Makayla’s Journey

After 7 and half years of testing, Makayla
was finally diagnosed with an extremely
rare genetic disorder called CTNNB1
happloinsufficiency.

Makayla is the 6th case in the entire world
and the first in North America.

After a particularly difficult year health wise, Makayla is back at McMaster for an
unknown amount of time (Day 14 so far...).
Our sweet girl is in so much pain and no one
knows why. She is currently undergoing
numerous procedures daily trying to find
answers.

As you could imagine this is an extremely
difficult and stressful time for
Fraser (mother). She is a single mother, and is the most amazing super mom to Makayla.
EVERY moment of her day is dedicated to her-24 hours a day, 7 days a week.

This Go Fund Me page is being set up for
some financial relief, so she doesn’t also have to worry how she’s going to pay her bills
while going through this most difficult time.

Prayers are welcome! ❤️
Thank you!!!