Consistent Outcomes Using Ryoncil as First-Line Treatment or Salvage Therapy in 309 Children With Steroid-Refractory Acute GVHD – BioSpace

NEW YORK, Feb. 24, 2020 (GLOBE NEWSWIRE) -- Mesoblast Limited (Nasdaq:MESO; ASX:MSB) today announced that aggregated results from 309 children treated with Ryoncil (remestemcel-L) were presented atthe American Society for Transplantation Cellular Therapy and the Center for International Blood & Bone Marrow Transplant Research (TCT) meeting in Orlando, Florida on February 22. The data showed that treatment with RYONCIL across three separate trials resulted inconsistent treatment responses and survival outcomesinchildren with steroid-refractory acute graft versus host disease (SR-aGVHD).

Key findings and conclusions were:

Mesoblast Chief Medical Officer Dr Fred Grossman said: These aggregated data from three studies demonstrate consistent efficacy and safety of RYONCIL in children suffering from steroid refractory acute graft versus host disease. If approved, RYONCIL has the potential to be an effective and safe therapy to improve survival outcomes in the most vulnerable population of children with severe forms of this disease who can have mortality rates as high as 90 percent.

In January, Mesoblast filed a Biologics License Application (BLA) to the United States Food and Drug Administration (FDA) for RYONCIL for the treatment of children with steroid-refractory aGVHD. The Company has requested Priority Review of the BLA by the FDA under the product candidates existing Fast Track designation. If approved, RYONCIL is expected to be launched in the US in 2020.

About Acute GVHDAcute GVHD occurs in approximately 50% of patients who receive an allogeneic bone marrow transplant (BMT). Over 30,000 patients worldwide undergo an allogeneic BMT annually, primarily during treatment for blood cancers, and these numbers are increasing.1 In patients with the most severe form of acute GVHD (Grade C/D or III/IV) mortality is as high as 90% despite optimal institutional standard of care.2,3. There are currently no FDA-approved treatments in the US for children under 12 with SR-aGVHD.

About Ryoncil Mesoblasts lead product candidate, RYONCIL, is an investigational therapy comprising culture- expanded mesenchymal stem cells derived from the bone marrow of an unrelated donor. It is administered to patients in a series of intravenous infusions. RYONCIL is believed to have immunomodulatory properties to counteract the inflammatory processes that are implicated in SR- aGVHD by down-regulating the production of pro-inflammatory cytokines, increasing production of anti-inflammatory cytokines, and enabling recruitment of naturally occurring anti-inflammatory cells to involved tissues.

References1. Niederwieser D, Baldomero H, Szer J. (2016) Hematopoietic stem cell transplantation activity worldwide in 2012 and a SWOT analysis of the Worldwide Network for Blood and Marrow Transplantation Group including the global survey.2. Westin, J., Saliba, RM., Lima, M. (2011) Steroid-refractory acute GVHD: predictors and outcomes. Advances in Hematology.3. Axt L, Naumann A, Toennies J (2019) Retrospective single center analysis of outcome, risk factors and therapy in steroid refractory graft-versus-host disease after allogeneic hematopoietic cell transplantation. Bone Marrow Transplantation.

About MesoblastMesoblast Limited (Nasdaq: MESO; ASX: MSB) is a world leader in developing allogeneic (off-the-shelf) cellular medicines. The Company has leveraged its proprietary mesenchymal lineage cell therapy technology platforms to establish a broad portfolio of commercial products and late-stage product candidates. Mesoblasts proprietary manufacturing process yields industrial-scale, cryopreserved, off-the-shelf, cellular medicines. These cell therapies, with defined pharmaceutical release criteria, are planned to be readily available to patients worldwide.

Mesoblast has filed a Biologics License Application to the United States Food and Drug Administration (FDA) to seek approval of its product candidate Ryoncil (remestemcel-L) for steroid-refractory acute graft versus host disease (acute GvHD). Remestemcel-L is also being developed for other rare diseases. Mesoblast is completing Phase 3 trials for its rexlemestrocel product candidates for advanced heart failure and chronic low back pain. If approved, RYONCIL is expected to be launched in the United States in 2020 for pediatric steroid-refractory acute GVHD. Two products have been commercialized in Japan and Europe by Mesoblasts licensees, and the Company has established commercial partnerships in Europe and China for certain Phase 3 assets.

Mesoblast has locations in Australia, the United States and Singapore and is listed on the Australian Securities Exchange (MSB) and on the Nasdaq (MESO). For more information, please see http://www.mesoblast.com, LinkedIn: Mesoblast Limited and Twitter: @Mesoblast

Mesoblasts Forward-Looking StatementsThis announcement includes forward-looking statements that relate to future events or our future financial performance and involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. We make such forward-looking statements pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995 and other federal securities laws. Forward-looking statements should not be read as a guarantee of future performance or results, and actual results may differ from the results anticipated in these forward-looking statements, and the differences may be material and adverse. Forward-looking statements include, but are not limited to, statements about the timing, progress and results of Mesoblasts preclinical and clinical studies; Mesoblasts ability to advance product candidates into, enroll and successfully complete, clinical studies; the timing or likelihood of regulatory filings and approvals; and the pricing and reimbursement of Mesoblasts product candidates, if approved. You should read this press release together with our risk factors, in our most recently filed reports with the SEC or on our website. Uncertainties and risks that may cause Mesoblasts actual results, performance or achievements to be materially different from those which may be expressed or implied by such statements, and accordingly, you should not place undue reliance on these forward-looking statements. We do not undertake any obligations to publicly update or revise any forward-looking statements, whether as a result of new information, future developments or otherwise.

