This gallery contains 59 photos.
A wealth of information to us all about the corrupt healthcare system and clueless doctors–or actually in this case criminal acts on the part of doctors! Please share!
This gallery contains 59 photos.
A wealth of information to us all about the corrupt healthcare system and clueless doctors–or actually in this case criminal acts on the part of doctors! Please share!
This post has nothing to do with clueless doctors but a lot with clueless people.
I have joined LinkedIn while I was still a student at Stanford and LinkedIn just started. At that time it was a fun site for networking and finding jobs. Over the years it has become more of an information exchange place as well but still remaining within the circles of the particular professionals of the subjects being discussed. Anyone can start a conversation and henceforth that person is immediately what is called a “group moderator.” Being a moderator means that any person of the moderator’s dislike may be moderated out of the group–moderating out pretty much means banned in this case, albeit you may stay in the group, but you cannot open your mouth without the moderator checking out if what you said was to his or her liking.
At one point of my career, about two years ago, I was invited to join a group discussing photography that stirred up my interest in a new kind of camera they were discussing. The group owner was a guy who moderated about 15 other groups, owned and bankrupted about 10 firms, attended 10+ colleges but never got his PhD hard as he tried but in his opinion he “had earned his PhD” and that was that–these are all on his personal bio.
So when I joined the group and the conversation, the topic of PhD came up–I no longer remember the circumstances–but he started to feel stifled that I had a PhD for real, while he did not so he did not like the color of my eyes and I was moderated out no matter what I said. All is well you say; he has the right to not like me for having a PhD. What you may not realize is that he moderated me out of the entire LinkedIn, globally!
Yep, LinkedIn is set up in such a way that a single moderation in one group will lock you out of all other groups. There is one group that is in fact for those alone who have been moderated out of other groups and there are hundreds of people in there. I know many people who start their own groups because they were moderated out of all others and that is the only way they can communicate with people of like mind and interest!
Thus a single person with questionable motives can moderate every single member out of every single LinkedIn group by a single click on the button per person!
So write a note to LinkedIn you say? Complain? Yes… I did.
I have been writing now for over two years, getting absolutely nowhere and still not able to comment anywhere. Today I tweeted to the CEO of LinkedIn to change this and today I officially filed a BBB complaint. If it comes down to having to sue them, I may start a class action lawsuit against LinkedIn with all those who have been moderated out of all conversations by a single person who did not like the color of their eyes!
It is ridiculous how LinkedIn has this moderation set up that a single person can kick every single other member out of basically any activity based on one comment that he/she may not have liked, or like in my case, a personality trait. I even wrote to Linked in that this person harassed me–I have emails of that for proof… no one gave a damn!
Well let us all change that! And let us start changing that now! Join the group I just created called OutModerated. 🙂
While I wrote the book, I tried hard as I may to incorporate all migraine types since migraine affects the brain initially the same way and for the same reason: the brain cells’ (neurons’) lack of ability to work as a result of inappropriate quantity of voltage generating and hydrating ions. Simple you think; just add more.
While the book’s method works very well for people in the US, I find that in the case of two other countries, UK and Australia, where there seem to be enough life style differences in comparison to the US, the standard method does not appear to work effectively. At the time I wrote the book, I tried to join migraine groups of these countries but it seemed that they were not interested in an American scientist and what she had to ask or say and so I never really had the chance to understand these differences.
The Fighting the Migraine Epidemic book by now has achieved quite a bit of success with US migraine sufferers will create a testimonials link as soon as I can. However, it has not yet been as successful in the UK and in Australia. Part of the reason is that people in these countries seem to have different types of migraines! In the US most migraines are classic (just horrendous pain, sick to stomach, dizzy, etc.,) or complex (comes with aura as well). Only a fraction of a percent of the US migraineurs has what is called a Hemiplegic Migraine. This is a form of migraine that starts typically with a blind spot and aura as the complex does but then it progresses into muscle weakness to downright muscle paralysis of one side of the body in whole or in part.
Hemiplegic Migraines are a lot more serious migraines than classic or complex ones because there is a higher risk of stroke and seizure with possible permanent effects.
