From the world of natural healing looking at Keppra

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Googman

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GREETINGS,

I decided today to look into the idea of changing meds to see if there was anything newer and less damaging these days ?

I spent most of my American life since the age of 8 surviving without seizure medications, changing my diet and learning how to stop seizures when I felt the auras arriving.

Due to taking care of my parent for years before they died, I was forced back into the electrical activity that brought the seizures back and so I had to start pills once again without having insurance.

This all happened near the time of America's second great depression and so As a man over 40 yrs old, my options became very short for survival which are still slim but at least I can think once again after reading one article about the (overdosing of medicines).

Times were completely dull for over 5 years and then Within 3 weeks, I became clear enough in order to start to think about some sort of future in 2014...

I became expert in the eating of higher-fat foods and staying away from the processed ones that have chemicals to keep them on the shelf almost forever by the mfgrs.

But, recently, after many years, I had a guest visit me and allowed myself to eat some of these things and had a seizure problem after so many years.


I have studied (The therapeutic level) within the Big Pharma world and feel that too many pills are given to too many Americans still and actually even more today.

I was taken into the hospital recently, seen by a nice young ER doc and offered another neuro clinic to get treatment/pills from.


I was suggested (keppra) but, I refused it due to my knowledge of my diet mistake and just agreed to set up a future appointment.

So, what I am wondering is if anyone here knows about the side-effects of keppra and how well it really works?

Also, are there anymore new pills that have less effects and are somewhat affordable by cash to buy in the USA ?

I realize that nobody lives forever but, I have the ability to go beyond typical medical suggestions and I'd like to stick around a little longer to show some others what I've learned over the past 30 years...

Be Well Always,

Googman
 
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Hi Googman, welcome to CWE. :hello:

The efficacy of any given AED is highly variable from individual to individual. What works fantastic for one person might be a nightmare for another. There really isn't any way to know if Keppra is going to work for you unless you try it.

Side effects for Keppra and every other AED are well known. You can find them discussed here in the forum or look up the clinical info from sites like drugs.com.

I think Dilantin is probably the least expensive AED available right now because the patent on it expired some time ago. It's not a good drug for long term use though as it does present undesirable side effects (affecting balance, gum/teeth, etc.).
 
I think Dilantin is probably the least expensive AED available right now because the patent on it expired some time ago. It's not a good drug for long term use though as it does present undesirable side effects (affecting balance, gum/teeth, etc.).

I have taken brand name Dilantin for over 40 years. For the last 20, I have been paying for it out of pocket, buying a years supply at a time on the suggestion of my doctor. What I pay for a years worth of brand name Dilantin is similar to what people pay for a month or so of the new drugs.

As to the side-effects, every AED has them. It is a matter of knowing about them and being vigilant in dealing with them. I had gum problems 30 years ago, was told to use an electric toothbrush and have not had problems since. As to the balance, that's an indicator of overdosing so it just requires a blood test to verify and then a change in dosage. I've tracked my blood levels for 15+ years so I can look back at my dosage levels and discuss the change with my doctor. The most important part of this for me was finding a very good GP who watches over all the various potential issues to help prevent future problems.

Most important, whatever you are doing, you must understand how you are being affected. These drugs affect so many people in so many different ways that a doctor wont know how it will affect you precisely, only you can know that.

Best of luck in your search.
 
A Great Site And Thanx For Your Responses...

I really appreciate you folks responding to me .


I agree that many react differently but, it only took about 30 mins to find the same bad side effects including (THE KEPPRA RAGE) here....

What I have to tell you from over the last 40 yrs of study is that if a person finds a way to (lower) the amount of seizure medicine they take, the more apt they are to not feel the overdosing that gives them many side effects.

Try to remember that in America, health care is a for-profit business and the more pills doctors sell, the more free vacations they go on each year.

When I was a kid and had my first seizure after an accident, they started me on a pill trip that landed me inside of 2 psycho wards where they could call me some sort of mental case and try new mental pills on me.

As a child guinea pig, they observed my reactions until my father drew up a court order from his legal co workers and rescued me out of the medical system before it was too late.

He started me on a ketogenic diet and I grew into a teenager lifting weights and playing football while I learned to stay away from coffee,soda pop and sugars such as candy bars.


Being in the mental wards and facing the traumas given there to young kids being abused by ignorant guardsmen, caused me to become angry and powerful around others until I went into a councelor to give me a clue as to how I looked to others.

