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Thanks for the article. I was recently diagnosed with fibromyalgia and have been...sm

Posted By: Melissa on 2005-08-29
In Reply to: Fibromyalgia - upcoming new treatments - good read (see article inside)

having trouble adjusting and trouble finding a doctor who understands. If others with fibromyalgia wish to correspond, I will post my email address. There are no fibromyalgia support groups in my area and corresponding with someone who understands would be great!


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Fibromyalgia
Just visited my doctor today.  I have many indications of fibromyalgia.  Of course there is no test to diagnose this, he wants me to try process of elimination by first trying a wheat free diet.  I'm kinda bummed about this.
Fibromyalgia
Don't be too bummed. I am reading a book called "The Yeast Syndrome", and the M.D. author states in it that fibromyalgia may be related to a yeast overload in the body. So the wheat-free diet may be very helpful to you.
Fibromyalgia
I was diagnosed with this in 1993. the first two years were terrible. I spent alot of money on tests and drugs.

Finally the last 6 years have been good to me requiring little or no medications. I was so proud of myself.

This year winter hit and along came the fibro. My line count fell 3 months in a row. I ended up loosing my current MT job for this reason.

Has anyone else had this experience?
Fibromyalgia - upcoming new treatments

Copyright 2005 Los Angeles Times
All Rights Reserved

Los Angeles Times

August 22, 2005 Monday
Home Edition

HEALTH; Features Desk; Part F; Pg. 1

2286 words
On pain's trail;
Exploring
fibromyalgia's mysteries, researchers look to the central nervous system,
gaining deeper insight into why we suffer.

Shari Roan, Times Staff Writer


FOR years, pain, stiffness and fatigue clung to Lauren Armistead like an
invisible shroud. It was tough enough to live with fibromyalgia -- but
the skepticism she encountered when she discussed her condition was intolerable.

"Throw out a word like fibromyalgia and you'll get this blank
stare," the 28-year-old said recently, sitting in her Santa Monica apartment.
"For so long, it was my own private battle."

Today, however, Armistead is slowly, tentatively opening up about a
disease that is simultaneously emerging from its own mysterious black box.

A groundswell of research has begun to expose the underpinnings of the
baffling disorder that affects an estimated 6 million to 10 million Americans,
most of them women. Not only do the findings have the potential to ease the
condition's stigma, they also may provide clues to other illnesses for which
there is no clear clause.

Fibromyalgia, experts now believe, is a pain-processing disorder
-- arising in the brain and spinal cord -- that disrupts the ways the body
perceives and communicates pain.

"There was a time when it was thought to be psychosomatic," said Dr.
Robert Bennett, a fibromyalgia expert at href=http://www.mtstars.com/medical_transcription/Oregon/>Oregon Health
& Science University in Portland. "We now understand the pain in
fibromyalgia is an abnormality in the central nervous system in which
pain sensations are amplified."

Now doctors are more likely to acknowledge fibromyalgia as a real
illness. Because patients are being diagnosed and referred to specialists more
quickly, they're finding relief, and acceptance, easier to come by.

Pharmaceutical companies have jumped on the new theory of the disorder
too. The first prescription drug approved specifically for fibromyalgia
will likely be approved late next year or early in 2007, and at least half a
dozen pharmaceutical companies are developing other treatments. Meanwhile, the
federal government is funding 10 studies of the disease.

"It's very rewarding," said Dr. Stuart Silverman, medical director of
Cedars-Sinai Medical Center's Fibromyalgia Rehab Program. "I was seeing
patients before because no one else wanted to see them. Patients would tell me,
'Everyone has told me there is nothing I can do.' "

*

The difficulty of diagnosis

Fibromyalgia typically is defined as unremitting pain in multiple
areas of the body -- at least 11 of 18 specific tender points -- accompanied by
fatigue, difficulties with concentration and other vague physical discomforts.
The illness is called a syndrome because the cluster of symptoms lacks the clear
markers of disease, such as changes in the blood or organ function.

