Thursday morning brought a snow storm to Cincinnati…not necessarily a snow storm by Michigan standards, but everyone was on edge on Ohio! It ended up being a little slippery by the late afternoon but as long as we went slow, everything was fine. Paul and I had spent hours hashing out what may happen at this appointment and making sure that the two of us were on the same page as to how we wanted things to progress. Those conversations were not easy ones..rather heart wrenching actually, but I am glad that we could present ourselves as a united front. So, the appointment did not bring any earth shattering news, but it was a very important appointment that helped everyone get onto the same page.
In a nutshell, she has continued to loose weight which now needs to stop. She NEEDED to loose the first 10 pounds but we don’t want her to loose any more so the doctors will tweak her TPN and hope to keep her weight stable. The other topic of discussion was a plan to get her off of the TPN. TPN is the IV nutrition and unfortunately it is not a long term solution as it does damage to the liver and kidneys and is a breeding ground for infections. However, the past three months were the first time in Keyan’s entire life that we did not work on advancing her intestinal feeds…and by far these past few months have been the best quality of life she has ever had. The proof is in the data! We have always said the Keyan’s body is happiest when she is not being fed, but we have never done a long term test of that and the last three months showed us quite a bit. She did have a lung infection when we increased from 7 to 8 mls an hour which could be circumstantial…although I tend not to lean that way. So, we talked at great length about what all this means and came up with a VERY SLOW plan to increase her feeds…and I mean REALLY slow. I won’t go into the details because it is a lot of medical jargon, but they have worked out some ideas to deal with her intolerance, depending on the symptoms, and we will go from there. The overall message from the docs was that while we would all love to get her off of TPN next week, her very complicated body is not going to allow that. She is in control of what happens and her body will direct our path. Furthermore the doctors stated the while TPN is by no means an ideal therapy, in some kids, it is all they have. You deal with what you have! We still have no root cause for this intestinal failure so to push forward with the same things we have been doing in the past would be negligent. None of us are willing to sacrifice the quality of life that she has right now, so that means that the plan is a work in progress. It is one that Paul and I are pleased with, and one that does in fact keep Keyan’s wellbeing in mind.
As we were leaving the hospital hours later, our minds were trying to keep everything straight and our hearts were trying to absorb the impact of the decisions that had been made when we came across a sign. It read..
“Cincinnati Children’s Medical Center has been ranked by U.S. News and World Report #1 in the nation for their Gastrointestinal department”
