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Funny Bone — Toledo: Another Example of Disabled People Being Treated as an Afterthought by an Entertainment Venue

Bruce Gerencser 11 Comments
trae crowder bruce and polly gerencser cropped
Trae Crowder, Bruce and Polly Gerencser

My partner, Polly, and I traveled to Toledo, Ohio, last night to listen to Trae Crowder at the Funny Bone Comedy Club and Restaurant in Levis Commons — a sprawling outdoor shopping center. Big fans of Crowder, we’ve been looking forward to hearing him for months. We listen to his weekly podcast, along with the short videos Crowder puts out several times a week. Crowder, an agnostic, calls himself the “Liberal Redneck.” While Crowder, age 37, currently lives in Los Angeles, he came of age in rural Tennessee. Crowder attributes his liberal/progressive political and social beliefs to his family’s abject poverty during his childhood years.

somerset baptist church 1983-1994 2
Our hillbilly mansion. We lived in this 720-square-foot mobile home for five years, all eight of us.

Having grown up in similar circumstances in the 1960s-1980s, I find Crowder’s humor appeals to me in ways other comedians don’t. When Crowder talks about “white trash” or “trailer trash,” I understand. When uttered by people who have never experienced real poverty, I bristle and often give them a buffet-plate-loaded-up-on-seafood-night response. However, when someone from the poverty fraternity satirizes these experiences, I laugh — been there done that — but the trauma of those years still lurks in the depths of my being. I no longer live in abject poverty. I am more “fashionably dirt poor” these days. Roof over our heads, food on the table, bills paid (albeit a few days late here and there), and taxes up to date. Life is good, even if the Bengals are 0-2.

Crowder delivered as advertised. We got the opportunity to meet him afterward, shake his hand, and have a picture taken. We live in an area where seven out of ten voters voted for Trump in 2016 and 2020. God, Trump, Guns, and Evangelical Christianity rule the roost. For godless liberals such as Polly and I, we are foreigners in the land of my birth and the home of our six children and grandchildren. Hearing Crowder was a brief respite for us from incessant right-wing extremism.

Unfortunately, the “experience” itself was, to put it mildly, less than optimal, and, at times, downright frustrating and painful.

We arrived at Funny Bone at 6:00 p.m. Unable to find a parking space, we were forced to park three city blocks away from the venue. Neither the sidewalks nor the parking lot were ADA-compliant. We entered the doors for the club around 6:15 p.m. The doors were challenging to enter. Technically, ADA-compliant, it took Polly several attempts to get my wheelchair through the glass doors (there was no automatic door opener). Once in the lobby, we found no staff to assist us. The club itself is on the second floor. On the desk sat a sign that said there was an elevator in “back.” Back where, exactly? No directions, no arrows pointing to the elevator. Being first-time visitors, we were left with figuring out what “back” meant. Polly walked the stairs to the second level, hoping to find anyone to help us. After being unable to find someone to help us, Polly came back to the lobby and told me that she was going to walk around the back of the building to see if she could find the elevator.

With the elevator found, we thought we were home free. Little did we know, the worst was to come.

Out of the inadequate doors we went, around to the elevator, only to find more doors we had to contend with. Barely wide enough for a standard wheelchair, none of the doors had automatic door openers. Fortunately, we had the elevator to ourselves. Easy in, easy out, straight. . . to . . . the . . . venue . . . now, right? Nope, there was another door we had to enter to reach the club. Thanks to boxes stacked near the door, Polly could not push my wheelchair through the door. She had to move the boxes so we had enough room to barely navigate through the door. This door gave way to a hallway that led to the hostess station. The hallway was narrow, and ADA compliant only if there were not boxes or people taking up space. In other words, it was difficult to navigate.

Finally, we made it to the hostess station. I had called Funny Bone the night before to remind them that I was in a wheelchair and would need accommodation. “No problem,” I was told. A few feet in front of the hostess station was a transition between flooring types. Paying no need to ADA compliance, Funny Bone used a raised transition instead of a flat one. Of course, hitting this speed bump nearly tipped over my wheelchair (with me in it). Thoroughly embarrassed, Polly eventually righted my chariot, and onto the main floor we went. The Funny Bone is laid out like a supper club. They could have parked my wheelchair in any number of out-of-the-way places, but the staff decided to sit me at a table that was pushed up next to another table, near where there would be a lot of foot traffic. I spent the rest of the night being bumped into by patrons and employees alike. Telling the crippled guy “sorry” might make you feel good, but it does nothing for the person physically harmed. I suspect if Funny Bone received a spot fire inspection or ADA compliance inspection, they would have failed miserably.

Crowder was as advertised. Afterward, we waited for most of the venue to clear out before leaving. We do this to avoid having to deal with rude, thoughtless people. That and the fact that it is impossible to push a wheelchair anywhere in a crowd. So we waited to make our escape. After retracing our steps, we finally made it to the parking lot at the back of the Funny Bone. We started out on the sidewalk, only to find out it was a dead-end, running into a metal gate. This forced us to take the parking lot, complete with speed bumps to our automobile. Adapt and persevere, right?

Polly wheeled me about ten feet into the parking lot, when all of a sudden my chair stopped, Polly screamed “Oh no!” and I went flying head-first onto the pavement. As I lay prostrate on my right side in the parking lot, Polly steadied herself and came to my aid, Others were nearby, but ignored what was playing out in front of their eyes, Finally, a young man rushed up and asked if I was okay; if I needed any help. Filled with embarrassment and pride, I thanked him and said I would be fine. He waited while I climbed on my knees to the wheelchair, locked the wheels, and pulled myself up. Polly apologized repeatedly as we made it back to the car. I told her, “It’s not your fault.” While on my knees I found the culprit, a chunk of asphalt was missing, and one of the front wheels on my chair sunk into the hole, sending me flying into the crisp fall night.

For those of us who use wheelchairs, walkers, and canes, doing simple things can prove to be a challenge — sometimes, dangerously so. I am not a disabled person who expects the same treatment as able-bodied people. I do, however, expect reasonable accommodations. Levis Commons and Funny Bone failed on this account.

How do I feel today? Time for a shovel and a six-foot rectangular hole. Either that or lots of pain meds and muscle relaxers. Polly couldn’t find the shovel, so we are going the medication route. 🙂

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Bruce’s Top Ten Hot Takes for September 14, 2023

Bruce Gerencser 14 Comments
hot takes

I have never been an Aaron Rogers fan, but after watching him on Hard Knocks, I’m more sympathetic towards the man. Rogers blew out his Achilles tendon minutes into the Jets’ first game and is done for the year. I genuinely feel sorry for him.

