Michael Wright:
CLASS OF 1977

University of Missouri - ColumbiaClass of 1977
Columbia, MO
Purdue University - EngineeringClass of 1974
West lafayette, IN
Indiana University - Purdue UniversityClass of 1970
Indianapolis, IN
North Central High SchoolClass of 1966
Indianapolis, IN
Westlane Junior High SchoolClass of 1963
Indianapolis, IN
Michael's Story
In my past posts here I have urged cancer patients to consider contacting Dr Rigdon Lentz, MD in Prien am Chiemsee, Bavaria, Germany and seek out his apheresis treatment prior to allowing their US doctors to treat their cancers with radiation and chemo. Dr. Lentz, a US born and trained physician, is a former US Naval Surgical unit commander and a respected immunologist who had an astounding 75% success rate with patients who had healthy immune systems, (that is, were naive to chemo and radiation treatments). That is the lesson I learned too late to save my wife's life. She died 19 July 2014, only 55 years of age and otherwise in perfect health. My biggest regret is that we blindly, stupidly followed our local oncologist's advise and allowed them to treat her with chemo drugs and radiation for a year. The radiation helped a little. The chemo only resulted in the cancer blowing up and spreading like wild fire. Chemo killed her quicker than the cancer would have had we left it untreated, and what is worse, it made her ineligible for Dr. Lentz to treat successfully. He only had about a 25% success rate with patients treated with chemo and radiation first. You had to have a normally healthy immune system to be able to benefit from his immunoaphoresis treatments. This is an update on the status of Dr. Lentz's practice in Bavaria, Germany.
Basically, I am sad to report that Dr. Lentz's practice became a victim of the COVID pandemic and of his age. He is 78 this year and at the end of 2019 he was faced with mounting losses as patients stayed away and travel restrictions clamped down on those who would have taken the chance of catching COVID in order to access his treatment. Upon realizing the gravity of the spreading COVID virus, especially to his type of patient, he made the painful decision to discontinue operations, file a world wide patent on his equipment designs and treatment procedures (See patent WO2019 / 053031A1) and retire back to his home in Tennessee, USA. Although he has closed his practice and retired, his patent stands ready for someone else to take up the treatment approach he invented. To date, no one has approached him about doing that in any meaningful way. We are left only with his ideas about how to beat cancer at this point. If you care to know more about those ideas I would refer you to a pair of You-Tube videos he produced that demonstrates the medical basis for his treatment ideas. You can find them by searching for "Dr Rigdon Lentz onco apheresis video"
The success of Dr. Lentz's procedure depends on your own immune system's natural ability to find and destroy the cancer cells. Therefore, you have to have an immune system capable of a normal response to foreign proteins before it works. What his procedure does is reduce the cancer cell's ability to mask its presence by removing the cloud of soluble tumor necrosis factor receptors (sTNFRs) a cancer cell produces in its immediate microlocation. The concentration of sTNFRs in your blood and interstitial fluids are reduced through the apheresis process so that your normal immune cells can find the tumor and are not overwhelmed by high concentrations of sTNFRs in the area of the cancer cell.
As a result of a number of parallel scientific developments, the sophistication of his equipment took dramatic leaps between 2013 and 2019, greatly increasing the patient comfort during the apheresis process. However the high cost of that instrumentation development was also a factor that led to the closure of the practice. It became clear that the pandemic years were not going to provide adequate "catch up" funds to create a reasonable return rate on the investment in instrument improvement. To persist in the practice at that point would have led to eventual bankruptcy before any turn-around in the arch of COVID infection rates subsided.
As an analytical biochemistry scientist, this immunoapheresis procedure, now patented by Dr. Lentz, is the only cancer treatment protocol I have seen which makes complete sense to me from a metabolic and technical feasibility point of view. I fully subscribe to Dr. Lentz's view that it makes no sense in treating cancers to try to kill the cancer before killing the patient with chemo and radiation nor does it make any sense to give a patient immuno-boosting drugs if their immune system is normally functioning, nor is it a high probability of success approach to giving drugs that are specific for cancer genetic flaws when so few cancers actually display such flaws. What does make sense is an approach that relies on normal immune system function by reducing the small molecule sTNFRs concentrations in a patient's blood and interstitial fluid with apheresis procedures so that the immune system can do its normal job unimpeded by the cancer cell's ability to mask its position by shedding sTNFR proteins in high concentration. Wish I'd known this when my wife was first diagnosed with inoperable non-small cell lung cancer.
Still, too little knowledge & to0 late awareness for my Jeannie.
Jeannie and I were married 28 years and one day. She was my business partner and best friend. We owned & operated an analytical laboratory and consulting business based in Texas. We were what the Agrochemical industry identifies as "contract regulatory research chemists". We were together 24/7 and specialized in conducting food safety and pesticide residue evaluation studies in raw agricultural products, processed food, animal feed, meat, milk, eggs, water and soil. The data from our studies have been used for dietary exposure risk assessments by regulatory agencies, such as EPA, from around the world. Something different every day and a good woman with whom to share it. What more could a lucky guy have ever asked for. Our glory days are gone and in the past now.
