Monday, December 22, 2008
Kisses
Friday, November 28, 2008
Black Friday
Alex seems grumpy again. All night and again this AM he is squawking at Sophie. We think it may be the medication, but who knows. He has no appetite, loud noises are bothering him again. Loud, to the extent if you carrying on a conversation while he is sleeping or in bed, he will squawk ‘non!’.
Thursday, November 27, 2008
Thanksgiving
We were joined by both Megan and Malinda along with their significant others, Efrin and Chris. Malinda and Chris had actually come down Tuesday evening. Wednesday they took Alex to ride the Zoo train and then went to Sonic near Walker Ranch. After lunch they strolled through the park as it is in the airport flight path. It affords a great viewing point for airplanes landing. And being the day before Thanksgiving Day, the number of planes was very high.
We had our meal about 2 PM as Malinda and Chris were going to the Texas vs Texas A&M game, in Austin, 7 PM. Marycke, as usual, made a fantastic meal. Our blessings were so bountiful we totally forgot the Tomato and Feta salad. But we had more then enough with the green beans, mashed potatoes, sweet potatoes, rolls, stuffing, turkey and gravy.
After dinner we retired to the living room and got to watch Dallas beat Seattle. Some fine apple pie with ice cream, or perhaps a slice of pecan pie with whipped cream, and we got to watch Texas beat A&M. No need for dinner but Alex and I did get to go look for trains. And we found one. Woo woo!
Sunday, November 02, 2008
Seizures & Trains
An hour or so later Marycke got him up, fed him a waffle and then showered him off. I loaded up the car, got his meds together and we are over by the airport waiting for a train. So far several planes, one malfunction of the train crossing guard and no trains yet.
Saturday, November 01, 2008
Trains & Football
Over near the East yard we picked up several trains and followed them all around the city. Of course we needed to make another stop at Mac Donald’s but he is looking well and may come with me on a service call.
But Mom’s calls in and agrees to pick Alex up while I install a wireless network. The install went better then expected and with 4 hours left in the day we agree to go try and see the Blue Angels. Alex and I travel to the Southside of SA and enjoyed a wonderful air show.
Time for Texas vs Texas Tech football. Alex piles in next to me on the lounger and smiled every time he heard a whistle blow. It took a couple weeks but he finally did decide he want to wear his whistles again. He did not want to eat Pizza but did eat a BIG plate of Cheddar Chez Its, Mixed Nuts and cubes of chunk cheese.
Near 10 PM now and Alex seems a little woozy. So he will spend the night with Marycke just in case he has seizures. I stayed up late and watched a great game, won by Tech with 1 second in the game!
Friday, October 31, 2008
Halloween Fun
Saturday, October 25, 2008
Drug change
Sunday, October 19, 2008
A Little Progress
Doctor Visit
Alex has gotten a rash. And along with the fever our Doctor wnat to see him. Marycke thinks it may have been the additives she has been putting in the smoothies.
Sleepy Sunday
Marycke is hoping it is not the Pehnobarb but something is no sitting well with Alex.
Saturday, October 18, 2008
Seizure Saturday
Whatever it is it is making for a stressful time. For the last 3 weeks Alex has been sleeping in our King size bed, with Marycke. Then unfortunately, more often then not, when Alex seizes, we pees in the bed.
But we did get a chance step out for an hour or so and attend the Epilepsy 'Day in the Park'. The park is in the flight path near the end of the runway. Alex enjoyed the planes but only for about 15 minutes.
He asked for Mac Donald's and at first said he wanted fries AND nuggets. But by the time we arrived to the drive through he only wanted a coke and fries.
Alex crossed the long bridge to the Park.
Then he 'signs' airplane as one passes over.
Thursday, October 16, 2008
Fortune Cookies
Then he grabs another and another. Out of fortune cookies Marycke finds a serving of Apple Jacks and another of Lucky Charms. Wow neat to see him eat!
Bummer, time for bed and he has a seizure. Maybe it was not good for him to eat. From Biblical times to the present, epilepsy has been a disease shrouded in mysticism and fear. Seizures, which are now known to be a neurophysiological phenomenon, are the defining characteristic of epilepsy.
It has long been known that starvation is an effective, if impractical means of controlling seizures. There is even a reference in the Bible to starvation controlling "fits." Mark 6:29 "cured by fasting and prayer." The first scientific study of fasting as a treatment for epilepsy was conducted in France in 1910. The researchers concluded that seizures were improved by absolute starvation.
