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Why some HPV infections go away and others become cancer

hpv-virusThis is what we’ve all wondered: Was it a weak immune system that led to my or my partner’s HPV throat cancer? Turns out, not so much.

For people infected with the human papilloma virus (HPV), the likelihood of clearing the infection and avoiding HPV-related cancer may depend less on the body’s disease-fighting arsenal than has been generally assumed. A new study finds that the body’s ability to defeat the virus may be largely due to unpredictable division patterns in HPV-infected stem cells, rather than the strength of the person’s immune response.

via Why some HPV infections go away and others become cancer.

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Acupuncture for Dry Mouth (Xerostomia) after Radiation

Acupuncture needles are hair-thin and relatively painless.

Acupuncture needles are hair-thin and relatively painless. Thomas Del Brase photography

 

John and I are both Licensed Acupuncturists, in practice for over 25 years. In a strange coincidence while John was in the process of getting the lump on his neck diagnosed (we knew it was cancer; we just didn’t know what kind yet) a patient came to see him for loss of saliva after radiation for, yes, HPV+ tonsil cancer. He had just finished his 6 weeks of radiation and was having trouble eating and swallowing. The first treatment stimulated saliva flow immediately, and after a couple more follow-ups he was greatly improved.

When John was diagnosed a few weeks later, this man became a tremendous source of information on what to expect.

Fortunately, there is research available on the efficacy of acupuncture for radiation induced xerostomia, carried out in San Diego, California. At the time we relied on research carried out in China.

John had an acupuncture treatment every day during his 35 radiation sessions. Now, while not everyone has the luxury of having their very own live-in acupuncturist, everyone can benefit from either preventative or restorative treatments, as John’s experience with his patient showed. Frequently during John’s treatments he would feel saliva beginning to flow.

Saliva is not only necessary to help moisten food for chewing and swallowing. It is equally essential for its anti-bacterial effects for preventing tooth decay. John’s dental health was good, and in addition to his daily acupuncture treatments he wore a mouth-guard device that fit over his teeth and was filled with fluoride gel. While he has had several cavities filled in the past year his teeth have apparently been re-mineralizing.

Acupuncture releases one’s own endorphins, which are like having your own little internal opiate factory. The treatments are deeply relaxing. While John did finally lose a great deal of the thinner saliva he never lost his saliva production altogether, which made it easier for him to continue swallowing and get back into eating solid food as soon as he possibly could. His radiation oncologist noticed and commented on the fact that he never completely lost his saliva as so many did.

Our local cancer center offers weekly acupuncture sessions. Check with your oncologist for a reputable Acupuncturist in your area. This works.

In case you would like to share this information with your own acupuncturist, here is the treatment we did on a daily basis:

Bilateral ear points: Shenmen, Point Zero, Salivary Gland 2′ and Larynx.
Bilateral: Lung 7, Kidney 6
Ren 24
Affected side: Alternating. One day Stomach 5 threaded to Stomach 6, the next day Small Intestine 17. These were discarded later in the treatment series as these areas became to painful to treat due to radiation burns.

2013: The Year of Clean Up

John and ColleenA year ago today we were still waiting for after the first of the year for the biopsy that would identify the worrisome lump in John’s neck as metastatic HPV + squamous cell throat cancer.

With the past year of crisis behind us (and I am working on a post that details our journey through 2012’s diagnosis and treatment) we are now facing what we’ve come to think of as The Year of Clean-Up.  Throat cancer hit our lives like a devastating natural disaster, plunging a 54 year old physically fit and healthy man into surgery, the strongest and longest dose of radiation given for any cancer, chemotherapy and recovery. The crisis has passed, and continuing to clean up the mess will be tho focus of our next year.  We focus on this with gratitude for the doctors, friends and family that made it possible to be here right now.