Jeannie died the day following our 28th wedding anniversary, at 2 p.m. on the 19th of July 2014 after an 11 day stay as an in-patient at Hospice Brazos Valley, Bryan, TX. The memorial service was at Holy Cross Lutheran church in College Station Texas on 23rd of July 2014. A second memorial service was held 12 Aug 2014 at her home church, St John's Lutheran in Westboro, MO where most of her childhood friends and family still live. Most of the immediate family tended to Jeannie during her hospice stay, they all attended the service in College Station and the service in Westboro, MO. In lieu of flowers we are asking that anyone moved to make a memorial gesture, please make a donation to Hospice Brazos Valley, 502 W. 26th St, Bryan, Texas 77803. Please do so in memory of Jeannie K. Wright. This is the oldest and only hospice in the Brazos Valley area of Texas with an in-patient facility capable of handling the difficult lung cancer patients and others with acute respiratory problems who are in the terminal stage of their disease. The doctors, staff and volunteers are the very best and deserve far more support than they are getting. As part of my grieving process I intend to volunteer there as soon as and for as long as I am able.
In previous posts I have recounted our family's medical odyssey with my wife's inoperable, non-smokers, non-small cell, stage IV lung cancer with which she was diagnosed 17 Feb 2013. By July 2013 she was recovered sufficiently from the simultaneous radiation/chemo treatment side-effects (resulting pneumonia and the nagging cough) that the Dr.s felt it was time to do another CT scan to see how they did in treating "Alice", as my wife called the golf ball sized tumor growing around her aorta in the medial hilar region of her right lung. The July 2013 contrast CT scan confirm that the inoperable tumor that had her aorta in its grip was less than half the original size and there were no signs of mediastinal or hilar lymphadenopathy present. However there was a new area of "ground-glass opacity" in the medial and lateral aspect of the right lung that could have been residual effects of radiation induced edema and resulting pneumonia or it could have been signs that the carcinoma had begun to metastasize to those regions of her lung. So things looked much improved over what we saw in the initial February 2013 CT and PET scans. The doctors wanted to wait until early October, 2013 to do another contrast CT scan to determine if things were the same, clearing up or changing in some other manner. So we waited until late October 2013 to get the CT scan done and because Jeannie had recently had some unexplained soreness in her right hip, we also did a bone scan.
28 Oct 2013 we sat down with her oncology team and discussed the results of those follow-up scans. The news was not what we had hoped to hear. Alice probably didn't live in her right lung anymore, but before she died she had babies; lots of babies. There were, at that time, a number of small 1/4 inch spots in both lungs that were probably cancerous and the cancer had also very clearly metastasized to her right ilium.
On the basis of the Oct 2013 scans, my wife was given a life expectancy of from 6 to 12 months. We had high hopes in July, 2013 that we had discovered her lung tumor and gotten into treatment in time to save her life....Expand for more
By Oct it was obvious that our hopes were quite thoroughly dashed. Another 10 radiation treatments in early Nov. 2013 to deal with the bone cancer in her ilium left her with a fist sized hole in that portion of her pelvic girdle and in a wheel chair. Lung cancer with metastasis to the bone is not curable, according to conventional medical wisdom, and without major bone resection the prospects of long term survival were nil. In my wife's case the doctor's opinion was that the amount of bone resection/replacement she would have to undergo would probably destroy what quality of life she then had and might actually hastened her demise. We were told that if we undertook stepped up nutritional therapy in conjunction with an altered chemo therapy and targeted radiation therapy, we might expect the longest life expectancy. That was so long as she didn't fall and break a bone or something like that. We believed them and agreed. Regardless of all of that, we were told that sometime within the next year I should expect to become a widower. The reality is that we split the difference at 9 months.
We were prepared to hear this ugly news and to begin to live out the remainder of our time together in the best possible manner we could manage. We did try chemo a second time in the Dec 2013 through April 2014 time frame but she only got worse and the cancer continued spreading at an accelerated rate. Before it was done in April, the cancer had collapsed her right lung, metastasized to #7-#12 vertebra, squeezing off the nerves to her left arm, and left her a bed-bound invalid. She clearly didn't have long to be with us, so we made the best of a bad situation. We gathered the family for one last good time together in late June-early July, before she just could not do anything on her own, and we had a good time, including watching a 4th of July fireworks display with Jeannie in a wheel chair and on portable oxygen.
2023 After 9 years I am still processing the events of July 2014 as Jeannie lay in Hospice trying to prepare her family for what was at hand. Despite the trauma of that time, what was clear to me then and still is clear as daylight is that we might have saved her if we had gone to Dr. Lentz first. I have been a long time living with that gem of hindsight with my only satisfaction being to live long enough to witness the Pharmaceutical Industry make a slow turn toward immunotherapy drug development in favor of platinum based immune system killing drugs and a pitifully small patchwork of genetics based intervention drugs.