Jets quarterback Zach Wilson will not lead the team to the Promised Land. The Jets need to sign a seasoned quarterback; someone who is a caretaker. Don’t throw the ball away and let the defense do the rest.

Last night’s low was 45 degrees. Where did summer go? I wanted to turn the furnace on. My bed partner didn’t want to crank up the heat. Who won? I froze.

I introduced my five-year-old grandson to newspapers — a sales insert from a farm supply business. Made his day. Sadly, children born over the past ten years know no little to nothing about newspapers.

Our six children grew up in a home that received a morning and evening newspaper every day. They especially remember Dad’s paper rule: keep the sections in the proper order. They also remember that on Sundays no one read the paper before Dad (though I think they sometimes ignored this rule, reading the comics and sports sections, and then putting them back in place — Dad none the wiser).

I no longer subscribe to any newspaper, getting my daily news from a plethora of online sites. I miss not physically reading a daily newspaper. Both local papers are dying. Outside of finding out who died or what Ney’s council did at their meeting, local newspapers offer little value to me.

I set a record yesterday: 12 vials of blood were drawn from my left hand — over $1,000 in tests. The pessimist in me wonders if any of this will matter. Every specialist interprets the numbers differently.

I’m anemic, with low potassium, B12, and testosterone numbers. Supplements keep these numbers hovering around low normal. I reminded the doctor that I was taking significant levels of supplements to keep these numbers out of the basement. Without the supplements, I would be dead. The question, then, is why I have these deficiencies. So far, no doctor has a clue.

Ohio State will not play in the national championship game this year. Neither will Alabama.

My youngest grandson found a cricket in the living room and freaked out. I stopped him from killing it. At Grandpa and Nana’s house, if necessary we capture and release. Spiders? More often than not, we ignore them. Polly swears a big wolf spider is stalking her. Maybe. 🙂

Bonus: Out of all the serious health problems I have, nausea is the worst. I’m nauseous every day, often without relief. You can’t escape nausea. Eating is one of the few pleasures I still enjoy, but nausea often ruins this pleasure. Hard to enjoy eating when you feel like throwing up. I take Zofran to limit the vomiting, but that dull, achy nauseous feeling remains.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Will the War on Chronic Pain Sufferers Ever End?

Bruce Gerencser 20 Comments
pain to stop

Recent years have brought an endless stream of rules, regulations, and demands from governments, doctors, and pharmacies meant to battle the evils of opiate addiction. What was once between a chronic pain sufferer and his primary care physician is now a multi-person group fuck. I don’t blame doctors or pharmacists. Government has forced upon them numerous rules that make it harder and harder for chronic pain sufferers to receive relief.

I am required to see my primary care doctor every three months to continue to receive narcotic medications. I currently take Vicodin (Hydrocodone), five tablets per day. Three scripts at a time are sent to the pharmacy. I can’t fill the prescriptions early. They must be filled on the day listed on the script. This means you are typically out of medication on the day you fill your prescription. Of course, if you don’t get to the pharmacy at the right time or they are OUT of your medication, you are screwed. Long-term narcotic pain meds users are not addicts. They are, however, physically dependent on narcotics. When pain medications are suddenly stopped, the patient goes through horrific withdrawals.

Last year, the pharmacy I use was out of Vicodin. Well not “out.” They had enough of the drug to give me a partial fill, but according to the pharmacist, CVS was not permitted to give patients partial fills for narcotics.

“Fine. Please transfer my prescription to another pharmacy.”

“I’m sorry, but we are not allowed to do that either.”

“You do know what happens if I suddenly stop taking Vicodin”?

“I understand, but there’s nothing I can do. We won’t have any Vicodin until Wednesday (four days).”

This was on a Saturday. My prescribing doctor was out of town until Monday. I knew calling the on-call doctor was a waste of time. He would think I was a drug-seeking addict.

Fortunately, I only went without Vicodin for thirty-six hours. I borrowed some Percoset from a dear friend of mine to tide myself over. Of course, doing so was a crime. On Monday, my primary care doctor was able to fix the problem for me by sending the script to a different pharmacy.

Keep in mind ALL narcotic prescriptions are tracked with software. All doctors and pharmacists have access to this system. It is IMPOSSIBLE to abuse legally prescribed narcotics. I can’t think of one way a patient can game the system. Scripts are no longer handwritten. They are transmitted digitally, straight to the pharmacy. The prescriptions can’t be filled early. There’s simply no way for me to abuse the narcotics I take five times time a day. Yet, here I sit tonight, unable to fill my August 8th prescription until August 13th.

My doctor prescribes me a thirty-day prescription of one-hundred-fifty tablets every twenty-nine days. This means I have an extra five tablets each month. Five. Not twenty. Not fifty. Five. These five tablets provided me a monthly buffer in case of a pharmacy problem or I have a really, really, really, really, really bad pain day. Five tablets. Unbeknownst to me, the pharmacy was tracking these five extra tablets, and today was the magic day when they decided to bring the hammer down on me.

The pharmacy will not automatically fill a narcotics refill. Even though my doctor digitally sends the script to them, I must call them to have it filled. That’s what I did today, only to find out that they would not fill my prescription until August thirteenth. Five days of no medication. I have nine tablets on hand, so I have to cut my medication by seventy-five percent — two tablets a day. Why? Five tablets. Five tablets each month for six months is thirty tablets, the pharmacist informed me. I tried to explain things to her, but it mattered not. All she saw is what she called a “retention issue.” Those tablets I “retained” were actually used when needed. Long-term chronic pain sufferers learn to manage their narcotic meds, adapting usage to pain levels. None of this matters. Fundamentalism rules supreme when it comes to prescribing pain medications. “These are the rules. Obey. Don’t obey, we will punish you.”

Will the War on Chronic Pain Sufferers Ever End? I ask in the title of this post. Death, that’s what will put an end to this pernicious war against chronic pain sufferers. Patients who have their medications suddenly cut off have a higher risk of suicide. Despair sets in when you think, and often know, no one is listening to you. Allegedly, the goal of the medical profession is to alleviate pain and suffering. My primary care doctor had that as his goal when I first started seeing him twenty-seven years ago. And he still does today. The only difference, of course, is that twenty-seven years ago no one stood between us. Today, the FDA, the state of Ohio, pharmacies, pharmacists, and insurance companies stand between us, materially affecting the prime directive: alleviate pain and suffering.

