DDA Chapter 23

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so it turns out not only did LUMC mess with me while I was there....it continues on. They don't have to pay into the unemployment coffers so I can't get any at all. :guilty:

I have to do 40 hours of volunteer service for us to keep our food stamp benefits.....and I had less than 15 days to do it this month (and I was sick last week, so there goes another 5) and working within the parameters of the Work Force Center and Goodwill is going to drive me nuts....basically I have to work 4-9 hour days before Thanksgiving and they don't allow for but a few volunteers on Wednesday (which I found out today:sad2:) and it has to be during the traditional work week.

I did have an interview today for a job I had put in for yesterday after I got home (so less than a 2 hour turnaround.....4:30 resume sent....6:30 phone call asking for interview)
:grouphug::grouphug::grouphug::grouphug:
 
No work for me today as my back went out again. This time it was just bending over to get clothes out of the dryer. It has been acting up the past 2 weeks & yesterday it hit full force. Such is life I guess.

Hope your doing better Janet. :grouphug::grouphug:
 
I cannot believe I am coming here to post something horrible again. The father of two of my students died suddenly today. He had knee surgery six weeks ago and apparently this pulmonary embolism was related to that surgery. He was just in class Monday night! My heart is breaking for these fatherless children. Please hug your husbands and children extra tight tonight.

I have no words Elin.:grouphug::grouphug::grouphug::grouphug:
 
Stephanie & Terry I am very excited for you :woohoo::woohoo::woohoo::woohoo:
 

Elin, I am so sorry you are dealing with another tragic loss. Prayers lifted up to that family!

Janet, I'm glad you're back is feeling better today.

Deb, I hope you get some answers today. Prayers being said for you all, too!

Theresa, any word on the interview? Thinking of you! :wizard:

Hi everyone! :wave2: TGIF!

Hope all of you who have seen or are going to see New Moon have fun! :teeth:
 
Where is everyone tonight? I came home and took a nap myself. I will be working all weekend and then will have Wednesday-Friday off.
 
Sorry that I couldn't check in earlier. Our internet was down and then we had company. Anyway the update.
We saw 2 neurologists today. They took a complete history, did a neuro exam and read his chart. Given the history, our stories and their findings they feel that he has juvenile epilepsy. Puberty can trigger the onset and unfortunately if they are correct it is something that will stay with him for the rest of his life. The good news is that they have very good meds that can control the seizures, leaving him seizure free once they find the right combination. They were unable to schedule an EEG until Monday and the EEG is the key to confirming their diagnosis. The EEG will take about 1 1/2 hours and they would like him to arrive tired (at 10 AM :confused3) we won't be able to see the doctors again until Wednesday. At that time they hope to be able to prescribe a medication to stop the seizures. Until that time he could have one (or more) at any time. We do have a med that we can give him if he starts to have convulsions or multiple seizures.

It appears now that what they have been calling low blood sugar episode was more likely due to the early stages of epilepsy. This makes us angry because we have spoken to numerous doctors on numerous occassions and they have all made the same assumptions/diagnosis. He has probably had multiple petit mal seizures that we were unaware of or did not recognize as such. They also assured us that they do not suspect any sort of brain abnormality as he is a straight A student, althletic, coordinated and he had a completley normal neuro exam and blood workup. That is a huge relief in itself. They also assured us that while watching him have a seizure is very traumatic for us, it does not in any way damage his brain and as long as he doesn't physically injur himself in the process they are completely safe for him.

We are feeling better about things tonight though the next few weeks could be hard depending on his seizure activity.

I have decided that I cannot devote my entire day tomorrow to ski patrol training. I sent an email to the head person explaining my situation and asking to be trained at a later date after things settle down. I have no idea how that will work out, but I know that I need to be here, now. It is truly amazing how entire lives can change in the blink of an eye and how quickly priorities change. My children are all clingy now and I certainly understand why. I can't remember the last time we have spent so much quality time together or when they needed to be within arms reach of me. I know this will fade over time, but I intend to nurture it for now.

