Guest guest Posted January 5, 2007 Report Share Posted January 5, 2007 You need to report these problems to your State Medical Board. They have the duty to review the problem and admonish or punish the physicians. Not the HMO. Did you not miss work for some time etc due to missed Dx and were treated with incorrect drugs for some time. You may need to see a different lawyer. I dont recall your story in detail. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2007 Report Share Posted January 5, 2007 Guess we need to be looking for PA patients with strokes, etc. Still going to the Med Lic Board is a start. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2007 Report Share Posted January 5, 2007 I certainly agree that this should be reported to the State Medical Board, but don't get your hopes up on a malpractice action. First keep in mind that I'm not an attorney, but am familiar with this in general. You should seek real professional advice. Here's my dose of reality for the day. If anyone has better news, frankly I'd love to hear it. Any successful hyperaldo cases out there in recent years?? From a legal point of view, these cases seem very hard to pursue. In many states, including mine, the statute of limitations begins at the time the initial malpractice took place or initial injury resulting from malpractice. So, for example, with a 2yr statute as it is in my state, the initial malpractice in my case took place 4yrs ago. Even though I continued to see the same doc until 1Q-2006 and there was in essence continued malpractice, it doesn't matter because the courts (at least in GA) consider the first failure to diagnose irrespective of whether there are subsequent failures to Dx the same thing. Secondly, if we look at time point of injury, with HTN related injury, unless there is a specific event such as stroke, heart attack, death, etc, with tort reform as it is, there is great difficulty in defining initial injury time. A specific and really ugly example was a woman suffering from neuropathy as a result of a physician missing an obvious B-12 deficiency in her blood work. Subsequently, the physician Dx drugs and procedures that were inappropriate for the actual problem and provided no help to the patient (sound familiar???). 4 years after the initial malpractice while seeing the same physician, the patient becomes paraplegic due to B-12 deficiency with no hope of recovery. Even though action was filed less than one year after onset of paraplegia, the court rules that the malpractice and injury began 4 years ago, so that's when the clock starts running. Even though there is a clear correlation between the B-12 deficiency and the end-state injury, it is irrelevant. That's the real world in many states...most particularly those in which tort reform has occurred. In all jurisdictions, unless you can get a very " special " jury, the more troubling issue for those of us with PA and SA related injuries due to misdiagnoses is that there is often not a clear causation between injury suffered and the misdiagnosis. Let's take my white matter lesions, for instance. I'm pretty confident, and my medical team is as well, that they were a results of poorly managed HTN and elevated aldo. However, there is no clear causation. In general, these can be caused by HTN related vascular events (silent mini-stroke), vasculitis, demylenating disease such as MS, traumatic injury, or even viral injury. It is easy to eliminate MS and trauma, but how do you eliminate viral injury? Worse yet, how do you eliminate injury from vasculitis...the -potential- biggie in many of the non-HTN impacts of aldosterone? Although there is substantive evidence in animal models, with the lack of human studies of aldo related vasculitis, the plaintiff can't say the vasculitis was caused by aldo. Legally, vasculitis could have been caused by any number of things, and aldo, for now, is not one of them. Even if it were, you have to disprove a bunch of negatives here. Yes, the doctor was an idiot and misdiagnosed, but it may be very difficult to prove causation of injury. With many injuries you can't demonstrate a loss. Say I -can- correlate the wml's and vascular damage from aldo with the malpractice (not likely). If they are not making me obviously ill right now, how do I prove that the vascular and brain injuries these will diminish my quality or length of life and to what extent? While it is more likely that I will have dementia and/or a shortening of life, it certainly is not a sure thing, and there are many things that I can do to mitigate future consequences...at least in theory. In any case, I'm sure as heck not drooling on myself at this point...might be later, but then it is too late to file a case. That does leave an obvious cause of damages, loss of work time and perhaps loss of career. Loss of work itself is not nearly enough money to make it worth pursuing such a complicated case (unless the attorney is bored and has nothing better to do...you don't want that attorney). Depending on what the career and income was, if the malpractice caused you permanent loss of livelihood, maybe you've got something there. Again, an attorney would spend the huge amount of resources to pursue the case unless the monetary loss is substantial. With hyperaldo being such a " rare " disorder, there are few malpractice teams that even know what it is and even fewer clinicians that would be available as expert