My MVD so far. Performed on 10/18/16

My name is Krissie by the way :slight_smile:ļø Nice to meet you guys.

Nanooo48,
Iā€™m so glad my words and experience are helping you. Honestly, Iā€™m a little worried about you going back too if you canā€™t ease into it and itā€™s a high stress job, but hopefully if you take as much time as you can and rest enough now, youā€™ll be fine.
I never had liquid come from my ears but I was told that itā€™s normal for some Craniosachral fluid to be swishing around, sort of outside where it normally would be. At least thatā€™s what I understood from what my NSā€™s nurse said after the surgery and from my continued (but diminishing in frequency and intensity) experience of hearing a pounding that is similar to how it would sound if I had water caught deep in that ear and I was hearing my heartbeat. It was far worse right after the surgery and will show up even now if I overdo it, and/or have a lot of pain on my left side (side which did not receive the MVD), or sometimes just randomly. The weird thing for me is that I never heard the pounding in the right ear (side which did receive the MVD). Iā€™m really glad you went to the ER and am sadly not surprised that they treated it like nothing; Iā€™m sure making you feel invalidated and possibly like you shouldnā€™t have gone. Such a******s sometimes. Hello people! Someoneā€™s just been working on my brain; loss of hearing can be a side effect of this procedure, and now I have FLUID coming out of that ear! Could you please show a little concern or at least some compassion? :wink: Oy.

Oh, I also think I know what you mean about your brain feeling tight. First of all, after the surgery I could tell someone had been messing with my brain. I could physically feel my brain it seemed. I didnā€™t express it as, ā€œtight,ā€ per se, but in retrospect that term wouldā€™ve been just as accurate as any I was using to try to explain it to my (ex) boyfriend and sister. Now, my scar will feel tight as well sometimes too.

Nanooo, Iā€™m worried about your work. On the other hand, I have to remember that I was, and am, still dealing with daily ATN on my left side, in addition to the surgical after affects, and of course, individuals are different. I ended up quitting my more stressful job because I simply couldnā€™t concentrate or focus like I could pre-op, nor did I have the energy I had. The energy really started coming back for me at about the 6 month mark, but Itā€™s only now, almost exactly 1 year later that I feel more able to focus and to concentrate for longer periods of time again. My memory is alsoā€¦different. I had to write things down before but theyā€™d mostly stay in my head too. Now, I absolutely have to write things down. I guess my main message here is to be ready for some things to be different for you, possibly for longer than you expected. Then, if theyā€™re not, great! If they are, youā€™ll know itā€™s normal and for how long you might have to deal with whatever side effect. I wish someone had let me know.
Nanooo, I wish you the best of luck with everything in your recovery. Iā€™m happy to be the reassuring voice that you need to hear. We all need that, whether weā€™re on this site or not, but ESPECIALLY if weā€™re on this site. :wink: Iā€™m happy to answer any questions, based on my own experience, as you continue to heal. Good luck! You sound great!

:sunrise_over_mountains: Christy

PS Krissie, I just saw your name! Nice to meet you! You too Liligirl!!
Also, omg, the clicking. I totally forgot about the clicking! It was the strangest sensation because Iā€™d hear it and then kinda feel it coming through my nose. I have awesome sinuses and it felt like it was air bubbles around my brain that escaped through my nose! I donā€™t know. Iā€™m sure itā€™s a little different for everyone whoā€™s had this, but itā€™s like nothing you can explain to anyone who hasnā€™t! :slight_smile: