A Doodle Kind of Day


Today was a perfect day.
The Doodle was happy and seizure free.
I was getting ready for our garage sale tomorrow and came across his Backyardigan's Tyrone costume from last year. The Doodle loves the Backyardigans. He couldn't wear the costume or go trick or treating because he had just broken his leg and was in a full leg cast. I guess he could have gone as a "Toddler with a Broken Leg" but how overdone and completely unoriginal. I wanted to put this on him before he outgrew it and get a picture to scrapbook.

Ta Da.He doesn't mind the hat, I guess since he wears a helmet every day, he's pretty used to having something weird on his head. He just looks up to something in this one. Like he's plotting something shady. Like how he's going to stay up all night and make us watch cartoons.It's almost 11:00 pm, do you think he's even close to going to sleep???
I wish every day could be a seizure free Doodle kind of day.

Now You See It...





Now you don't.

Thank you for all of your emails. I've received an overwhelming number of emails concerned about the "shower door" incident and how Jimmy is so I thought I would give a quick update and post a couple of pictures of what used to be the shower door. If you look closely you can see the spots where his feet were underneath the broken glass before I picked him up and shook the glass off of him.

I get a little sick to my stomach to even think of how bad it could have been. I would call this a freak accident but you would need to know the story behind our contractor and our experience building this house to fully understand.

Jimmy was very lucky. Someone was watching over him because he walked away with just a few small cuts from so much broken glass. He's a little traumatized and now prefers baths, but completely fine. I can't even imagine if the Doodle would have been in there. He wouldn't have known to stay still and even though I would have probably been in there with him, I don't know how I could have stopped him from cutting himself on the millions of pieces of broken glass.

All Jacked Up and No Where To Go


Not sure what to do about divvying up the dosage of the Doodle's medication. When I give him the larger dose in the night, he won't sleep for HOURS. He lays in bed thrashing around, kicking, crying, screaming. It's not so bad when I give him the morning dose because, well, he's busy being 3. But at night, within 5 minutes of giving it to him, he's climbing the walls and he doesn't come down off his Depakote/Keppra Cocktail High for at least 2-3 hours.

Tonight around 8:00 pm I had to drive to my bosses house which is about an hour away. My mom drove with me and we brought the Doodle since I had just given him his medicine and we knew he wouldn't be going to sleep anytime soon--he was freaking out in his car seat; doing a weird scream, covering his ears and shaking his head back and forth so fast I thought he might jar something loose. My mom got in the back seat with him and tried her best to entertain him. She fed him and played with him. I couldn't get home fast enough. What was I thinking? I keep having these moments where I can't believe I brought him somewhere and regretted it but it was too late to un-do it.

I've read on the Epilepsy.com website from real people with epilepsy how mind altering these drugs are; that they cause ringing in the ears, anxiety, irritability, insomnia, blurred vision and many more side effects. How can I possibly begin to tell what the Doodle is feeling or which side-effects are affecting him? I know they make him crazy. I know they make him anxious and unable to sleep. But what else?

I've talked to the Doctors about spreading out his dosages, so that I am not giving it to him all at one time but they don't think that is a good idea. I could try switching his medication to a different one...but the side effects of those are said to be even worse and could be more life threatening.

His seizure activity has been much less than usual. We had a few completely seizure free days and then just a few break-through seizures here and there on the other days. Today he only had one that we know of. Much better than the previous 40-60 per day we were seeing.

Although, I'm still waiting for that other shoe to drop.

There's No Place Like Home



I convinced Jimmy with a little motherly guilt and some bribery to come home a night early. I told him I would take him to the Fair tonight and then we could go to Scandia tomorrow if we came home.

It took us 4 hours to get home from Gilroy. Traffic was brutal. We walked in the door and immediately had to grab the Doodle and get back in the car to go to the fair. Not my first, second or five hundredth choice of what I really wanted to do tonight. Especially with the Doodle and no help to bring with me.

Two words: OVER STIMULATED. Between the noise, the flashing strobe lights, crowds and being locked in his stroller, the Doodle wasn't having a very good time either. Luckily most of his autistic screaming was drowned out by the loudness of the crowd, the music and the rides. I couldn't see the Doodle's face but could tell he must be freaking out pretty bad based on the stares and bewildered faces made at him by the on-coming people in the crowd.

It was especially fun sitting down on one of the crowded benches trying to empty 3 sprinkle capsules of Depakote onto a spoon full of applesauce carefully being balanced on my knee. I guess people aren't used to watching a child get dosed anti-seizure medication at the fair.

Good times. And then it got even better.

Most of the kiddie rides the child has to be 36", which criteria the Doodle meets. Granted, most of the kiddie rides the parents are too big to go on the ride with the child, and the child is supposed to ride by themselves. That might be the case for a typical 3 year old but not a special needs child.

No way was I putting the Doodle Bug on a ride alone. He doesn't have the emotional capacity or understanding to handle it. He's pretty impulsive and would most likely jump out when the ride got up to speed. He's a trained escape artist and can wiggle his way out of even the best seatbelts and straps.

Then there were kiddie rides where the parents could go on the ride which was a great solution because I thought I could have Jimmy ride along with him and I could have at least gotten some cute pictures to scrapbook. But the non-English speaking Carnival workers wouldn't let him even though he's 5' 2" and bigger than some parents. I think maybe because he wasn't old enough but I'm still not sure with the language barrier and all. It's times like these I wish I would have paid better attention in Sophomore Spanish class or at least retained the properly effective curse words to use at such opportune times.

Reluctantly, I took the Doodle myself in full screaming mode on the Flying Elephant. I sat there with anxiety that the Elephant might not be able to fly with my weight on his back.

The waiting part was the hair-puller-outer. I guess they like to wait for the ride to get full before they take off, so we sat. And waited. And waited. The problem is, the Doodle doesn't have a patient bone in his body. The only thing he knows about waiting is that he doesn't like it.

He actually loved it (look at that little face) once they finally took off.

Since Jimmy was too big for the kiddie rides, he was bored out of his mind and he had no one to go on the big rides with since we brought the Doodle. Once I told him about the gang related stabbings after dark and he could see the police population ramping up, he was ready to go too.

By the time I got off the poor, overworked flying Elephant, I was ready to go. I'd had my fill of fun. $50 for one and a half hours of autistic behavior torture and I'm still trying to figure out how many Weight Watchers Points are in a Fair Corn dog. I had my heart set on my favorite food of all time, Fair Tacos. The soft, greasy rolled up kind with lettuce and some kind of unidentifiable meat, but they are gone. Ido. Terminado. No más.

