I have question whether epileptic attacks do occur frequently with CBD.
My wife has CBD since 2017 and as husband I take care of her since then. Just last week she experienced something that looked like an epileptic attack that took about 3 minutes. Thereafter she just want to sleep and that still after a week.
We see a neurologist and have anti epileptic prescibed.
I want to know whether these kind of attacks are common with CBD and what trigger may cause this.
Written by
Tindb
To view profiles and participate in discussions please or .
Hi my husband had epileptic seizures, but he had PSP, he used to have them about once or twice a month, one time he had 7 siezures in one day. He would sleep a lot afterwards and be very vacant aswell.
The doctors never prescribed him any medication for it as it was not regular enough, but they did last for about 3 minutes and then his breathing was affected for about 30 minutes afterwards.
I don’t think siezures are very common with either PSP or CBD as when he started having them I asked on this forum and there wasn’t anybody going thru the same.
Hi my husband had CBD and suffered epileptic seizures lasting a long time and each time ending up in hospital medication helped for a while but in the end They could not control the seizures and was put on palliative care and sadly passed away But everyone is different and as your wife’s only last a short while will be better controlled with meds
my Mum had CBD and started having seizures in her last 2 years. I can't say what the triggers were as Mum was in hospital when they first started but they weren't that frequent and didn't seem to bother her too much other than, similar to your wife, she would be very tired for a few days after. Unfortunately, it does seem to be another symptom of this disease.
My husband had CBD and sadly he had seizures during the last 18 months of his life. They didn’t appear to upset him too much and he was prescribed a sedative. The only issue was trying to keep him safe. He was in a hospital bed luckily by this time so couldn’t fall out as they often happened in the evening. . I think it may just be the progression of the disease. I wish you all the best. xx
I have PSP. I do have a form of Epilepsy that is brought on by stress but haven't had an episode in decades (early 1980's). However, since PSP I have developed what my Movement Disorder Neurologist calls Myoclonic Jerks over my entire body. I don't have them longer than a minute and was having them 3 or more times a day. I'm now under a medication that can treat epilepsy and it has my Myoclonic Jerks down to about 2 a month.
Can I ask what medication you are on, because while I do not have PSP, I personally have epilepsy and any medication I have ever taken only stops the major seizures, but have never done anything for the jerks. I also involuntarily scream - its rare, but it does occur say on a bi-monthly basis and more when stressed.
Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.
Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.