Wrenn Leigh

As many of you know, Hannah Musselman and Ian Brewster welcomed their beautiful baby girl Wrenn Leigh Brewster, on June 28, 2024.

Wrenn was diagnosed this week with Pierre Robin sequence of events. Basically in utero her jaw didn’t pull forward, which caused her tongue to stay tied and the roof of her mouth not to form.

They have been told the jaw will either grow on its own or will need plastic surgery to extend. They will then cut the tongue tie (she has both an anterior & posterior tie which is actually very good, as this is stopping her from swallowing her tongue all together and suffocating) and around 9-12 months old if she’s growing at a normal rate they will then repair the cleft palate (she has no roof of her mouth at all, her nasal cavity is 100% exposed giving her only one airway instead of the two she needs to breath properly). She will be on feeding tube for time being as she isn’t able to control swallowing reflex and was aspirating when eating orally. We will learn more next week about feeding & rate of growth of what to expect of jaw.

Ian, Hannah and Willow are currently in Saskatoon with Wrenn while she is in the NICU at the Jim Pattison Children's Hospital.

Any contribution, no matter how small, will make a difference and help them focus on what matters most- Wrenn’s health and recovery.

Your generosity and kindness means the world to Hannah and Ian.

Nicole