Community Forum Archive

The Epilepsy Community Forums are closed, and the information is archived. The content in this section may not be current or apply to all situations. In addition, forum questions and responses include information and content that has been generated by epilepsy community members. This content is not moderated. The information on these pages should not be substituted for medical advice from a healthcare provider. Experiences with epilepsy can vary greatly on an individual basis. Please contact your doctor or medical team if you have any questions about your situation. For more information, learn about epilepsy or visit our resources section.

emergency room care for seizures

Thu, 03/01/2007 - 02:04
"I'm mad as hell and I'm not going to take it anymore..." I dont have a clue if my experiences are similar to anyone else's, anyone else at all, in my region, in my state, in the USA, in the world, etc. I think it would be a good idea if I found out. I know for sure that I have been incompetently treated in the emergency room when in for seizures. I really think its mostly a matter of the nursing staff not having a clue what to do. Seizures are scary for those who have them, but perhaps more so for those who have no idea what its like and how it works. I sympathize, however, these people are supposed to be PROFESSIONAL CAREGIVERS. My complaints are as follows, just from my visit today: 1. I was beginning to seize and they asked me to sign a form. The effort to try and sign the form brought on the full blown seizure. And my signature ended up taking up the whole page. Totally unuseable. 2. I was in the midst of a full blown seizure and they were asking me to do things like move my arm over here, etc. 3. They hauled me out of the wheel chair during my seizure and then screamed at me "You're too heavy! You are going to hurt somebody!" when I couldnt walk to the stretcher. 4. At no time did anyone even after the seizure and everything had calmed down did they show me where the call button was. I held my urine for over an hour waiting to ask someone to go (in case they needed a urine sample), ended up ripping electrodes off myself so I could get up and go to the nurses' station to ask. The nurse said yes. Within 1/2 an hour a nurse came and told me they needed a urine sample. I told her about having already gone and that I had no call button. She said that a urine sample was what the doctor had been waiting for, and this was the same nurse who told me I could go before. I told her I had no call button. She hauled one out from behind some drawers and wires and left without a word. 5. People turned on and off my light without saying a word to me. 6. When they were taking me to get a CT scan the nurses talked to each other as if I wasnt there...the only thing they said to me was, as if I was 2 years old, "the doctor wants to look at your head now" as her way of informing me we arrived at the radiology department. 7. Four times I requested my family to be with me, to which they said that they were going out to tell them come in. The nurses never approached my family, even though they were in the waiting room. The time my Mom asked to see me, they claimed that the doc didnt want me to have any extra stimulis. The only way I got my Mom in was to catch someone coming in the door visiting someone else. 8. When I get myself up to go to the bathroom, my bed tipped at the end I got up from because the side bars were up and had been up for 3 hours even though I had not had any seizure activity during those three hours, and I could not put them down. I believe thats actually considered an illegal restraint. I understand the necessity of ascertaining whats happening with the physicality of the person having a seizure, but moving and asking them to walk themselves I think is a gross misunderstanding of whats going on with someone having a seizure. I think a little respect for an epileptic's dignity and humanity is also a necessary improvement. I would like to know if others have similar experiences or tips on re-educating hospital care staff, to facilitate activism to remedy this problem.

Comments

Re: emergency room care for seizures

Submitted by gwen48 on Sat, 2007-03-03 - 11:21
beaconeer: emergency rooms are overflowing these days, too many patients, not enough help. Your family needs to go back with you when you are there, be more dependent on a family member to be your "spokesperson" than the staff. EXAMPLE; "hey I got a urine sample here for you nurse". You get the idea. Here in the U.S., emergency rooms are adequate at best, and have become a doctors office for our "visitors" from other countries. This has caused a tremendous strain on hospitals. So, it is not a matter of educating the staff, they already know. The individualized care has suffered due to understaffed, over worked hospital employees. Hope this helps - Gwen

Sign Up for Emails

Stay up to date with the latest epilepsy news, stories from the community, and more.