Category Archives: Stem Cell Doctors


34 years with a new heart and counting – MDJOnline.com

Whenever Harry Wuest has a doctors appointment in northern Atlantas hospital cluster dubbed Pill Hill, he makes sure to stop by the office of Dr. Douglas Doug Murphy for a quick chat.

And Murphy, unless hes tied up in the operating room, always takes a few minutes to say hello to his former patient. Remember when ... ? is how the conversation typically starts, and its always tinged with laughter, often joyful, sometimes bittersweet.

Its a reunion of two men who shaped a piece of Georgias medical history.

Almost 35 years ago, Murphy opened the chest of Wuest and sewed in a new heart, giving him a second shot at life. Wuest was the third heart transplant patient at Emory University Hospital.

Tall, lanky, with short curly hair and a quiet demeanor, Wuest is the longest-surviving heart transplant recipient in Georgia and one of the longest-surviving in the world. The 75-year-old accountant still plays golf twice a week and only recently went from working full-time to part-time. My heart is doing just fine, he says.

Murphy is now the chief of cardiothoracic surgery at Emory Saint Josephs Hospital and still in the operating room almost every day. He has moved on to become the worlds leading expert in robotically assisted heart surgery.

Harry Wuest is originally from Long Island, New York. After a stint in the Air Force, he moved to Florida to work and go to school. He wanted to become a physical education teacher. Then, in 1973, he fell ill. It started with some pain on his left side. He didnt think much of it, but when he got increasingly winded and fatigued, he went to see a doctor.

Several months and numerous specialists later, he received the diagnosis: Cardiomyopathy, a disease of the heart muscle that can make the heart become enlarged, thick and rigid, preventing it from pumping enough blood through the body.

They didnt know how I got it, says Wuest, sitting back in a brown leather armchair in the dark, wood-paneled living room of his Stone Mountain home. Maybe it was a virus. And back then, there wasnt much they could do to treat it, except bed rest.

For the next 12 years, Wuest lived life as best as he could. He got a degree in accounting from the University of Central Florida and worked for a real estate developer. There were good days, but there were more bad days. He was often too weak to do anything, and his heart was getting bigger and bigger.

Emorys first transplant surgeon

The first successful human-to-human heart transplant was performed in Cape Town, South Africa, in 1967 a medical breakthrough that catapulted the surgeon, Dr. Christiaan Barnard, onto the cover of Life magazine and to overnight celebrity status.

This highly publicized event was followed by a brief surge in the procedure around the world, but overall, heart transplants had a rocky start. Most patients died shortly after the surgery, mainly due to organ rejection. Back then, immunosuppressive drugs, which can counteract rejection, were still in their infancy. Many hospitals stopped doing heart transplants in the 1970s.

That changed with the discovery of a highly effective immunosuppressive agent. Cyclosporine got FDA approval in 1983 and altered the world of organ transplants.

It was shortly thereafter when Emory University Hospital decided to launch a heart transplant program, but none of the senior surgeons wanted to do it. Even with the new drug, it was a risky surgery, and mortality was still high.

Its an all-or-nothing operation, Murphy says, as he sits down in his small office overlooking the grayish hospital compound. Hes wearing light blue scrubs from an early morning surgery. At 70, he still has boyish looks, with a lean build and an air of laid-back confidence. If you have a number of bad outcomes initially, it can be detrimental to your career as a surgeon, he says.

But Murphy didnt really have a choice. He remembers that during a meeting of Emorys cardiac surgeons in 1984, he was paged to check on a patient. When he returned, the physicians congratulated him on being appointed the head of the new heart transplant program. He was the youngest in the group and had been recruited from Harvards Massachusetts General Hospital just three years before.

Yeah, thats how I became Emorys first transplant surgeon, says Murphy.

He flew to California to shadow his colleagues at Stanford University Hospital, where most heart transplants were performed at the time. Back home at Emory, he put together a team and rigorously rehearsed the operation. The first transplant patient arrived in April 1985. The surgery was successful, as was the second operation less than a month later.

Around the same time, Harry Wuest wound up in a hospital in Orlando. He needed a transplant, but none of the medical centers in Florida offered the procedure. One of his doctors recommended Emory, and Wuest agreed. I knew I was dying. I could feel it. He was flown to Atlanta by air ambulance and spent several weeks in Emorys cardiac care unit until the evening of May 23, when Murphy walked into his room and said, Weve got a heart.

I could finally breathe again

The heart, as the patient later learned, came from a 19-year-old sophomore at Georgia Tech who had been killed in a car crash.

Organ transplants are a meticulously choreographed endeavor, where timing, coordination and logistics are key. While Murphy and his eight-member team were preparing for the surgery, Wuest was getting ready to say farewell to his family his wife and three teenage sons, and to thank the staff in the cardiac ward.

I was afraid, he recalls, especially of the anesthesia. It scared the heck out of me. He pauses during the reminiscence, choking briefly. I didnt know if I was going to wake up again.

The surgery took six hours. Transplants usually happen at night because the procurement team, the surgeons who retrieve different organs from the donor, only start working when regularly scheduled patients are out of the operating room.

Despite the cultural mystique surrounding the heart as the seat of life, Murphy says that during a transplant surgery, its not like the big spirit comes down to the operating room. Its very technical. As the team follows a precise routine, emotions are kept outside the door. We dont have time for that. Emotions come later.

Waking up from the anesthesia, Wuests first coherent memory was of Murphy entering the room and saying to a nurse, Lets turn on the TV, so Harry can watch some sports.

Wuest spent the next nine days in the ICU, and three more weeks in the hospital ward. In the beginning, he could barely stand up or walk, because he had been bedridden weeks before the surgery and had lost a lot of muscle. But his strength came back quickly. I could finally breathe again, he says. Before the surgery, he felt like he was sucking in air through a tiny straw. I cannot tell you what an amazing feeling that was to suddenly breathe so easily.

Joane Goodroe was the head nurse at Emorys cardiovascular post-op floor back then. When she first met Wuest before the surgery, she recalls him lying in bed and being very, very sick. When she and the other nurses finally saw him stand up and move around, he was a whole different person.

In the early days of Emorys heart transplant program, physicians, nurses and patients were a particularly close-knit group, remembers Goodroe, whos been a nurse for 42 years and now runs a health care consulting firm. There were a lot of firsts for all of us, and we all learned from each other, she said.

Wuest developed friendships with four other early transplant patients at Emory, and he has outlived them all.

When he left the hospital, equipped with a new heart and a fresh hunger for life, Wuest made some radical changes. He decided not to return to Florida but stay in Atlanta. Thats where he felt he got the best care, and where he had found a personal support network. And he got a divorce. Four months after the operation, he went back to working full-time: first in temporary jobs and eventually for a property management company.

After having been sick for 12 years, I was just so excited to be able to work for eight hours a day, he recalls. That was a big, big deal for me.

At 50, he went back to school to get his CPA license. He also found new love.

Martha was a head nurse in the open-heart unit and later ran the cardiac registry at Saint Josephs Hospital. Thats where Wuest received his follow-up care and where they met in 1987. Wuest says for him it was love at first sight, but it took another five years until she finally agreed to go out with him. Six months later, they were married.

Harry Wuest and his wife, Martha. She was a head nurse in the open-heart unit and later ran the cardiac registry at Saint Josephs Hospital. Thats where Wuest received his follow-up care and where they met in 1987. Wuest says for him it was love at first sight, but it took another five years until she finally agreed to go out with him. Six months later, they were married.

Having worked in the transplant office, I saw the good and the bad, Martha Wuest says. A petite woman with short, perfectly groomed silver hair, she sits up very straight on the couch, her small hands folded in her lap. Not every transplant patient did as well as Harry. And I had a lot of fear in the beginning. Now he may well outlive her, she says with a smile and a wink.

Wuests surgeon, meanwhile, went on to fight his own battles. Two and a half years into the program, Murphy was still the only transplant surgeon at Emory and on call to operate whenever a heart became available. Frustrated and exhausted, he quit his position at Emory and signed up with Saint Josephs (which at the time was not part of the Emory system) and started a heart transplant program there.

At St. Josephs, Murphy continued transplanting hearts until 2005. In total, he did more than 200 such surgeries.

Being a heart transplant surgeon is a grueling profession, he says, and very much a younger surgeons subspecialty.

