- Joined
- Jun 7, 2011
- Messages
- 109
My daughter, aged 4, has a MicKey button gastrostomy stoma, and has had surgeries which stop her being sick (which mean she cannot burp too) and also to let her stomach empty faster.
She is due to start school in September, and so far through preschool she has dealt amazingly with having a stoma and a button, as she has done all her incredible little life (she's had the stoma since since she was 9 months old). She acts, understands, and feels emotionally like any other child her age, but knows she is different because of the stoma. Her preschool has only a fraction of the kids she will encounter at school and I'm so worried about how she will cope with it, and also how other children are going to respond to her, as they will see her stoma when she changes for PE each week.
She knows it's her special button and that it's special because it kept her alive, but it doesn't stop me worrying about teasing or stressful situations that may start to occur in a school, which may make her feel left out or isolated.
I know she may be a lot younger than many of the children who have/had stoma's on this site, but any advice on how you or your child dealt with it at school would be greatly appreciated. There aren't many kids her age with stoma's that aren't going to a SN school in this area so there isn't a lot of support available for us.
Thanks in advance
She is due to start school in September, and so far through preschool she has dealt amazingly with having a stoma and a button, as she has done all her incredible little life (she's had the stoma since since she was 9 months old). She acts, understands, and feels emotionally like any other child her age, but knows she is different because of the stoma. Her preschool has only a fraction of the kids she will encounter at school and I'm so worried about how she will cope with it, and also how other children are going to respond to her, as they will see her stoma when she changes for PE each week.
She knows it's her special button and that it's special because it kept her alive, but it doesn't stop me worrying about teasing or stressful situations that may start to occur in a school, which may make her feel left out or isolated.
I know she may be a lot younger than many of the children who have/had stoma's on this site, but any advice on how you or your child dealt with it at school would be greatly appreciated. There aren't many kids her age with stoma's that aren't going to a SN school in this area so there isn't a lot of support available for us.
Thanks in advance