If there’s one thing we’ve learned from this past year of crisis and challenge, it’s respect and amazement for how adaptable human beings are to drastically changing circumstances.  John went from hale and hearty to months of being unable to work, eat, or even literally see the world as he was used to seeing it.  If you had told John a year ago that he would lose function in his shoulder, would be unable to work out as he used to, would need a machine at night to breathe properly and would see the world like something out of a Peter Max illustration he would have been utterly freaked out; but then, a year ago at this time he was freaked out about potentially dying from cancer.  After the first flush of relief that his cancer was treatable and curable he was then freaked out about some of the worst side effects of throat cancer treatment that never came to pass, like losing his ability to speak or swallow or work again. Nobody knows how they will be physically, emotionally or spiritually tested in a crisis like throat cancer, and nobody knows what they will face or how they will face it.  But I am here to tell you that however this journey plays out in your life you can and will adapt and resume your life, however changed it might be.

John’s journey began with a biopsy on Jan 4th, 2012, a lymph node dissection surgery on January 26th, and the last of his 35 radiation treatments on April 20th.  Instead of three chemotherapy sessions he only had one, due to an unusually neurotoxic response I’ll describe below.  His follow-up PET scan was NED, sweet-talk for “No Evidence of Disease.”  Our term for this is, cured.

THE EXPECTED ISSUES

John is dealing with some of the expected outcomes.  His sense of taste, while improving, is not all the way back.  Eating is still more of a chore than a pleasure, and meat remains the hardest substance to chew and swallow, having a consistency like cardboard.  With the exception of strongly spiced or peppery foods, though, he can eat just about anything, and amazed me over Thanksgiving week in Mexico on the occasion of our 25th Wedding Anniversary by eating an entire Mexican platter including chile rellenos!  

Thanksgiving and 25th Anniverssary in Puerto Vallarta

Thanksgiving and 25th Anniversary in Puerto Vallarta

He’s back at work full-time, off of all medications, and has started working out at the gym again.  So there is a lot to grateful for!

Dental Issues

John was lucky to have a great set of chompers going in, with only a few cavities filled over a lifetimes.  During the radiation treatments he wore a custom-fitted dental appliance usually used for teeth whitening.  This was filled with fluoride gel and held in place for 20 minutes, used daily during radiation.  Since the end of radiation he’s had gum recession for the first time in his life and still can’t use toothpaste with strong mint flavors.  He uses Sensodyne toothpaste and rinses with Xylitol, as recommended by his dentist and which has anti-bacterial properties.  While John never entirely lost his saliva during or after treatment (thanks to regular acupuncture treatments) he is still deficient in the thin saliva, which makes it much easier to get cavities.  We discovered that John was also clenching his teeth at night die to sleep apnea (discussed below) and this was causing the rims of his front teeth to become jagged with little bits of tooth breaking off…an alarming development to be sure.  His dentist sanded off the rough edges and filled nine cavities in the front teeth that had suffered breakage, and his smile looks normal again.  In the process, though, his dentist found five more cavities along the sides of the molars where the gums had receded, so there’s another round of cavity-filling coming up soon.  We expect to see more cavities and more fillings in the coming year, but at least he has teeth to fill!

THE UNEXPECTED ISSUES

Ironically, the greatest problems John has had as a result of treatment were unexpected, unpredictable, and highly unusual, to say the least.  He tends to react strongly to medical treatments; something we didn’t know because he’d never been sick with anything worse than bronchitis before this.  Some of these problems are clearing up, but with others it’s unclear to what degree there will be recovery.

Nerve Damage

While recovering from the lymph node dissection on January 26th John complained about shoulder pain on the side of the healing incision, and it was difficult for him to raise his arm up over his head to brush his hair.  Amazingly, he was back to chopping wood for the fire within a week of his surgery, so we thought this pain and limitation would be temporary. Turns out, we still don’t know.