He then shifted his focus and became a pioneer in robotically assisted heart surgery. He has done more than 3,000 operations with the robot, mostly mitral valve repairs and replacements more than any other cardiac surgeon in the world.

Heart transplants "remain the gold standard"

Since Murphy sewed a new heart into Wuest 35 years ago, there has been major progress in the field of heart transplants, but it has been uneven.

There is improved medication to prevent rejection of the donor heart, as well as new methods of preserving and transporting donor hearts.

Yet patients requiring late-stage heart failure therapy, including transplantation, still exceed the number of donor hearts available. In 2019, 3,551 hearts were transplanted in the United States, according to the national Organ Procurement and Transplantation Network. But 700,000 people suffer from advanced heart failure, says the American Heart Association.

New technologies and continued research are providing hope to many of these patients. There has been significant progress in the development of partial artificial hearts, known as Left Ventricular Assist Devices, or LVADs. They can be used as bridge devices, to keep patients alive until donor hearts are available, or as destination therapy, maintaining patients for the remainder of their lives.

Also, total artificial hearts have come a long way since the first artificial pump was implanted in a patient in 1969. The technology is promising, says Dr. Mani Daneshmand, the director of Emorys Heart & Lung Transplantation Program. But its not perfect.

Long-term research continues into xenotransplantation, which involves transplanting animal cells, tissues and organs into human recipients.

Regenerative stem cell therapy is an experimental concept where stem cell injections stimulate the heart to replace the rigid scar tissue with tissue that resumes contraction, allowing for the damaged heart to heal itself after a heart attack or other cardiac disease. Certain stem cell therapies have shown to reverse the damage to the heart by 30 to 50 percent, says Dr. Joshua Hare, a heart transplant surgeon and the director of the Interdisciplinary Stem Cell Institute at the University of Miamis Miller School of Medicine.

All of these ideas have potential, says Daneshmand. But none of them are ready to replace a human donor heart. A heart transplant remains the gold standard, because you cant accommodate the same success with a machine right now, he says.

Efforts around expanding the donor pool are really the best way to address this problem, while we wait for technology to catch up, he adds.

Besides Emory, other health care systems in Georgia that currently have a heart transplant program are Piedmont Healthcare, Childrens Healthcare of Atlanta and Augusta University Health.

Organ rejection remains a major issue, and long-term survival rates have not improved dramatically over the past 35 years. The 10-year survival is currently around 55 percent of patients, which makes long-term survivors like Harry Wuest rare in the world of heart transplants.

The United Network of Organ Sharing, or UNOS, which allocates donor hearts in the United States, doesnt have comprehensive data prior to 1987. An informal survey of the 20 highest-volume hospitals for heart transplants in the 1980s found only a scattering of long-term survivors.

In for the long haul

Being one of the longest-living heart transplant recipients is something that Wuest sees as a responsibility to other transplant patients, but also to the donors family, which hes never met. If you as a transplant recipient reject that heart, thats like a second loss for that family.

Part of this responsibility is living a full and active life. Both he and Martha have three children from their previous marriages and combined they have 15 grandchildren. Most of their families live in Florida, so they travel back and forth frequently. Wuest still works as a CPA during tax season, and he does advocacy for the Georgia Transplant Foundation. In addition to golf, he enjoys lifting weights and riding his bike.

Hes had some health scares over the years. In 2013, he was diagnosed with stage 1 kidney cancer, which is in remission. Also, he crossed paths with his former surgeon, and not just socially. In 2014, Murphy replaced a damaged tricuspid valve in Wuests new heart. That operation went well, too.

Murphy says there are several reasons why Wuest has survived so long. Obviously, his new heart was a very good match. But a patient can have the best heart and the best care and the best medicines and still die a few months or years after the transplantation, the surgeon says. Attitude plays a key role.

Wuest was psychologically stable and never suffered from depression or anxiety, Murphy says. Hes a numbers guy. He knew the transplant was his only chance, and he was set to pursue it.

Wuest attributes his longevity to a good strong heart from his donor; good genetics; great doctors and nurses; and a life that he loves. Im just happy to be here, he says.

Quoting his former surgeon and friend, he adds: Doug always said, Having a transplant is like running a marathon. And Im in for the long haul.

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34 years with a new heart and counting - MDJOnline.com

Lil Nas X surprises the kids at Berts Big Adventure 2020 – Atlanta Journal Constitution

Atlantas Lil Nas X joined Berts Big Adventure Saturday night to sing and entertain the 13 chronic and terminally ill kids at a Disney hotel Saturday night.

TheOld Town Road singer also popped into a wedding in the same hotel and got some TMZ love.

Wouldnt ya know thats the thing that gets publicity, mused Bert Weiss by text Sunday morning.Lol. He was actually in our green room ready to perform for the kids. He had a few extra minutes and popped into their wedding before he performed.

Weiss said his group simply asked Lil Nas X for his availability and was pleasantly surprised he said yes.

The Berts Big Adventure social media team wrote:Lil Nas X surprised us at our dance party! The kiddos promptly lost their minds, and everyone was on their feet and singing along while the rapper performed his record-breaking hit, Old Town Road. He was so kind and thoughtful arriving with an autographed hat for each kiddo to wear during his performance. In addition, he graciously posed for so many photos and commemorated the evening by having the Berts Big Adventure kiddos and siblings sign his hat too! It was an experience to last a lifetime!

This is just one more feather in the cap for Weiss organization, which he started soon after he joined Q100 in 2001.

Inspired by his mentorKidd Kraddock, the morning radio host brings the kids to Disney World for a whirlwind trip. This year, he was able to bring in 13 families from around the country.

It changes every year because the families are different, Weiss said.

Some received bonus gifts as well. BBA is paying for a stepdad to adopt his four-year-old child. They are giving a child VIP treatment at a Falcons game in a $6,000 suite. They also introduced the stem cell donor who saved a kids life.

Bethany and George Van Winkle of Cumming have a nine-year-old Sam with Downs Syndrome and a congenital heart defect. Sam has had two surgeries and appears to be on his way to a healthy life.

The family was saving money for a Disney trip but then Bethany had breast cancer and all the savings disappeared. (She is in remission). Berts Big Adventure solved that problem and gave Bethany and George a bonus trip to the Bahamas as well.

This Disney trip will enable us to be present, Bethany said.We are always worrying about hours ahead, weeks ahead, about money. Now we have a place to stay, the itinerary isset up for us. There are two doctors on call and a wheelchair for him if he needs it.

The organization also holds events and programs year around for 200 alum families featuring reunion gatheringsand a Fairy Godmother program where volunteers visit kids who are in hospitals.

For many years, Weiss has had a salaried full-time executive director Molly Darby and a raft of loyal sponsors such as Carters, Moes and Jersey Mikes. Endeavor Air flies the kids gratis to Orlando.

The most recent 990 available on GuideStar for Berts Big Adventure shows his organization raised $935,661 in 2017, up from $811,469 a year earlier. Based on the financials, it appears to be a very healthy organization.

Here are some more photos from the kickoff party from both the Hilton Airport and the hangar where the Endeavor plane departed.

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Rodney Ho

Rodney Ho covers radio and television for the Atlanta Journal-Constitution.

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Lil Nas X surprises the kids at Berts Big Adventure 2020 - Atlanta Journal Constitution

The Top BioHealth Capital Region CEOs to Follow on Social Media – BioBuzz

The BioHealth Capital Region (BHCR) is evolving quickly and it can be tough to keep pace with the latest news emerging from the host of biotech, medical device and cell, and gene therapy companies in the area. BioBuzz, when combined with some strategic social media follows, can help you stay on top of the latest developments, news and thought leadership coming out of the BHCR.

If youre reading this, you already know about and hopefully, follow us (@BioBuzzMaryland).

To add to your social media sources, weve handpicked several key industry CEOs, founders and thought leaders that are must follows to stay in the loop with all of the excitement, innovation, and milestones that are sure to come in 2020 and into the next decade of the regions evolution as a top global BioHealth cluster.

Jeff Galvin is the CEO of American Gene Technologies (AGT) (@americangene). AGT is a cell and gene therapy company that utilizes a proprietary lentiviral platform to develop potential treatments for HIV, liver cancer, Phenylketonuria (PKU) and inherited genetic disorders. In October 2019 the company announced it had submitted an Investigational New Drug (IND) to the FDA for its HIV cure program, AGT103-T, which is expected to start clinical trials in 2020. Galvin is a dynamic presence on the BioHealth Capital Region speaking circuit and a leader in fostering a world-class community of cell and gene therapy companies here in Maryland that he sees becoming a future DNA Valley.

