This blog, of course, cannot only be about Jennifer!! I did say in my profile you’d hear about Ben’s ears and Sam’s allergies and heart. So, I figure I’d better give you the background on those so you know it when you get the updates.
Benjamin had his first ear infection at 5 months old along with a bout of bronchiolitis. He had to do breathing treatments then too. He got better and we figured it was just a winter bug and all was over. Unfortunately, that was just the beginning for him and his ears. He had another ear infection at 7 months old. The poor thing would be inconsolable with these ear infections too. This started a pattern of ear infection leading to an antibiotic then a recurrance of the ear infection about 2 weeks later.
After 4 ear infections in a row like this he was put on a preventative antibiotic that he took daily to prevent further ear infections to get him to summer when ear infections are supposed to go away. All the while he also had a chronic yellow-green runny nose. This would also clear up with each course of antibiotics and restart once they were finished. He stayed on this daily preventative antibiotic for about 6 weeks. Within 4 days of being taken off it his nose started again and within 8 days he had a raging ear infection with a high fever. At this point he was sent to an ENT doctor.
At 11 months old he had his first surgery where he had a set of ear tubes placed and he had his adenoids taken out. The adenoids were removed in hopes that they were harboring the bacteria that was causing the chronic runny nose that was then leading to the chronic ear infections. His nose did continue to run for awhile even after the adenoids were removed and he was tried on several allergy medicines without success. Eventually after his second birthday it finally just spontaneously stopped. He continued to get ear infections even with the ear tubes but he was a different child with an ear infection at this point. No longer was he in terrible pain and no longer did we have to do antibiotics by mouth. Now just a few drops twice daily into his ears. What a welcome relief.
We were lucky that he was one of the kids that the tubes stayed in instead of them falling out quickly. Though this luck later turned into them really staying in!! At 3 1/2 they had to be surgically removed!! This was due to if they are in too long it can lead to scarring and perm hearing loss. At this point it was noticed that his tonsils were quite large too. Feeling that eventually he would have to have them removed due to some sleep apnea issues he was scheduled for surgery again. The ear tubes were removed and the tonsils were removed. He had a rough time for about a week with tons of pain, thrush, refusing to eat and drink, and some nerve issues in his jaw but then went on to recover quite well.
In Ben’s style about 4 weeks later he got an ear infection. This was quickly followed by a second one so a tube was placed again. Unfortunately, only the ear that got the infection had healed from the first set of tubes so only one tube was able to be placed. Several months later the second ear drum finally healed and sure enough (just as Mom had predicted) he got an ear infection in it. Knowing his history we didn’t wait and immediately scheduled him for a tube in that ear too. So he is now 4 1/2 and on his second set of ear tubes and doing quite nicely. Hopefully this will be his last. Hopefully this set will stay in as long as his first set did (but then fall out on their own!!) and by then his ears will have grown enough to be able to drain on their own without more infections. Only time will tell I guess.
Samuel is Jennifer’s twin brother. He had reflux as a baby too but fortunately outgrew it by 8 1/2 months old. He spent some time on prevacid too but didn’t have nearly as hard of a time as Jennifer had with it. When Sam was born he had a heart murmur. Being 5 weeks early this wasn’t entirely unexpected but it wasn’t heard by the pediatrician on his first day of life but was heard on the second day. To just be safe they did an ultrasound of his heart. It showed that his foramen ovale was still open. This is common in preemies and we were told it should close in his first few months.
He was hospitalized along with Jennifer (full story in last entry under Jen’s story) at 3 weeks old and they were both given another heart ultrasound since they both still had murmurs and fevers. Both still showed patent foramen ovales. Again, ok. At each well check up the pediatrician and I would talk about their murmurs and Jennifer had outgrown hers somewhere between 4-6 months old. Sam never did.
Just prior to his second birthday we saw a different pediatrician for a sick visit as I thought he had an ear infection. He looked in his ears and said they looked fine but then spent a long time listening to his chest and then referring back to his chart. At that point I knew something was coming!! He said that even if he still had the patent foramen ovale we shouldn’t still hear the murmur from it. He then wanted him to have another heart ultrasound. This time, however, he wanted a pediatric cardiologist to read it. The others hadn’t been read by one. He made it clear that he didn’t want Sam seen by the cardiologist, just that he wanted his ultrasound read by him. We had the ultrasound done about a week later on a Thursday and that Friday afternoon one of the other pediatricians from the office called and said that the cardiologist’s office would be calling to set up an appointment for Sam to be seen by the cardiologist sometime in the next month. And I was like, “what, I thought he wasn’t supposed to be seen by the cardiologist?”
Tuns out he has a condition called a subaortic membrane or subaortic stenosis. It is pretty rare but it is a heart defect and needs to be followed by a cardiologist. We saw the pediatric cardiologist in August 2007, the same month he turned 2. He actually told us that this isn’t usually diagnosed until between ages 2-3 as this membrane needs time to grow and cannot be picked up until it grows big enough to be seen. For now he isn’t symptomatic with it so he just needs to be followed yearly with heart ultrasounds and visits to the cardiologist. If he were to ever become symptomatic then he would need heart surgery to remove the membrane. They don’t routinely just do surgery to remove them because of several reasons 1) it is a big surgery that comes with risks and 2) the membrane tends to grow back.
Now, for Sam’s allergies. This one is easy!! He had the same chronic runny nose like Ben but minus the ear infections so I kinda figured he wouldn’t really respond to any allergy meds either and put it off awhile. But after going through tons of boxes of kleenex in a month I took him to the pediatrician. She suggested claritin and after 2 days on that I have barely seen anything come from his nose again!! Yipee!! So, he obviously has some sort of environmental allergy. Hopefully it is only to pollen and not dust and dust mites like his momma!! Though his nose started much sooner than pollen season so only time will tell I guess.