Because patients often look healthy, doctors have sometimes diagnosed
fibromyalgia as a muscle problem or an autoimmune disorder. It can also
be a "wastebasket" diagnosis, attached to people with inexplicable pain
problems. Some have even dismissed it as the complaints of emotionally troubled
women.

Many fibromyalgia patients stumble around for years seeking help
for their symptoms -- even after receiving a diagnosis. Always athletic,
Armistead first experienced back pain when she was a child, but
she assumed the discomfort was a part of playing sports.

By the time she had joined the UCLA volleyball team in the mid-'90s,
however, Armistead knew something was seriously wrong. After games, she would be
racked with pain. She sometimes took as many as 15 over-the-counter pain pills a
day.

Coaches and trainers, alarmed at her use of painkillers, insisted she
undergo medical tests. Over a year, Armistead saw numerous doctors but got no
answers.

"Eventually everyone started doubting whether or not I was really in
pain," she said. "My coach couldn't understand how I could play one day and be
bedridden the next."

Debilitated by pain and fatigue, Armistead quit the team and began to cut
back on classes. She lost 35 pounds in eight months. It was a time in her life
"so painful, I've tuned a lot of it out."

In 1996, however, a doctor diagnosed her problem as ankylosing
spondylitis, a type of arthritis affecting the spine, and
fibromyalgia.

Today Armistead takes an arthritis medication, two sleep
medications, vitamins and herbs. She undergoes acupuncture, exercises moderately
and works only a few hours each day doing freelance marketing.

"With each passing year I've accepted the cards I've been dealt," she
said. "I'm not giving up. I keep trying new treatments."

*

The evolution of treatment

Armistead, like many fibromyalgia patients, is a long way from
being pain-free. But the new research on fibromyalgia's causes offers a
blueprint for more effective treatments.

For years doctors had been looking for a cause of fibromyalgia at
the site of the pain: the head, back, hands, neck, gut or elsewhere. And their
treatments focused on soothing pain in these locations. As their understanding
has grown, however, these treatments have begun to change and new ones are in
development.

Fibromyalgia is now thought to arise from miscommunication among
nerve impulses in the central nervous system, in other words the brain and
spinal cord. This "central sensitization" theory is described in detail this
month in a supplement of the Journal of Rheumatology. The neurons, which
send messages to the brain, become excitable, exaggerating the pain sensation,
researchers have found.

As a result, fibromyalgia patients feel intense pain when they
should feel only mild fatigue or discomfort -- such as after hauling bags of
groceries. They sometimes feel pain even when there is no cause.

"The pain of fibromyalgia is not occurring because of some injury
or inflammation of the muscles or joints," said Dr. Daniel Clauw, a
fibromyalgia researcher and director of the Center for the Advancement of
Clinical Research at the University of Michigan. "There is something wrong with
the way the central nervous system is processing pain from the peripheral
tissues. It's over-amplifying the pain."

Recent studies show multiple triggers for the amped-up response to pain.
Fibromyalgia patients have, for instance, elevated levels of substance P,
a neurotransmitter found in the spinal cord that is involved in communicating
pain signals.

They also appear to have lower levels of substances that diminish the
pain sensation, such as the brain chemicals serotonin, norepinephrine and
dopamine. Growth hormone, which helps promote bone and muscle repair, is also
found in lower levels in fibromyalgia patients.

New therapies are aimed at these abnormalities. The experimental drug
pregabalin, for example, can reduce the release of brain chemicals involved in
the pain response. Other medications might encourage the deep, restorative sleep
during which the body secretes growth hormone to nourish tissues.

Although antidepressants that increase just serotonin have been a
disappointment in treating fibromyalgia, a new class of drugs may provide
better pain relief by boosting both serotonin and norepinephrine. The pain and
depression of fibromyalgia are caused by abnormal levels of these
neurotransmitters, doctors now believe, not simply by the inability to live life
normally.

"What we have realized is there is a very strong relationship between
depression and pain physiologically," Bennett said.

Medications approved specifically for fibromyalgia will
dramatically change treatment, Silverman predicts.

"Fibromyalgia will get a lot more respect," he said. "People will
think there must be a disease if there is a medicine for it. It must be
treatable."

