Bit of a background. My daughter is 16 months, has had silent reflux and failure to thrive as well as mild development delays and constant feeding issues.
We have been seeing a public paed every 3 months through a big children's hospital. She sent us to the feeding clinic/speech therapist today. They have said that she sounds like she has sensory issues to do with feeding, her hands and mouth. They will be sending info/activities to do to help her.
My question is (before I get the info letter), who has been through this, what can I do and does it get easier/better?