Commonly Known as a Heart Attack

I shouldn't have being playing golf Thursday. I woke that morning feeling lethargic. I had a nagging pain in the middle of my upper back. But with my history of pericarditis, and more recently, arthritis, I seldom go through the week without some pain here or there. I decided to ignore the way I felt and play golf. That was my first mistake.

I took an Ibuprofen, threw my clubs in the car and drove to the course. I was playing with my good friend, who'd invited me to play at his club at Meadow Springs, a beautiful course nested along the Amon Basin creek watershed. The sky was overcast as I parked and checked in. By the time we were standing on the tee, about 12:00, a slight drizzle had started. My friend asked if I wanted to take the golf cart. I told him I wanted to walk the first Nine to get some exercise. That was my second mistake.

Because course maintenance was taking place on the Front Nine, the pro shop started us on No. 10, which is an elevated tee crossing Amon Creek at the bottom of the hill. After that, the course regains altitude at a steep rate. By the time I'd negotiated the first six holes, I was having trouble catching my breath. At the No. 16 tee I had a pressing feeling in my chest. Did I quit? No, I struggled on. That was my third mistake. You know what they say about three strikes.

I finished the round, joined my friend for lunch, which I couldn't finish, and went home. I lay down for an hour, took a shower, and joined my wife on the couch. This was about 5 pm. By this time I was experiencing a severe throbbing pain radiating up my left carotid artery into my neck. I went back and lay down.

My wife came in and asked me what was happening. She said I should go to the emergency room. I said I'd take an aspirin and wait it out. Another mistake.

I couldn't sleep. I tried elevating my head and back, something I'd done when I had pericardial pain. It didn't help much. I continued to have the throbbing pain up my left carotid artery, into my neck, and over to my shoulder. I was sweating. I took 3 more aspire @ 325 mg ea over the next 8 hours.

The next morning, a Friday, March 29th, I called my primary care physician and speaking to the receptionist asked to have an appointment ASAP. She said she could get me in Monday. I said okay. She asked me why I needed the appointment. I said, "I'm having chest pain." She said just a minute. Then she came back on the line and said, "Go to the emergency room." This time I followed instructions.

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As it turns out, if you're experiencing chest pains, the best advice is to call 911. This way you'll get directly to the ER, you'll get there quickly, and you'll likely get emergency treatment along the way. Going to your primary care physician first is poor policy, if you are having a heart attack. Learn to recognize the symptoms and be smarter about taking action than I was. The longer you delay, the more heart damage you'll have, and the longer your recovery will be -- assuming you recover.

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My son drove me to the nearest emergency room, which was at Kennewick General Hospital (now Trios). When I told the person manning the reception desk my problem, he took me right to the triage nurse; the first time I hadn't been asked for ID and insurance when going to the hospital. I was with the triage nurse for no more than 3 minutes before I was taken to a room and placed on an examining table.

Before I knew it, a lab tech had taken blood, I had an IV in my right arm near the wrist, and had been wired for an ECG. After the ECG a technician wheeled in an X-Ray machine and did a chest X-Ray. At some point, a nitroglycerin patch was placed on my chest. The IV contained a blood thinner, easing the blood pumping burden on my heart.

The attending physician came in to see me about 20 minutes into this process. He told me indications were that I'd had a heart attack. KGH didn't have a cardiac specialist available to do a catheterization, so they were transferring me to Kadlec. He asked me who my primary doctor was, I told him, and he said he'd notify him.

Someone from the hospital business office came by and finally collected my insurance cards (Medicare and TriCare), and then I was visited by a social worker. Before the social worker could finish his interview, the EMTs showed up to load me into the ambulance.

I was transferred to Kadlec by ambulance. One of the EMTs sat in the back with me and monitored my vital signs. It took 18 minutes to get from KGH to Kadlec. On the way I learned the EMT liked to read and promised him a signed copy of my soon-to-be-published novel, The Lion and the Sun. I was assuming I'd be alive to sign the book when it was published. I'm an optimist.

At Kadlec I was taken directly to the cardio ward, where ECG sensors were attached to my chest and connected to a transmitter that sent signals wirelessly to a display at the side of the bed. 

