Joyce 🐝 Bowen Brand Ambassador @ beBee

4 years ago · 6 min. reading time · ~10 ·

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Killer Drugs [Updated]

Killer Drugs [Updated]


Richard Nixon passed an Act in 1973 allowing Medicine to become a for-profit industry. Let’s face it—there’s no profit in Healthy People.

Joyce Bowen
me



There are plenty of street drugs that can kill, but what about prescription meds? More and more drugs cause medical consequences endured by people who take them. More doctors are prescribing meds for off-label uses, resulting in complications not revealed to the patient.

Richard Nixon passed an Act in 1973 allowing Medicine to become a for-profit industry. Let’s face it—there’s no profit in Healthy People.

Joyce Bowen

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I give you my travels through the prescription drug realm.


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As I have gotten older, my body has become more susceptible to side effects. I have implored doctors not to give me drugs that impact blood sugar and blood pressure. This has often fallen on deaf ears.

It seems doctors wish to help, but the pen can be mightier than the sword when it comes to that damned prescription pad. I have suffered at the hands of this mindset. Many drugs create problems rather than solve them.

One drug I have been put on was Lamictal.

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I started on a low dose. Twenty-five milligrams. I had a doctor’s appointment four days after I started the drug. My blood pressure had jumped 20 points on each end. I googled Lamictal and there it was—high blood pressure. I stopped the drug immediately, and my blood pressure went back to my normal.

There were a few drugs I was put on that boosted my blood pressure. I cannot remember them all.

There have been some drugs that I have tried that boosted my blood sugar. Doctors seem to love these drugs. I keep telling them,

“I have Autoimmune Disease. I don’t need another major disease (Diabetes).” Most doctors agree, but they still pull out that prescription pad.

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I had one Physician’s Assistant who lied to me and told me Geodon would not cause blood sugar spikes. I looked it up on 

Web MD and lo and behold—it causes diabetes. It is a drug that is often used for PTSD, but trading PTSD for Diabetes is not the direction I want to go in. My blood sugar spiked 20 points in just four days. I stopped the drug. The PA told me Web MD was wrong. But the truth lies in the results.

Then I discovered a drug I was already on combined with the above caused pre-renal failure in 100% of 60+-year-old women. That’s me.

The most recent catastrophe [2016] was a drug by the name of Aricept.

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An appointment at the doctors recommended the pneumonia shot [Prevnar] and a flu shot. I asked if it was safe to get them both at the same time, and the nurse said,

“Su-u-ure—we give them in different arms.”

 Well—hey—I gotta tell you: It was a very bad idea. Aluminum in one arm and mercury in the other. I took a cognitive hit I thought I’d never recover from. It was autistic-like. I’d be writing, trying to find a word in my mind, and find that, not only could I not find the word, I could not grab any related concept. There was a black hole in my mind.

I had stopped writing from 2010, pretty much, thru 2016 because my hands had become so crippled. I had seen a neuro-psychologist who recommended I go back to writing and that I should also take a drug by the name of Aricept.

I periodically experienced what I called word-abysses and could not remember a word. More significantly, I could not verbalize any concept relative to a word, so no replacements were available to my lips [or my fingertips…].

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A simple example could be the word: tree [although the usual words were more complex]:

Think of all the words used for tree—tree, oak, maple, wood, and on and on and on…

Where that word [and all its relations] resided in my brain turned into a black hole. I could get none of them from my brain to my lips [or my fingertips for that matter…]. I had been getting sicker and sicker, so I thought what I was experiencing was part of a dying process. I thought it was the beginning of my loss of language. I thought it was over for me.


I was uneducated as to the state of medical affairs at the time, so I let the doctor convince me it was early dementia. Off went a prescription for Aricept to the pharmacy.

Aricept is an Alzheimer’s drug. Some doctors have told me it’s not much good for Alzheimer’s. It’s being promoted off-label for a myriad of things. God help patients that have this drug thrust upon them.

