So excited that we have finally managed to get an appointment for my poor DS (5yrs)who has had atopic dermatitis since birth. He was begrudgingly referred to paedderm at hospital last year but we have only seen her once and she barely checked him over. Very blasé about it all, and pretty much spoke down to us saying parents were always worried about steroids , etc and that it’s incurable but we have to manage it. 🙁
Asked about wet wrapping and she sort of sniggered with the eczema nurse and similar when we asked about allergy testing.🤨
She just whacked a few more steroids on prescription and wrote a letter to gp saying what happened and sent us on our way. In the letter it said to contact them if we needed anything meanwhile.
After about 3 months of aggressive ezcema flares 2 does of antibiotics and no sleep we finally decided go go private and managed to get a remote consultation with this dr. It cost and arm and a leg even though some of it will be paid for thru DH a work health insurance .
Please tell me things will get better , feel like this is out last resort now to help poor little DS have some sort of life back😔