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#1 | |||
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Magnate
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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.
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Anybody who doesn't think a dog can smile has never dropped a piece of bacon. |
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"Thanks for this!" says: | sugarboo (02-14-2008) |
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#2 | ||
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Member
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Thanks for the commiseration and the good example! ![]() I LOVE the "sorry movie reviews" comparison!! Nancy |
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#3 | |||
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Member
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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 ![]() 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 |
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"Thanks for this!" says: | sabimax (02-15-2008) |
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#4 | |||
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Member
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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.... ![]() ![]() tante
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tante |
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#5 | |||
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Member
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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] |
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#6 | ||
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Member
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Hell has officially frozen over! Nancy T. has found a GOOD DOC!!!!!
![]() Yes, this fresh young whippersnapper of a family practice doc is going to be my doctor forever! (I hope.) I was right--the very new doctors are still actually paying attention to their patients! Not only did he ask me more questions at my appointment today--and examine me, which hasn't been done for MANY years--I left the office with a referral for ENT, PT, follow-up bloodwork (for cholesterol/meds), and the little stool-testing cards and sigmoidoscopy order (the last two are yuck, but at least this doctor noticed that I'm past 50--my internist was not on the ball about ANYTHING except the BP and cholesterol). They checked up on EVERYTHING!! When I told him about the walking problems, he tested the range of motion in my hips and knees (NO doctor EVER did this--not even the rheumatologist to whom I complained about this) and gave me a PT referral--WOW!!! Maybe, after 7 years, someone will finally TRY to figure it out, instead of saying "you're just deconditioned" or "bursitis", neither of which made sense, but they weren't listening... This guy is so bright, nice, efficient (types everything into the computer right there in the room--Kaiser really has its act together, I'm VERY impressed with their whole system), and is seriously addressing all my concerns and requests. With nary a hint of smirk, not a hint that he knows what's going on with me before I open my mouth (like previous doctors). Straightforward and helpful, like a real doctor!! Is this possible?? I had given up thinking so, after going through five PCPs in nine years, all of whom were either totally uninterested (1), arrogantly presumptuous (1), had blinders on (2), couldn't be reached or relied upon (2), didn't talk to me or let me talk because they thought I was a hypochondriac (3), and one who was a semi-airhead. Right now I could even believe in the Tooth Fairy, the Easter Bunny, and a balanced federal budget! ![]() Tante: Actually I do not blame the ENT department for leaving me with the impression that the BAHA (bone-anchored hearing aid) would likely be covered--I was just trying to feel them out on the phone (since the membership department wouldn't tell me anything), and they had no authority to promise me anything, I knew that. ("Bait and switch" was the wrong term for me to use--it was just the mood I was in when I posted that.) The policy may have changed since I talked to them last year anyway. In any case, I'm seeing the ENT March 11 and will hope to find something out. The BAHA (bone-anchored hearing aid), developed in Sweden where "hearing aid" is not anathema to insurance companies, is now called things like "bone-anchored implant" or "bone-anchored hearing system". Here's a link to the US manufacturer that bought out (?) Entific, the Swedish developer: http://www.cochlearamericas.com/Products/2013.asp My hearing loss is strictly one-sided, being normal up to 500 Hz and then waterfalling down to a 75-110 Hz loss, which is bad enough that I have very poor speech discrimination in that ear and would not be helped by a regular hearing aid. The loss occurred in 1999 when I sneezed hard one day. Cause unknown, but obviously something traumatic happened in my inner ear. Well, what a day it's been! I feel like I won the lottery!! A huge psychological burden has been lifted, after many horrible years of awful internal churning, the doctors' attitudes literally eating away at my insides. Everything is different--just because someone listened--really listened, and addressed things with me in a straightforward and proper way. Good luck to everybody, undiagnosed and diagnosed... feel better and good luck with new treatments! Nancy T. |
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