FAXING HEALTH INFORMATION TO THE WRONG PEOPLE

Nova Scotia – 2006 – 2016

For over 10 years dozens of highly sensitive mental health records were faxed to Lisa Belanger’s Bedford spa; faxes which should have gone to a mental health referral office. “She estimates she receives between eight and 14 a year.” (1)  She contacted the doctors offices that sent the fax, and “an official at the former Capital District Health Authority, hoping someone there would take action to stop it.”(1)  They said memos were sent to all doctors offices telling them to carefully enter fax numbers and to have “the proper preset fax number on the fax machine” (1)  But Ms. Belanger continued to receive faxes.  Really, how hard is it to preset a fax number?

“She says she subsequently called Health Minister Leo Glavine’s office, the College of Physicians and Surgeons and the office of Nova Scotia’s privacy commissioner.” (1) * “Belanger was concerned about the personal information on the documents.” (5)  She said “she’s been repeatedly assured by health officials the problem would be fixed, but the faxes continued.” (5)  “She has even made suggestions on improving the way faxes are transmitted.” (1)  Finally, in 2016, in frustration she contacted the CBC. (5)

“Everton McLean, a spokesman with the Nova Scotia Health Authority, said doctors are independent and the authority can’t tell them what to do.” (1)   And yet, “Nova Scotia’s Personal Health Information Act says it’s an offence to fail to protect personal health information in a secure manner. Anyone found guilty may be subject to a fine of up to $10,000 or imprisonment for six months, or both.” (1)  I think if you start enforcing the law there would be change.  Also, doctors are paid from tax dollars so, I believe, the government can put conditions on receiving those funds.   “Halifax privacy lawyer David Fraser” said “‘The larger concern for me is the apparent casualness with which these documents are being faxed and also what seems to be the response when they’re told that they’re going to the wrong place,”‘ Fraser said. (1)

When this issue hit the media, the privacy commissioner started to pretend to do something (they do like their name in the media). Privacy commissioner Catherine Tully made recommendations (5) which the doctors are free to ignore.  In fact, I suspect that most doctors aren’t aware that a report was written much less read it.

 

“Tully said if the information had ended up in the hands of someone who knew the patient, the harm would be ‘close to irreparable.'” (5) We don’t know that some unreported mis-faxed information hasn’t gone to people who know, or will know, a patient and the patient just hasn’t heard about it.  We only know about the faxes reported to the media.

“Privacy commissioner Catherine Tully wrote in a report… that momentary inattention and human error by those sending the faxes are to blame for the three cases her office examined.” (5) But, between 80 and 140 faxes went to Ms. Belanger’s spa over 10 years.  Were all these human error?  And, at what point, does human error become incompetency or just disregard for people’s rights?

“The report says doctors notified each of the patients whose privacy was breached.” (5) Were these just the patients in the three cases Tully received or all 80 to 140 patients whose personal/health information was received by Ms. Belanger?  The report also does not say when or how the patients were notified, nor is there any verification that it is true.  A victim of the breaches, whose name was not given, said “he only learned of it this week when Belanger herself contacted him to say his information had been faxed to her last fall.” “‘This is pretty serious stuff,” he said. “This can ruin people’s relationships, careers, a whole myriad of things.'” (2)

As of June 1, 2013, “’The Personal Health Information Act does require that notification goes to somebody,’ (bolding mine) said Robert Bay” (a Nova Scotia privacy commissioner spokesperson).   “So the question is: Is the notification to the individual whose privacy has been breached or is the notification to our office? The determining factors are the degree of harm or embarrassment that would result from the breach.” “He says if the” ‘custodians’ “who hold the personal information”, the doctors, “determine there is no potential harm or embarrassment, then the person whose information was mishandled may not be told.”  “The commission said it has no way of knowing how many breaches resulted in notification to patients.” (2)  In essence, unless the commissioner has been notified, they have no way of knowing if anyone was notified.  And, why would you notify the commissioner if there is no potential of harm or embarrassment to the patient and not when there is?  Why are the doctors given the right to make this decision?  Isn’t that a conflict of interest?  How often do you think doctors will decide “no harm done” and not inform patients that their privacy was breached and not inform the privacy commissioner.  Not that notifying the privacy commissioner is any great help.  All they can do is write a report and/or encourage/recommend as they have no enforcement powers.

