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| Alan and Gloria, on his 70th birthday. |
It's kidney disease as Toy Story and the blogger as Buzz Lightyear: from dialysis to transplantation – and beyond!
Wednesday, November 16, 2022
I Really Give a Whitt About This Guy; I’m Hoping That You Will, Too
Thursday, November 18, 2021
Happy Kidneyversary to Me: Celebrating A Decade of Death Defiance
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| Beewee and Me, Just Out of Kidney Surgery |
On November 18, 2011, a decade ago today, my life changed forever. I was lying in a bed at Barnes-Jewish Hospital in St. Louis, drifting in and out of anesthesia and thinking about a 6-year-old girl I didn't know and had never met, and how her parents' unbelievably selfless act might add some overtime to my game of life here on Earth.
Three years earlier, to my great surprise, I was diagnosed with Stage IV kidney failure. They say that at Stage V you should start checking your insurance policies and consulting morticians, so all in all Stage IV wasn't so bad.
But once your kidneys start heading south, they won't see the Mason-Dixon Line again. I was going to need a transplant, sooner than later. And prior to that I probably would have to go on dialysis.
Here's the point where I can't understand why everybody doesn't believe in God. When I received my dire diagnosis I was living alone in Detroit, divorced and downsized out of a high-paying job, unable to afford COBRA insurance and barely holding on to my rental house. This is generally what's known as rock bottom.
Then, on an online dating site I was canceling the next day, I met this indescribably wonderful woman named Karen. She lived two states away in Champaign, Ill., so I knew there was little chance of ever meeting her, much less launching a relationship. But we had tons in common, eventually began talking and/or texting daily, and before I knew it I was on a plane to central Illinois to hold her in my arms. She knew everything that was going on with me health-wise and never batted an eye.
A year later we were married.
Wait, it gets even better. I moved out of Michigan for the first time in my life and relocated to Champaign so that Karen – better known today on social media as BeeWee, abbreviation for "Best Wife Ever" – and I could be together. She works for the University of Illinois, and I am firmly convinced that the main reason the State of Illinois is in such constant financial peril is because the health insurance for its state employees is so phenomenal. I had barely set foot in the state as the spouse of an employee, and it was like, "Oh, you need a kidney transplant? Hundreds of thousands of dollars? No problem! Welcome to the Land of Lincoln."
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| Kidney Crusading at a Local Hospital |
For more than a year I was placed on peritoneal (pair-it-on-NEE-uhl) dialysis, the gentler, less invasive form of assisting your kidneys I have since championed for renal patients old and new. Then, after a few false alarms, we finally received THE CALL: a kidney had been found for me from a deceased donor, and it appeared to be an ideal match. How fast can you get to St. Louis?
How fast can this car go?
As I was getting prepped for surgery, I remember the nurses must have broken every HIPAA regulation in the manual, so eager were they to tell me about their donor. "Do you know whose kidney you're getting?" they kept asking. Uh, no, I didn't, but apparently I was the only one.
The story was all over the news in St. Lou, and one nurse called it up online to show me: a 6-year-old girl, apparently in perfect health, suffered a brain aneurysm on the playground one sunny morning and died on the spot. And her parents, in the midst of their sudden, devastating grief, made the decision to donate her organs to others.
As my transplant surgeon suggested to me, I was receiving "the perfect kidney:" it was a flawless blood and tissue match, and at age six her experimenting with smoking, alcohol and drugs was probably minimal.
I named my kidney Cheyenne, in her honor. She's a teenager now, and sometimes she can get a little rebellious, but for the most part she has seemed completely content and productive in her second home. I take tacrolimus (tack-crow-LEE-muss), a leading anti-rejection drug, twice a day, every day, exactly 12 hours apart since 2011 to try to keep her happy. (Anyone who knows my commitment to punctuality can imagine how challenging that has been.)
I have never met or communicated with her parents, by their choice. However, I may try to reach out to them once again on this 10th anniversary. I have always wanted to hug them verbally, if not physically, to let them know what their gift has meant to me. Many times I think about all the things I would not have accomplished or experienced had I not been here for the last decade:
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| BeeWee and Me, at Our Son's Wedding |
The experience of being a father, as we shepherded Karen's brother, Jordan, through his high school years.
The two books I have ghostwritten, and the fascinating one I'm working on now.
