Hi,
Just wondering what you guys have experienced with this.
DD has a cows milk allergy and is on a fully excluded diet and on neocate.
She was on the CDA, at her review the Dr ticked the box saying she had a serious disability, but then ticked "no" to the boxes saying that she doesn't require any extra care (which I didn't notice - long story - actually think Dr made a mistake!!).
Anyway as a result she has been declined the CDA. I'm gutted!
She still reacts badly when she has anything dairy based, even the smallest amount is enough to set her up. I know this from both the last challenge and her dad giving her some ice cream

(but we wont go there!!!!!!).
She goes all lethargic and sleepy, then vomits for the next 24 hours. Her reflux kicks in and for a week she is a very unhappy girl, with a sore tummy (and the reflux). Last time - the ice cream incident, her face also broke out in hives where it touched her skin (a new reaction).
So I believe she does require extra care, in that I have to watch what she eats, by providing an exclusion diet and special foods (also watch her while she eats so she doesn't steal her brothers food) and when she either has a challenge or accidentally has some dairy she requires extra care while she is sick.
I have friends who get the CDA for lesser conditions!!
We rely on this as I am on the DPB and use the extra money to buy her neocate. Without it it's almost impossible to find the extra $$ to buy the milk

I was especially upset when they declined it, as a friend gets it who's DS has a very mild allergy as he has almost grown out of it (she even admits this!) and her DH earns over a 100K!!! And here is me struggling

I am going to take it to review, but WINZ have become very tight on all benefits and I don't like my chances. I have to get something signed by my Dr too.
Has anyone been through a review? or had any bad experiences trying to get the CDA? Any advice or help would be appreciated.
TIA