 

North West Territories – 2010

On four separate occasions, in a two month period, confidential files were mistakenly faxed to the CBC from the N.W. T.’s main hospital. If this weren’t so serious, it would be funny.

The hospital then imposed a faxing freeze “on any medical documents unless it is an emergency”. (4)

“In addition to the freeze, the hospital has also implemented a temporary policy requiring two staff members to oversee the faxing of confidential documents, Lewis said” (CEO of Stanton Territorial Hospital). (4)

“This ‘double-checking’ policy, which is meant to ensure the faxes reach the right destination, will stay in place until a permanent solution is found, she said.” But, as usual for the government, “she wouldn’t give specific details about any measures being taken”.(4)

In 2012 the CBC received its 6th sensitive medical fax in two years. (6) This came from Kugluktuk, Nunavut health centre.  “The fax included information about the patient and their sexual health history.”  “In a statement, the department said it’s investigating. It added that health centres are required to use pre-set speed dials for confidential patient referrals”.  (6)

“At the time, Health Minister Tom Beaulieu said a summer student sent that fax. The department has not yet said if any action was taken, or why the faxes continue to come to CBC North in Yellowknife.”  (6) It certainly illustrates how important privacy is – the faxes continue and very sensitive patient information is given to a summer student.  But the government/medical business will tell you that it takes your privacy very seriously — just propaganda.

 

Alberta – 2014

“Entering incorrect telephone numbers into fax machines is being blamed for more privacy breaches of personal health information by Alberta Health Services.” (3)

“Documents obtained by CBC News through access to information show that Alberta Health Services were regularly (bolding mine) sending faxes intended for Strathcona Home Care to a custom home builder in Sherwood Park over a two-year period.” (3) “At one point the builder was receiving as many as one fax each week.” (3)  “Despite repeated calls, the faxes continued until company owner Dianne Ingram sent AHS a fax of her own.” “She scrawled, “You have the wrong fax number!! Stop faxing us!!.” (3)  Also faxes were sent to a manufacturing company. (3)

“Patients often go uninformed when their information is disclosed.”  (3)

“While AHS is not obligated to report breaches, Hamilton (Brian Hamilton, with the Office of the Alberta Information and Privacy Commissioner) said his office encourages AHS to inform all patients whose privacy has been breached.” (3)  Sorry, but, in my opinion, “encourage” is essentially meaningless.

“’This is highly sensitive information and an issue of public trust,” privacy commissioner Frank Work said. “How can the public have faith in public bodies if they can’t provide security for personal information?”‘ (7) (Bolding Mine). He was referring to laptops but it is just as relevant to faxes.

‘”It’s surprising,” Hamilton said during an interview. “The health sector in particular, spends millions of dollars on information systems with secure access, and yet people keep faxing.”‘ (3)

“Sending personal information by fax is a less secure method of transferring information compared to encrypted emails, he said.” (3)

Dr. Verna Yiu, with Alberta Health Services said “We do rely on cooperation of the recipient to let us know that” (they have received a mis-fax), “and I would have to say that in general (italics mine) people are pretty co operative about that.” (3)  This is NOT a privacy policy.  This is NOT how you protect patient information.

 

Some Questions:

  1. In all these cases, the doctors offices, violating patients privacy, were not identified. Should they be? Would you want to know who is not taking care of your information?
  2. Most people who violate people’s privacy are either not disciplined, disciplined (ex. A day or more off without pay), or fired. Should the penalties be stiffer? Do we have a right to know what disciplinary action is taken under what circumstances so we can determine if this is sufficient or excessive?
  3. Don’t you think THE PATIENT should be notified in all cases so the PATIENT can decide the degree of harm in violating the patient’s privacy?
  4. Should there be a central phone number that people can call when they receive medical information that belongs to someone else?