My advocacy for kidney transplantation and peritoneal dialysis (I'll never forget the man who gave a knockoff Jimmy Choo – or was it Jimmie Chew – handbag for my wife as thanks for recommending peritoneal dialysis, which gave him more freedom to sell purses out of his trunk), which led to me serving two years as the ESRD (End-Stage Renal Disease, or kidney failure) Patient Representative for the State of Illinois. The whole freakin' state.
That being one of the factors leading to my being named a Distinguished Alum by my Alma Mater, Hope College in Holland, Mich., in 2019. As the first McFarlin to attend college, how I wish my parents had been alive to see that.
Uniting hundreds of couples in my role as a wedding officiant (under the business name Wholly Matrimony 4U), including the marriage of my son Jordan and his fiancée Graycie last summer.
Emceeing my 50th high school reunion.
Finding an amazing church, Mattis Avenue Free Methodist, that has deepened my love of God and my daily walk with his son, Jesus.
And having more time to spend with you, my readers and friends who mean so much to me, and writing this blog post to you today.
Cheers to us all. God bless. Here's to another 10 years!
Monday, April 12, 2021
It May Not Be the Bee's Knees, But I Hope My Knee Will 'Bees' Better
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| This is about how my knee feels now. Every day. |
• This will be my first major operation since my kidney transplant at Barnes-Jewish Hospital in St. Louis on November 18, 2011. (Great Googly-Moogly! That was 10 years ago! I just realized that. Suppose I should think about doing some sort of anniversary tribute later this year.) And to tell you the truth, I really don't know how I feel about this week's procedure.
• My surgery initially was scheduled for March 2020, about a week before the world as we knew it flipped upside down and corona became way more than the name of an imported beer. My joint replacement was canceled due to a sudden, urgent need for hospital beds. Then it was aborted a second time in November when the virus spiked again. As a result, I have been in relentless, agonizing leg pain for more than a year, Biofreeze and IcyHot my constant sidekicks.
I have not been a happy cowboy.
As another result, I find myself approaching this week's operation with a feeling of...well, really, no feeling at all. I'm not excited or anxious or nervous or relieved. I was bitter for quite some time over the cancellations and the knowledge that my suffering continued through no fault of my own. But when you've been in pain day after day for months, it sadly becomes part of your normal existence. You learn to live with it. If you can call that living.
(Many deep thanks to Danny McFarlin –– absolutely no relation, unless his family once owned mine –– the physician's assistant who kept me reasonably sane between surgical disappointments with a series of cortisone injections in my knee. He really gave me a leg up.
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| My Surgeon: 'No-Pain Bane?' |
And while I'm told the pain will be worse after the procedure, at least initially, at this point it's all relative. Besides, fool me twice, shame on everybody. When I'm actually on the gurney with an IV in my arm and being wheeled into the OR, then I'll know it's really going to happen. Until then, I'm keeping my emotions on lockdown.
• The orthopedic surgeon performing my procedure (a total left knee arthroplasty) is one Dr. Robert Bane, who by all accounts is the Dr. Kildare of east central Illinois. I am not exaggerating when I tell you every single person who's asked about my operation has broken into a broad, knowing smile when I answer, "Doctor Bane," followed immediately by, "He's the best."
OH! I misspoke. One woman at my church replied, "I tried to get Dr. Bane, but I couldn't get onto his calendar. (Pause.) He's the best, you know."
Even other doctors praise his holy name, which is rare indeed. Last week my cardiologist broke into a broad smile when Bane's name came up. "You're in good hands," he reassured. Ironically, I have yet to meet him: we conversed briefly via Zoom many months ago, but due to COVID I will not meet the man in person who's going to cut into my flesh until I'm on the table preparing for the anesthesia. I'm in the hands of a near-total stranger. He is, quite literally, the Bane of my existence.
I am absolutely positive I am not the first one to come up with that.
• I know times change over the course of a decade, but I don't remember ever jumping through as many pre-surgical hoops as I have for this procedure. I have had a complete pre-op physical, new X-rays, bone density screening, blood pressure monitoring, a consultation with my cardiologist. Bathe with a special soap the night before and the day of surgery. Sleep on clean sheets. Stop taking vitamins and all supplements. And, of course, the obligatory COVID-19 test.
Good news: here you can take the COVID test without having to leave your car. Bad news: It entails pulling into a line as long as the ones giving out free food these days and enduring what seems like a drawn-out, confusing and disorganized process. Very good news: The Carle system requires patients to simply run a Q-Tip around both nostrils, rather than jamming a stick past the eye and into the brain. Extremely good news: I tested negative, so we can continue to communicate.