During starvation, the body first burns all of its glycogen. It then begins to burn body fat and protein for the specific purpose of supplying the brain with glucose. As fasting continues, the body shifts into a state known as ketosis. The brain begins to use ketones from the metabolism of fats as energy rather than glucose. This shift in metabolism also correlates with a reduction in seizure activity.
Tuesday, October 14, 2008
Doctor Visit
Alex has gotten a rash. And along with the fever our Doctor want to see him. Marycke thinks it may have been the additives she has been putting in the smoothies.
Yeah! He is over 100 lbs again. Still not eating much more then smoothies and Ensure but at least he is not loosing more weight.
Meanwhile, Sophie continues to be very interested in Alex. Always trying to play with him. And when he has seizures she seems to know something is wrong. She comes over and licks his face or lies on top of him.
She is getting so big. She also is loosing her baby teeth and chewing on EVERYTHING. I always seem to have only one shoe. So Marycke went and got her a BIG bone. She seems to enjoy it!
Friday, October 10, 2008
Little Progress
Sunday, October 05, 2008
Play time for Sophie
Sophie has discovered the sprinklers. I never knew a dog could have such a fun time with a couple of sprinklers.
Better
Meanwhile, ran across this video from last month. Sophie was trying really hard to wake up alex. But Alex sleeeps... he SLEEPS!
Neal
Still not eating
We are coming up on day 21 of Alex not eating (His only nutrition is Ensure that we giving him 3 times a day squirting it into his mouth with a syringe and hoping he does not spit it back out.) Not eating makes him very susceptible to infection. So Doctor Martin’s office wants to monitor him closely. We may also have to have a feeding tube put in.
On Thursday they determine his medication levels to be 200% of the therapeutic level which may account for his lack of appetite and sleeping 15-20 hours a day. The doctors are now backing off on the drug levels.
On the upside, no seizures for the past 8 days!
Thursday, September 25, 2008
Alex Home
Yeah. Alex was allowed to come home late yesterday afternoon. Marycke called and said the docs saw no reason to keep him in the hospital and it would be okay to come home. Alex agreed and was ready to go right then.
As ususal it took a few hours but we finally did make it home. Sophie was happy to see him but Alex was not ready for sophie.
We thought he may eat more at home but not so far. He would not even drink anything. Maybe later today.
We are just happy to be home.
Alex Day 11
Early on yesterday afternoon Alex was up and doing well. we expected to go home today.
Marycke said he was waiting for 'Neal to call.' He kept the phone with him all night.
Well we have reached day 11. And does not look like we will be going home.
Last night Alex did pretty well. Nothing to drink still but ate some chunk cheese.
Then this AM he had seizures at 6:11 and 8:15. So I feel the doctors will want to keep him another day or two.
Alex recovers after seizure #2 this AM.
The tech agrees to remove his 'hat'. Alex is happy!
For the past few days he has been sitting in a chair. No longer does he want to be in 'that bed.'
Thanks your all your care, prayers and notes.
PS. Marycke’s phone was damaged during one of the seizures so reach her at 210.358.1252
Monday, September 22, 2008
Day 8
We watched the Cowboys play football and then finally we got to sleep just before midnight. However Alex stayed up to nearly 3 AM. Every 20 minutes or so he tried to pull something off or out of his body. He just is not a happy camper right now.
Come Monday morning, Alex is up earlier than I expected (7:10 AM) so we sat around waiting on Mom to bring breakfast. Of course the breakfast was for Neal as Alex still has not eaten anything nor has he gone to the bathroom on his own. Until those two things are accomplished we will not be able to leave.
I am going home for a shower and to check on PSU. But on the way back, Marycke called to say Alex has had 3 seizures. Maybe that is why he was not willing to eat. Needless to say with all those fluids being pump in and him not going to the potty, everything came out during this latest episode.
They have given him 2 does of Ativan and as of 2:30 PM, Marycke reports he has not had anymore. He is sleeping and may do so for sometime. So I imagine for now Marycke does not want any visitors.
Thanks again for all the notes and comments of the blog. Looks like we will be there even longer than we expected.
Neal
Neal and Alex discuss what can can cannot be removed.
Alex 'converses' with his faorite nurse, Rebecca.
Sunday, September 21, 2008
Alex Update
Alex did well last night. Sitting up and ‘playing’ with the nurses until after midnight.