Once I knew, it was easy to (unlearn)

I spent decades without pills and only had to live a clean life cooking for myself and avoiding canned and fast foods.

It wasnt until my father became ill with parkinson's disease that I felt it was not safe to be without some sort of pill to make it thru the years of caring for him and appearing infront of hospital mgrs/owners as Power Of Attorney for him as he lived his last years.

The part I had no clue for after decades without pills was that I would be prescribed an amount for my weight that would be toxic to my brain at that level and would go on for years being basically disfunctional and unable to realize there was a problem until I came across an article about how American doctors do (over-prescribe) medications often.

After 3 weeks and the lowering of my dosage, I was finally able to see things in the real light once again, my teeth were not numb and my ear hurt once again if I pinched it.


A note here...

My current doctor will not accept health insurance for payments yet is affordable.

In my opinion, Americans need to have another friend be their pill-buddy if they are going to take neuro pills and to check in with them from time to time or, you may become subject to side effects that you may take as (normal) in order to avoid seizures.

Seizures large or small take you out of control which is scary but....

Having a Gran Mal is very close to what doctors do to you when they try to shock your system into mental health from what I have studied.

These days, there are more fast foods and canned foods that will cause toxic effects onto you than anything else in my opinion and many are taking the full dose of neuro pills simply to be able to tolerate the bad effects from the foods...

I am truly interested in more reactions here from you that will support pills like Keppra but, after reading about (Keppra Rage) I won't be thinking about taking that.

Also, if you are having emotional problems you seem to not understand, tell me here and if the owners of this site don't mind, I will build a blog for you all.


I feel that if I can live without pills or with a lower dosage than the (Therapeutic Level) so can others....

Be Well Always,

Googman
 
Here is what I found in 30 mins here....

Here is what I found in 30 mins here....


INFO FROM HERE...


KEPPRA



If the dr completes the Rx as "fill as prescribe", they have to use brand name. My dr's office has not used that option previously as there was no generic, but now they are changing their procedures on prescriptions.
My understanding that without insurance,

Keppra is between $250 - $300 for 30 days of pills. Ouch!



My current prescription of Keppra is just under $700 for a 30 day supply and my Lamictal is about $300 without insurance coverage! I found that out when my husband changed jobs and we were without insurance for a month...Ouch! I did the math once, and the Keppra cost me approximately $4 per tablet and the Lamictal about $5 per tablet that month. With the insurance, my co-pay for brand name is $50 each drug; the generic is $25 each drug, but if I wanted (or my doc ordered) me to take the brand name now that the generics are available I would have to pay the difference between the cost and my co-pay for the generic. (for keppra, it would be about $675)




I use generic keppra (on assistance and never been able to afford brand names), and it's worked well for me (the first 3-5 weeks, though I was really sleepy, and would have screaming rage about dumb things like dropping lunch meat on the ground or being late for an appointment that lasted only 30-90 seconds). However, my seizures are not severe, so I'm probably not sensitive to minute variations.

I did have preoccupation about death and dying, sort of an existential depression (not again!) But I was able to use the thoughts to develop a more productive philosophy about life to enrich each moment, but I can see how at a different time or for different circumstances it could've become suicidal depression, so that's something to watch and report to doctors, especially if you have a history of mood disorders.

ETA: also, I'm prescribed folic acid, which apparently helps.



Hello,
If you've been having these thoughts, it can indeed be due only to the current stressful issues in your life.. but it's likely keppra can be influencing how you're handling these situations. I would talk to your neurologist or doctor as soon as you get the chance.
I was in a very similar situation only a month ago - I've been recently diagnosed with epilepsy and was taking keppra (1500 bid) along with Clobazam to help me sleep. But I had noticed, and other people as well, that my mood wasn't normal, and I was having massive swings in my mood. I switched about a month ago to Valproic Acid, which has so far been a great alternative. I think it's too early yet to tell if this medication will prove more effective and lighter on my mood, but I can tell you from experience that the keppra certainly had very negative effects on my mood when I took it. I've been working through a lot of academic stress, and with valproic acid it's been a lot easier to handle. Keppra, stresses in my life were blown way out of proportion than they needed to be, from what I found. I started seeing a psychologist but I now find it unneccessary.


FROM C GIRL COLORADO 2012


Changing to generic Keppra XR really screwed me up!! Especially at first, it's better now, but I still have little panic attacks over nothing and I was never like that on brand name Keppra XR.


