Keppra And CBD Oil Interaction

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Hello! Advice needed ASAP! I'll give you a quick run down I am 24 years old and recently diagnosed with generalized epilepsy. Being diagnosed is literallu my biggest fear coming true ive always been afraid of having seziures and all these years ive had minor moments of blackkng out but never thought tbey were seziures until this year theyve gotten worse and my EEG showed Keppra And CBD Oil Interaction Pharmacokinetic and pharmacodynamic interactions occur with multiple ASMs. Pharmacokinetic interactions are frequently attributed to CYP2C19 and CYP3A4. Known “We’ve tried it all” AN EMPTY FEELING. With saliva leaking from his mouth, Preston experiences an absent seizure, which looks and feels like it sounds: He stops interacting and stares into

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Hello! Advice needed ASAP! I’ll give you a quick run down I am 24 years old and recently diagnosed with generalized epilepsy. Being diagnosed is literallu my biggest fear coming true ive always been afraid of having seziures and all these years ive had minor moments of blackkng out but never thought tbey were seziures until this year theyve gotten worse and my EEG showed seziure activity on both sides of my brain. My neuro prescribed me 500mg keppra (generic form) twice a day to start but I am so scared to start it due to everything I’ve read and heard about it and it’s side effects. I’ve done research on CBD and wanted to give it a try but I don’t know how effective it will be. I just want to do something that I know will work, also I had recently been trying to conceive and am worried what my new diagnoses means for TTC. Any advice on ether keppra or CBD would be great. Thanks in advance.

Comments

There is a host of
Submitted by epihelp on Tue, 2017-09-12 – 12:31

There is a host of information that is well known about Keppra and other seizure medications, but very little on cannabis or CBD. While a few research studies to date look positive for a pharmaceutical grade cannabadiol, we don’t know how it will work in all seizure types. Side effects can occur so it’s important to look into these. Talk to your health care team about options. What’s known about helpfulness, side effects and safety. There are concerns about safety of different products grown. Here is a section on cbd -http://www.epilepsy.com/learn/treating-seizures-and-epilepsy/other-treatment-approaches/medical-marijuana-and-epilepsy

There is a host of information that is well known about Keppra and other seizure medications, but very little on cannabis or CBD. While a few research studies to date look positive for a pharmaceutical grade cannabadiol, we don’t know how it will work in all seizure types. Side effects can occur so it’s important to look into these. Talk to your health care team about options. What’s known about helpfulness, side effects and safety. There are concerns about safety of different products grown. Here is a section on cbd -http://www.epilepsy.com/learn/treating-seizures-and-epilepsy/other-treatment-approaches/medical-marijuana-and-epilepsy

There is a host of information that is well known about Keppra and other seizure medications, but very little on cannabis or CBD. While a few research studies to date look positive for a pharmaceutical grade cannabadiol, we don’t know how it will work in all seizure types. Side effects can occur so it’s important to look into these. Talk to your health care team about options. What’s known about helpfulness, side effects and safety. There are concerns about safety of different products grown. Here is a section on cbd -http://www.epilepsy.com/learn/treating-seizures-and-epilepsy/other-treatment-approaches/medical-marijuana-and-epilepsy

I’m just nervous because I’ve
Submitted by Melissa1992 on Tue, 2017-09-12 – 18:03

I’m just nervous because I’ve never taken anything so serious and alot of people have said negative things about keppra and have told me to try CBD. I just don’t know which to do

I’m just nervous because I’ve never taken anything so serious and alot of people have said negative things about keppra and have told me to try CBD. I just don’t know which to do

I’m just nervous because I’ve never taken anything so serious and alot of people have said negative things about keppra and have told me to try CBD. I just don’t know which to do

