Hunter Thomas Reeve was born on March 12, 2009 at 2:38 in the morning at St. Thomas Elgin General Hospital. Hunter weighed 6 pounds and was four weeks early but appeared to be a healthy baby boy.Although Hunter was eating well he was steadily losing weight. Three days after his birth Hunter was released from the hospital and made the trip home. Due to the weight loss Hunter was brought back to the St. Thomas hospital and after a series of tests it was found that Hunter was severely dehydrated. An IV line was started in the top of Hunter’s head because he was too dehydrated for the nurses to find veins anywhere else in his body.Hunter was rushed by ambulance to the Children’s Hospital in London, where he stayed on the IV while doctors and nurses diligently tried to determine what was causing the dehydration. By this time Hunter was down to almost four pounds and struggling to stay alive. Hunter fought hard (even managing to rip out the lines that the nurses kept putting in) and was stabilized thanks to the staff in the Pediatric Critical Care Unit. Without their care Hunter would not have lived through the night.After exhausting all of the non invasive tests, doctors from many specialty units were brought in to try and find out what was causing Hunter’s illness. Dr. Bax of the Pediatric Gastroenterology team was brought in, and in Hunter’s first week of life, he had his first surgery. A sample of Hunter’s small intestine was obtained through a biopsy and sent off for analysis. This is a rare procedure to have done on a baby and is not part of routine testing. Miraculously enough, this procedure determined the cause of Hunter’s decline: his small intestine was not absorbing any nutrients from his food. In fact, Hunter was outputting more than he was taking in.Hunter was diagnosed with an extremely rare and potentially life threatening disease of his intestines called Microvillus Inclusion Disease (MID). This disease prevents Hunter from absorbing any nutrients through his small intestine making him completely dependent on Total Parenteral Nutrition (TPN). TPN is very hard on Hunter’s liver but the only other option is a small intestine transplant.At first it seemed like a very grim prognosis as the complications with transplant are many. But there is hope: an experimental treatment called Omegaven. Omegaven couples Omega 3 fatty acids with TPN which greatly reduces the risk of liver damage and may assist in its repair. Unfortunately, Omegaven is not currently covered by the Ontario Health Insurance Plan (OHIP) or independent insurance companies.This disease only affects one in five million people. Hunter is the twelfth known person suffering from this disorder in North America right now. Currently there is no cure for Microvillus Inclusion Disease. Hunter needs constant medical care and the cost can be overwhelming to a family. There is very little coverage for in home support for families battling MID; as this disease is rare it is not typically covered by OHIP. Although Hunter’s Omegaven is currently being paid for it is unknown how long it will remain covered and what challenges this little boy will face in the future. Because MID is such a rare disease more research is needed to find other treatment options that are not as detrimental to the health of those affected. Hopefully someday this research will lead to a cure. Hunter needs your help to stay home. With your support we hope to make this dream a reality. Please help – because every baby deserves to grow up.

Wednesday, March 31, 2010

More Milestones!

Hunter took his first couple of steps yesterday..and he seems to want to keep the momentum going today!!!! He doesn't really seem to care that he's doing it.....he looks at us like "what's the big deal"! I can't wait to see him full out walking...it seems that all of my friends kids who walk have a distinct character walk..for example...one little guy does the "Bill Cosby" and the other does "Ed Grimley"...it's hilarious...I can't wait to see what Hunter's character will be!!

Hunter is up to 19lbs 10oz and his blood work is back to being perfect...we are going to try him with 7 hours off of his TPN tomorrow...a nurse will come and check his blood sugar level when we lock him off and then again just before hooking him back up 7 hours later to see if his body can sustain the additional hour. I can't wait since he naps through a good 2-3hrs of his "off" time already.

Going to be beautiful out the next few days....
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Tuesday, March 16, 2010

Hunter's First Birthday!!











Hunter's first birthday was March 12! Had a party and he was great...wasn't too sure about the cake though....I wanted him to get right into the cake and make a mess but he didn't...easier clean up for us!

We started the IV metoclopramide and it seems to be working. His vomiting is reduced but he seems to have a seasonal allergy or something because he is sneezing a bit and coughing...when he does vomit it is very mucousy like he has a cold...but as always...he is super happy! The blood work for his stomach salts etc came back normal although his lytes were out for about 2 weeks. They are back to normal this week thankfully and he has put on some weight...he's up to 19lbs 3oz!!!!
Hunter is still not walking but he's so close...if he could get over the fear of standing on his own! He is getting more brave but not quite there yet...more teeth coming in but nothing right out yet....

We were given some suggestions for his oral aversion and he is doing much better with it...they said his aversion is very minimal, which we knew, but we want him to progress so we were happy with the consultation.

The weather is beautiful so we are getting outside....
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