I'm going to expand on what I said earlier and give you my history with name brand vs generic, and this is long.
I started Keppra about 7 years ago after bad side effects from lamictal, tegretol, neurontin, depakote, and a few others I can't even remember now. But I had tried a lot, got pregnant by accident while on hormone birth control and was told that depakote and lamictal would make my baby be born with horrible congenital birth defects so had an abortion, then said screw this and dropped all meds for a few years. Had lots of seizures and finally had a horrible day with many grand mals (as well as the partials distracting me all day long) and decided to get back on meds. So I started Keppra under my neurologist's direction because if I got pregnant accidentally again I would know it was safer than those meds. The first few weeks were tough with tiredness and all day head fog and a difficult time waking up - it seemed like I was comatose. But I got over it, and life was so much better! I had to keep upping the dose and finally at 2000mg I was stable again. I found that I have had some rage at times but overall it made me a normal person again. Generic Keppra came on the market and I was forced to take it due to the insurance copay BS I have to deal with making it more pricey and the difference was amazing. All of a sudden I had horrible headaches every single day and I stuttered!!! What I was thinking is not what came out of my mouth, and what I tried to say was interrupted by uh uh uh and t.t.t.t... I just couldn't spit it out. After one month I called my neurologist and he told me that Keppra XR had come out on the market so I made the switch, because that could be covered at the copay price since no generics were available. The only problem I had was that my neurologist prescribed me to take it in the morning and the all day fog returned, so once I took it before bed and slept off the worst of the tiredness I was fine. Hello normal self again! I got pregnant by accident (again, but on barrier birth control) but had a perfectly healthy pregnancy, labor, delivery, and baby, and breastfed him for 15+ months with absolutely no problems. I had to take a lot of folic acid with him and still take 800mcg but life was great. Fast forward to last September. Levetiracetam ER hits the market, my brand name medically necessary prescription doesn't matter anymore and I am forced to take the generic or pay a dispensed as written penalty, so my price goes from $25 for 3 months of meds to $465.81 for 3 months. Figured I'd give the generic a chance. First brand, Actavis, made me break out in hives and get super edgy and freak out over stuff. Anxiety over nothing. I filed an appeal with my insurance company to receive the name brand at copay price since I was having side effects and it was denied. So I decided to pay for the brand name for Keppra XR but only had $155.27 to spend on one month so just did that and decided to try Watson Labs brand the next month. So, I did, and this time no hives. But, the very first night I started having seizures again, the anxiety was amplified by 1000x, I was having full blown panic attacks, my face started to break out like a teenager, fat tongue feeling, couldn't talk right, tingling and numbness in my hands and feet, inability to straighten out my hands and use them correctly, extreme exhaustion (like someone had sucked the life out of me), and migraines again. So, I had a bunch of blood work done to figure out if something else is causing this and everything looks good. My neurologist upped the dose to 2500mg to get the seizures under control. I filed another appeal with insurance, and an external review was denied. They have granted me 4 months of the name brand but only that and in the meantime, no one can tell me anything about the second appeal, if it's been approved, denied, etc. It's like it never happened and they skipped right over that to this external review that was denied. Anyway, in the midst of the worst of the symptoms, I became pregnant accidentally again. I say accidentally because these have all happened while on birth control and through different types of BC. We had many many fears about the baby and at a 9 week appointment discovered that it had died but I had not miscarried yet. I have no idea if the generics caused it ... people say it should not have... but for how messed up I've been, how can I ever be sure? Anyway, after the miscarriage, I decided that I'm not taking the generics anymore. I want to have a healthy baby now and on purpose. So, I have weaned myself down from 2500mg to 2000mg to 1500mg to 750mg and now 500mg. I figure if my insurance will give me 4 months of a 2000mg daily dose, I can make it last 16 months - long enough to get healthy enough to get pregnant again and have a healthy pregnancy. I really hope the 500mg controls the seizures. So far I haven't had any problems and actually feel really good again, which is surprising considering I had a miscarriage one week ago tomorrow morning. Of course the fear remains with having a seizure while pregnant, but... I don't know what to do since even with my insurance I can't afford my meds and it seems like the appeals are all going to be denied.

