Oh vacation, how I have missed you so. Our family had a great time visiting family in Connecticut, playing in Bar Harbor, Maine and exploring Boston between doctor appointments. Here are some of our highlights:
Boating in Connecticut. Zack’s first time on a fishing/lobster boat and he loved it! He was a man of many questions and is forever bonded with Captain Don.
Bar Harbor adventures. Jim, Zack and I took a 4 hour sea kayaking tour. See those islands in the picture above? We paddled to the third and took a break. Then we went around the third and back into shore. We saw some porpoises and bald eagles. Happily, we did not see any of the sharks that also inhabit the harbor because that would have freaked me out.
We rode the carriage trails in Acadia National Park on bikes. We ate popovers at Jordan Pond, frolicked on Sand Beach, drove around the entire island and shopped and ate and had a grand old time. Zack and I also went on a date on Diver Ed’s boat. Diver Ed scuba dives into the harbor and videos the ocean floor as he goes. The video is broadcast on board. Then he comes up with some of the creatures he finds down there and the kids get to touch them all before releasing them back to the ocean. Zack was so enthralled with the whole thing until the touching part. He finally worked up the nerve to touch a few things. Can you tell how hard it was for him to do it?
After a week of fun, we headed to Boston to see Zack’s doctors. First we met with Zack’s surgeon. It was strange to see her in a new hospital, but she was as awesome as ever.
While Zack is currently doing better than he has in years, we still have some concerns. You may have noticed that I have been talking about how his stoma has been swelling which constricts his output during the day and then goes back to normal when he rests. His surgeon and doctor here both feel he is prolapsing internally. One thought is that where his stoma was stitched down internally actually worked this time, but his intestines before that point internally are still trying to get out. We think they are getting stuck at that point, cutting off the flow. Thankfully things have been resolving well so far, but it is not supposed to be happening. We have a plan in place now for IF things go wonky.
Today we met with one of the leading pediatric motility experts in the nation. He asked us lots of questions. He said that Zack’s case is interesting because there is a lot going on that does not make sense….yet. He is hopeful he can figure out what is happening with Zack. He did say that just because Zack’s small intestine manometry test was normal does not mean his small intestine is functioning normally, just that things are being pushed through. We talked about Zack’s biopsies that showed eosinophilic ganglionitis, the possibility of autoimmune issues and other things, but he wants to review all biopsy slides, testing, fluoroscopies, manometries, CT Scans…basically everything that has already been done…for himself before giving his opinion. Jim and I appreciate that and think it is a good idea. Of course, Zack’s files from both Cincinnati and Walter Reed are so incredibly large that it will take some time for him to get through it all.
The doctor said that there are several drugs we can try to help slow down Zack’s output. He wanted to talk to his surgeon about a few things first, so we do not have a plan for that yet either. Even though we left without a plan, Jim and I felt that he was very thorough and we really appreciate that he wants to understand why Zack’s body is behaving this way. Why does he have secretory diarrhea? Why doesn’t his colon work? Is there also a problem with his small bowel? All questions his other doctors have asked before and have not been able to answer. Somehow I feel good about his method of investigation and have hope that perhaps he will be able to narrow things down a bit more. It is good to have hope.
While we were in Boston we were able to connect with some of dear friends that we had not seen since 2011. We spent a great day at their home catching up. Why do we wait so long to do these things? Oh yeah…intestines. We were also able to see a friend from our time in Minot. Her daughter has been in the PICU since DECEMBER! December people! I am happy to say that her daughter is getting close to getting out of the PICU and to finally going home. It is amazing to see her faith and strength. It was a blessing to me to be able to spend the evening with her.
So there you have it, an exceptionally long update. We are so thankful for our vacation and our time in Boston. We are thankful that we had a fun time as a family. We are happy that we were able to come to Boston for a non-urgent visit. We are happy to have scoped out the area, found a hotel close to the hospital and to know we have friends close by. While we did not have time to see all of our friends here, we know we will be back! Until then…