An IV drip was started, and additional blood work was done. Another ECG was performed. My cardiologist walked into the room a few minutes later. Friday was normally his day off. He'd be in checking on me the next two days, Saturday and Easter Sunday.

My cardiologist put his stethoscope on my chest and as he listened to my chest he told me that my ECG was abnormal -- I had an inverted t-wave -- and blood work indicated I'd had a myocardial infarction, commonly known as a heart attack. I asked how blood work indicated a heart attack. The doctor told me that my troponin level was elevated.

The troponin test measures the levels of certain proteins called Troponin T and Troponin I in the blood. These proteins are released when the heart muscle has been damaged, such as a heart attack. The more damage there is to the heart, the greater the amount of Troponin T and I there will be in the blood. An increase in the troponin level, even a slight one, usually means there has been some damage to the heart. Significantly high levels of troponin are a sign that a heart attack has occurred. Cardiac troponin levels are normally so low they cannot be detected with most blood tests. Test results are usually considered normal if the results are between zero and 0.10 ng/mL. My Troponin I was 2.64.

Another test that showed evidence of an heart attack was Creatine Kinase-MB (CK-MB). A CK-MB of more than 2.5 to 3 is indicative of heart damage. Mine was 10.7.

This doctor had been my cardiologist for many years. I saw him regularly because of my history of pericarditis. Even though I'd had my pericardium removed, I had over the years experienced pain of the type I experienced when I had a pericardium. I'd assumed it was from residual pericardial tissue left around major arteries. My cardiologist wasn't so sure. He said it might be from that, or from an unrelated cause, such as arthritis, sprains, congestion, infection, or imagination.

Over the years my doctor had performed a myriad of tests to monitor my heart function, including ECGs, Echocardiograms, stress tests, nuclear stress tests, ultrasound scans, and regular blood work to track my cholesterol. Despite my checkered medical history, and high cholesterol, my heart function was essentially normal (I had moderate mitral valve regurgitation, meaning the valve wasn't closing completely and blood was leaking back out). In my most recent stress test, I'd gone 11.5 minutes, which was essentially what I done twenty years ago.

My doctor knew that I was proficient with the Internet and did a considerable amount of research on medical issues. He had always been very open with me and willing to discuss matters associated with my history of heart problems. I'd even offered to will him my heart (I was sure to stipulate, after my death) to use in research on long-term survival of pericardectomy survivors (he wasn't interested).

The doctor told me that he wanted to have coronary angiography performed. I wasn't anxious to have this done, mainly because I didn't like the risk involved in having a wire inserted into my coronary arteries and I wasn't sure the test was required. My doctor convinced me otherwise by pointing out my history of high cholesterol and the fact that I'd gone off my cholesterol medication several months previously because of myopathy brought on by the statins in the medications. He said that with the test we could determine if my heart attack had been brought on by clogged arteries or something else. This would help determine the course of therapy. I couldn't argue with the logic.

I was wheeled to the "cath lab" around noon Friday. My wife and my son accompanied me as far as the prep room, where my groin area was shaved. An angiogram can be done by inserting the catheter through the femoral artery in the groin (most common), or through the radial artery in the forearm. I had the former procedure. An estimated 3 million coronary angiograms are performed in the United States each year to look for blockages in coronary arteries. The radial artery is currently used in less than 5% of them. However, a recent study suggests angiography using the radial artery is just as effective as the technique using the femoral artery, and patients report finding the procedure less uncomfortable. I did not experience any significant pain during or after the procedure.

Cath Lab

During coronary angiography, special dye is released into the bloodstream. The dye makes the coronary arteries visible on x-ray pictures. This helps doctors see blockages in the arteries.  Cardiac catheterization is used to get the dye into the coronary arteries. For this procedure, a thin, flexible tube called a catheter is put into a blood vessel in your arm, groin (upper thigh), or neck. The tube is threaded into your coronary arteries, and the dye is released into your bloodstream. X-ray pictures are taken while the dye is flowing through the coronary arteries. Because the dye can cause nausea and or stuffiness, I was given medication to prevent stomach upset (Pepcid) and nasal passage blockage (Benadryl) prior to the procedure.

