Get some sleep

This article I found on Epilepsy.Com contains some interesting info on sleep & epilepsy. Check it out.

Off Topic: Excuses To Miss Work

As if I didn't have enough to do... I started yet another blog. Excuses to Miss Work. My hope is that this might actually be useful to someone. ;) As opposed to my other blogs with topics such as: an obscure furniture maker from the Victorian era, my own ramblings about epilepsy, random philosophical quotes, family vacations to Oahu, family vacation to Finland, and contributing to a blog dedicated to solving the worlds problems "one beer at a time".

PET....

I'm still awaiting the report from Baptist Hospital regarding my PET scan. I'll probably call tommorow to find out what is taking them so long.

PET Scan Pics

Here are a selection of my 147 PET scan images that they put on a CD for me. I can't really tell much from them... so I will have to wait for a Dr. to analyze them for me.

Epilepsy Awareness Day

The local epilepsy awareness group with which I participate, NC EASE (North Carolina Epilepsy: Awarness Support Education) has organized an Epilepsy Awareness Day in November:

NC EASE and the Epilepsy Institute of North Carolina invite you to join us for our first annual Epilepsy Awareness Day.

The event will take place at the Epilepsy Institute, 1311 Westbrook Plaza Dr. Winston-Salem. From 10 A.M. to 2 P.M. on November 3rd, 2007.

There will be activities for children.

We will have a number of presentations and information on the following topics:
* Epilepsy and seizure disorders.
* First Aid instructions for seizures
* Tests for epilepsy
* New treatments for seizures
* Clinical trials for new treatments for epilepsy
* College scholarships for people with epilepsy or their family members
* Epilepsy support dogs

If you have any questions please contact us via email: coordinator@epilepsysupportnc.org

One month...

I am seeing my Dr. today. Hopefully the PET scan will provide some information of use. I have tried looking through them myself, but am obviously not qualified... as I can't tell a thing by examining the images. I'll try to get some posted soon.

My last seizure was exactly 1 month ago. Hopefully I can make it a few more decades without another. Wish me luck!

8 Thousand Hits

I got my 8 thousandth page hit today. Someone visiting from Proberta, California.

I started this blog so that I would not have to call up everyone I know to tell them what was going on with my seizures... they could all just check on me here. I never thought I would end up getting 8 thousand hits. This new-fangled Internet thingy is pretty cool. ;)

PET PICS

Here are the pics of me with my EEG leads wrapped tight to my head.

And the two techs who wrapped it.

This is me about to go into the PET scanner.

The PET Experience

I just got back from the imaging center at Baptist Hospital. The procedure was not that bad. Here's how it went:

I went and got EEG leads placed. They then wrapped my head tightly with gauss so that the leads would not fall off as they took me over to imaging. I get there and go over some paperwork and they request some cash before doing the test. Then they stick me with some saline fluid and a "butter-fly" needle. After a wee-bit of saline, the tech brougt out the radio-active stuff, glucose with radioactive flurine. Not much... just a few ml. He had to bring it out in a case about the diameter of my arm and perhaps 10" high. After inserting that, they had me sit in the dark for 45 minutes. The instructions were to try to rest and not think too much. THAT was rough. After about 30 minutes my head started hurting really bad. I'm not sure if it was lack of food, the EEG leads pressing into my head, or the radio-active positrons flying out of my head. But I made it through and then they removed the portable EEG & Leads. Then they put me in the tube detector thingy. It was a bit larger than an MRI, but not nearly as loud. I only had to stay in that for 10 minutes. And that was it!

I got a copy of the images. I'm still figuring out how to get the things off the disk and onto the net. Soon as I figure it out, I will post. I won't know any news about the test until my dr. or another Dr. gets to do the analysis.

Food v. PET scan

For this PET scan, they have instructed me to not eat after 7:00 A.M. All I get is water! I am going to be so hungry. But Christa said she would take me out for food after the test is done. I am thinking of a Texas Jack burger from Back Yard Burgers. Yum!

I suspect that they will attach the radioactive material to glucose and then since I have not had anything to eat, my body will send the sugar to where it is most needed in the brain. From there, the radioactive stuff should emit the positrons which are detected by the PET gizmo. I'll ask the techs and let you all know if I am correct.

