I am about 33 weeks and have been going UP up til now but I think I may have this condition. I've looked at a few sites, and I have all of the symptons they list: constant itching of the hands, arms, feet, and soles, general unwell feeling, loss of appetite and nausea, insomnia.
Starting about a week ago I have been itching badly and I'm developing a bumpy rash on my hands, arms, legs, and neck. My itching is mainly on my arms, hands and legs and it's pretty intense, and for the last week or so I really haven't had much of an appetite. Every time I do eat I get an upset stomach afterwards {like I want to throw-up or I'm going to have diaherra} plus I've been really tender in my upper right abdomen about where the liver is located. Of course Aidan also sits on my right side and usually has his butt jammed up in my ribcage, so that could be the cause of the tenderness. I also read on one site that insomnia is common with ICP and I have had the most random sleep schedule lately. I'll sleep for about 3-4 hours then be wide awake, stay up for about 5-6, then go back to bed for another 3-4 hours. Unless I take a sleeping pill I can't stay asleep for longer than 4 hours and at this point with my dd I was sleeping 9-10 hours a night plus taking a 2-3 hour nap everyday.
And of course I read a scary statistic that says that 10% of untreated cases of ICP result in stillbirth. So now I'm really unsure what to do. Obviously I don't want to do anything that will endanger the baby, but at the same time I don't want to get thrown into the over medicalized freak out mode and do a bunch of unnecessary monitoring and the early induction that is given as pretty much the only treatment option. That is completely the opposite end of the peaceful UP/UC we have been planning, but of course the health of the baby is the most important thing.
I guess I'm trying to find out from a natural minded birth professional stand point how worried should I be about complications from this condition? Is there anything I can do on my own to minimize the chances of harm to the baby? Will getting the blood tests and NSTs every week that I read are the usual treatment actually help reduce the risks?
Sorry if I'm rambling! I have so many conflicting thoughts right now!
TIA
Starting about a week ago I have been itching badly and I'm developing a bumpy rash on my hands, arms, legs, and neck. My itching is mainly on my arms, hands and legs and it's pretty intense, and for the last week or so I really haven't had much of an appetite. Every time I do eat I get an upset stomach afterwards {like I want to throw-up or I'm going to have diaherra} plus I've been really tender in my upper right abdomen about where the liver is located. Of course Aidan also sits on my right side and usually has his butt jammed up in my ribcage, so that could be the cause of the tenderness. I also read on one site that insomnia is common with ICP and I have had the most random sleep schedule lately. I'll sleep for about 3-4 hours then be wide awake, stay up for about 5-6, then go back to bed for another 3-4 hours. Unless I take a sleeping pill I can't stay asleep for longer than 4 hours and at this point with my dd I was sleeping 9-10 hours a night plus taking a 2-3 hour nap everyday.
And of course I read a scary statistic that says that 10% of untreated cases of ICP result in stillbirth. So now I'm really unsure what to do. Obviously I don't want to do anything that will endanger the baby, but at the same time I don't want to get thrown into the over medicalized freak out mode and do a bunch of unnecessary monitoring and the early induction that is given as pretty much the only treatment option. That is completely the opposite end of the peaceful UP/UC we have been planning, but of course the health of the baby is the most important thing.
I guess I'm trying to find out from a natural minded birth professional stand point how worried should I be about complications from this condition? Is there anything I can do on my own to minimize the chances of harm to the baby? Will getting the blood tests and NSTs every week that I read are the usual treatment actually help reduce the risks?
Sorry if I'm rambling! I have so many conflicting thoughts right now!
TIA









