My little boy is 8 weeks old and was put on Aptamil Pepti 1 at around 4 weeks old because of suspected CMPA, mainly due to a persistent nappy rash and frequent poos. It was never formally confirmed that he had CMPA.
His symptoms did seem to improve on Pepti, particularly the rash and diarrhoea, but we’ve since had a lot of issues with reflux, spit-up, wind and constipation, especially since introducing Gaviscon. I’m finding it difficult to know whether these symptoms are related to CMPA, reflux, the formula itself or just normal baby behaviour.
I’m wondering whether he ever actually had CMPA in the first place, and I’d really like to establish this rather than keep him on specialised formula unnecessarily.
Has anyone else had a baby with suspected (rather than confirmed) CMPA and done a milk challenge by reintroducing standard formula to see whether symptoms returned?
I’d particularly love to hear from people who:
- Were prescribed Pepti or another extensively hydrolysed formula based on symptoms alone.
- Did a reintroduction challenge to confirm or rule out CMPA.
- Found out their baby didn’t actually have CMPA and successfully returned to normal formula.
- Or tried a challenge and found their baby’s symptoms did return.
What symptoms originally made you suspect CMPA, how did you go about confirming or ruling it out, and what was your experience when you reintroduced normal formula?
I’m not looking for medical advice on how to do the challenge, as I’ll discuss that with our GP/dietitian. I would just really appreciate hearing other people’s experiences, particularly with babies who were diagnosed based on suspected symptoms rather than a confirmed allergy. ❤️