You may have noticed the trend by the government/medical system: it’s someone else’s responsibility, there is nothing we can do, false promises to fix it or we’ll look into it but the people never hear if anything was ever done to fix the problem.  And if it hits the media, the “problem” is sent to the privacy commissioner, who writes a report.  The report may say “Order No.” but it is not an order, it is a recommendation which the medical system is free to, and I suspect in most cases does, ignore.  So what changes – NOTHING.  Mistakes are made, and I think people would be mostly forgiving, if they knew concrete steps had been taken to fix the problem.  Instead we get propaganda – we’ll fix it, trust us, trust us.  Save the money from all these useless, money-sucking,, reports and put it into software/training for something positive such as end-to-end encryption and enforcement; privacy might be protected and money saved.

And, these violations are only the ones that are reported to the media. These are, no doubt, the proverbial tip of the iceberg.  I suspect there are some medical people who are very careful about patient’s privacy.  But, we don’t know who they are, therefore all are suspect.

I am deeply grateful to Ms. Belanger and Ms. Igram for sharing the information with the media; and to CBC News for publicising the problem. It is the only way we are learning that our information is not protected.  And, until we know the truth, we cannot try to fix the problem.

* I contacted a Minister of Health, Victor Boudreau, twice and requested an organizational chart/description of the health system in a province (who reports to whom and what are their responsibilities). Never got a reply (see future post tentatively titled “My Story – Part II).

 

  1. Mental health records sent to Nova Scotia spa in error over last decade – Yvonne Colbert, 07 Apr 2016, CBC News
  2. Victim of mental health privacy breach in Nova Scotia feels “very exposed” – Yvonne Colbert, 08 April 2016, CBC News
  3. Unsecure faxes put health data of Albertans at risk – Kim Trynacity, 10 Feb. 2014, CBC News
  4. N.W.T. Hospital clamps down on medical faxes – 07 Jul 2010, CBC News
  5. Privacy commissioner says doctors should move faxing patient referrals – Yvonne Colbert, 23 Nov. 2016, CBC News
  6. CBC Yellowknife newsroom gets 6th medical fax in 2 years – 30 Jul 2012, CBC News
  7. Security on stolen laptops was inadequate: privacy commissioner – 24 Jun 2009, CBC News

 

COLLECTING MEDICAL INFORMATION (OR NOT) – MY STORY

I started to get copies of my medical information that I didn’t already have.

(1). My primary doctor’s office first demanded to know why I wanted a copy of my records.  I told them “because I want them”.  I didn’t feel I needed to provide an explanation; a reasonable office employee told the other to just give them to me.  But the other one said that I would have to talk to the office manager, who wasn’t in the office.  I finally contacted her and she said some of the records might be stored in the back and they would have a hard time getting them.  I asked for them anyways.  In fact, if she had checked the computer she would have known that I had started seeing the doctor after they started computerizing their records.  But some doctors do all they can to avoid giving out copies of records to patients.

Then she demanded to know why I wanted the records. She said there were different prices depending on whether they were for me or for my lawyer.  I asked what the difference in price was and she refused to tell me.  Is it legal to charge different prices for the same thing (assuming she was telling the truth)?   And are they legally allowed to refuse to give me a copy of my information unless I tell them why I want it?  Are they legally allowed to do everything they can to discourage me from getting a copy of my records?  Oh yes this is the medical business who don’t seem to care about the law, unless it suits them.

All my information was, if fact, in their computer. My primary doctor charged $27 and as the office manager said, they just printed it off the computer; is this expensive paper, another way to discourage people from getting their records or just a money grab?  My medical records were put in an envelope, unsealed, and left at the front desk for a few days;  Staff and patients are all round the desk.  Another middle finger given to privacy.

