I know I haven’t written in awhile.  This little one in my belly is causing a  severe case of lethargy and a mild case of nausea.  The dishes don’t get done every day as they usually do, the laundry has been known to sit on the couch an extra day before being folded, and the kids have been loving chicken nuggets.  Thank goodness they like veggies and salad!

Life has been humming along.  As of last week I have begun my many doctor visits.  I had my normal ob visit and my first with the perinatalogist.  We talked about what the protocol will be for my treatment.  He said somethings have changed in the last 3 1/2 years.  I will probably only have to have one cordosyntesis at 32 weeks instead of one also around 20-24 weeks.  That brought a smile to my face because that procedure freaks me out.  I knew NAIT was rare, however I don’t think it really sank in.  He told me he has treated 6 women with this in the last 20 years, and 3 of those were while he was at university!  He is supposed to be a specialist too!  It hit me how rare this really is.  I was reading some material from a yahoo group I am a part of.  Not until the mid/late 80’s was there much successful work done on this condition.  Reading the reports was very sobering.  I didn’t realize how new this treatment and recognition of NAIT is.  Just one generation back and I would only have one child with my other kids dying soon after birth.  I couldn’t imagine my life without a house full of kids.

On a lighter note, I will be having “the” ultrasound on January 7th along with the usual appointment.  I have to go back on the 8th for my visit with the perinatologist.  We are going to nail down the exact protocol.  We are pretty sure what it will be but he wants to check the medical journals so he has the most updated info.  Also I started feeling a little bean movement at the end of week 16 (about a week and half ago)!