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Ive never tried the Generic of Keppra, Ive only been on name brand seizure medications all my life. But I have tried lamotrigine AKA Lamictal. I tried that in April of last year and had a really bad experience. It changed my mood, making me feel really depressed, and I also had an allergic reaction to it. I had to get off of it. Since then, Ive been on Keppra XR 3000mgs a day. I also take a Vitamin B-12, and Vitamin B Complex each morning. For me, ive had no problems with the Keppra for the past 13 years.




G Girl, Im so sorry you're going through all this crap with the insurance! Is crap like that, that just pisses me off! So far, ive been lucky enough to get the insurance to pay for brand name, as long as my dr doesnt approve the generics. My neurologist is pretty good at letting me make those kind of choices. Once I was put back on the Keppra XR after my first video EEG in march of last year, they let me decided it I would like to try the generic of Keppra XR. After thinking about it, I chose to stay with the name brand, because first off, Ive never tried a generic seizure medication before, and Ive known for years that the name brand Keppra has worked, so I didnt want to screw up and take the chance of the generic not working. But when my dr tried to wean me off of keppra in April of 2011, he had to put me back to the Keppra, and not the Keppra XR. I went from 3000mgs a day down to 2500mgs a day, and suffered from really bad headaches and tingling and numbness feelings in my hands and feet. My dr didnt think nothing was up, at least that It was seizure related. But when the end of May came around, I got to see the dr's assistant and told her about it. I was determined to make this stuff go away! I brought it up, and asked if he was planning on leaving me on the Keppra, (In april his plan was to put me on Lamictal, and wean me off of Keppra, but I had an allergic reaction with the lamictal, and once I was told I was having the allergic reaction, I was down to 2500mgs of the Keppra, the dr thought the 2500mgs a day would hold me over, so he left me there, despite having the tingling feelings in my hands and feet, and headaches) if they could switch me to the Keppra XR and back to 3000mgs? She asked the dr himself, he said sure. Within less than a week, all those symptoms went totally away! I told my mom I knew that stuff wasnt all in my head! My mom then started to see where i was coming from, and she really thought it was in my head too, but after seeing the change in what took place, just going to Keppra XR from Keppra and bumping the dose up 500mgs more a day, it changed me for good!




SIDE EFFECTS: Common side effects associated with levetiracetam include headache, sleepiness, weakness, dizziness, and infection. Difficulty walking or moving, hostility, irritability, mood swings, anxiety, hallucinations, and delusions also have been associated with levetiracetam. A small number of patients may experience a decrease in red or white blood cell counts. Like other antiseizure medications, levetiracetam should not be discontinued suddenly because of the risk of increased seizure activity.

Has anyone experienced the Keppra Rage?

I have been on Keppra for almost 11 years now and during that time I was also on Carbatrol. I was taken off the Carbatrol March 7th and since then Ive been experiencing alot of different emotions.

Anger, sadness, feeling of just not caring, no desire to even want to get up out of bed, crying spells, you name it, I have it!

Today was the worst! I felt like not even wanting to spend another day of dealing with this again!

I had to contact my dr, which he told me he thinks its Keppra Rage. He thinks that since my body was so use to the Carbatrol, that the carbatrol was like a sedative and helped with the irritability, and moods. Now that Im no longer on the Carbatrol, the emotions are getting worse!




I am 125 lbs and am on 2000 mg of Keppra 2x/day. I do have rage issues that appear to be connected to Keppra.
I take 1000 mg of time released B12 in the morning along with 100 mg of B6 (not time released). This gets me through the work day. If I felt like I needed it, I would take another 100 mg dose of B6 in the afternoon, but that is my time to chill out. I feel it makes a big difference in my mood.



I understand the Keppra Rage thing completely and not wanting to be with someone cause you always feel like your treating them like shit. Some times I don't even mean too but I just can't help it you know. fecking sucks. I also take Keppra I may not have mentioned that. And your right not everyone is a jerk. I still talk to the one guy I dated years ago and were friends now I think. I just wish we could have normal relationships without the extra baggage I guess. =(
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Keppra makes me, and a lot of others, very irritable and angry. We call it keprage.

One thing with meds is it may be helping control your seizures but the side effects are just too much to handle and you need to stop taking it, which sounds like is what's going on here. I've had to stop taking different meds several times because I couldn't deal with the side effects.

I'd deffently call your neurologist tomorrow and tell him about the problems. You'll have to be weaned off of it. You can't just do it cold turkey because that can be very unsafe.