What may be the reason for the US having fewer Hemiplegic Migraineurs than the UK or Australia?
Migraine is genetic but genes mean nothing until their switch is turned on–the gene gets expressed. It is unknown at this point if a particular type of migraine is represented by a particular type of gene or if particular lifestyles turn on a gene in a different way at a different time–we do have information on several types of genes in Hemiplegic Migraine cases but not everyone with those genes comes down with migraines, and if they do, not everyone comes down with Hemiplegic ones. It is not clear from the point of genetics how and why a migraine becomes Hemiplegic.
Now the book is also available in the UK and in Australia. Since I encourage private conversations with my readers to make sure they have no other health conditions that may interfere with my recommendations, I have been able to obtain more information on the possible causes for why people in the UK and Australia suffer different migraines and why those migraines are not responding as well to the standard US treatment.
Thus I am writing this note to those who live in the UK or Australia.
One of the reasons why the standard methodology in the book is not working as well in these countries is that some of the minerals, such as salt, are not available in many of the foods in these countries. I was talking to one of the book users in the UK and I suggested that she buy some crackers with salt. She advised me that there are no more crackers with salt in the UK and the whole country is salt free. Furthermore there are no sport drinks without artificial sweeteners, etc. Artificial sweeteners can often be migraine triggers. Also, since they are toxins the body doesn’t know what to do with, they may leave the brain with serious problems (you can read about it in Fat Chance by Robert H. Lustig). It seems that the whole country of the UK went salt free and sugar-free in the name of “health” creating a huge migraine epidemic of a very serious kind that cannot even be easily remedied because of the lack of availability of proper minerals in everyday food items. Yes, heart health is a concern but even the heart cannot function without salt–it too has pumps that depend on salt. Lack of salt can have immediate, adverse consequences and can even be fatal in a relatively short time, whereas too much salt may be harmful (not lethal) in a long time, over 20-40 years. Which would you choose?
Furthermore, in the UK in particular, the first line of treatment for any migraine is still vascular, meaning vasoconstrictors (drugs that reduce the size of blood vessels to increase blood pressure) or vasorelaxers (beta blockers and similar that reduce blood pressure). There are two problems with this approach:
So if you have migraines in the UK or Australia, please note that drinking tea means a ton of caffeine that reduces blood volume while increasing pressure and constricting the veins. This is a major problem since anything with caffeine is diuretic-it chases water out of the body. Thus people in these countries who suffer from migraines are so dehydrated and the drugs they often take are so much the opposite of what they need, that this alone would explain the frequency of Hemiplegic Migraines in comparison to the US and why the process described in my book does not have a chance of working as effectively.
My book assumes that each person knows how much water to drink a day–there are plenty of apps for smart phones and also plenty of online calculators. I, for example, need to drink 10 glasses of water in the winter and 12 in the summer based on my location (hot and dry), age, elevation, physical activity, etc., and that I neither drink alcohol nor soft drinks or tea, only one small espresso a day.
When I ask UK or Australian people how much water, soft drinks, coffee, tea, alcohol they drink, I get answers like: I drink 2-4 glasses of water a day, 2-3 glasses of soft drinks, 2-3 teas, 1 coffee, and I may have an alcoholic drink a day.
Since soft drinks have some salt, they are halfway diuretic because of the sugar or sugar substitutes: tea, coffee and alcohol are fully diuretic. So for each cup of tea, coffee, and alcohol, there better be equal number of cups of water added just to make up for their diuretic effects and a half cup of water for each cup of soft drink. Thus, someone drinking 4 glasses of water and 3 glasses of soft drinks, 3 teas, 1 coffee, and 1 glass of alcohol, is drinking negative 2.5 glass of water–that is, rather than gaining the body is losing water.
In terms of the other minerals in the book, like salt, my book assumes some salt in the diet since the US diet is full of it. If food in the UK and Australia is without salt, just to be at the US baseline for my book, salt must be added.
Yesterday I asked a mom from Australia, whose daughter just had her first episode of Hemiplegic Migraine, what food her daughter eats and her response was: oh she eats a very healthy diet. Yep… healthy diet typically means minimal salt. Vegetarians are the most likely to get migraines and be dehydrated since vegetables only contain trace amounts of salt.