Think a little. Do people
Submitted by just_joe on Sat, 2017-09-16 – 17:45

Think a little. Do people that have been prescribes and taking a medication go to a forum and talk about their medicatins if they are working? THe answer to my question is NO they are out with friends or with family and doing other things since the medications are working.Side effects do happen. They happen with any and all medications including over the counter meds. Aspirin has killed some people.I have been using keppra for about 15 years now and have had no problems with it. I have used about 20-23 other medications or couplings of medications. Keppra is th best medication I have used in the 50+ years I have been living and dealing with seizures. CBD is being researched. But just like medications it too has side effects.Recently diagnosed means you have researched forums and used the web to find out about side effects, Have you asked your neurologist about said side effects and how many patients he has had that got them? If not Why not talk to him? I know it sounds weird but I do believe I would take the medication since it was created to stop seizures. It was tested for years before ever going on market. Generally about 8% of the people taking the medications get a side effect. Which would equate to 92% not getting a side effect. I personal never thought about side effects since when I was diagnosed there were no computers. Research was done in real physical libraries. You listened and did what your doctors said to do. If you had an issue then is when you talked to your doctor. I did have an issue with the very first medication I was given. But it was not a side effect that cause my issue. It was the dosage was too high. I was taken off it and the next week was put on the same medication at a lower dosage and it worked well

Think a little. Do people that have been prescribes and taking a medication go to a forum and talk about their medicatins if they are working? THe answer to my question is NO they are out with friends or with family and doing other things since the medications are working.Side effects do happen. They happen with any and all medications including over the counter meds. Aspirin has killed some people.I have been using keppra for about 15 years now and have had no problems with it. I have used about 20-23 other medications or couplings of medications. Keppra is th best medication I have used in the 50+ years I have been living and dealing with seizures. CBD is being researched. But just like medications it too has side effects.Recently diagnosed means you have researched forums and used the web to find out about side effects, Have you asked your neurologist about said side effects and how many patients he has had that got them? If not Why not talk to him? I know it sounds weird but I do believe I would take the medication since it was created to stop seizures. It was tested for years before ever going on market. Generally about 8% of the people taking the medications get a side effect. Which would equate to 92% not getting a side effect. I personal never thought about side effects since when I was diagnosed there were no computers. Research was done in real physical libraries. You listened and did what your doctors said to do. If you had an issue then is when you talked to your doctor. I did have an issue with the very first medication I was given. But it was not a side effect that cause my issue. It was the dosage was too high. I was taken off it and the next week was put on the same medication at a lower dosage and it worked well

Think a little. Do people that have been prescribes and taking a medication go to a forum and talk about their medicatins if they are working? THe answer to my question is NO they are out with friends or with family and doing other things since the medications are working.Side effects do happen. They happen with any and all medications including over the counter meds. Aspirin has killed some people.I have been using keppra for about 15 years now and have had no problems with it. I have used about 20-23 other medications or couplings of medications. Keppra is th best medication I have used in the 50+ years I have been living and dealing with seizures. CBD is being researched. But just like medications it too has side effects.Recently diagnosed means you have researched forums and used the web to find out about side effects, Have you asked your neurologist about said side effects and how many patients he has had that got them? If not Why not talk to him? I know it sounds weird but I do believe I would take the medication since it was created to stop seizures. It was tested for years before ever going on market. Generally about 8% of the people taking the medications get a side effect. Which would equate to 92% not getting a side effect. I personal never thought about side effects since when I was diagnosed there were no computers. Research was done in real physical libraries. You listened and did what your doctors said to do. If you had an issue then is when you talked to your doctor. I did have an issue with the very first medication I was given. But it was not a side effect that cause my issue. It was the dosage was too high. I was taken off it and the next week was put on the same medication at a lower dosage and it worked well

epilepsy community fears
Submitted by [email protected] on Sun, 2017-09-17 – 12:34

epilepsy community fears medical pot . keppra made my seizures worse, / six weeks in medical pot smoked daily is helping me . think for yourself

epilepsy community fears medical pot . keppra made my seizures worse, / six weeks in medical pot smoked daily is helping me . think for yourself

epilepsy community fears medical pot . keppra made my seizures worse, / six weeks in medical pot smoked daily is helping me . think for yourself

I believe we are in agreement
Submitted by epihelp on Sun, 2017-09-17 – 13:22

I believe we are in agreement for people to think about pros and cons. My point is to get the right information so people make informed decisions. There is quite a bit of research done on cannabis in scientific ways so we can learn more..

I believe we are in agreement for people to think about pros and cons. My point is to get the right information so people make informed decisions. There is quite a bit of research done on cannabis in scientific ways so we can learn more..