John’s course of 35 radiation treatments was done on a new protocol, 6 times a week instead of 5 days a week.  This meant he had radiation treatments twice on Thursdays, once in the morning and once in the evening.  About three weeks into his radiation, and two weeks after his one (and only) chemotherapy infusion, the muscles around his right shoulder quite suddenly atrophied, looking quite deflated.  His right shoulder drooped and his right clavicle stuck out dramatically.  During this time John wore a tank top to his various appointments as his skin was becoming quite red and painful, and when he took off his outer jacket to show his ENT the sudden change in his right shoulder I saw the sad, worried look in Dr. Sprague’s eyes. “I hope that comes back,” he said quietly.   No one could agree on why it was happening.  His surgeon said the he’d had to “stretch” the accessory nerve a bit to get it out of the way of cancerous lymph node but thought the radiation was responsible but the sudden atrophy.  The radiation oncologist thought it was from the surgery.  I thought it was from the chemotherapy, since he’d had so many other neurotoxic effects from it (see below).  Neither of us cared at that point what caused it– what we wanted to know was what to do about it.  Everyone agreed he would need physical therapy, and that couldn’t start for several weeks until the radiation was over and his skin healed.

John started physical therapy three weeks after the end of radiation, and at my insistence had an EMG (electromyogram) at the end of May to test nerve transmission.  He shoulder hurt dreadfully from just hanging there, but he had full use of his hand and lower arm.  He couldn’t reach up over his head without “assisting” with the other arm.  After testing the nerves he was told that there was no reason why the muscles couldn’t recover within a couple of months.

scapular brace

John models the brace that keeps his right scapula from “winging” out

But they didn’t.  John has been to two physical therapists, a shoulder specialist in the San Francisco Bay Area, a neurologist, and has had another EMG.  Three of the muscles around the shoulder girdle (the trapezius, supraspinatous, and rhomboid) are non-functional due to accessory nerve disorder.  There is no corrective surgery to be done, no special exercises or workouts to bring back the muscles.  They are unaffected by acupuncture.  Once of the long-term side-effects of intense radiation is the formation of fibrous tissue, and John works with a rolfer who does deep massage to break-up the fibrosis in his neck and shoulder on a regular basis to prevent further damage or construction.  He has ordered a brace to hold his scapula in place because it “wings” out without muscles to stabilize it. We work on moving his arm through range of motion exercises nightly so that his shoulder maintains its mobility and doesn’t freeze up.

We haven’t given up on it, though.  The neurologist he saw in early December  said that he shouldn’t give up hope for up to two years, and to keep working with it and encouraging any signs of life.  John feels certain that he will “get his arm back.”  This will be our greatest clean-up project over the next year.

Without regret, and knowing he made the best decision he could at the time, John says that knowing what he knows now he would not choose to have the lymph node dissection surgery, since that isn’t part of the standard treatment protocol and it appears that is where  the original damage to the accessory nerve occurred.  While this doesn’t interfere with his work, his shoulder aches all the time, he’s learning to use his left arm for lifting and reaching, and he’s having to find other ways to work out, as his old weight-lifting and pilates routines are no longer possible.

Sleep Apnea

During treatment John began snoring but in the summer the snoring took on a truly alarming timber.  He’d gasp and thrash and sometimes hold his breath for long periods of time.  I would wake up to see his entire abdomen jerking up and down spasmodically,  shaking the entire bed, and I’d shake him until he’d finally take in a huge gasping breath.  Around this time he was becoming discouraged and not feeling any better, at feeling foggy all the time and “not in his body.”  In what was a major cause of frustration for me this took a ridiculously long time to get seen to, diagnosed, and treated.  It was just assumed that of course he didn’t feel like himself with all he’d been through.  He needed to give it time, up to a year, to recover.  Here’s  what I want to say to fellow caregivers:  If something doesn’t feel right, it’s because it isn’t right.  Trust your instincts and continue to push for answers.  We finally got John in for an overnight sleep study at a local clinic.  They woke him up two hours into the study (he’d had 99 “events” of  stopping breathing and of his blood oxygen dropping to dangerous levels that can lead to heart attack and organ damage) and put a CPAP mask on him. His sleep study showed that he wasn’t ever getting into the deeper levels of sleep.  No wonder he felt so terrible!