The doctor performing the procedure came to the side of the operating table and introduced himself. He described the procedure for me, and kept me informed throughout it. A nurse applied local anesthetic (1% lidocaine) to my right groin. The doctor said, "You're going to feel a slight pinch," and inserted the arterial sheath through which he'd thread the catheter. The pain I experienced from this was what I'd describe as a lower case ouch. My wife told me later that the procedure took twenty minutes. I was awake throughout. Afterward, the doctor came out and told us that my coronary arteries were clear.

The doctor also told us that I had a significant gradient between the apical segment and mid segment of the left ventricle. He thought this likely due to segmental hypertrophy cardiomyopathy (thickening of the muscle). The doctor thought it advisable that I undergo a cardiac MRI and OTE. Hypertrophic cardiomyopathy (HCM) is a genetic cardiac disease that can cause sudden death, or go undetected for the affected person's lifetime. Unless my lifetime is 75 years, I fall into the latter group.

Aside: Even after my 1965 pericardectomy I experienced fairly regular chest pain, reminiscent of the pain I experienced with pericarditis. This has continued with reduced severity all my life. Given this heart attack and the results of tests associated with it, I am curious as to whether the "thickening" noted might be due to recurrent inflammation.

My hospital stay was uneventful -- no "Code Blue" -- and as is generally the case -- little sleep. Hospitals are noisy, and lab techs wake you at all hours. In addition, this hospital had a system of alerts that when initiated, sounded in all rooms, just in case needed staff were away from station. This is a really annoying system -- haven't they heard of pagers? In addition, the bed was programmed to change angles and slopes in order to prevent bed sores for bedridden patients. The movements occurred every 40 seconds (I timed them) and were accompanied by a low 'growl." Eventually, I got used to the bed growling at me and growled back. My second night in the hospital I asked for Ambien (zolpidem), and that helped significantly (I took half at 10 pm, and the other half at 3:30 am, after the lab tech woke me for blood work).

Prior to my release from the hospital on a bright, sunny Easter morning, I underwent an Echocardiogram. According to my cardiologist, the results showed a thickening of the ventricular wall (from the lab report, "moderate concentric left ventricle hypertrophy"), and some other segmental thickening (again from the lab report, "sigmoid shaped septum with focal hypertrophy of the basal septum"). My ejection fraction (EF) was normal, at 60-65% (percentage of blood pumped from the heart's ventricles). This is interesting, since thickening generally results in reduced heart efficiency.

My instructions from my cardiologist were to go home and take it easy. He put me on Coreg to slow my heart, which would aid healing, and Ibuprofen twice a day for pain. He said my recovery might take 6 to 8 weeks. I am scheduled to see him again on May 10th.

One week after my release from the hospital, I'm essentially free of pain, I have no shortness of breath, or dizziness, and I'm going stir crazy.

Living without a Pericardium

The Pericardium

I was trying to give my heart to my cardiologist, let’s call him Dr. Sing.

“Why would I want your heart?” he asked in his soft, sing-songy voice, a little smile on his round, brown face.

“For research,” I said, holding out my hands as if they were holding the very heart I was offering.

“I’m not doing any research,” Dr. Sing protested. “Besides, there are plenty of hearts to be had if one is to be looking.”

“But my heart has been without a pericardium for over forty years now,” I said. “Surely that means something to medical researchers.”

I had chronic pericarditis as a young man and my pericardium had to be removed. Without going into all the gory details, think of the pericardium as a partially inflated balloon into which the heart is shoved. The balloon, the pericardium, forms around the heart and acts (I’m guessing here) as a kind of shock absorber. Pericarditis is an inflammation of the pericardium. It can have a variety of causes. Mine was caused by an unknown and very persistent virus. After many episodes, my pericardium had begun to constrict the heart and so had to be removed. Think of peeling a peach; a peach that has a lot of arteries attached to it.

Performing a pericardiectomy. That evil looking device is a rib stretcher.

“Medical researchers are very much acquainted with pericarditis,” Dr. Sing said. “In fact, last week I had a man come in with chest pain and as soon as I listened to his chest I knew what it was.”

“You heard a rub?” I said, showing off my knowledge of the so-called pericardial friction rub caused by the outer and inner walls of the inflamed pericardium rubbing against each other.