Galvin comes from the West coast where hewas a successful tech entrepreneur and executive. After living through theindustrial revolution first-hand in the microcomputer and software industry,Galvin is driven by his passion to see that the work they are doing in cell and gene therapy brings forth what hedescribes as, the software revolution for the next 100 years: reprogrammingDNA in cells to improve health. With nearly 1,900 followers on LinkedIn and350 followers on Twitter, keeping tabs on Galvins social media will help youkeep your finger on whats happening at AGT (@americangene)and the cell and gene therapy industry.

Greg Merril is the CEO of Adaptive Phage Therapeutics (APT), which is a clinical-stage biotechnology company founded to provide an effective therapeutic response to the global rise of multi-drug resistant (MDR) pathogenic bacteria. This is an exciting company to follow with a remarkable founding story that is chronicled in the memoir, The Perfect Predator. Earlier this month APT was selected as one of the TOP 1% of startups at the 2020 Startup Grind Global Conference, making the cut to be one of just 54 companies selected from 4,000 total applicants from 133 countries. Merrill was also featured last week on NPRs On The Record podcast where you can learn more about their technology and story.

APTs core asset is a large and continually expanding phage library (PhageBank) deployed with a companion diagnostic to achieve a rapid response and cost-effective therapy for otherwise recalcitrant bacterial infections. Merril is very active on social media and has been a regular panelist and speaker on the regions event circuit. Join his more than 2,500 followers on LinkedIn and stay in the loop on the latest APT and BHCR happenings.

Jon Rowley is the founder of Frederick, Marylands RoosterBio and is the companys Chief Product Officer. RoosterBio is rapidly becoming Marylands most well-known stem cell company based on Rowleys vision for plug and play stem cell products and a culture that is attracting a flock of loyal employees (a.k.a. Roosters) and customers to them. The work that Rowley and his team do at The Roost is focused on developing products that help simplify the translating cell therapy and tissue engineering technologies into the clinic and onto the market. The company is at the leading edge of designing products that will accelerate research and development, which will create a sustainable regenerative medicine industry that can deliver more life-saving therapies to patients. Rowley founded the company in 2013 in the FITCI Incubator located in Frederick and is another thought leader who keeps his more than 2,800 LinkedIn and nearly 1,700 Twitter followers in the loop about the latest RoosterBio and bioscience news.

Crystal Icenhour leads Aperiomics, which is a biohealth data science company. The companys Xplore-BIOME bioinformatics algorithms and Deep Shotgun Metagenomic Sequencing technology help physicians identify the causes of their patients infections which are traditionally not identifiable through other testing. Icenhour co-founded Aperiomics in 2014 and the company, with support from the National Science Foundation, identifies every known, sequenced bacteria, virus, fungus, and parasite through deep shotgun metagenomic sequencing, using its world-renown database containing over 37,000 microbes. Icenhour and her team are on a mission to revolutionize the way doctors around the world identify infections. Nearly 4,600 LinkedIn and almost 1,800 Twitter followers stay connected to Icenhour for the latest biohealth data science news and announcements from Aperiomics.

Robert Kramer is CEO of Emergent Biosolutions, a leading developer and manufacturer of medical countermeasures for public health threats like Anthrax or the Coronavirus. Kramer became CEO in April 2019 and has a long history with the company going back to 1999, holding positions that include CFO and most recently COO. With the disappearance of MedImmune last year, Emergent has taken the help as Marylands largest, home-grown biotech companies employing more than 1,300-employees globally and over 500 in Maryland between its headquarters and product development facility in Gaithersburg, two manufacturing facilities in Baltimore, and a manufacturing facility in Rockville.

Historically, Emergents leadership had been quite dormant on social media but Kramer seems to be taking a much more modern approach to communicate the great work that the company and its employees are doing, both with their public health portfolio of products as well as their volunteer work in the community. With more than 1,100 followers on LinkedIn, Kramer is a cant miss follow to keep track of whats going on at Emergent, the biodefense industry and within the biotech and pharma industry at large.

Steve has over 20 years experience in copywriting, developing brand messaging and creating marketing strategies across a wide range of industries, including the biopharmaceutical, senior living, commercial real estate, IT and renewable energy sectors, among others. He is currently the Principal/Owner of StoryCore, a Frederick, Maryland-based content creation and execution consultancy focused on telling the unique stories of Maryland organizations.

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The Top BioHealth Capital Region CEOs to Follow on Social Media - BioBuzz

Local News: Calculating the costs of beef production (2/19/20) – Monett Times

A panel of doctors of veterinary medicine attended the recent annual Beef Cattlemens Conference, hosted by the Monett Chamber of Commerce, the University of Missouri Extension and the Southwest Missouri Cattlemens Association, to discuss cattle health issues that can impact productivity and profit. From left, are: Dr. Ted Dahlstrom, of Monett; Dr. Darren Loula, of Clever; and Dr. Voyd Brown, of Cassville. Melonie Roberts/reporter@monett-times.com

The 51st annual Beef Cattlemens Conference, held Feb. 4 at the Monett National Guard Armory, posed some tough questions for producers attending the program.

One of the first topics, on calculating the cost of the operational costs for varying sizes of beef farms with a panel of successful producers, broke the costs of production down to a per cow basis.

Nathan Isakson, of Ash Grove, spoke of his beef cattle production at the 51st annual Beef Cattlemens Conference, hosted by the Monett Chamber of Commerce, the University of Missouri Extension and the Beef Cattlemens Association on Feb. 4, at the Monett National Guard Armory. Melonie Roberts/reporter@monett-times.com

Nathan Isakson, of Ash Grove, said he runs 2.5 head of cow-calf pair per acre on his farm, the majority of which is Show-Me Select, on a rotational basis.

We stockpile fescue for strip grazing from mid-November through the first week of February, Isakson said. We do feed hay in the event of snow or ice, because of trampling. We also feed hay through the month of September to allow the farm to rest for 30 days.

In lieu of building a barn, Isakson stores his tarped hay on a three-inch bed of gravel.

Cherry Warren, of Exeter, runs his Angus operation on 2,000 acres: 1,500 of which he owns and another 500 that he rents. Warren advised young producers to take care of the ground first, and the ground would, in turn, take care of the cattle. He also urged producers to precondition their cattle before taking them to the sale barn in January. Melonie Roberts/reporter@monett-times.com

Dont pay for a barn you never build, he said.

By using a scheduled plan of operation, grazing fertilized regrowth October through mid-November; feeding hay from February through April, Isakson said he has a higher percent of cows re-breeding faster, generating uniformity of calves at market time.

If we were able to graze through December without stockpiled forage, we would spend an additional $5,463 to provide the nutritional requirements of the herd, assuming a 750-pound [round] bale is valued at $40, he said. However, there is a difference in quality between lush fescue and baled hay.

Weaver Forest, of rural Verona, discussed how his Oleo Ranch because its one of the cheaper spreads, runs on a rotational grazing system. With 750 acres, Forest has practiced rotational grazing since 1966, and his advice to young farmers attending the 51st annual Beef Cattlemens Conference in Monett was, to have a supportive wife with a job off-farm, a good CPA, a good banker, and a good salesman. Mentor with other successful producers and learn what works for them. Melonie Roberts/reporter@monett-times.com

Isakson also advocates for soil testing, and fertilizes his fields based upon those test results.

Im a firm believer in dont guess, soil test, he said.

In accounting for the cost of feed, veterinary supplies, chemicals, veterinary labor, farm services, pasture rent, marketing fees and other expenses, Isakson said it costs him $589 per year per cow.

Weaver Forest, of rural Verona, said he follows a rotational grazing system on his 750-acre farm, and has since he started in the cattle business in 1966.

Ive used a number of different protocols, he said. Sometimes, you win. Sometimes, you lose. Thats the cattle business.

Forest said he had purchased most of his land since 1980.

But, I use pasture rent as an opportunity cost, he said.

Forest said he fertilizes his fields with chicken litter, but cautions young farmers.

Keep cattle off of mature fescue, he said.

Forest uses another practice that is not typically mentioned.