Jimmy


Today was the start of a mid-week couple of days off mini-vacation with Jimmy. Last year we came down to Gilroy to stay a couple of nights with Jim while he worked and we went to the outlets and to the Santa Cruz Beach Boardwalk. We brought the Doodle on the trip last year and it wasn't easy. Or much fun. So this year, Jimmy and I came down for a couple of days Doodle-free. Grammy is watching the little monster and I sure miss him right now; so much that my heart aches. I just played a slide show for myself of his pictures on my laptop.
I'm bummed we just missed the famous Gilroy Garlic Festival, it was last weekend. But, Jimmy is having the best time. He gets to pick and decide everything we do, where we stay, and what we eat. I am completely on Jimmy time. Right now it's 11:00 and we're watching Hannah Montana in our hotel room, we're burning the midnight oil. I love Hannah's song so I put it in on the Doodle's blog for you to enjoy. It makes me cry, I'm such a wuss.
We spent most of the days shopping for school clothes at the Gilroy Outlets. He's a dream come true because he likes to shop as much as I do. I gave him a budget this year and I told him he can spend it anyway he wants to on his school clothes. Now that he has to part with "his" money he is much more thoughtful and careful about what he buys. We went to all of his favorite stores so it was worth the trip: Volcom, Fox, Etnies, Quicksilver, Hurley, Puma, Nike, Echo, Calvin Klein, DC Shoes, and so many more. He was in heaven. Here's what Jimmy bought...
Here's what I bought...Another hat to put in the rotation, can you believe it?

We had a nice date night out to dinner at Chevy's (boy do I love their Salsa!) And then we came back to the hotel and went in the hot tub. Yes, I got in a bathing suit...we met some nice people from Canada, aye.
Not even sure what we are doing tomorrow. We will sleep in, go to breakfast and play it by ear. I'm trying to talk him into going home early and going to the fair; the Doodle could go to the fair with us. He's pushing for Raging Waters Water Slide Par, where I would be required to shave my legs or I might scare the kids and then put on a bathing suit which is equally as frightening.

You'd think I would sleep great tonight, I've only had a few nights away from the Doodle and I can't help but worry. When I say away, I don't mean just away, but not sleeping next to me, touching me and kicking me in the back all night long waking up screaming. I've got black-out curtains, a no disturb sign on our door, a queen bed with high thread count sheets and a down comforter all to myself and I probably won't get any sleep tonight thinking about the Doodle.

Tipping the Scale


As nervous as I've been, I was being so optimistic and hoping that the last two seizure free days meant something wonderful. Like maybe the medicine was working or we had a miracle cure. Hopeful that the Doodle was finally getting a break. And then it just happened. Minutes ago, sitting here on my bed with me, he just had a head-drop seizure and within minutes another one. Does this mean they're back in full force? There is NO way to tell other than we will just have to watch and wait. The Doodle's seizures are totally unpredictable and completely random. No rhyme or reason to them, makes me want to eat a cookie.

Speaking of cookies, I went to my first Weight Watcher's Meeting and Humiliation Weigh-In this afternoon. I sat in the intervention section and I felt like I didn't have to say anything to the group, it was pretty obvious why I was there. So I just listened and clapped for all of the people with willpower just saying no to Chocolate for breakfast.

What I'm hoping works about Weight Watchers is that as bad as I am with math and keeping track of points, at least I can eat real food. I'm not required to be really strict with what goes into my mouth, just how much and when. So if I want to eat a donut, I just know I will have to make up for it later with some points reduction. I tried Weight Watchers about 6 years ago when I was hooked on Starbucks Vanilla Frappucinos and I would drink 2 or 3 of those in the morning and be out of points by lunchtime. So, we'll see.

It's a little bit humbling standing on the scale in front of a complete stranger. When she told me to get on the scale I started taking off my hat, jewelry and shoes. I handed her my tiny earrings and then I looked at her deadpan and asked her if it was OK if I got naked for my weigh in. I think she thought I was serious. I can't believe what I weigh. Our scales at home have to be so off, maybe it's the altitude. If I want to lose an instant 6 pounds, I just have to weigh myself at my mom's house.

So right now, I'm doing a tally of points in my head for my daily points and I think I'm already over. But there's always tomorrow, right?

P. Doodle


Look out P.Diddy or Puff Daddy, whatever you are calling yourself these days...there's a new Gansta in town. Check out this little Homey.

He's still coming down off his birthday cake high. Jim affectionately refers to him as his little shortie.

The Doodle's Birthday Party

Today was a remarkable day.

Doodle Bug turned 3 and we had a little party for him. It was just close family and our new friends Jill and Peyton. It was a fun day and the perfect sunshine weather. The best part of the day was the Doodle was SEIZURE FREE! It's been 2 weeks since the big storm of seizures and I've been biting my cheek every day waiting for more. Today we were blessed with a perfect day. My mom was a tremendous help today and I am so very grateful to have her here. Thanks Mom, I love you and I would never give you away.

The Doodle loved his cake. He doesn't blow very well but he can sure do a raspberry to beat the band! So, instead of blowing he did raspberries. He kept trying to grab the candles, no sense that they might burn him. He liked that people sang to him and then clapped their hands at the end. He's a bit of a ham.

He's pretty exhausted right now, we broke out the jumpy for the kids and he had a ball. I think the cousins had fun too--they even played some baseball.

We never did our fire in the pit to make s'mores so now I have a ton of s'mores kits sitting here calling my name. Who's coming over for s'mores?

And, of course I had to have favors...

I'm glad we had the party afterall. It was a huge success.

Happy Birthday Doodle

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My 100th Post

Drum roll please...this is my 100th post here at Doodle Bug Chronicles.

I wanted to take a moment to thank all of you fabulous readers and followers for your support, kind words of encouragement, hugs and prayers. You do not know how much they mean to me and my family and they keep me going on even the toughest day.

It's amazing to me how this little blog about our Doodle Bug has been such a therapeutic release and sounding board for me to get my thoughts, feelings and, YES, complaints out there to our world. Our family is very lucky, under these circumstances, to have such kind and genuine people in our lives who care about this little guy so much. And thank you also for hanging in there even when I bitch, curse and talk about poo.

I've met some really nice people after beginning this blog and I appreciate all of your emails. I'm saving all of the touching notes I get from you and I will someday put them together in a book for the Doodle to read when he gets old enough to understand all of this.

From the bottom of my heart and the Doodle Bug's heart, we thank you.

Love,
Angela, Jim, Jimmy & Doodle

Papa Steve




The Doodle Shows Papa Steve His Helmet.

What great timing the Doodle has. I think you can tell when he is really comfortable around some people because he poops his pants. My Dad, Papa Steve and Kathy, Dad's Better Half, stopped by this evening to bring the Doodle his birthday presents because they will be out of town for his party on Saturday. They got the best Doodle greeting he could muster since he was engrossed in his SHAPE appointment with the Dora the Explorer lady.

Papa Steve was nice enough to wear his helmet too. It always make the Doodle feel like one of the guys when he sees a fellow helmet wearer. And, he loves his wooden groceries that they brought him. I'm so happy that they are made out of wood because he would most definitely rip them to shreds if they were the cardboard kind...not sure how Kathy knew that. But, good call! I must now unhide his shopping cart that I put away when he started having his seizures again so that the groceries can go in his cart.