• I suddenly came to realize one reason so many pre-op tests are required is because I'm not as young as my brain keeps telling me I am. I was blown away by the number of contemporaries who responded to my Facebook announcement of impending knee replacement with comments like, "Had mine done years ago," "Had both of mine done" or "You won't regret it." One friend even sent me a book of healing techniques after surgeries! Good Lord – my friends are getting so OLD! So thankful I'm retaining my youth.
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| My knee, without a scar. For posterity. |
• I was grateful that my pastor, Herb Coates, specifically mentioned me and my upcoming surgery during his congregational prayer last Sunday. Prayers are always welcomed. However, since I was manning the Welcome Desk next to the front door after the service, I was an easy target for every parishioner who wanted to inquire about the operation –– which seemed like every parishioner. I swear, I think some of them seemed to care more about my surgery than I do. Is that a good thing?
• I am also so, so grateful for the advancements in medical science. Knee replacements are commonplace now but practically unheard of in America until the 1970s. I think of my Aunt Carrie in Palmetto, Ga., God rest her soul, who made her living by cleaning the local movie theater. In those days you were lucky to have any job, so she worked on her hands and knees, picking up candy and all manner of filth brooms couldn't reach, well into her 80s. What unbearable pain she, and so many other laborers, must have endured!
I'll think of you Wednesday, Auntie. Just before the lights go out.
Thursday, March 11, 2021
Taking My Best Shot: Pondering the COVID Vaccine Controversy
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| They even give you a sticker! |
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| A Shot in the Arm for America. |
Thursday, November 5, 2020
Can Kidneys Create Comedy? I'm Trying to 'B Positive'
Hey, this is a joke, right?
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| Transplant Pals. (by Pamela Littky, Warner Bros.) |
Thursday, June 4, 2020
I Can Feel That Knee On My Neck, Too
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| Now THAT'S Symbolism. |
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| Memorials to George Floyd Are Going Up Across the Nation. |
COVIDQuarantineJoblessnessKobeTrumpBreonnaAhmaud: it all runs together. A steady stream of 2020 indignities. Simmering, churning anger. Pressure. Time on our hands. We can't breathe.
Friday, April 10, 2020
Please Say a Prayer For My Man, Alex the Great. He's Got IT.
| Alex and Me at the Book Launch Party for "The Booster" in '19 |
I posted some goofy photo on Facebook the other day that made vague reference to the coronavirus, and among the comments was a totally unexpected response from Alex Kimbrough's wife, Rosalind. It simply said, "Call Your Buddy Alex!"
These days, when anybody says "Call your buddy" who lives in disease devastated Detroit, you do it.
So I did.
And he does.
They say it's only a daily, brain-numbing drumbeat of numbers, advisories and Trump denials until someone you love is stricken by "the virus." And I see now that it's true.
Because while I have been moved by the recent deaths of distant friends and notable names in my former Detroit home, people like the amazing drama educator and devotee Brenda Perryman, former Aretha Franklin intimate Willie Wilkerson, and legendary restaurateur Otis Knapp ("Mr. FoFo") Lee, this is now a entirely different dimension entirely.
Because you see, Alex Kimbrough is my boy, in that inflection African American men use to describe another man who inhabits his innermost circle.
And Alex Kimbrough has COVID-19.
I suppose Rosalind wanted her husband to tell me himself. My late afternoon call woke him up, which was not completely uncommon: as morning news director for Detroit's FOX2 (WJBK) for as long as anyone can remember, more than 30 years at the station in all, his workday typically begins in the wee small hours.
But once I sensed that his weak, gravelly speech was more than the sound of someone being awakened from a deep slumber, I immediately felt guilty. I could feel the tears welling up in my eyes. My own breathing was becoming sporadic.
"She didn't tell you?" Alex asked me. "Well, it's good to hear your voice."
He doesn't know when or where he contracted the illness, but who does? He had just been released after spending five days at Providence Hospital, and never needed to go on a ventilator. Thank heaven for all blessings, great and small.
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| Alex in His Element, Here Directing Aretha's Funeral Coverage |
But Alex almost was at a loss for words –– which for him would be literally unheard of –– when trying to describe how much pain he was, and continues to be, in.