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I believe we are in agreement for people to think about pros and cons. My point is to get the right information so people make informed decisions. There is quite a bit of research done on cannabis in scientific ways so we can learn more..

So you haven’t even tried it,
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:18

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it,
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:21

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

Just forget about meds. Your
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:20

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

So you haven’t even tried it,
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:22

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

Just forget about meds. Your
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:21

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

What state do you live in if
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:22

What state do you live in if I could ask?

Just forget about meds. Your
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:26

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

Just forget about meds. Your not the type of person to take them. Go to a doctor who will help you live your life WITH seizures. You might handle that better.

What state do you live in if
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:26

What state do you live in if I could ask?

You have to try Melissa then
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:26

You have to try Melissa then you’ll know.

So you haven’t even tried it,
Submitted by SeizingLisa on Mon, 2017-09-18 – 00:26

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

So you haven’t even tried it, is that what I read? It could be the one. Try it first at least if you have any side effects that will stop you from using it then stop it and call your Dr. Everyone reacts differently to meds. If you don’t at least try the meds the Dr. gives you then why are you going. Stop going to the Dr. Try some herbal remedies they might work for you. Good luck Melissa.

Try the medication, because
Submitted by sindarintech on Mon, 2017-09-18 – 23:39

Try the medication, because it has a long documented history of helping people. Give it a couple of months for your body to adjust. Usually a good neuro will ease up your dosage over a period of time, so expect some periods where you just feel weird. Keep in mind that YOU are the final authority of what you put in your body. Different meds work different ways on different people. I got off the Keppra because it was making me too tired and groggy. That’s not an acceptable ‘remedy’. especially with so many other options, medication-wise. If Keppra doesn’t work for you, or has negative side-effects, insist on changing your medication. But give it sufficient time for your body to adjust first. CBD is still an unproven option and is not really something you want to try all by itself. There are also a lot of variations in production, which makes it difficult to gauge dose-wise. If you want to see if it helps, use it as a supplement to your primary medication. Be careful not to overthink things. you now know for sure that you have an epilepsy diagnosis, and can plan accordingly. It’s a treatable condition. I went for 20+ years not even knowing what was happening to me.

Try the medication, because it has a long documented history of helping people. Give it a couple of months for your body to adjust. Usually a good neuro will ease up your dosage over a period of time, so expect some periods where you just feel weird. Keep in mind that YOU are the final authority of what you put in your body. Different meds work different ways on different people. I got off the Keppra because it was making me too tired and groggy. That’s not an acceptable ‘remedy’. especially with so many other options, medication-wise. If Keppra doesn’t work for you, or has negative side-effects, insist on changing your medication. But give it sufficient time for your body to adjust first. CBD is still an unproven option and is not really something you want to try all by itself. There are also a lot of variations in production, which makes it difficult to gauge dose-wise. If you want to see if it helps, use it as a supplement to your primary medication. Be careful not to overthink things. you now know for sure that you have an epilepsy diagnosis, and can plan accordingly. It’s a treatable condition. I went for 20+ years not even knowing what was happening to me.

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Try the medication, because it has a long documented history of helping people. Give it a couple of months for your body to adjust. Usually a good neuro will ease up your dosage over a period of time, so expect some periods where you just feel weird. Keep in mind that YOU are the final authority of what you put in your body. Different meds work different ways on different people. I got off the Keppra because it was making me too tired and groggy. That’s not an acceptable ‘remedy’. especially with so many other options, medication-wise. If Keppra doesn’t work for you, or has negative side-effects, insist on changing your medication. But give it sufficient time for your body to adjust first. CBD is still an unproven option and is not really something you want to try all by itself. There are also a lot of variations in production, which makes it difficult to gauge dose-wise. If you want to see if it helps, use it as a supplement to your primary medication. Be careful not to overthink things. you now know for sure that you have an epilepsy diagnosis, and can plan accordingly. It’s a treatable condition. I went for 20+ years not even knowing what was happening to me.

