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Two febrile seizures in less than 30 hours

Yes, you read the subject line correct. Life here at Chez Angel has been turned upside down since early Saturday evening. When we left the ER Saturday night with no answers and over 24 hours to go before seeing our doctor I was beyond nervous. As the parent of two children that have had febrile seizures, I know that the following 48 hours are the most common for a repeat.

NHL had his febrile seizure when he was 11 months old and is now almost six years old. Finally getting out of the danger zone. When I was little I had three, but none were back-to-back. JL had two as a child and to my knowledge both were seperated by time.

JSL apparently had to be different. 

Everything from Sunday night is a blur. I went to sit in bed with my computer and got tired, so I turned off the light. The little guy was next to me to make it easier to medicate him during the night. At 10:30 we opted to let him sleep, rather than wake him for the fever reducers. This decision would soon come to bite us in the you know what.

The next thing I remember is it being midnight and SCREAMING for JL to come quickly. I do not even recall waking up. I just remember pulling JSL to me as he was once again rigid, thrashing/shaking and frothing from the mouth. 

After a few seconds (not that I actually timed it), he was done with the seizure. He was burning up. I got Motrin for him and called my parents to come over. I thought that we would be going to the hospital for sure and needed someone to be with NHL. Next I called the doctor at about 12:30 and waited to hear from him. He called back after everyone else was here. He did not want us to go to the ER. Instead our main goal was to give JSL fever reducing medications every two hours the rest of the night.

We did just that and brought him to see the doctor yesterday morning. We believe that he has a sinus infection and may have a hidden ear infection. JSL is now on an antibiotic to try to kick this in the butt. Of course the fever is still hanging in there. Every two hours we are dosing up one fever reducer or another. Here is the little guy after he returned home from seeing the doctor.

Tired and sick little guy

To add to the excite, NHL has been on a steroid for his breathing troubles the last three days. He finishes this up today. Then yesterday, his allergist called back with more detailed results of his adenoid/sinus x-rays from Wednesday. The adenoids still look great, but he did not like the way the sinuses looked. Given that he was still very stuffy and actively blowing mucus out of his nose, he is now on an antibiotic as well.

This is medicine chart central and our own personal mini pharmacy. 

Medicine charts for the boys      Our own pharmacy

This morning JSL’s temperature started to go way up again. So, it will be another day of fever reducers every two hours and the second dose of antibiotic later this afternoon. With any luck we can kick this thing and stop worrying about more nightmare moments. Of course you know that I will forever worry given how quickly these last two febrile seizures came out of no where.

TheAngelForever

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13 Months later – the nightmare returns

My body is completely numb and my mind is still racing. Just before sitting down to eat dinner last night my worst nightmare came true again. Almost thirteen months after it happened before, JSL stopped breathing and turned blue.

One minute he was chasing after his big brother, the next he slumped over on the floor next to my legs. It all happened so quickly it seems like a blur to me.

JL and I were helping NHL to try on a new bike helmet. JSL was sitting on the floor behind my legs watching Sesame Street. Suddenly we heard JSL grunting. We thought he was a little constipated and doing his business. Then I looked a little closer and his head slumped forward. I picked him up and honestly thought he was gagging on something. I tried to do back blows and other things to get something out of his mouth. When I tried to reach into his mouth I could not open it.

This should have been a light bulb moment. Of course I was not thinking. I was in a panic. My 22 month old son was rapidly turning blue. First his face and second later his hands. His life flashed before my eyes as we prayed that the emergency personel would arrive soon. O could not get his mouth open. His jaws were clenched down on my fingers as I tried with all my might to get into his mouth. Then I noticed his entire body was rigid.

By the time everyone arrived, I was pretty sure he was not choking on something. I was positive he had another serizure. When the EMT came in he seemed a little warm, but nothing too alarming. Problem was, he was unresponsive. His eyes were glazed over and he was not respnding to my voice. The lights were barely on and nobody was home. We quickly determind that he had to go via ambulance to the ER. I sat on the stretcher with him in my arms.

The ride to the hospital was awful. Nobody said anything to me. They worked on their papers as I sat there talking to JSL. He was starting to respond some. If I asked where Mama was he was able to move his hand to point in my direction. He would also point to the lights inside the ambulance when I asked. Slowly he was showing signs of my little boy.

After we arrived in the ER and were taken to a room they did a rectal temperature. It may sound horrible, but I was relieved to see that he was extremely feverish. At that point his temperatuer was 103.5. JL and my mother were there with me as we waitied to see the resident. She came in and looked in his ears and checked him out.

