of our Baby Boy. We had our big U/S today and instead of walking out on clouds I am now on pins and needles while I wait the results of a quad screen. And then we go from there if it is nothing they will monitor it and if I don't know what we go to a specialist.
Re: There is a Cyst on the Brain
I am so sorry, I will be thinking of you and hoping everything turns out okay. ::HUGS::
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It can and that is what we will find out on Friday after the result from my quad screen. YES I am so pissed that my Ob talked me out of it earlier in the pregnancy. I am so unsure what my OB means when if the results comeback bad that I have to to the M? specialist ( I was so overwhelmed that I did hear all the letters).
If the results comeback okay, we will monitor it through u/s the rest of the pregnancy.
I guess right now, I am on pins and needles waiting to hear back.
T&P that its something that can resolve itself and that yor Baby Boy will be fine. I'm so sorry you guys are going through this right now. (((hugs)))
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I am so sorry, waiting for the results must feel like forever. ((Hugs)). My T&P will be with you and your LO.
Can you recall if they said it was a choroid plexus cyst?
If so, then we've just been through a very similar experience. Our baby has an echogenic intracardiac focus (EIF) -- a bright spot in her heart on ultrasound that is also one of the common "soft markers" for chromosomal issues like Down Syndrome.
My understanding is that, on their own, these "soft markers" can be present in a small percentage (but significant number) of normal babies & aren't necessarily anything to panic about (easier said than done, right?). Part of the problem when trying to figure out how significant these things are is that these markers have mostly been studied in women/babies who are already labelled as "high risk" (meaning they have other reasons to suspect a problem). So a lot of the research/info. you're going to find is in a skewed population & can make things look a lot worse than they really are.
While I was looking up research on our baby's findings, I came across this website, which may be of some help:
https://choroidplexuscyst.org/
But keep in mind that the research may be misleading & I'd take everything with a grain of salt until you can ask your doctor(s) more questions.
The specialist they're going to send you to is called an MFM doctor = Maternal Fetal Medicine. They will likely do a more detailed (level 2) ultrasound with a better machine just to redo all of your son's measurements, recheck on the cyst, & make sure they're not seeing anything else of concern. They can also give you the option of doing an amnio at that point to find out for sure what's going on. In your case, the results of your quad screen should really help to put the u/s findings in perspective (we didn't have one, either, so it was less clear if there was anything else going on), but they can only tell you for sure if there's a chromosomal defect by doing the amnio.
I'm sorry this is so long, but I just had my MFM appointment yesterday (see post below) & wanted to give you an idea of what to maybe expect! I really hope that the cyst resolves itself & isn't an indication of anything more serious. I know this is going to sound impossible, but try your best to stay relaxed until your MFM appointment.
((BIG HUGS)) & best wishes for good news on the way.
My baby has this, too. The doc explained that the cysts themselves are perfectly harmless and don't have any effect on functioning, personality, or memory. She said they do usually resolve themselves, and that they alone are not a reason to worry. She is an MFM doc, too, since my doc doesn't do those screenings. My blooodwork came back fine, and there were no other markers for any chromosomal issues, so she said the cysts are probably just an anomoly. I go back for another ultrasound in a few weeks to cehck amniotic fluid levels and the doc said the cysts will most likely be gone by then.
I know how scary it is to hear those words, but try not to panic! Sending good thoughts your way.
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(((((HUGS)))))
I'm so sorry you guys are going through this, I can't imagine how scary it must be.
Fingers, toes, and everything else crossed that everything turns out just fine.
If it makes you feel any better I was born with a cyst right near my spinal cord in my brain. It's still there and I'm fine. The neurologist noted it on my records during a migraine work-up and said that I would have lived my whole life and never knew it was there. He stated he saw it was found in utero but has not moved, changed or impeded my life at all.
T&P that everything is fine!
The quad screen will basically give you odds on a couple of diseases/disorders. If I remember correctly, it gives you odds on Cystic Fibrosis, Down's and Trisomy 18. If your odds are within normal range, you'll get a "negative" result. If they're not, then you'll get a "positive." Be aware though that they do have a false positive issue (my doc said 5-10% get false positives), so they're not infallible. They also have a false negative issue, though it may be less. My Mayo Clinic book mentioned it, but didn't give statistics. However,it's basically a (mostly) non-invasive test to help figure out if you might need a more invasive one (amnio).
I'm sorry you're going through this. It has to be really scary. I have read that a lot of these are simply soft markers for disorders and go away prior to birth, so hopefully yours is one of those. Big ((((hugs)))) and T&Ps for you and your LO.
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I am sorry. I hope that this turns out to be nothing serious. I will be praying for your baby boy. Lots of (((((HUGS)))))