*

A multifaceted model

The "central sensitization" model of fibromyalgia may even be used
to help explain and treat other chronic pain conditions that have stumped
doctors, such as irritable bowel syndrome, chronic low back pain,
interstitial cystitis and vulvodynia, Clauw said. All may be variations of
central sensitization and the resulting imbalance of chemicals and hormones.

Although fibromyalgia is thought to affect mostly women, he
believes many men are afflicted but are instead diagnosed with chronic low
back pain.

"These enigmatic chronic conditions are all probably central pain
syndromes," he said. "People were taught that there is one kind of pain, a pain
that occurs in the area of the body where people are experiencing pain. But this
notion of central pain, that's where we really need to move."

Others aren't so sure, however. Many questions about central pain
disorders remain, including why some people are afflicted and not others; why
symptoms can vary so widely among patients; and whether the emerging chemical
markers -- high levels of substance P and low levels of serotonin and
norepinephrine -- cause the exaggerated pain or are its result.

The central sensitization theory hasn't convinced everyone that
fibromyalgia is a real illness, said Dr. Nortin M. Hadler, a professor of
medicine, microbiology and immunology at the University of North Carolina.

It's possible that fibromyalgia patients simply have a different
mind-set, he said. They tend to catastrophize small burdens, exaggerate minor
discomforts and quickly lose hope. This psychic despair, he said, can alter
neurotransmitters and influence other central nervous system functions.

"Is central sensitization something we want to label as a pathological
process or is this something we are all capable of doing if we prepare ourselves
intellectually?" he said.

Hadler is the author of the 2004 book "The Last Well Person," in which he
said that too many normal human characteristics and conditions are "medicalized"
into problems that require treatment.

Once fibromyalgia patients are treated as if they have a disease,
he said, "they never return to wellness."

*

A hard disorder to treat

This perception of fibromyalgia, while falling out of favor among
many doctors, nevertheless strikes a nerve in patients and among doctors
specializing in its treatment.

Fibromyalgia patients are difficult to treat, Bennett said,
requiring much time and attention. Some patients never get better, although
about 80% improve with a dedicated treatment plan and lifestyle modifications,
he said.

"There is no recipe for treating fibromyalgia patients. The
treatments have to be fully individualized, and that takes a lot of time,"
Bennett said. "Most patients aren't getting the treatment they need."

Armistead, however, has reached a turning point. Now she sits down with
loved ones and friends and explains to them, one on one, what her illness is
like, how she must be flexible when making plans, that she may not feel well
even though she looks fine.

"The name 'fibromyalgia' is recognized now," she said. "I think
someday people will be shocked that anyone thought it was all in your head."

On a recent day, as the clock approached 6 p.m., Armistead pushed herself
through a 90-minute yoga class at a sunny Westside studio. She slowly picked up
her mat, towel and water and left the studio looking tired and moving gingerly.
Her back throbbed. Her neck hurt. A headache was coming on.

But she did it. She made herself do the stretching exercises her doctor
said are necessary. She enjoys the small satisfaction of knowing that she did
her best.

"Living with any chronic illness is not easy," she said. "It's a constant
battle. My saving grace is I know there will be a day when I'll wake up
pain-free."

*

New options for treatment

As understanding of fibromyalgia has grown, so too have options
for treating the condition. These medications are under study:

* Pregabalin (brand name Lyrica): This antiepileptic drug, also approved
for diabetic nerve pain, appears to be effective in reducing pain and disturbed
sleep in fibromyalgia patients. If late-stage trials prove successful,
Pfizer plans to ask the FDA to approve the drug for fibromyalgia.

* Milnacipran: Marketed outside the United States as an antidepressant,
this drug increases the brain chemicals norepinephrine and serotonin. Early
studies showed it to be successful in reducing fibromyalgia pain, and
data from the first phase-three trial is due out this fall. Cypress Bioscience
and Forest Laboratories hope to seek FDA approval late next year.

