A network to share best practices for children with special needs
My grandson is disabled. I came in contact with a co-worker in another country via our web page at work who has a disabled child and we have been sharing stories, heartaches, difficulties.
I don't have the details but she was mentioning feeding times are terrible. He only eats about 5 things and apparently makes a terrible mess with each meal, he is about 2 1/2 years old.
I told her I thought there were or should be Internet groups of parents with disabled children helping other parents?
Is this a place for her to get some tips, ideas? She has been to the "experts" who have apparently not thought it was "as bad as she thinks" and not offered much in the way of solutions.
I wanted to find out who, what, how, this site works before giving her the false hope that there is such an Internet site where she might get some tips, ideas, on feeding problems with a disabled child.
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Corrine: You are a wonderful source of support for this mom. You don't mention this child's specific diagnosis. Is it possible he has some type of sensory processing disorder? Many children who have issues like this are super sensitive to touch, textures, sound (even crunching something in their mouth may be very loud for them) and smell. If this is the case, then I would hope that her local team of "experts" that you mentioned might or should include an Occupational Therapist and/ or Speech/Language Pathologist that could at least give some home program recommendations to work on these types of sensory over responsiveness issues. In addition to Tobi's creative ideas, I might also suggest a book called Just Take A Bite that may give some additional suggestions. I hope this information is helpful and please give her our best wishes for success!
Corrine: You are a wonderful source of support for this mom. You don't mention this child's specific diagnosis. Is it possible he has some type of sensory processing disorder? Many children who have issues like this are super sensitive to touch, textures, sound (even crunching something in their mouth may be very loud for them) and smell. If this is the case, then I would hope that her local team of "experts" that you mentioned might or should include an Occupational Therapist and/ or Speech/Language Pathologist that could at least give some home program recommendations to work on these types of sensory over responsiveness issues. In addition to Tobi's creative ideas, I might also suggest a book called Just Take A Bite that may give some additional suggestions. I hope this information is helpful and please give her our best wishes for success!
Corrine, Cecilia is right. YOU have already done so much by being a good listener. Thanks for being a Grandma that is involved in such a positive way and welcome to the network! As Tobi is suggesting, when a child is not eating or has difficulty eating...it is the most primally distressing things to a mother. In our hearts we internally biologically know that this is our first job with our child. Millions of years can not undo instinct. No matter what any physician reassures us with!
Also, please know that there is no such thing as false hope! At 2 and 1/2 years, there is so much your grandson will teach you. Cecilia is correct in suggesting that there is so much that can be accomplished using a sensory approach to feeding. Let us know your grandson's diagnosis. If his Mom has time to join our network, it may be useful and encouraging for her, too. Welcome!
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