To summarize, if you are from the UK or Australia please note that the recommendations of my book need to be modified depending on how much tea you drink, artificial sweeteners you eat or drink and how little salt you eat.
Please contact me for more information and for help calculating your needs. Please join the Facebook migraine group I created or send me an email: angela@migraine-book.com
Wonderful dreamy art. Sherri is all dreams. Wonderful gallery. 🙂
I received a phone call today from the CA Board of Medicine, where I filed against many doctors who messed up during the treatment of my mother. The mess-up ended up in her death for no reason. There were many medical malpractice type issues but there was this one case I want to bring your attention to since this can happen to you any day and anywhere.
There was this one “doctor” who appears to have practiced without license as I later found out. When I filed the complaint with the CA Board of Medicine (there is a complaint form to fill out with standard questions), it included space for the license number of the doctor. I called the medical office where he was employed and asked for his license number. I was told “oh he works under doctor Y’s license number.” So I immediately knew that there is something fishy here. Next I asked for Dr. Y’s license number and I was refused.
Just so you know, the doctor’s license number is public information and they have no right to refuse to provide it. This further underlined my suspicion of stinky fish.
Thus in the form where it asked for X’s license number, knowing he did not have one, I placed Dr. Y’s name! Submitted the form and waited. I received a confirmation letter from the CA Board of Medicine confirming the complaint against Dr. Y! What??? I filed for X and not Y. Clearly X has no license so what happened here?
The CA Board of Medicine switched the names!
Meaning I filed against X who appears to not have a license and is working under the license of doctor Y. So they changed my complaint against doctor X to Y who had a license and dropped X since he was not in the database!
I sent them a fax–which the case worker said he has not yet seen–reminding them that it is X who I had a problem with and if he practiced medicine without a license, that is a criminal act, and I need to know that so I can throw his case to the DA for criminal charges. And if this is the case, doctor Y is also guilty and will have to face the law since he knowingly employed someone without a doctor’s license and sent him to act as a doctor, writing prescriptions!
I need to know this because these are federal crimes!
I had to repeat this 3 times–I hope he understood… I may have to repeat it a few more times before the CA Board of Medicine realizes that I am filing a medical fraud case against a person who is not a doctor or is acting without a license… they will not understand it because if he has no license, his name will not be in the database and will come out as “no charge against him is possible;” I bet you!
The law and all the people in it are clueless and the people in medicine are corrupt. This is a system that will be very hard to change but we must! If you have similar stories, do not let it go without action! You must do something so we can change the system. The least you should do is send me a note so I know about it. I do not use names as you can see but if no one does anything about this, the system will continue to get worse!
Please send me notes in private: angela@migraine-book.com or comment in public here or join the closed group CluelessDoctors on Facebook and post your experiences there. I am going to collect all kinds of stories to point out our clueless doctors and corrupt medical system!
Angela
I have for years been wondering why I know so many people with multiple knee replacements who would normally not do anything that would warrant even one, let alone multiple knee replacements, get them until one day I had a back injury. I herniated 3 discs in my back to such extent that I could not lay down flat in the MRI. The doctor had to send me to what is called a “stand-up” MRI, which is an MRI standing vertically and the patient, me in this case, sits in a chair outside of the MRI, sort of next to the two sides of it. It is an open MRI.
I never gave it a second thought until I started to heal and started to remember some of the things that happened and which made a huge impression on me and finally I was able to connect a few dots. Here you see the dots connect.
I back up now several years; in fact over 30 years. I used to have this pain behind my left knee and visited my doctor several times. He ran all kinds of knee tests (never a back tests!) and never found anything wrong so he just said “oh well.. go home, here are some pain killers.” I did.
Then about 10 years later we moved and the place we moved to was a very dusty one inside the house–it was a rented house on a termite hill as I later understood–and the dust really bothered my allergies so we invested in a humidifier, and then a larger humidifier so that I did not need to change water several times every day. But this humidifier was very big; it came with two huge water tanks, each many gallons. I used to fill them in the shower and carry them to the machine, load them up and go. One day, I popped my back doing this and ended up taking massive doses of NSAD medications for pain and inflammation and also going to physical therapy.