He was playing with the giant Hummer, which he broke the doors off and showing them how the Daddy guy would go inside. He then put all the groceries in the car, not knowing his Dad doesn't ever actually go to the grocery store. Still no sign of a Mommy person, the one that actually does all of the grocery shopping.

So, in the end, he did what any excited kid would do, he opened his presents and then dropped a load. And, on their way out he blew them a kiss. It was really nice to see my Dad and Kathy.
Check Spelling

TURNING


Jim told me tonight that we don't tell each other we love each other enough. I had to agree. We know that we love each other and when it feels like we are living in crisis mode, taking things day by day we forget to tell each other.

I love you Jim.

Here's something I wrote for you a long time ago and I still feel the same way. I'm not sure if you will remember it or not.


TURNING


Turning in circles, turning around,

We turn to each other, making no sound.

The night becomes morning, as chill becomes warm.

Turning to you, to clear up the storm.

Turning my life of lonely regret,
into a moment of happiness yet.

Even one moment of feeling your love,

rekindles my feelings from somewhere above.

Of knowing how happy we both truly will be,

by trusting in you, you trusting in me.

Turning my life to a new founded course,

of strength and support from a warm, loving source.

Of friendship and kindness, our time to unfold.

Turning sadness to smiles when it's you that I hold.

Clean Up On Aisle Upstairs Bathroom


What a day.

Jimmy decided to finally take a shower. The one he takes once a week, whether he needs it or not. He usually, albeit infrequently, takes his showers downstairs in our bathroom. I told him today to try his own shower. I think he's only used it once. So to make my long story even longer....

I was downstairs visiting with the Doodle and one of his favorite visitors in the world, Betsy. All of a sudden we heard a crash and then screams from upstairs. It was Jimmy screaming so I ran as fast as I could upstairs to find him standing in the shower covered in glass and blood dripping everywhere. He was freaking out and screaming and I had no idea what to do or what had happened. There was glass everywhere, covering his bloody feet, all over the floor. It was a real nightmare. I kept yelling for him not to move.One of the glass shower doors had completely shattered. I didn't have shoes on but I walked over to him and lifted him out of the shower, he weighs 90 pounds and is over 5' tall, so my mother warrior super strength must have kicked in. I set him down on a towel and tried to assess the severity of the cuts. I carefully pulled little pieces of glass out from between his toes. His beautiful brown hair was still soapy.

All I could think about is how could this have happened? Then I remembered our shitty contractor cutting every corner he possibly could and a bell went off in my head. Yes.

Jimmy swears he was just sliding the door over with the palm of his hand--it's not like he has a ton of strength, he's only 9. It wasn't as if he slammed it or anything else, the entire glass door was in millions of tiny pieces. The weight of the glass falling on him is what cut him. He has many tiny little cuts and one pretty big one on his arm.

The whole time he's screaming, "I never want to take a shower again" and "Am I going to die?"

Thank God Betsy was there to sit and watch the Doodle while I dealt with the shattered shower door aftermath.

I put Jimmy into the bathtub and tried to wash the blood off so I could see how bad the cuts were. All I could see was blood all over his arms, legs, hands and feet. I didn't know yet if he needed to go to the emergency room.

He was still crying and now he was shaking.

All I could do was curse our cheap ass contractor.

Once the bleeding stopped and I was able to see the cuts, they were minor. Thank goodness. I guess my boy is just a bleeder. He was still crying and I could see that there were pieces of glass still in his cuts. I had no idea tempered glass could break into such tiny shards. I had to get a pair of tweezers and pull the glass out one piece at a time. You should know I am not good with blood and guts and have been known to pass out in places like the Veterinarian's office.

We bandaged him up and I did what any scared shitless mom might do. I kissed him and hugged him, told him how sorry I was and gave him an extra good behavior point out of guilt...

Never a dull moment.
On a brighter note, we have a Peacock. We don't own it, but it's been coming to visit. I'd take a picture and post it but it's a little camera shy. As beautiful as peacocks are, they have the loudest and shrillest voices ever. The peacock sounds a lot like our cat when she was in heat.


Maybe I'm Autistic

Having an autistic child has been a challenge and with that challenge comes new experiences I had never prepared for. As grateful as I am for all of the Doodle's therapies and autism programs he has been blessed to receive, it is hard keeping up with the intense daily schedule and the many different people involved on his constantly changing TEAM and making their schedules fit with ours.

Yup. I think I might be complaining again. I went a whole day without complaining but now it's back.

The Doodle has been in the Shape program and receives services from our Regional Center where they send an assistant to work with him for two hours a day and other types of therapists. They set goals with us and they come to the house and do a lot of floor time and play-based therapy with the Doodle. We were blessed to have been assigned a wonderful lady, Betsy, who loved and worked with the Doodle every day for almost a year. Once the school year was over we lost her, although we still keep in touch.

In Betsy's place, they sent two other ladies to split up the week but it wasn't the same. Sure they showed up with bins of things to do, which the Doodle loves. If you ever come to the door and the Doodle answers he will be most certainly looking to see if you brought a bin for him. He only gets this in home service until he turns 3 so the summer time has been quite challenging because we no longer have the other two ladies either. They left. So we had some confusion and had a couple of weeks skipped and then they just sent another one out. While this one is nice enough, she barely speaks any English. I don't think the Doodle really cares much, he thinks Dora the Explorer is here to play with him. And if his first word is going to be Spanish--I'll happily take it. I'm all about diversity.

The Doodle also has a speech therapist that comes weekly, although we don't have a very good track record with her actually showing up. He needs a speech therapist more than anything and it's what he gets the least of. His physical and occupational therapists are outside of the home, once a week for an hour each--although they have been combining his appointments and doing them together, so he's getting a little jipped there too. I'm supposed to be his advocate yet I feel guilty when I complain about his "free" services.

It's hard for me, because you spend so much time getting a good team assembled and maybe my expectations have been set too high--but we haven't had much consistency since Betsy left. Betsy was here even on the days the Doodle felt crappy and had seizures.

In addition to keeping all of these appointments in between and during seizure activity, doctor appointments and naps--it's hard counting on these people, getting to know them, getting to trust them, letting them into your home and life and then they're gone.

It takes a lot of energy and social skills to get to know people. Lately, I feel like these people (pre-Betsy) that have been coming, just want to get in and get out. They know they are not going to be here for any length of time, so it's felt very disconnected. I'm probably going to get shot for saying this or want to eat my words but it's hard having a revolving door of people coming through here. Since the Doodle has been in the program we have had 11 different people on his team in 1 1/2 years. With each new person, comes an orientation process. It's hard to orient someone who is only going to be here five times. One of the new last assistants we had told me the Doodle was saying words. I don't think she was told or knew he couldn't speak. Then she left me scratching my head when she asked me if I thought he was autistic. OK. What did she think she was here for exactly?