I have the vet pelvic measure every cow on the place, he said. Believe me, thats the cheapest $5 youll ever spend.

At the end of the season, when Forest calculates his operating costs, he estimates he invests $900 in each calf before it goes to market.

There are several things youll need to succeed in this business, he said. A supportive wife with a job off-farm, a good CPA, a good banker, and a good salesman. Mentor with other successful producers and learn what works for them.

The third panel member, Cherry Warren, of Exeter, said he operates his rotational grazing operation on 2,000 acres, 1,500 of which he owns and the remainder of which is leased.

I rotate the cows every two to three weeks, he said. It helps prevent fescue foot.

We calve both in the spring and in the fall. We background all calves. I keep about 100 heifers a year for replacements.

Warren attributed his success in his Angus cattle operation to his off-farm job of 18 years in the banking industry.

Thats where I learned about farming, he said. I talked with successful operators and learned from them.

Warren uses both chicken and turkey litter to fertilize his acreages.

Last summer, I couldnt put enough cattle on to eat the crab grass, he said. I do plant wheat as a cover crop, but fescue is still the main base.

In addition to making sure his cattle has plenty of lush fescue on which to graze, Warren also uses DNA testing results before buying a bull.

Those tests are more accurate, he said.

Upon calculating his annual costs of insurance, feed, fertilizer, vet costs, chemicals, wages, taxes fuel, utilities and supplies, Warren broke down his operational costs, based on a 90 percent calf crop, to $725 per calf.

Summing it up, Warren told younger producers why he doesnt mind aiding a laboring cow in the middle of a cold winter night.

We start calving in the fall and continue through January, he said. I dont mind it at all if I need to be out at midnight with a cow about to calve. I have a passion for cattle. Thats why I do this.

The next topic, the alternative protein market, was addressed by Dr. Byron Wiegand, a professor of animal science at University of Missouri in Columbia.

Wiegand noted there are a number of vegetable sources in todays marketplace by which people can meet their protein needs. However, there are some that are utilizing stem cells from inside a cows mouth, animal blood product, which is collected from a slaughterhouse, and grown in a lab.

They take satellite cells from a living animal and the product is proliferated in strips, to mimic skeletal muscle, he said. Its grown on a scaffold, instead of a skeletal structure, fed a nutrient-rich medium and then stretched for exercise, to achieve the texture of a meat product.

The product takes 21 days to mature in a bio-reactor, and there are guestimates that predict it will hit retail shelves by 2021.

The upside for local producers so far?

It costs $18,000 a pound to reproduce beef, he said. But [beef producers] will have competition when the technology catches up. What we dont know is if the marketing can catch up.

For those who believe that cultured meats will save the planet, Wiegand posed a reality check.

Cultured products are highly processed, which goes against the whole concept of clean labels and simple labels, he said. For example, the Impossible Burger, sold by Burger King, contains 19 ingredients to make it taste like meat. Meat only has one. And the Impossible Burger is $1 more expensive than the Whopper.

Weigand said many food processors, including Tyson Foods, Cargill and Archer Daniels Midland, have invested in the alternative meat industry.

Why? he asked. Because they want diversified portfolios; first-hand knowledge of the technology; secondary pick-up of brand loyalty; and millions in short-term revenue.

During his travels, Weigand ran into at least one individual who expressed his irritation with those trying to replicate a meat-flavored product to attract the vegetarian and vegan markets.

The man said he was aggravated that companies were doing this, he said. The guy told me he had willingly given up [meat], and did not see any reason behind companies trying to mimic a plant-based product targeted toward those who had made that choice.

Finally, Weigand questioned what agency or entity was going to be required to oversee the food safety aspect of cultured meat products.

Who is going to be responsible for ensuring the consumer is protected? he asked. That has not yet been determined.

Those issues, along with legislation that has not caught up with the technology, truth-in-labeling and other issues are currently working with local producers.

Right now, the motivation for companies is to make money from this process, Weigand said. That will take awhile.

Three doctors of veterinary medicine, Dr. Darren Loula, Dr. Ted Dahlstrom and Dr. Voyd Brown, rounded out the evenings presentation with a discussion on herd health.

Loula, of Clever, reported an increase in pink eye infection in cattle, citing flies, lack of shade and other contributors to the disease.

We now use a combination vaccinations, as well as talk to producers about other ways to reduce the potential for cattle to develop pink eye, he said.

Dahlstrom, Monett, spoke of the many benefits of using multi-strain vaccinations for herd health.

You have to give a booster after the initial0 pink eye vaccination, he said. It boosts protection from 65 to 95 percent. There is also a pink eye impact that contains the initial dose as well as the booster. It is highly successful, but a little inconvenient. You still have to use fly control. But we have the tools to enhance pink eye protection.

Loula also recommended producers take an hour to sit down with their veterinarian and develop a herd health plan.

Customers should tell their vet what they have been battling for the past couple of years, he said. We take that information and make a plan that works for you.

There has also been an increase in hairy heel warts in beef cattle.

Traditionally, this is more common to dairy herds, Loula said. However, our practice has a seen more cases in beef herds in the last few years.

The bacteria results in painful ulcerations and erosion of the heel of the foot, along with significant lameness.

Topical treatment is most effective, but keeping a clean environment and promoting a strong immune function in your herd is the best practice, he added.

Other suggestions included moving bale rings when the ground around them becomes muddy from weather and feces. The bacteria, which is highly contagious, thrives in damp dirty conditions, so keeping fields clean and minimizing cow contact with slurry reduces the risk of infection.

Dahlstrom said mycoplasma is not getting enough attention for current preventive practice strategies.

The bacteria is constantly mutating and changing, he said. It is an untreatable disease. Commonly used antibiotics do not work. They are a waste of time.

Mycoplasma has been classed as a highly contagious disease. The bacteria can cause a number of ailments to cattle, including mastitis in dairy cows, arthritis in cows and calves, pneumonia in calves, and various other diseases likely including late-term abortion.

The best thing you can do is take a bunch of calves to the back 40 and go back a couple of weeks later and pick up the live ones, he said. If your calves are sick, its already too late. There is no way to get them healthy.

Concerning open cows that did not become pregnant through natural methods or artificial insemination, Brown indicated economically, they are best culled from the herd.

She has to earn her spot on the farm, he said. If she has been a slow breeder the first time, shell be a slow breeder afterward.

When I am culling, if a cow has not produced that year, I get rid of her, Dahlstrom agreed. My wife will say, shes been a good cow, and has been is the key phrase. When you, the producer, are paying us to pregnancy check your cows, and one comes up open, they need a bus ticket. That is the way to stay ahead in the game.

Dahlstrom also noted that his practice also does vaccine compounding, using the right quantities of medications after cell culturing in his lab in Monett.

With the vaccinations we have made, we have identified 21 different strains of mycoplasma organisms, cultured from local farms, he said. The only way to know if your cattle have the same strain as your neighbors is to have them swabbed. These bugs mutate. They find a way to adapt to the environment and survive.

We have the tools you need, Brown said. You just have to implement and utilize those tools at the proper time in production.

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Local News: Calculating the costs of beef production (2/19/20) - Monett Times

Stem Cell Therapy Market Competitive Analysis and Forecast 2017-2025 – News Parents

Stem Cell Therapy Market: Snapshot

Of late, there has been an increasing awareness regarding the therapeutic potential of stem cells for management of diseases which is boosting the growth of the stem cell therapy market. The development of advanced genome based cell analysis techniques, identification of new stem cell lines, increasing investments in research and development as well as infrastructure development for the processing and banking of stem cell are encouraging the growth of the global stem cell therapy market.

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One of the key factors boosting the growth of this market is the limitations of traditional organ transplantation such as the risk of infection, rejection, and immunosuppression risk. Another drawback of conventional organ transplantation is that doctors have to depend on organ donors completely. All these issues can be eliminated, by the application of stem cell therapy. Another factor which is helping the growth in this market is the growing pipeline and development of drugs for emerging applications. Increased research studies aiming to widen the scope of stem cell will also fuel the growth of the market. Scientists are constantly engaged in trying to find out novel methods for creating human stem cells in response to the growing demand for stem cell production to be used for disease management.

It is estimated that the dermatology application will contribute significantly the growth of the global stem cell therapy market. This is because stem cell therapy can help decrease the after effects of general treatments for burns such as infections, scars, and adhesion. The increasing number of patients suffering from diabetes and growing cases of trauma surgery will fuel the adoption of stem cell therapy in the dermatology segment.