Why the hell are you getting
Submitted by Stephen L on Fri, 2017-09-22 – 17:28

Why the hell are you getting so defensive to her? Your passive aggressive tone isn’t needed nor wanted on a place like this. -_-

Why the hell are you getting so defensive to her? Your passive aggressive tone isn’t needed nor wanted on a place like this. -_-

Why the hell are you getting so defensive to her? Your passive aggressive tone isn’t needed nor wanted on a place like this. -_-

Keppra And CBD Oil Interaction

Pharmacokinetic and pharmacodynamic interactions occur with multiple ASMs.

Pharmacokinetic interactions are frequently attributed to CYP2C19 and CYP3A4.

Known interactions may not alter the ASM level outside the therapeutic range.

There is limited evidence currently for many ASMs.

There is limited evidence for the clinical relevance of many interactions.

Abstract

Objective

Cannabidiol is efficacious as an adjunctive treatment in children with epilepsy associated with Dravet and Lennox-Gastaut syndromes. As its role is currently adjunctive, we reviewed the interactions of cannabidiol with other antiseizure medications (ASMs).

Methods

A search of Cochrane, Pubmed and Embase databases from January 2015 to April 2020 was performed. All original research papers discussing interactions between cannabidiol and ASMs were included. Bibliographies of review articles were searched to identify further papers. Adverse events and side effects were excluded.

Results

Cannabidiol interacts with ASMs through both pharmacokinetic and pharmacodynamic mechanisms. Thirty studies were identified (eighteen observational cohort studies, two randomised-control trials, three case reports/series, three animal studies, two briefing reports, an analysis of cohort data and a clinical trial simulation). There is potential for pharmacokinetic interactions between CBD and brivaracetam, clobazam, eslicarbazepine, lacosamide, gabapentin, oxcarbazepine, phenobarbital, potassium bromide, pregabalin, rufinamide, sirolimus/everolimus, stiripentol, tiagabine, topiramate and zonisamide. Pharmacodynamic interactions were identified for clobazam, valproate and levetiracetam. An animal study identified that the brain concentration of ASMs may be altered while the serum concentration remains the same.

Conclusion

Pharmacokinetic and pharmacodynamic interactions exist between cannabidiol and ASMs. The cytochrome p450 system in particular has been implicated in pharmacokinetic interactions, although not exclusively. The existing literature is limited for some ASMs by studies having relatively small cohorts. As increasing numbers of patients use cannabidiol, specialists need to monitor closely for interactions clinically and with blood levels when required.

“We’ve tried it all”

AN EMPTY FEELING. With saliva leaking from his mouth, Preston experiences an absent seizure, which looks and feels like it sounds: He stops interacting and stares into nothing.

Inside Children’s Hospital Colorado, Ana Watson stares across the small exam room at the woman in a white lab coat quizzing her. Banzel? “Tried it,” Ana says. Keppra? “Is that the one that causes the rash?” Ana asks. “Keppra often causes behavioral issues,” the doctor responds. “Yes, that’s what we got with that,” Ana says. The doctor continues down the list of anti-epilepsy medications, collecting the medical history of Ana’s 12-year-old son, Preston, whose seizures cause such unrelenting brain damage that he functions at the level of a 2-year-old. The doctor ticks through 13 medicines, but Preston already has tried each one, to little effect.

That’s why Ana moved her family across the country to Colorado, where Preston could try a treatment that’s not on the doctor’s list. Three days before the doctor’s appointment in mid-July, Ana gave Preston his first dose of an unregulated medical marijuana extract that is high in a compound called CBD. Hundreds of families like Ana’s have moved to Colorado for the treatment, hoping it will calm their children’s seizures.

A desperate hope and well-publicized stories about kids who have responded to the drug drive the families here, despite scant research on CBD’s overall efficacy. Scientists know so little about the treatment that it’s not even clear what CBD might do in the brain to impact seizures.

So, the entire day after that first dose, Ana watched Preston like a poker player looking for a tell.

Preston yawned. Did that mean the marijuana made him sleepy? Preston ate. Did the extract make him hungry? Preston didn’t seem to seize as often.

Then the next day, Preston suffered a grand mal seizure that left him writhing violently. He had another one the day after that. Getting him to eat or drink had become nearly impossible, and that meant he wasn’t getting consistent doses of either the CBD treatment or his traditional medications, both of which Ana tried to hide in Preston’s food or sweet tea.