“Yes, of course,” Dr. Sing said, handing me a slip of paper. “This is an order for a chest X-Ray.”

I took the X-Ray order without looking at it. I’d derailed my argument by trying to show off. I tried to get back to it. “Yes, there’s a lot of information on pericarditis, but what about information on what happens to the heart when it has to get along without a pericardium?”

“Well, your heart seems to have done just fine,” Dr. Sing said. “Look at your stress test.”

The stress test involved hooking me up to an EKG and having me run on a treadmill, on which Dr. Sing kept increasing the incline until I was about to fall off the back. When I quit, breathing hard and drenched in sweat, Dr. Sing said, “I’m disappointed.”

“Why?” I asked. “I went longer than I did last year. What was it, eleven minutes? More?”

“Well, I had a man do almost twenty minutes,” Dr. Sing said. “Of course he was half your age and a tri-athlete,” he said, chuckling.

He was beginning to get on my nerves.

I was seeing Dr. Sing because I had been experiencing a recurrence of upper back pain, mostly under my left scapular. I have had chest and back pain on and off ever since my pericardiectomy in 1965. My doctors over the years had explained it as very probably inflammation of pericardial tissue remaining around major arteries.

“They can’t get everything,” one doctor told me, squeezing my shoulder reassuringly.

When I asked about why I got back pain from inflamed tissue around heart arteries, I was told the pain was “referred.”

I learned that referred pain happens when nerve fibers from one region of the anatomy converge with nerve fibers from another region at the spinal cord. Nerve impulses apparently jump the track and cause, for example, that horrible, aching pain that runs down the arm during a heart attack.

Pain felt in one area of the body does not always represent where the problem is because the pain may be referred there from another area. For example, pain produced by a heart attack may feel as if it is coming from the arm because sensory information from the heart and the arm converge on the same nerve pathways in the spinal cord.

But I digress. After all these years of living without a pericardium, I was wondering why we have it in the first place. Maybe, I thought, it’s vestigial, like the appendix. If so, removing it would probably have about as much impact as removing the appendix, although recently, medical researchers may have changed their mind about the usefulness of the appendix, describing it as a little factory that manufactures “good bacteria.” Surely the pericardium has a useful function, as well. Maybe it manufactures good acne. Wouldn’t it be useful to know what happens when a person has to get along for most of his or her life without a pericardium?

The pericardium is said to be a tough, two-layer membranous sac enclosing the heart. The outer layer, called the fibrous pericardium, protects the heart from contact with the chest wall, ribs, sternum, and lungs. The pericardium wraps completely around the heart, extending around the bases of the great vessels; the aorta, superior and interior vena cava, pulmonary artery and vein as they arise from the heart. Two ligaments attach the top of the pericardium to the back of the sternum. Other ligaments loosely connect the bottom of the pericardium to the diaphragm. These structures anchor the heart in its place in the chest.

I started researching the question of what effect removal of the pericardium might have and came across an abstract in the International Journal of Cardiovascular Medicine that began, “The removal of the pericardium does not appear to have…” This could be what I was looking for. I brought up the article itself and read on. “The removal of the pericardium does not appear to have any deleterious effect in the normal dog.” Well, that was a start, wasn’t it?

A study performed in Spain (Departamento de Cardiología y Cirugía Cardiaca, Hospital de la Santa Creu i de Sant Pau, Barcelona, España) found that of those patients who survived the initial procedure (16% did not), 82% were still alive after 9 years, and 64% after 10 years. Pericardiectomy improved or alleviated their symptoms. A study performed in France of long-term survival of pericardiectomy patients was not so positive. It found that pericardiectomy allowed a clear functional improvement, but following pericardiectomy more than 60% of patients died within 10 years of the diagnosis being made.

A Japanese study followed 24 post-pericardiectomy patients for up to 27 years, with surgeries taking place between 1966 and 1990. Survival rates were 85% at 5 years, 67% at 10 years, and 58% at 15 years. As in other studies I reviewed, the causes and complications encountered in the patient population varied considerably, making any definitive conclusions difficult.

