Magic days with Morgan

In February 2023 the Bashall’s welcomed their third daughter Morgan into their family. Her two beautiful sisters were smitten. Morgan is happy, loves a wrestle with her sisters, playing with Jock the family golden retriever and has a smile that lights up the room.

In March 2024 Chris and Candice received a heartbreaking diagnosis that no parent could prepare for.

Morgan has Sandhoff disease.

There is no treatment. There is no cure. Her development will be greatly impacted and her health with deteriorate over the next 12 months.

You can read more about the disease at The Rare Find Foundation (https://www.rarefindfoundation.org/the-diseases/sandhoff-disease/)

This page and fund has been set up to support the Bashalls during this difficult time. Funds will go towards providing special experiences for Morgan, memory making with her family, meals and cleaning and anything else needed to support this amazing family.

A list of the experiences that the Bashalls have put together will be shared here soon. If you have any connections or can help facilitate these experiences please let us know.

How can you help?

Time is of the essence as Morgan’s needs will become more significant over the coming months.

Donations are welcomed through this page or you can contact James via the contact button at the bottom of this page to donate direct to the family.

Meals are being coordinated through Meal Train. You can find more information and volunteer for a date at the following link Provide a meal here

Any other ideas and questions can be directed to James.

Thank you for your support as we work together to alleviate some of the burdens of everyday life and take a small weight off the Bashalls as they navigate this uncertain and challenging journey with their girls.