I had dizziness and would stumble quite a bit when I first started Keppra. It was weirdest in the night and morning. I also noticed that my seizures changed. Once my body adjusted I stopped stumbling and feeling dizzy. The only thing I'm noticing is that PMS essentially renders the drug useless for me. I'll be great and then the PMS comes and the seizures are back. I don't think that part will be an issue for you, though.



END
 
What I have to tell you from over the last 40 yrs of study is that if a person finds a way to (lower) the amount of seizure medicine they take, the more apt they are to not feel the overdosing that gives them many side effects.

Try to remember that in America, health care is a for-profit business and the more pills doctors sell, the more free vacations they go on each year.

Googman,
I've had epilepsy for 34 years and have tried many meds myself. I even had a temporal lobectomy, to no avail. But I needed to find something to control my seizures because I experienced nearly every type of seizure there is. After the lobectomy, my seizures were worse than before, so we needed to increase the dosage in order to help with the overwhelming seizures. And yes, I did experience many serious side effects from those meds.
I do agree somewhat that health care is a profitable business here in America and Drs. prescribe meds for their benefit, but not always. There are some caring docs. Many times back in the 90's, I would see a pharmacy rep in my neuro's office and that would really piss me off because they would take more time from my neuro.


When I was a kid and had my first seizure after an accident, they started me on a pill trip that landed me inside of 2 psycho wards where they could call me some sort of mental case and try new mental pills on me.

As a child guinea pig, they observed my reactions until my father drew up a court order from his legal co workers and rescued me out of the medical system before it was too late.

After my lobectomy, I ended up severely depressed, suicidal as said before. The never put me in a psycho ward. My neuro called in a neuropsychiatrist who specialized in depression and epilepsy- they often go hand in hand. At the time this dr. said I was his most difficult patient because nothing would ease the depression and at times I wanted to kill myself. But no way would I go to some psycho ward. Why did your parents allow it in the first place?

He started me on a ketogenic diet and I grew into a teenager lifting weights and playing football while I learned to stay away from coffee,soda pop and sugars such as candy bars.

Their are several members on CWE who have their kids on the ketogenic diet.

Being in the mental wards and facing the traumas given there to young kids being abused by ignorant guardsmen, caused me to become angry and powerful around others until I went into a councelor to give me a clue as to how I looked to others.

Once I knew, it was easy to (unlearn)

I spent decades without pills and only had to live a clean life cooking for myself and avoiding canned and fast foods.
A young kid having seizure should never have been put in a mental ward to begin with. Why did your parents allow it, especially if you learned to function without pills for decades? :ponder:


The part I had no clue for after decades without pills was that I would be prescribed an amount for my weight that would be toxic to my brain at that level and would go on for years being basically disfunctional and unable to realize there was a problem until I came across an article about how American doctors do (over-prescribe) medications often.
There are books out about the American pharmaceuticals continuing to get our nation "hooked" on prescription drugs. One is entitiled,
"Our Daily Meds". I have it right here on my own book shelf. Go to Amazon.com and you will see it.

After 3 weeks and the lowering of my dosage, I was finally able to see things in the real light once again, my teeth were not numb and my ear hurt once again if I pinched it.
Great, let's hope the seizures don't increase.


In my opinion, Americans need to have another friend be their pill-buddy if they are going to take neuro pills and to check in with them from time to time or, you may become subject to side effects that you may take as (normal) in order to avoid seizures.

Seizures large or small take you out of control which is scary but....

Having a Gran Mal is very close to what doctors do to you when they try to shock your system into mental health from what I have studied.
First of all, regardless of which type of seizure(s) anyone has, they need to have a friend or family member check in with them to make sure they're getting the meds and ask how they feel: Are they depressed?, Are they suffering from headaches?, Any new aches? Any new falls within the last month? These are the questions I get asked every time I see my docs.

Secondly, having a grand mal, (now called tonic-clonic) is nothing like ECT (Electroconvulsive Therapy). Sometimes, having a TC does help alleviate the symptoms of deep deep depression.

I am truly interested in more reactions here from you that will support pills like Keppra but, after reading about (Keppra Rage) I won't be thinking about taking that.

Also, if you are having emotional problems you seem to not understand, tell me here and if the owners of this site don't mind, I will build a blog for you all.
I feel that if I can live without pills or with a lower dosage than the (Therapeutic Level) so can others....