So now Ana is sitting in the hospital whose doctors have been the most outspoken in Colorado in urging parents not to use marijuana to control seizures — it’s too risky, they say; there are too many unknowns — and she is hoping for advice on what to do.

Ketogenic diet, the doctor asks?

“Basically, we’ve tried it all,” Ana says. “That’s why we moved here for CBD. His doctors said we can’t go up in his meds anymore, and we were at a stopping point.”

The doctor looks at her list. She looks sympathetically at Ana.

“Have you tried Stiripentol?”

“Yes,” Ana sighs, “we’ve tried everything.”

No recommendations

The CBD rush to Colorado is a movement that divides patients from doctors.

Even as families flock to the state, few doctors here condone the use of marijuana to treat seizures. And that means the very people on whom families depend for medical advice are often silent when it comes to critical questions about the new treatment.

The state health department, which manages the patient registry that all children using medical marijuana must join, offers almost no guidance.

“What I always tell people is you have to be really careful,” said Dr. Larry Wolk, the executive director of the Colorado Department of Public Health and Environment. “They have to know that it’s outside of the regulatory process, outside of the (Food and Drug Administration), and it’s very much ‘Buyer beware.’ “

Many of the families arriving in the state for medical marijuana — as well as those already living here — seek out the care of specialists at Children’s Hospital Colorado. About 100 kids who see doctors at the hospital have tried a CBD treatment.

But no doctor at Children’s recommends using cannabis or gives more than cautious advice about it.

“We don’t make recommendations about the marijuana therapy because we don’t have the information to do that,” said Dr. Amy Brooks-Kayal, the head of pediatric neurology at Children’s. “We feel very strongly that we need to act on good medical and scientific evidence, and that doesn’t exist.”

A national survey of doctors by the American Epilepsy Society found that while 94 percent said they have been asked by a patient about using cannabis to control seizures, fewer than a third would actually recommend that patients try it. Another 13 percent said they would support its use but would rather have another doctor provide the recommendation needed to obtain it.

“For the doctor to know what they need to know about an illegal drug is a very high expectation,” said Dr. Jacqueline French, an epilepsy specialist at New York University’s Langone Medical Center. She said CBD is “driving the conversation” many doctors now have with their patients.

The result of that one-sided conversation, though, is that parents who give CBD to their children must turn to one another and their medical marijuana providers for help. Facebook has become a crowd-sourced doctor’s office. Colorado’s sometimes ragtag community of medical marijuana growers acts as a de facto human services agency.

By not engaging more with providers, doctors often lack an understanding of the types of marijuana products their patients are using and are unaware of the sometimes contradictory advice their patients receive.

For instance, CBD providers commonly tell newly arrived parents that they should reduce the level of an anti-seizure drug called Onfi before starting CBD because the two could have a dangerous interaction. Parents often reduce the medicine without consulting their doctors. Doctors at Children’s, though, say they haven’t seen conclusive evidence that CBD has an impact on Onfi levels. Meager research makes it impossible to know who is right.

Some physicians are now stepping forward to work with providers on clinical trials for CBD, and doctors at Children’s have begun recording more specific details of the CBD products their patients are using — who is providing the medical marijuana and how much the child is taking, for instance. But the broader dynamic still hinders the study of CBD’s effectiveness. And that only increases the uncertainty that hangs over families such as Ana’s in their Colorado exile.

Leaving Children’s after the first visit, Ana still has questions about CBD. But doctors there have set up several new appointments to address other aspects of Preston’s care. He soon will have a feeding tube inserted into his stomach, allowing Ana to give him food and medicine consistently. She’ll take him to get fitted for a new helmet to protect him in falls.

A plan is taking shape.

“I thought it went really well,” she says.

Parents hope to see progress

Two days later, they’re back again. A blue line squiggles furiously up and down on a computer screen.

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Preston is talking.

“Silly mommy,” he says to Ana, as she snuggles into a single hospital bed with him.

“Silly Preston,” she says back.

He leans in to give her a kiss on the cheek. A maroon line on the computer screen jumps to life.

A bundle of 21 multicolored electrical wires poke from the top of a wrapping on Preston’s head, running off the bed and to the computer. Every gesture, every word, every eye blink shows up as activity on the screen, where blue, maroon and green lines measure Preston’s brain activity. It is one answer to the question that has vexed Ana for the past 12 years: What is happening inside her son’s head?