It was during that second round of Chemo with an Eli Lilly drug called Alimta, that I heard from a long time colleague of mine about an alternative cancer treatment called immunoapheresis as performed by a former California U- Berkley physician, Dr. Rigdon Lentz, now retired. My colleague claimed Dr. Lentz saved his wife's life 18 years ago when all else had failed to control her breast cancer. About that same time, the Exeter Green Committee of the Aurora Foundation issued a report in December 2013 on Dr. Lentz's treatment procedures as he was then practicing in Germany. Their report gave a strong recommendation for it as an advanced cancer treatment protocol with a 75% cure rate to full remission with an additional 15% of patients who are able to maintain a remission state with additional follow-up treatments. It seems to work no matter from what type of cancer the patients suffered.
It was about that time that the WHO induced the English manufacturer of Dr. Lentz's equipment to find ways to lower the cost of the machine and expendable supplies so the WHO could afford to put one of the immunoaphoresis machines and trained staff into every third world clinic in Africa and Asia. The roll out was terribly slow and far more expensive than originally envisioned but it did result in the equipment Dr. Lentz's team was using when they closed their clinic being far superior to anything previously available for therapeutic oncoapheresis. Again, too little, too late for my Jeannie.
At least we got to celebrate our 28th wedding anniversary on Friday the 18th of July. It was a miracle that she was awake and alert enough that morning to know what the occasion was, and be able to respond a little bit to it so that we knew that she knew the significance of what was going on. At that point in her hospice stay Jeannie had not eaten anything in 9 days, had only about a quart of fluids to drink in all that time, was so weak she could not hold her head up, could not read her anniversary card (I read it to her as she struggled mightily to make out the words) had use of only her right hand (which she used to hold the card) and she could not articulate words Intelligibly. But after I read the card to her, the family presented her with the fabulous flower arrangement our Belgian daughter had send (she couldn't get plane tickets to come back to us) and then the ice cream anniversary cake the nursing staff bought was presented to us in a perfectly choreographed manner at which point we all joined together in singing a made-up happy anniversary song. Jeannie indicated she fully understood what was going on by raising her one good arm, made a little fist and waving it gently as she uttered a triumphant, Yahhhay! with just about all the strength she had left. Later that Friday afternoon, having been given a bath and shampoo by the nursing staff, and resettled in her "Cloud Chair" with clean linen and nightshirt, the hospice staff started a new course of sedation (Jeannie was resistant to opiate sedatives). She drifted off to sleep about 4 p.m. and slipped into a coma late that evening or early Saturday morning from which she never awoke until sitting up suddenly at 2 p.m. Saturday with a surprised look on her face, threw up her arms and almost as quickly wilted back onto the cloud-chair with me steadying her by her right arm and her sister holding her left to help ease her back down. Six minutes later the body she had left behind stopped breathing altogether and she was pronounced dead at 2:06 p.m. At peace at last, Thanks be to the Lord.
The next 18 months I went to hell and back trying to come to terms with all the changes that losing her required I undergo. Carrying on the business was the most difficult, and ultimately, most impossible task of all. We did manage to complete all of the work that was ongoing at the time of her death. I then elected to retire and close the business. I no longer wanted to do the work and the number of people I would have had to hire to replace what Jeannie did for us made the business plan unworkable for the long term. Rather than re-invent ourselves a fifth time, There were other things I could still do. I had church work and other charitable work with children to which I did give my full attention. At the same time, I turned greater attention to a genealogy book I had been working on for almost 15 years. I wanted to bring it to a close & publish before I died. I also owned some rental properties that needed attention before my tenants begin to be too annoyed with me! There was still much to do.
Life is very different now, but it is still good and there are still a few people, young and old, who are counting on my help, so, feeling sorry for myself is not an option. I must continue building relationships with others & keep living a life that is helpful to others. That is what we were put on this earth to do and what I have always vowed I would do until my turn here is done. In doing that, I know there are still adventures to be had, and that I can embrace them with joy, so long as my attitude remains solidly rooted in hope.
I certainly pray the pandemic years 2020 to 22 treated all of you well, that you found it easy to stay healthy, and found ways to keep in touch with your social network and whatever remains of your youth. As for me, I am feeling better, stronger and more at peace with having had my life ripped apart in 2014. Things could have been so much worse. We could have been partying down at the Bataclan concert hall in Paris that year when it was bombed. At lease Jeannie got to choose how she passed on and was able to do it with dignity and tranquility surrounded by her family and dearest friends, rather than in the helpless terror experienced by those who lost their lives at Bataclan in Paris and in all the mass shootings we have had in recent years. What utter insanity! So I pray you all take care, stay alert, make wise choices & be well.
One last note. About 8 years ago I had occasion to reincarnate my laboratory service business one final time. It has been turned into a very profitable one man operation. It was not my doing, but at the insistence and with the assistance of some of my past clients. I am blessed at 78 to be getting paid to do what I love to do once again. I'm healthy and employed and I'm quite OK. I just wish more people knew about and believed in Dr. Rigdon Lentz's therapeutic onco-apheresis procedures and in particular someone in a position to take up his procedures and turn it into a practice where cancer patients could go as an alternative to chemo and radiation and gene based treatment.
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