Nick's appointment was pretty much a waste of time. He has had this cold/cough/sore throat for 2 weeks, but they won't treat unless he has it for another week :sad2: He did get the seasonal flu shot.

Colby's 7 year check was good. He grew 3 inches and about 10 lbs in the last year and the doctor feels that he is on a good growth curve even though he appears a bit heavy to us. She is still unconcerned that he is not completely night trained, but attributes it to being a heavy sleeper since he does not have accidents when he is awake. He also got the flu shot and unfortunatley he now has a temp of 100.2 :sad2: Hopefully he'll feel better in the morning.
 
Sorry that I couldn't check in earlier. Our internet was down and then we had company. Anyway the update.
We saw 2 neurologists today. They took a complete history, did a neuro exam and read his chart. Given the history, our stories and their findings they feel that he has juvenile epilepsy. Puberty can trigger the onset and unfortunately if they are correct it is something that will stay with him for the rest of his life. The good news is that they have very good meds that can control the seizures, leaving him seizure free once they find the right combination. They were unable to schedule an EEG until Monday and the EEG is the key to confirming their diagnosis. The EEG will take about 1 1/2 hours and they would like him to arrive tired (at 10 AM :confused3) we won't be able to see the doctors again until Wednesday. At that time they hope to be able to prescribe a medication to stop the seizures. Until that time he could have one (or more) at any time. We do have a med that we can give him if he starts to have convulsions or multiple seizures.

It appears now that what they have been calling low blood sugar episode was more likely due to the early stages of epilepsy. This makes us angry because we have spoken to numerous doctors on numerous occassions and they have all made the same assumptions/diagnosis. He has probably had multiple petit mal seizures that we were unaware of or did not recognize as such. They also assured us that they do not suspect any sort of brain abnormality as he is a straight A student, althletic, coordinated and he had a completley normal neuro exam and blood workup. That is a huge relief in itself. They also assured us that while watching him have a seizure is very traumatic for us, it does not in any way damage his brain and as long as he doesn't physically injur himself in the process they are completely safe for him.

We are feeling better about things tonight though the next few weeks could be hard depending on his seizure activity.

I have decided that I cannot devote my entire day tomorrow to ski patrol training. I sent an email to the head person explaining my situation and asking to be trained at a later date after things settle down. I have no idea how that will work out, but I know that I need to be here, now. It is truly amazing how entire lives can change in the blink of an eye and how quickly priorities change. My children are all clingy now and I certainly understand why. I can't remember the last time we have spent so much quality time together or when they needed to be within arms reach of me. I know this will fade over time, but I intend to nurture it for now.

Nick's appointment was pretty much a waste of time. He has had this cold/cough/sore throat for 2 weeks, but they won't treat unless he has it for another week :sad2: He did get the seasonal flu shot.

Colby's 7 year check was good. He grew 3 inches and about 10 lbs in the last year and the doctor feels that he is on a good growth curve even though he appears a bit heavy to us. She is still unconcerned that he is not completely night trained, but attributes it to being a heavy sleeper since he does not have accidents when he is awake. He also got the flu shot and unfortunatley he now has a temp of 100.2 :sad2: Hopefully he'll feel better in the morning.

Yikes Deb. Glad you at least have a diagnosis I bet you will be spending this weekend researching the internet. Congrats to Colby on growing 3 inches. Olivia sleeps so hard that she also wets herself.

Poor Nick I hope he gets well soon.
 
Yikes Deb. Glad you at least have a diagnosis I bet you will be spending this weekend researching the internet. Congrats to Colby on growing 3 inches. Olivia sleeps so hard that she also wets herself.

Poor Nick I hope he gets well soon.

I've had intentions of researching on the internet, but everytime I come near my computer the boys ask me to sit on the couch and snuggle so I'm not making progress.
 
