I have 3 DC, 2 with SN. When we are out it is clear that DS is disabled, (SN buggy, no clear speach at nearly 4, repetitive behaviour, wears ear defenders etc) DD is 6 and mobile but flaps, toe walks, falls often, tactile and uncoordinated.
When asked what's wrong with them. I simply say they have Special needs and are both registered disabled. Of course I much prefer people asking rather than staring but I think that's enough information. The conversation can move on from that but people seem fixated on finding out what exactly is 'wrong' with them.
People will push for more information that I'm just not comfortable with telling, partly due to them both having multiple diagnosis so it's not as simple as saying autism or SPD. It's also DCs personal information and as their parent I feel I should protect that until (and if) they are able to share it themselves. I think it makes them more vulnerable if it's common knowledge.
I see so much about autism awareness etc and that we should be raising awareness and explaining but I just can't. I wouldn't go round telling everyone about DD anaphylaxis to nuts unless it was important the situation. So can't see why I should with DCs other medical conditions.
Should I just put aside my feelings and start explaining more to help educate others about these conditions or continue and understand that we will aways be an unknown to others wanting to understand our situation.