Rylan's seizures seem to be getting more frequent while on a low dose of meds :-( It's so stressful. . .because while i want his neuro to up his meds i am scared to at the same time, because of his last reaction. I wish i could just take it all away from him so he doesn't have to go through this. I see friends and family having healthy kids all the time so I sometimes wonder why my son has to go through this. It's very hard to accept it sometimes. But, there is a reason God wanted to put Rylan with me and I know we can all get through this. He is a strong little guy and so far these seizures have not kept him down. There are some days that are harder than others but he always has a smile at some point in the day. Mommy loves you little man ♥
And I have posted a video of what rylan's seizures look like
http://www.youtube.com/watch?v=BV44CErEN1s&feature=g-upl&context=G20d8027AUAAAAAAAAAA
Tuesday, February 28, 2012
Wednesday, February 15, 2012
Somebody Please Wake Me Up :/
A lot has happened since my last post a few weeks ago. First, the last post I have on here was about taking him to E.R. for strange behavior. . .well a week or so after that we took Rylan to the doctor because he was doing the exact same thing and he started vomiting (sorry tmi). He looked horrible and he was just so tired had no energy and the nurse right away knew this wasn't good. She looked very concerned about him. So dr. chen came in and looked him over and seemed very concerned as well, I had told her my concerns that i thought it could be his meds causing it and right away she agreed with me. So she sent us over to the e.r. so they can get his levels checked right away because he was getting sicker. They checked his levels and it was within normal range. Well they explained to me that some kids are more sensitive to medications than the average kid (which is what the results were based off) so they said that was what is going on with my son, and they drove him in an ambulance to Cardinal Glennon and kept an eye on him over night. He was fine again the next day so they said it was the meds causing it and kept him off it and sent us home.
A couple days later we are back in the same hospital because we had a scheduled 72 hour video eeg. It was pretty uneventful except maybe two seizures, and one weird eye rolling episode when he was watching a movie with flashing lights. The first seizure i marked down they checked it on the EEG and came back in and said it didn't register as a seizure, so the rest of the time we were there i had it in my head that these episodes were not seizures after all. So i started thinking what else it could be and decided maybe it's an eye thing, and that when we got the test results back that were going to be normal i was going to get him into see an eye doctor. . .well it took two full weeks for them to get the results back to his neurologist. I had called earlier that week and his nurse told me that so far from what she gathered his EEG was reading normal, but she couldn't officially say until he got the results back. Well last Friday I get a call from Rylan's Neurologist himself (Never a good thing) and when i heard his voice my heart sank because i knew it wasn't going to be what i was expecting and what i was told previously. . .He preceded to tell me that my son was in fact dealing with seizures. He was concerned that these could turn into the convulsing type of seizures and wanted to get him back and meds right away. He even told me that in parts of the EEG there were seizure tendency's ( where they could have turned into seizures but did not). I felt so numb. I know i have to be strong for my son but hearing these results just tore me up. I am more worried now because i don't want him to have to deal with this, and I was hoping that for once my mommy instincts were wrong, but they weren't. So if you are a mother please listen to your mommy instincts when it comes to your child because we know our children best ♥♥
A couple days later we are back in the same hospital because we had a scheduled 72 hour video eeg. It was pretty uneventful except maybe two seizures, and one weird eye rolling episode when he was watching a movie with flashing lights. The first seizure i marked down they checked it on the EEG and came back in and said it didn't register as a seizure, so the rest of the time we were there i had it in my head that these episodes were not seizures after all. So i started thinking what else it could be and decided maybe it's an eye thing, and that when we got the test results back that were going to be normal i was going to get him into see an eye doctor. . .well it took two full weeks for them to get the results back to his neurologist. I had called earlier that week and his nurse told me that so far from what she gathered his EEG was reading normal, but she couldn't officially say until he got the results back. Well last Friday I get a call from