"It's worse than the worst flu you could ever have," he rasped. "Don't get this, Jim. Do NOT get this. You don't want this."
Alex said the higher-ups at FOX2 have advised him to take all the time he needs to recover, to not even think about returning to the control room until he feels 100 percent. Wise decision. The station wants to protect one of their, and Detroit's, great natural resources.
In addition to his work at WJBK, in his "spare time" Alex has freelanced directing programs for Detroit Public Television (WTVS) for more than 20 years, and freely lends his talents to other Metro Detroit productions as well. For a brief period he even worked for the Detroit Lions. When Aretha Franklin's sudden death in 2018 left local and national broadcast outlets without someone to coordinate the TV media pool, Alex was recruited to spearhead the coverage, more than eight hours live and nonstop.
He is so highly regarded by his peers that he has served as president of the National Association of Black Journalists' (NABJ) Detroit chapter, vice president of the local branch of NATAS (National Association of Television Arts and Sciences, the Emmy people), and has long been active in the local chapter of the Directors' Guild of America.
And you would be hard-pressed to find a more devoted or passionate alum of Detroit's famed Cass Technical High School: Alex's regular "Cass Tech Moments," usually connected to a fellow grad who appeared on a FOX2 morning show, are the stuff of social media lore. His proposed documentary on Cass Tech, which he's been working on almost as long as I've known him, has become a permanent agenda item whenever we talk.
And atop it all, Alex Kimbrough is a loyal and loving husband to Rosalind, and a doting dad to their only son, Brandon. He's been a BMW –– Black Man Working –– for an entire career, committed to providing for his family. He's just a good brother.
I almost feel guilty or selfish asking you to pray for someone who appears to be on the back end of coronavirus when so many have lost so many to this disastrous pandemic. However, like I said, the abstract becomes achingly real when it suddenly affects someone you know and care about.
So, if you are so inclined on this Good Friday, and beyond, please ask God to lay His healing hand on Alex Kimbrough and help him to make a full recovery.
After all, who else is going to finish that Cass Tech documentary?
Monday, January 6, 2020
And He Was in the Skeet Shooting Hall of Fame, Too
Celebrities. Sports legends. Relatives. Close friends. Relatives of close friends. Almost every day, it seemed, I was saying goodbye to someone who occupied at least a small corner of my mind and heart. Have you ever felt that way?
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| A Wide-Screen Tribute to Morrie at a December NKFI Forum. |
So rapidly were souls "leaving this Earth," as my mother used to say, that I didn't have time to mourn them individually. It was as if I were in a constant state of grieving. However, since we're in that annual period of "Remembering Those We Lost" in the previous year and starting anew, I didn't want the window to close without acknowledging one loss that hit me particularly hard: Morrie Funkhouser.
After all, how can you not remember a guy named Morrie Funkhouser?
Morrie –– or Morris E. Funkhouser II, if you please –– was one of the first people I met after I was encouraged to join the local transplant support group, hauntingly named "Second Chance," shortly after my kidney transplant in November 2011.
Now Frank Veach, the longtime leader of the group, is a delightfully engaging and salt-of-the-earth fellow, a bit of a goofball, difficult not to like. I accepted his welcome into the fold with gratitude.
However, if memory serves I was the only person of color in the group when I joined. (Dave Freeman and his wife Mara have since come on board to help even the odds.) I had only moved from Detroit to the middle of corn and soybean country a year or so before, and most of my time in my new prairie home was consumed by medical appointments, surgery and recuperation. I really didn't know the lay of my land very well.
I think most black people know that feeling of being the only in the room. Stranger in a strange land, I had no idea what to expect.
Then I see Morrie: older, weathered, a factory machinist all his life. The guy at the end of the bar. I stereotyped his gruff exterior the moment I saw him, I'm sure.
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| Morrie, in a Glamor Shot. |
And I could not have been more wrong. In how many situations could an African American writer from Detroit and an instrument maker from central Illinois become chuckle buddies?
Morrie was warm, wonderful and wise. He was the longest surviving kidney transplant recipient in our little band, 27 years and counting before other causes took him from us last June at the age of 72. He was afflicted with polycystic kidney disease, a genetic disorder in which fluid-filled sacs, or cysts, grow in the kidneys and disrupt their ability to do their job in filtering waste products from the blood. About one in 1,000 people worldwide have the condition, including Morrie's son, Anthony, who inherited it.
