the name means absolutely nothing
Over the years I’ve seen many of you pediatric and internal medicine physicians at Vanderbilt Univeristy Medical Center. You may be employed at a hospital renowned for being the best and largest hospital and employer in Middle Tennessee but you, the doctors, are way behind the times. You are not like the doctors of Seattle Grace, you are not like McDreamy (or McSteamy), you’re not Luka from ER, you’re not Jack from Lost, you’re not even House.
You probably wouldn’t remember me and I know you wouldn’t remember my name, much less how to spell it (even if you’re my PCP). I’ve seen so many of you over the years that I might not remember your name either–so I guess we’re even on that front. You may think you’re groundbreaking researchers and physicians in many areas, and you may well be, but let me tell you this: YOU FUCKING SUCK with bedside manner and chronic pain patients.
Doctors can get a little cocky, I know because my father is one of them, and they can assume they know your case and your problems and your story before they take the time to listen (if you’re lucky enough to snag one that actually listens). Reporting that you’re in pain and need medication to ease it means you are a junkie, you are faking it, and you are just groveling for some meds to get your next fix. And dear god, if you’re underage and you need pain killers well then you’re doing the dirty work for your junkie parents or you’re just exaggerating, after all children can’t have chronic pain disorders, right? You guys are so behind the times that you don’t even have A PAIN MANAGEMENT CLINIC, which nearly every hospital does nowadays. Hell, even small practices are taking on pain management with fervor, but not a rich, educated hospital like Vanderbilt.
In the area of Reflex Sympathetic Dystrophy/Complex Regional Pain Syndrome you really are clueless, once more. You think what the Children’s Hospital of Philadelphia says about their study with RSD and exercising for eight hours a day is the Word Of God, and that’s all you can try out. Don’t do your own studies or give your patients any options, go ahead, leave them feeling like they’re doomed, after all, they are junkies.
You think I’m exaggerating by now, I can tell. The last paragraph was just for one doctor, Dr. Lawton (a pediatric rheumatologist), who told me about an exercise program for minors with RSD (drop out of school and exercise constantly, see if it rewires your brain, don’t give them any relief for the massive amounts of pain they’re enduring just for your study). He also suggested my RSD (which he diagnosed) was just “emotional”. Bullshit.
I haven’t even moved on to those assholes at the very new Vanderbilt Children’s Hospital Emergency Room. That’s a totally different entry.
But I just want to say one thing to the brilliant young doctor (Dr. Kristine Ehst, Internal Medicine) who suggested my pain that causes me to writhe and scream and moan and yell and sob in pain was just ‘growing pains’, and prescribed some ‘Bengay’ for it (and nothing else), and who told me one afternoon when I was leaving her office to “go out and have some fun this weekend”.
Well damn, Dr. Ehst. I was planning on sitting at home watching Passion of the Christ, hitting my legs and arms with hammers so I could be in that chronic pain I keep telling you about, reciting the Illiad, and maybe even giving myself an enema, but since you told me to “go out and have some fun this weekend” I guess I’ll have to change my plans.
I'm Lizzy. Or Liz. I'm a seventeen year old from Nashville. I write words here. I like it when people comment on the words I write. Want to know more about me? Carry on my wayward son. (see what I did there? HA.)
KC
February 12th, 2007 at 6:41 pm
I feel your pain. Literally.
And I have bad news. Chronic pain sufferers receive no better treatment as we get older. My life is currently a war with pain and the doctors who refuse to treat it.
Desiree
February 14th, 2007 at 8:39 pm
I was hit hard when I raed your message. I am a 44 y/o otherwise healthy woman who has suffered with RSD for about the past 2 years. My pain is unbearable at times and as for the doctors, I have had to take phographs of my legs during a flare up to prove to even my pain management doctor, that the condition exists. Then , once he did, I endured over 40 sympathetic nerve blocks, the last of which, during sedation, made me “code blue” and aspirate landing in the hospital with double pneumonia. The funny thing is that I am a Therapist/ social worker so I know all the alternative treatment methods they say work, have tried them with no help. I often feel alone and judged bu even my peers, especially when it comes to the medication taking part, with some alluding to that I may have a potential “problem” YES…the problem is that I can bearly walk a few feet without the soles of my feet and my legs feeling as thoiugh I am walking on hot coals. Enough complaining, just wanted to thank you for your letter.
Carrie
February 16th, 2007 at 8:25 pm
Just wanted to say kudo’s and I feel your pain litterally. I was diagnosed 2 yrs ago and it’s been hell ever since. The self ritous, self important Dr.s who all seem to agree its real pain but none are willing to help!!!!!
I am not a med seeker or a junkie, I AM IN PAIN!!!! If they would only listen.
I do have a specialist appt. #3 next week so we shall see if things get any better!So a big thank you for saying out loud what atleast I know I am felling.
Duane
February 19th, 2007 at 8:05 pm
Sorry to hear your story I’ve have Reflex Sympathetic Dystrophy in my feet for about 8 years, keeps getting worse! I just read this aritcle about injections to the lower spine, is anyone familiar with this and did it work.?Thanks,
Duane
Richard Qian
December 7th, 2007 at 8:36 pm
Hi, I know your pain too. and My wife is RSDer and I was a doctor. Best wish to you. Richard
————————-
Discovered the primary pathophysiological mechanisms of CRPS
Richard Qian of the Medical College of Wisconsin.
————– Present diagnoses criteria are over-strict too far away from truth.
Oct. 4, 2007
Dear every RSD/CRPS patients and medical professionals:
I have discovered the primary, major pathophysiological mechanisms of Complex Regional Pain Syndrome (CRPS/RSD). These new mechanisms can give 95% explanation of all issues of CRPS and its mystery. The “Complex” is only number two which include only two easy-understanding mechanisms.