Rylan's Neurologist himself (Never a good thing) and when i heard his voice my heart sank because i knew it wasn't going to be what i was expecting and what i was told previously. . .He preceded to tell me that my son was in fact dealing with seizures. He was concerned that these could turn into the convulsing type of seizures and wanted to get him back and meds right away. He even told me that in parts of the EEG there were seizure tendency's ( where they could have turned into seizures but did not). I felt so numb. I know i have to be strong for my son but hearing these results just tore me up. I am more worried now because i don't want him to have to deal with this, and I was hoping that for once my mommy instincts were wrong, but they weren't. So if you are a mother please listen to your mommy instincts when it comes to your child because we know our children best ♥♥
Tuesday, January 10, 2012
Med side effects
My son had a very rough day yesterday. I feel so bad for him that he has to go through all this. His baby sitter calls me while I am at work and was telling me that he was starting to sleep all day again, he slept all morning then she woke him up for lunch and meds and she said was very disoriented he couldn't even sit up right for lunch and he was crying to go back to sleep. She said he wouldn't walk and when he tried he just fall down and was very unsteady. So we rushed him to the E.R. because his pedi couldn't get him in right away. And when we got there he was fine by the time the doctors seen him. So i am waiting on a call back from his neurologist because E.R. did nothing for him. I really want a different med for him, but i have a feeling that he is just to sensitive to the higher doses :( Today however he is fine and himself again ♥
Monday, January 9, 2012
One Seizure at A Time
It's so hard dealing with this, and i can't understand why it has to happen to my sweet little boy. He has done nothing to deserve this. I love him and i try to stay as strong for him as i can, but sometimes it's really hard. These seizures are just stealing my baby boy from me :( Maybe i am looking for answers in the wrong spots. I know God is in control of everything but I haven't really been that good at praying and talking to God lately :/ I was going to go to church yesterday, but decided not to because Rylan wasn't doing well at that point. He was extremely tired and emotional and it just wouldn't have been good. And at that same time he had his first seizure of 5. It didn't last to long but it was there. So my mom picks us up from my friends house so she can take us to meet hubby in St. Clair, and Rylan falls asleep so it was about 1 o'clock then. We get him home and he stays sleeping for 5 hours. I had also upped his meds over the weekend per the doctors request. So 5 O'clock rolls around and he is fine up until bed time which was at 9. Rylan was playing with his IXL from fisher price and he suddenly stops playing-looks up and stares for about 10 seconds-then resumes playing with his toy. He is getting pretty tired at this point, so the rest of them follow up until he falls asleep at 10. I think because of his seizure activity at bedtime it usually takes him about an hour to fall asleep. I really don't understand why his seizures are becoming more frequent. But, I know we are just dealing with it one seizure at a time.
Wednesday, December 28, 2011
This Sucks!
So Rylan was almost seizure free a MONTH! On Dec. 22nd would have been a month without a seizure, but then he had one on the night of the 21st (so close!) and ever since he has been having them. And now he has developed a new type it seems. . .
Yesterday we dropped him off at our babysitters (which is my hubby's cousin) and she sat him at the kitchen table to eat breakfast she heard him start crying and went to check on him he was gripping the high chair arm so tight she had to pry his hands off the high chair and when she got him out and picked him up he was so stiff he was still in the sitting position. I called his neuro and the nurse said it definitely sounds like a seizure :( I am so bummed right now, i was hoping his seizures wouldn't change at all. Please keep my little man in your thoughts and prayers, he has been dealing with a lot lately.
Yesterday we dropped him off at our babysitters (which is my hubby's cousin) and she sat him at the kitchen table to eat breakfast she heard him start crying and went to check on him he was gripping the high chair arm so tight she had to pry his hands off the high chair and when she got him out and picked him up he was so stiff he was still in the sitting position. I called his neuro and the nurse said it definitely sounds like a seizure :( I am so bummed right now, i was hoping his seizures wouldn't change at all. Please keep my little man in your thoughts and prayers, he has been dealing with a lot lately.
Wednesday, November 30, 2011
EEG and Seizure Activity?
