Corewell Health Lakeland Hospitals

Corewell Health Lakeland Hospitals At our core, we are here to help people be well so they can live their healthiest life possible.

Corewell Health is a not-for-profit health system that provides health care and coverage with an exceptional team of 60,000+ dedicated people—including more than 11,500 physicians and advanced practice providers and more than 15,000 nurses providing care and services in 22 hospitals, 300+ outpatient locations and several post-acute facilities—and Priority Health, a provider-sponsored health plan serving more than 1.3 million members. Through experience and collaboration, we are reimagining a better, more equitable model of health and wellness.

We are proud to introduce the residents selected to serve as Chief Residents for the 2026-2027 academic year. These indi...
03/23/2026

We are proud to introduce the residents selected to serve as Chief Residents for the 2026-2027 academic year. These individuals were chosen for their demonstrated leadership, commitment to academic excellence, and dedication to advancing the mission of our training programs.

Emergency Medicine: Abbey Goodman, MD & Nick Wilson, DO
Family Medicine: Paige Moreno, DO & Yousuf Siddiqui, MD
Internal Medicine: Chris Naco, MD & Yousef Hasanain, DO

Our Chief Residents play a vital role in supporting their fellow residents and strengthening the educational experience across our programs. We look forward to their leadership in the upcoming year.

Congratulations and welcome to our new residents! We are excited to have you join us!
03/20/2026

Congratulations and welcome to our new residents! We are excited to have you join us!

Happy  ! Today, medical students receive their letters sharing which hospital program they’ve matched with as they take ...
03/20/2026

Happy ! Today, medical students receive their letters sharing which hospital program they’ve matched with as they take a huge step in their careers toward residency.

We asked a few of our current residents for their advice for our incoming matches. Here’s what they had to say:

"You're going to learn so much and have a blast doing it!" - Jacky Sarette, MD - Emergency Medicine Resident

"This is a wonderful community filled with wonderful people. Your training goes by a lot quicker than you think so make sure to enjoy the community and people around you while you are here!" - Dominique Gutierrez, MD - Family Medicine Chief Resident

"Come with a good attitude, the humility to admit when you don't know something, a desire to learn, and a willingness to work hard, and you'll do just fine! We can't wait to work with you!" - Alyssa McCue, DO - Emergency Medicine Resident

Evelyn Brimite embodies what it means to “Be Exceptional Everyday.”Her compassion and advocacy ensure that patients feel...
03/09/2026

Evelyn Brimite embodies what it means to “Be Exceptional Everyday.”

Her compassion and advocacy ensure that patients feel safe and truly cared for. Evelyn’s dedication inspires those around her and strengthens our unit and we are honored to celebrate her as our BEE award winner. Congratulations, Evelyn!

Not only are our patients rare disease warriors, but so are the families, researchers, and physicians who stand alongsid...
03/06/2026

Not only are our patients rare disease warriors, but so are the families, researchers, and physicians who stand alongside them every step of the way. To every single one of them, we are grateful.

Thank you for your advocacy, research, and tireless dedication. You make progress possible every single day. Together, you are changing lives.

Let’s give a high-five to Marley. 🙏 Our last, but certainly not least, rare disease warrior. Magnificent Marley was born...
03/05/2026

Let’s give a high-five to Marley. 🙏 Our last, but certainly not least, rare disease warrior.

Magnificent Marley was born with a head full of silvery hair that many said mimicked X-Men superhero Storm's shimmery locks. But little did her parents know the kind of battle that really lay ahead for their mighty warrior. In 2018, Marley was the first patient ever to be diagnosed with Bachmann-Bupp Syndrome (BABS) by Corewell Health physicians and researchers and since her diagnosis, she has overcome superhero challenges thanks to the treatment her team of doctors discovered shortly after diagnosis.