It remains to be seen how the next five days will go. Polly is fearful that I might kill myself, but I told her as she left for work, “Don’t worry. I’m fine.” She asked me “Why aren’t you more upset over this?” I replied, “I have no control over any of this. None! Yes, I am angry, beyond angry, but all the rage in the world won’t change the fact that my prescription will NOT be filled until August thirteenth.”

My singular goal is to make it to the thirteenth. Will one tablet every twelve hours, lots of Tylenol, and aspirin be enough to stave off the worst of withdrawal? I doubt it, but what else can I do? Maybe drink Jamison for breakfast, lunch, and dinner?

I plan to take a drive to Michigan where marijuana is legalized. According to state law, I can’t legally buy cannabis, but Michigan dispensaries will sell it to Ohio residents. Rumor has it that the Ohio sheriff’s departments that border Michigan — particularly Williams and Fulton — are using off-book undercover officers to write down the license plate numbers of Ohio residents who dare to visit Michigan dispensaries. Yes, indeed. Crimes of the century are taking place just over the state line.

Writing helps distract my mind from my ever-present pain, so if you see a flurry of new posts, you will know why.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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How the Use of Subjective Measurements by Doctors Affects Patient Care

Bruce Gerencser 6 Comments
bmi chart

Twenty years ago, the U.S. government forced doctors to move from paper to electronic records. The result? Many doctors spend more time staring at a computer screen than they do interacting with their patients. The goal becomes inputting data, and not attempting to understand why the patient is there and what treatment plan is best for him.

This move to data-input medicine has led to doctors increasingly relying on numbers to measure patient health. I want to talk about some of these numbers, sharing my experiences and concerns.

Pain Chart

“On a scale of one to ten,” the nurse or doctor asks, “how bad is your pain?” Instead of talking to the patient about his pain, he is expected to diagnose his pain on a subjective scale. First, pain is subjective. My pain is very different from your pain. As a redhead, I have increased sensitivity to pain. All pain is relative. Remove a bandaid from my grandson’s leg and he will scream bloody murder, saying, “doctor, it’s a ten!” To my grandson, his pain is very real, but he has no real-world experience with actual pain. Grandpa has sixty-six years of experience with pain — horrible, debilitating pain. I have had tests that were painful; procedures that have left me in tears. Polly gave birth to six children. She understands pain. Three years ago, she had major abdominal surgery and spent twenty-one days in the hospital. Again, lots of pain.

I have had family and blog readers minimize my pain. They believe if I can walk or stand, I must not be in pain. Never mind the fact that walking and standing require psychological and physical contortions from me. One look at my face will tell you everything you need to know. But, people don’t make eye contact much these days. We no longer read body language. If they see me getting out of the car or walking in the store, they assume I must be fine. I’m not fine. And I am never, ever going to be “fine” again. Life for me is pain and endurance; of wondering whether I want to keep living,

Second, people with chronic pain quickly learn that if you tell a doctor nine or ten for your pain level, he will automatically think you are a drug addict looking to score some narcotics. Tell the doctor one, two, or three, he will wonder why you are there. So, I typically say five or six. Bullshit numbers; meaningless numbers, but there ya go doc, you have a number you can input in your digital records program.

Third, I can’t tell you the last time I had a doctor sit down with me and comprehensively talk to me about my pain. Where? How severe? What makes it worse? Do medications help? What physical activities are you able to do, not do? How does your pain affect your sleep; your sex life? Of course, doctors don’t have time to interact with patients this way, especially primary care physicians. They have patients scheduled every 15-20 minutes. No time for personal connection and investigation.

Weight and Body Mass Index (BMI)

I’m obese. The BMI number for me on the doctor’s digital screen is a blinking red number with an exclamation point. This tells the doctor that his patient is fat, as if his eyes couldn’t tell him that already. According to the BMI chart, my “healthy” weight is 140-170 pounds. I weighed 160 pounds at age eighteen; 180 pounds at age twenty-one; 225 pounds at age twenty-five. Was I obese at 225 pounds? Is that even a relevant question? At age twenty-five, I was physically fit. I played basketball and softball. I hunted, hiked, and fished. I cut wood in the fall. I was a physically strong man, yet according to the BMI chart, I was obese.

The BMI number says nothing about the fitness of a person. Most NFL players are obese. Are they unfit? Of course not. I have a big frame. I lost 100 pounds over the past three years, yet I look the “same.” Why? I don’t have a beer belly or ass. I’m built like a fireplug. Certainly, I knew I had lost weight. I dropped two shirt sizes and eight inches in my waist. Yet, to the casual observer or inattentive doctor, I look just like I always have — fat.

Squeeze My Hand

When doctors want to check my strength, they ask me to squeeze their hand. Without fail, they will tell me “Good. You are strong.” My complaints about weakness and debility are dismissed, all because I passed a subjective hand squeeze test.

How does this test tell doctors about the level of my strength? First, isn’t the doctor judging my strength based on his subjective measurement of strength? Second, shouldn’t the measurement of strength be based on how strong or weak I was in the past? Using that criterion, I have lost over half of my physical strength. Sure, I can still squeeze your hand, doc, but there was a day when I could have broken your fingers.

Temperature

“Normal” body temperature is 98.6 degrees, patients are told. That’s what mine was for the first thirty-four years of my life. And then, I contracted mononucleosis and almost died. Mono can be deadly for adults. Afterward, my “normal” body temperature dropped to 97.0 degrees. And thus began a never-ending fight with nurses and doctors about my body temperature. “Doc, I have a fever.” “Your temp is only 99.0. It’s normal.” But . . . he’s already stopped listening. I can’t have a fever, in his mind, because 98.6 is the standard. He doesn’t believe me when I explain mono changed my body temperature. Dare to object and his notes will say, “difficult patient.” And since every other doctor in the practice can see his note, soon the other doctors you see will deem you a “difficult patient.”

Blood Pressure and Glucose Levels

While these numbers can be helpful in diagnosing and treating a patient, they are only a snapshot of a moment in time. Typically, my blood pressure and glucose levels are normal, even exceptional. I get a star by my name for 120/80 and 90 blood sugar level. But, do these numbers tell the whole story about my health? Of course not. I have landed in the ER twice with sky-high blood pressure for no known reason. I have had several instances where I woke up in the night, only to find my blood sugar level was 48 and 50 respectively. Not good. Again, no explanation for the low numbers.