But, even now, the seizures from a rare form of epilepsy known as Dravet syndrome remain a mystery. Some little eye-flutter seizures cause leaping spikes on the screen. Some seem to skip by without a change in the pattern. So chaotic is Preston’s brain that, looking later at the electroencephalogram, or EEG, doctors will have a hard time telling from the readings when he was awake and when he was asleep, when he was seizing and when he was still.

At the end of their first visit, Dr. Kelly Knupp, Preston’s new neurologist at Children’s, suggested the EEG so that the hospital could have some starting record of Preston’s brain activity. The timing worked; Preston was already in the hospital, after the feeding tube surgery the day before.

But, to get a true starting level, the EEG meant Ana would need to take Preston off CBD temporarily. She had spent seven months planning how to get to Colorado for the treatment. She was pausing it after five days.

“The point of this is to get a baseline,” Knupp had told Ana, “so that after you’re on CBD, you can have a baseline to look at.”

While doctors at Children’s don’t exactly want their patients on CBD, they are eager to find out what it’s doing. Knupp told Ana that doctors at the hospital now recommend all patients have both an EEG and a bloodwork exam prior to starting CBD. They would like to run follow-up tests every three or four months.

The results from the first batch of CBD kids tested made their way into a study that Knupp and two other doctors will present this week at the American Epilepsy Society conference in Seattle. Of the 58 children tested, 31 percent saw their seizures reduce by half, the study found. About 50 percent of the patients saw at least some seizure reduction.

But the results were ultimately even less conclusive.

The doctors relied on parents to report how much CBD reduced seizures. And that opened the door for the study’s two most intriguing findings.

The hospital didn’t see any improvement in the before-and-after EEGs of four kids whose seizures appeared to lessen significantly. That may have been due to something called “electroclinical dissociation,” where the seizure still occurs but its outward indicators disappear. It also might be that parents can pick up on smaller improvements than an EEG can, said Dr. Kevin Chapman, a pediatric neurologist at Children’s who was a co-author on the study.

But the study also calls into question parents’ ability to be objective. The doctors found that parents who had moved to Colorado for medical marijuana were much more likely to report that it had helped their children significantly than those who were already living in Colorado — 52 percent compared with 17 percent. In other words, the greater the leap of hope it took to try CBD, the more likely a parent was to see progress.

“We worry about all the stresses that families had to go through to start the treatment,” Chapman said. “That desire for it to be effective may cloud their recognition of seizures.”

Supporters of the CBD treatment say Children’s sample was skewed because the hospital might not be seeing the kids doing best on medical marijuana. State health officials have recommended that Children’s receive nearly $1 million in grants for further research.

Even if the treatment is successful, though, no one knows what will happen if kids who have seized their whole lives suddenly stop. Do they develop normally? Or does their underlying condition continue to inhibit their growth?

Including the new Children’s study, the nine studies or surveys looking at whether CBD controls seizures in humans form a scientific crazy quilt.

They look at different forms of epilepsy, different kinds of seizures and different measurements of success. At least five types of CBD-rich marijuana therapies are represented in the studies.

The results swing wildly: The studies show 30 percent to 80 percent of children seeing a significant seizure reduction while on CBD. And now even some doctors involved in the research question the findings.

Dr. Edward Maa, an epilepsy specialist at Denver Health Medical Center, worked with the most famous CBD provider in Colorado, the Realm of Caring, and a Colorado Springs medical marijuana doctor on a patient survey — one of the earliest studies on the efficacy of CBD in the state. The study found that nine of the 11 families surveyed saw at least a 75 percent reduction in seizures. It was an overwhelming success rate.

But now Maa wonders whether families who tried CBD with little success quit using the treatment before they could be included in the study. The Realm of Caring says only one patient had stopped using CBD at the time the survey was conducted. Maa is working on a genetic study trying to determine why some kids respond to CBD and some don’t.

“The vast majority of people, if they were going to respond, had a dramatic reduction of seizures,” Maa said. “That doesn’t represent the larger, global number of people who had exposure to it. We don’t know those true numbers yet.”