After me going thru brain surgery, trying 12 different meds going thru depression and still having seizures, I now have the VNS and still take 3000 mgs. of Keppra along with an anti-depressant. After seeing the neuropsychiatrist who was well-known in the world of epilepsy, I think I understand my emotional problems and don't need a blog. Nor can I live with a lower dosage of AEDs. Been there, done that and ended up facing a fence in my car. No thanks.
 
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Thanx for your input I appreciate it...

See, for years while I was on that (Therapeutic Level) while helping my father as he faded, there was no way I could have arranged the thoughts you did here in the order you replied without frustrating me into quitting.

Now, on a lower dosage and eating correctly, I am able to think much more clearly and helped two suicidal people back up that were obviously over-medicated and helpless to change.

They were so drugged-out that being quiet was all they knew until it becomes unbearable and then they explode...

It was the (unlearning of behaviors/habits) and the correct level of natural nutrients inside that allowed them to live once again.

Now one can go to a place like weedwirefederaldotcom and see seizures stopped with maryjane...

Be Well Always,

Googman
 
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That website, weedwirefederal.com is all about cannabis. Here in my state of Colorado, it is now legal locally, but not federally. But no way will I do it unless I know for sure it can "cure" or at least stop the seizures. How the hell can you arrange your thoughts while smoking this? Like I said in my last post, I still take a HIGh dosage of KEPPRA, 3000 Mgs. along with Topomax and some Potiga along with a high dose of Zoloft. And even on all that, I can still write sensibly, although I do suffer from aphasia and dyslexia.

I also eat correctly because I also have Type 1 diabetes, so I have no other choice. Otherwise, I could pass out or seize. So on top of my seizure meds and eating correctly, watching my carb intake, I also have to give myself daily insulin injections and check my glucose level numerous times a day. All that can be unbearable at times, but no way will I try smoking weed again. The young renters living above me do it every weekend in the summer. The smell makes me want to puke.

So using this "pot" for a "natural cure" is a bunch of bull, IMO. If not used properly and getting the THC levels lowered, it can do a lot of harm.

http://www.drugabuse.gov/publications/drugfacts/marijuana
The highest density of cannabinoid receptors is found in parts of the brain that influence pleasure, memory, thinking, concentration, sensory and time perception, and coordinated movement. Marijuana overactivates the endocannabinoid system, causing the “high” and other effects that users experience. These effects include altered perceptions and mood, impaired coordination, difficulty with thinking and problem solving, and disrupted learning and memory.

Marijuana also affects brain development, and when it is used heavily by young people, its effects on thinking and memory may last a long time or even be permanent. A recent study of marijuana users who began using in adolescence revealed substantially reduced connectivity among brain areas responsible for learning and memory. And a large long-term study in New Zealand showed that people who began smoking marijuana heavily in their teens lost an average of 8 points in IQ between age 13 and age 38. Importantly, the lost cognitive abilities were not fully restored in those who quit smoking marijuana as adults.

What Are the Other Health Effects of Marijuana?

Marijuana use may have a wide range of effects, particularly on cardiopulmonary and mental health.


Marijuana also raises heart rate by 20-100 percent shortly after smoking; this effect can last up to 3 hours. In one study, it was estimated that marijuana users have a 4.8-fold increase in the risk of heart attack in the first hour after smoking the drug. This risk may be greater in older individuals or in those with cardiac vulnerabilities.

A number of studies have linked chronic marijuana use and mental illness. High doses of marijuana can produce a temporary psychotic reaction (involving hallucinations and paranoia) in some users, and using marijuana can worsen the course of illness in patients with schizophrenia. A series of large studies following users across time also showed a link between marijuana use and later development of psychosis. This relationship was influenced by genetic variables as well as the amount of drug used, drug potency, and the age at which it was first taken—those who start young are at increased risk for later problems.

Associations have also been found between marijuana use and other mental health problems, such as depression, anxiety, suicidal thoughts among adolescents, and personality disturbances, including a lack of motivation to engage in typically rewarding activities. More research is still needed to confirm and better understand these linkages.


Additionally, because it seriously impairs judgment and motor coordination, marijuana contributes to risk of injury or death while driving a car. A recent analysis of data from several studies found that marijuana use more than doubles a driver’s risk of being in an accident. The combination of marijuana and alcohol is worse than either substance alone with respect to driving impairment.