Dr Sprague looked down into his throat and said that the trouble breathing at night was caused by obstruction from ongoing swelling at the back of the tongue and in the throat. Apparently John didn’t have a lot of clearance to begin with, and when he relaxed at night and his tongue fell back and obstructed his breathing. Sprague guessed this will clear up in 6-12 months as John’s throat continues to heal.

John was initially reluctant about the whole C-PAP idea.  What he had heard was that it is noisy, uncomfortable, and your wife won’t sleep in the same room with you any more once you’re using it.  I pointed out that I was  already spending far too many nights int he guest room trying to get some sleep of my own while he bucked and thrashed and gasped.  Finally, two weeks ago he brought home a portable CPAP machine.  CPAP stands for Continuous Positive Air Pressure, and it works by forcing room air into the mouth and throat to keep them open and unobstructed.  Rather than the huge mask covering his mouth and throat, he was given a small mask with straps around the head and two soft silicon plugs that go up into his nostrils, much like the oxygen cannula you get in the hospital but that completely covers and seals the nostrils.  Once in place, the machine itself makes not a sound.  Water is added to the unit for a misting affect so that the device doesn’t create more dryness in the mouth and throat.

And here’s the thing…John sleeps all night now without bucking like a bronco.  All is calm and peaceful, he is beginning to dream again, and wake up refreshed, and feel like himself again.  What a difference a good night’s sleep makes!

John’s dentist also guessed that the damage to his front teeth was happening during the apnea episodes when his teeth would come together with a snap, shearing off small bits and wearing away the enamel each time this happened.  I haven’t heard of anyone else having this issue after radiation, but be aware if you’re hearing breathing problems at night.  It’s worth looking into!

Weird Visual Aftereffects

One of the stranger things that happened was an extremely rare side effect of Cisplatin that happens in less than .12% of patients.  John was given Cisplatin overnight in the hospital so it could be dripped in slowly and his reactions closely monitored.  Nausea was controlled and his kidneys were fine, so he was sent home on Saturday morning.

On Sunday he was sitting in the reclining chair looking out the big picture window on a clear sunny day and asked me if it was raining.  Whaaaaa???  In his visual field he was seeing what looked like diagonal sheets of water pouring across the sky….only he also saw it when he looked away from the window.  His ears were ringing and his feet were burning and numb.  Because Zofran, the powerful anti-nausea medication John was given could also cause serious visual disturbances (“hopefully temporary”) he was taken off of it and as a result spent the rest of the night vomiting, becoming dehydrated.  I got him in to his oncologist the next morning who had never seen anything like this.  It was, he said, as if John was reacting to months and months of chemotherapy instead of to a single session.  The truth is, people vary in their ranges of sensitivity to drugs, and we discovered that John is highly sensitive to drugs.  He tends to react on the far end of the spectrum.  The oncologist checked John’s bloodwork (all of which was normal)  and set him up for an infusion of fluids, and when John’s vision didn’t clear up that day or the next it was decided that this would be his only chemotherapy infusion.  (“Common sense dictates that when a patient has a severe and unusual response to a drug you don’t repeat it,” his oncologist noted dryly.)

The diagonal sheets of water in John’s visual field gradually became more like a light rain, then a mist, and then the “watery” aspect of the disturbance slowly abated.  His vision is normal enough that he can drive, read, and carry on, but it is in no way “normal.”  He can’t describe how odd and different it is other than to say it’s as if everything has a “neon halo” around it and all colors are weirdly brighter and stronger, but he’s gotten used to it.  The tinnitus is also still there but most of the time he manages to ignore it.