These are hypotheses with evidences rather than imagination. It does mean I have know 90% the reasons of CRPS and how to prevention and treatment with cure goal when very few pathological change of CRPS has been know in the world. When we all know the real pathophysiological changes in RSD patients, it become easy to let everyone know CRPS (awareness), to prevent from CRPS to EVERYONE in the world.
Complex Regional Pain Syndrome (CRPS/RSD) has been diagnosis by medical professional for about 20/70 years, the relative medical history is over a century, human being have suffered from it over three thousands years. The detail symptoms are known very well, but little of the pathological mechanism is known. After eight months continuously thinking and clinic research, I have discovered the primary/major pathophysiological mechanisms of CRPS. I have evidences to show them NOW; All Data are from Medical College of Wisconsin and Froedtert hospital. These mechanisms result in tremendous spontaneous burning pain (can last life-long), swelling, discoloration, muscle atrophy, movement dysfunction, disabled, pathological spreading, and other sympathetic change. These discoveries are followed by absolutely useful prevention (90% cases can be prevented), diagnosis, differential diagnosis, and treatment (90% cure rather than present pain-killing treatment.), and prognosis. I like to give 30 minutes presentation any time to show my discoveries’ authority and easy understanding by medical professionals and patients). They are totally different from present ones, from any information of PubMed. Two objective tests can be set up and be gold standards for CRPS/RSD. Two animal models can be set up which can mimic the pathological changes of patients 100%. Two treatment regimens will be standard to cure CRPS. A prevention procedure will be benefit to everyone in the country, including those patients going into surgery room. “The well-known CRPS mystery” will become past. I have had enough data and confidence; you will have same confidence too after my presentation. It deserves Nobel Prize. This research will benefit to 0.2–2.0 million of CRPS civilian patients and veterans cases in USA and the triple number in the world at least. My personal opinion will double or triple this number, because more than 50% RSD patients have been staying home without diagnoses and benefits——– It has been over-strict too far away from truth and missed and will miss very high percentile of patients anytime that the present diagnosis criteria without understanding pathophysiological mechanisms. Another reason is any surgeons don’t like to say their patients suffering RSD pain, so they use brain to skip the RSD diagnoses. I think you know why.
I have designed all procedures, animal models and objective tests. I will setup best clinic and research center in the world in Medical College of Wisconsin in three to five years.
Now I have my MD background abroad and graduated from famous medical school, 10 years full-time scientific research, seven years research in USA, 12 years surgeon training and practice abroad, 21 years talking with a physician and PhD, eight months of CRPS patient’s husband, and more. My unique background has given me a one-to-century chance to find the CRPS major pathophysiological mechanisms and treatments.
These are private scientific discoveries without any business activity. I have sent my mail to vice president of the American Medical Association (AMA), NIH research office, couple of Dean of some university, and lots of famous CRPS medical Doctors and specialist. According my opinions, a lot of previous treatments will become useless and harmful to CRPS patients. I will show my discoveries to everyone any time by presentation after NIH official know this idea is from Richard Baogang Qian. By the way, I am living with my wife and 5-year-old son David in Milwaukee.
Please feel free to spread my letter out to everyone and Senators. We, CRPS patients and family, can get better treatment and recover after we work hard to let everyone know this. Any one is welcome to talk by air or person to person.
Sincerely thank you for your consideration.
Richard Baogang Qian, MD. Research Associate.
(Co-author Rong Zhao, MD, PhD.).
The Medical College of Wisconsin
Physiology, Room 545
8701 Watertown Plank Road
Milwaukee, WI 53226
414-4568553 (O)
414-6303727 (M) (Personal using)
bgqian@mcw.edu
bgqian@yahoo.com
Richard Qian
January 25th, 2008 at 9:44 pm
Etiology/Cause & pathology of CRPS/RSD/Causalgia (Chronic pain) Discovered
Richard Qian of the Medical College of Wisconsin.
————- The discoveries lead to cure and prevention
Dec. 10, 2007
Dear RSD/CRPS patients, veterans and medical professionals:
Hi, I am Richard Qian, Scientist of Medical college of Wisconsin. 148 years after the RSD discoverer, Dr SW. Mitchell, the Father of American Neurology, described RSD and left all relative questions to us, I have answered these questions. I have discovered Complex Regional Pain Syndrome (CRPS/RSD/ Causalgia) etiology (Causes or origins), objective diagnosis tests, cure treatments and prevention. It is first time for human being to know this in the world. It means I have discovered the primary, major pathophysiological mechanisms of Complex Regional Pain Syndrome (CRPS/RSD). These new causes/mechanisms can give 95% explanation of all issues of CRPS and its mystery. The “Complex” is only number TWO which include only two easy-understanding mechanisms. I am medical biologist and working in Medical College of Wisconsin. I like to give 30 minutes presentation any time to show my discoveries that are easily understood by medical professionals and patients.
I have read thoroughly Dr S. Weir Mitchell’s original books about RSD/Causalgia (1864 and 1872. Dr Mitchell is the Father of American Neurology and discoverer of RSD/Causalgia), all of RSD papers from Pubmed and keep any details in mind. I have tried to answer any possible questions for my discovery, and have gotten 99% answers. This gives me one hundred percent confidence about my discovery.
Richard Baogang Qian, MD. Research Associate.
(Co-author Rong Zhao, MD, PhD.).
The Medical College of Wisconsin
Department of Physiology, Room 545
8701 Watertown Plank Road
Milwaukee, WI 53226
414-4568553 (O)
414-6303727 (C)
bgqian@yahoo.com