Posts in Blog
Meet Logan

On November 25, 2017, our world was turned upside down. Our son Logan, who was 5 at the time, was diagnosed with T-Cell Non Hodgkins Lymphoblastic Lymphoma. Late in the night he had kept saying his throat hurt and felt funny. We let him sleep with us and are beyond thankful we did. A few short hours later he was panicking and jumped out of bed and tried to let out a cry but couldn’t. We very quickly turned the light on to find him blue and unable to breathe.

Read More
Meet Sara + Nathan

At the very beginning of this long journey we were told about The Dream Factory. We met with them when Sara was first diagnosed and their kindness was so comforting during such a terrible time in our lives. We spent many hours and days over the next year taking about all the amazing possibilities for dreams they might want to experience. It gave them something fun to focus on and look forward to. S

Read More
A Sushi Dream Come True - Thanks to the Manitoba Restaurant and Foodservices Association

For Karmyn and her family, sushi has been an important part of her battle with a rare form of leukaemia. In fact, during her intensive chemo treatments, one of the only foods she would ask for was salmon sashimi. It’s no surprise that one of Karmyn’s biggest dreams is to visit Tokyo to sample all of the incredible sushi Japan has to offer. It’s a big dream - and one that we can now bring to life thanks to the support of the Manitoba Restaurant and Foodservices Association (MRFA).

Read More
Meet Apollo

The minute our son was born, the doctor asked us what his name would be and we said Apollo! She immediately said that it was quite the strong name to live up to. Apollo has never been a sickly child (quite the opposite!) but just before the age of 2, he started to have recurring ear infections. This continued for a while and at first we thought they were from swimming class, but when it persisted it was evident he needed ear tubes.

Read More