In most kidney transplants, the failing kidneys are left inside the body because, hey, they still may have some function left, and what could it hurt? In Morrie's case, his cyst-covered kidneys became so huge and invasive –– nearly 13 pounds each –– that both organs had to be extracted.
He never complained, and almost never said no to an opportunity to serve, inform or assist in some organ donation drive or renal-related campaign on behalf of the National Kidney Foundation of Illinois (NKFI), Gift of Hope, or Illinois Secretary of State Jesse White's Life Goes On crusade.
I remember spending many delightful hours chatting with Morrie under a canopy or in a tent somewhere in the region, encouraging people to become donors and answering their questions as living examples of what transplants can mean to people's lives. He was an outstanding ambassador for the cause, and at an NKFI "Living With Kidney Disease" seminar last month in Champaign, a moment was set aside to honor his life and dedication. Class move.
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| My Friend, the Hall of Famer. |
And yet, as is sadly the case with even our closest friends, there were several things about him I did not know until I read his obituary. For example, even though we talked about music, I had no idea he was a talented, longtime musician who played more than a quarter century in a band called The Variations. And he never once mentioned to me his gift for skeet shooting, a passion that led to his induction into the Illinois Skeet Shooting Association Hall of Fame in 2011.
Glad he liked me; he probably could have picked me off at 1,000 feet.
He was blessed to find love again after his first wife, Ann, died in 2005. I did not know Ann, of course, but his second wife, Sandy, was something special. Bubbly, blonde and vivacious, she's the kind of person who brightens a room just by entering it.
She clearly loved Morrie very much and they planned to care for each other well into their golden years, a scenario that tragically was cut short far too soon. Morrie's health declined so rapidly that by the time I heard he was hospitalized and hurried home from my summer vacation, he was gone.
I understand Sandy has since relocated out of state. Good for her, bad for us. I got to visit with her at his visitation, but she often accompanied Morrie to our monthly support meetings and I miss her. She is quite a lady.
Strangely, Funkhouser was the second "Maurice" who had a seminal impact on my life. The late Maury DeJonge (say "DeYoung") was a legendary political reporter for the Grand Rapids Press who later went on to become the county clerk for Kent County in West Michigan.
My first job out of college was at the Press, and I was given the desk directly across from his. He was a close personal friend of Gerald R. Ford, knew everything taking place in local government almost before it happened, and it was a revelation for this cub reporter to watch him work.
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| What a Handsome Young Morrie! |
For reasons I never understood, DeJonge took a liking to me and placed me under his wing. I'll never forget the day we were walking out of the newsroom together to our separate assignments and I happened to glance at the wall clock. "Looking at that clock?" he intoned. "Forget it. The news doesn't keep a 9-to-5 schedule."
I have been truly blessed. The Morrie the merrier, I guess.
We will gather in January for our next "Second Chance" group meeting, and undoubtedly we will miss Morrie again. I'm not certain when, or if, we will ever stop.
Memorial contributions may be made in Morrie Funkhouser's name to the Polycystic Kidney Foundation at https://pkdcure.org/tribute-donation, or at 1001 E. 101st Terrace, Suite 220, Kansas City, MO 64131.
Wednesday, December 25, 2019
It's the Most Wonderful Gift of the Year
Sometimes it's an average Joe or Joanne, unknown to everyone except family and friends, who strolls into a hospital, walks up to the information desk and declares they want to donate one of their kidneys.
They don't necessarily care who it goes to. They just saw a story on the news, or know somebody with renal failure, or just became overpowered with the Christmas spirit. They want to make a difference in someone's life, to enhance the quality of somebody else's time on this planet. It's called "living non-directed donation."
This year it happened in (among other places, we pray) Illinois. According to the National Kidney Foundation of Illinois website, an anonymous donor stepped forward this month whose blood and tissue types were compatible with a 16-year-old teenager named Jonathan Guitron. And shortly thereafter, the Guitrons received the gift every family struggling with kidney failure longs to receive:
The Call.
"We were definitely not expecting to get it," says his mother Nicki, referring to the call from the hospital or transplant center announcing that a matching organ has been located. "But we're beyond grateful."
So this year on Christmas Day, instead of spending the day combining their joy with undercurrents of concern and fear for Jonathan's health, the Guitron family will be at the hospital helping him get prepped for surgery. If all goes according to plan, he and his donor will undergo simultaneous surgeries the morning of Dec. 26th, proving the adage that it's more blessed to give than to receive.