witness (and they will be needed). As such the costs of litigating will be increased. Here's the best part, if you win, not only do you have to pay off your attorney's cut, but g-d help you if your insurer(s) gets wind of the case. They will want their cut of your winnings for unneeded proceedures, hospital stays, etc. So you win $500K. Of that $200K goes to the attorneys and the insurer get $150K or whatever. You get the $150K that is left...less federal and state taxes. So you are left with maybe $90K. Is it really worth it??? > > You need to report these problems to your State Medical Board. They have the > duty to review the problem and admonish or punish the physicians. Not the > HMO. > > Did you not miss work for some time etc due to missed Dx and were treated > with incorrect drugs for some time. You may need to see a different lawyer. > > I dont recall your story in detail. > > > > > > May your pressure be low! > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2007 Report Share Posted January 6, 2007 > >> > Here's my dose of reality for the day. If anyone has better news, > frankly I'd love to hear it. Any successful hyperaldo cases out there > in recent years?? > >> What you have written is what I have discovered, without permanent damage there is no case. It doesn't matter that I was not able to work for almost two years, it doesn't matter that I was misdiagnosed for 13 years, and as you said, the physician who first gave me the essential hypertension diagnosis without ever doing testing and refused to refer after multiple meds were tried and my BP worsened AND who ignored the significance of a 3.1 potassium on a potassium sparing diuretic in Jan 2004...that is over two years ago, I cannot touch him. The next PCP had to play " catch-up " as I was 51 and hadn't even had a routine EKG after 10 years of HTN. My symptoms were so severe and varied by then that I was sent to referals for everything BUT Hypertension. I feel it is time to move on as it only upsets me to see all the indifference out there. Doctors need to take back their practices, too many have become complacent, only follow the dictates of the age specific health practice guidelines given to them by the insurance companies. Referral seems to be discouraged, when they can't come up with an answer to a patient's problem they don't seek consult unless the patient is hospitalized or lab results are significantly off withthe patient having identifiable symptoms. Routine diseases, such as diabetes, seem to be handled well but anything complex never seems to be adequately addressed at an office visit. I know, I've seen it , I have worked in healthcare for 33 years. When managed care took over medicine changed, and not for the better. It is the most mis-managed system I have ever seen! Of course I am not saying ALL docs are like this but, unfortunately, I have come in contact with my share who were. I was sent for consults where no info was forwarded as to why I was there, no tests that had been done were sent. That is when I learned to obtain and carry my own binder of my records. Docs became impatient with me when I couldn't answer their rapid fire questions due to the trouble I had concentrating. Few ever even bothered to listen to the response, they had already summed me up and decided the treatment course that would be covered by my insurance plan. I was diagnosed with Fibromyalgia and Hypermobility Syndrome by a physician who stood in the doorway after his intern had examined me. Because I refused to take medications I was dismissed, nothing he could offer me but come back in a month to see how things are. I could go on forever, but these are things that are known by the medical community but ignored. Try to find a local doc who will speak out about another. It just doesn't happen. I have to live and work here, at least for now. I need to bury this and go on. Sorry to sound cynical but that is how it is, at least in my area. I cannot change it I can only take care of myself, my family and my friends. I hope for a physician revolt but don't see that in the future either. Patients need to be able to take care of themselves or find someone else to advocate for them. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2007 Report Share Posted January 6, 2007 I look at this very simply. If I don't have a personal relationship with the doc, he won't see me as a person and won't treat me that way. Its as much human nature as it is managed care. The doc has to manage his time very carefully. So, if he refuses to talk to me as a colleague, I walk. In fact, I did that with a guy that is considered to be one of the best endocrine surgeons in the southeastern US. I thought he was a prick and I was a number, so I walked. Yes, surgeons don't always have the best personalities, but if he won't listen to his patients, it is likely he is not listening and learning from his peers as well. Thank g-d I'm not on an HMO. Not to say this always works out to the best. I had an excellent relationship with my former internist. and he really did listen to what I had to say. He even checked for PA early on...he just screwed up the protocol. These things can happen and you have to be very educated as a patient to ask the right questions as well as provide the right info. I was not educated at all at the time. If I had been, given the nature of our relationship, I would have been cure of Conns as much as 4 years