Aricept was a wild ride. I should have known better when my pharmacy called me and refused to fill it until they spoke with the doctor about interactions with other medications I take. One drug I had to stop was for anxiety. The other, Trazadone, treats my insomnia. Sleep is important to me, so, at first, I did not give up the Trazadone. That was a mistake. I took my Trazadone at night, and my heart practically walloped out of my chest. Yes—Aricept and Trazodone interacted with each other and impact the heart. The interaction can be life-threatening. I doubt my neurologist even checked on what I was taking.

I backed off the Trazadone until my heart stopped screaming. Sleep went with it. But what I didn’t know was that Aricept could cause a pretty damned intense insomnia.

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There is desperation entwined with trying to keep your thought process. I did not look up side-effects. I only knew my blood pressure and blood sugar were fine so I was happy. I attributed my insomnia to having to back down on the Trazadone, but there was a tickle in the back of my mind this insomnia was more intense. I attributed it to hypervigilance [which is just the result of being so damned smart.]

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Doctors sought to alleviate my insomnia with more drugs. One was Remeron. It is also used to treat Depression [which I didn’t have.] After six weeks on that drug, I woke in the morning to find I could not read anything on my computer. My vision would clear up after a few hours, but for about three hours upon awakening, I was legally blind. I thought something had finally taken my vision initially. After three days, I thought about what had changed in my life recently. On a whim, I googled Remeron and vision and came up with something like this. The piece I found was more specific in that it can cause blindness in my age group. I dumped Remeron and recovered my vision. I brought the article to my doctor, and he said,

“Oh my; I have a lot of people on Remeron.”

Other drugs were added to no avail—with no consideration that my difficulties may have been a consequence of another drug.

By this time, I had dumped my neuro and found a new one. He continued the Aricept. He left that practice, and I was forced to find yet another neurologist. By this time, I was experiencing severe muscle spasms all over my body. I had had spasms for years, but the rising intensity was more than I could bear. I had informed the dwellers of my building that if they heard me screaming they were not to call 911. I was put on Baclofen for spasms. The occasional relief was welcome.

My first visit to my new neurologist brought with it the message that Aricept could be causing my spasms. By this time I was thinking, brain be damned. I cannot take the pain.

Now that I was off the Aricept, I could increase my Trazadone to treat my insomnia. I called the doctor treating this condition, and he ordered increases in small increments to start immediately. When I increased the dose, I noticed my heart racing straight away. The Aricept is not out of my system, I thought. I wandered back to Google and discovered Aricept does not leave the body for 16 days. I wondered why my doctor did not know this. I waited for 16 days.

As I waited for Aricept to wean out of my system, I found myself passing out in the most inopportune places. I was exhausted. It had been a wild ride for eight months. It was over. I feel like a fool for trusting that a doctor would give me helpful medications rather than hurtful ones. It is disturbing that the several doctors I saw for the myriad of difficulties that Aricept introduced did not know that simply removing a drug from my repertoire rather than adding more would be more helpful.

It took over a year to recover from the devastating effects of Aricept on my brain.

Sleep comes easier now. I am relieved. A part of me misses that energy I felt. But I don’t miss all the problems that came with it.

It’s now been about three years since I wrote this article. I’ve learned much. I wish I had learned more sooner. I am stuck with a myriad of medical issues caused by prescription pads and MDs’ orders. I would be healthier had I never gone to a doctor. I do have one honest doctor in my corner, and apologies beam from her eyes when I visit her office. 

I’m still struggling with a lasting infection given to me by one medication I have not taken for 2 years. We just discovered [my doctor and I] that I can not even take antibiotics. I held on to the hope that antibiotics were sacrosanct—they are not. I found a homeopathic answer on my own.

Health insurance only covers conventional medicine. No sense in paying for something I can’t use. I’ve been conditioned to believe I need these things for a long, long time. But for me, they’re suicide. I’d like to keep breathing.


