Ben is HAPPY to be THREE!
Monday, April 4, 2005
Sunday, February 20, 2005
Make A Wish
February 2005
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On February 6th, the Orton Family left for Walt Disney World. We were picked up in a stretch white limosuine that took us to the airport. From there we caught our plane to Orlando, FL. We were met by a "Give Kids The World" volunteer. (only wish kids are able to stay at GKTW) He collected our luggage, brought us to our rental van, gave us directions to GKTW and sent us on our way. We stayed for a total of 10 days and were able to take in many sites and attractions. GKTW in itself was like it's own theme park. They had a huge movie theatre, mini-golf, a merry-go-round, ice cream parlor, face painting, Disney characters that came to the village special to see the wish kids and much more. We visited EPCOT, MGM, Magic Kingdom, Sea World, Universal, Adventure Islands and of course Ben's grandparents who were staying in Tampa, FL at the time. It was an unbelievable, unforgettable and magical trip of a lifetime! We want to thank our wish volunteers, Maureen and Kim, who made it possible. We love you
Sunday, January 30, 2005
January 2005 PICU Stay
What a crazy month January was. We were scheduled to leave on the 6th for Ben's "Make A Wish" trip to Disney World. The kids were SO excited! Unfortuanately Ben got sick on the 4th - two days before we were to leave. I still had great hopes that we would make it home in time to leave. (wishful thinking) I took Ben to the local ER like I always do and there they did all the regular tests and blood work before calling for DHART to come pick him up. On the way to Dartmouth, Ben got worse and they ended up putting him on the vent to rest him until he arrived in the PICU. There we found out that he had pseudomonas - something he probably is colonized with - but when his immune system is compromized, it can infect him and make him really sick. He actually looked really good for being so sick. The doctor's tried to wean him off the vent the next day so that he could fight this on his own but Ben would have no part of that. He was on a small amount of pressure support, just enough to make life a little easier while coasting through his illness. He had IV access for ceftazidine which they treated him with for 14 days. For some reason, we couldn't wean Ben off the vent. After the first week the doctor's began thinking that maybe Ben's brain was deteriorating and shutting down slowly. All his numbers continued to get lower and lower the longer he was on the vent. He was hypothermic, had bradycardia, low blood pressure and his CO2 levels were really low as well. I had my hunch that the vent was causing all of this and not his brain. After 3 weeks there I wanted them to push him more and get him off the vent so that he could bring up all his numbers. That is exactly what they did and sure enough his numbers came back to normal. We were prepared to go on his wish trip with a vent - which we were trained on - but thank goodness that did not have to happen. We were so happy. After 23 days, Ben went home!
Friday, October 15, 2004
2004 Surgery
October brought yet another surgery to Ben's history. (sigh....) Dr. Moen is Ben's orthopedic doctor and when we went for our annual visit in August, she decided that the time had come for Ben to have some release and lengthening done on his muscles because they had become so contracted. We actually tried botox first, but it never really worked for Ben. As you can see above, Ben's legs were placed in removable casts so that we could watch his skin carefully. (he has very sensitive skin) His feet were actually casted from his knees down. Ben spent a total of four days in the PICU where he recovered marginally. He had his usual post-operative respiratory issues but other than that he did fine. They had him weaned down from morphine for the pain to just tylenol. The doctor had us do a few trial hours of getting him out of bed and into his chair to make sure the pain wasn't too bad. He passed with flying colors.
Wednesday, August 4, 2004
Trach Change
Every two weeks I used to take Benjamin up to Dartmouth to get his trach changed. Laura Cogswell would usually changes Ben's trach although Dr. Gosselin, Ben's ENT doctor occasionally would do it too. The reason we had it changed up at Dartmouth and not at home is because since he has a cuffed trach it is much more difficult to pull it out and to put it in and usually causes a good amount of bleeding. These changes use to cause Ben to have some major coughing spasms but now they spray lidocaine into his airway before the change to prevent these spasms. These pictures are from a visit in May of 2004 when both Laura and Dr. Gosselin did it together.
Sunday, April 4, 2004
Sunday, August 10, 2003
Sunday, July 20, 2003
Summer Surgeries 2003
Summer of 2003, Ben had two major surgeries. The first one was performed in June by a pediatric surgeon, Dr. Latchaw. The name of the surgery was a "Fundoplication" or Nissan wrap. This is where they take the top of your stomach and wrap it tightly around your esophagus so that the food in your stomach won't "reflux" or travel back up the esophagus into your mouth. This surgery was done to prevent Ben from aspirating food into his lungs. He stayed 8 days in the PICU at Dartmouth and recovered quite nicely from the surgery. The only drawback was that his swallowing capabilities were changed and so when his secretions would pool in the back of the throat he would start coughing, choking and turning blue. We tried so hard to fix this problem but in the end, the only thing that helped was to have a "Tracheotomy" done.
Friday, April 4, 2003
First Birthday
April 2003 was such a milestone for us. I just kept thinking that if we could make it to his first birthday that everything from there on out would be okay. Well, Steve and I planned this really big party with all our friends and family that have been so monumental in our lives and wouldn't you know that the night before his big day Ben catches RSV. I remember not having such a great feeling the night before because his oxygen levels were slowly dropping and by morning they were around 83%. I packed our bags and headed to the local ER where they then prepared to have us transported to Dartmouth by the DHART team. This was Ben's second go around with RSV and it was worse than the first time. We spent a total of 11 days in the PICU that time and it was eerily similar to exactly a year before when he was born. We spent the same exact days in the ICN there, the 5th through the 15th of April two years in a row.
Tuesday, March 4, 2003
Benjamin's First Year
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