At one point the therapist set up some cage like trick where he tied himself to me and leaned back so that his weight pulled my lower half away from my upper half, letting my back get a little room between my discs so the fluid sacs could fill.
This treatment was so amazingly comforting that I remember giving this huge smile and it was only hours later that I realized that the pain behind my knee was gone!
I was still too young and way before my doctorate so I gave it little thought only I remember the moment of realization. Then came the big discovery after my doctorate when I popped 3 of my vertebrates in my back. It was at this time that the points started to connect and the knee replacements of so many people suddenly appeared in a different context.
You will not like to read what I write… so if you are looking for a happy ending, close the page. This will not have one. In fact it will end on the note of corruption.
Back to my back. When I injured my back, my left leg said good bye to me for 2 months. I was in a wheelchair. It took several additional months to be able to walk without any walking aid of some sort but part of my leg was still not feeling touch. It was at this time that I remember thinking “what would a doctor say if today, with impaired left leg, I would end up visiting one and not tell the doctor about my back. Would that doctor know it was my back?” Particularly as I started to heal and like now I only get a few toes hurting. If I went to my doctor today saying I had 3 toes on my left foot hurting and said nothing else (I am no longer in a wheelchair), would he have any ideas where to even send me to check what is wrong?
I can tell you right away that yes, they would all, without exception, send me to a podiatrist. Why? It is logical: podiatrist is in charge of pain in the foot and toes. If I have my toes hurt and nothing else, it must be my toes. Right? But if I went to a podiatrist and he looked at my toes that hurt to the touch but show absolutely no defect in any other way, would he send me to a back doctor? Absolutely not!
And here we come back to the knee surgeons who do multiple knee replacements for people who need none: what is their interest to send that patient to a back surgeon even if the pain is actually caused by a pinched nerve in the back? It is money out of their pocket! If they get paid for a knee replacement by the insurance company of the patient, why would they not offer to give one? The Hippocratic Oath says nothing about not replacing a knee that is healthy. It does not harm the patient. It does not cure the patient but causes no harm! And the knee surgeon can get paid. If the knee surgeon sent the patient to the back surgeon, the knee surgeon would get no payment. It is not in his/her interest to send a patient to another doctor!
This is why my doctor–as good a doctor as he was–had no concept of checking my back when the area behind my knee hurt! There was nothing in there for him to send me to a back surgeon–and perhaps he did not realize that it was a pinched back nerve either, since he was an internist. An internist would not have to know–or should they? I think they should. Bu they are not treated and paid accordingly and so they do not make the effort.
Is this legal? Absolutely! Do we all pay for it? You bet. We do pay in multiple ways: First we pay because many people who get these knee replacements (or hip replacements for that matter) are medicare patients and the tax payers pay for medicare. Secondly we pay for it because none of us gets proper medical treatment and we remain sick and get sicker. And we also pay for it because we keep alive industries upon industries that are not needed.
If there were only 2 knee replacements and 2 hip replacements needed per year, it would not have to be a specialty by thousands of doctors who make their living out of it. Of course if the medical system worked fine and we all got healthy faster, there would be less need for doctors and so the oversupply we now have would mean longer unemployment lines. It would also mean less money to insurance companies since healthy people pay less than sick people do so many jobs would also be lost there! Medical schools would suffer since fewer students would apply to a field that is over saturated already. And finally the pharmaceutical industries would take a huge blow since healthy people need no medicines!
Do you still believe your doctor?
I look forward to your comments and opinion.
Angela
I watched two very interesting videos today. Both perfectly align with my thoughts on the title of the website: clueless doctors. It is not so much that they are clueless–albeit many really are–but rather that they are helpless.
Quick: name one medication that cures any illness:___________________
If you cannot name one, nor can any doctor. So if doctors prescribe medications that do not cure your disease, what the heck are the medications for and why do we go to see a doctor anyway? Granted, on those occasions when you break a bone or need a surgery, yes, those may be “cures” but note those are not medicines. We do not have any medicine that cures an illness. What medicines take away are our symptoms until our bodies heal themselves.