I can take no—and I mean no—pharmaceutical products.  They caused all sorts of problems: crashing kidneys; liver inflammation; legal blindness; cognitive whacks; 24/7 pain; high blood pressure; high blood sugar; infections; severe cough [AKA lung damage]; autoimmune disease; insomnia; anxiety; etc. Now almost all gone. I still have some liver inflammation problems, and I’ll die with the autoimmune disease, but I can’t go to today’s MDs. I can’t take pharmaceuticals, and that will inevitably be his or her answer.

And MDs do not treat damages from medications. They’ve got a new mantra:

“Just because it’s on the list doesn’t mean it happens.”

So if side-effects from pharmaceutical products do not exist for these people calling themselves MDs, it’s best to avoid them.


Whether we like it or not, we live in a drug culture. Street vendors sell drugs that kill, and so do doctors.

I’ve spoken to a few people with Parkinson’s who have said their medications hurt rather than helped.


Do you have a story to tell that might help others?


About the Author: Joyce Bowen is a freelance writer and public speaker. Inquiries can be made at crwriter@comcast.net

Copyright 2017 Joyce Bowen

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https://joyce-bowen.com/

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Comments
Royce Shook Here is the article I wrote, which was submitted for publishing and approved. https://www.bebee.com/producer/@joyce-bowen/needham-7-some-other-place-in-cambridge-ma-and-thank-the-lord-for-2018
Royce Shook yes. I'm glad you have a council. I think my time there was one of my most terrifying experiences. I lay in my bed while they coaxed my incoherent roommate into signing a DNR. She signed a wrong name and they had to tell her what her name was. I was horrified. On the day I left, they sent a physical therapist who demanded I "do the stairs." I told her I had already done them twice, had passed, and it was documented; in hindsight, I think they would have refused to let me go home on the basis of not doing them well enough no matter how well I navigated them. Fortunately, I escaped, but I think if I had had more in assets, they would have found a way.
Debasish Majumder Thank all of you for your shares and your "likes."

Royce Shook

4 years ago #11

Hi Joyce, the nursing home issue is a concern in Canada, but in BC where I live, we have a Senior's Advocate (I am on here Advisory Council) who is actively investigating nursing homes and pressuring the government to act where the nursing homes get out of line. I was not aware of the guardianship issue but I will be looking into it for my jurisdiction. Thank you for the links above.
Royce Shook Funny--or not funny... I just wanted to let you know that that same hospital that caused my hemorrhage was [or still is] connected with 4 nursing homes. They stuck me in one after calling it "rehab" for a bum knee. I barely escaped, but my roommate did not. My understanding is that this "nursing home" thing is quite bad in Canada, too. I felt certain they were after my assets--but I couldn't be positive until I saw this last week: https://www.esquire.com/entertainment/tv/a31847699/netflix-dirty-money-guardians-inc-guardianship/ https://www.netflix.com/watch/81005050?trackId=14277283&tctx=0%2C4%2Cd08fd1e5-45bf-4a4f-81b3-02a743859025-30496136%2C%2C Damn--it never ends.
Royce Shook Oh--don't let them do it. Whoever is pushing for these changes is backed by the pharmaceutical industry. I call our doctors here drug pushers with prescription pads--not all--but most. As I said, I have a doctor who is greatly apologetic, but that MD can say nothing. I know if that MD speaks out the risk is loss of license. That whole office is behind me. I am grateful, but more needs to be done.
Royce Shook Oh--don't let them do it. Whoever is pushing for these changes is backed by the pharmaceutical industry. I call our doctors here drug pushers with prescription pads--not all--but most. As I said, I have a doctor that is greatly apologetic, but that MD can say nothing. I know if that MD speaks out the risk is loss of license. That whole office is behind me. I am grateful, but more needs to be done.

