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.

Monday, July 25, 2011

New addition







The summer is flying by and alot has happened...most significant is Hunter became a big brother to little sister Regan...she was born on June 13, 2011...Regan was born with a full head of dark hair unlike Hunter who did not have hair until he was almost 2!! Hunter loves her...wakes each morning saying "baby". He likes to mimic her when she cries and help burp her after a feeding....I'm exhausted but its the cost of parenting I guess...
Hunter has had a couple of low grade fevers over the last couple months...we took him to the hospital for blood work and each time its been an ear infection....thankfully not a line infection.
Hunter continues to eat...he more so mouths the food and spits it out..a little messy but we are glad he has continued to progress with the eating.
Hunter is talking more and more each day...he talks in little sentences and will start singing certain songs when he hears them on the radio....I think everyone knows the song with the lyrics "it's not about the money money money"...well Hunter heard it one day and without prompting started singing "money money money"! It was pretty cute...I've taught him to sing "feeling hot hot hot"...and a few other old songs like "Barbara Ann", he especially likes the high pitches parts! hahaahah.....when we bring him to his appointments at the hospital he says hello to his doctor by saying "hi doctor Paul" and of course his dietician "hi Suzanne"....and he always has kisses for Suzanne! He's a little flirt that's for sure.
Hope everyone is having a great summer....its stupid hot here!
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Sunday, March 13, 2011

Happy 2nd Birthday Hunter

Happy 2nd birthday Hunter!!! Well it was yesterday March 12 but we were so busy I did not get a chance to post it! He had a great day with family and friends....he was exhausted by the end and so were we!! haahaha

His new line has been working great in his back/shoulder area....we are happy we made the decision to go back to the broviac and put it in that area...

I'll try and post some bday pics but I find they sometimes won't upload so I end up giving up on the waiting!!
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Sunday, January 23, 2011

New Central Line

We are booked and ready for Hunter to get his new central line this week...in the last day or so we decided we are not going to get a port but a broviac like he had the first year of his life. Hunter is so active that we feel the port will stick out too much and likely get hit like last time which caused some of the damage. Also we are going to have it put in his back so this will hopefully avoid infections from stool. Hunter is a belly sleeper and wakes up every morning with a wet belly which we feel is the source of the 3 infections he has had in his life.

Since we made the decision and spoke to his doctor about it we feel really good about it. We know he can still swim with the broviac although its a bit more complex than having the port, we have to cover it and make sure water does not get under the dressing. We are not opposed to Hunter having a port when he is older and can understand that he has to be more careful with it but at his age he just can't comprehend that.

So Hunter will go to the hospital this Tuesday and is booked for the procedure on Wednesday...if all goes well he will be home after the procedure....the interesting part will be getting him used to laying on his belly during the dressing changes once a week! He learns so quickly that we don't foresee a huge issue....fingers crossed ;))
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