Rylan just had his second EEG and he did not take it well at all! He was good up until we had to leave and the whole ride up there all he wanted to do was sleep :( so i had to keep waking him up and he would get so upset with me. He tried to hit me a couple of times, but wasn't successful. Then when we got there he was okay up until we had to hold him so they could get the electrodes on his head (which was alot). He got so upset that when it was time for him to go to sleep he had a hard time. At one point he was messing with the electrodes on his head so she had to wrap him up in a blanket so his arms were in the blanket and then he fell right asleep. I think he just wanted to cuddle. We did all that and his results came out normal which is good, just wishing we had more of an answer to his issues :/
I have been asking around and it seems that his eye rolling when he gets water in them is not normal for most. I have not talked to the neuro about this yet, but will the next time i call up there. I also have a video of him having a CPS with hand movement too that i want to email to them and have them check it out.
Good News is: He hasn't had a seizure for 8 days now! :) But, i'm not sure if i am reading to much into this, sometimes he has weird breathing when he is sleeping (which i noticed the day of his eeg when we got home) and he has been having a lot of saliva in his mouth, last night it just kept coming out, and i am not sure what to think of it, because he also fell asleep for a few minutes at 8 o' clock and that was not like him. I am hoping it wasn't seizure activity, because before he fell asleep he was acting weird a few minutes before. I couldn't get him to stay straight up he was kind of acting like a drunk person, and he kept falling down to the ground.
Well for now that is all the update i have on my baby boy ♥
I have been asking around and it seems that his eye rolling when he gets water in them is not normal for most. I have not talked to the neuro about this yet, but will the next time i call up there. I also have a video of him having a CPS with hand movement too that i want to email to them and have them check it out.
Good News is: He hasn't had a seizure for 8 days now! :) But, i'm not sure if i am reading to much into this, sometimes he has weird breathing when he is sleeping (which i noticed the day of his eeg when we got home) and he has been having a lot of saliva in his mouth, last night it just kept coming out, and i am not sure what to think of it, because he also fell asleep for a few minutes at 8 o' clock and that was not like him. I am hoping it wasn't seizure activity, because before he fell asleep he was acting weird a few minutes before. I couldn't get him to stay straight up he was kind of acting like a drunk person, and he kept falling down to the ground.
Well for now that is all the update i have on my baby boy ♥
Tuesday, November 22, 2011
Updates
I last posted about Rylan's doctor appointment and how they upped his medication to 7.5ml twice a day. I have been noticing a pattern with upped meds. . .it works for about a couple of weeks and then they start slowly coming back! I hate it. It's not affecting him to bad right now, but if we don't get this under control it could affect his learning :/ I don't want to see him struggling through school. It just breaks my heart. This may be because he is only two years old but sometimes he is so tired all he wants to do is sleep, i am really hoping he outgrows that stage because he can't be sleeping in school when he gets school aged. I am planning on putting him in preschool when he is 3-4 years old, hoping that helps him.
He is also scheduled for another sleep deprived EEG for Monday morning at 10:45 a.m. I was hoping for a longer one so we have a better chance at catching one but for now i will take what i can get for my little man. He apparently may be having them at night while he is sleeping. My mother in law had him over night one night she seen him have one. His eyes opened and he was staring then his eyes started rolling back, and then he fell back asleep. I just want real answers. I am tired of not knowing if these are really seizures or not because now the neuro has put doubts in my head. He is pretty positive these are seizures but there is still that doubt lingering there.
It sucks to see your child not be there :( Every time he has one my heart stops. I am calm on the outside and freaking out on the inside and it is just a horrible feeling to have. No child should have to go through this. But i do have a lot to be thankful for. It could be a lot worse.
He is also scheduled for another sleep deprived EEG for Monday morning at 10:45 a.m. I was hoping for a longer one so we have a better chance at catching one but for now i will take what i can get for my little man. He apparently may be having them at night while he is sleeping. My mother in law had him over night one night she seen him have one. His eyes opened and he was staring then his eyes started rolling back, and then he fell back asleep. I just want real answers. I am tired of not knowing if these are really seizures or not because now the neuro has put doubts in my head. He is pretty positive these are seizures but there is still that doubt lingering there.
It sucks to see your child not be there :( Every time he has one my heart stops. I am calm on the outside and freaking out on the inside and it is just a horrible feeling to have. No child should have to go through this. But i do have a lot to be thankful for. It could be a lot worse.
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