Global Stem Cell Therapy Market: Overview

Also called regenerative medicine, stem cell therapy encourages the reparative response of damaged, diseased, or dysfunctional tissue via the use of stem cells and their derivatives. Replacing the practice of organ transplantations, stem cell therapies have eliminated the dependence on availability of donors. Bone marrow transplant is perhaps the most commonly employed stem cell therapy.

Osteoarthritis, cerebral palsy, heart failure, multiple sclerosis and even hearing loss could be treated using stem cell therapies. Doctors have successfully performed stem cell transplants that significantly aid patients fight cancers such as leukemia and other blood-related diseases.

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Global Stem Cell Therapy Market: Key Trends

The key factors influencing the growth of the global stem cell therapy market are increasing funds in the development of new stem lines, the advent of advanced genomic procedures used in stem cell analysis, and greater emphasis on human embryonic stem cells. As the traditional organ transplantations are associated with limitations such as infection, rejection, and immunosuppression along with high reliance on organ donors, the demand for stem cell therapy is likely to soar. The growing deployment of stem cells in the treatment of wounds and damaged skin, scarring, and grafts is another prominent catalyst of the market.

On the contrary, inadequate infrastructural facilities coupled with ethical issues related to embryonic stem cells might impede the growth of the market. However, the ongoing research for the manipulation of stem cells from cord blood cells, bone marrow, and skin for the treatment of ailments including cardiovascular and diabetes will open up new doors for the advancement of the market.

Global Stem Cell Therapy Market: Market Potential

A number of new studies, research projects, and development of novel therapies have come forth in the global market for stem cell therapy. Several of these treatments are in the pipeline, while many others have received approvals by regulatory bodies.

In March 2017, Belgian biotech company TiGenix announced that its cardiac stem cell therapy, AlloCSC-01 has successfully reached its phase I/II with positive results. Subsequently, it has been approved by the U.S. FDA. If this therapy is well- received by the market, nearly 1.9 million AMI patients could be treated through this stem cell therapy.

Another significant development is the granting of a patent to Israel-based Kadimastem Ltd. for its novel stem-cell based technology to be used in the treatment of multiple sclerosis (MS) and other similar conditions of the nervous system. The companys technology used for producing supporting cells in the central nervous system, taken from human stem cells such as myelin-producing cells is also covered in the patent.

Global Stem Cell Therapy Market: Regional Outlook

The global market for stem cell therapy can be segmented into Asia Pacific, North America, Latin America, Europe, and the Middle East and Africa. North America emerged as the leading regional market, triggered by the rising incidence of chronic health conditions and government support. Europe also displays significant growth potential, as the benefits of this therapy are increasingly acknowledged.

Asia Pacific is slated for maximum growth, thanks to the massive patient pool, bulk of investments in stem cell therapy projects, and the increasing recognition of growth opportunities in countries such as China, Japan, and India by the leading market players.

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Global Stem Cell Therapy Market: Competitive Analysis

Several firms are adopting strategies such as mergers and acquisitions, collaborations, and partnerships, apart from product development with a view to attain a strong foothold in the global market for stem cell therapy.

Some of the major companies operating in the global market for stem cell therapy are RTI Surgical, Inc., MEDIPOST Co., Ltd., Osiris Therapeutics, Inc., NuVasive, Inc., Pharmicell Co., Ltd., Anterogen Co., Ltd., JCR Pharmaceuticals Co., Ltd., and Holostem Terapie Avanzate S.r.l.

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Stem Cell Therapy Market Competitive Analysis and Forecast 2017-2025 - News Parents

Survivor Legend Ethan Zohn Discusses His Journey Through Cancer and Back to the Island – Parade

This past Wednesday, millions of Survivor fans got to see 20 previous winners from the reality shows storied past return for another shot at victory and a $2 million prize. And while each of them had a journey to getting back to the island, season 3 winner Ethan Zohn may have the most inspirational story of them all. Because up until seven years ago, not only was it up in the air whether Ethan would be playing Survivor again in 2020, it was unlikely he would even be alive to see season 40.

In 2009, five years after his last Survivor appearance, Ethan was diagnosed with a rare type of cancer called CD20-positive Hodgkins lymphoma. He underwent several treatments since his diagnosis and was declared cancer-free in late April 2010. Then, after nearly 20 months of remission, cancer returned in his chest. Not to be deterred, Ethan continued to undergo stem-cell transplants, all the while doing charity work to promote his cause, as well as his charity Grassroot Soccer, which uses soccer to raise money and awareness to fight HIV/AIDS. In March 2013, Ethan officially declared he was cancer-free once more and has been in remission ever since. With a clean bill of health, hes now ready to return to the game that changed him forever, with a new outlook on life.

Ethan talks with Parade.com about the experience of engaging with both Survivor and the fandom after more than a decade away, the struggles he underwent after becoming cancer-free, and his decision to use his time in the spotlight to give back.

Related: Survivor Season 40: Everything We Know So Far (Including Who Was Voted Out)!

This time last week, you got to watch your return with a special screening of the premiere on the big screen in LA What was that experience like, the culmination of everything you went through to this point?Watching myself, I cant believe they make us run around in our underwear! Ill just put that out there. Im like, Jeff, they know were not shipwrecked. We get it. Give us some bathing suits, buddy! Nobody wants to watch anyones junk flop around. (Laughs.)

But watching myself on TV was a rush. Its a snapshot of my life. Its my highlight reel, and this is my song. Being here is just another chapter in this incredibly blessed life that Survivor has given me. Ive never watched the show with such a live audience, with fans cheering for different people and moves. It heightens the excitement for me. I realize how lucky I am and the moment we have right here. Im just trying to drink it all in and have so much fun.

Whats it been like to engage with the fan community, considering how different it looks between now and when you first played?When we played the game, it was like we were playing underwater compared to now. We had no idols, no clues, no ways to get back into the game, nothing. To take that one step further, we had no social media. We had printed media, radio, maybe some television spots. The way in which information is passed around is like light speed. That is indicative of the way the world works and how the games played. We delved deep into personal relationships, honor, integrity, trust, teamwork, and survival. We depended on each other to survive daily out there in Africa. Now its like boom, boom, blindsides, backstabs, idol clues. Its fast-paced, rocket fuel injected into the game of Survivor both inside and outside the show.

For me, just trying to keep up with social media is a thing in and of itself! (Laughs.) Im trying to figure out whats going on right now. But its been fun to interact with it because, surprisingly, a lot of fans Ive been connecting with are young. They were either extremely young or not alive when I was on the show. So to see a new generation of fans getting excited about the greatest show on earth is pretty exciting.

Youve been considered one of the most well-liked and revered players in Survivor history. What has been your reaction to that label?It feels wonderful, to be honest. (Laughs.) It lets me reminisce about my past in a way thats really fun and exciting for my family and me. I definitely didnt drop off the face of the earth, but Ive been in the public eye recently more as a cancer survivor than a Survivor player. So its really fun and exciting. Im very appreciative of what this show has enabled me to do in my life. So coming back on was wonderful. Its also paying tribute to the life the show has given me, to everyone who has come before and after me who made this show what it is today.

I specifically remember the first second of the game, when we lined up on the beach. I looked down and saw $21 millionbecause Sandras won twiceas well as a history lesson. Youre looking at each person and seeing 20 years of my life, of Jeffs life, of everyones lives. Its rare that any TV show has the shelf life Survivor has. I remember in season 3, people say, Oh, this is the last season. Theres no way this is going to go another season. (Laughs.) September 11th happened, and nobody wanted to see a show called Survivor and see people suffer. Now look at us, 20 years later!

Though youve been away from Survivor for a while, you certainly havent strayed away from reality television at large. What drove you to want to appear on other shows, even if they werent on an island?Right place, right time. It was the start of reality television as a genre. All these new shows were coming out, and having been on Survivor, most of the time, they were celebrity reality shows. I just said yes to everything. I never thought it would last that long. So I thought, Im going to get in and have as much fun as I possibly can. Because I never know when this is going to end. So I said yes to every single opportunity possible. Why not?! (Laughs.) Plus, its always a good opportunity for me. I could wear a Grassroot Soocer t-shirt, or talk about my experience with cancer.