* Duloxetine (brand name Cymbalta): This antidepressant, already on the
market, increases the activity of serotonin and norepinephrine. It was
successful in reducing fibromyalgia pain in early-phase studies, and
plans for a phase-three study are underway. If successful, Lilly may seek FDA
approval of the medication for fibromyalgia.

* Xyrem: Approved for narcolepsy with the complication of weak or
paralyzed muscles, the drug might be able to increase deep sleep in people with
fibromyalgia. The results of an initial study on fibromyalgia are
due later this year. It's made by Jazz Pharmaceuticals.

* Provigil: Approved for daytime sleepiness associated with narcolepsy
and shift-work disorders, or sleep problems in those who work nights or on
changing schedules, the medication might help treat fatigue related to
fibromyalgia. The manufacturer, Cephalon Inc., has no plans to seek
approval for the drug for this purpose, but it can be used off-label.

* Mirapex: Approved for Parkinson's disease, this drug works by
increasing the neurotransmitter dopamine. The manufacturer, Boehringer
Ingelheim, has no plans to study the drug for use in fibromyalgia, but it
can be used off-label. An independent study showed it was promising for reducing
fibromyalgia pain.

--

Fibromyalgia's link to other disorders

The recent fibromyalgia research might also lead to a greater
understanding of several other disorders. The suspected cause of the condition
-- central sensitization, in which nerve impulses in the central nervous system
malfunction -- may also play a role in:

* Irritable bowel syndrome

* Chronic fatigue syndrome

* Gulf War syndrome

* Interstitial cystitis

* Vulvodynia

* Chronic low back pain

* Chronic headaches

* Endometriosis

PHOTO: (no caption) PHOTOGRAPHER: JONATHAN WEINER For The Times
PHOTO: REGIMEN: Yoga is part of 28-year-old Lauren Armistead's treatment plan
for fibromyalgia. Before she was diagnosed with the condition, she
sometimes took up to 15 or more over-the-counter pain pills a day. PHOTOGRAPHER:
Perry C. Riddle Los Angeles Times

August 22, 2005

This is the best site I've found about treating fibromyalgia. It works for me, maybe it will for

Diagnosed w/deQuervain's
I've just been diagnosed this week with deQuervain's tenosynovitis.  I've gotten a splint (very awkward!) and have been prescribed anti-inflammatories.  Are there any exercises to do to help w/this?   My doctor mentioned PT, but I wasn't ready to go just yet.  Surely don't want to have to undergo surgery--thanks very much for any information or personal experiences!
Have you been diagnosed with occipital neuralgia?
I have been diagnosed with every headache there is. I have had 7 surgeries this last 1 1/2 years plus am on multiple medications. I even went so far as to have a C2 neurectomy, which was unsuccessful. My next surgery is hopefully my last. I have an occipital stimulator placed, which works wonders for the headaches and pain in the back of my head. I have to have it hooked up agan, as they removed the wires due to an 8-month long postop infection when I had the wire revised. For frontal ones, I get Botox injections every few months. Not only am I a sufferer but I transcribe for a headache and pain clinic. Feel free to post to me.

You can get rebound headaches, especially if you are using Excedrin Migraine or more than two Fioricet a day. For other people like me, it is a combination of things that are causing them.

Good luck!
Just diagnosed with type 2 diabetes...sm
I would really love to hear from others who have diabetes and any tips on how to live with it.  I just got my testing supplies, a diet guidelines, but now have no idea what to do from here.  Of course my health insurance as of tonight at midnight ends for two months, as I had to switch companies, so hope that does not cause any problems, but we will have to see.  Please feel free to email me or post here.  Thanks. 
Coffee is a stimulant. My oldest was diagnosed with

severe ADHD.  Meds didn't work and made his heart race to the point that he was very uncomfortable.   He is now 16 and learned coping skills, but he has been off meds since he was 8.   I always tells parents of newly diagnosed children to try giving their child coffee or Mountain Dew on a weekend when they have nothing else going on.  Sometimes it works, sometimes it makes the kids bouncing balls, which is why you don't want to have any other plans that day.  