To add more people into the mix, we have added a Nurse. We are going through an in-home nursing agency for his nurse for 4 hours a day, and we have come to like our Nurse very much. She is a great fit and we are very comfortable with her. You have to be comfortable with someone who is spending 80% of their time in your master bedroom...But, she just went on vacation. For three weeks. Now we are getting sent 5 different nurses to replace her shifts. I have no idea who these people are or how they are going to fit with our family. They aren't here long enough to really find out. Everybody brings their own personalities and ideas with them. Then I think as long as they are good with the Doodle, it doesn't matter and it will be OK.

One big and general trait of most people with autism is that they need consistency and like familiarity. They are very into structure, patterns and schedules. That includes, for the Doodle, meeting and working with so many different and new people.

My social skills are a little rusty and lacking--which brings me to the title of my post. For the most part, I haven't been wanting to be around people lately. I haven't felt like socializing. I don't like meeting new people or expending the extra effort and energy it takes to get to know people. I've suddenly become a bummer at parties. Until yesterday when I met my new friend, I was Debbie Downer. She was the first new person I was excited about meeting.

Maybe I'm Autistic.

Kindred Spirits


Can you believe it? I have nothing to complain about today.

The Doodle is status-quo, just a handful of the head drop seizures today--last count was 4.

I'm feeling lighter today and definitely not because I ate all that cheese cake last night. My soul feels lighter. Besty introduced me to the most wonderful woman and today I finally got to meet her in person. She has a 3 year old and we took our little guys for a walk around Spring Lake. What I love about her is how much we have in common and how much she gets IT and ME. She is a wealth of information and understanding and her little guy couldn't be any cuter and sweeter. The Doodle made a new friend and so did I.

I suddenly feel like I have met my match. She is a genuine kindred spirit. And, even though the walk kicked my butt, I had a great time. Things felt as normal as they could feel. So today was one of the first days I didn't feel overwhelmed with sadness. I had moments of true joy and remembered to count my blessings for all of the good that is in my life. It hurts to dwell so much on the negative and watching your baby suffer makes it hard to remember to do that.

When I came back from our walk, my mom was hosting a lunch for some of her Corvette Club friends. My mom has some great friends. She is lucky to have friends like that. And, I too am lucky to have met them too. One lady, Dottie, has been saying prayers for the Doodle in her prayer group. Today when I saw her she had some nice words of wisdom and encouragement for me and gave me a beautiful silver coin with a passage written on it. The coin says: "Lord help me remember that nothing is going to happen today that you and I can't handle together".She said He has a plan for us and the Doodle...I know it's asking a lot but I'd really like to know what that plan might be.

Worth Every Last Bite

The Doodle loves to take baths. All you have to do is say, "Do you want to take a Bath?" And he immediately shrieks and tries to take off his pants. Here's a picture of him sporting nothing but his helmet getting ready for a bath.

No garage sales today. I had to work. I look so forward to my Saturday morning coffee and perusing through other people's crap for treasures. So I had to go down to Marin tonight and do some work related things and I brought my Mom to help me and she took me to dinner afterward at The Cheese Cake Factory. We officially decided that when we hit the lottery or she hits another Jack Pot up at one of her Indian Casino's that we are going to be opening a Cheese Cake Factory here in our city. Hold your applause please. We even know where we are going to put it. In the old Gottschalks space--plenty of parking.

Of course we were too full to order dessert so we both declined the Cheese Cake. Can you even believe it? But then as we made our way to the door and saw all of those incredible cheesecakes calling out to us from the glass case, we stopped and bought $30 worth of cheese cake to-go. Waiting for our little slices of heaven to be boxed up, I noticed all of the calorie contents listed on each cheese cakes. The calories were over 1,000 calories on most all of the decadent perfection. Surely they meant that many calories for the whole cheese cake right? Can you really eat 1,079 calories in one slice of cheese cake? Suddenly I felt a little sick about it. I was wondering how many Weight Watchers points would be in a 1,000 calorie slice? I tried asking myself what Tori Spelling would do? And then they put a gorgeous and generous dollop of their fantastic whipped cream on the side. The whole way home I kept wondering if the whipped cream calories were included in that very large number. It's really great that the marketing geniuses at the Cheese Cake Factory got together and decided to list the calories on the cakes themselves. How very Jenny Craig of them. But, and I have a big BUTT, why ruin the fun?

So the cheese cake made it home safely without being devoured in my car. And I proceeded to pace myself and only eat half of the chocolate mousse cheese cake. Which means, I only had about 500 calories. Jim ate the rest.

The Doodle only had a couple of head drop seizures today. But the undigested Depakote sprinkles are still showing up in places they should not be if you get my drift.

I spend so little time doing normal things now that tonight when I tried actually having a conversation on the phone with someone, a real live grown up, it was another eye opener for me that our life has forever been changed. Simple things like talking on the phone are no longer easy to manage when you have a Doodle screaming, crying, wanting to be held, jumping on the bed, torturing the cat and getting scratched in the mouth. Luckily this person is very Special and I know that she completely understands.

Doodle Free


Today was a Doodle-Free day. A fun day planned just for Jimmy. I took the day off, actually traded since I had to work last weekend and some this weekend, so that we could go to Six Flags Discovery Kingdom. It will always be Marine World to me.

Not to be an elphant's ass, but you know I pretty much can't post without complaining about something so here it is. Remember the good old days when it was ride at your own risk and you were responsible for holding onto your belongings? So I was really careful and only brought a tiny shoulder purse that could hold my money, ID, camera and park map. I had it carefully attached to me, wrapped over my head and one shoulder so that I could ride. It wasn't going anywhere. NEW STUPID RULE...Now you are not allowed to ride with any belongings at all. The Belonging Police kicks you off the ride. They have mandatory lockers you must purchase at each major ride unless you have someone who can hold your stuff. These lockers do not have KEYS. You can only get back into them once and then you have to buy it again. You can only leave your items in these lockers for 2 hours or you lose your valuables in it, so it's not like you can get one locker for the day unless you have a lot of pockets or want a permanent locker which are located at the front gate. You would be watching your watch and having to high tail it all over the park back to your locker in time if you kept your stuff in the little lockers by each ride. Irritating.

I'm just saying, today we had to purchase at least 6 lockers. Just one more way for Six Flags to make a buck. It's not like $12.99 for a Souvenir Cup is a good deal...Thank goodness my super nice and generous friend Jessica gave me a free ticket! Thanks Jessica.

So besides the mandatory locker rip-offs and completely but expected over-priced food, we had a fabulous time! Jimmy brought a couple friends and I think he had fun too. Jimmy and I both love scary roller coasters and neither one of us gets sick so we can just keep on going. I love that he's old enough and tall enough to go on big rides with me.

It's been so long since I've been to a Six Flags amusement park that I was not aware of this wonderful yet costly convenience called a "Flash Pass". It's a pass where you reserve your seats for the big, popular rides so that you don't have to wait in line. I splurged and bought a Flash Pass for 4. It was $82.00 well spent! We did not have to wait in the hot, miserable 2 hour lines. We got to walk straight up to the front of the line and ride. We never waited longer than 5 minutes for a ride. Because of the Flash Pass, we were able to ride so many rides. The kids, if they really liked a ride, would get off and just get right back on. We had it down to a science. It's the only way to go.

I let Jimmy drive the Go-Cart and I sat in the passanger seat. Let's just say that will never happen again. He scared the bee-jesus out of me and my life flashed before my eyes at least 6 times. Jim will be teaching this boy to drive and driving in the car when he has his learner's permitt, NOT I. I do not have the stomach or blood pressure for it.

We also saw the Shoaka the Killer Whale show. She wasn't cooperating with her trainers. They had to give her a time out. The water rides were fun too. We got soaked! 3 times!!! What fun to be a kid again. In the end, it was worth every penny. And, I've got some great pictures to scrapbook!

Needless to say, we're all exhausted. I wish I would have brought my pedometer so I could have seen how many miles we walked. Just the walk to and from the parking lot was a jaunt, I needed a nap before we even got into the park. It's hard keeping up with 2 nine year olds and a 13 year old jacked up on Starbucks.

Grammy and our nice nurse watched the Doodle today. I couldn't stop thinking about him and hoping that he was OK. I know it sounds pathetic, but it's almost hard for me to have fun when I'm feeling guilty for leaving him. He had 5 or so head-drop seizures. Almost tripling the Depakote has not stopped them. I'm wondering if we need to switch medications again.

What's the Point?

I've been given the gift of counseling. There is a program the Doodle is in through our Regional Center where they have allotted us 20 hours or 20 sessions with a therapist that specialize in issues with raising children with special needs. It has been a blessing. I've been taking Jimmy with me because I thought it would be good for him to have a professional non-bias person to talk to. She is very nice, warm and friendly. Her office is completely kid friendly. We've even brought the Doodle with us and she has some great things for him to play with while we get our counseling.

I love her.

We've been most recently talking about what it must be like to have a little brother with special needs. It's great because Jimmy is completely honest, sometimes brutally so and he lets his feelings out about how he feels like we pay way more attention to the Doodle than him. Which might be partly why he has become so mouthy and feels like he has to have the very last word. I know it must be hard to to be the Doodle's big brother.

And as hard as it is to be the Doodle's brother, I tell Jimmy to think about how hard it must be to be the Doodle...

But it is hard on Jimmy. Before we only had the autism to deal with and that was a challenge. Add epilepsy and things have become much more stressful with the health issues and seizures. It's a lot for anyone, including a 9 year old.

We do our best to make Jimmy feel special. We try to carve out special one on one time with him. I take him to movies, lunch and his favorite thing to do with me is go to the mall. Jim takes him riding almost every weekend and sometimes they spend the night in the motorhome and have a boys camping trip. And most recently, we've been going to the Lake in the boat with him. We have a skateboarding camp scheduled for him and special Jimmy only trips planed. We can only do so much; there's only so much time in the day and we both work full time and the harsh reality is we have a very sick little Doodle.

This nice therapist lady has also been helping us with devising a points system for Jimmy so that he can feel rewarded and acknowledged when he does something good...instead of only when he does something bad. The points system is a little incentive program to get him to stop talking back and do what we ask, the first time.

We all signed a contract and while it was not notorized, it's pretty damn official. Here is the points system which we have already found a serious flaw in after only working with it for less than two weeks:

Each day is divided in 3 segments:
8:00 a.m. to 12:00 p.m.
12:00 p.m. to 5:00 p.m.
5:00 p.m. to bedtime

Jimmy is able to earn 1 point for each segment of time if he doesn't talk back or screw it up somehow- that would give him a maximum amount of 21 points for the week.

Depending on how many points he has at the end of the week, he gets a reward. Here are the rewards, he can only chose one from each reward group:

15-17 points = a snack/meal type of item of his choice such as Togos, Subway, Burger King, Juice Shack, Candy Bar, etc.

18-20 points = $5.00 cash OR a play date OR rent a movie/video game

21 points = An outing of his choice: Ice Skating, The Movies, The Mall, Lunch in a nice restaurant, something that would take a couple of hours.

Sounds pretty good right. Can you spot the MAJOR FLAW in our system?

Here is where the points system becomes counterproductive and does not work for ME.

The nice therapist lady said that you can't take away earned points. Apparently that is a NO NO. However, once Jimmy has screwed up and gets a point taken away, there is NO MORE INCENTIVE TO BEHAVE FOR THE REMAINING TIME IN THE SEGMENT. So, if he talks back to me at 12:01 p.m., I can look forward to him acting up the rest of the time period until 5:00 p.m. when the reward's clock resets so that he can earn another point....Hmmmmmmmm. Jimmy plays us like a deck of cards and completely knows how to work the system in just a short period of time.

I'm all for positive reinforcement...when DUE. But, Jim and I are both in agreement that we should be able to take points away; otherwise what is the POINT.

Bring on the Raspberries!



10 head-drop seizures today and counting but we have a much happier and with it Doodle so that's a good thing. I've just found out that the Doodle is on a prayer list at a couple of churches. How cool that complete strangers that have never even met the little monster are praying for him. I hope God is listening.

Doodle Poo

Now that we got to experience a week of almost no seizures, it Pisses me off that they're back. It used to make me sad, confused, anxious and helpless when he would have the seizures. But now that I've experienced the Doodle seizure free, even though it was only a week, and now that they are back, now I'm freaking Pissed. What is so frustrating is that I have no idea why they're back. Or should I say, why they decided to leave for just that one week? What was the trigger? What did we do differently last Friday to bring them back. Was it something he ate? Was it the heat? Did his body get used to the medicine already? Was he getting sick? Was it a full moon?

Then I thought I cracked the case!!!

Not to get completely disgusting and graphic on here but I noticed something very interesting yesterday. I was changing a Doodle Poo and it was very soft...the glycerin suppository they gave him in the hospital on Saturday finally did the trick.

Well, are you on the edge of your seats right now?

So I change his pants and in the Doodle Poo are hundreds of white sprinkles. His Depakote medication comes in sprinkle capsules--filled with tiny white granules. The tiny little beads of medicine were not dissolved which means that his body had not absorbed the medicine. I only noticed because of the soft poo. He's been so constipated over the last couple of weeks that I haven't noticed whether or not the little Depakote granules were in there...there has to be a connection somehow about this and the seizures coming back so strongly.

Nope.

I talked to the very nice UCSF Doctor and he said he's probably still getting the medicine, just not all of it and that the poo thing probably had nothing to do with the bombardment of seizures. I'm not sure how if I'm looking at them the same way they went in...then the Nurse Practitioner told me if he has any kind of immediate poo or diarrhea after eating or taking the medicine, it is not getting absorbed.

Hmmmmmmmmmmmmm. We have a Doodle Poo mystery on our hands.