Its good to have something valuable in your life that isnt reality TV. I went on reality TV because it was a crazy adventure. I wanted to compete at the highest level in front of millions of people. Youre never going to get that anywhere. I didnt grow up watching Survivor dreaming of being on, like an Adam Klein. People like him, Michele, Wendell, and Ben grew up on when I was on the show, and here they are coming out to play again because its been their lifelong dream to be on Surivor. My lifelong dream was to be a professional soccer player. Once I accomplished that, this was the icing on the cake.

Its interesting you talk about never knowing when your reality TV career would end, given the way your life went. I cant imagine what your first thought was when you received your initial cancer diagnosisGetting diagnosed as a young adult at 35 years with a rare form of blood cancer was completely shocking to me. My only connection to cancer was through my father, who passed away when I was 14. So I only thought, Cancer = death. I was completely frightened and confused, as you can imagine. At that point, all my other friends were just starting their lives. They were beginning jobs and families, moving to new homes and towns. I was forced to press pause on my life, while everyone else was starting theirs. That was difficult for me. But coming out of the cancer diagnosis was more difficult for me personally.

Related: Survivor Winners at War: Lex van den Berghe on Amber Mariano and Old School Tactics

Can you elaborate on that?When you get diagnosed, and the doctor tells you to do something or youll die, you do it. Theres no choice; its not that hard. But then, when youre deemed healthy and in remission, all the doctors and nurses go away. And your friends start to pull away. Thats when it really got hard. Dealing with the anxiety and the fear of relapse, the dump trucks full of uncertainty, the scars that need healing. Now Im a young adult with no job. Im infertile; whos going to marry me? Is it going to come back? Theres all this stuff in your mind as a young man that an older adult doesnt face. I had to get to a point in my life where I was mentally clear, physically strong enough, and spiritually open to having an experience like Survivor. Thats the win for me. Just getting to the starting line is probably harder than anything Ill have to do for the rest of my life.

Obviously Survivor and fighting cancer are like apples and orange. But is there anything you pulled from that experience mentally or emotionally that helped you during your treatments?I do think my time on Survivor enabled me to learn how far I can push my body. Mentally, physically, spiritually, environmentally, socially. On Survivor, you push yourself to the max, and then you have to go even further. Coming into cancer, Im like, Okay, Ive suffered before. I know this is going to suck, but Ive been here before. Youve just got to take it day by day and minute by minute. You never know whats around the corner, whether it be an Immunity Challenge or a clinical trial.

Survivor is a game of relationships. Youve got to make friends with these people, but friendship is based on trust, and you cant really trust anyone. With cancer, you are surrounded by so many people who love you. But it is a lonely feeling. No one knows what its like to have cancer unless youve been through it yourself. Even then, everyones experience is different based on who you are. There is loneliness out there on Survivor. Even though you have a tribe and alliances, the result is having fewer and fewer people around you. The concept of community exists at a level. But in the back of everyones minds, they want you dead. (Laughs.) So does cancer. There are surprisingly some parallels.

When you get the call to go out for season 40, what went through your head, considering how much your life has changed from the last time you played?The game has changed, and so have I. (Laughs.) Its not better or worse now; its just different. Any good player in any sport has to adapt and be open to playing with the rules that exist for that specific game at that moment. I had gotten to a point where I was comfortable in life, with my wife and my two cats in New Hampshire. Im not the 27-year-old who doesnt care what happens to him anymore. Im now playing with the fact that Ive had to go through cancer and stem cell treatment twice. No one else has brought that kind of baggage into the game. Yes, everyone out there has a story and challenges weve overcome to get to where we are. I dont think anyone has had the health challenges that Ive had going out there. I was a little nervous about leaving the world I lived in to play that game, to be honest.

Once you made that decision, how did you make sure you were ready to go back into the game?I knew I had to do some catching up! I knew I had to get off the couch and stop smoking weed; cannabis and CBD have been huge in helping my post-cancer anxiety medically speaking. I left New Hampshire, because they called me in January and I knew I couldnt swim in a frozen lake. My wife and I moved down to Atlanta and I started training outside. I was swimming, doing puzzles, reading body language and lip reading books. I met with my shrink; my wife hid idols in the forest for me to find every day. I thought, If Im going to do this, to ease my fears that Im an old-schooler who has no place in the modern game, I want to get ready.

Related: Survivor Winners at War: Reed Kelly Talks Natalie Anderson and the Power of Partnerships

What role has the show served in your life, especially as the years passed between appearances? I know youve told the story about receiving a stem cell treatment while you were watching the Heroes vs. Villains premiere.Survivor is a wonderful word to describe me for a lot of different reasons. Its been a constant in my life. Im still known as the Survivor guy. I do a lot of speaking engagements, and my notoriety comes from the fact that I was on Survivor. Im not trying to hide that fact. Survivor changed my life. It sent me on a trajectory and enabled me to do so many things I would have dreamed of doing. I am incredibly grateful and appreciative of what this show has offered me.

Not only is the show creating fans around the world, but they are also saving lives. This show is completely responsible for the fact that I was able to co-found Grassroot Soccer. I played professional soccer in Zimbabwe leading up to my time on Survivor: Africa. During the show, I played hackeysack with the children in a local village. It was a real-life moment in the middle of this cutthroat game. When I won the money, I wanted to do something great with that. I met up with some buddies of mine, and we co-founded Grassroot Soccer. Were an adolescent health organization that has programs running in 63 countries and graduated 2.3 million kids, all because of Survivor.

Let me take that one step further for you. When I got cancer, we had just lost [Palau contestant] Jennifer Lyon. We were battling at the same time, and she didnt make it, unfortunately. In response to that, I created Survivor Stand Up to Cancer, which was a partnership between the show and the cancer research organization. Every year, props are auctioned off, and the proceeds go to cancer research. Some of the money raised from 2009 to 2012 was used to fund an experimental new drug that saved my life. Talk about full circle! This show is so much bigger than people imagine, especially in my life.

You get the chance to come back to the show that has meant so much to you. Your feet hit the sands of Fiji, and you realize youre playing Survivor again. Describe that feeling for me.Just thinking about it gives me chills. Theres so much emotion. My heart was pumping; my brain was going crazy. Theres a lot of pressure that Im putting on myself, the pressure to perform well, make alliances, not look stupid, and win. All this stuff is going through your head at that exact moment. The games about to start; Jeff Probsts waiting for you. Youre just walking into one of the most uncomfortable comfortable situations. Ive dreamed of this moment, hoping it unfolds positively. It was emotional. Its a perfect little bow on this amazing life that Survivor has given me.

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Survivor Legend Ethan Zohn Discusses His Journey Through Cancer and Back to the Island - Parade

Lawyer thought her tiredness was down to jet lag until she visited doctor – Mirror Online

A high-flying lawyer who thought she had jet lag after relocating to Hong Kong was actually suffering from an aggressive form of leukaemia.

Alexandra Simpson has spoken out about her cancer battle to encourage others to be mindful of their bodies and to ask their doctors for a blood test if they are worried about any persistent symptoms.

The 26-year-old from Llandudno, north Wales, is now in remission but, to lessen the risk of relapsing she is also having a stem cell transplant, having started a week of chemotherapy before having the procedure on February 21.

Alexandra was 25 when she started suffering from fatigue and blamed her tiredness on her massive career move from London to Hong Kong.

It was only when mysterious bruises popped up all over her body that Alexandra saw a doctor, reports WalesOnline.

Still believing she had the world at her feet, Alexandra relived her horror when she received her blood test results the following day, saying: "The doctor told me, Its not great news, today'."

Alexandra had acute lymphoblastic leukaemia (ALL) cancer of the white blood cells- and her life was under threat so she needed treatment immediately.

The doctor told me hed booked an appointment with a specialist for me at midday, then wished me luck, she said.

I left in floods of tears. It was the middle of the night back home, and I knew I had to tell my mum, but I wanted to give her a few more minutes of not knowing her child had cancer.

I wandered around the city, which was still quite unfamiliar to me, with no idea where to go, she continued.

Eventually, I called home and Mum just kept saying, No.

She saw me as this strong, healthy girl it was shocking that cancer could suddenly hit me so aggressively.

You sometimes imagine how it may feel to be told you have cancer.

"On TV, people always seem to go numb their hearing fades and the room around them swirls. I actually became hyper-aware. I still remember every word the doctor said to me, even now.