Testing Tommorow

I'm getting a PET Scan and EEG test done tomorrow at Baptist Medical Center at their Epilepsy Monitoring Unit. I've never had a Positron Emission Tomography scan before, but as I understand it, they pump some radioactive stuff in your body and then use a detector to determine where it went... well, it is a bit more complex than that, so here is some info off a Radiology site.

Before the examination begins, a radioactive substance is produced in a machine called a cyclotron and attached, or tagged, to a natural body compound, most commonly glucose, but sometimes water or ammonia. Once this substance is administered to the patient, the radioactivity localizes in the appropriate areas of the body and is detected by the PET scanner.

Different colors or degrees of brightness on a PET image represent different levels of tissue or organ function. For example, because healthy tissue uses glucose for energy, it accumulates some of the tagged glucose, which will show up on the PET images. However, cancerous tissue, which uses more glucose than normal tissue, will accumulate more of the substance and appear brighter than normal tissue on the PET images.

I'll post more tomorrow. Hopefully with some pictures!

Grateful for the Past 11 Days

Scott had another tonic clonic seizure this evening around 6:00 pm while at the Epilepsy Institute. He did not injure himself (thank the Lord!) but had to be put on oxygen for a while. He is resting now. We are grateful for the past 11 seizure free days and realize that 11 days is more than most epileptics have without a seizure. Dr. Dean is going to send him for some more tests - presumably some time later this week. I'll keep you posted as soon as I learn more. Please join us in saying a prayer of thanks that Scott was not injured this evening. Please also keep him in your prayers as he undergoes additional testing.

Thanks everyone,

Christa

3 days...

Well, I have to start again... 3 days no seizures. Discouraging, but a lot of people would be thrilled to make it that long. I count myself fortunate. :)

Another Day.... Another Seizure

Scott had another tonic clonic seizure this evening. Our son found him seizing around 8:00 pm in our living room. During this seizure he only stopped breathing for a minute or so. Luckily Scott's only injuries seem to be a bruise on his right jaw and a slight headache. He is resting now. We will try to update everyone again tomorrow on his condition.

Christa

RNS Discussion with Dr. King-Stephens (Part 5)

Part 5 of my RNS discussion with Dr. King-Stephens:

The RNS is able to detect brain activity that could indicate a seizure. How does it know the difference between normal activity and seizure activity?

The physician decides what is normal and abnormal for that individual. By looking at a number of records of brain activity from that patient, the physician can identify the specific patterns that characterize that person’s seizures. The device is then programmed by the physician to detect those specific patterns. Thus, the device is programmed differently for each individual.

If the RNS is able to distinguish between different types of brain activity it is essentially reading your mind. Can it detect emotional responses?

The RNS detects the brainwave activity but does not "read the mind". It would probably take a supercomputer with millions of electrodes placed over every cell in the brain in order to be able to "read" peoples thoughts. After all, the mind is the expression of all the brain cells activity at any given time.

For what other purposes is the RNS technology being used?

Right now, the RNS is only being used in a clinical trial for refractory epilepsy. It may be used for other conditions in the future.

Previous Posts (Part 1 Part 2 Part 3 Part 4)

If you have epilepsy and are interested in finding out if you are a good match for the RNS clinical study, Call: 1-866-904-6630 or go to: www.seizurestudy.com

RNS Discussion with Dr. King-Stephens (Part 4)

Part 4 of my RNS discussion with Dr. King-Stephens:

How does the RNS “know” to send an electrical pulse to the brain?

The RNS uses very sophisticated computer programs to recognize abnormal brain electrical activity and distinguish it from normal activity. The data (or EEG) is stored in the RNS and by communicating with a laptop computer, similar to a heart pacemaker, it can be retrieved and sent to a computer at NeuroPace and stored for future review.

Once the patient downloads the activity that is stored in the device to the main computer at NeuroPace, the doctors can review it and make changes in the detection programs to improve the ability of the device to recognize the seizure activity. The better the device gets at distinguishing the abnormal from normal brain activity, the better it works at blocking the seizures and improving the control of the epilepsy.

The RNS must acquire a significant amount of data about your brain. How is that data stored and how is it sent to your physician?

The data is stored on servers and is password protected, that is, the physician can access the information only for his or her own patients.

The pulse of a VNS has to be powerful enough to reach the activation threshold of the Vagus nerve and cause it to “fire”. How powerful do RNS pulses have to be in order to interrupt seizure activity in the brain?