The video above is by a doctor describing that doctors can only treat symptoms and why. All medicines treat only symptoms.
Medicines that may actually cure, like for example a new drug for Hepatitis C that was just FDA approved, are impossible to pass by the medical industry because of their price. And they are so expensive because once you are cured, you won’t need them anymore! So they must include in the price of each drug the cost of losing you as a future patient as well!
Here is another video, this one from TEDx, in which the doctor explains if medicine is really helping you or killing you.
I think medicines do more harm than good. I will enjoy your thoughts and comments!
Both videos are posted originally on http://failuretolisten.com/2014/04/06/wtf-is-wrong-with-medicine-tedx/ and I shared from there.
Originally posted on May 17, 2014 by Angela A. Stanton, Ph.D.
Revised on March 2, 2019 by Angela A. Stanton, Ph.D.
I posted this note in my FB migraine group, so you are all aware of a few important things when you start your recovery from migraines. Some of these points assume you are familiar with the book I am talking about so if you are not, please consider reading “Fighting The Migraine Epidemic: A Complete Guide: How To Treat & Prevent Migraines Without Medicine” (available e-book and paperback)
Assuming you read the book, please make sure you follow these guidelines: Continue reading
A story for you that is hard to believe. It starts sad and then it becomes really ugly so stick with me until I get to the point. My mom died in April and of course, lots of malpractice, incompetence, ignoring power of attorney, wrong drugs without permission, etc. These stories for another day but I now want to introduce you to another subject.
My mother belonged to a large HMO through a major senior organization in Southern California–not giving names but I am sure you know what I am talking about. Few seniors do not belong to this HMO. After my mom died and I received all the medical records from all the hospitals, skilled nursing, etc., (for a lot of money mind you!) I started to suspect that something is not right.
Today I received a call from another woman who went through the same thing–with the same hospital in one case–with the same outcome: dead mother for no reason. She had something I did not have: Medicare summary copies of medicines and treatments her mother received so she could see that there was fraud. The hospitals charged Medicare for things her mother (blind and demented) could never do, medications she never got, etc.
She tried everything and though she could not break the system, she educated me on what so far she has learned. Well. Let me tell you this is not pretty!
On her urging I called the Senior Medicare Patrol in Orange County who dutifully will investigate all charges that were submitted by individuals to examine hospitals and medical providers in what they submitted to Medicare and then compare those with the data files of the patients to find discrepancies–sort of like a Medicare watchdog. Awesome. Great service! So after we talk, I called Medicare and gave them my mother’s information and asked them to send me the medicine and treatment records they have from the hospitals so I can compare what she got versus what was claimed on the medical records and then, like an autumn fly, I hit the hard wall of stupidity.
I call it ADA, short for “absolute dumb act,” on the part of both Medicare and also on the part of the California legislature.
First let’s look at Medicare’s dumb act: when someone dies, Medicare immediately purges all records so there is no chance in heaven or hell to find out what medications and treatments were claimed by hospitals or doctors and what the deceased actually received. This is an amazing opportunity for fraud and I bet your pants off that there is plenty of fraud as a result. There is just simply no way to check who received what and what was claimed–this is invitation to cheat as you like.
Dumb act two is even dumber: HMOs file to Medicare in “bulk” meaning that if they have 15 patients who receive morphine, they will bill Medicare for 15 doses of morphine but Medicare will have no clue who actually received that morphine–perhaps no one did! So in theory, any HMO hospital or medical center can claim any amount of any expense of any drug given to any patient for reimbursement that they have never ever given to anyone!
Are you angry? You must be! It is your money these HMOs are taking! It is your tax dollars they are spending–no wonder our government is bankrupt! I will open my window and yell as “I am mad as hell and will not take it anymore!” until I can get the ears of someone who can help me change the system!
If you have information of any kind that is helpful so I can start breaking the system down, please send a note, email, comment, whatever. I want this ADA to end!
Angela
This story does not appear perhaps on the surface to have anything to do with clueless doctors but it does… Prozac? Really? How clueless is that! She was priceless.. her doctor is clueless.
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