Two hours after we arrived we were told it was time to go home. His temperature was down to 100.8 with Motrin. The part that leaves me freaked out – we do not know what caused the sudden, freak spike in temperaure. Actually, we do not know what continues to keep his temperature up. This morning it was up to 102. So today we are staying home, keeping him cool and rotating different fever reducing mediations to the little guy. Tomorrow we will follow up with our doctor to see if anything is suddenly visible in his ears or elsewhere.

 

TheAngelForever

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Quest for allergy relief

Over the last two to three weeks, NHL’s allergies have been acting up. At one point he actually had his first ever asthma attack during the night. We pulled out the nebulizer and within minutes he was breathing easier and no longer wheezing. After several days of symptoms getting worse, we opted to take him in to see the PA at the ENT/Allergy office that we went to. She diagnosed NHL with allergic asthma and gave us a bunch of new items to try to get things under control. We were not to start the one medicine until we saw how he did with the other. Three days later things were worse, especially behavior wise at school. The PA told us to immediately begin the new medicine.

The new medication was the Asmanex Twisthaler. If you have never seen this before it is an interesting medication. The problem is that it is hard to inhale and teach a five year old to use. The pharmacist told us he was floored that a young child was given this and warned that often children get thrush from it. Lovely!

Last Friday NHL’s teachers were very concerned with his behavior. They directly related it to the recent allergy attack. I called the doctors office and asked for assistance since I was not sure if NHL was getting the Asmanex in properly. Nobody called me back. I made a return call and was asked to leave another voice message for the medical assistant to remind her to return my call. What? 

After quite some time, the MA called me back. She was extremely snotty on the phone. When I tried to explain something to her she cut me off and told me "No need to tell me the history, I read his entire chat and know what is going on."   Pretty cocky statement if you ask me. She went to try to get NHL an appointment to see the doctor, but he had no openings for several weeks. She came back to the phone and asked me the following question, "Has NHL tried Singulair?"  

This was the wrong thing to say. I was too angry to yell, I simply cried because I felt like I was failing my child. I have seen NHL’s chart and know there is a huge section all about his adverse reaction to Singulair. She told me that she was going to talk to the doctor again to see if he wanted to fit in an emergency appointment or just switch things up and see us at the end of the month. Things were switched, but my mind was quite uneasy about everything that had happened.

I started to do research for pediatric allergists in the area. Our family doctor and the school nurse both recommended the same person. We received a referral from the doctor and I called the new office. They had an opening in less than a week. I immediately took that time. Next, I called the allergy/ENT office to get the items faxed to the new doctor. They sent something Friday morning to JL to sign and fax back to them. Monday morning I called the new office and they had nothing. I left a message at the allergy/ENT office and 24 hours later did not hear back and still nothing at the new office. The new allergist’s office suggested calling our family doctor to see if they had records that could be sent. Much to my horror, when they checked NHL’s file there were only two tiny notes from the allergy/ENT group. He had been a patient there for almost a year, been allergy tested and had a horrid reaction to a medication – yet nada! To make a long story short, I called to speak with the office manager to explain the three major issues that had cropped up over the past week. End product, she was very sorry and told me that the doctor was disgusted with what happened.

Yesterday was our appointment with the new doctor. It did not start off very well. He asked me to explain what has been going on. When I said that NHL’s allergies were acting up, he stopped me and said "Well, it is very rare that children under 7 have season allergies"  Please picture me rolling my eyes. I have heard this before, so it was nothing new. Then he asked about how we have been treating NHL. I mentioned the previous medications. When I stated the adverse reaction to Singulair, he told me that the FDA and latest reports indicate that there is no connection with pediatric patients and changes. I looked him right in the eyes and said the following "I do not care what the report says, I KNOW what it did to my child!" 

The subject was quickly changed and he got the point that I am observant and so are NHL’s teachers. We see changes and know what is going on with him. In the end we saw mostly eye-to-eye on NHL. A lot of this happened when we agreed that he was very nasal. He believes that  NHL has bad rhinitis that is being caused by at least three things. Some are allergic, some illness related (virus and things from school), stress, and potentially his adnoids. He was upset that the other group was treating him the way they were (specifically the Twisthaler) and switched his medications after doing some breathing tests. We are back to using the nebulizer once daily, keeping up with the OTC antihistamine and watching things for the next month. We go back on St. Patricks Day and will talk about knocking the nebulizer to every other day.

I am glad that I did not leave after the first statements becuase I do believe that the doctor started to listen to me. He heard that I was not just some mother trying to medicate my child. That I am part of a group of people that have carefully watched my son and seen things that trigger him. With any luck this will be the start of some relief in breathing symptoms and behavior for my kindergarten kid.

TheAngelForever

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Feeling frazzled

Lack of sleep, an ambulance ride and visit to the emergency room can leave a family quite frazzled. I would be one of those family members this morning.