The magnitude of the electrical activity delivered to the brain to control the seizures is much lower with RNS than VNS, (probably around 15% of what is needed for VNS). Since there are no pain nerve fibers in the brain, the patient does not feel the "shock" applied by the device.

Previous Posts (Part 1 Part 2 Part 3)
More tommorow.

If you have epilepsy and are interested in finding out if you are a good match for the RNS clinical study, Call: 1-866-904-6630 or go to: www.seizurestudy.com

RNS Discussion with Dr. King-Stephens (Part 3)

Part 3 of my RNS discussion with Dr. King-Stephens:

The VNS has a number of possible side-effects, the main one being that it affects your voice. What are some possible side effects that you have already discovered during your studies?

Some patients have had mild tingling and/or pain of the scalp or face but by reducing the intensity of the stimulation or repositioning the electrodes, the symptoms disappear. So far, the side-effect profile has been excellent, i.e. few side-effects, and the patients do not have any sensation when the brain is receiving the therapy, which averages about 600 very brief pulses a day!!!

One of the things that most concerned me when deciding to get a VNS is the whole concept of being a Cyborg: Part man – part machine. The RNS seems to be more invasive and more “cyborgish”. How would you address these concerns to potential study participants?

The RNS in no way can change the personality of the person or "take over" their feelings or thoughts because it is only stimulation; less than 1% of their brain. There is no chance of becoming the "Terminal Man".

If you had epilepsy, what treatments would you try before electing to have a RNS implant?

If I had epilepsy, I would try at least 2 medications, alone or in combination, before looking at the possibility of having "curative" surgery. If I was not a candidate for curative surgery but could have the RNS, I would go for it. If not a candidate for surgery or RNS, then I would try VNS or an investigational medication.

Previous Posts (Part 1 Part 2)
More tommorow.

If you have epilepsy and are interested in finding out if you are a good match for the RNS clinical study, Call: 1-866-904-6630 or go to: www.seizurestudy.com

RNS Discussion with Dr. King-Stephens (Part 2)

Part 2 of my RNS discussion with Dr. King-Stephens:

I have generalized tonic-clonic seizures. My EEG shows that the electrical activity does not start at one point in the brain and spread, but occurs on both sides of the brain at once. Would I be a good candidate for an RNS?

At this time, only patients who have focal onset seizures, 1 or 2 foci, are candidates for the study. It might be that in the future, people with generalized seizure onsets might be candidates for this therapy.

The VNS has been around since the nineties and has been implanted in over 30,000 patients. It is well studied and effective for many people. Why would I want to consider an RNS as opposed to the VNS?

VNS is indicated for patient in whom we do not know where the seizures are coming from, have more than 2 foci or have generalized onset seizures. Thus, the indications for using VNS or RNS are very different at this time.

How do you find the specific point on the brain at which to place RNS leads? Is an EEG or regular MRI sufficient?

In order to determine where the seizures are originating in the brain, we do EEG, MRI and occasionally PET studies. If the non-invasive studies can not give us the answer, we sometimes introduce (implant) the EEG electrodes into or placed on the surface of the brain, to capture the seizures and investigate whether we can find the focus or foci. This requires a surgical procedure and observation in the hospital for 7 to 10 days.

Once you have received a VNS, Cyberonics recommends that you not have any further MRIs as the strong magnetic field could heat up the leads wrapping around the Vagus nerve. As an MRI is required to determine the locations to place RNS leads, could a person with a VNS have an RNS implanted?

A person with a RNS generally should not have a MRI scan of the brain because the device creates so much artifact that the information given by the scan is often useless. Also, the MRI may cause heating of the leads. If an imaging procedure is necessary, x-ray based technologies such as a CT scan should be used whenever possible. Hopefully, future RNS devices will be MRI compatible.

The study website indicates that the leads & electrodes are implanted in the brain and that the neurotransmitter is placed in the skull. When you say “in the skull”, does that mean in the cavity with the brain or under the scalp?

The device is embedded in the skull and does not go into the brain. It is then covered by the muscle, fat and scalp and is therefore not visible. The EEG electrodes do go into and/or sit on the surface of the brain and therefore are under the skull.

Previous Posts (Part 1)
More tommorow...

