tat and have read the whole thread. I also said a few pages back that it was not about who it was harder for. I am not having a go, I have asked over and over again what information people want but am yet to really see an answer to that question really. Lots of information is available from our health board if you ask. Same with BF info, it is there if you ask.
We're not talking about that. We're talking about information given to FF mums by HVs and MWs being restricted to only being given when asked and also the information is very basic (ie: not being able to recommend a certain type for a refluxy baby etc).
Not everyone has access to the internet to look at health boards and forums. Not everyone is able to purchase pregnancy and baby books. Not everyone is able to access antenatal classes (for example, I couldnt make the NHS ones and couldnt make the NCT ones, some people cant afford the NCT ones).
The basic point of this thread is mothers who FF only can access advice re: FF when they ASK. And also HVs and MWs are restricted in the info they can give. Im aware not all trusts are the same and some do give info leaflets to pregnant women etc without asking. I never got any info on FF but had plenty of BF leaflets given to me. But in general, the restriction of information is there
And that restriction is discriminatory and prejudiced against those who FF.
People have answered what info FF mums need quite clearly actually as you would see from previous posts.
Info on making up bottles correctly and storing bottles are vitally important as if done incorrectly it can be harmful to babies. Yes it is on the back of the tin but imagine a mum whose own mother FF her. Back then, her mum could make up the entire days bottles.
The new mum may ask her mum about bottle making and think making 12-14 hours worth of bottles is ok and choose to ignore the tin because she trusts her mother's advice...when it isnt ok at all!
Like I said, we're not asking for promotions, for workshops, peer support workers or anything like that. But to be able to access the basic information regarding FF from the HCPs that guide us through pregnancy and early childhood surely is an unreasonable ask? To restrict information is not only potentially dangerous to those who may not comprehend the new guidance for FF but also unfair and prejudiced against those who FF. I think its the principle of the matter.