The drugs are so bad if you can come up with an alternative it would be so much better.  The nurse at our doctor's office told me to take a pill one time to see what my child was experiencing and it was not pleasant.


 


 


 


In time past my child was diagnosed
with a disease that is catastrophic. He was in college and quit that day. I was employed in hospital setting and immediately sat up Cobra, and carried it for about 4 months I think until which time he got a job and got his own medical insurance. My insurance covered as long as the child was in college. I knew with the disease if no insurance bridge would never be able to be covered again and with the cost of the medications needed just an overwhelming thought and even though I have money, would never be able to cover the costs of thousands every month to be paid out.
I have diagnosed myself with motivation necrosis, possibly secondary to DQS. SM
I hope it's not terminal.  Not old enough to retire yet.  Anyone else with this sickness?
Has anyone noticed lately that there has been a lot of people diagnosed with breast cancer?
or is it just my imagination?
I'm wondering how you came to the conclusion that she has manic depression. Was she diagnosed

with this?  From what I read, it doesn't sound like manic depression to me.  Sure, she has some issues going on there, major depression would be a pretty good guess, but does she have any manic episodes?


My ex-husband and ex-mother-in-law were both bipolar which is the new and improved way to say manic depressive and they were the exact opposite of hypochondria.  During the manic phase, they felt like they ruled the world.  According to them, they had never felt better, thought more clearly, or got more done, but the exact opposite was true.  They never slept.  They never finished anything they started.  They were incoherent at times, basically jumping from one subject to the next so you could not carry on any kind of coherent conversation with them.  Sometimes they were even delusional - my mother-in-law thought she was in love with a televangelist and divorced her husband and moved to be closer to the televangelist.  My ex-husband thought he was the victim racism when he got a speeding ticket.  He claimed the officer had something against Hispanics.  Nevermind that my husband was maybe one-eight Mexican on his mother's side and has a German last name.


Those are just a couple of examples of manic behavior.  It can even be more bizarre.  I could write a book based on what I've seen first hand and it can be very scary.


My son was diagnosed as an infant. Prevacid helped tremendously! Hope she gets better. nm

Cold fingers often - diagnosed with Raynaud syndrome many years ago.
I usually try warm water first - if that doesn't help, I have these little packets, normally found in the camping section of stores called hand warmers. One is called Hothands-2(up to 10 hrs of heat), another one called MEGA warmer(12+ hours). One you shake to activate, the other just expose to air - then place them in a pocket or glove. I wear sweats with pockets - put them in my pockets and warm up my hands.

Found these several years ago as we go camping; however, hubby loves going out in late Sept & I'll swear would go all winter if he could. When he's comfortable, I'm turning blue!! He found these for me - and, they also have foot warmers (6 hrs heat), which sometimes I will use in the winter if I'm wearing my moccasins - with socks - while transcribing!!


NO... Just recently.....

my sister came home to a real disaster.  She left for work at the beginning of a thunderstorm and came home to find everything blown out in her house and scorched burnt wallpaper in places on the walls.  Apparently the lightening hit the Invisible Fence wire around the perimeter of her property, traveled into the garage where the power box for the fence was, and breached her circuit box and traveled up into the sockets in the house.  She lost TVs, her computer, all sorts of items which were destroyed.  I'd unplug and wait it out.


i just recently became SE
and all i can tell you is that when i talked with my accountant about what to do with the 401k that i already have, knowing my situation, she gave no indication of there being a problem maintaining this as an SE.
I recently got one because I could not
adjust to the earphones my company sent.  I got mine from the Dictation Store and they were $9, but shipping is about $8.  I just got standard shipping and I think it took 2 days to get it, though I'm on the same coast. 
I had one of those recently.
Foot pedals wouldn't work (I tried several). Keyboard keys (F1, etc.) wouldn't work. I ended up using the mouse on media player to stop, start, and back up the dictations. Obviously it takes much longer to transcribe anything that way because it's a pain in the neck to use the mouse to operate the player, and you're much more prone to make mistakes because of the clumsiness and hassle involved.

