French mother of 3 children, my life took a turnover when my daughter Alexia was diagnosed with Smith magenis Syndrome in 2010 when she was 15 months old.
Part of this genetic disorder is that you have to deal with speech and motor delay,severe sleep issues and behaviour problems like head banging. To improve my daughter's life and the whole family's, I've been looking for affordable and easy products since she was diagnosed.
I've now decided to share all of what I've found for the past few years through my society "Sweet Home Alexia", a society that knows your needs coz she daily lives with the same problems !!!