CARRIEANNE-here's my story:
I had RNY 4/02. I've had "headaches" since I was a teenager (stoneage), but got worse a couple of years post op...got prevention meds...headache control somewhat better...no adverse reactions...was poorly controlled Diabetic..off Insulin by 10 months post op, then off all Diabetes meds by 12 months..blood sugar readings have remained within normal limits...
Fast forward...
July, 2011...headaches more frequent...having periods of 'brain farts"..would lose little periods of time...5-10 minutes...would be somewhere I didn't recall going to..I blamed it on stress and being almost 54..then one morning, at work, I had rambling speech/crawling on the floor/and alot of other stuff. Lucky, for me, I'm a nurse, and work with very smart nurses, who got me to the hospital. All I remember is having a really bad headache and going to work. I have NO recall of the whole rest of that day/the ER/all the tests/nuthin'. From reading the hospital records I HAD to be talking SOME sense, because they had "history" that they could not have known unless I was the one to tell them. I was in the hospital 4 days-still with headache-had every neuro/cardiac/Diabetic/etc test known to modern medicine... Results? Nadda...Nuthin'..Even had GI doc in and EGD, since I'd not had one since the day after my RNY-all my guts still intact...good to know...but still was having brain farts...
Present day: now, 7 months later I am seeing a very "seasoned" Neurologist who was "intrigued" by me, so he started a research study with me and some other people with similar stories. Due to our continued negative neuro tests, he has us now checking our blood sugars when we get the smallest feeling of "just not right". You may have been hearing alot about "reactive hypogycemia"--if not-google it-it sure can mimic seizures
For ME: My co-workers still see me "check out" occasionally, but it's only moments at a time, and I haven't crawled under my desk anymore. I am taking 2 low dose "anti-seizure" meds, but they have secondary usage as migraine meds, so guess it's a win-win.
My doctors did not give me a "seizure disorder" diagnosis, due to all the negative EEGs, CT scans, etc, even though the probable seizure activity was noted at work/then in the hospital/etc, so it's not a "label" on my insurance/medical file yet. I am happy to be taking part in a study that will help not only me, but others-like you
There's SO much still to be learned about "afterlife" of RNY...I think we're still just screatching the surface. I'm one of those peeps who has always been diligent about vitamins/labs/etc...so...you just never know...
But...I'd still do it..WLS..every year, if I had to !!