You can tell the Doodle is feeling better today because he is back to doing raspberries. He's done a few today, not the usual 872 per day we've been used to getting, but it's a good start. He's more alert and his eyes are better focussed. He didn't have a grand mal today but had around 10 of the head drop type of seizures so he's still a little wobbly. The carts have been hidden from him so as to not torture him by wanting them. He's pretty bored and wants to run around. He escaped out of the carpeted room a couple of times today and boy can he run fast. Now when he runs away from me he thinks it's really funny.

We're really loving the Doodle's new nurse. Jimmy has a little bit of a crush on her. She takes really good care of the Doodle and he's genuinely excited to see her every morning. She's going on vacation for 3 weeks so we will have 3 different nurses coming in to take her shifts. Ugh. It's hard having strangers in your house and trusting them with your most precious things, like your children. It takes me time to warm up to new people and feel comfortable with them. It's a lot of energy of which I'm not in abundance of lately.

My Husband


With all of the craziness and stresses of life I sometimes forget to acknowledge Jim. He's the love of my life and it's during these incredibly hard times when he pulls it together and becomes my rock. He usually handles these types of stressful hospital situations better than I do. While he might be in touch with his sensitive side and cry at country music videos and while watching Oprah, he's a pretty strong and big guy. So when he broke down in the hospital over the weekend while holding the Doodle, it brought me to my knees. I'm so wrapped up in the day to day issues that I forget who else this is deeply affecting.

Together for more than 16 years, we've been through a lot and I mean A LOT. I could write a screenplay just about us. Oh wait, I did that already. It's a romantic comedy drama.

I'm glad he is my partner through this because he is a really good dad to both of our children. He is the most loving, affectionate and tolerant father they could ask for. I know the Doodle's health issues have been hard on him and because he is at work all day I sometimes find my self resenting that I am dealing with most things by myself. But when push comes to shove and I really need him, he is there.

Some men couldn't handle this and would be out of here. That's not Jim and I admire him for that.

Both boys completely adore him, especially Jimmy. Right now, Jimmy looks up to his father so much. Sometimes I feel a little bit left out of their boys club, but I know it is for the best.

There are things I might wish Jim would do more of or help out with but he's giving all he can right now. To watch him holding the Doodle in the hospital over the weekend, crying, made everything so much clearer for me. I had to remember that I'm not the only one hurting. They say special children have special parents and I know that to be true.

I love you Jim. Thank you for being a great husband and father; and even though you suck at holidays, that is the best gift I could ever ask for.

Because it Can't Always Be Just About the Doodle


Not that I ever forget, but I need to be careful to not let Jimmy feel like the world revolves around the Doodle. Jimmy has very important chronicles in his life too and I feel bad that I don't have a Little Peanut Chronicles dedicated to Jimmy. So I let him start his own (well monitored) blog. This way he has to carefully plan what he is going to write about. It's like his online journal. His fan base is already huge!

So I'm going to take a minute and gloat about what a wonderful little 9 year old he is. He is very sensitive and right now wants to be with us more than anything. I know there is going to come a time where he soon wants nothing to do with us so I want to remember these moments.

Jimmy is a great athlete, a straight A student and a Brown Belt in Karate. He's the best big brother the Doodle could ever ask for. I know it must be hard to have a sibling with special needs...so many special needs and he handles it all so well. I think it has really taught him a lot about people being "different" and why you shouldn't make fun of people who have handicaps of any kind. Today he was teaching him how to play with his skateboards and ramps and even tolerates him in his room sometimes.

He also has done some modeling and is with an agency in San Francisco. He's done Pottery Barn, National Geographic Toys and most recently Dell Computer. He's on the Dell Computer website and a Bonus...he's in the Costco July Coupon Book.

I know it's just the back of his head but what a cute head. I absolutely love and adore this young man and I couldn't be any prouder of him.
http://www.costco.com/Service/FeaturePage.aspx?ProductNo=11487019&cm_re=1-_-Quad5-_-Mailer

Standards


The Doodle is completely out of it. He can barely walk on his own; he's very wobbly. I can tell he doesn't feel good because he didn't want to get his picture taken. He just looks very sad.

Since the weekend hospital drama I'm feeling like my standards have been lowered where my happiness is concerned. I had to go to work this morning at 6:30 a.m. so I called my mom a couple of times to see how the Doodle was doing. When she told me he had one grand mal, I found myself relieved that it was only one. Never before would I have been relieved to hear that he had a grand mal. I guess I've lowered the bar. Now if we don't land in the hospital I will consider it a good day.

At least our nurse was here this morning when he had the seizure. She was able to time it and check his vital signs during and after the seizure. He is not the same baby he was last week. I watch as the seizures chip away at his already medically altered personality. He looks severely drugged and tired and is cranky yet unresponsive. His eyes look vacant and his dark purple circles look like they might hurt. He could barely clap his hands. He is going in and out of sleep fighting it every step of the way; not sure if this is from the multiple seizures or the high potency drugs in his system; probably both. It's almost like he is afraid to go to sleep because he knows what is going to happen to him.

If you would have asked me last week, I would have optimistically told you I didn't know how much longer we would need a nurse since he had gone the whole week without either kind of seizure.

I'm waiting for a call back from UCSF so that we can see what our next step is going to be. With such limited options, I have a pretty good idea what they are going to tell me.

They will tell me to just sit back and wait.

A Shit Sandwich for Breakfast, Lunch and Dinner

Are you comfortable?

Get a cup of coffee and sit back this is going to be a long one.

11:00 p.m. last night and the Doodle was still wide awake. He had just had another seizure so when I say wide awake, please don't confuse that with being alert, aware or with it. He was just very awake. His eyes were heavy and you would think that he might fall fast asleep at any moment. He looked drunk. Just as he would start to dose off, he would startle himself back awake or a Nurse would do that for him.

They wanted to try more Benadryl. I said no. The first two doses had not worked and now we were just overdosing him. He'd been so pumped with sedative and anti-seizure medication that he was freaking out. In the Doodle's 3 years on this planet, I can honestly say I have never seen him behave that crazy or yell that loud. He was kicking, screaming, biting his hands, hitting himself in the head and thrashing his body around the hospital bed while I tried to hold him. They had to remove his IV.

So they decided to try a sleeping agent, Chloral Hydrate. The name reminds me of Chloroform that you always see the bad guys use on a cloth to knock out their victims in the movies. It just sounds toxic like something you should not give a three year old. I was so nervous that it would have the paradoxical effect on him. But, at this point I was willing to try just about anything. I have to confess when they brought in the sleeping medication, I had thoughts of how nice it would be if I could have some too. At this point I would settle for a Tylenol P.M. and some bad chamomile tea.

So the Chloral Hydrate worked, kind of. He slept pretty soundly from 11:30 p.m. to 3:00 a.m. and then he woke up screaming. He was awake but still pretty out of it from 3:00 a.m. to 5:00 a.m., and he had seven of the little head drop seizures during multiple reruns of Dora and the Wishing Star. I had some wishes of my own for Dora.; like shut the &^%$ up! That little girl can talk.

He fell back to sleep until 8:00 a.m which was great except it was hard for me to get any real sleep; I never knew my body could still contort that way. The Doodle likes to sprawl out.