Some Final Thoughts:

If there’s one thing you learn from all this, it’s how adaptable human beings are to changing circumstances.  If you had told John a year ago going into this that his shoulder wouldn’t be working, he wouldn’t be able to work out, he’d need a machine at night to breathe properly and his visual world would look like something out of a Peter Max illustration he would have been utterly freaked out; but then, a year ago at this time he was freaked out about potentially dying from cancer.  After the first flush of relief that his cancer was treatable and curable he was then freaked out about some of the worst side effects of throat cancer treatment that never came to pass, like losing his ability to speak or swallow or work again. Nobody knows how they will be physically, emotionally or spiritually tested in a crisis like cancer, and nobody knows what they will face or how they will face it.

But face it you will, one step at a time.

“Road to Recovery” Provides Rides to Treatments

The American Cancer Society’s Road to Recovery program was the most incredibly helpful service for us.

John thought he would be able to drive himself to his daily radiation treatments. And, for the first week, he could.

We live 40 miles from the cancer center that housed the recommended specialized radiation therapy machine. The machine had only been in use for two weeks, and John’s treatments were long– sometimes he spent as long as 50 minutes on the table, strapped down in his mask, while they precisely calibrated the machine to focus on the tiny lesion on the back of his tongue.

At the end of his first week of radiation John had his first chemotherapy infusion, done overnight in the hospital in order to keep him hydrated to protect his kidneys. He sailed through it, but the next day when he got home very strange things began to happen. I won’t go into the details here because first, I don’t want to scare anyone and second, the visual side effects John encountered happen in less than 1% of people getting Cisplatin. Driving was out of the question for him, and I was working full time covering the practice for both of us.

We had plenty of friends who were ready to help John with rides, but none of them lived in our town. This meant someone would have to drive up the hill from Chico, pick John up, drive him the 40 miles back to the Cancer Center in Chico, bring him back home, and then drive back to Chico. It was just too much to ask people to do every week day for six weeks.

On top of this, John was the first person to receive a new radiation protocol. On Thursdays he was getting two radiation treatments, 7 hours apart. This meant two trips to Chico on Thursdays.

This is where the incredible Road to Recovery program kicked in for us.

The American Cancer Society matches up volunteer drivers with cancer patients who need rides to their treatments. The volunteer picks up the patient in their own car. I really doubted they would be able to find drivers for us who would be willing to take up to two hours to take John to Chico, wait while he had his 30-50 minute session, and drive him back.

But they did.

I called the Road to Recovery Program at 1-800-227-2345. Their requirements were few.

First, they needed a week’s notice to coordinate volunteers.

Second, the patient must be ambulatory, meaning they must be able to get in and out of a car by themselves.

Third, they can’t drive patients later than 5:30 pm, during American Cancer Society hours. So I did call on friends to drive John to and from his Thursday evening treatments.

I gave them John’s schedule, and a few days later they sent me a calendar print out with the names of John’s volunteer drivers filled in. They weren’t able to fill in every single day, but they did fill in as often as four days a week some weeks. This made it much easier for me to ask friends to fill in the remaining trips.

John’s volunteer driver called him the night before to get directions and to confirm what time they should pick him up. Each of his drivers refused any compensation for gasoline and were beyond happy to be able to provide this service.

I kept a whiteboard in the kitchen with the names and numbers of friends and volunteers, and every day I would write in big red letters, YOUR DRIVER TODAY IS _____.

When our lives get more back to normal I’ll be signing on as a volunteer for this incredible service. It will feel great to give back!

BUT WAIT– THERE’S MORE!!

In addition to the Road to Recovery service, the American Cancer Society also helps with your own gasoline expenses. All you have to do is keep a mileage log of all medical-related trips, and the Cancer Society reimburses you so many cents per mile in the form of a debit card, for use only at gas stations. Because all of John’s doctors and providers were at least 40 miles away, and because he needed physical therapy after he healed up from his treatments (by now he was able to drive himself again), and because gas was over $4.00 a gallon, these gasoline debit cards were extremely helpful.

