To see Maëlys grow up
Hello everyone,
We are launching this fund to support Maëlys’ parents and give them a little hope.
For those who don’t yet know her story, Maëlys is a little doll born on 24 April 2021 to her parents Alizée and Guillaume.
After 3 months and her first epileptic seizure, her parents realised that things were not going to be a smooth ride: they learned that Maëlys had multiple disabilities with neurodevelopmental disorders and was still awaiting a genetic diagnosis.
Alizée and Guillaume’s long battle began with many sleepless nights full of anxiety, severe epileptic seizures and frequent hospital stays.
Maëlys needed a lot of attention and care, so her parents had to organise full-time care for her. Her mum gave up her job to devote herself 1,000% to her little girl.
At almost 21 months old, Maëlys still has no autonomy: she can’t hold her head, can’t sit up, is fed through a nasogastric tube… yet her body is continuing to develop and daily life is becoming increasingly difficult without suitable equipment.
So even if money isn’t everything, a small gesture will be PRECIOUS to help her parents feel SUPPORTED and to help them finance the many appliances and therapies necessary for Maëlys’ development.
Funding for psychomotor therapy sessions, self-help courses and adapted seats are just a few examples of the many PRIMARY needs for Maëlys’ healthy development.
Your help will be most welcome in the extraordinary struggle of this ordinary family who deserve all our support.
We also invite you to share this fund with others.
Hello everyone,
We are launching this fund to support Maëlys’ parents and give them a little hope.
For those who don’t yet know her story, Maëlys is a little doll born on 24 April 2021 to her parents Alizée and Guillaume.
After 3 months and her first epileptic seizure, her parents realised that things were not going to be a smooth ride: they learned that Maëlys had multiple disabilities with neurodevelopmental disorders and was still awaiting a genetic diagnosis.
Alizée and Guillaume’s long battle began with many sleepless nights full of anxiety, severe epileptic seizures and frequent hospital stays.
Maëlys needed a lot of attention and care, so her parents had to organise full-time care for her. Her mum gave up her job to devote herself 1,000% to her little girl.
At almost 21 months old, Maëlys still has no autonomy: she can’t hold her head, can’t sit up, is fed through a nasogastric tube… yet her body is continuing to develop and daily life is becoming increasingly difficult without suitable equipment.
So even if money isn’t everything, a small gesture will be PRECIOUS to help her parents feel SUPPORTED and to help them finance the many appliances and therapies necessary for Maëlys’ development.
Funding for psychomotor therapy sessions, self-help courses and adapted seats are just a few examples of the many PRIMARY needs for Maëlys’ healthy development.
Your help will be most welcome in the extraordinary struggle of this ordinary family who deserve all our support.
We also invite you to share this fund with others.