I was delayed picking up the envelope because I wanted to pick up this information and the “d”’s at the same time. Of course, I had expected the envelope to be sealed.

(2) The first surgeon I had seen refused to give me a copy of the information that had been collected.

(3) No problem with my surgeon. I just had to go in and sign off at the desk that I had received the copies which was fine.  Except that there had been communication between the surgeon and the “d’.  The surgeon wasn’t sure the information could be released without the other doctor’s approval so he didn’t give it to me (he could have just phoned the “d”).

(4) I phoned the “d”s office and asked for a copy of my medical records and if he gave my information to the registry.  I had asked my primary doctor and surgeon but neither of them knew who gave my information to the registry (or so they said).  At the “d”s office I was told that I had to make an appointment to get this information.  Now you know where some your tax dollars get wasted.  As I am entitled to a copy of my medical records I made an appointment.  When I went into his office he started taking the conversation in a different direction so I stated, again, that I just wanted my medical records and to know if he gave my information to the registry.  Again he took the conversation in different directions, probably trying to justify the visit, but when I wouldn’t play ball, he finally said essentially “So, you just want a copy of your medical records and to know if I gave your information to the registry.”  He said he didn’t have any records so apparently there was no record of my first visit or the so-called checkup.  He also said that he hadn’t given my information to the registry but he mentioned who might have.  Also, when I mentioned the communication between him and my surgeon I got the same response as my surgeon.  Now these are two people who, based on age, have been in the business for a lot of years and I would think would have encountered this before and so should know whether they could share the information or not.  In any case, he said he would check with the other doctor and get back to me.  Of course, being the medical system, he never did.  He just LIED.  It would have been interesting to find out what they were hiding.  I walked out of his office in absolute disgust, AGAIN.

I also wrote letters to the hospital and anyone else involved in my health care, requesting copies of my files. And I wrote to the appropriate organizations with questions (this included treatment in the new province).  I did not receive a response to several letters, so I mailed another copy, after a few more months and no answer, I sent the letters by registered mail.  I got answers.  Now it is possible that ONE letter got overlooked but when it happens to several letters and to different people/organizations, in the same business, it begins to look like a tactic.

Some answers I received to my questions made sense in relation to my direct health care. Others did not (I do not include those mentioned in other posts).  These are some of the non-answers from William Findlay, Michele Stanton and John Garratt:

  1. What are your living arrangements? They said that they want to know if someone will be at home when you get out of surgery. So, why don’t they ask “will someone be at home to care for you when you leave the hospital”?  You may be living with someone but that doesn’t mean that, for a variety of reasons, they will be there when you get home.  You may live alone but that does not mean you will not have someone at home when you leave the hospital?  The non-answer I got from Findlay was “yes, that is a broad question”, which means they will continue to ask the questions for reasons they refuse to state.
  2. I asked who sent my information to the registry? I was told it was nobody specific; it’s just entered from a variety of sources at the hospital. And researchers have access to this information.  My surgeon said researchers would only have access if I went for further treatment which I didn’t.  The “d” said they were only counting a number.  Now, I am being told that the registry staff and “researchers” have access to my information (no limits mentioned). You just can’t get an honest answer from these disgusting “people”.

I asked William Findlay how much of my information was put in the registry. He refused to answer and referred me to the organization that owns the agency that has the registry.  That organization refused to answer my question.  I sent letters again to the organization and to Findlay insisting on an answer since it was the hospital sharing my information.  Findlay’s secretary said, in essence, that they refused to answer the question.  I got no response from the organization.  I sent a letter to the agency and they refused to answer my questions.

I have to assume that all my information/body parts is being shared/traded/bartered with all their unsavoury friends (the only kind who steal from the vulnerable/sick people) until I hear otherwise and, so far, no one will tell me; I just get the run-around. Obviously, these vultures have something truly horrendous and very evil to hide.