The test I took was very easy (radiology). They graded it the same as if I had had full use of a foot pedal and no technical difficulties. There were a few simple errors that were obviously the result of not being able to quickly back up and re-listen to things. They also counted off for minor stylistic "errors" even though they did not make it known anywhere that they required the use of a specific set of style guidelines on the test (presumably the BOS). I now regret taking that test at all under those ridiculous circumstances.

In the end I concluded that they either didn't know how to administer a test or it was all designed to be an ambush to stifle the MTs they had decided they didn't like and weren't about to sign a contract with. Or both. In any case, I would never choose to work with a place that incompetent or that nasty anyway.
I have done several recently and
every single one of them required you to type it into Word 2003 and email it in so that they can read it.

Maybe you were testing with bigger companies than I was, though and they have some other way to test.
Why does it seem that VR/SR has just recently taken off
it just really seems like in the last few months everyone on here has been forced to go VR (I know not ALL of you), but the majority. My work had one account on VR last year and now ALL accounts are within the just the past months. Why all of a sudden are we getting bombarded with it. It doesn't seem to matter what company or what platform, but it is taking us by storm. I happen to like VR myself, but WOW its exploding!! Want your opinion as to why "all of a sudden"?
From what I have seen recently,
they are hiring people with little or no experience and getting rid of the ones who have tons of experience and can learn quickly and can start producing at the get go. They advertise for experienced MTs with acute care experience but they are not keeping them.  They even laugh and joke about it.  
I have investigated recently-
checking up the corporate ladder and with tech people, all of us in MQ get paid for spaces within a section/paragraph, naturally not the blank line between sections/paragraphs. That was one of the motives for insisting we stop double spaces after periods and colons(:). It adds up.
I've seen the same recently...

"work pools were changed recently" was what I was told and now finding myself with the accents....luckily since I work on 85% during my full time job during the day the accents on this part time account are a piece of cake.  I did have a funny experience last night on my last report...


I pulled in an echo that someone apparently abandoned because they couldn't do it.  It was an ESL but not a difficult ESL.....


The doctor dictated....."Normal mitral valve........NO MORE MITRAL VALVE was transcribed....then pericardial effusion.....THE PATIENT WANTS DIVERSION was typed.....  !


 


I was just recently hired by
Transcend and am receiving the equipment today or tomorrow, will train next week. I would not worry about the interview if I were you.  She was very nice and we had a nice talk.  I am leaving MQ.  Welcome.
I checked it out recently (sm)
If I weren't already in my senior year of college and on a different path, I'd definitely check it out. The average income was something like 45K (salary.com).

I'd not worry about competition. MT is considered hard for newbies to break into, but we did that, didn't we? Where there's a will, there's a way.

I'd definitely consider it if I were you. Frankly, getting out of the house sounds really nice to me.
I think there was something recently posted about this
company.
I recently met someone who has a friend who took a
6-week course, is working at home with all the work she can handle.  Of course I don't believe this, but this is what she said.  
I found this recently (sm)
See link
Not unless something has changed recently...
I have worked at a job where I had to use both the Lanier and a Dictaphone.  They are two very separate things.
anyone recently take the cmt exam?
thank you.
Oh, they did for me! I just recently plugged my

instead of my junky speakers, and what a difference!!!  Can't believe I've gone this long thinking that it was DQS that was all the problem with the degradation in sound quality since going from using a C-phone. 


I assume that better speakers would have to make a difference, because mine are super cheap.  But for now I'm just staying with my headphones through the computer speaker plug (and with a Turtle Beach Audio Device as well now). 


Someone asked this recently and several
mentioned the same reasonably priced vacuum (yes, some also loved their Dyson's, but I'm with you on the price). Sorry, I can't remember which one it was (maybe a Eureka something???), but I do remember the same one coming up three or four times in the thread. Search the archives. Good luck to you! (p.s. I'm coming back to search the archives myself when I'm ready to buy again).
this happened to me recently :)
Hold down either the Ctl key or the Alt key and then hit either your right or left arrow depending on which way you want it to move. It only happened to me once, so if that doesn't work, play around with holding Clt+Alt and possibly Shift with the arrow, but that was how I got mine back after my 3 YO granddaughter played with it.