earlier. End of the day, though, if your plan gives you the flexibility to be a consumer, you must be an educated consumer and expect to be treated as an equal. If you are on an HMO and have the option of fleeing, do so. HMOs are simply not appropriate for complex care. Just ask my father-in-law...oh right, you can't because he died from a cancer that shouldn't have killed him but for the repeated denial of service from his HMO. -Jeff Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2007 Report Share Posted January 7, 2007 In a message dated 1/6/07 3:28:21 PM, shotzie@... writes: > >> > Here's my dose of reality for the day. If anyone has better news, > frankly I'd love to hear it. Any successful hyperaldo cases out there > in recent years?? > >> What you have written is what I have discovered, without permanent damage there is no case. It doesn't matter that I was not able to work for almost two years, it doesn't matter that I was misdiagnosed for 13 years, and as you said, the physician who first gave me the essential hypertension diagnosis without ever doing testing and refused to refer after multiple meds were tried and my BP worsened AND who ignored the significance of a 3.1 potassium on a potassium sparing diuretic in Jan 2004...that is over two years ago, I cannot touch him. You can file a formal complaint with the Medical Board and with the health care group he is in. The next PCP had to play "catch-up" as I was 51 and hadn't even had a routine EKG after 10 years of HTN. My symptoms were so severe and varied by then that I was sent to referals for everything BUT Hypertension. I feel it is time to move on as it only upsets me to see all the indifference out there. Doctors need to take back their practices, too many have become complacent, only follow the dictates of the age specific health practice guidelines given to them by the insurance companies. "All HTN guidelines state how to evalutate low K and HTN. Referral seems to be discouraged, when they can't come up with an answer to a patient's problem they don't seek consult unless the patient is hospitalized or lab results are significantly off withthe patient having identifiable symptoms. Routine diseases, such as diabetes, seem to be handled well but anything complex never seems to be adequately addressed at an office visit. I know, I've seen it , I have worked in healthcare for 33 years. When managed care took over medicine changed, and not for the better. It is the most mis-managed system I have ever seen! Of course I am not saying ALL docs are like this but, unfortunately, I have come in contact with my share who were. I was sent for consults where no info was forwarded as to why I was there, no tests that had been done were sent. That is when I learned to obtain and carry my own binder of my records. Docs became impatient with me when I couldn't answer their rapid fire questions due to the trouble I had concentrating. Few ever even bothered to listen to the response, they had already summed me up and decided the treatment course that would be covered by my insurance plan. I was diagnosed with Fibromyalgia and Hypermobility Syndrome by a physician who stood in the doorway after his intern had examined me. Because I refused to take medications I was dismissed, nothing he could offer me but come back in a month to see how things are. I could go on forever, but these are things that are known by the medical community but ignored. Try to find a local doc who will speak out about another. It just doesn't happen. I have to live and work here, at least for now. I need to bury this and go on. Sorry to sound cynical but that is how it is, at least in my area. I cannot change it I can only take care of myself, my family and my friends. I hope for a physician revolt but don't see that in the future either. Patients need to be able to take care of themselves or find someone else to advocate for them. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2007 Report Share Posted January 7, 2007 > > I look at this very simply. If I don't have a personal >relationship >with the doc, he won't see me as a person and won't treat me that >way. >Its as much human nature as it is managed care. The doc has to >manage >his time very carefully. I couldn't have established any more of a relationship with both my prior PCPs, I worked with them in both the hospital, then in their offices. The second one sought me out to offer me a position in their office, yet when I became too ill to work they couldn't see me as a patient but as an employee who was of no use to them. I tried to suggest treatment, I did research and brought in material that was not read. I was told that I researched too much and directed my care too much and at one time was even told " you will not ever tell me how to prescribe for you. " That is probably why when I asked for the nephrology referral it was delayed. I had also asked for help in finding a place that would evaluate me as a whole, I was willing to pay out of pocket but didn't want to waste my money. Shoulders were shrugged and no suggestions made or effort made to find what would help me. Why did I stay at all? Physician choice around here is limited, many affiliate with certain clinics and facilities I want no part of. I felt that I was better off with someone who knew me than a stranger but I have now changed that opinion. > If you are on an HMO and have the option of fleeing, do so. HMOs are simply not appropriate for complex care. Just ask my father-in- law...oh right, you can't because he died from a cancer that shouldn't have killed him but for the repeated denial of service from his HMO. > > -Jeff > I am sorry for your loss, I have also seen patients suffer needlessly We did abandon our HMO but had to wait for my husband's employers " open season " to do so. I have strongly discouraged my kids from choosing the HMOs at work, I hope to see their power reduced in the future, some patients are becoming fed up with the restriction on choice of physician and necessity of referrals. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2007 Report Share Posted January 7, 2007 > > > In a message dated 1/6/07 3:28:21 PM, shotzie@... writes: > > > I feel it is time to move on as it only upsets me to see all the > > indifference out there. Doctors need to take back their practices, > > too many have become complacent, only follow the dictates of the age > > specific health practice guidelines given to them by the insurance > > companies. > > > " All HTN guidelines state how to evalutate low K and HTN. > US HTN eval and treatment guidelines: http://www.nhlbi.nih.gov/guidelines/hypertension/jnc7full.htm Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2007 Report Share Posted January 8, 2007 P.A. and its variants is only one of the " not well understood " diseases or conditions deregulation has allowed to " fall through the cracks " of the system. The managed care system was an early attempt to skirt strict regulation that existed before 1979 - but then Reagan (bless his otherwise recalcitrant heart) gave it to the bigger entities on a platter whose name was deregulation. The " less government " ideology may be right for may areas hobbled by bureaucratic boondoggles, but medical care? Since then, the so-called neoliberals have also taken up this pro-corporate ideology, calling it " free trade. " Bipartisan dereliction of governments' duty to protect citizens becomes non-partisan. One physicians' action group on CNN wondered, in the words of their keynote speaker, " why voters seem keen to dismantle the protections consumers and individual citizens had struggled so hard for since the days of Theodore Roosevelt? " Why the populist and progressive reforms that culminated in regulatory and administrative protection for " the little guy " were being abandoned. I wonder if many voters see a connection between their vote and the " free trade " cult that has seized many in public policy. " Free Trade " advocates " market correction " to take care of any problem. " Market " means sales. There are physician groups lobbying for reform (re-regulation of medicine, in essence, or taking the power to decide back from the pharmaceutical companies), but imagine. Re-regulation will mean more paperwork, more practitioner & institutional insurance and more " continuing education. " More costs in time and money on top of already crippling increases doctors and smaller facilities who cannot " buy big " suffer in this economy. The corporations who currently benefit from deregulation are poised for such new sales, just in case the Democrats or somebody else wakes up (or, more likely, find it the only new marketing strategy that will get the media going on something else), but compared to the amounts of money involved with patient care coverage, those new sales will be minimal. Worse, they will burden physicians and medical schools, certifying boards and research institutions more. But as long as we have something as " newsworthy " as Iraq and terrorism to distract the public (and law enforcement), how can some little 'rare disease' get anywhere in the mix? The answer - lawyers. Our unelected guardians. Finally, it will take the burgeoning civil law " contingent liability protection " sales deregulation put in the hands of mid to large-sized lawfirms and put those back in the hands of individual attorneys and their clients. Do you think the big money legal eagles will just let that go by? No, it is us, the patients and their families, the consumers who must foot the bills - even if many must die from unpopular diseases in the meantime. Dave On Jan 6, 2007, at 1:21 PM, shotzie wrote: > > > > >> > > Here's my dose of reality for the day. If anyone has better news, > > frankly I'd love to hear it. Any successful hyperaldo cases out > there > > in recent years?? > > > >> > > What you have written is what I have discovered, without permanent > damage there is no case. It doesn't matter that I was not able to > work for almost two years, it doesn't matter that I was misdiagnosed > for 13 years, and as you said, the physician who first gave me the > essential hypertension diagnosis without ever doing testing and > refused to refer after multiple meds were tried and my BP worsened > AND who ignored the significance of a 3.1 potassium on a > potassium sparing diuretic in Jan 2004...that is over two years ago, > I cannot touch him. > > The next PCP had to play " catch-up " as I was 51 and > hadn't even had a routine EKG after 10 years of HTN. My symptoms > were so severe and varied by then that I was sent to referals for > everything BUT Hypertension. > > I feel it is time to move on as it only upsets me to see all the > indifference out there. Doctors need to take back their practices, > too many have become complacent, only follow the dictates of the age > specific health practice