I stopped checking my BP and glucose levels every day. I found the varying numbers too stressful. Occasionally, I will check my numbers, but I typically leave it to my body to tell me what’s up or down, especially my blood sugar levels.

Advice to Doctors

Stop typing. Look your patient in the eye and let him know you care. Ask lots of questions. Pay attention to what his body language is telling you. Use your gifted hands to touch and probe, interacting with the patient all the while. See him as a fellow human being. Never forget, you will be in his shoes one day.

Of course, doing these things takes time, and therein is your problem. Corporate medicine demands efficiency, treating patients like they are line entries on a spreadsheet. The bottom line is more important than the welfare of your patients. Surely, this is not why you got into medicine.

Several years ago, I wrote about a doctor named Bill Fiorini. He’s the kind of doctor I’m talking about. You can read this post here.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Your comments are welcome and appreciated. All first-time comments are moderated. Please read the commenting rules before commenting.

You can email Bruce via the Contact Form.

I’m Tired of Judgmental Doctors

Bruce Gerencser 15 Comments
fat shaming

Medical doctors are very much a part of my life. I see my primary care doctor four times a year, a dermatologist twice a year, a cardiologist once a year, and other specialists, as needed. Today, I saw an orthopedic doctor for pain in my left hip and a carpel tunnel-like problem in my left hand; a problem I had surgically fixed in 2010. While I was lying on the cold table for an X-ray of my hip, the festering cyst on my upper back — which I had removed a few months ago, but has returned — burst, leaving a wet, bloody, puss stain on my tee shirt. “Wonderful, right?” I have an appointment with a dermatologist tomorrow to figure out what, exactly, to do about the cyst. (I have an ongoing problem with cysts here and there on my body. I have spent thousands of dollars getting them drained and incised. More often than not, the cysts make repeat appearances.)

The orthopedic doctor walked into the room, and after we exchanged pleasantries, I told him why I was there today. The doctor, whom I have seen before, had no recollection of my medical history, including the fact that I have widespread osteoarthritis, and was diagnosed two years ago with:

  • Disc herniation (T7,T8)
  • Disc herniation (T6,T7)
  • Central spinal canal stenosis (T9/T10, T10/T11)
  • Foraminal stenosis (T5,T6)
  • Disc degeneration/spondylosis (T1/T2 through T10/T11)
  • Facet Arthropathy throughout the spine, particularly at T2/T3, T3/T4, T5/T6, and T7/T8 through the T12/L1 levels.
  • Hypertrophic arthropathy at T9/T10

The orthopedic doctor was unsure what the problem was with my hand. Scar tissue from my previous surgery? A new problem? He ordered a new EMG — a nerve conduction test. As far as my hip was concerned, he decided my pain was caused by the aforementioned back problems. Solution? Live with it.

And then came the lecture . . . “have you thought about losing weight?” I told him I had lost one hundred pounds over the past three years . He asked, “How?” I replied, “Gastroparesis.” I added, “Nausea, lack of appetite, and vomiting, will do that to you.” I quickly determined that he knew little to nothing about gastroparesis. This, of course, is not surprising since bones and joints are his specialty. His cluelessness didn’t stop him from suggesting I see a different gastroenterologist to get a “second opinion.” Second opinion, for what?

Gastroparesis is an incurable stomach disease. The treatments are limited: medication to manage symptoms, feeding tubes, and experimental procedures. I hate when doctors think they always need to be the expert in the room. I have no doubt that I know a hell of a lot more about gastroparesis than my orthopedic doctor did. I have read the relevant literature, and know gastroparesis is a miserable disease; that no miracle is forthcoming. I take medication, vomit, forego eating, and I had an experimental procedure done under anesthesia last year (to no effect).

Ignoring everything I said, my orthopedic doctor suggested I contact the practice’s weight loss clinic for a consult. He said, “You know, if you lose more weight, it will lessen the pain in your back.” By this point, I wanted to scream. “Are you not listening to me? “Or do all you see is the fat guy?”

Had my orthopedic doctor asked, he would have learned that I started having back problems at age twenty. I was first diagnosed with narrow disc space in my lower back when I weighed 225 pounds and still played competitive sports. My spine is literally falling apart. Losing weight won’t fix structural problems. I have had back problems at various weight points throughout my life. Lose, gain, it matters not, the pain remains. I am a living study that shows that the idea that losing weight will fix whatever ails you is untrue. As I mentioned, I have lost one hundred pounds. The only thing losing twenty-five percent of my body mass did was improve my glucose levels and provide me a new wardrobe. That’s it. My debility and pain remain the same. But, hey, I love my new Charles Tyrwhitt shirts.

I am comfortable in my own skin. Lecturing me about my weight is not helpful, nor will losing weight magically cure my fibromyalgia, osteoarthritis, or gastroparesis. While there certainly could be benefits from losing more weight, I doubt dropping another twenty-five to forty pounds will lessen my pain.

What I most wanted my doctor to do today is see “me;” to listen to me; to consider the totality of my health. Since that was beyond his “expertise,” he is no longer my doctor. In fact, I am done with doctoring. When I leave their offices worse off than when I came in, I wonder “why bother?”

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Your comments are welcome and appreciated. All first-time comments are moderated. Please read the commenting rules before commenting.

You can email Bruce via the Contact Form.

Updated: Local Southern Baptist Pastor Steve Eyers Opposes Helping People Suffering From Chronic Pain

Bruce Gerencser 7 Comments
medical marijuana suffering new jersey
Cartoon by Drew Sheneman, featuring anti-marijuana crusader Chris Christie

Four years ago, the Village of Hicksville, Ohio banned the establishment of medical marijuana facilities within its borders. The Defiance Crescent-News reports:

On Monday evening the Hicksville Village Council passed an ordinance prohibiting the establishment and operation of medical marijuana facilities within the village limits.

This is in response to previous sessions in which the possibility of such facilities coming to town was addressed, although no definite plans had been revealed to council by any such entities. Council had received strong support against these facilities by Police Chief Mark Denning and pastor Steve Eyers; no one has spoken out in their favor at any recent council sessions.

