Stef
Mummy to Olivia & PG #2
- Joined
- Jan 23, 2007
- Messages
- 6,321
- Reaction score
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TJW - Im so sorry to hear about the situation with SD
I havent been on much myself. Im feeling really sensitive at the moment, DD is being a nightmare with her behavior, feel like im constantly shouting at her for the same things every day. I feel like im generally being a crappy mum and also feel like im struggling to cope. I dont feel as though I am enjoying the time I have with Isla because im constantly on at Olivia.
I had the results of Isla's heel prick this week, she too like my first daughter is a carrier of an unknown hb type. When Olivia's came back with this they recommended blood tests etc to determine what it was only when I got there they decided not to follow it up. Im now feeling really angry at this. I know I should be thankful that both my children are carriers rather than affected by this unknown hb type but how (and I know its gona be a fair few years yet) do you tell your children there is a chance if they have children they could be disabled. They have given me a number for somebody at the hospital to contact to try and get more info so im going to do that this week.
I hate being in the house at the moment, but I also hate going out, but I need some form of distraction, i dont know what from. Perhaps from how my home life really is.
I havent been on much myself. Im feeling really sensitive at the moment, DD is being a nightmare with her behavior, feel like im constantly shouting at her for the same things every day. I feel like im generally being a crappy mum and also feel like im struggling to cope. I dont feel as though I am enjoying the time I have with Isla because im constantly on at Olivia.
I had the results of Isla's heel prick this week, she too like my first daughter is a carrier of an unknown hb type. When Olivia's came back with this they recommended blood tests etc to determine what it was only when I got there they decided not to follow it up. Im now feeling really angry at this. I know I should be thankful that both my children are carriers rather than affected by this unknown hb type but how (and I know its gona be a fair few years yet) do you tell your children there is a chance if they have children they could be disabled. They have given me a number for somebody at the hospital to contact to try and get more info so im going to do that this week.
I hate being in the house at the moment, but I also hate going out, but I need some form of distraction, i dont know what from. Perhaps from how my home life really is.