Shaye Ganam

A place to talk. To come together. To be heard. Shaye Ganam is taking the conversation province-wide on 880 CHED in Edmonton and QR Calgary - 770 AM, creating a collective town square to rehash the old and imagine the new for every part of this province. Tune in Monday to Friday from 9 a.m. to noon to join the conversation. Follow Shaye Ganam on Twitter to keep up with your host wherever he goes.

News
776
Canada lagging behind U.S. in adopting drones f...
9 min
777
Weekly Economic Recap 
9 min
778
Carney announces plans to ‘transform’ Canada’s ...
9 min
779
Ultra Processed, Justice, EV's
78 min
780
Empty nest, full house: These parents are sick ...
8 min
781
Ultra processed foods like sodas and sweets sho...
10 min
782
Danielle Smith says Alberta will withhold fundi...
13 min
783
Alberta legislation could pave way for two-tier...
9 min
784
Could your electric vehicle pose a cybersecurit...
9 min
785
Federal union warns Canadians will be affected ...
11 min
786
Electric Vehicles, Federal Union, Justice System
57 min
787
 'Capital Conversations' with Melissa Caouette ...
19 min
788
Hybrid Work, Olympics, Jason Kenny
66 min
789
Calgary among diminishing number of locations c...
9 min
790
Iran weighs nuclear diplomacy with U.S., Foreig...
10 min
791
The case for hybrid work is clear, so why are s...
8 min
792
The 2026 Grammy Awards
9 min
793
Separatists' math doesn't add up, warns Edmonto...
8 min
794
Provinces have too much power, and Canada's eco...
13 min
795
Canada is funding its own economic decline
12 min
796
Conservative Leadership, Separatists, Economic ...
69 min
797
Corus Radiothon in support of the Stollery Chil...
Sam has been living with an undiagnosed genetic syndrome. From multile genetics tests to procedures like strabismus correction, radiology with sedation, hip surgeries and the development of osteopenia and epilepsy, the care and support Sam and our family receives is unmatched. After a 10 year wait, Sam was officially diagnosed with ReNU syndrome in August 2025. Sam has been followed closely by Dr. Caluseriu in genetics since he was an infant in the NICU. This is a remarkable development and step for Sam’s family, and a testament to the importance of genetic research and testing.
8 min
798
Corus Radiothon in support of the Stollery Chil...
At 10 weeks old, Marigold began showing signs of breathing trouble. She was struggling to breathe without extensive effort. Her family brought her into emergency, and she was admitted right away. At that time, doctors suspected a cold and discharged them five days later. They quickly returned but this time via ambulance. Marigold was immediately admitted to PICU on high flow oxygen, and she was diagnosed with aspiration pneumonia. This began the family’s feeding journey.
8 min
799
Corus Radiothon in support of the Stollery Chil...
Aubree was born 24 weeks and five days, weighing 680 grams. She had a long road filled with overcoming a PDA, brain bleed, surviving NEC, surgery, cardiac arrest, multiple infections and, of course, needing to grow. Her family still uses the Stollery today for her follow-ups and when she gets sick requiring additional support.
6 min
800
Corus Radiothon in support of the Stollery Chil...
Jace’s family knew he would be born with a kidney condition, and at six weeks old, theyfound out his left kidney didn’t work. In June 2018, Jace was having fevers, not eating, not sleeping and complaining of pain in his tummy all the time. Urology tests didn’t show anything was wrong but they could see things weren’t good. Later that year, Jace’s parents approved a surgery to remove his kidney and ureter, not knowing if it would solve Jace’s health issues. Since his surgery, Jace has grown like a weed and is back to being his funny, silly self! Jace’s parents know surgery was the right choice for their son, and feel like to have the Stollery so close to home.
10 min