“At first, I placed a lot of the blame on myself because the medical community didn’t give me any answers. Having a name to the disease doesn’t necessarily solve anything either. So many rare diseases are under researched and there’s such little information available. Sometimes having a rare disease doesn’t give you answers but opens a whole new world of questions. This is why supporting rare disease research is so crucial, because there’s a lot of rare individuals out there searching for more information and more answers.” Kelly Berthoud – Marley’s mom

Can we get a shout out for rare disease warrior Liam?From the moment he was born, Liam started having seizures and his m...
03/04/2026

Can we get a shout out for rare disease warrior Liam?

From the moment he was born, Liam started having seizures and his mom Tammy knew something was wrong from the start.

After coming to Helen DeVos Children’s Hospital, Liam was diagnosed with SCN8A, a rare neurological disorder that can cause severe epilepsy, developmental delays, and other complex medical challenges. Now, at 11 years old, Liam’s personality is on full display thanks to his doctors, nurses and so many more involved in his care.

“I feel like the luckiest person in the world to be his mom. I would never change our lives. He’s our sunshine boy. I wish that people knew that just because my child is rare, he still matters. Research is important, even though our numbers are ultra rare. I wish people knew how hard this life can be but also know I would never not choose him. He is our warrior and I wish I had as much strength as he does every day.”

Say hello to Caroline. Another one of our awesome rare disease warriors.In early 2023, sweet Caroline was diagnosed with...
03/03/2026

Say hello to Caroline. Another one of our awesome rare disease warriors.

In early 2023, sweet Caroline was diagnosed with Neurofibromatosis (NF), a rare genetic disorder that causes tumors to form along nerves throughout the body. While the tumors are typically non-cancerous, they can cause significant medical complications for young patients.

Caroline is the “why” her mom, Danielle, founded Give NF a non-profit that recently gave a gift to support our Steensma Lab to further research in NF.

“As a parent, particularly a parent of a child with a rare disease, you are your child's best advocate. You sometimes have to do the research because there isn't a ton out there. You have to piece together the medical team that's the right fit for your child and your family, particularly with how specialized the medical field is these days. Yes, there's a point when you're "going down the rabbit hole" and it's not helpful, but it IS ok to advocate and research.” – Danielle Grover, Caroline’s mom.

Meet Jameson, a rare disease warrior.In 2020, Jameson was diagnosed with Bachmann-Bupp Syndrome (BABS), an ultra-rare ne...
03/02/2026

Meet Jameson, a rare disease warrior.

In 2020, Jameson was diagnosed with Bachmann-Bupp Syndrome (BABS), an ultra-rare neurodevelopmental condition. The diagnosis came after years of uncertainty, until one day, the work of our physicians and researchers brought answers. Today, Jameson is making remarkable progress, even taking his first steps without help not too long ago!

For those just starting their rare disease journey... “Reach out to the rare disease community however you can- social media, groups in your area or even around the world. Connecting with families who have rare diseases can be a huge asset to have. Not only does it help to feel not so lonely, but there is strength in numbers when it comes to research and the ability to learn more about rare diseases.” - Kayla Jibben, Jameson’s mom.

02/28/2026

Behind every rare disease diagnosis is a face, a family, a physician and a story worth sharing.

On this Rare Disease Day, we celebrate the incredible resilience of our rare disease warriors who remind us what strength looks like.

Follow their journey throughout the week as we share more about Liam, Marley, Jameson, and Caroline.

Every day, our residents bring compassion, commitment, and strength to their work.On Thank a Resident Day, we take the c...
02/27/2026

Every day, our residents bring compassion, commitment, and strength to their work.

On Thank a Resident Day, we take the chance to recognize all that you do and the lasting impact you make.

Thank you to our incredible residents!

02/12/2026

Innovations like VR learning help Corewell Health ensure our rural communities have access to leading healthcare practices. Regional President for Southwest Michigan, Natalie Baggio, joined Health Care Rounds to discuss how Corewell Health is finding new ways to provide top-of-the-line healthcare for all communities. Listen to the full episode here: https://www.darwinresearch.com/health-care-rounds

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1234 Napier Avenue
Saint Joseph, MI
49085

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