Happy Holiday!

I recently did this and went back to being
IC status. I did not enjoy being an employee, yes the tax thing is a pain in the butt, but being an employee with this particular company was horrible!! I vote for the IC position unless you don't mind being restricted on time off, emergencies etc. Just my opinion though, good luck with your decision.
just recently transitioned myself
from decades of being an 'employee' to a SE. I just wish i would have done it many many years ago. The freedom from time clocks, schedules etc is well worth the bene's i gave up. If one puts it all together (add bene's to gross pay), i don't make as much money, but that's really my fault, because now many days i work 6 or 6-1/2 hr instead of 8. But my quality of life is so much more. You sure want to set aside money for taxes though, and i made a savings acct for just that. Hope you make the right decision for you!!
Recently started using

Meditech for a new hospital account (acute care and rad)  Compared to WP and/or Word,(or even DocQscribe)  it's like pushing a truck up hill with one hand.  Easy to use but very cluncky and requires more Keystrokes for any function than any other platform that I've used.  No doubt it (or you) gets faster with use, but I'm not impressed.


PS It has an awkward spell check - not case sensitive, does not pick up transpositions, takes 3 keystrokes to make a correction instead of 1 as in WP or Word.


At my age plus the fact recently
paid off every debt I have, could get social security - I am glad I do not have to worry about will it be this way or that- much too unnerving for a person supporting family, bills, etc. I work part by my own desires and if that is the way it goes, that is that. I hated the first time I was ever outsourced but after the 2nd time used to it. Times change.
I knew anyone could look at it but I did not know until recently (sm)
that it would come up in search engines. I accidentally found something I posted months ago when doing a search for something else!
I saw saw one recently; I think it was Nicholas
Transcription, but can't remember for sure.
Anyone take the CMT test recently?
I was just thinking about taking it and wondered if anyone had any advise. 
I have been on both sides and recently sm
I had a team and their QA to oversee. The "recruiter" would hire anyone she knew who could type. This was a teaching hospital, very large, very difficult and a challenge to those of us with plenty of experience. I could not fire an MT and if I told the MT manager that this so and so could not do the job, I was told to TEACH HER to do it and in the mean time, fix her reports.

I did have some MTs who wanted to learn, had had a bit of experience, and were anxious to progress. I spent a lot of time on them because they took to suggestions and they worked hard. The ones who not MTs, hadn't studied and were clueless, I had the option of assigning them very little work, which is what I did and I did out of self-preservation. There are only 24 hrs in a day and I was working 20 of them!

I have two jobs right now and QA at one I know very well, having worked with her for years. She only sends back a corrected a report in its entirety. The blanks she filled in are changed to a red font. I can see it, I can learn and I keep every one of her reports in a special folder in my email. I am trying to learn 3 doctors who chased away several other MTs on this account. One has a speech impediment and talks very very fast, one has an accent and talks too fast in the face of it and the third is a speed dictator who doesn't think that words need to be pronounced to be understood. The rest of the physicians don't present a problem. It has been difficult because I have had these 3 doctors about twice each and not enough to tackle the learning curve YET. In any case, this QA is patient and she never ever offers personal comments of a derogatory nature.

The other company I work for, I think that QA is nonexistent, other than when they are throwing their weight around. I had one particular report, an I&D of a sebaceous cyst. The doctor followed with this "cheesy material" which is what I transcribed. They called me on the phone to tell me that the doctor "never would have said that" and I said I'd stake my reputation as an MT that he did! She said, well...you're still wrong. Ummm no, I am not. That is lack of experience, knowledge or even a decent ear. No wonder we are on the verge of losing the account, yet again.

Now, I worked for a company where the QA person treated everyone like they were about 2 yrs old. I had her call me names like $toopid, moronic, an imbecile and whenever she used a word of 3 syllables, told me to look it up since I was not bright enough to understand what she was talking about. The owner, when I complained, said that is just how she is, but that she is so good at what she does... I said look, she represents your company and what you stand for. If this is all you have to offer, I am leaving, and I did.