guidelines given to them by the insurance > companies. Referral seems to be discouraged, when they can't come up > with an answer to a patient's problem they don't seek consult unless > the patient is hospitalized or lab results are significantly off > withthe patient having identifiable symptoms. > > Routine diseases, such as diabetes, seem to be handled well but > anything complex never seems to be adequately addressed at an office > visit. > > I know, I've seen it , I have worked in healthcare for 33 years. > When managed care took over medicine changed, > and not for the better. It is the most mis-managed system I have > ever seen! > > Of course I am not saying ALL docs are like this but, unfortunately, > I have come in contact with my share who were. I was sent for > consults where no info was forwarded as to why I was there, no tests > that had been done were sent. That is when I learned to obtain and > carry my own binder of my records. Docs became impatient with me > when I couldn't answer their rapid fire questions due to the trouble > I had concentrating. Few ever even bothered to listen to the > response, they had already summed me up and decided the treatment > course that would be covered by my insurance plan. > > I was diagnosed with Fibromyalgia and Hypermobility Syndrome by a > physician who stood in the doorway after his intern had examined me. > Because I refused to take medications I was dismissed, nothing he > could offer me but come back in a month to see how things are. > > I could go on forever, but these are things that are known by the > medical community but ignored. Try to find a local doc who will > speak out about another. It just doesn't happen. I have to live and > work here, at least for now. I need to bury this and go on. > > Sorry to sound cynical but that is how it is, at least in my area. > I cannot change it I can only take care of myself, my family and my > friends. > > I hope for a physician revolt but don't see that in the future either. > Patients need to be able to take care of themselves or find someone > else to advocate for them. > > __ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2007 Report Share Posted January 8, 2007 Type " most underecognized cause of hypertension " into PubMed. Do the same at TIME magazine. The medical articles written after 2003 are filled with it. Eve the AMA has coined this term. Armed thus, you can dump a pile on their desk, highlighted on the phrase " under-recognized. " They've seen lots of cases - just didn't recognize them. Besides hypertension, there are lots of other symptoms in the 'syndrome.' From Dr. Grim's summary of Dr Conn's findings : • hypernatremia (high sodium in blood) • heart rhythm irregularites thought " non-specific, " or PVC's (premature ventricular contractions, and others including a-fibs, which can kill suddenly). • intermittent muscular weakness • periodic, localized paralysis • nocturnal polyuria (peeing at night - and/or having to vacuate 2-3 times for one bladder emptying). • episodic tetanic manifestations (muscl spasms or 'tics' minus actual tetanus - a central nervous system disorder from low K) • headache (recurrent, unexplained or remedied) • hypertension that is labile (atypical periodicity when measured 4 x day B4 breakfast, lunch, dinner & bedtime, and recorded) • alkalosis (excess persipring, white powder residue) • alkaline urine w/mild proteinuria (24-hr test) • positive Chvostek and Trousseau signs (calcium metab. spasm, 'pins & needles' gotten easily) • LVH (left ventricular hypertrophe - too thick or stiff muscle) • anxiety/depression not following situational causes • sleep fractionation - restless leg syndrome, multiple wakeups at night (Dr. Jerome W. Conn, after whom is named " Conn's Syndrome " ) Dave On Jan 5, 2007, at 2:12 PM, shotzie wrote: > Dr Grim > > You constantly comment that we should all educate the medical > providers we have come in contact with. > > I have tried to be an informational source for all medical personnel > I come in contact with. I reported my previous PCPs for their > negligence in finding a cause of my rising and uncontrollable BP and > steadily falling K despite good diet and supplementation. I sent > them info while I was being tested by the nephrologist and met > resistance from them causing me to leave their practice. They could > have killed me by forcing me to take diuretics with a low potassium > level while I had all the symptoms of hypokalemia AND they delayed my > referral to a hypertension specialist. > > I wrote a detailed complaint to my HMO before my surgery. They > dragged out my authorization for surgery for over a month, they > refused to pay for the AVS although, to this date, I haven't been > billed. It is supposed to be up to the physician and facility > performing the procedure to provide the info to dispute the denial of > payment. We'll see, that bill was 27,000. > > I sent your article along with Dr Young's article to the HMO before > my surgery and I spoke with a local case manager so I would be spared > the aggrevation of more denial of treatment. > > Today I received a letter that my HMO referred my case to a > " Healhcare Recoveries " agency that tries to prove that the payment > should be made by someone other than them. The women at that agency > had absolutely no idea what PA was or why an adrenalectomy was needed > She stated that they wanted to be sure it hadn't been