![]() |
Quote:
Different kinds? I know it can be caused by different things (MS, Devics, some think it can be a prelude to MS..). You'll find out more when he looks at the test results and (hopefully) calls you back. |
Quote:
BTDT (been there done that, wore out the T shirt). I got to the point that when I finally found docs who listened, believed, tried to help, I cried real tears all the way home - was it all a dream? Was I gonna wake up and then have the real appt of disappointment? hmmm. And after all that, I will not read the erroneous scribblings about me - what do I care? I treat all that like those sorry movie reviews, as if I were an arrogant actor. It's what the fans think, not the critics, It's what the tests say, not the idiot docs who think it's all in my head and I'm some desperate housewife. I was never that girl. Either you want to be my doc and help me or you can get out of the way. Next? And I agree - quality, not quantity. My great gran lived to be 94. A good 94, and died in her sleep. She was a fiest old broad in every sense. If I could do as well, that would be fine. But 50 more years like me? Um, no thanks. |
Quote:
I hope you have an amazing time! :) What the docs do not get is that all we want is to get back to our lives. We all have better things to do than look at their mugs. and better things to spend our money on than meds, tests and their boats. We really are still living in the dark ages where diagnostics are concerned. What I would do, if I were Bill Gates rich, is set up a clinic where NO one goes home without an answer. How cool would that be? :cool: |
MomX7 - glad you finally got to the eye doc. I guess he should know, but I never heard that before, more than one kind of ON.
:confused: I hope you get more info on that so you can share and we all can learn a thing or two. I also hope he can help you out with that - eyes are one of the most important things, I hate to think of you dealing with that. How are all those munchkins? Better I hope? Sarah - most of the 1,000's of people I've*met* on these forums - like you - are pretty good at saying their sx, tests and results etc and comparing with others. and you get a real good idea of if one disorded fits you or not, or if somebody else fits your disorder. Docs may not get that, but we know how it works. It's the only way I can tell where my sx are coming from, and what is not coming from my neck. The sx are so much alike form so many things. It's so frustrating when YOU know and the docs will not listen. Hey, if they are right, then why do none of them agree? Which one is right? That's WHY we have to figure it out. They told me I have ms, then no I don't yes I do, no I don't yes I do... I hate it. They act like I am the crazy one, where did I get the idea I have ms... maybe from them telling me I do? LOL. Why can't they make up their minds, tell me what it IS and stick with that? |
thanks Brain, I am having a awful morning of sxs....snowing pretty out there..but the humidity kills me....:(
I do have a new pcp, that seems to listen like my last pcp that I LOVED>..and miss, she moved away....but this one too listens...and think she believes me persay..hehehee anyhow, gotta run get ready for the day..hugsss,sarah:D |
Oh man, I just remember the eye is closed on Thursday so I guess I want be hearing from them today. I hate waiting SO much. :thud:
|
Quote:
Thanks for the commiseration and the good example! :) I LOVE the "sorry movie reviews" comparison!! Nancy |
I feel for all of you in limboland...
Hi everyone...
I just want to say that I feel for all of you in limboland.... After reading some of your experiences, I can feel your pain (and disgust) at what some of you have been put thru for years....and I've heard similar stories of people who have thru that only to have gone from possible to probable to confirmed MS dx. I am not sure if I should be thankful that my MS came with a bright neon flashing sign that said "MS here: Vacancy" (I guess the big black holes left lots of room for visitors?!) - I never had problems until December 22....and of course with the holidays and all...didn't make it to a doctor until Jan 2 (at which point I went to see a dental specialist b/c I was certain it was my TMJ acting up - as the right side of my face was numb) - and he said go to a neuro...so on Jan 4 I went to neuro, who immediately sent me for an MRI...it was a Fri - and when I left his office to go get the MRI - I told him if he left for the weekend without calling me to let me know what was going on, I'd hunt him down...well, I'm not sure if I regret telling him that or not...because when he called on that Friday afternoon to say, "You have MS" - it kinda blew me out of the water. I had no idea. I thought I had a pinched nerve in my face! My life has been pretty intense for the last 6 weeks - sheesh, I can't believe it's only been 6 weeks :( my life has been pretty rotten. Part of me wishes I was in limbo land - b/c then I could just be in the pain I'm in (pretty bad exacerbation right now) - but with my head in the sand and not having to deal with treatment, etc. Switching from copaxone to tysabri right now. Anyhow - point of this was to wish you luck - b/c I personally believe in importance of treatment....so I wish you all well... ~Keri |
Nancy T, I would be so fried if I were you, particularily about the insurance and hearing device surgery.
You might not want to talk about the procedure, or the type of hearing loss, but if you're up to it, could you post a link? To know there is something tangible, something that works, something almost within reach that is not subject to the maybes and I don't think sos of medical subjectivity, and to then have it snatched away....:( :hug: tante |
Might Have An Answer!!
Hey folks, a WARM and melting-snow-SPRING LIKE kind of welcome!!!
I saw my "other neuro" yesterday. THe one who I saw incase I was having seizures. He's a sleep specialist and conducted a sleep study with me. I DO Have sleep apnea and my oxygen levels keep dropping all night. i am going back to have a 2nd study to determine what level of Cpap? I need. He thinks this may be the source of why I have so many problems, incuding uncontrolled BP/HR. and get this NARCOPLESY with catyplexy or sleep paralysis. I dont have the typical drop down kind of narcorlepsy but have sudden weakness, "altered consciousness" where it looks like I am unconscious or going "out" gradually. I then cannot comprenhend cognitively and eventually cannot move my body or talk at all !! I lOOK unconscious. THis had ended in several ER visits over 10 years and many inpt stays. I present like a TIA as one side is weaker or I cannot walk, as I loose my balance. An MS MIMIC? hmmm.. no one knows. AND its not completely ruled out. Told him I still have buzzing tho my balance and cog problems have improved with nutrition. Any way it will be nice in a month or so, to finally get enough oxygen while I am sleeping!! And not to be so tired during the day. MANY MANY have sleep apnea and it goes untreated. OH, he thinks my head shaking while I sleep (it wakes me up) is essential tremors, not related to this apnea/narcolepsy. OH well, still have neuro problems,but not as bad as before. Again the nutrition for the brain ALONG with detoxing toxins have really helped me neuro problems. THought I would share all this... ya never know. So much for the fibro DX. I really dont think the Lyrica helps with pain and it makes me sleep in a paralyzed way. I sitll take the baclofen that helps my spasticity. Stay tuned... MISS and LOVE you all !! I am on your side Jan[/SIZE][/COLOR] |
All times are GMT -5. The time now is 07:40 PM. |
Powered by vBulletin Copyright ©2000 - 2025, Jelsoft Enterprises Ltd.
vBulletin Optimisation provided by
vB Optimise (Lite) -
vBulletin Mods & Addons Copyright © 2025 DragonByte Technologies Ltd.