we have just been told our DD (2 + 2 months) has CMA. I was wanting some advice from other parents like us, as the doctor who "diagnosed" her doesn't seem to know much about it.
she has only been tested for lactose intolerence which came back as "some significance" only to be told the test was pointless in her case. doctor doesn't want to test for anything else, but has told us to treat her for CMA and we are being refered to a nutritionalist.
Im a bit wary of cutting a large part of her diet out without a test backing it up. is it normal to not be tested?
any info on diagnosis and early treatment would be a great help to us.
thanks!