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Hello, my name is Christine. I wanted to join a forum because even though my seizures are controlled now, I have so much anxiety about it. I started having tonic clinic seizures when I was 7 years old, I'm 25 now. I take lamotrigine and recently started increasing the dosage because I started feeling like I was going to have one way more often. I have a great neurologist and she always listens when I tell her how I feel. Something really cool happened recently that kind of changed how I think about my brain and seizures. There's a science show called breakthrough and they had an episode about the brain. They had a graphic of what happens in the brain during a seizure. The visual has really helped me understand what's going on in there. My triggers are not eating combined with photosensitivity (at least that's the usual pattern). I look forward to meeting everyone and sharing experiences!
 
Welcome Christine,

We are glad to have you here. This forum was made by Bernard out of love for his wife Stacy. That love permeates throughout the whole forum.

I am on Lamotrigine too. I take only 200 mg a day.
 
Thanks for the response Ruth. I am slowly working up to 150 twice a day. Since starting the increase I've been feeling kind of moody and a little sad. I hope it levels out at some point.
 
Hi Christine,

Tell your doctor your side effects and any seizures that you are having.
 
Hi

My name is Gilles.

My question that I always had is what does is normal? I am on 150mg of lamontrigine twice a day.
 
Hi Giles,

I am on 200 mg of Lamotrigine. I do not think that there is a normal dosage. It is different for each individual.
 
Welcome Christine and Gilles!
This forum is wonderful, full of great info, support and awesome people!
I also lamotrigine 100 mg twice a day along with Keppra XR.

Cindy
 
Cindy
Do you have any side effects from the lamotrigine?

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For me, I think the mood stabilizer in it will keep me in a good mood or a bad mood for a while. I also think I'm having some hair loss but I haven't talked to the neurologist about it yet. I go back soon though. When I was on keppra, I thought I was losing my mind lol. Other than that I don't have side effects from lamotrigine.
 
Hi gnault and Christine, welcome to you both.

There's no standard dose for Lamotrigine, just a suggested range. Some folks will fall on either side of that range. Individual reaction in terms of side effects can vary quite a bit. In many cases, side effects lessen or go away after the brain adjusts to the med. (That's been my experience). For others, the side effects can be problematic.

Lots of good discussions and feedback can be found at the links below (which will take you to threads that discuss Lamictal/Lamotrigine):
http://www.coping-with-epilepsy.com/forums/tags/lamotrigine.html
http://www.coping-with-epilepsy.com/forums/tags/lamictal.html
 
Hi gnault,

Sorry it's taken so long to answer.

The lamotrigine actually made me feel better and more alert. Vimpat and KeppraXR made me feel foggy and tired and very uncoordinated. I'm now on lamotrigine and Keppra.

The only side effects of lamotrigine is insomnia and a low dose of trazodone before bed has taken care of that. I'm also experiencing hair loss (yikes) but it could be from Keppra. There's no way to know. I'm going to see my dermatologist next week to see if there's an organic reason for the hair situation.

Cindy
 
Welcome I'm glad to see that someone has been able to control their seizures, I've about given up hope of controlling mine.
 
Christine,
I didn't realize that there was a mood stabilizer in the Lamotrigine. I don't think that I necessarily have a sense of indifference, but I seem to have a sense of quietness in most situations. It at times seems hard to fully connect certain situations. It is a bit hard to describe. Many different side effects, issues that you don't realize or understand until you exchange information or stories with others in a place like this.
 
Hi Christine, welcome :)
I take Lamotrogine too, along with topirimate and occasionally clobazam.
I also have been taking Charlottes Web cbd oil for a month now.
I started having seizures when I was 15 and they have never been controlled, I am 22 now.
The medication stops them hurting so much and cut them down from everyday to every few days, but has never stopped them completely.

Great to meet you :) welcome

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Hi Zara,

I have not been around the rooms for awhile. Yet, I have found great efficacy with CBD and the other non-psych-active, THCA...not to be confused with THC. This reply will be lengthy, yet it addresses some issues I'm aware of in the drug profile you described.

I have juvenile myoclonic epilepsy. Yet, before all this, my conventional drug beforehand was Depakote. It gave me full efficacy for many years until major side effects forced me to go off and onto Zonisimide. That brought back a small amount of the myoclonis that had been gone completely along with my tonic clonic.

The drug titration off of Depakote and onto Zonisimide was no picnic. I had a choice of other drugs since the Zonisimide was not working as well as expected. However, I was not feeling the love after what I endured. Perhaps much had to do with the research I was doing into GW Pharmaceutical's CBD formulation, Epidiolex. This is what Realm of Caring and all the other CBD vendors researched and modeled their platforms on. Plants with a high yielding CBD like AC/DC, grown organically or veganically are much better for seizure control. Although, CBD is not the only cannabinoid with efficacy. THCA is much cheaper and it is top notch for some. Still, your CW is a very potent and successful CBD cannabinoid.