And while its been incredibly difficult both for me and the people that have walked alongside me, seeing the horror of it all I wouldnt undo any of what Ive been through.

She added: Before, I think I was a little lost, almost sleepwalking through my twenties.

"But now, Ive learnt to appreciate the little things all those beautiful moments youd otherwise take for granted and have a purpose and a passion in raising awareness of leukaemia.

Doctors now believe that cancerous cells first started to invade Alexandra around January 2019, when she had seen a GP in London because she was feeling rundown and had concernes she was anaemic.

Working in a busy law firm, when she had noticed dark circles around her eyes, she assumed it was her fast-paced lifestyle taking its toll rather than anything more sinister.

She said: I almost got used to having very little energy. I was working long hours and still managing to get myself to the gym three times a week, so I didnt think it was anything overly worrying.

I blamed city life. I kept telling myself Id be moving to Hong Kong soon and would feel better in a new place, with a bit of sunshine.

Alexandras doctor agreed she could be anaemic so suggested she eat more red meat, or try an iron supplement to get her levels up.

Assuming that would be the end of it, Alexandra turned her thoughts to her big move in early March 2019.

When her fatigue did not lift, she said: I kept telling myself Id just moved around the world and that feeling tired was natural but I just wasnt bouncing back from the jetlag.

As I became more comfortable with the new friends I was making out there, they remarked that I still looked pale, despite being in the sweltering heat every day.

Agreeing she could be anaemic, Alexandras doctor suggested she eat more red meat, or try an iron supplement to get her levels up.

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So, assuming that would be the end of it, she turned her thoughts to her big move in early March 2019.

When her fatigue did not lift, she said: I kept telling myself Id just moved around the world and that feeling tired was natural but I just wasnt bouncing back from the jetlag.

As I became more comfortable with the new friends I was making out there, they remarked that I still looked pale, despite being in the sweltering heat every day.

It was at the end of March when Alexandra banged her leg getting out of the bath one day and noticed a dramatic bruise forming within minutes that she thought something sinister was happening.

She continued: It kept developing, getting larger and larger, to the point where I was embarrassed to show it, as I could feel people staring, wondering what Id done.

That seemed to almost trigger something in my body and, before long, clusters of bruises sprang up all over, with no explanation as to where theyd come from.

Alexandra looked up her symptoms online and was shocked when almost all of them pointed towards leukaemia.

So, using healthcare benefits she had through work, in April she booked a private appointment to see a doctor, who gave her a blood test with the results back the next morning.

Id just sat down at my desk when my phone started to ring, recalled Alexandra.

I dont think the receptionist even said hello. She just asked, Where are you? and told me to come in right away.

The urgency in her voice was really worrying. When I got there, I was trying to analyse the doctors face. I knew that something serious was going on, as he couldnt quite look at me. Then he told me I had leukaemia.

After wandering around the city and phoning her mum, feeling shaken and disorientated, Alexandra returned to her office and broke the news to her colleagues.

A colleague came over to ask if I was okay, as I was visibly upset. I think she assumed itd be a break-up, or homesickness a more normal problem for a 20-something who had moved across the world to be facing, she said.

When I told her, I watched the colour drain from her face. She sat with me and we talked it all over then, bizarrely, I actually wanted to do a bit of work while I waited for my midday appointment. My colleagues thought I was bonkers, but I needed a distraction.

When Alexandra she saw the specialist later that day she realised how gravely ill she was.

She recalled: He told me I wasnt well enough to fly back to the UK, and I needed to go straight to hospital.

I said, 'Okay, Ill just go home to get some things'. But he told me no, that if I somehow fell or knocked myself on the way, that my blood didnt have enough platelets to form clots, so I could bleed to death.

She continued: "He said, 'You need to go to hospital right now, and just to warn you, youll be there for at least a month'. He was good at keeping me calm, but also making me realise how much danger I was in.

Admitted to hospital, Alexandra was given a bone marrow biopsy, which confirmed her official diagnosis.

According to the charity Leukaemia Care, ALL is a rapidly progressing form of the disease, with almost 350 cases a year diagnosed in UK adults.

Symptoms can include fatigue, fever, frequent infections, unusual bleeding, unexplained weight loss and small purple spots on the skin known as purpura.

Three days after her diagnosis, Alexandra began the first of four gruelling cycles of chemotherapy.

It all happened so quickly, I didnt really have time to consider what I was about to put my body through. I was just focused on getting the cancerous cells eliminated, she said.

"When I look back at that part of everything, it doesnt feel like my life. Its like Im looking at another girl thinking, 'Poor her, shes been through so much'.

As well as the obvious side-effects, like losing my hair and having to deal with everybody staring at me, knowing I was sick, there were all these other little ways it impacted me.

For example, my fitness level plummeted to the point where Id have to take a rest when walking upstairs.

It was like being locked out of my own life. The chemo made me sicker than the cancer, in a way but I knew it was the cure, and I had to keep going.

By May, Alexandra had stabilised enough to fly home, where she continued the rest of her chemotherapy at Manchesters Christie Hospital, finishing in September 2019.

Later that month, she began immunotherapy, where the bodys own immune system is used to fight off cancerous cells.

She said: The form I had targets a specific antigen in the leukemic cells, and uses my own immune system to kill the cancer. The drug I take is slowly infused over a 28-day period, so I carry around a pump that delivers a very small dose every minute.

Now in remission, Alexandra described how her journey has made her re-evaluate life, and find value in small things she may have once taken for granted.

She said: I know now I wasnt prioritising the right things, like chasing that deal at work, or buying the latest designer handbag. Those things do have a place in life, and they are important, but they arent the be all and end all.

Now, things like sitting around the table with my family laughing, or feeling the sun on my neck in the garden those are the moments that mean the most.

For a long time, I put what happened in a box, only to be opened at certain times.

Now Ive gone from being obsessed that nobody would know to look at me what Ive been through, to being proud of my scars.

Ive worked through that denial to find a place of peace. Ive found my cause in life and am so proud to be a part of the cancer community.

Urging people to be mindful of the bodies, she said: You know your body better than anybody, so if you feel something has changed however minor then ask your doctor for a blood test, she said.

The likelihood is it will be something much more minor than leukaemia, but if it is serious, its important to catch it early. Going through this has completely changed my mindset, and Im so glad to still be here to appreciate the little things that make life so beautiful.

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Lawyer thought her tiredness was down to jet lag until she visited doctor - Mirror Online

Family honors the memory of loved one by collecting teddy bears for families dealing with cancer – KTIV

SIOUX CITY (KTIV) - For five years now, the Ruehle family has held a teddy bear drive in memory of Mike Ruehle, who passed from cancer in 2014.

The teddy bears are given to adults and children with a cancer connection, in Mike's memory.

Family and friends knew Mike as "Bear."

The family asks people to consider donating a teddy bear in memory of a loved one, or in honor of healthy family members.

If you'd like to donate, every bear must be new with the tag still attached. The donations will stay in Siouxland.

There are five different locations where you can drop off the bears:

Ruehle's family says the teddy bear drive has donated more than 3,000 stuffed animals to several Siouxland agencies.

But who is the man who inspired the teddy bear drive?

"Very thoughtful person, very giving, he always took the time to listen to other people, just a really compassionate, kindhearted person," said Kerry Ruehle, Mike's Widow.

Mike Ruehle, or as his family called him, Bear, passed away six years ago, after a 12 year battle with cancer.

The family said he was very active in the community and was often coaching numerous sports teams.

They said he had a big heart, and always did what he could to make others feel better, even while he himself had cancer.

"If there were any patients his doctor had, who were having a difficult time with the news or with the adjustment. He would reach out to my dad, and see if my dad would sit down with them and talk about what was going on with them," said Rhett, Mike's son.

Part of the reason the teddy bear drive was started was because of Bear's compassion towards children who were also dealing with cancer.

"He would see a young child going through similar things that he was going through. He would always go out of his way to talk to that little kid and brighten their day a little bit," said Rhett.

Mike had had three different kinds of cancers, and due to the chemotherapy, eventually was diagnosed with MDS, which is a bone marrow failure disorder.

Doctors determined that the best treatment would be a stem cell transplant. The transplant surgery went well, but months later his body began rejecting his brother's stem cells, and within five weeks he had passed away.