Royce Shook

4 years ago #6

Hi Joyce, your story is shocking and as you said, what is happening in the US is criminal yet we have many powerful people in Canada wanting us to go to a US type medical system. So far they are no succeeding but they are slowly making inroads. Thank you for sharing.
3/3 Royce Shook The PHQ forms are copyrighted by Pfizer. Pfizer's biggest division is its psychiatric drugs. I was so shocked, I took all their forms with me and refused access to any medical records. As you can see--I was pretty angry. They say you can amend records in this country, but you can't. It's a lie. The doctor who wrote the initial record has to review your request and can deny the amendment. And Medicine can now change or alter health records anytime they want. A lesion on my cervical spinal cord was edited out in a record from 2010, and I was vigorously denied access to the original. Medical test results will leave out information. I had an MRI for a 6-month-long headache. The ER I went to told me I was fine. Six months later, I was sitting at that MDs office in Tufts while she looked at the MRI online, and the MD said, "You have an old cerebral hemorrhage here." The hospital I had the MRI at, I suspect, caused the cerebral hemorrhage with heparin shots. They covered themselves by telling me I was fine. Medicine has been "corporate captured" way too much in this country. The pharmaceutical industry now also runs our hospitals. In some cases, if you refuse pharmaceutical treatment, you are declared suicidal and committed for treatment. This has happened to patients declining chemo. We need to take back our schools and train our MDs ourselves [not pharmaceutical companies]. Medicine is very nearly a disaster here. What is happening in the US is criminal and shocking.
2/3 Royce Shook The co-author sent back this: "From: Sent: Saturday, October 13, 2018 10:56 AM To: crwriter Subject: RE: pfizer I am sorry to hear a diagnosis of depression was made solely on the basis of the PHQ-9. It is not intended to be a diagnostic measure for depression. The 9 symptoms simply measure the criteria for depressive disorders but, as you mention, some of the symptoms can also occur in a number of medical conditions and other diseases. Thus, it is incumbent upon the clinician to determine whether the symptoms endorsed on the PHQ-9 are due to an underlying medical illness, to depression (or in some patients a combination of both). Also, it is important when a PHQ-9 score is obtained, to incorporate the patient’s perspective since she or he often has salient insights about the potential underlying cause of the symptoms that can complement (or override) what the clinician believes may be the cause. As I occasionally teach about recognizing and treating depression, I will continue to remind the audience that a simple score on a brief self-report scale is nothing more than a measure of symptoms and not a diagnosis of depression. I have typically communicated this but your experience and words convey more poignantly this caveat. Professor of Medicine Regenstrief Institute
1/3 Thanks, Royce Shook. It may be harder in the US. MDs are trained by the pharmaceutical industry here. I went to the prestigious Tufts, and they had a pharmacy tech sitting in the room with the doctor and I, eagerly waiting to order any prescriptions the MD might order on the laptop sitting on his lap. They also had the PHQ-2 form sitting atop of all the forms they want a patient to sign which is comprised of 2 questions to determine your level of depression. It used to be the PHQ-9 form until I sent this: "From: crwriter Subject: pfizer Regarding the phq-9 form. I have Autoimmune Disease. I fell for this form in my neurologist's office. Of course, with all my physical symptoms, I qualified for major depression. If you could read my mind right now, you’d probably cover your ears and eyes and run and hide. I AM NOT ******* DEPRESSED, but I sure am angry. They are refusing to determine depression any way other than with this form. I hope Pfizer paid you lots of money for what you did to people. Oh—wait… I see Lilly paid you a few bucks. Joyce Bowen"

Royce Shook

4 years ago #2

Hi Joyce, thank you for sharing your story, I am sure it will help others. In Canada, there is a movement to help patients get off drugs, called Deprescribing Network. The Canadian Deprescribing Network is a group of health care leaders, clinicians, decision-makers, academic researchers and patient advocates working together to mobilize knowledge and promote the deprescribing of medication that may no longer be of benefit or that may be causing harm. The web site is here https://www.deprescribingnetwork.ca/ and they have good tips.

Debasish Majumder

4 years ago #1

extremely helpful buzz indeed Joyce \ud83d\udc1d Bowen Brand Ambassador @ beBee! read and shared. thank you very much for the buzz.

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