“Uncontrolled experiment”

A faint smell of cow manure wafts in the breeze as Ana pulls her minivan up to a house in eastern Boulder County.

In the five weeks since Preston left the hospital, Ana has restarted him on CBD — now shooting it efficiently into his feeding tube. Preston went the first two weeks without suffering a grand mal, but his blinky seizures remained.

“But they don’t seem to me to be as long,” Ana said.

The CBD oil she was using then was a roughly 35:1 mixture of CBD to THC. But Ana, concerned that she wasn’t using the best formulation, sought out the opinion of a Denver doctor who specializes in making medical marijuana recommendations. The doctor, Alan Shackelford, suggested Ana try a mix with more THC.

“In a way,” he told Ana, “it’s an uncontrolled experiment. Which I don’t necessarily like. But we are pressed into this circumstance.”

So Ana visited her CBD provider, who gave her oil at a 10:1 ratio of CBD to THC, and the next day she watched as her son ate better than he had in months: a plate of fried okra, a plate of potato chips smothered in barbecue sauce, a stick of string cheese, a Frosty and, most surprising of all, tuna salad with crackers.

Preston’s grandmother, Milly, thought he had the munchies.

“But you have to be careful that you’re not making things in your brain,” she said. “We’re all watching him and his behavior.”

While Preston played later in the backyard August sunshine, his eyes seemed to roar.

The toy was a Slip ‘N Slide, on which he and his sister, Sydney, were supposed to be shooting across the tarp and under an inflatable shark’s mouth that held a spraying hose. Instead, Preston grabbed the hose and became the shark.

His hunting spared no one. He drenched Milly. Sydney escaped back inside, water dripping down her hair. And Preston laughed with such big gulps of air that it sounded as if his own joy might strangle him. Until, suddenly, his laughter stopped.

Preston’s legs folded under him, and he crashed hard to the ground. Milly burst from her chair and ran over to him, reaching him in time to see his eyes roll toward his brows. And then, lying there in the grass he had soaked, Preston began to shake violently.

“It’s OK,” Milly whispered into his ear, trying to talk him out of the seizure. “It’s OK.”

Milly gathered Preston and sat him on her lap in a chair. He breathed heavily, wheezing in and huffing out. His eyes were shut.

“It’s OK,” Milly whispered again. “It’s OK.”

The shaking calmed.

“We pushed that too far, didn’t we?”

Preston’s breaths grew quieter.

“You were being a big, mean shark. It’s OK.”

His muscles relaxed.

“It was fun, though, wasn’t it, Preston?”

A roller coaster

The seizure — the second grand mal in a week — flustered Ana. And that’s why she finds herself back at the house in eastern Boulder County. Jason Cranford meets her on the porch.

Although he owns a medical marijuana store and several licensed cultivation warehouses, Cranford provides CBD to young patients out of his home under the state’s less-stringent regulations for medical marijuana caregivers. He says it keeps the cost down for patients and creates a more personal atmosphere.

After he harvests his marijuana plants, he hangs them over the arms of a weight bench in his front room, ready to be trimmed. He extracts the oil in a lab he assembled in his garage. When families arrive, his German shepherd is there to greet them.

Soon, Jason hands Ana new bottles of cannabis oil. This time, he’s giving her one bottle of high-CBD oil and another bottle containing high-THC.

Now she can make any ratio she wants, Jason says. It’s the third formulation change since Preston started the oil six weeks ago.

She asks about the amount she’s giving. “Should I up it?”

“Are you seeing any results?” Jason asks.

Ana’s reply is quiet.

“Then you need to up it,” Jason says.

In the next week, blinky seizures will overwhelm Preston each afternoon. A week after that, Ana will write on Facebook, “Preston started a new ratio oil yesterday higher THC, today only being on it for the second day we saw 70-80 percent seizure reduction. BAM. Bite that seizures. ” And then a week after that, Preston will have three grand mals in a day. A roller coaster, Ana will call it.

But for now, she walks back to her minivan and returns home to try again.

She’s learning that when it comes to Preston’s treatment, traditional medicine and marijuana have at least this much in common: There are still far more questions than answers.

John Ingold: 303-954-1068, [email protected] or twitter.com/johningold

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