Sorry that I couldn't check in earlier. Our internet was down and then we had company. Anyway the update.
We saw 2 neurologists today. They took a complete history, did a neuro exam and read his chart. Given the history, our stories and their findings they feel that he has juvenile epilepsy. Puberty can trigger the onset and unfortunately if they are correct it is something that will stay with him for the rest of his life. The good news is that they have very good meds that can control the seizures, leaving him seizure free once they find the right combination. They were unable to schedule an EEG until Monday and the EEG is the key to confirming their diagnosis. The EEG will take about 1 1/2 hours and they would like him to arrive tired (at 10 AM :confused3) we won't be able to see the doctors again until Wednesday. At that time they hope to be able to prescribe a medication to stop the seizures. Until that time he could have one (or more) at any time. We do have a med that we can give him if he starts to have convulsions or multiple seizures.

It appears now that what they have been calling low blood sugar episode was more likely due to the early stages of epilepsy. This makes us angry because we have spoken to numerous doctors on numerous occassions and they have all made the same assumptions/diagnosis. He has probably had multiple petit mal seizures that we were unaware of or did not recognize as such. They also assured us that they do not suspect any sort of brain abnormality as he is a straight A student, althletic, coordinated and he had a completley normal neuro exam and blood workup. That is a huge relief in itself. They also assured us that while watching him have a seizure is very traumatic for us, it does not in any way damage his brain and as long as he doesn't physically injur himself in the process they are completely safe for him.

We are feeling better about things tonight though the next few weeks could be hard depending on his seizure activity.

I have decided that I cannot devote my entire day tomorrow to ski patrol training. I sent an email to the head person explaining my situation and asking to be trained at a later date after things settle down. I have no idea how that will work out, but I know that I need to be here, now. It is truly amazing how entire lives can change in the blink of an eye and how quickly priorities change. My children are all clingy now and I certainly understand why. I can't remember the last time we have spent so much quality time together or when they needed to be within arms reach of me. I know this will fade over time, but I intend to nurture it for now.

Nick's appointment was pretty much a waste of time. He has had this cold/cough/sore throat for 2 weeks, but they won't treat unless he has it for another week :sad2: He did get the seasonal flu shot.

Colby's 7 year check was good. He grew 3 inches and about 10 lbs in the last year and the doctor feels that he is on a good growth curve even though he appears a bit heavy to us. She is still unconcerned that he is not completely night trained, but attributes it to being a heavy sleeper since he does not have accidents when he is awake. He also got the flu shot and unfortunatley he now has a temp of 100.2 :sad2: Hopefully he'll feel better in the morning.

I'm very glad to hear that it sounds like you are on the track to the right diagnosis. I'm sorry that it is possibly a lifetime condition but knowing what you are dealing with will help with that. I know that you have been worried about what was really wrong and that seems to be coming to an end for you.

I can understand the boys being clingy. Life is too short. We all need to remember that at all times. Enjoy every minute that you can. Tell those you love what they mean to you.

All of the DDA mean a lot to me and I thank you for your friendship. Deb, I really meant it when I said Call ANY time. I'm here for you.
 
Sorry that I couldn't check in earlier. Our internet was down and then we had company. Anyway the update.
We saw 2 neurologists today. They took a complete history, did a neuro exam and read his chart. Given the history, our stories and their findings they feel that he has juvenile epilepsy. Puberty can trigger the onset and unfortunately if they are correct it is something that will stay with him for the rest of his life. The good news is that they have very good meds that can control the seizures, leaving him seizure free once they find the right combination. They were unable to schedule an EEG until Monday and the EEG is the key to confirming their diagnosis. The EEG will take about 1 1/2 hours and they would like him to arrive tired (at 10 AM :confused3) we won't be able to see the doctors again until Wednesday. At that time they hope to be able to prescribe a medication to stop the seizures. Until that time he could have one (or more) at any time. We do have a med that we can give him if he starts to have convulsions or multiple seizures.