A retrospective analysis of the records of 60 patients who underwent pericardiectomy over a 10-year period (1980 to 1990) at Johns Hopkins showed differential operative and long-term survival rates based on the cause of the disease. A history of malignancy, previous pericardial procedure, and preoperative New York Heart Association class IV were found to be predictors of poor survival. The operative mortality rate for pericardial effusion and constriction was 4.2% and 5.6%, respectively. Follow-up (median follow-up, 56.9 ± 38.2 months) was obtained on 56 patients (93.3%). Actuarial survival at 1 year, 5 years, and 10 years for all patients was 82.1% ± 5.1%, 71.7% ± 6.7%, and 59.8% ± 12.2%, respectively. All patients who underwent operation primarily for effusion with associated pain were found to be alive and had improved functional capacity without steroid use. The researchers concluded that pericardiectomy can be performed with low mortality and can result in good long-term survival and improved functional capacity. Patients who are seen primarily with pain refractory to steroid therapy can be relieved of symptoms with operation.

The most interesting study from my standpoint was one performed at the Cleveland Clinic, in Cleveland, OH, titled: Constrictive pericarditis (CP): etiology and cause-specific survival after pericardiectomy. In this study, the etiology of CP was idiopathic in 75 patients (46%), prior cardiac surgery in 60 patients (37%), radiation treatment in 15 patients (9%), and miscellaneous in 13 patients (8%). Long-term survival after pericardiectomy for CP was found to be related to the underlying etiology, LV systolic function, renal function, serum sodium, and PAP. The relatively good survival with idiopathic CP emphasizes the safety of pericardiectomy in this subgroup.

One has to be careful about how to interpret findings that survival rates after pericardiectomy are best when the cause of pericarditis is "idiopathic," i.e., unknown. This isn't a case of, "The less we know, the better your chances." What this means to me is that ruling out known serious illness/injury as an underlying cause of pericarditis, such as tuberculosis, cardiac surgery, cancer, etc., results in a patient population for whom pericardiectomy is more straightforward and less likely to result in follow-on complications, thus improving survival.

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I woke up on a sunny Tuesday morning in July of 1962 at Chanute Air Base in Rantoul, Illinois, feeling tired and slightly feverish. I had pain in my left shoulder and a dull ache in the middle of my chest. I dressed and went to my Aircraft Maintenance Officer’s training class. By noon, the ache in my chest was sharp and constant, and I was having trouble breathing. I went to Sick Call at the infirmary, where they checked my temperature (97), blood pressure (145/80), and pulse (88), listened to my chest (“clear”), and sent me home with a tube of Bengay heat rub.

By 1700 that evening my chest pain was severe and got worse if I tried to take a deep breath. I couldn’t lie down, because the pain became much worse and breathing was more difficult. It was a struggle getting back to the infirmary, as any exertion caused greater pain. When I shuffled into the infirmary gasping for breath they immediately put me in a wheel chair and took me to an examining room, and then admitted me with, “Chest pain, undetermined etiology.”

It was two or three days before a doctor brought in from the teaching hospital at the University of Illinois at Urbana-Champaign diagnosed my problem as pericarditis by identifying the rubbing sound he heard while listening to my chest as a “friction rub,” the sound of the inner and outer layers of the inflamed pericardium rubbing against each other. This was my first case of pericarditis. I was 24 years old. I would have another 9 episodes of pericarditis before my pericardium was removed at Wiesbaden AFB, Germany, in January of 1965.

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I was a 2nd Lt when I first came down with pericarditis at Chanute. I had a second episode while there, was admitted to the hospital again, and after a few days, was permitted to attend class during the day and return to the hospital in the evening. I completed training with the class behind my class and received my assignment to the 36th Tactical Fighter Wing at Bitburg Air Force Base, Germany.

Medical tests failed to reveal the underlying cause of my pericarditis. It was recorded as "idiopathic," and presumed to be viral in nature. An interesting footnote was appended to the medical record, which stated that I had been quartered with Arab officer maintenance training students and one of them, an "Ahmed Gandi," had been hospitalized with "precordial pain." He was in the hospital 2 weeks, and then again a second time for 4 weeks. He did not finish the training course, and nothing more was known about his condition. The doctor at Wiesbaden preparing the clinical record preceding my pericardial window, an F. Steichen, wrote that, "It might be interesting to write to Chanute AFB Hospital to get the diagnosis of Gandi's disease." It's puzzling to me why Dr. Steichen would think this information relevant, since everything I've read indicates that viral pericarditis is not contagious. In any case, to my knowledge, no follow up was done on the matter.