In February 2019, the Hicksville village council held a hearing on the matter. The Crescent-News reported at the time:

Pastor Steve Eyers of Lifeline Connect Church stated he has done sizeable research on medical marijuana since the last meeting and believed the jury to still be out, with no solid documentation existing substantiating positive claims about such facilities; he did observe that medical marijuana is not on the “approved” list of the Food and Drug Administration.

Eyers suggested council speak to state lawmakers and those in other municipalities which have approved medical marijuana production facilities about the results of such places, noting, “Once you open the door it will be difficult to close.”

As readers will note, the main objector to medical marijuana was Steve Eyers, pastor of Lifeline Connect Church. At a previous council meeting, Eyers, a Fundamentalist Southern Baptist, used the “slippery slope” canard to argue against medical marijuana. In Eyers’ world, every perceived negative (sinful) behavior is a step farther down the slippery slope that leads to Hell. I am sure Eyers believes that marijuana is a gateway drug, and once people start toking mary jane they will soon be hooked on crack, cocaine, heroin, or other highly addictive drugs. Funny how Eyers’ “sizeable research” didn’t turn up any evidence to the contrary:

The “gateway hypothesis” or theory refers to the idea that one substance — marijuana, in this case — leads to subsequently use and/or abuse other drugs. If [Governor Chris] Christie’s point is simply that the use of marijuana tends to precede the use of other drugs, then he is correct — but that’s not the whole story.

Though studies of large populations of people have indeed found that those who smoke marijuana are more likely to use other drugs, these studies show a correlation without showing causation — a commonly misunderstood phenomenon in science. In short, just because marijuana smokers might be more likely to later use, say, cocaine, does not imply that using marijuana causes one to use cocaine.

A 1999 report from the Institute of Medicine, which is part of the National Academy of Sciences, laid out this issue clearly (see pages 100-101): “In the sense that marijuana use typically precedes rather than follows initiation into the use of other illicit drugs, it is indeed a gateway drug. However, it does not appear to be a gateway drug to the extent that it is the cause or even that it is the most significant predictor of serious drug abuse; that is, care must be taken not to attribute cause to association.”

We spoke with several experts and reviewed the available scientific literature on gateway theory. Christie’s definitive statement is unsupported by evidence — there is some evidence in favor of a gateway effect, but the scientific community shares no consensus on the issue and there is little evidence on the underlying cause of that effect. — Factcheck.org.

Evidently, the good pastor was absent the day his teacher covered correlation and causation in science class.

There is no question that medical marijuana can and does help with many medical maladies, including chronic pain. Numerous readers of this blog can testify to medical marijuana’s efficacy and how it has improved their quality of life. It is absurd to oppose any drug (or treatment) that will reduce pain and suffering. But, Bruce, people might get “addicted’ if they start using medical marijuana. So what? Should it matter that a drug is “addictive” IF it’s helpful? Shouldn’t the goal be reducing pain and improving quality of life? Besides, moral crusaders such as Eyers usually confuse addiction with dependency. Addicts misuse drugs, using them for the sole purpose of getting high. Most people who use medical marijuana (and opioids such as Hydrocodone and Oxycontin) are not addicts. They use the drugs as prescribed to relieve pain and improve the quality of their lives. Long-term users can become dependent on such drugs, but, again, why does that matter? I have been on narcotic pain management drugs for fifteen years. Does this make me an addict? Of course not. I take the medications as prescribed by my family doctor. I have taken a variety of pain relievers over the years, but I have not, one time, abused them. Using these drugs for long periods has certainly made me physically dependent on them. If I were to stop taking Hydrocodone, for example, I would go through withdrawal. And believe me, that’s not fun. Several years ago, I stopped taking Tramadol. I had been using Tramadol on and off for managing mild pain for over a decade. It took months of suffering to successfully wean myself off of the drug. The withdrawal symptoms were so severe that I had to sleep in the living room so my thrashing and crying wouldn’t keep my wife awake. Yes, I survived, but at no time was I addicted to Tramadol. Dependent, yes. Addicted, no.

Count me as one person who is fucking tired of moralizing preachers such as Steve Eyers. First, they are hypocrites. Why did Eyers decide to take a stand against medical marijuana and not the drugs that are widely abused by Hicksville residents, including nicotine, caffeine, alcohol, and religion? Alcohol, in particular, causes all sorts of physical and social problems. Yet, crusading preachers are eerily silent on the subject — outside of an occasional anti-booze sermon. Why is that? Second, they attempt to force their personal or sectarian moral codes on others. There are times I wish that the Steve Eyerses of the world would come down with a debilitating, painful disease; one where relief could only be found through using narcotics or marijuana. Then, and only then, would they understand why chronic pain sufferers need drugs. Of course, I wouldn’t actually wish that on anyone, but there’s nothing like first-hand experience for revealing ignorant beliefs.

If Eyers and others like him want to live in pain, have at it. Taken literally as a moral prescription for living, the Bible encourages enduring pain and suffering. Just pray to God and trust that Jesus will be with you every step of the way, right? No thanks. As a humanist, my goal is to reduce suffering and pain, not only for humans, but all living animals. The greater goal is happiness and well-being for all. While suffering and pain can and do teach us valuable lessons, only Evangelical/Catholic sadomasochists think pain is desirable or necessary. Of course, when you believe the world is a shit hole ruined by sin, that all humans are born sinners/haters of God, that life is to be endured until the rapture, and that the grand goal is eternal life in Heaven, it should come as no surprise, then, that you don’t put much emphasis on the here and now.

Medical marijuana sale and use is legal in Ohio, and there’s movement towards making all use of weed legal (it could be on the ballot this November), All praise be to Shiva. Sadly, some Republican state legislators — who are overwhelmingly Christians — and regulators have gone out of their way to impede the opening of medical marijuana growers, processors, and sellers. Just over the border in Michigan, marijuana use is legal and much cheaper than Ohio’s medical weed. Sellers abound. Further, here in the Land of God, Guns, and Republicans, most doctors refuse to write prescriptions for medical marijuana. The insane government war against opioids has scared the shit out of medical professionals — fearing the loss of their licenses — so they refuse to act in the best interest of their patients. Ohioans can go to one of the few doctors approved to write medical marijuana prescriptions, but this could cause them all sorts of problems with their primary care doctors — including the refusal to treat in the future. (Please see How the War on Opioids Hurts People With Chronic Pain, A Plea From a Chronic Pain Sufferer: Please Be Aware of Others, Medical Marijuana and Relieving Pain and Suffering, How Fundamentalist Prohibitions Cause Needless Suffering and Pain,  and Understanding and Helping Those Who Live With Chronic Pain.)