It appears now that what they have been calling low blood sugar episode was more likely due to the early stages of epilepsy. This makes us angry because we have spoken to numerous doctors on numerous occassions and they have all made the same assumptions/diagnosis. He has probably had multiple petit mal seizures that we were unaware of or did not recognize as such. They also assured us that they do not suspect any sort of brain abnormality as he is a straight A student, althletic, coordinated and he had a completley normal neuro exam and blood workup. That is a huge relief in itself. They also assured us that while watching him have a seizure is very traumatic for us, it does not in any way damage his brain and as long as he doesn't physically injur himself in the process they are completely safe for him.

We are feeling better about things tonight though the next few weeks could be hard depending on his seizure activity.

I have decided that I cannot devote my entire day tomorrow to ski patrol training. I sent an email to the head person explaining my situation and asking to be trained at a later date after things settle down. I have no idea how that will work out, but I know that I need to be here, now. It is truly amazing how entire lives can change in the blink of an eye and how quickly priorities change. My children are all clingy now and I certainly understand why. I can't remember the last time we have spent so much quality time together or when they needed to be within arms reach of me. I know this will fade over time, but I intend to nurture it for now.

Nick's appointment was pretty much a waste of time. He has had this cold/cough/sore throat for 2 weeks, but they won't treat unless he has it for another week :sad2: He did get the seasonal flu shot.

Colby's 7 year check was good. He grew 3 inches and about 10 lbs in the last year and the doctor feels that he is on a good growth curve even though he appears a bit heavy to us. She is still unconcerned that he is not completely night trained, but attributes it to being a heavy sleeper since he does not have accidents when he is awake. He also got the flu shot and unfortunatley he now has a temp of 100.2 :sad2: Hopefully he'll feel better in the morning.


Epilepsy is certainly a scary diagnosis but it is better to have a diagnosis and a game plan going forward. I had wondered if his blood sugar levels were actually pet mal seizures. Gran mals are terrifying for those who witness.

I am glad that you are seeing the upside (family time) to all of this.

You all will continue to be in my prayers.
 
Wow Deb, how scary. I'm glad you are so much closer to a diagnosis. They have really good drugs for seizures now. :goodvibes

Many, many hugs to you and your family.:goodvibes
 
Hey Stephanie & Terry, when are you at Disney World on your trip coming up in 14 days? Chuck is really serious about me trying to get us down there for a whirlwind trip.
 
Deb - I'm glad that you are on the path toward some answers, even if they are more serious. I'm glad that there are meds that can help him. You'll all remain in our thoughts and prayers. Enjoy your snuggle time with the boys while it lasts. :grouphug:
 
Hey Stephanie & Terry, when are you at Disney World on your trip coming up in 14 days? Chuck is really serious about me trying to get us down there for a whirlwind trip.

Vicki - They arrive 2 weeks from today. A bunch of us are meeting for lunch 2 weeks from tomorrow and then they leave on their cruise that Sunday or Monday.
 
Deb - I am delighted that you have a diagnosis of sorts. I have a student who had/has the same symptoms and diagnosis that you have for Hunter. Madi is now 15 and her meds control the seizures completely. I am hoping the same for Hunter.
 
Hey Stephanie & Terry, when are you at Disney World on your trip coming up in 14 days? Chuck is really serious about me trying to get us down there for a whirlwind trip.


Vicki, we arrive on Friday the 4th and go on the Wonder Sunday the 6th. Friday EPCOT is open until 12:30am and Saturday DHS is open early at 8:00 am! We can always squeeze two more for lunch! Oh please come on down!!:dance3::dance3::dance3:
 
Deb - Like everyone else, I'm so glad to hear that you finally have some answers as to what is going on with Hunter.
 
Good morning. :)

With this new schedule I am on, I can't sleep in anymore on my days off. But I guess when I get up at 3AM for work, I should realize gettting up at 7 when I'm off IS sleeping in.

I think we will do some shopping today. Alyssa needs a few pairs of jeans and a coat, and Nicholas could use some shoes. Alyssa also has to finish up her Indian project that is due on Monday. She has decided to make a poster of the life of the Powhatan Indians.
 
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