The donor will give, and Jonathan will be more than delighted to receive.
I can say from personal experience that recovery from transplant surgery is slow and excruciatingly painful, and there are some medications you will take every day for the rest of your life. But when the healing is complete, life is infinitely better than anything one can imagine while on dialysis.
Now, not everyone reading this may be willing or able to rush to the nearest hospital tomorrow and scream, "Take my kidney! Please!" That's a tremendous decision. But here's something you could do:
Sometime today, after all the presents have been opened and cooed over and your closest family members are gathered 'round, take a few minutes to talk about organ donation. Let them know you wish to be a donor after you've passed so there can be no mistaking your wishes, and ask if they've thought about what their intentions are.
And check your driver's license. Many states have some sort of symbol on their licenses indicating the driver wishes to be a donor. In Illinois, where I live, it's a small red outline of the state. In other states it can be a heart, a star, or even simply the words "Organ Donor." I've found that many people are organ donors and either forgot or didn't realize they had made the commitment.Please, make this the merriest, jolliest, happiest Christmas ever. I can bet the Guitrons will.
Merry Kidneymas.
Friday, December 20, 2019
Well, If This New Development Don't Trump All
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| Illustration by Global Village Space |
I can hardly believe it either. And on his Impeachment Week, at that. Will wonders never cease?
Then again, none of us is completely good or totally evil. Hitler built the Autobahn, and I understand he threw amazing parties.
You have to give the devil his due. So I must praise Twitler and his administration for putting some muscle this week behind a cause that is extremely dear to my heart: kidneys and increasing the number of available organs for the nearly 100,000 Americans waiting for a transplant.
In July, Trump signed an executive order –– the first executive order focused on kidney health since the 1970s –– launching an initiative aimed at improving the lives of Americans suffering with kidney disease. Among other things, the initiative seeks to help prevent renal failure in the first place through improved diagnosis, treatment and preventative care.
The federal action also seeks to streamline and speed up the process of kidney matching and modernize the existing system in order to increase the number of transplants. It wants to make treatment options more affordable and ramp up the development and placement of artificial kidneys.
Wow.
Then on Dec. 17, the Trump administration announced a radical new change to the kidney donation system that could result in as many as 5,000 more available organs every year.
To help make the system more transparent, the government wants to change the way it works with organ procurement organizations (OPOs), the federally-funded nonprofits Medicare and other agencies rely on to manage the process of obtaining kidneys.
In the past, OPOs have been largely autonomous and infrequently re-certified. Partly as a result of this, as you may have heard elsewhere, almost 20 percent of kidneys currently donated in the U.S. are routinely discarded. That's one out of every five!
They may have come from older donors or persons with pre-existing health conditions, but if you're on dialysis, stuck on a transplant waitlist, and feeling weaker every day, an imperfect kidney is way better than no kidney at all.
With ongoing advancements in medicine, many of these "imperfect" kidneys could work quite well. (By contrast, France only throws out about 9 percent of kidneys donated.) The new system would rely on independent data by the CDC (Centers for Disease Control and Prevention) that would be used to evaluate the OPOs in terms of their donation rates and the percentage of donors whose organs are actually transplanted.
In addition, Trumpster wants to make it easier for living donors to help save lives by giving one of their kidneys to another. Hospital expenses for donors have long been covered completely, but new rules also would reimburse donors for lost wages and, possibly, child and eldercare as well.
For a man who cheats on his wives, denies responsibility for everything but the economy, brags about everything but his tax returns, attempts to extort foreign leaders, and travels to Michigan to suggest that its longest-serving congressman in U. S. history may now be in Hell, this is an unusually compassionate act from Le Grand Orange.
Somebody must have told him to do it.
Regardless of the reason, however, for the 3,000 people who are added to the transplant waiting list each month and the 20 people who die every day waiting for their matching organ to be found, any step forward is a quantum leap.
And of course, Don the Con can't even do a good thing without opening his mouth and cramming his bone spurs in it. In signing the executive order last summer, he was heard by everyone within earshot rhapsodizing that 'The kidney has a special place in the heart. It's an incredible thing."
This, of course, sparked an avalanche of social media wisecrackers offering Agent Orange free anatomy advice. And for all we know, he may need it.
T-Rump often seems to have trouble finding his backside with both hands.





