caused by and > accident or injury!!!! > > I called my former HMO, we changed to a nationwide plan with no > referrals starting this month, I will never go through that nightmare > again. > I asked if my complaint had been acknowledged and I asked why my case > had been sent to this other agency. I commented it seemed that no > one there was aware what my disease was and that the surgery was a > cure of the disease. I got bumped to another person in the complaint > dept and had to leave a message. > > I am so tired of trying to explain myself to the rest of the medical > world. I seem to be cured which should be vindication in itself. > No one yet has admitted that I even had a delay of care or a > misdiagnosis. So much money was wasted sending me to specialists for > other things and I lost two years of income because I was too ill to > work. " Oh well, that's life " is the response, at least someone > FINALLY caught it. > > You also mention lawsuits. No lawyer wants to take this on as a case > since I do not have any documented permanent damage. I will work > again, I didn't stroke or have a heart attack although I had LVH and > mild retinopathy. They want big settlement cases. I am an > insignificant individual with a " rare " disease. Can't blame the docs > for not finding it, it really doesn't exist. > > I don't know how you can change the general concensus that Conn's > isn't out there, it is just something you read about. When it is in > front of their faces few still acknowledge it. You would think that > the doctors would be eager to see an actual case, so far only the > endocrinologist in another city seems at all interested. The > nephrologist also seemed to be interested but he left the area > suddenly with no explanation. He was the only one locally who gave > my symptoms and complaints any deep consideration. > > I am ready to go on with my life, I have printouts of everything to > give to my new PCP who I have yet to meet. The endo is managing > follow up labwork. I only need the local PCP for routine care. > I hope she is interested in PA and Conn's, we'll see. > > __. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 In a message dated 1/8/07 1:16:12 PM, riothamus20@... writes: I have tried to be an informational source for all medical personnel >Â I come in contact with. I reported my previous PCPs for their >Â negligence in finding a cause of my rising and uncontrollable BP and >Â steadily falling K despite good diet and supplementation. I sent >Â them info while I was being tested by the nephrologist and met >Â resistance from them causing me to leave their practice. good judgement. They could >Â have killed me by forcing me to take diuretics with a low potassium >Â level while I had all the symptoms of hypokalemia AND they delayed my >Â referral to a hypertension specialist. Dont like to admit they dont now about HTN. Everybody thinks they know about HTN but few have received much specific exposure to the details of high blood pressure. Also not many HTN speicalist for the 65 million folks with HTN in the US. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 In a message dated 1/8/07 11:50:32 AM, riothamus20@... writes: What you have written is what I have discovered, without permanent >Â damage there is no case. What we need to find then are some of the following: 1. Persons whos high blood pressure that was missed by bad measurement who then developed a stroke or MI or went on dialysis or got CHF. 2. Persons whos high blood pressure was falsely diagnosed becasue of bad measurement who then developed serious complications from drugs being used to treat a disease they did not have. 3. Persons who had a cardiac arrest due to low K. etc. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 In a message dated 1/8/07 11:50:32 AM, riothamus20@... writes: Â Routine diseases, such as diabetes, seem to be handled well but >Â anything complex never seems to be adequately addressed at an office >Â visit. HTN is about 4 x more common than diabetes. So it should be VERY routine. A Dr who is not an expert in HTN cannot be a good Dr. May your pressure be low! Clarence E. Grim, B.S., M.S., M.D. Specializing in Difficult to Control High Blood Pressure and the Physiology and History of Survival During Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 9, 2007 Report Share Posted January 9, 2007 The coroner's office would be a good place to start. Dave On Jan 9, 2007, at 9:28 PM, lowerbp2@... wrote: > > In a message dated 1/8/07 11:50:32 AM, riothamus20@... writes: > > > What you have written is what I have discovered, without permanent > > damage there is no case. > > > What we need to find then are some of the following: > > 1. Persons whos high blood pressure that was missed by bad > measurement who then developed a stroke or MI or went on dialysis or > got CHF. > 2. Persons whos high blood pressure was falsely diagnosed becasue of > bad measurement who then developed serious complications from drugs > being used to treat a disease they did not have. > 3. Persons who had a cardiac arrest due to low K. > etc. > > > > May your pressure be low! > > Clarence E. Grim, B.S., M.S., M.D. > Specializing in Difficult to Control High Blood Pressure > and the Physiology and History of Survival During > Hard Times and Heart Disease today. Quote Link to comment Share on other sites More sharing options...
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