He slept through the night and then got to enjoy breakfast with Grandpa.
Unfortunately it is the ‘eating thing’ that is keeping him in the hospital. He still has not eaten since Saturday night a week ago.
They tried the feeding tube of the nose without success. Next they are taking about a tube directly into the small intestine.
His seizures remain ‘below the surface’ but he is continuing to seize. His medicines appear to be working. The doc thinks we are past worrying about seizures from medicine withdrawal.
So we are focused on getting him to eat, walk around and then we could home. I expect with will be Tuesday or Wednesday at the earliest.
Thanks for all the notes.
Saturday, September 20, 2008
Saturday Morning
The Internal Medicine doctors have decided Alex needs to be feed through a tube up his nose.
On the better side, his lungs have cleared up. The docotors feel his pneumonia is clearing up. More than once Alex has pulled off his head bandage. Here Dale has to reapply it.
Last night around 4 AM he woke up and realized he had needles in the arms, a catheter, his head rapped, something clipped to his finger and both legs wrapped with something squeezing them to increase circulation. He let out a very BIG yell. Both RNs came running and I said, 'He is awake.'
Now we have to figure out how to keep him from pulling everything off. They considered restraints, we suggested some type of homemade sleeve, but the decided on 'boxing gloves'. Soon they went. The RN was very pleased with his work until 2 seconds later Alex had one off, had tossed it across the room and was proceeding to try and remove the wrapping from his head.
Okay back to last night. From 4 AM to 5:10 I am by his bedding trying to get him not to pull any thing off. He falls asleep. Sure enough 15 minutes later the nurses are in to 'turn him'. Alex gets
He is showing some signs of bedsores and inactivity.
Okay I get him settled back down and 10 minutes later it is time for 'vitals'. Once again he gets wakened. Again becomes agitated (mostly because I think he does not understand he can go 'potty' while still in bed.) So now we have got him back asleep a little after 6 AM. 6:15 it is the respiratory nurse. 'We have to give Alex his treatment." So now they hold a mask over his nose and mouth for 7-8 minutes and pump O2 and drugs into him.
Okay not so bad. I lay down to go to sleep (they have a chair with a pull out cot.) and Alex screams out again. Okay I am up. He is trying to pull stuff off and I think needs to go potty.
7:15 his Doctor (Joe David Bowers, who also happens also to go to my church.) tells me they need to put a feeding tube down Alex's nose. We give him more drugs, take a few more vitals, and now Marycke arrives... just in time to see them shoving a tube up his nose. 3 nurse and Marycke held his hands, legs and head, as the tube is inserted. Looking good, looking goods, BAM! Alex breaks the grasp of someone and yanks the tube back out.
Okay more staff is called and we go for attempt number two. Let's just say it did not work. Marycke was thankful I was not shooting video. The tube started down, there some screaming, some coughing and then lots a blood was spit across the bed and onto the doctor. Guess that says enough that they decided no to do the tube for now.
Marycke is with him now so I can come home, shower, check email and write some new posts. Then I am going back over. Grandpa was on his way up as I left. We have had several visitors and appreciate each and every one. Still, remember to call Marycke first. we are not sure what we will be doing to the boy.
Prognosis, we will be there 3-4 more days. The Dialantin and Phenobarbital are in good therapeutic ranges. However he is still have seizures that never manifest to the 'outside'. The EEG is seeing the activity. Marycke is noticing a few changes in his eye pattern. But a good Mom seems always to be able to do that.
Thanks again. Not sure when I can post again so here are some pictures and even some videos.
Neal
This video shows Alex waking up and me telling him he would have to ‘wait five’ before removing anything from his body.
This one shows a night time seizure. Pretty mild compared to the others.
Tuesday, September 16, 2008
Alex Hospital
Backing up a little let me say, Alex typically becomes refractory to his medication about every 18 months. This was the case near the end of May.
So we took him off of Felbatol and started him on Lyrica. He also did not do well on that. Seizures increased to about 4-5 per week and rather than only being at night, he started having them during the day.
So while we were in the course of getting this med adjusted it became harder and harder to stop his seizures. We have a drug called Diastat we could give him at home and it would stop them. But it is a strong drug and ‘knocks him out’ for the next 24-30 hours. Well over the past two weeks Alex appears to have also built up a tolerance to Diastat.