Years ago, I helplessly watched a devout Evangelical man suffer horrific pain as he slowly died of bowel cancer. He refused to take pain medications because he believed Jesus was better than morphine; that his suffering had some sort of redemptive value. My late father-in-law often went without pain relief because he believed drug “addiction” (I tried to explain to him the difference between addiction and dependence to him, without success) was sinful. As a pastor, I watched countless dying congregants forgo narcotic pain management because they wanted to be clear-headed when they entered the pearly gates. They needlessly suffered, and for what? Remove God and the afterlife from the equation, and I suspect most people will say YES to anything that reduces their pain.

If Steve Eyers wants to suffer for Jesus, have at it. All that I ask is that he not stand in the way of other people getting the help they need. Jesus is called the Great Physician. The gospels detail many of the healing miracles the Son of God purportedly performed while walking the dusty roads of Palestine. Be like Jesus, Steve, Be like Jesus. If you can’t heal people, Steve, at least let the sick and hurting among you have access to people and drugs who can.

Pastor Eyers lost his battle against weed. Four years after his lies and distortions before the Hicksville Village Council, a new marijuana dispensary opened this week ten miles from his church in the village of Sherwood. Hicksville said no to the dispensary, as did the village I live in. Both Ney and Hicksville council members put their religious and personal beliefs before what was good for their communities. Tax money that could have helped fund local services went — dare I say it? — up in smoke.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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I Have COVID-19 — Again

Bruce Gerencser 25 Comments
gone fishing

I have been thrice vaccinated, yet I contracted COVID in August 2022. I was quite sick, but I survived. Today, I tested positive for the virus again. I’m sicker than I was the first time — mainly respiratory problems.

I will likely not do any writing this week. If you are sitting on a guest post, now would be a good time to send it to me.

Thank you for your love and support.

signature

Chronic Pain: Living Life When There Are Few “Better Days”

Bruce Gerencser 6 Comments
pain and suffering
I am sure glad I am so close to Jesus 🙂

“I hope you will feel better soon,” is an oft-heard line by chronic pain sufferers from well-meaning people. There’s this idea that our pain is temporary; that a cure awaits somewhere beyond the next doctor’s appointment. “A better day awaits,” people confidently say. How they could possibly know this remains unsaid, but such thinking finds its impetus in the idea that all suffering is temporary; that deliverance awaits just around the next corner.

For chronic pain sufferers, however, there are few better days outside of death on the horizon. We know there will never be a day when we “feel better,” outside of the marginal relief we receive from medications and treatments. In our minds, “it is what it is,” and no amount of good thoughts, wishful thinking, or prayer is going to change that fact.

Why, then, do the family members and friends of chronic pain sufferers ignore, marginalize, or reject this fact? If the pain sufferer can live with “it is what it is,” why can’t they? Certainly, family members and friends want the pain sufferer to feel better. I never doubt that such people are sincere or that they want what they perceive is best for me. Others have warped understandings of medical science or the specific medical conditions chronic pain sufferers face. They deify science, thinking that no medical problem is beyond treatment or cure. Doctors, of course, know better. They know that they can actually cure a handful of maladies. Most often, pain is managed and controlled. I know my doctors cannot cure me. My health problems are beyond simply taking medication or having surgery. Everything my doctors do is in the hope of giving me quality of life during what time I have left. I told my primary care doctor that I don’t expect him to cure me. I want him to do what he can to make my life better: less pain, and more mobility, or at the very least, no increased pain or debility That’s the contract we have with each other.

Many well-wishers think that if pain sufferers can, they should. If there is a treatment or procedure that “might” help, we should do it. Such people are convinced that a “miracle” awaits if the pain sufferer will just swallow this pill, eat these foods, take these supplements, have this surgery, or go through yet another treatment. They are unwilling to accept that “it is what it is.” When concerned family members and friends think (often wrongly) pain sufferers are giving in or giving up, they lecture and badger chronic pain sufferers, prodding us as a farmer with a cattle prod, to move forward through the chute of life. In their minds, giving in or giving up is always wrong, even if doing otherwise leads to more pain and suffering. I have watched numerous people — including my wife’s father — go through horrific pain and suffering, all because family members didn’t want their loved ones to give in or give up. And in the end? They died anyway.

I take a stoic approach to life. I have had a lot of trauma, tragedy, and suffering in my life. All suffering is personal. I know that what I have experienced is less than what some people have faced, but more than what others have gone through. When one of my toddler grandsons gets a boo-boo, his pain is every bit as real as Grandpa’s. The difference, of course, is that I have had almost sixty-six years of trauma, tragedy, and suffering. My lived experiences are far different from that of grandchildren or people decades younger than I am. All I know to do is to empathize with people when they are suffering, even when I know their pain is less than mine. I know that pain is a great teacher. I have had numerous steroid injections over the years. Polly always goes with me when I get juiced up. She usually remarks about my stoic mentality when the orthopedic doctor is sticking a long needle into my shoulder, hips, or hands. I always tell her that I have experienced horrible pain in my life; that the injections are uncomfortable, but nothing compared to my day-to-day pain or some of the painful procedures I’ve had in the past. I have developed mental processes that help me embrace the pain; the mental version of gritting one’s teeth and clenching one’s hands.

As I sit sideways in my recliner typing this post, my body hurts — literally — from head to toe. Herniated discs in my spine and neck, degenerative spine disease, osteoarthritis in numerous joints, muscle pain from fibromyalgia, and nerve pain in my legs and feet have left me in constant pain. I take narcotic pain medications, NSAIDs, and muscle relaxers to cope with my pain. They help, to be sure, but these drugs do not magically deliver me from pain. That has never been the goal. Pain medications and muscle relaxers, at their best, tamp down pain spikes. Certainly, I could take high enough levels of narcotics to make my pain go away, but in doing so I would sacrifice living a meaningful life. You see, “not dying” is not my grand goal. I don’t want to spend the last months and years of my life so drugged up that all I do is sleep, hoping that doing so will add a few days to my life. I choose quality over quantity, even if it means more pain than I would otherwise have.