  1. I asked if my DNA was shared with researchers and I provided my care card number so they could look at my file. All I got was a non-answer that researchers may access the registry. So, I can only assume that researchers have access to my DNA for their use.  Just think they could clone me (like they have done to sheep, etc.) and then throw darts at me and otherwise torture me.  Anything is possible until the truth is known.
  2. I asked if researchers, biotech companies, etc. are allowed to patent my DNA. Again they had my care card number to check my file. Again, I just got the non-answer “This is very uncommon.  Should you wish to have your DNA patented you should contact your family doctor about that”. I guess he thought that was pretty funny.  So, although I gave him my personal health number (PHN) he could not/would not tell me if my DNA was, or could be, patented without my knowledge/consent.  So I can only assume that “researchers” can do whatever they want with my DNA.
  3. I was also told that when I was admitted to the hospital I signed an admission form basically giving them permission to do whatever they want. I checked my copy of forms from the hospital and did not find an admission form. I asked William Findlay, in two separate letters, to send me a copy of the signed admission form. The question was continually ignored and I have not received a copy of the form so I have to assume that it does not exist.  But, if it did exist it would only have been manufactured consent versus real consent.  Real consent is explaining exactly how they want to use information, especially in ways that are not directly connected with my specific care, with whom they want to share the information and requesting my consent (it implies respect for the patient). Manufactured consent implies contempt for the patient — Give us everything we want or die, we don’t care, we are the medical business.

Update: I found a consent form in with the copies from my surgeon.  When asked to sign the form I said that I didn’t agree with some of the “requests”.  I was told to just stroke out anything I didn’t like, which I did.  I don’t know if this is the hospital consent form but I suspect it is.  It may be why they refuse to send me a copy because I stroked out everything that was not directly related to my surgery, such as no sharing of information or body parts, etc.  But they probably just stole the information/body parts anyways.

William Findlay said that the confidentiality and security of my information was protected under the privacy act. Isn’t that disgusting.  My information is protected under the privacy act.  Let’s see, oh yes, the auditor general and the privacy commissioner have found, on several occasions, that the privacy act has not been implemented, much less enforced in the medical business.  They found that our information was/is being shared with every low-life.  But my information is protected under the privacy act.  How?  Oh yes, and when the medical business is caught illegally sharing patient information NOTHING happens.  The management is not sued, fired or held accountable in any way.  They just promise to change things, until they get caught again.  And then they just make the same lying promise.  But my information is protected under the privacy act.  The privacy act was meant to be, and is, just words on paper to be used to misdirect and con the public.  But my information is protected under the privacy act.  What a vile farce.

One medical person, when asked for specific information, about who my information was being shared with, told me, essentially, that if I didn’t like his (general) information I could contact the privacy commissioner.  I contacted the privacy commissioner who told me that such requests were outside their mandate.  But that’s what they do, run you in circles.

I had to laugh at the arrogance/narcissism of one medical person who said that I had his assurance that my information was protected. Obviously, he was still under the illusion that the word of someone in the medical business had value, that he could be trusted.  I wish that were true but it isn’t.

As for that registry, well, I tell people I wouldn’t give that organization my spit. But then they have probably STOLEN that too.

I received a letter from the staff of a doctor telling me that the doctor would like me to phone as the doctor had something to say to me. I asked that the information be sent in a letter.  I never heard from the doctor/staff again.

If I could trust the medical/government business I wouldn’t have to ask the questions. But they have proven they are not trustworthy.  And, if they were trustworthy, I would have gotten honest, complete answers, not non-answers, run-arounds or just blatant LIES.

So, now they have all this information on me, the truth and the lies. It will be shared with every scumbag because, in my opinion, that’s the only type that would access a patient’s information without their knowledge and/or their real consent.  Collecting information “anonymously” has been proven too many times to be another lie.

Again, I state, I am not against research, if done with respect. I am against stealing people’s information because only unethical, immoral fiends would do this.  If you can’t ask for information honestly, if you refuse to state who is using this information and for what purpose, if you have to hide in the shadows, in the gutters, then you must be doing something corrupt, vile and contemptible.