Last night, we went to Nana and Papa’s house to have an early Chanukah dinner with them, Mimi and Aunt T. We had a wonderful time opening presents, spending time with each other, and of course eating a delicious meal. After dinner, we decided to let the kids play. JSL loves to run around the large space at Nana and Papa’s house. At one point he was playing with my father and they were running through the kitchen. The rest of us were sitting in the living room and heard a gigantic THUD.

The night quickly changed at that moment.

That noise was JSL’s feet wiping out, his body flying into the air and him coming down on the back of his head. After a minute he cried and wanted JL. We figured the boys were getting tired, so we went to the table for cheesecake.

Of course after the fact, everyone else mentioned that they noticed the same thing when we sat down. JSL suddenly got very pale, stopped talking, was sweating horribly and then started shaking. Then the scariest part, he was unresponsive to us.

Nightmares of February came flashing back to me.

We got him out of the booster seat and took him into the kitchen. He was still not responding to us. Not to his name, tickles, nothing. He was trying to close his eye. When he did look at us, it was as if we were not there. I screamed for JL to call 911. He did and they sent out first responders.

During the time it took for them to arrive, JSL came in and out of it. When we tried to let him walk, he looked like he was drinking and could not walk in a straight line.

When the paramedics came into the kitchen we noted more odd behavior. Typically if a stranger tries to go near JSL he will recoil onto one of us and scream. Nada happened, he just sat there starring into space. They did vitals and said they were ok, but wanted to take him by ambulance to the hospital.

As I went running to get his coat and my boots I failed to notice all of the water from the paramedic’s shoes on the kitchen floor. I went flying into the basement door jamming my foot, hand and fingers. I was on an adrenaline rush and kept moving.

During the ambulance ride JSL was very quiet. He did move or do much. Finally minutes from the hospital he uttered "Mama" and pointed to the light. When we arrived into a room at the hospital the little guy started to perk up after about 30 minutes. He wanted to get down, explore and he was chatting up a storm.

When the PA came to see us you would never know there was anything wrong. The end product is JSL definitely had a concussion and may have had a mini-seizure. We have to follow up with our doctor Monday and keep a close eye on him today.

Last night he was up until midnight and was screaming and very restless during the night. Thankgoodness this morning he is in a great mood and playing nicely.

Today we will be staying in during another snow storm for a quiet day with the boys.

TheAngelForever

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My little monkey is growing up

I believe denial is healthy from time to time. For the last two weeks I have been trying to forget that JSL is now 18 months old. It is hard for me to believe that my baby has been here for a year and a half already. The time has gone by way too quickly.

Today I took JSL for his 18 month well baby visit. His stats for this visit:  26 pounds (50th percentile), 30 3/4 inches (10th percentile), and head was 51 cm (95th percentile). So basically as the doctor put it he’s a little short in stature with a good sized head! Clearly the poor kid got my short genes. Mommy is the classic recessive short gene in action. I am only 5’3" with two parents that were 6′.

The doctor is not concerned, although I wonder about the small amount of height growth. I guess we will see what happens over the next six months. I have a feeling we are due for a growth spurt since he’s been really restless and tired lately. Developmentally he is right on track with motor and fine motor skills, and talking more than a typical 18 month old.

We discussed the ear wax issue and how it seems to alter the way he hears. Her theory is it may not have been the wax and could very well have been the fluid from the infection.  I have been told what to do to try to help that. For now we just have to watch the ears, especially the one that was just infected and still has some fluid in it. Since he is just getting over antibiotics and a high fever less than ten days ago, the doctor opted to only give him one of the three immunizations that he is due for. Today he had the DTaP and will go back in a month for the Hib and HepA.

I also asked the doctor about milk and how we should approach introducing it to him given big brother’s allergy at this age. She said it was completely up to us. JSL is still nursing and shows no interest in stopping yet (this shocks me, but I am perfectly fine with it). We may try some little sips of pure cows milk here and there to see how it goes. The main concern is making sure JSL is getting enough protein. We are practically vegetarians (thanks to the obscene price of kosher meat) and she is worried that we do not know how much milk JSL is getting when he nurses. She is fine with him still nursing, but wants to increase meat/fish in his diet. Of course since I am back home I found that the grams of protein in the fake burger patties is almost identical to the chicken nuggets that she suggested. Thanks to that I am not too worried.

The poor little guy was tired after his shot and a quick trip to Target. We went there to get a new part of our family. Here it is with an explanation on JL’s blog

Something I never imagined buying

We shall see how it goes when we try it out later, perhaps when I go sneaker shopping.  For now I shall let the little monkey rest after a stressful morning that included a rough immunization. 

Tired after a shot today

Our next well  visit is not until May when the little guy will be two. On that note I am going back to my own little world away from the reality of my baby growing up. 

TheAngelForever

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