I try to educate myself about the various diseases and debilities that I have. When I was diagnosed with gastroparesis (an incurable stomach disease) two years ago, the first thing I did was study up on the disease and its treatments. Knowledge really is power. With knowledge, I can know what to expect and how to best treat symptoms. I work in partnership with my doctors, knowing that the person who best knows my body is me. Unfortunately, family members and friends aren’t going to do this, so they often say ill-informed, ignorant, and, at times, stupid things to chronic pain sufferers. Typically, I ignore them. Other times, I ask, what treatment or drug do you suggest? Well, uh, I heard, I read on Facebook . . . You see, they don’t have any answers either. Why? In my case, there are no treatments, drugs, or surgeries that will lessen my pain and suffering in meaningful ways. And if there were, don’t you think I would investigate them and act accordingly? Or do some family members and friends think I want to be in pain; that I enjoy crippling pain, debility, vomiting, and diarrhea?

I have accepted that “it is what it is.” Unless there is a major medical breakthrough, I know that my life tomorrow and the day after will pretty much be, pain-wise, as it is today. I have embraced this fact. Are there treatments that I could have done that would offer short-term, temporary relief? Sure, but to what end? In 2021, I had a procedure done under anesthesia that used Botox to paralyze a muscle in my stomach. Did it work? Did I find relief? Sure, for three days, and then I was right back to being nauseous and vomiting. The same goes for epidurals and nerve blocks. They last for a short amount of time and are prohibitively expensive. I tried all of these procedures, but I decided, in the end, I didn’t want to deal with the false hopes and highs and lows that come from such treatments. A while back I had a night when I slept for nine hours, only waking up twice. I hopefully thought, “is this a sign of better days ahead”? Of course not. It was an anomaly. The next night I got two hours of sleep, and after that, I had on-and-off sleep for ten hours, as is typical for me.

I have accepted the fact that “better” days are not on my radar; that if I want to live, write, and enjoy what life I have, I must embrace my pain, do what I can, and try to ignore the well-meaning well-wishers. And when I can’t, I write a blog post. 🙂

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Chronic Illness: Oh, What a Night!

Bruce Gerencser 12 Comments
oh what a night

There are days, and then there are DAYS; memorable days; unforgettable days. Yesterday, and into the early morning hours of today, was one of those unforgettable days. I have had a lot of bad, really bad, awful days over the past three years. Thanks to gastroparesis, fibromyalgia, and degenerative spine disease, every day is challenging. Most days are normal, but there are other days that stand above what has come to be my “new normal.”

About 7:00 pm last night, my battle with nausea kicked into overdrive. My goal is to avoid vomiting. I took some Zofran, hoping it would ratchet the nausea down to normal levels. An hour later, I realized that the medicine was not going to work (it usually works quickly). I finally felt that awful feeling, the call to bow before and worship the porcelain God. I slowly rose from my recliner, picked up my cane, put my right hand over my mouth, and made my way to the bathroom. I quickly knelt before the toilet and up came the contents of my stomach. I repeatedly vomited for what seemed like eternity. Once I determined that I was “safe,” I got up off the floor, washed my face and beard — which was covered with chunks of vomit — and returned to the living room. I still felt nauseous, so I took more Zofran, hoping that I wouldn’t have to throw up again. The medicine quickly kicked in. All praise be to Loki and modern medicine.

Surely, this is enough for one day, right? Right? I mean, right?

Polly came home from work at 2:30 am. She asked me if I wanted anything to eat. I told her nnnnnooooo! We watched a bit of TV and then headed for bed. The time was 3:45 am. Polly did her usual bathroom routine while I arranged my side of the bed in preparation for yet another titanic struggle with pain. I took my nightly medications, including Vicodin, Zanaflex, and Trazodone — all meant to reduce my pain so I could sleep. At 4:15 am, I told Polly “good night” and told her “I love you.” As is her custom, Polly gently patted my side and told me “I love you too. I hope you have a good night.” In a matter of minutes, Polly drifted off to sleep. I started watching a new series on Netflix, hoping to join Polly in dreamland one to three hours later.

Surprisingly, I fell quickly asleep, only to wake up an hour later. What could happen in an hour, right? Due to the excruciating pain in my back and neck, I typically sleep on my right side or on my stomach. This night, I started out on my side. Sometime during the hour I was asleep, my right leg fell off the bed (a common occurrence). When I woke up (the first time), I was alarmed to find that my leg and right arm were totally paralyzed (not numb, paralyzed — a first). It took me about ten minutes to get my leg back on the bed. I suspect the nerve (s) controlling my leg and arm had gotten pinched. Once I was properly situated on the bed, the paralysis eventually went away.

Surely, this is enough for one day, right? Right? I mean, right?

As I wrangled my body on the bed something didn’t feel right. Why do my back and legs feel wet? I stood up by the bed and surveyed the blanket and sheets. Water, maybe? Nope. Shit. Lots of shit. I had lost control of my bowels. Worse, in trying to get my body settled, I had rolled in the shit. The “wet” on my back and legs was shit. Think: vanilla ice cream cone rolled in chocolate. I said to myself, “are you fucking kidding me?”

Surely, this is enough for one day, right? Right? I mean, right?

As I made my way to the bathroom to get a wet washcloth and towel, I noticed I was really weak and lightheaded. Halfway to the bathroom, I passed out for a second, sending me careening into a white folding table in the living room. Fortunately, this broke my fall.

Surely, this is enough for one day, right? Right? I mean, right?

Nope. You see, when I used the table to break my fall, my glasses were on the top of the table, Of all the things I could have hit, I put my full weight on my glasses, bending them to such a degree that I can’t wear them.

I finally made it to the bathroom, got the towels I needed, and returned to the bedroom to clean up my mess. Amazingly, Polly slept through all of this. I didn’t feel I needed to wake her up, though I could have used some emotional support. “My shit, my problem,” I told myself.

After cleaning the bed, I sat on the side of the bed for 30 minutes or so, head in hands, wondering if I could go on. I finally decided I could, and snuggled back in bed next to Polly.

Surely, this is enough for one day, right? Right? I mean, right?

Finally, I can say yes.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Bruce, These Doctors Can Heal You

Bruce Gerencser 8 Comments
peanut gallery

Today, a woman named Sherryll left the following comment on the post titled The Tyranny and Oppression of the To-Do List. I have no idea whether Sheryll is a drive-by reader or a regular reader. I doubt she’s a regular reader for this reason: people who have been reading my writing for years know I have no use for unsolicited medical advice. Both on the comment guidelines and contact page, I ask people to not send me medical advice. I have an expert team of medical doctors caring for me. Beyond that, I have read scores of books, articles, and studies about the various diseases that afflict me. I have been tested, poked, scanned, and injected more times than I can count, including extensive work-ups at the University of Michigan and the Toledo Clinic. I’m confident that my diagnoses are accurate, as is my treatment plan.