From the Open Society Justice Initiative, printed by the Office of the BC Information and Privacy Commissioner, Right to Know Week, September 28th to October 5th, 2007,:

10 Principles that form the core of the right to know:

  1. Access to information is a right of everyone.
  2. Access is the rule – secrecy is the exception!
  3. The right applies to all public bodies.
  4. Making requests should be simple, speedy, and free.
  5. Officials have a duty to assist requestors.
  6. Refusals must be justified.
  7. The public interest takes precedence over secrecy.
  8. Everyone has the right to appeal an adverse decision.
  9. Public bodies should proactively publish core information.
  10. The right should be guaranteed by an independent body.

Just words on paper. Sounds good but not worth a damn because the medical/government business will not implement it.  But the privacy commissioner’s office likes to print it because it makes them look like they care.  Just propaganda by the government.

Simply put, privacy refers to an individual’s right to remain anonymous or control who, how, when, and where information that is used to identify them is managed. (source unknown). And we have a RIGHT to privacy, this is our information not theirs but these people flip their middle finger at our RIGHTS.

I still have to see medical “people” periodically, whether for healthcare or outside the medical business. But I don’t have to like them, I certainly don’t respect or trust them.  I look at these cannibalistic cowards who feed off the patients, whether it’s a pharmacist/technician/researcher/physician, etc. (with one or two individual exceptions) with the same disgust and contempt that they have for the patients.  The difference is — I don’t mask it.

COMPLICIT

If you have to lie, steal, and con to get information, then what you are doing is neither moral nor ethical.

I believe that everyone who knows about the lies and the theft of our information and body parts, and does nothing, is complicit.

I thought at first that these people might be pawns but, in fact, they are willing participants in the lying, conning and theft of our information, our body parts.

I was taught when I was a child that you don’t pick on those younger, weaker, more vulnerable; that’s only for cowards.  I have to assume that the people in the catholic/medical/government business and all they accomplices have yellow streaks up their front, their back and their sides.

Someone told me, when I was in front of St. Paul’s, that these people were just getting a pay-cheque, jobs were hard to find. Well, that’s what any thief would tell you  — it’s just a job.  The same for a hit man/woman, who just take the money and carry out the dirty deeds.  What you are doing is still unscrupulous, unethical and possibly illegal.  And if you are just getting a pay-cheque then there is no caring or compassion in what you do.  You do not care about the patients, only yourself.

I was told that I had a lot of support in the medical business for raising awareness of what was going on in the medical business.   Is this true?  I don’t know.  But, even if it is, verbal support, especially hidden, isn’t enough.  You have to DO something.

A few people did provide me with information, usually without evidence, so I had to be careful that I wasn’t being setup. But, for those who gave me information, it shows you care but you, and the others, need to speak louder.

Dr. Warren Bell, Salmon Arm, BC wrote Doctor’s Diagnosis: Pipeline Symptoms of “Social Pathology”, 04 Feb 2013, TheTyee.ca.  He states how he helped found the Canadian Association of Physicians for the Environment or CAPE because they wanted to improve health by improving the environment.  I find what I consider to be his hypocrisy mind-boggling.   “A 2007 Canadian Medical Association survey showed that 11 per cent of patients already admit to holding back information from health care providers because of privacy concerns.

A 2012 survey “indicated that 43.2% (of patients) have withheld or would withhold information from their health care provider because of privacy concerns, while 31.3% of Canadian patients have or would postpone care over privacy concerns, and 42.9% would seek care outside their communities for the same reason” [Medical privacy breaches rising, Roger Collier, 06 Mar, 2012. vol. 184 no.4, Canadian Medical Association Journal CMAJ)]. And I expect these numbers will continue to increase.  And note this refers to patients.  How many people don’t just hold back information but don’t even see a doctor because of privacy concerns?  But, do you see the doctors founding an association to “Protect People’s Health by Protecting Their Privacy Rights” so they can improve health.  NO.  And this is an area where they are largely responsible for the loss of privacy and trust.  So, what is it that they don’t want to give up to protect patients health; Is it pay-cheques, is it kickbacks, an attitude of arrogance/narcissism that patients privacy is irrelevant to medical people?