To PEG or not to PEG: Pros and Cons of using a Feeding Tube

As always, I am not giving medical advice here, just recounting why we chose to go with a PEG tube before John started radiation.

John was very fit and trim when he was diagnosed. He worked out with weights 3-4 times a week, took Pilates classes, and rode his bike regularly. At 5’7″ and 158 pounds he had very little body fat or weight to spare.

During the time between diagnosis and treatment we were able to add an additional 10 pounds to his frame, so he started treatment at 168 pounds.

Why John Chose the PEG Tube:

Going in, John was told he would lose 10-40% of his body weight from radiation. My biggest concern for him going in was weight loss. As I started reading blogs about dealing with side effects from radiation I first ran into the idea of a PEG tube. Punching a hole directly through your abdominal muscles and into your stomach sounded invasive and extreme, and I wasn’t sure John would go for it. As it turned out, he had no hesitation about it. John had just met a fellow who had gone through 6 weeks of radiation for HPV squamous cell tonsil cancer that was discovered in situ (that is, no spread to the lymph nodes) and he had chosen against the feeding tube. He ended up losing 40 pounds which actually brought him down to a normal weight. But John knew full well he didn’t have 30-40 pounds to spare!

John’s ENT and Radiation oncologist both recommended the PEG tube. John’s chemotherapy oncologist explained that the use of the tube is controversial to some. If a person becomes dependent on the tube and stops eating altogether they can have much more trouble regaining their swallowing ability after treatment. It was emphasized to John that even though he would have a feeding tube, he would have to regard it as an ancillary method of getting nutrition in him. He absolutely had to keep swallowing on a daily basis. John agreed to this. I had spoken with a local man who had undergone treatment for the same cancer 5 years earlier, and he had also used a PEG tube. He had gone for 5 weeks without swallowing at all, getting all his nourishment through the tube, and as a result five years later still had some difficulty with choking when eating. So John had a pretty clear idea that this was to be avoided.

John did continue to swallow every single day of his treatment and aftermath, even when it was excruciating to do so. He was told that water would be the most difficult liquid to swallow (thicker, more viscous liquids are easier), and so he made that his personal challenge and swallowed his morning pills with water every single day. As a result, he has had no difficulties with regaining his ability to swallow, as he never let it go.

It was recommended that John get the PEG tube “installed” at least three weeks before treatment started so that the wound would be completely healed up. He was warned that people who decided to “tough it out” without the tube would find it much, much more difficult to have one installed later.

Getting the PEG tube Installed:

John’s PEG tube was installed on 2.17.12. His first radiation treatment was scheduled for 3.12.12, so this gave him plenty of time to heal.

The procedure was done in the hospital under intravenous (not general) anesthesia. He was assured that this was going to be one of the simplest procedures with little downside or discomfort. Unfortunately, while this is true for most people, this proved not to be the case for him. I’m not describing this to scare anybody, but what happened to him has since happened to another acquaintance of ours who was subsequently diagnosed, and it is something that can be prevented.

John was sedated and taken into the procedure room. Briefly, a guide wire with a light on the end of it is run down the esophagus into the stomach. The surgeon then makes a small cut where he sees the light shining through the skin, and the plastic PEG tube is inserted through the hole. The tube is held in place inside the stomach by a small mushroom-shaped “cap” on the end. On the outside, the tube is held in place against the skin by a plastic hub.

When John awoke from the sedation he immediately had severe cramping. He was trying not to complain and to be a “good patient” but the cramps came in intense waves. He was given a shot of Dilaudid for the pain, but an hour later he was still having extreme waves of cramping. At this point somebody should have taken the bandage off his abdomen and checked the placement of the tube…but no one did. Instead, he was given another shot of Dilaudid. At this point John wanted nothing more than to get home and rest, and he assumed that the cramping would subside over time.

