Heaven, sweet Emma💜 Our hearts break that you aren’t celebrating 12 years with your sister. Life isn’t the same without you. It’s really hard to balance grief and joy at the same time. We know you are celebrating with Jesus and Great Grandma, eating all the cake and having a dance party. We miss you with every fiber in our bodies. Thanks for the glimmers you send us each day from Heaven💜

Dear Emma,1,825 days without you. Today, we sit at home without you, alone in the stillness, looking at the empty space ...
05/24/2026

Dear Emma,

1,825 days without you. Today, we sit at home without you, alone in the stillness, looking at the empty space where your laughter used to live.

You were six when the world fractured. Five years have passed since then, which means you have now been gone almost as long as you were here. That is a cruel kind of math. Abby is eleven now. She is growing tall, losing her baby softness, and becoming the most beautiful girl. Every time I look at her, I am hit by a breathtaking wave of gratitude, immediately followed by a quiet, aching phantom pain. Because I know exactly what you would look like right now, too. Your dark brown eyes would match your long dark brown curls.

Abby carries you forward in ways that breaks my heart and heals it all at once. You are talked about and your name is said every day.

People told me back then that grief changes shape. I didn’t believe them. In those first couple of years, grief was a jagged piece of glass in my throat. It was the suffocating weight of hospital and St. Jude corridors, the beep of monitors, the deterioration of your fragile body. It was the anger of watching a vibrant, fierce little soul be stolen by an illness too big for her small body.

Five years out, the glass has worn down into something smoother. It doesn’t scream anymore- it hums, as a permanent background noise. I feel it when I pack 1 school lunch, back to school shopping for 1, birthday/Christmas shopping for 1, etc.

I miss you every time Abby has something to celebrate without her built in best friend beside her. This absence will forever feel this way.

Amidst the missing, a strange profound beauty can sometimes be found among the wreckage. Loving you for six years was worth the heartbreak that followed. Your absence hasn’t made the world darker, it has made me look closer to the light. I love fiercely. I hold Abby a little longer. I don’t take quiet mornings for granted.

You are not here, my sweet girl. But you are never, ever gone. đź’ś

We will always say Emma’s name. She is a part of our every being. And we miss her terribly 💜https://www.facebook.com/sha...
05/04/2026

We will always say Emma’s name. She is a part of our every being. And we miss her terribly 💜

https://www.facebook.com/share/p/1DHZc1uDKY/?mibextid=wwXIfr

Today is a weird day. It's International Bereaved Mother's Day.

A day meant to create awareness, honor those of us with a child on the other side, and validate the grief that we carry every day.

But, I've always had a weird relationship with this day.

First, I never knew it existed until my own child died.

In those early years, I hated this day! It felt like one more thing I had to endure and find a way through. Like two Mother's Days back-to-back, which felt like torture.

If I'm honest, I'm indifferent about this day now - 10 years in.

We don't need a day to talk about our kids or our grief.
We don't need the burden of reminding or educating others.
We don't need a day to hold our grief and motherhood sacred.

We can do all of those things every single day!

Yet, today exists. And because it exists, we get to decide exactly how we want to engage with it.

Maybe for you, today is a quiet day of survival.
Maybe it’s a day of loud, proud remembrance.
Maybe you’re feeling a bit of both, or nothing much at all.

There is no "right" way to be a bereaved mother today. You don't owe this day anything.

But if you find yourself wanting a space to speak their name or show their face, I’d love to hold that space with you here.

If you feel like sharing, I’d love to see a photo of your child in the comments, and if you’re up for it, tell us one thing about how you’re navigating the "weirdness" of today.

Have a Bereaved Mother's Day. However that looks for you. ❤

Address

Normal, IL

Alerts

Be the first to know and let us send you an email when Embracing Emma posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share