But getting on the bandwagon of promoting the environment, and other issues, distracts the people from the fact that the catholic/medical/government businesses are adversely affecting people’s health by violating their privacy. I think it’s a diversionary tactic.  The pope is doing it and it diverts people’s attention away from the paedophile issue.  It’s purpose is the make the medical people/pope look good and it doesn’t cost them a thing.  They don’t have to change what they are doing, or give up anything.

Dr. Bell writes about the “structural pathology” in the governance system in Canada. But he ignores the “structural pathology” in the medical system. He adds other comments which, again, he fails to mention could also apply to the medical business.  I guess it’s a case of “look over there so you don’t see what I am doing”.

And Dr. Bell is not alone. Lots of other doctors and their organizations lobby the government for various reasons, such as increasing funding to the health care system.  But they don’t lobby about privacy rights for patients.  Instead they lie, steal and con.  Why?

The medical unions, at contract time, like to advertise what they do for the patients. What they fail to mention is how they steal patients privacy/body parts and the negative affects that may have on the patients health and safety.  They know privacy is important because, in their own contracts, they made sure their privacy was protected, but not the patients.  If privacy is important to the medical staff, why is it not considered important for the patients?

This is from a commenter named cyndi: “I am one of those nurses that is being forced to wear a mask for the next 4 months. I take umbrage against that policy. My rights as a human being are being held hostage to a Health Authority. Why dont they make it mandatory to just give every admitted patient the flu shot on admission to the hospital should be the question….that way all of us front line workers would be so called protected instead of forcing us to get the flu shot every year!!!  I think the real discussion here is Are frontline workers human rights being maligned….I am extremely insulted by this Health Authority policy!!!  And employees have the right to work in a respectful place free from discrimination.  (Are Flu Shots as Effective as Billed, Bill Tieleman, 08 Dec 2014, TheTyee.ca)  This is only one person’s comment but I include this because it represents an attitude I heard many times, from medical staff, in front of St. Paul’s.  It’s all about them.  They get very upset if they feel their rights as a human being are violated but don’t care about patients rights as human beings.  In fact, she said to do to the patients what they, the medical people, don’t want done to them, make the patients have the flu shot. Aren’t patients rights as human beings being stolen when the medical people steal their information/body parts?  She talks about discrimination against her but isn’t it discrimination when medical staff and their special friends have their privacy protected but patients don’t.  My response, to paraphrase a couple of sayings, is:  they came for my rights and you did nothing, so quite frankly my dear, I don’t give a damn about you.

I didn’t want to spend a lot of time standing in front of St. Paul’s taking all the abuse. I didn’t want to spend a lot of time researching and writing a blog.  But when I realized that the medical business was lying, stealing and conning the vulnerable, the sick, the newborns I couldn’t walk away.  I know the difference between right and wrong and my values say that you must speak up against injustice.  It cost me a lot, in a variety of ways.  That was a choice I made because the cost of doing nothing was much higher, to who I am as a human being.

Obviously I won’t be in front of St. Paul’s anymore which I’m sure makes “them” very happy. But I don’t have to be.  My blog is still on the internet, people have linked their social media sites to my blog; my blog has over 100,000 page views and counting.  It  has been, and continues to be, read not only by people in Canada but by thousands of people around the world who are learning how Canada treats its vulnerable, its sick, its newborns.   I am on twitter and I will keep raising awareness in one way or another.  The information is out there and they don’t get it back.  And it will continue to spread, a lot of it from their own unethical, immoral actions.

“In order for evil to flourish, all that is required is for good men (people) to do nothing.” – Edward Burke