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#1 | |||
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In Remembrance
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(((((Janet))))), what an airhead nimrod of a Neuro, you have..
![]() glad your Niece was there at the right time to be of help to you. I don't suppose Vegas is the place for top notch Docs, unless they're retired.. ![]() I hear you and you have every right to complain. I will pray that things ease up for you soon. You deserve a break!! Feel better soon.. ![]()
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~Love, Sally . "The best way out is always through". Robert Frost ~If The World Didn't Suck, We Would All Fall Off~ |
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#2 | |||
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Wisest Elder Ever
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I had to stop driving a few years ago.....but I did it on my own. Nobody told me or made me stop. In fact, I still have my driver's license but just keep it for identification purposes.
It's hard to stop driving. It was definitely an adjustment for me. But, my income has more than been cut in half so not having to make a car payment or insurance payment is really the only way I can make it through a month. The doctor should have told you that she contacted the DMV. That's just common courtesy. Sorry you had to find out the way you did.
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These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
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#3 | |||
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Wise Elder
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I'm so sorry this is happening to you.
![]() Did you actually see the neuro at all or was everything done over the phone? IMHO, they should have done some testing such and an EEG to make sure that it was truly a seizure and not something else. Granted, from your description it sounds as if it may have been but still.... And, she contacted the DMV without concrete proof (such as an EEG) that you even had a seizure. Nor did she investigate the reasoning behind it, such as what you mentioned - medication interactions. She didn't discuss contacting the DMV with you and by that she has impacted your quality of life. I think finding a new neuro may be a good idea if you are able to do so. I have had absence seizures before and the neuro didn't contact DMV. I was told to avoid driving for 6 months to make sure no more seizure activity occurred. If it did, then they would have to contact the DMV. I guess I was lucky that they didn't contact them. I am glad your niece happened to come by and help you. I hope you start feeling better soon. Let us know the results of your CT scan and how you are doing. ![]() |
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#4 | |||
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Senior Member
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I'm sorry all this happened to you, Janet. Hope you get to feeling better soon.
![]() So, all these medical professionals are taking you at your word that you had a seizure and a concussion? That seems odd. And wrong. Is it standard procedure for people who have experienced a seizure, or simply said they did, to be reported to the DMV? ![]()
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RRMS, diagnosed '00 Everything will be alright in the end. If it's not alright, it's not yet the end. |
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#5 | |||
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Grand Magnate
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i'm sorry you're going thru all this.
your "neuro" should have done some tests to substantiate that you really did have a seizure, and didn't have a head injury. maybe and eeg or something. use the ensuing time just to get her release for the dmv. then dump her. she's awful. and, please go to the er if anything like that happens to you again. please stay with us and keep us posted on how you are. we're here for you.
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Judy trying to be New Skinny Butt ______________________ You are a child of the universe, no less than the trees and the stars; you have a right to be here. And whether or not it is clear to you, no doubt the universe is unfolding as it should. -------------------------------------- "DESIDERATA" by Max Ehrmann |
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#6 | ||
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Junior Member
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Thank you for your kind words and concern. It means so much. Im sure she did it to cover her self. No tests, exam, scans, just report. By the time I saw her I was fine (still a bit hyper/anxious but much better when I saw her). Her parting words to me when I finally saw her were "you have bigger problems than MS"....and that was the END of the appt. I have an appointment with a neuro/psych tomorrow. Lets see what he says. All I know is that I've been there for mri's, and seen dr a couple of times and they have not really told me anything. a couple lesions on brain, a couple on spine, old lesions, bla bla. But nothing except "here try this pill". I really had high hopes that this dr would work out. But you are right, I will just do the best I can the next 3 mos and move on. Thanks so much for your concern and support. |
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#7 | |||
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Wise Elder
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Quote:
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Also, telling you that you have bigger problems than MS and just leaving you hanging like that was very unkind and somewhat harmful to your emotional state. I'd be asking her what she meant by that. I'm so, so sorry you are being treated this way. It makes me upset to hear about the medical professionals treating patients this way. I am sure that if you called the DMV and stated that you don't know if you have a seizure and that the dr just made an assumption that you did without further testing, maybe they'll work with you or something. And, maybe, like Judy mentioned, once the 3 months is up you can find a new physician that will treat you much better. Hang in there! I'm hoping and praying that all works out well for you. ![]() ![]() |
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#8 | ||
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Junior Member
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hi everyone
well, I did finally get a CT scan of my head....its normal. So it must've been a contradiction between the wellbutrin and my heart meds, specifically the arrhythmia drugs. I had a fainting/syncope type incident when I mixed Cymbalta with the heart drugs. Anyway, first wellbutrin. disaster. then keppra. bigger disaster (manic like I have never experienced in my life. I was off the charts. Never have I experienced anything like that in my life). Off keppra. Then on lamictal. 2 weeks of a very low dose (25 mg) and I was more depressed ..... I was in a very deep very dark very dangerous hole. My only saving grace was that I knew it was because of the med interaction. So I'm going to "just say no" to any more antidepressants. They contradict with my heart meds. Maybe not everyone has that happen, but I did. So I'm don't with that crap. I will deal with my chronic low grade depression (dr thinks I'm BPII because my mood swing goes from depressed to less depressed). Neuro was also unhappy that I refused tacfidera. I have pos JC virus and a 40% chance of a brain infection didn't seem like a good bet to me. She said well if you have a lot of bad luck maybe. (apparently she didn't read my file and the history etc.). Anyway, just thought I would catch you up. Thanks so very much for you caring and support ... this has been an awful experience. And now looking for a new neuro. Or, no neuro. Honestly, I was managing my MS and other issues better with just a visit with primary dr. But I made myself go. I hadn't seen a neuro in over 5 years and some things were progressing (eyes, legs, etc.) but nothing is worth the hell I went through this last month. janet |
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#9 | ||
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Junior Member
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Thanks for your questions and concern. |
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#10 | ||
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Junior Member
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It is what it is at this point I guess I just have to accept it and wait it out. Then, 3 mos and I'm done with Lou Ruvo Center |
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"Thanks for this!" says: | Kitty (12-02-2013) |
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