Hi Anna,
I'm sorry to hear that you're going through this. It might be nothing, but it's a worry you don't need! I don't really know anything about "protein in the blood", except what I've read about screening tests, but I imagine it's the same thing - that they picked it up during your elected screening for Downs/spina bifida? I refused these tests because they cannot tell you anything definite and can lead to unecessary worry (like you're experiencing now).
What you probably had a couple of weeks ago is the Alphafeto protein (AFP) test, which measures the amount of alphafeto protein (AFP) in your blood. This is the simplest way of screening large numbers of women for markers of spina bifida. If the level of AFP in your blood is
very high, this COULD "indicate" that your baby has spina bifida or anencephaly. This means that even if VERY high, it still does not tell for sure whether your baby has spina bifida. Also, it sounds like the AFP in your blood is not very high, so chances are, everything will be fine.
Here's something I picked up from the internet:
'Always remember that screening tests are
not very reliable. There are a number of factors which could influence their accuracy. For example:
If you are outside the 16-18 weeks optimum testing time
If you are very overweight or very underweight
If you are Afro-Caribbean
If you are pregnant with twins
If you have diabetes which is controlled by insulin injections
If you have recently had any vaginal bleeding
Anna, the last point would certainly apply to you. No matter what we say on here to try and reassure you, you are still (naturally) going to worry. The reason that they're probably making you wait a bit for your scan is that a detailed, anomaly scan is best performed around 19-20 weeks. Look on the bright side (even if it's only a slither of brightness right now) - at least you'll get to see your baby again next week
I hope everything goes okay, I'm sure it will. Let us know how you are.
Love,
Wendy
xxx