Callihan Marshall

Callihan Marshall New York State Regional Representative for PRISMS (Parents and Researchers Interested in Smith-Magenis Syndrome) I love my job. Shared with Public

I graduated with a Bachelor's Degree in Broadcast Journalism. I began my career in Grand Junction, Colorado as a reporter and fill-in news anchor at KREX. In 2016, I moved back to New York and worked at WKTV in Utica for four years where I anchored the weekends and reported during the week. Then in 2020, during the height of the pandemic, my career brought me to Syracuse as a reporter/anchor for W

SYR. I fell in love with Syracuse, and this is where I decided to stay. I work as the Director of Public Relations/Communications at a school district. Even though I'm no longer in news, I would like to use this page to promote something I'm passionate about...Smith-Magenis Syndrome. Many who follow this page know my sister Briahna who has SMS. I became a regional representative for the organization who does research on the genetic disorder, PRISMS. I will share any updates and valuable information with families who have loved ones with SMS, on this page. And of course, pictures of my sweet sister!

03/16/2026

Good ole March!

This is some very good insight into what reporters/anchors have to do to make it big. There’s eating ramen and cans of t...
02/27/2026

This is some very good insight into what reporters/anchors have to do to make it big. There’s eating ramen and cans of tuna and vegetables because you can’t afford anything else. There’s a lot of debt, a lot of moving, no lunch breaks. Savannah may have a glamorous job now, but she had to fight to get there.

02/10/2026

🎿 HISTORIC PERFORMANCE 🎿

Ben Ogden grew up in the tiny town of Landgrove, Vermont (just outside of Manchester).

He just won the SILVER MEDAL in the Olympics ‘mens cross country’ race.

It has been 50 YEARS since the United States won any medal in that category.

Way to go Ben… the Capital Region and all of Vermont is proud of you.

Landgrove, by the way, has a population of 177.

One of their hometown’s own just won at the Olympics.

01/17/2026
01/14/2026

IN MEMORIAM: Remembering Alan Rickman, beloved actor known for a range of roles, including in "Die Hard" and "Harry Potter," who died 10 years ago today. https://abcnews.visitlink.me/f7a7pP

01/03/2026

Three years ago, an NFL game between the Buffalo Bills and Cincinnati Bengals turned into a gut-retching moment when Bills safety Damar Hamlin suffered cardiac arrest and collapsed. Since then, Hamlin has made it his mission to increase awareness of CPR.

12/30/2025
How awesome!
12/13/2025

How awesome!

🏈 Carrying Something Special 🏈

I know we have some Bills fans on this page.

Josh Allen and his lovely wife Hailee Steinfeld are expecting 👩‍❤️‍💋‍👨 🤰

Thought you’d appreciate some happy news 🤗

11/16/2025

Smith–Magenis syndrome is named after the two pioneering clinicians who described the condition in 1986, namely, Ann C. M. Smith, a genetic counselor at the National Institutes of Health, and R. Ellen Magenis, a pediatrician, medical geneticist, and cytogeneticist at the Oregon Health Sciences University.

Other names people may use to describe Smith-Magenis Syndrome include chromosome 17p deletion syndrome, deletion 17p syndrome, 17p11.2 monosomy, partial monosomy 17p, SMS and 17psyndrome.

PRISMS Clinic Research Consortium, (PCRC), provides comprehensive care for people with SMS, who can consult with a multi-disciplinary team of experts. Learn more about the PCRC here: https://www.prisms.org/about.../living-with-sms/sms-clinics/

11/14/2025

There is no cure for Smith–Magenis syndrome. Children with SMS often require several forms of support, including physical therapy, occupational therapy, and speech therapy. Support is often required throughout an affected person's lifetime. PRISMS has curated a series of medical management guidelines and treatment recommendations to help support families and the clinicians who care for individuals with SMS.

11/14/2025

Because rare doesn’t mean small. SMS may be rare, but discoveries made through SMSRF research reach far beyond one condition — advancing understanding of neurodevelopment and genetics that benefit millions.


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Dewitt, NY

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