Hi there Bruce! I’m so sorry you’re dealing with such pain!

I have been dealing with chronic pain for twenty-five years. My pain is widespread and diverse, from the bottoms of my feet to the top of my head. I have muscle pain, nerve pain, joint pain, eye pain, and bowel pain. This pain is not the normal aches and pains expected at age sixty-five. I have three types of days: less bad pain days, bad pain days, and screaming, off-the-charts pain days. I don’t have pain-free days.

Most of my pain is structural. I have osteoarthritis in virtually every joint in my body. Eighteen months ago, I started having severe pain in my upper back. This pain later spread to my neck. An MRI of my back revealed:

  • Disc herniation (T7,T8)
  • Disc herniation (T6,T7)
  • Central spinal canal stenosis (T9/T10, T10/T11)
  • Foraminal stenosis (T5,T6)
  • Disc degeneration/spondylosis (T1/T2 through T10/T11)
  • Facet Arthropathy throughout the spine, particularly at T2/T3, T3/T4, T5/T6, and T7/T8 through the T12/L1 levels.
  • Hypertrophic arthropathy at T9/T10

An MRI of my neck revealed similar damage.

These issues are structural in nature. No medication, supplement, or exercise is going to “cure” me. I recently saw a neurosurgeon at Parkview Hospital in Fort Wayne. There’s nothing that can be surgically done for me, especially my back. The surgeon’s notes state: the patient will have to live with it.

I too have suffered through the years with similar issues but I fortunately found a doctor in Dallas Texas that helped me. He died three years ago, but his associates are carrying the torch and assisting others in their personal healing process!

Doctor Sherryll, who stayed at a Holiday Inn Express last night, says that she had “similar” problems as mine. I doubt it. She doesn’t know enough about me to make such a judgment, but that doesn’t matter in this Internet age. She sees that I have chronic pain; she had chronic pain; she was healed; I can be healed too.

The doctors in question operate the Environmental Clinic in Dallas (Richardson)Texas. The front page of their website lists their primary service offerings: allergy testing, immune support, nutrition, and detoxification. Does anyone smell “alternative medicine?”

Environmental Clinic’s website states:

Did you know that many common ailments may be traced to substances you are exposed to in your everyday environment? Thirty years ago, even medical science was not broadly aware of the extent the environment affected health. But, thanks to much research and the work of pioneering physicians, doctors now recognize such maladies as headaches, sinusitis, fatigue, joint aches, blood vessel abnormalities, asthma and chronic infections may be caused by environmental factors. The Environmental Health Center-Dallas is one of the oldest and most advanced centers in the world addressing health and disease as it relates to the environment. The center provides full-service medical care with a special emphasis on the impact of environmental factors on the human body.

According to Dr. William J. Rea, the surgeon who founded the Clinic in 1974, various exposures may cause sleep disturbance, learning disorders, blood vessel, colon and bladder inflammation, as well as a host of other inflammatory problems. The “environment” involves all of our surroundings, including everything we breathe, eat, or touch. It consists of thousands of substances we are exposed to each day, but often do not even know exist. They are substances like the air-pollens, molds, and animal danders in the air, machinery, carpets, cleaning supplies, perfume and smog produces chemical by-products.

For those unacquainted with the effects of the environment on our lives, this process can be compared to carrying a load of bricks. Just as we might fill our arms with bricks, our bodies are being filled with a variety of stressors, including biological, chemical, emotional and physical. As long as the amount of bricks, or stress factors, stay within a range our bodies can manage, everything is fine. But, when the load becomes more than our bodies can handle, down come the bricks. This collapse is represented physically as symptoms.

New patients begin by completing a detailed patient questionnaire and meeting with the physician. Lab tests are often recommended, as is sensitivity testing. In the latter, the patient is exposed to or injected with low levels of various substances which help to identify the cause of their sensitivity.

When the triggering agents are pinpointed, the physician determines an individualized program to help each patient achieve a state of maximum health. This program includes educating patients about their sensitivities, nutrition and environmental exposures as well as getting them actively involved in their treatment. Some patients also receive immunotherapy, a specialized type of vaccine treatment that may provide substantial relief.

At this point, I say sigh. (Why I Use the Word “Sigh.”)

It takes being pro-active though consisting of adopting a healthy diet and exercise within your present capacity.

Note the judgmental presumptions Sherryll makes about me. She assumes, without evidence, that I am not being proactive about my health; that I am not eating a “healthy” diet; that I am not exercising enough. How could Sherryll possibly know these things? In her mind, she thinks that I am not “healthy,” so these must be the reasons why. Would it matter to Sherryll if I told her that I AM proactive; that I eat a vegetable-filled well-balanced diet; that I do what I can physically within the limits of what my body will tolerate and allow? Of course not. Much like religious Fundamentalists, food fundies, homeopathic fundies, and alternative medicine fundies think they have THE truth; that all other viewpoints are lies bought and paid for by big pharma, rich doctors, and hospital conglomerates. These people want us to stay sick, keeping from hearing the true gospel of glorious health. This, of course, is bullshit.

When I look at prospective treatments, all that matters to me is the science. Not anecdotal stories; not sketchy studies; not medical professionals who have an axe to grind.

I realize you feel as if you’re knocking on heaven’s door(as an atheist, you still get the picture) but I am hoping with your drive—- albeit diminished via the illness—you could be up to the challenge! If interested look up Environmental Clinic in Dallas Texas! My best to you!

Sherryll wrongly thinks that she is providing me a “challenge”; that if I really want to get well, I need to accept her challenge. What, are we in grade school? I did look at Environmental Clinic’s website, including its extensive offerings of woo and pseudoscience. No thanks.

Bruce Gerencser, 66, lives in rural Northwest Ohio with his wife of 45 years. He and his wife have six grown children and thirteen grandchildren. Bruce pastored Evangelical churches for twenty-five years in Ohio, Texas, and Michigan. Bruce left the ministry in 2005, and in 2008 he left Christianity. Bruce is now a humanist and an atheist.

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Your comments are welcome and appreciated. All first-time comments are moderated. Please read the commenting rules before commenting.

You can email Bruce via the Contact Form.

Bruce Gerencser