He woke up a little cranky and hung-over and had another grand mal this morning. After 45 seconds the Nurse was screaming for someone to bring her a shot of Ativan STAT!!! I kept waiting for her to grab the crash cart and paddles like I've seen in my doctor shows.

Then he came out of it. This one barely lasted a minute. He was laying on his side, coming out of the seizure and she was still asking for the shot. I was like, "Uhm excuse me? You are not going to give him that are you?" And she said, "Yes." And I said, "NO! He stopped seizing. He doesn't need it." She said, "No, he's still seizing and it's almost been two minutes."

"No. He's not. I've seen him have almost 100 of these now and he's done.", I snipped.

She said, "No. He's not responding..."

And then I lost it a little bit. Shame on me.

In my best, most stern and tactful voice I could muster without being the Bitch I'm known for I said, "No! You don't get it. He's always out of it after a big seizure. He's postictal. It's what happens after he has a grand mal."

I couldn't believe I was talking to a Nurse.

She told me since his eyes were rolled back when she lifted his eye lids, he was still seizing. Then we argued some more. I told her we needed another opinion.

She put the syringe down by her over-zealous side and called for the other Nurse. A nurse I actually know outside of the hospital and trust. The Trusted Nurse came in quickly and asked, "What's going on?"

The Other Nurse, still armed with the shot, said, "He was still seizing and I need to give him this Ativan but the mother doesn't want me to."

The Trusted Nurse looked at him.

"He's not seizing anymore." she said.

I just looked at her and said, "Thank you. She wanted to give him more narcotics that he doesn't need and I can't have another day and night like yesterday unless it's going to save his life."

The Other Nurse immediately got defensive; trying to explain why she thought he was still seizing. I just held him and told him it was going to be alright, even though I know it is not.

Hospitals are pretty good for the most part. It's the closest thing I've been to a Bed and Breakfast in a while so maybe my expectations are little high. And I'm not just talking about the bad food. I see the bill and it's the most money I've spent for a nightly stay anywhere in my life time so I guess I want it to be the best it can be. You want to at least feel like you got the best care possible.

My biggest complaint with hospitals, and if there are any nurses out there please listen. This is just my feedback but have you ever heard the saying, let sleeping dogs lie? Well, if you have a wound up insomniac Doodle Bug who has not slept for 24hours, it might be a good idea to tread a little lightly. You don't need to enter the room every 14.5 minutes like gangbusters-- marching around, flipping on lights. If at all possible, do everything you need to do at once--take the vitals, change the IV bag, give the medicine, reset and reprogram the really loud beeping machines, take out the trays or what-have-you and GET THE HELL OUT and stay the hell out unless it is absolutely necessary to come back in. I'm not sure why all of that needs to be spread out so much. Multitask.

Every time the Doodle would finally fall to sleep, the nurse would barge in. I know she was just doing her job but it seems like it could be done more respectfully and mindfully.

Late morning came and all I could wish for besides and improvement in the Doodle's health was to get the hell out of there. There was nothing that they were doing for him that I could not do at home. I can just as well watch him have seizure after seizure and save the $2687 per day ++ in the comfort and privacy of HOME.

The worst part about epilepsy is that it is individually based. It affects each person differently and to varying degrees of severity. There are different causes and triggers for everyone. Each individual responds differently to the medications. Each epilepsy case is different. Like finger prints, no two are exactly alike. Doctors do not know much about it. There is so much to learn.

So we're home. The Doodle has not had another grand mal since this morning but he continues to have the head drops and now he's severely constipated to top it off. He was always a pretty regular kid when it came to pooping. Now, with all of the influx of sedative and anti seizure medication, it has slowed down his system. His stomach pain and discomfort is just one more thing we can add to the Doodle's list of health issues. He's so backed up that even a glycerin suppository did nothing last night.

Two steps forward, three steps backward. We're back to square one, hoping he doesn't hurt himself on the tile. Praying he doesn't have another 10 grand mals in a row. Looking for answers. Relying on doctors and medicine. And, my favorite one...

Waiting.

The Calm Before the Storm

I'm sitting in a hospital bed right now holding a very sick little Doodle. Things went from bad to worse last night after his second grand mal seizure. He had seven more. This is the Doodle's record. Nine big ass-kicking grand mal seizures in 12 hours. He is fried.

We called UCSF and they told us to bring him to our local hospital's emergency room so that they could give him a sedative drug meant to stop or interrupt the seizures. They were coming almost every hour and they were horrific.

The Doodle is very sensitive to sedation drugs. They have the opposite effect on him. Valium hypes him up. So now we sit here, watching the Doodle bounce off the walls not sleeping. Our little insomniac is screaming, totally freaked out yet so tired he can't stand it. All he wants to do is pull his IV out. He didn't sleep all night. None of us did. The irony is being tired can bring on seizures...

The last week he had virtually no seizures. It was awesome. We had our baby back. His entire mood and spirits were up! He got a taste of what it must feel like to feel good.

I thought the medicine was finally working. Part of me, the wishful part, thought maybe he had outgrown them. It's possible right? Possible but not likely.

It's as if the anti-seizure medicine had been suppressing the seizures but then pissed them off in the meantime. Hell hath no fury like a pissed off seizure. Now they were catching up. Never, ever, has the Doodle had this many grand mal seizures in one day. His high score was 4 in one day and that was rare and then he didn't have another one for a week and a half.

The two doses of Ativan have done nothing. You would think they would have knocked him out. Nope. Wide awake. They even tried some Benadryl. Nope. Still awake. Every time he starts to fall asleep, he jolts himself awake and then screams. Almost like he's getting an electric shock or having another seizure. We can't tell and they do not have him hooked up to an EEG; so we do not know.

They told us they were going to transport us to UCSF because they do not have a Pediatric Neurologist here and now our nice new doctor is there anyway. But UCSF declined. They said there is nothing they can do for us there that they can't do here. Basically, there is nothing you can do for seizures except watch and wait and then throw medicine on them and hope for the best. I'm not going to take this personally.

I wish they could at least tell us why this is happening. What is causing these seizures? There is something very wrong with the Doodle and we do not know what it is. The seizures are not the disease but a symptom of another disease or so I read.70% of epilepsy cases never learn the why...it just is.

They've once again increased his medication dosages, so we will have to wait and see. As for how long we will be in here, I do not know. He's already had two grand mal's here at the hospital. I'm not sure the pissed off seizures are ready to stop any time soon.

They are talking about doing a spinal tap. I can't imagine that so I am trying not to think of that right now. This would be to see if he has Meningitis. Wouldn't he have some other symptoms? He has none. Just seizures. I had Jim google Meningitis. It's a pretty scary viral infection.

Please say a prayer for the Doodle. He can use all the prayers he can get right now.

Thank you.

