thanks for all your support. It means a lot right now. So far still no AF, so testing tomorrow AM, although not very hopeful so I am using a dollar store test (peeing in a cup in case I need to use a different test).
I caved the need to pee on something tonight. so I peed on an OPK, completely stark white. I have no feelings about it because I know that doesn't mean anything. I just need to pee on SOMETHING! So it worked to help with that crave.
I am having a tiny bit of cramping, but doesn't feel like AF really. Some seconds I am like total AF, why am I testing and at other times I am like happy I am testing.
Well today the doc called again (calls from the doc = bad news, no call = good news). We took genetic testing to make sure we wont produce a baby with an awful life threatening disease (we didn't do testing to find out eye color or anything like that). Well DH's tests came back (still waiting for mine, so doesn't mean a whole lot with out my genetics involved) but we found out he is a carrier for spinal muscular atrophy. Which means if I am negative then there is a 50% chance our kids will be carriers (which isn't a big deal, they will just want to do genetic testing when they have kids). If I am a carrier then we have a 25% chance our kid will have it (and it means the kid will die as an infant). So we are crossing our fingers I am not a carrier. So I am not freaked out until my testing comes back. Some of you might be wondering why we even bothered with genetics, but apparently Jewish decent are known to be carriers for the most amount of life threatening disease... and I am Jewish. So we wanted to make sure.
Kyla enjoy your trip!!!!! I will be testing around 8am (mountain time) tomorrow and will post ASAP the results. so hopefully you will be clued in before you leave.