If you have epilepsy and are interested in finding out if you are a good match for the RNS clinical study, Call: 1-866-904-6630 or go to: www.seizurestudy.com

RNS Discussion with Dr. King-Stephens (Part 1)

I recently had the opportunity to candidly speak with Dr. King Stephens about the Responsive Neurostimulator (RNS), a new treatment for epilepsy that is currently in clinical trials. Dr. King-Stephens is the Director of Clinical Neurophysiology at the California Pacific Medical Center in San Francisco.

(As the discussion was quite long, I'll split the transcript into 5 posts.)

Neurology is probably the most complex of all sciences. The amount we know about the brain is far outweighed by the amount we still have to learn. So what in the world possessed you to go into neurology? Surely you could have chosen something more lucrative and less frustrating… like podiatry or plastic surgery?

My interest in neurology is due to the complexity of the brain. Every patient is challenging and keeps the work interesting. Having the opportunity to do research and take care of patients is a privilege and rewarding when we can improve someone's life.

How much have you been involved with the development of the RNS?

I was not involved in the preclinical development of RNS but have worked in the clinical study for almost 2 years.

Experiments with direct neurostimulation and neuro-feedback to the brain have been going on for many years now. What technology specific to the RNS has moved the device to the point where you think it will be practical as an implant.

Improvement in the microprocessors (smaller size and increased speed), reduction in the size of the battery and specially in the algorithms that help recognize the seizure activity have made possible the development of this device.

I had brain surgery about 15 years ago to remove some tissue that was hemorrhaging on my brain and was causing simple-partial seizures. The surgery involved opening a hole the size of a playing card in order to remove the tissue. I had to stay in the hospital for 5 days! What size hole is required for the RNS leads to be placed? And have brain surgery techniques advanced much in the last 15 years?

The size of the (burr) hole to implant the electrodes is about the size of a quarter. The opening of the bone for embedding the RNS device is about 1 x 1/2 x 1/4 of an inch. The advancement in surgical techniques has involved better and safer anesthesia medications, MRI studies during or after surgery and post-operative care.

More tommorow.

If you have epilepsy and are interested in finding out if you are a good match for the RNS clinical study, Call: 1-866-904-6630 or go to: www.seizurestudy.com

ADA Restoration Act of 2007

On July 26, the anniversary of the passage of the Americans with Disabilities Act, House Majority Leader Steny Hoyer (D-MD) and Representative James Sensenbrenner (R-WI) introduced the ADA Restoration Act of 2007, H.R. 3195.

Recent court decisions (Sutton v. United Airlines - 1998) have dramatically limited the scope of the Americans with Disabilities Act (1990) such that most people with epilepsy are deemed not to have a disability and therefore cannot seek legal recourse if they are discriminated against because of their epilepsy.

Why are they deemed not to have a disability? Because the Supreme Court decision in Sutton v. United Airlines required that the effect of mitigating measures (such as taking medication) be considered in determining if someone has a disability under the ADA... Of the more than a million people living with epilepsy, about 60 percent have their seizures controlled by medications. That is great, but anti-epileptic drugs (AEDs) by their very nature are designed to reduce brain activity and the potential side effects of these medications can go on for pages. Many times, the negative side effects of AEDs can exceed the advantage of having seizure control. But let's assume that one has a seizure at work, goes to the Dr. gets on meds that control the seizures completely with few side effects. Well, the person is still likely to be discriminated against because his boss is scared he will have another one.

Take John Roberts for example, you can bet that when court gets back in session, even if he is not diagnosed with epilepsy, those other 8 Judges are going to be quite apprehensive that their Chief Justice might just have another seizure. A perfect example of the discrimination he already faces are all the questions posed by the media concerning his ability to perform his job. If he did not already have the top spot on the bench, chances are that if he was diagnosed with epilepsy, he would be less likely to get promoted.

Until 1999 there was little fanfare about whether a person with epilepsy is covered by the ADA, or its model counterpart, the Rehabilitation Act of 1973. Most cases presumed that epilepsy was a covered disability.

Since then, courts have recognized that epilepsy is a disability in only a few cases. As a result, people with epilepsy are questioning whether they are even entitled to the protections of the law. Even more troubling is that employers, public accommodations, schools and state agencies have also begun to ask the same question.

Many people who are trying to work despite having an impairment are not being given a fair chance. The ADA Restoration Act of 2007 would correct this injustice. This legislation restores the basic right of people who have a disability to be judged based on performance – just like women, minorities, and the rest of the American workforce.

The Epilepsy Foundation of America makes it easy to take action by sending your Representative the ADA action alert.