Living With A Terrorist

I’ll never forget September 11, 2001. I remember exactly where I was when the tragic life changing event of our century took place. I remember watching the first tower burning on the news with astonishment. I remember sitting with Jim on the edge of the bed and holding Jimmy while I sobbed. I remember being in complete disbelief and then it happened again…another plane flew straight into the second tower. I remember brushing my teeth with Cinnamon Close Up toothpaste and feeling sick to my stomach. I still can’t brush with Cinnamon Close Up without feeling queasy. There was so much confusion, commotion and speculation and it was still unclear as to why the first plane hit the first tower, and then the second plane hit. As the day’s horrific events unfolded, and more reports came out about the other planes—the one into the Pentagon and the one that crashed into the field in Pennsylvania, it was obvious that it was the sinister work of Hijacking Terrorists.

I remember not opening our store that day, being afraid that this terror attack could strike in more and more cities throughout the day. I was glued to the news. I remember not wanting to leave our house and being scared about not having enough food and supplies should this turn into some kind of horrifying and devastating World War on American soil. Those events that day shook all of us.

We took Jimmy out in the boat again tonight so that he could knee board. Grammy was home from her vacation house so we asked her to watch the Doodle. He’s been doing so great with the seizures this last week. And then we got a call from Grammy. He had a grand mal tonight around 5:30 p.m. He was having a good time jumping in his bouncy house and then it happened. He likes to climb in and out of the jumpy and he fell down and went into a seizure. My mom doesn’t know if the seizure caused the fall or the fall caused the seizure…It was the bad kind. She said it lasted about a minute. Usually after he has a big seizure, he is out of it and exhausted. He sleeps and you can’t wake him up for at least 20 minutes to a half hour. This time he screamed and cried for a long time right after. She said she couldn’t calm him down. I’ve heard from people who have had seizures that they can wake up from a grand mal and be nauseous, agitated or have a headache. Since the Doodle doesn’t talk, he can’t tell us what he is feeling.

It’s 11:17 p.m. and the Doodle is laying next to me and Jimmy watching the Backyardigans while I type. He’s all wound up and won’t sit still since he slept for a couple of hours tonight with my mom after the seizure. Out of the blue, he just let out a yelp and went into another grand mal seizure. This was one of the worst one’s I’ve seen, his face was contorted with his eyes rolled back into his head. It’s hard for me to watch and then I looked over and saw the look for terror on Jimmy’s face. Even though he’s scared, Jimmy is trying to be so strong. He said, “It’s OK Mom, I’ll go get Dad.” And then he ran in the other room to get Jim. The full body convulsing lasted about a minute and now the Doodle is sound asleep, exhausted from the reign that just took over his precious brain, body and soul.

Jim told me the other night that he felt like the Doodle’s body and brain had been invaded by a Terrorist. He was right on the money.

Although the Doodle’s seizure disorder is not as gravely morbid, economically and politically devastating as 9-1-1, living with Epilepsy is similar to living with a Terrorist. Once the seizure strikes you are scared, effected and confused. You’d do anything for the seizure to stop. You pray, making desperate deals with God. Once it finally stops you are hopeful that it will not return. Then the seizure returns…and your hope has been crushed and there is nothing you can do but wait. First you wait for the seizure to stop and then you spend the rest of your day or week waiting and watching for the seizure to return. You can’t relax. Even if the seizures have gone away for a few hours or days…you know they are coming back; planning their attack at the perfect and unsuspecting time where they can inflict the most terror, damage and pain. This type of terrorist is not concerned with age or innocence. It leaves bodily injury, brain cell destruction and confusion in its path for all close to it.

You cannot rest living with this terrorist called Epilepsy, it’s all you can think about. Even when you aren’t thinking about it, you are thinking about it. Things are no longer up to you. You have no control over the situation or the seizure. The Epilepsy Terrorist feeds on your despair and anxiety while you wait for the other shoe to drop.

I still don't know which seizures are worse, the big ass kicking seizures or the quick drop you to floor seizures. We get both.

I will sleep with one eye open tonight as I listen to the breathing patterns and watch the Doodle’s movements in the glow of our dim night light.

Daddy


Today we gave the Doodle a Playskool play garage. We like to give him things that he can play with on the floor because of the seizure activity. It's better when he's sitting down playing on the carpet than running around pushing his carts.

It is a two car garage and came with a Jeep Wrangler like ours, a trailer and a boat. It even has an automatic garage door opener. Coincidentally, the garage came only with a Dad guy.

No Mom.

There's a lawn mower, a basketball hoop, a hose, some trash for the trash can, a BBQ with steaks, and what else? A chainsaw. I did notice there was no beer.

When I told Jimmy I thought the garage was chauvinistic and after taking 15 minutes to explain what chauvinistic meant he came back and said, "We can get a Mom for the garage that is always telling the Dad to get in here and help with the Doodle."

The Doodle can relate to this obvious man cave where Daddy likes to hang out. The only thing missing would be some dirt bikes and a lot of junk the absent Mom's brought home from the flea market.

We taught the Doodle how to put Daddy in the hammock so that he can relax and take a nap when he's not sawing things with the chain saw. Of course the Doodle's favorite thing to do is open and close the garage doors.

My Letter to Oprah


Even though I know She is on vacation, I wrote to Oprah yesterday in hopes that she would do a show about (raising a child with) Epilepsy.

Here's my letter, keep in mind my penchant for over-talking. I get a little wordy and I had to cut it down from 6,200 characters to 2,000 characters. That was hard because you all know how much I have to say.

Dear Oprah:

Epilepsy is life changing for all involved.

Can you please do a show about Epilepsy and how it affects the quality of a person's life? How sometimes the seizures themselves aren't what are so dangerous but how the falls and consequences from having a seizure is what kills. How difficult it is to raise a child with epilepsy when anti-seizure medications do not work and the child is not a candidate for brain surgery.

Epilepsy takes lives, not only in the form of dying, but by robbing people of their independence, dignity and ability to become fully-functional. Epilepsy is crippling even though the person affected might be able to walk.

I have a 3 year old little boy with severe epilepsy (and autism) and am living in a state of constant fear and hopelessness. He is having 60+ seizures a day and cannot be put down. He cannot run, play, or attend preschool. The seizures have greatly affected his cognitive learning ability. He doesn't understand what is happening to him and either do I. He has to wear a helmet and might soon be confined to a wheel chair. The irony is without being able to use his arms and legs, he is losing all muscle tone, coordination, balance and strength in his body. Seizures are now not just affecting his brain, they have immobilized a once happy and healthy toddler.

We have been to two of the top hospitals in the Nation, Stanford and UCSF and we are still without answers as to why or how to help him. He has been on seven different anti-seizure medications since February of this year, sometimes multiple medications at once...up to FOUR at a time. The side effects from the medication is almost worse than the seizures. The seizures have taken over his body and brain. The more seizures a person has determines how many they will continue to have. The brain has a way of multiplying them if they are not under control. It is amazing to me that we really know so little about this devastating disease.

To see photos of my little epileptic or read our story about raising a child with epilepsy please visit my blog: http://doodle--bug.blogspot.com/

Warmest,
Angela