Peridot Kids

My August babes and their issues: ear tubes, laryngeal cleft, MSPI, cyclic vomiting syndrome and a congenital heart defect. Join us for the ride of tears and joy.

Tomorrow is the day October 8, 2008

Tomorrow we go back to Boston to find out if Jennifer’s surgery was a success.  She will have her post op swallow study.  It will have been almost 3 months since her surgery.  (I think it will end up being 2 months and 3 weeks to be exact).  

I’m nervously excited about it.  She’s been on thin liquids since this post and is doing well. She does still cough but more as a protection than choking like before the surgery.  And it is pretty infrequent.  I really do think the study will still show some penetration into her windpipe but no real aspiration.  I think when the penetration happens is when she coughs.  This is a huge step for her as it means that her body has started to recognize that fluids are coming there and triggers her cough reflex.  I *think* if this is all that’s happening then they will clear her to stay on thin liquids.  As long as there is no aspiration.

Another exciting thing about going tomorrow is that I will get to meet one of my online friends that has a kiddo with aspiration too!!  She found me through this blog and we have been emailing for a few months now.  Her daughter is today going for a G tube placement and to be scoped to see if she also has a laryngeal cleft.  Please say a prayer for them today.