"It was a shock because he had been ahead of schedule and everything else. And he had come through things beautifully, so it was quite a shock. But it was god's plan I guess," said Kerry.

But Mike's family wanted a way to keep Mike's memory alive, and that's what also helped start the teddy bear drive.

"My oldest granddaughter is five, she never met her grandpa. But in some ways, she feels as though she did, because of talking about him and she helps me with the bear drive," said Kerry

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Family honors the memory of loved one by collecting teddy bears for families dealing with cancer - KTIV

Transplanting the immune system: Easier on patients than medication? – WNDU-TV

There are nearly 35,000 organ transplants done in the U.S. every year. Once patients receive their transplant, they face a lifetime of medications that keep their body from rejecting the new organ, but those medications can cause serious side effects.

Now, a groundbreaking procedure has successfully changed that for one woman.

Having breakfast together was nearly impossible for Barb Okey and her husband after her kidney transplant. The 24 pills she took before breakfast ruined her appetite, and the side effects left her tired. But that's all in the past now.

In 27 years doing transplants, Dr. Dixon Kaufman has never done one like Barb's. Her sister's kidney was a perfect match, but then both women took part in a second pioneering transplant to give Barb her sister's immune system.

"We had the transplant and the next day I started radiation. I had to do radiation for 10 days," Barb recalled. "That was to suppress my immune system. After the 10th day, they gave me my sister's stem cells."

"The immune cells start to multiply, so she has not only the kidney from her sister but a little bit of her sister's immune system, and we call that phenomenon chimerism a,nd that's where you have a dual immune system," Kaufman said.

The immunity accepted the new kidney and left Barb drug-free.

"It's the start of hopefully a long progression of trials that will allow more and more people to, if not completely eliminate the medicines, significantly reduce them," Kaufman said.

"I feel very, very lucky. Very lucky," Barb said.

Barb is just the second person in the U.S. to take part in the national trial pioneering the duel transplant. The hope is that the procedure will one day be available to transplant recipients who are not perfect matches with their donors, and possibly even to those who have had transplants in the past.

MEDICAL BREAKTHROUGHSRESEARCH SUMMARYTOPIC: TRANSPLANTING THE IMMUNE SYSTEM: EASIER ON PATIENTS?REPORT: MB #4700

BACKGROUND: Organ transplantation is sometimes necessary when one of a patient's organs has failed. This can happen because of injury or illness. The organ may come from a living donor or one who has died. Transplants can include heart, intestine, kidney, liver, lung, or pancreas. Often patients must wait a long time for an organ transplant and doctors must match donors to recipients to reduce the risk of transplant rejection. (Source: https://medlineplus.gov/organtransplantation.html)

REJECTION RISK: The immune system usually protects you from substances that may be harmful, but it can also simply attack anything that enters the body, which the immune system detects as "foreign", and this includes transplanted organs. When a person receives an organ in transplant surgery, their immune system may recognize that it is foreign if the cells of the organ are different or "not matched". Mismatched organs can trigger a blood transfusion reaction or transplant rejection. To help prevent this rejection, doctors try their best to match similar proteins known as antigens between the donor and recipient. Tissue typing ensures the organ or tissue is as similar as possible to the recipient's tissue. The match is usually not perfect, as only identical twins have identical tissue antigens. Doctors use medicines to suppress the recipient's immune system with the goal of preventing it from attacking the newly transplanted organ. If these medicines are not used, the body will almost always launch an immune response and destroy the foreign tissue. Some exceptions include cornea transplants, because the cornea has no blood supply. Also, transplants from one identical twin to another are almost never rejected. (Source: https://medlineplus.gov/ency/article/000815.htm)

NEW RESEARCH: Medeor Therapeutics is now developing cell-based therapy to reprogram an organ recipient's immune system to accept the transplanted kidney without the need for long-term use of immune system suppressing drugs. The study is in Phase 3 and is working to demonstrate the efficacy and safety of how transplanting some of the stem cells from the organ donor into the organ recipient after transplant surgery could cause an immune tolerance; preserving the organ donation and preventing kidney transplant rejection. It would also eliminate the need for immunosuppressive drugs for the rest of the patient's life. (Source: https://clinicaltrials.gov/ct2/show/study/NCT03363945?show_locs=Y#locn)

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Transplanting the immune system: Easier on patients than medication? - WNDU-TV

FHSU partners with Be the Match for bone marrow registry event – hays Post

Brynn Niblock, FHSU junior in pre-med from Hoxie, swabs her cheek as part of the sign up for the Be the Match bone marrow registry Feb. 6 at Gross Memorial Coliseum.

By CRISTINA JANNEYHays Post

Usually Tiger basketball games are a time to have fun cheer the home team, eat some popcorn but students and community members at Feb. 6 game took a few minutes to stop and potentially save a life.

FHSU student health sponsored a Be the Match bone marrow registry drive.

Potential donors ages 18 to 44 answered a list of qualifying health questions on their smartphones and then swabbed their cheeks to be matched with a potential cancer sufferer in need of bone marrow transplants.

Kathy Pyke of Hays knows too the well the importance of the registry. Pyke was at Gross Memorial Coliseum the night of the drive as a volunteer handing out information to potential donors.

Her husband, Tom, was diagnosed with leukemia on March 1, 2014. Family members were tested, and they were not matches. Doctors were also unable to find a bone marrow match on the national registry. There were 6.2 million people in the registry at the time.

In lieu of a bone marrow transplant, Pyke was given donated umbilical cord blood.

Initially the treatment improved Pyke's condition. However, he ultimately died as a result of the disease on Feb. 12, 2015 at the age of 62.

Kathy said the family was rocked by Tom's illness. He was playing golf and went fishing the week before he was diagnosed with cancer.

Kathy said she wishes she could be on the registry to help another family, but her age prevents her from doing so.

"Not only for my husband," she said of the importance of the registry. "I did pray there had been a match. We stayed at the Hope Lodge that was run by the American Cancer Society in Kansas City. There were 45 apartments there and everyone there has someone who has cancer plus a caregiver in it. You just see so many lives being touched. ...

"If this is something that can help somebody, it is just an easy thing to do."

Kathy said she had a good friend who had a family member sign up for the registry, and he was able to donate to someone who had cancer in England.

Pyke said she would also like to see more hospitals participate in the cord blood bank, which is what helped her husband. At the time of Tom's illness, HaysMed was not participating in the umbilical cord blood bank.

Michelle Toogood, BSN, RN, supervisor of Hays Meds Women's andInfant Care Center/NICU, said parents wishing to participate in cord blood donation should initiate the process prior to delivery. HaysMed staff will then aid in the collection of the specimen.

"I just can't express how much people need to do this," Pyke said of signing up for the registry. "It is just so easy to swab test and they could potentially save more than one person's life. It is so easy to do and so important."

If you are identified as a match to someone suffering from cancer, you would be contacted through the registry and asked if you are willing to donate,Amanda McCord, RN at the FHSU student health center.

"Finding the perfect match is essential for people who are fighting this type of cancer," McCord said. "The closer the match the better their chances of remission and beating whatever cancer they are fighting."

There are over 70 diseases that can be treated by bone marrow transplants, according to Be the Match.

Physicians will usually look for matches among relatives first, but only 70 percent of the time are matches made from family members, McCord said.

Statistics also indicate minority patients are less likely to find matches than Caucasian patients. Be the Match is trying to boost minority participation as there are fewer minority participants in the registry at this time, McCord said.

Donating bone marrow is a little bit different for every donor, McCord said.

Most give through a Peripheral Blood Stem Cell (PBSC) donation. A machine draws blood from one arm, extracts the cells it needs, and returns the remaining blood through your other arm, according to the Be the Match website.

Others give through a marrow donation. Liquid marrow is withdrawn from the back of your pelvic bone with a needle. In this case, youll receive anesthesia and feel no pain during the procedure, the Be the Match website said.

According to Be the Match,PBSC donors may experience headaches or body aches several days before collection, but these disappear shortly after donation. Most donors feel completely recovered within a few weeks.

If you missed the Be the Match event at FHSU last week, you can contact Be the Match though its website, and the organization will send you the cheek swab kit to sign up for the registry.

The Be the Match website also has information on the donation process and a link to make monetary donations to the Be the Match program.

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FHSU partners with Be the Match for bone marrow registry event - hays Post