I had my first "overseas attack" of pericarditis on the 15th of February 1963 and this time I told the examining physician at the hospital exactly what the diagnosis was. He had my medical records and gave me no argument. While hospitalized I developed an effusion and was treated with ACTH (prednisone).

Air Force Hospital, Wiesbaden, Germany

On March 5th, I was transferred to Wiesbaden, the main hospital in Germany, for further evaluation. I was there for almost a month undergoing one test after another; blood work, EKG, X-Ray, and lymph node, bone marrow, blood vessel, and muscle biopsies. Finally, I underwent surgery to make a "window" in the pericardium, and allow doctors to obtain pleura and pericardial tissue samples, and to preclude constriction. All test results were normal, except for fibrosis of the pericardium, which was caused by scarring due to pericarditis.

I was returned to Bitburg to convalesce from surgery and returned to full duty after two weeks. I had another attack of pericarditis on the 24th of April, then on the 19th of November, and the 14th of December. My next attack wasn't until August 3rd, 1964. I married my nurse in September 1964. We were spending so much time together we thought we might as well formalize the arrangement.

When I wasn't in the Bitburg Air Base hospital, I was working in my specialty as an aircraft maintenance officer, first on the flight line, then as Chief of Maintenance, then as an assistant maintenance control officer. I worked 12-hour days regularly, and we were subject to frequent alerts, when the horn would sound at 0300 hours and we'd sprint to the flight line, not knowing whether it was another drill, or whether the Russians were charging across the Fulda Gap.

My frequent bouts with pericarditis effected me in three ways. First, I was less physically fit than I had been going into the Air Force. I'd been active in sports and was in excellent physical condition. I enjoyed running, but after several episodes of pericarditis, I found I had no "umph" in my legs. I remember starting to run on the air base track and staggering to a stop, bent over, hands on my knees. It was a very discouraging experience.

Second, my officer evaluations had been downgraded from outstanding to excellent by the reviewing officer, and my recommendation for a Regular Air Force Commission had been refused by the reviewing officer, on both counts because of my frequent attacks of pericarditis. I'd been hospitalized or confined to quarters a third of the time I'd been at Bitburg. I couldn't blame the reviewing officer for thinking that my boss was inflating my evaluation.

Bitburg AFB Hospital

Third, I was for the first time in my life concerned about my health and the implications for my future and that of my family. My new wife was pregnant with our first child. If the Air Force decided I was physically unfit for duty, what then?

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The Superior Vena Cava and the Inferior Vena Cava both bring deoxygenated blood to the heart. Generally, the Superior Vena Cava carries blood from the upper part of the body while the Inferior Vena Cava carries blood from the lower part of the body. Like all veins, the Superior and Inferior Vena Cava are made of smooth muscle. Unlike arteries which require their elasticity to withstand the pumping of the heart, veins are more inelastic. These two large major veins feed into the right atrium.

On the 25th of January 1965, "through a left thoracotomy a pericardiectomy was performed with removal of the pericardium to include the area of the superior and inferior vena cava, anteriorly and posteriorly and to the base of the heart."

The surgeon performing the procedure was Dr. Dale E. Dominy, a 39 year-old Air Force major. In his operation report he wrote, "the left pleural space was entered through a left anterior chest incision [Dr. Dominy noted that I already had a previous right thoracotomy] with finding of considerable adhesion of lung to pericardium." Dr. Dominy went on to describe the surgery as, "excision of the pericardium to the region of the right phrenic nerve, the aorta and pulmonary artery..." Dr. Dominy stated that, "the left phrenic vessels and nerve were preserved."

Dr. Dominy wrote that I tolerated the procedure satisfactorily and was taken to recovery in excellent condition. My wife, who saw me leave surgery after what she thought was 4 to 6 hours, said I looked, "gray."

I returned to Bitburg to convalese, and then returned to duty. Unfortunately, my struggle with pericarditis was not over.

