Guest guest Posted November 4, 2001 Report Share Posted November 4, 2001 I know what you mean about the drs. poo-pooing what we tell them about the diet and it's effects on our children. I have made it my mission to let every doctor we come in contact with know that the diet has made the most significant improvement in our daughter's PDD. Maybe if they hear it enough times... I told the pedi neuro last week when I took my younger son there. He knew about the diet and even said to continue it for my NT son who has had seizures. That gives me hope. I will be interested to hear what the allergist says re. diet. In Jan. when we saw him for a peanut allergy(also pre PDD dx)he seemed skeptical about diet impacting anything! I will give him an earful this time. (-: BTW this same allergist said my daughter didn't need an epipen for her peanut allergy (a 4) bc since she had come in contact with it via cross cont. and had not had a anaphylactic rxn, she would be fine. She reacted with red, swollen face after I wiped peanut butter off the knife before putting it in the jelly to make her a jelly sandwich. She has always refused pnt butter. Our bodies know, don't they!? That just goes to show you that cross contam. is a real issue. I had every visible speck of pnt butter off the knife. Now that we know about her peanut allergy, we don't keep it in the house. Unfortunately I like cashew, almond, etc.. butter much better!!! I find the fact that she " doesn't need " an epipen to be questionable, esp considering what I have learned about repeated exposure. I will tell him I want a prescription this time, no matter what, but just curious if any of you have a child with level 4 peanut allergy and " 2 tsp of benedryl " will suffice it in the case of ingestion? Janelle Quote Link to comment Share on other sites More sharing options...
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