I apologised for replying to the thread from just the title, in one of my previous posts.
It is because time and time again on here, I find myself having to explain in full, hurtful detail just how it felt to give birth to my SB baby boy because of CP.
It stuns me that people can be so ignorant about how dangerous CP can be, probably because given my family history (Great Nan having chemo for ovarian cancer when I was 4/5, Great Aunt dying of breast cancer after chemo when I was 7/8, Nan having breast cancer and chemo when I was 10/11, Cousin having kidney transplant when I was 12/13, me being hospitalised with CP when I had it for the third time at 14, me losing my baby, my DS2 being immunocompromised by his prednisolone for his severe asthma, my DD 's friend having chemo for leukaemia), it has just ALWAYS seemed like a severe illness to me.
I appreciate that not everyone has had the experiences that I have had which makes me more aware than most about just how severe an illness CP can be, but when it is the 15th time in a year you have had to bare your soul to try to get people to understand just how important it is to keep a child with CP indoors until they are completely crusted over, every last spot, on here, occasionally you do just jump in feet first and respond to the thread title.
Which I accept is unfair on an OP who is just looking for information. But when the thread is also in AIBU rather than _Chat, or General Health, or Children's Health, I tend to get a bit
that anyone has to ask if they are being unreasonable, rather than asking politely in another section what the risks to their child and to others might be from taking a DC with still-infectious CP might be.
I think the way that the question was posed hot my back up a bit, for that I apologise, OP.