Three months after my pericardiectomy, March 1965, I was readmitted to the Bitburg hospital with pericardial pain. I was again treated with ACTH, my condition improved quickly, and I was released. I was told that whatever virus had caused the pericarditis in the first place was probably attacking bits and pieces of remaining pericardial tissue. The doctor told me, "They can't get everything."

I had another episode of pericardial pain in October 1965, and was treated as an outpatient.

In May of '66 I was notified that I had again been disqualified medically for a regular commission. Also in May of that year I was granted a waiver by the flight surgeon and given medical clearance for an altitude chamber flight.

In June of 1966, 3 months prior to my reassignment date, I experienced pain in my right shoulder, across my chest, and into my rib cage. Deep breathing exacerbated the pain, as did lying flat. This was all very similar to my experience before the pericardiectomy. Serial EKGs revealed "evolutionary changes of acute pericarditis with minimal improvement noted in later tracings." Not a good sign.

At the beginning of July1966, I was transferred to Wiesbaden Hospital for further evaluation and possible medical board. The prospect of being discharged from the Air Force at this time was distressing.

I had been responsible for a major transfer of our three squadrons F-105 Thunderchiefs to Vietnam and replacement by the F-4 Phantom. This was a massive undertaking, because we had to ensure each aircraft had undergone periodic maintenance and been prepared for overseas flight. At the same time we had to bring in the F-4s, run them through acceptance inspection, and schedule any maintenance necessary. While doing this, we had to fly regular sorties as part of our mission. I worked long hours and spent most nights with scheduling charts spread on the living room rug trying to work out the details of the transfer and replacement (if only I'd had today's Mac and an Excel spreadsheet).

I had been receiving outstanding performance evaluations (this time not overturned by the reviewing officer), I had been promoted to 1st Lt, and then captain, and I had been selected to attend the Air Force Institute of Technology (AFIT) to study for an advanced degree in human factors engineering at Texas Tech starting at the beginning of the school year, September 1966. My wife was pregnant with our second child and was expecting in October.

Thinking myself fit for world wide duty, I had also volunteered for Vietnam, something I had yet to tell my wife. It didn't seem that this was going to be a problem.

My wife and I decided that she and our 18-month old son should return to the States ahead of me and stay with her parents while I underwent the medical board at Wiesbaden. It was a very difficult trip for her. For me, it was a month of examinations, consultations, waiting, and wondering what the doctors at Wiesbaden would determine about my future in the Air Force.

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The Wiesbaden medical staff decided that I was fit for worldwide duty, so informed my commander, and my permanent change of station (PCS) orders were cut, and was on a flight to McQuire Air Force Base, where I'd shipped my Volkswagen Beetle 2 months earlier.

Amazingly, the VW started right up, and I drove immediately to Florida to see my wife and son, and then on to Lubbock, Texas, to start school at Texas Tech, leaving my wife in Florida with her parents and under the care of her brother, who was a doctor.

Texas Tech

I checked into the BOQ and fell into bed. I needed sleep. But there was a lot to do and I was up early the next morning and making up a list of action items. I had to register at Texas Tech, find a house, manage shipment of my household goods, meet with my advisor, and come up with a slate of classes that would meet leveling requirements (my BS in Aeronautical Engineering didn't cover all the prerequisites for my degree work in IE/Human Factors), and keep me on schedule for degree completion in the time allotted by AFIT (1966-68).

I kept in virtually constant touch with my wife and was troubled to learn that she'd had some bleeding and had been put on bed rest awaiting delivery. She was bored, but otherwise seemed okay, or at least she made me believe that was the case.

My Air Force sponsor helped me locate a modest, three bedroom house in a quiet neighborhood and I located my household goods and had them shipped. In the meantime, I started attending classes. Our second son was born 5 weeks prematurely on September 19, 1966. He was being kept in the hospital for observation. My wife was okay.

On October 25, 1966, I was required to report to the local AFIT commander, who handed me a letter from the Air Force Surgeon General disapproving the recommendation of the Wiesbaden medical board and requiring that I undergo another medical evaluation board. My fight to continue my Air Force career without my pericardium was not yet over.

Continued -- click here.