Does anyone find the repeat the same sentence more than once or/and fine themselves talking to themselves.
Ive been having that pins and needles feeling in my hands and feet, mostly my left hand, and i dont know why.
I was under the impression you could not realistically quantify brain damage in a tangible way, especially with epilepsy ?
anyone neurologist explain seizure brain damage ?
I have percieved notions of seizures causing brain damage : urinary incontinence , drooling sometimes , asperating my own spittle ,vomiting at wired times and bloody noses rare but super bad bad
idk if that is from seizures or brain damage from uncontrolled seizures
I was wondering in regards for myself , as I have uncontrolled… read more
Is this epileptogenic dysfunction only something that happens to uncontrolled (intractable ) and/ or ( pseudointractable ) seizure disorders, epilepsies . if it is truly epileptic in nature ?
I have a high metabolism and intense seizures. Downside I live off basically fat, proteins, carbs, sugars and dairy this is due to the caloric intake seems to be what my body needs. I haven't gained weight since high school. I don't seem to gain anything even though what I eat is basically I eat all the stuff people shouldn't and never gain. I also have a high metabolism that probably is needed to ensure this but am I eating what my body truly… read more
My nan and myself both have nocturnal epilepsy. I got diagnoised at 11 and nan at around 80. Im starting to believe my cousin now has it too. Shes 19, she collapsed and her hands were shaking also got a friction burn on her face. She went through a phase of collapsing a few years back and drs said just low blood pressure. However she used to sleep walk like i did but after i would have a seizure (from what were aware of she didnt)… read more
Been on a roller coaster ride diagnosed with epilepsy nov2 this year medication overload trying to balance out. Just want to know how many different meds did you all try and how quick before the correct one and dosage. The second part is how much dose stress and anxiety effect the meds
My sense of smell returned about the same time as I got Epilepsy ( I hadn't had a sense of smell for 20 years). Just curious if anyone else has had a similar experience?
(And I wish people would go easy on perfume/cologne haha)