C.S. Mott Children's Hospital

C.S. Mott Children's Hospital U-M Health C.S. Mott Children’s Hospital – one of the nation’s best children’s hospitals.
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Sharing a powerful voice for children and families on Capitol Hill12-year-old E’Shon Guy, a patient at C.S. Mott Childre...
06/09/2026

Sharing a powerful voice for children and families on Capitol Hill

12-year-old E’Shon Guy, a patient at C.S. Mott Children's Hospital, recently traveled to Washington, D.C. to share his healthcare journey with lawmakers and discuss how health policy decisions affect kids like him.

E’Shon has a severe form of sickle cell anemia that led to frequent illness and repeated hospitalizations before lifechanging treatment at Mott.

He and his parents, Eric and Virona Guy, met with members of Michigan's congressional delegation and their staff as part of the Children’s Hospital Association’s Family Advocacy Day.

The family had the chance to speak with Congresswoman Hillary Scholten, Congresswoman Debbie Dingell and Congressman Tom Barrett as well as staff from the offices of Congressman John Moolenaar and Congressman Tim Walberg.

Thank you, E’Shon! 💙💛

06/08/2026

Would you know what to do if someone's heart suddenly stopped?

Although national CPR and AED Awareness Week has ended, the importance of knowing these lifesaving skills lasts all year.

Mott pediatric cardiologist Dr. Jeff Zampi provides step-by-step instructions on how use an AED. You never know when you may need one.

Meet Lincoln one of our Little Victors from our 2026 calendar. “Lincoln has a super rare genetic disorder called NONO-as...
05/30/2026

Meet Lincoln one of our Little Victors from our 2026 calendar. “Lincoln has a super rare genetic disorder called NONO-associated X-linked intellectual disability syndrome. He is one of 24 people in the entire world diagnosed with this genetic disorder. C.S. Mott Children's Hospital has dealt with one other case of this genetic disorder, which is his big brother, Hudson. This genetic disorder causes so many unknown answers due to its rarity. There is no cure for this since it's based on genetics.” Hail, Lincoln!

Meet Tommie one of our Little Victors from our 2026 calendar. “At just five days old, Tommie had heart surgery to repair...
05/29/2026

Meet Tommie one of our Little Victors from our 2026 calendar. “At just five days old, Tommie had heart surgery to repair her coarctation of the aorta. Then at just 2.5 weeks old, she had open-heart surgery.” Hail, Tommie!

Meet Bentley one of our Little Victors from our 2026 calendar. “Bentley was diagnosed with a germinoma brain tumor in Ju...
05/28/2026

Meet Bentley one of our Little Victors from our 2026 calendar. “Bentley was diagnosed with a germinoma brain tumor in July 2024. He has received chemotherapy, radiation, surgery, etc. He completed active treatment on Christmas Eve that year and he is currently stable as a 12-year-old middle schooler. He is currently receiving services from ophthalmology, oncology, neurology, genetic oncology, endocrinology, and audiology, all at C.S. Mott Children’s Hospital.” Hail, Bentley!

💕☀️A summer kickoff party for Little Victors and their families made possible by Event on Main. Ice cream, popcorn, bubb...
05/27/2026

💕☀️A summer kickoff party for Little Victors and their families made possible by Event on Main. Ice cream, popcorn, bubbles, chalk, rocket launchers and music from our talented music therapy team. THANK YOU Event on Main for launching summer at Mott.

Learn more about Event on Main and how to support at https://michmed.org/enyKv.

Meet Brynlee one of our Little Victors from our 2026 calendar. “Brynlee was diagnosed with medulloblastoma (group 3) in ...
05/27/2026

Meet Brynlee one of our Little Victors from our 2026 calendar. “Brynlee was diagnosed with medulloblastoma (group 3) in April of 2025. She has gone through 30 rounds of radiation and rang the bell in June! She’s currently going through maintenance chemotherapy and is going on her fourth cycle with 42 rounds and counting. She is the bravest, funniest, most polite, amazing little girl there is.” Hail, Brynlee!

Meet Ethan one of our Little Victors from our 2026 calendar. “Ethan was diagnosed with cystic fibrosis when he was four ...
05/26/2026

Meet Ethan one of our Little Victors from our 2026 calendar. “Ethan was diagnosed with cystic fibrosis when he was four weeks old, but he doesn't let that define him. He is very active, and you can almost always find him on a field or court. His favorite is tackle football, but he also plays baseball and basketball, and plans to run track this year. His dream is to become the first player in the NFL with CF. Thank you, Dr. Saba, the respiratory therapists, the clinical team, the 12 East team, Colin from Child Life, and anyone else who has been involved in his care, for having such a big impact on his life. Because of all the amazing people that we deal with at appointments or for inpatient stays, Ethan remains positive about having CF and handles his treatment like the Victor he is. Because of them, he is able to dream of his future.” Hail, Ethan!

Meet Jesus one of our Little Victors from our 2026 calendar. “Jesus battled retinoblastoma and received his diagnosis at...
05/24/2026

Meet Jesus one of our Little Victors from our 2026 calendar. “Jesus battled retinoblastoma and received his diagnosis at only 10 months old. Doctors discovered he had three tumors in his left eye. This led to him undergoing six months of chemotherapy. Thankfully, his body was receptive to the chemo and today, Jesus is cancer free. Jesus has a wonderful team starting with his oncologist Dr. Hakan Demirci and his whole team, as well as the oncology department, Dr. Laura Sedig, and nurse practitioner Amy Edmonds.” Hail, Jesus!

Meet Cole one of our Little Victors from our 2026 calendar. “Cole was born with eosinophilic esophagitis, a chronic immu...
05/23/2026

Meet Cole one of our Little Victors from our 2026 calendar. “Cole was born with eosinophilic esophagitis, a chronic immune system disease that causes inflammation in the esophagus. When Cole started eating solid food at 6 months old, we knew something wasn't right. After almost every meal he would vomit, and this went on for five years. He had seen different doctors and specialists and tried many different medications. Nothing worked and we had no answers and were told he might be doing it on purpose. After that we decided to get one more opinion at Mott in pediatric gastroenterology. We finally got answers and the right diagnosis. Cole is now receiving the proper medication and is in remission! We are truly thankful for Dr. Grace Lee and the entire pediatric GI team at Mott!” Hail, Cole!

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1540 E Hospital Drive
Ann Arbor, MI
48109

Telephone

+17349364000

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