Unfortunately, while it did subside somewhat, the pain was still severe. When I came home from work that evening he was flattened in bed, unable to move an inch without intense pain. Sitting up in bed was impossible. He could slowly, with much painful effort, roll over on his side and I could then help him sit up. The waves of intense cramping were getting further apart but he was miserable.

Long story short, he spent an exceedingly miserable night in his reclining chair, hoping for respite. We knew we could go back to the emergency room, but we knew that would be an ordeal and that he would wait 6-8 hours in the waiting room.

I spent the evening searching the internet for an answer. I found two blogs where two men had the exact same experience. What they had in common? Both were lean, fit, muscled men with very little body fat. In one case the man went to the emergency room and the hub on the PEG tube was loosened by a GI doctor. In the second case, the man figured out how to loosen the hub himself, relieving his pain.

The following day we took the bandage off and studied the feeding tube. We tried fiddling with it a little bit to see if we could loosen it, but the mechanism for doing so wasn’t apparent. I called the on call number for the gastroenterologist who placed the tube, but instead of the call going to an answering service with a live operator, I got his office’s voicemail. Clearly I wasn’t going to get a call back before Monday (This turned out to be true, as the doctor’s office has neglected to switch their phone system over to the operator for the weekend).

What happens next shows the power of patience and persistence. I called the hospital and asked for the gastroenterologist on call. I was transferred to the emergency room, spoke with a nurse, and was transferred to the charge nurse, who couldn’t believe we could not contact John’s gastroenterologist. She even tried calling his office herself. She suggested we come to the emergency room. I explained that while John was very uncomfortable this was not a true emergency, that I didn’t want to make the 40 minute drive if I could help it, and that I didn’t want to sit in a waiting room for several hours with a cancer patient in the middle of a flu outbreak. She took my point and said she would contact the GI doctor on call.

15 minutes later the GI doctor on call called back. He had John’s records in front of him and saw the two Dilaudid shots that had been given. I explained John’s slim build and “wondered” if perhaps the tube was too tight. He agreed that John’s symptoms were likely muscle spasms from the tube being cinched down too tightly. He suggested we come to the emergency room. I explained again why I didn’t want to use the limited resources of the emergency room for a non-emergency. I explained that we were both medical people and understood the need for keeping the wound clean. I asked if he could simply talk us through the process of loosening up the tube ourselves. Thankfully, he decided to trust us, and explained how to go about releasing the pressure on the tube. It took us about 15 minutes of working with it, but once we loosed the hub on the tube and backed it out 2 cm, John’s relief was immediate and profound.

What am I suggesting here? I am not in any way, shape, or form suggesting that you fiddle around with your own PEG tube. I do suggest that, if you have it done:

1) Don’t have it placed on a Friday afternoon. If there’s a problem you don’t want to have to go to the emergency room.
2) Don’t leave the facility if you’re having pain or cramping, no matter how “difficult” a patient this makes you seem.
3) If you are slim or don’t have much body fat around your abdomen, report any cramping immediately. From what I can tell (and I realize this is only anecdotal), thin healthy men seem to have more trouble with their PEG tubes.

A couple of weeks ago I heard from a man about John’s age who weighed 130 pounds going into his treatment. There was no question he needed a PEG tube. He had the same experience as John, experiencing severe cramping and pain. He did end up in the emergency room until the gastroenterologist on call could come and loosen up the hub on his tube.

The feeding tube was a lifesaver.

One of the best resources I encountered was a blog called “You Start With a Tube.” The writer here was dealing with a long-term disease that rendered him unable to swallow, and he quickly grew weary of canned guck as well. Look for more information about him, about how to put all kinds of foods down a PEG tube, and how to deal with a clog if it happens.

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Support for those supporting people with HPV+ throat cancer

You start with a tube...

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HPV Origin Throat Cancer

Diagnosed July 6, 2012 via Tonsil Biopsy

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Support for those supporting people with HPV+ throat cancer