Living in a MM state, I was doing my best back then to track down CBD rich plants. This was long before Sanjay Gupta's Weed episodes. But what I found out while doing this was more important than CBD. And, this is the point I wanted to bring to your attention. You mentioned using Clobazam, ONFI. If you use any benzodiazapine for seizure control, you risk building tolerance, dependency and greater seizure issues and a myriad of other symptoms which may develop when choosing to go off of the benzo. Many of the CBD children living in the MM states with intractable seizures are having to wean off of their benzo drugs before they can realize the true effectiveness. Klonopin (Clonazepam) and ONFI (Clobazam) are two of the common benzo's they are on. This reaction of going of of either is one that has to take its course and can take months, even years before the Central Nervous System calms back down. I know this for myself.

Back in 2011 while trying to track down a reliable source of CBD to control my myoclonic head shakes - which some higher strains were doing - I ended up going onto Klonopin after having a huge 35 minute myo episode one night. My brain was almost like gel. There was no such thing as a regular supply of CBD back then. Very rare to find a high strain in those days. At the time, I had not been doing CBD for practically 3 weeks.

The episode was so bad I could not get hardly any sleep without shaking as soon as I closed my eyes. The second night I had another episode. All I knew is that I needed something to calm my brain or another huge episode would hit and it felt surely as if it would go tonic clonic and I might not come out. I called the doctor and it resulted in a klonopin scrip. It worked great, calming all these shaking nerves. From then on I took it "As Needed". Yet, I knew something was not right as not all neurologists were on-board with prescribing k for seizures. Took it occasionally for about 1-1/2 years. It set me up for what was to become the worst experience of my life. And, I only was taking it about once a month....and then it changed to maybe every two weeks or so...then finally to every week.

Everything was starting to feel weirder and my myoclonis was getting stranger in its activity. Felt like I needed Klonopin much more frequently during stress times which I normally would not require. Slowly these changes were taking place. I was scared as I watched myself act differently and get myo attacks more frequently. Enough was enough and I went for the Hail Mary play and hurriedly rustled up a one day commitment to quit cold turkey.

This cold turkey move was the biggest mistake, and I only did so since I was not using daily. Benzos are insidious and there is more power in those tiny pills than anyone could ever imagine. But I used cannabis flowers as my rescue and hoped for the best. And, at about 9 months after, I recognized the first big sign of relief that it was all coming very close to an end. I came out of this, but it was the slowest process and at times did not seem like it would ever end. This is a normal feeling for many sufferers. And, just after a year of going off, the majority of myoclonis and symptoms were practically all gone. Slight bit of anxiety left, yet compared to the hell I lived in, this tiny aspect deserves hardly any mention. It took months, but for a cold turkey, this was impressive...especially for an epileptic.

Most people who go off benzos do it the wise way - they taper off of them. Otherwise, you can die attempting to go off cold turkey.

I am just over a year off the k and life with a CBD/THCA protocol is unbelievable. The efficacy is stable and efficient when benzos were not in my body. Taking a benzo occasionally is almost as bad as taking them daily. It creates what is called "inter-dosing". And, being on any dose of benzo's causes you to build tolerance, unlike most of the other seizure drugs. The paradoxical effects of coming off the cold turkey for me was just plain wicked for many months.

Lucky I had cannabis protocols to save my ass and calm it down. After tapering off a benzo, you can also risk "kindling" if you go back on the benzo to rescue. It's a very difficult drug to get off of safely. Cannabis did not interfere with my healing as it does not have an affinity for your GABA receptors.

Benzos do serve a purpose for short term like issues like surgery and life threatening one-time seizure use - but long term seizure control has negative consequences when using over time. Although the pharmaceutical companies do see a more important economic need to continue getting patients on them for sleep, anxiety, restless leg syndrome...and the list goes on. It's a $80 billion dollar industry. Going off benzos means you may have to contend with symptoms which worsen to sometimes unbearable levels while in withdrawal.

Also, when using CBD, one must observe the CYP-450 Cytochrome potential for drug interactions. The CYP interference can have reactions when you metabolize certain drug combos. CBD does inhibit the class of benzodiazapines and its inducing ability, just like grapefruit. It can potentiate the benzo's actions. Ask your doctor to learn more about all of this.

Wish you the all the best in your journey and hope you can find the relief you need and deserve.

Check out the following links for more info:

The Ashton Manual - The Gold Standard for Withdrawing from Benzodiazapines

http://www.benzo.org.uk/manual/

History of Benzodiazepines: What the Textbooks May Not Tell You
http://www.psychmedaware.org/HistoryBenzodiazepines.html

Recovery and Tolerance - https://www.facebook.com/notes/benz...ce-and-dependency-definitions/958439544237472


Tips to Finding a Doctor to Assist you With a Taper/How to Talk to Your Doctor
https://www.facebook.com/notes/benz...ses-of-tapering-off-of-benzos/716838248397604

BenzoBuddies Online Forum

www.benzobuddies.org

Beyond Meds - Start Slow Taper Plan

http://beyondmeds.com/2013/09/18/listen-to-your-body-taper-plan/
 
Hello Christine how are you ? It is so nice to meet you . I have had episepsy since I was in Jr. High School . Boxing was the cause of it . My seizures are very well controlled Thank GOD but I only wish my Meds had Zero side effects . You mentioned Photosensitivity, I have to always were Polorized glasses if I am in a store . But other than that I am doing good .
 
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