SOME QA gals seem to have a chip on their shoulders. I am of the opinion that those who can do this job, do it and those who are knowledgeable, but can't do the job, do QA. I know several QA people who have CTS and can't type anymore, so they QA and I think that is a bit different.

It is widely understood that the very best MTs are not QA people, they are still MTs. I could not, would not take a 50% or better pay cut to be a QA person. I am far too fast and too capable for that. Neither company I work for presently would ever put me on QA because I am extremely valuable as an MT. Transcribing is my stock and trade and I can't see giving that up for anyone.

Remember as well, there are reasons that we work at home, and I am talking psychological reasons. I can't stand office politics and I don't like people. I am told I don't play well with others, and this is a correct assessment. Others have their issues too, and some of these issues creep up with QAs who seem to need some therapy and help dealing with people. This seems to attract people with a decided need to be the biggest fish in the smallest pond and throw their fins about to get attention.
When I did my resume recently (sm)
I listed the companies and underneath put a brief summary of my duties. One company I had worked for a very long time and held multiple positions in the company based on my "life needs" at the time, you know, MT, supervisor, part time at home with little ones, etc. I just kind of briefly stated that I had held multiple positions within that company.

Seems like resumes used to also contain a "position sought" or "goal" line and in that line I would clearly state that I was looking for supplemental income and to maintain my active transcription skills. Perhaps that will be enough of a "continuing ed" spin that any recruiter worth their salt would surely understand.
I recently asked the same
question (about a week ago) with little reply. Only one other person replied and suggested Bose noise reducing earphones. I just purchased a pair of Glimmer Insight from transcriptiongear.com. They also do not have a seperate volume control, which would be nice. I also purchased a pair of earmuff style headphones just in case the others hurt my ears, Skullcandy lowriders. I don't care for the "urban" design of them, but the sound is very crisp and clear. Again, no volume control on those.
I've seen a few recently that are sm
upgraded to work with Vista, but not many.  I think there are too many quirks with Vista (my opinion) and not everyone is ready to upgrade their systems to be compatible. If you work IC, buy a computer with XP and write it off on taxes.
Wasn't there a gal recently who was getting out of MT and going to

I wonder how that's going.  That's what I REALLY want to do.  I have just about reached the camel's last straw with this job.


My clinic has gone to this recently...sm

Our clinic went to this in October.  The doctors started using it for their clinic notes in November.  Right now my dictation has been cut down to less than half of what it was and they still don't have all the appropriate templates set up yet, so I am expecting in the next 3-6 months there will be no more dictation at all.  Right now I am having to find other things to do because the dictation is so sporadic.  I don't have any experience doing anything other than medical transcription my entire adult working life (30+ years), so needless to say this is very difficult for me to adapt to. 


My MTSO has recently been
emphazing this. As I understand it from what I was told, 99.9% of the time there is a comma before "which." An example of now to use one is "The patient has a cold for which she is being treated with ....."

When used as "the patient had a chest x-ray, which showed ..." you use a comma. I really don't understand what difference it makes, but we hvae been told to use it. In fact, they gave us a way to enter it in our autocorrect so it automatically puts one in, which can be irritating at times when you don't need it.
I recently typed an EGD....sm.
The patient had choked on a piece of meat and had it lodged in his throat. The whole report for some reason by hands did not want to type food...always foot. I felt pretty confident that I did a good job correcting all of them and sent the report on.

Two days later the doctor sends it back and asks me to change it. No big deal, must have made a different mistake....NO I was so mad at myself that I sent this report that stated "foot was removed from the esophagus". It was embarassing then but now it is pretty funny to me.
Anyone recently worked for Amphion?
I am curious about what kind of work they have.  I read in archives that there were a lot of clinic notes, letters and correspondence type work.  What I want to know is whether this has changed and if I went to work for them would there be acute care/hospital work?  What is the program they use?
Until recently my experience was great
Now all of the sudden many accounts have no work. When there is work, the money is good. Really a lot alike many of the other nationals, IMO.