Had my twelfth ECT yday. Doc said sometimes the effects come on over time .... 🤔 and she wants me to come weekly. I dunno that I feel any different, if anything I fell into deep depressions after treatments. Also the ketamine has made my head feel funny, even today.
ECT : Had my twelfth ECT yday. Doc said... - Anxiety and Depre...
ECT
You should trust your doctor .
A I was hoping you'd feel a difference. May I ask, have you seen maybe just a hint of relief after the depression lifts between the treatments. Or has the depression gotten worse and does not lift? Where do you think your at compared to what you and the doctor discussed prior to beginning ect.?
Discuss your concerns with the dr and take someone with you that could help with the concerns if you haven't already. A second opinion?
No need to answer unless you care to and I apologize for putting a lot of questions out there. I know I find it hard to think thru things and by no means do I want to cause you more stress.
My questions are just food for thought.
Big hugs for you!
nicetry, with your doctor wanting to see you every week, is that
for ECT or therapy? xx
For ECT & ketamine.
nicetry, that's true in that it can take time before it starts to turn
things around. Others will probably notice before you do.
My best to you with your treatment. xx
Thank you Agora1. I have a treatment tomorrow morning & am DREADING it but trying my best to understand that to reach the truly positive outcome I must work through the not-so-positives.
Tell your doctor about this stuff and if they keep pushing you to do this then find a diffrent one. This doctor sounds like they don't have your best intrest in mind.
I want to hear more about the ketamine therapy. Makes your head feel funny? Pass it over here! Sounds like a party to me. I'd tell doc no more ECT if you're not feeling it. That can permanently mess you up.
It’s a really strange feeling. I don’t happen to like it — gives me a headache — but some people do.
I had ECT and ketamine injections as well. I had a series of ECT and didn’t feel any improvement. They pushed for me to continue the ECT as well (once a week for 4 months then once a month for maintenance) but I opted to discontinue. I don’t regret it because I honestly did not feel any difference. The ketamine injections didn’t work either unfortunately. I’m back to different med trials.
Unfortunately we can not trust everybody. Maybe your doc does have your best interests at heart but if I were you, I’d get a second opinion. I would also do some more research on ECT myself.
Give yourself some time to think and make a decision re her recommendation and time to evaluate how much it has helped you thus far. What’s the rush ? Doesn’t it often take time to feel the benefit of ECT ? I really do not know much about the subject.
Look out for yourself if you possibly can. Be informed. It will be worth it and you will gain confidence in making decisions along with your doc to take care of yourself in the future.
Good luck.
Thinking about you!!
I think following the treatment regimen as prescribed is standard protocol. How many ketamine injections have you gotten? I got 8 and supposedly if you are going to respond positively then you will see it by the 4th treatment. It’s sooooo frustrating....waiting and trying different treatment approaches. Keep me posted on how you are doing.
My experience with ECT was not great, lost short term memory, IQ dropped by more than 20 points. I would not recommend it to anybody. I would try everything else, but I see you have had 12 treatments. Trans Cranial Magnetic Stimulation is fairly new, and there is also the fisher wallace machine. With TMS, they take a scan and can see what part of the brain is not working, up to par. Look up TMS, before and after images on google. I hope this helps, and good luck.
Heyyyy how's the ECT going??
Well I’ve had 12 sessions, 10 of them with ketamine added. I feel very strange. Not certain it’s doing anything but my husband says I’m different.
ECT is an extremely difficult procedure to go through, in so many different ways. The fact that you have been going to every treatment, and to the TMS treatments before that, goes to show how strong and determined you are. Its so easy to throw up your hands and give in to the illness. But it sounds like you are willing to do whatever it takes to get better and you should be proud of yourself for that. Keep it up and give that wonderful husband of yours a big hug!
Thanks. This is just what I needed at this moment — for some reason I fell into a panic attack about 10 mins ago, crying and crying and crying ... anxious about tomorrow’s treatment & just wanting it to be over. I feel really tired and drained.