So last week, after multiple seizures Saturday and Sunday, it became apparent Diastat was not going to work. So Monday afternoon we took him to the ER. Normally they administer Ativan and seizures stop. Not this time. Alex continued to have 70 seizures over the next 14 hours. The ER never was able to get them to stop. So we checked him into University Hospital (Room 1252) and they gave him super doses of anti seizure (AED) medications. We had gone near the point of having to possibility putting alex into a ‘chemically induced coma’. But fortunately, just after midnight Monday, Alex stopped seizing.
Now, we have been trying to wake him up for the past 2 days. No luck so far. The doctors have taken him off 3 of the five AED he was on but will not know his reaction to the change until we get him to wake up.
And now they have decided his larnnyx is drying out. Them have had to put on a mask to add moister to this O2
Sunday, September 14, 2008
Seizure weekend
but by the afternon he had rturned to his room, gathered al lhis favorite items, and has now fallen alseep on the floor.
Then Sunday AM, seizures again. Marycke has given him Diastat but they still are not controlled. If we can not ge tthem to stop by 2 PM we will have to go the ER.
Oh good. All done for now. Let's see what tomorrow brings.
Neal
Thursday, September 11, 2008
Welcome Sophie
We are hoping she will become a good friend and guardian to Alex. So far they are still getting aquainted.
Sometimes she takes a break from chasing her tail, eating and sleeping to help Marycke with office work. So please forgive any invocies with paw prints.
And of course nap time is important for puppies.
From the back of the couch to sitting on the dishwasher door, Sophie has figred a way to be in the middle of the action.
Friday, August 15, 2008
Up early
We can not find his dot box, his favorite puzzle. Mom picked it up yesterday so the new puppy would not chew on the pieces. Anyway, we go back and forth from the LR to his bedroom. The whistles are jangling around his neck. I am afraid the puppy will hear us and want to get up as well.
Tuesday, August 12, 2008
On our own
So I could not get him to eat a normal breakfast but he did have Mac and Cheese again. Then we went off to the showers. He still needs help with every aspect. I guess he sort of can wash his own hair. But otherwise we have to wash him down. He also does not dry himself.
Before going to The ARC, we stop over by the runway and watch a few planes land. Even after all these years he use the word, ‘orange’ for any airplane. I guess it was because of all the orange Southwest planes we use to see.
Monday, August 11, 2008
Early Night for Alex
Well it is 7:40 PM and Alex has already had meds is asleep.
He had a seizure this AM, 5:33, but then got up on his own around 6 AM. He has stayed up the entire day. We had to have MAC and cheese for breakfast but he had no problem going to The ARC.
I picked him up early, stopped by the house to say hi to Grandpa, and then out to Fiesta Texas again. He was very excited about riding the train, and the horses on the carousel, and then sat and watched the airplanes. After about 20 minutes he finally said he wanted to go on the plane. But alas he was too tall.
But, while waiting, we were near the White Water log rise. He expressed an interest in going. So off we went. And again. And again. Wow he was wet but said he still wanted more. I expected to bring him home and let him get to sleep. Here we are coming down the big drop.
Then we got home and there was a water rise right in our own street! Water main brake.
Sunday, August 10, 2008
Sunday Seizures
Now we have decided to go look for trains, stop by Mac Donald and maybe bring along some Mac & Cheese.
We indeed got Mickey D’s and then stayed along the tracks by Whetmore, at the end of the airport run way, but had to wait nearly an hour for a train. During that time he finished on 32oz Diet Coke and we got a refill at the Broadway Mac.
Back to the tracks. Here is the train? There it is! But wait, it is going backwards. There is no engine. Alex thinks that is just too funny. Lots of laughing. Then they crash couple with a loud – bang!
Mickey D's
Now we have decided to go look for trains, stop by Mac Donald and maybe bring along some Mac & Cheese.
We indeed got Mickey D’s and then stayed along the tracks by Whetmore, at the end of the airport run way, but had to wait nearly an hour for a train. During that time he finished on 32oz Diet Coke and we got a refill at the Broadway Mac.
Back to the tracks. Here is the train? There it is! But wait, it is going backwards. There is no engine. Alex thinks that is just too funny. Lots of laughing. Then they crash couple with a loud – bang!
Saturday, August 09, 2008
Saturday with Dad
Of course, had to stop by Mac Donalds for a biggie breakfast. We could just eat pankcakes while watching the planes.