Rising Potency

The amount of THC in marijuana samples confiscated by police has been increasing steadily over the past few decades. In 2012, THC concentrations in marijuana averaged close to 15 percent, compared to around 4 percent in the 1980s. For a new user, this may mean exposure to higher concentrations of THC, with a greater chance of an adverse or unpredictable reaction. Increases in potency may account for the rise in emergency department visits involving marijuana use. For frequent users, it may mean a greater risk for addiction if they are exposing themselves to high doses on a regular basis. However, the full range of consequences associated with marijuana's higher potency is not well understood. For example, experienced users may adjust their intake in accordance with the potency or they may be exposing their brains to higher levels overall, or both.

Is Marijuana Addictive?

Contrary to common belief, marijuana is addictive. Estimates from research suggest that about 9 percent of users become addicted to marijuana; this number increases among those who start young (to about 17 percent, or 1 in 6) and among people who use marijuana daily (to 25-50 percent).


How Does Marijuana Affect a User’s Life?

Research shows marijuana may cause problems in daily life or make a person's existing problems worse. Heavy marijuana users generally report lower life satisfaction, poorer mental and physical health, more relationship problems, and less academic and career success compared to non-marijuana-using peers. For example, marijuana use is associated with a higher likelihood of dropping out of school. Several studies also associate workers' marijuana smoking with increased absences, tardiness, accidents, workers' compensation claims, and job turnover.
 
The Maryjane look for seizures...

Thanx I appreciate your responses ...

Its the CBD weed I am interested in, the sort without the high like they voted through here...

JUST GOOGLE THIS IF YOU CARE TO

Tenn. medical marijuana bill fails, but CBD-only bill goes forward
Scope of cannabidiol approval limited to clinical tests


"We’ve heared from some physicians and patients that small does (less than 5 milligrams) of a CBD-dominant tincture or extract (15>:1 CBD:THC) can be very helpful for depression and overall health. LESS IS MORE! is often the case with regard to cannabis therapeutics. The challenge is to find =good-quality medicine — a lot of what passes for CBD Hemp oil is not good quality. Good luck." projectcbd dot org


Be Well Always,
Googman
 
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Its the CBD weed I am interested in, the sort without the high like they voted through here...

And this has been discussed here, too. Did you see Dr. Sanjay Gupta's program about? Now here is an American neurosurgeon who changed his mind about "pot" and told the nation about it. Check it out:
http://www.cnn.com/2013/08/07/health/charlotte-child-medical-marijuana/index.html

The strain was low in tetrahydrocannabinol, or THC, the compound in marijuana that's psychoactive. It was also high in cannabidiol, or CBD, which has medicinal properties but no psychoactivity. Scientists think the CBD quiets the excessive electrical and chemical activity in the brain that causes seizures.
 
Welcome, I agree in regards to big pharma and haow criminal it is that they make the money they do charging what they do. I have been on quite a few meds and have had bad reactions to them. I am very petite and often docs just prescribe the adult dose rather than weight based. I am a former RN, I don't think it is all too conducive suffering from grand-mal seizures and going back into the ICU. But I have adjusted my diet and am starting to research through the back door of course how marijuana would be better for me than the rampant chemicals made up in a lab and than into my bloodstream to screw with my own natural brain chemicals.
 
Keppra. Well, I've been on this for at least 8 years. In all that time, I've noticed I just can not get my words out of my mouth! It's as if something has taken the sentence I was waffling on about out of my head....only to finish it when I remember what I was talking about to begin with! I tend to slump around dinnertime too, although that could just be because I need something to eat....but I'm not diabetic. I've also developed a 'can't be bothered' attitude & so I try setting a deadline (even though I don't need one) when there are things that need doing. I do get frustrated at times, for no apparent reason, so maybe that's down to this 'Keprage'.
As for using cannabis, I did try this twice. The first time, it set off a partial seizure. So! Thinking it might not be related, I tried it again, only to find it happened again. Obviously I've kept well clear from that smelly stuff since, although lots of people I know smoke it morning, noon & night.
 
This is an old thread . . . but since it has been ressurected, I think it always bears mentioning that one person's evil drug is another's savior. Like most of us, I've run through a long list of AEDs and found keppra to be one drug that gives fairly decent seizure control with virtually no side effects, and very few if any cognitive side effects. No Kepprage either. It's worked well for me. On the other hand Topamax almost killed me through electrolyte imbalances, probably due to low-grade chronic acidosis, whereas it's a great drug for many. One never knows what they personally will experience until they try!
 
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