Release authorized by the Chief Executive.

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Consistent Outcomes Using Ryoncil as First-Line Treatment or Salvage Therapy in 309 Children With Steroid-Refractory Acute GVHD - BioSpace

Stem Cell Alopecia Treatment Market Size, Current Trends, Business Opportunities, Market Challenges and Analysis by 2026 – News Parents

The report carefully examines the Stem Cell Alopecia Treatment Market, with a focus on most of the major players and their business strategies, geographical scope, market segments, product landscape and price and cost structure. Each section of the research study is specially prepared to investigate key aspects of the Stem Cell Alopecia Treatment market. The area of market activity, for example, drivers, restrictions, trends and opportunities in the global market for Stem Cell Alopecia Treatment is explored in detail. Through qualitative and quantitative analysis, we support you in a comprehensive and comprehensive analysis of the Stem Cell Alopecia Treatment market. We also focus on the five forces analysis of SWOT, PESTLE and Porter in the Stem Cell Alopecia Treatment market.

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The main Companies operating in the Stem Cell Alopecia Treatment Market are listed in the report.

Stem Cell Alopecia Treatment Market: Competitive Landscape

The players who lead the Stem Cell Alopecia Treatment market are analyzed taking into account their market share, the latest developments, new manufacturers, associations, acquisitions and markets. We also provide a comprehensive analysis of your product portfolio to explore the product and the applications that you focus on while operating in the Stem Cell Alopecia Treatment market. In addition, the report offers two different market forecasts: one is the production side and the other on the use side of the Stem Cell Alopecia Treatment market. It also provides practical advice for newcomers, as well as for established players in the world of smart camera market.

Stem Cell Alopecia Treatment Market: Segment Analysis

This chapter focuses on the different segments in the Stem Cell Alopecia Treatment market. The report segments the market by type, application, product, service and end user. This division enables a detailed view of the motif. It helps to understand the changes in production and the general needs of consumers that are likely to affect these segments.

Stem Cell Alopecia Treatment Market: Regional Analysis

The chapter on regional analysis highlights the political scenario in emerging and industrialized countries that is expected to affect the dynamics of supply and demand. Regional analysis also helps identify the changing needs of the population that have a critical impact on the general market for Stem Cell Alopecia Treatment . This part of the research report also took into account labor costs, raw materials and production costs by region.

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Table of Content

1 Introduction of Stem Cell Alopecia Treatment Market

1.1 Overview of the Market1.2 Scope of Report1.3 Assumptions

2 Executive Summary

3 Research Methodology of Verified Market Research

3.1 Data Mining3.2 Validation3.3 Primary Interviews3.4 List of Data Sources

4 Stem Cell Alopecia Treatment Market Outlook

4.1 Overview4.2 Market Dynamics4.2.1 Drivers4.2.2 Restraints4.2.3 Opportunities4.3 Porters Five Force Model4.4 Value Chain Analysis

5 Stem Cell Alopecia Treatment Market , By Deployment Model

5.1 Overview

6 Stem Cell Alopecia Treatment Market , By Solution

6.1 Overview

7 Stem Cell Alopecia Treatment Market , By Vertical

7.1 Overview

8 Stem Cell Alopecia Treatment Market , By Geography

8.1 Overview8.2 North America8.2.1 U.S.8.2.2 Canada8.2.3 Mexico8.3 Europe8.3.1 Germany8.3.2 U.K.8.3.3 France8.3.4 Rest of Europe8.4 Asia Pacific8.4.1 China8.4.2 Japan8.4.3 India8.4.4 Rest of Asia Pacific8.5 Rest of the World8.5.1 Latin America8.5.2 Middle East

9 Stem Cell Alopecia Treatment Market Competitive Landscape

9.1 Overview9.2 Company Market Ranking9.3 Key Development Strategies

10 Company Profiles

10.1.1 Overview10.1.2 Financial Performance10.1.3 Product Outlook10.1.4 Key Developments

11 Appendix

11.1 Related Research

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When Treating Women With Ovarian Cancer, Gynecologic Oncologist Emphasizes Openness And Dedication Throughout Journey – Forbes

By Jodi Helmer

When Heidi E. Godoy, D.O., gynecologic oncologist, sees new ovarian cancer patients for the first time, she starts preparing them for the likelihood their cancer will return.

Dr. Heidi E. Godoy, gynecologic oncologist

For those unfamiliar with the disease, Godoys early focus on recurrence may seem premature. But she believes that being upfront about the realities of ovarian cancer is as important as discussing the initial treatment, which is typically surgery followed by platinum-based chemotherapy.

Ovarian cancer is difficult to diagnose, increasing the odds that it wont be discovered until it reaches an advanced stage. And in 85% of late-stage ovarian cancer cases, the disease recurs, according to research published in the International Journal of Surgical Oncology.1

One of the first conversations I have with patients outlines the relapse that often happens with ovarian cancer, said Godoy, who works in private practice in New York State and is affiliated with several hospitals there. I dont want it to be a surprise if the cancer returns.

Godoy also makes it a point to reassure women living with ovarian cancer that she will be with them throughout their cancer journey. Gynecologic oncologists, she explained, generally provide complete care, from diagnosis to surgery, for cancers affecting the ovaries, uterus, cervix, vulva and vagina. Holistic care is one of the reasons she pursued the subspecialty.

When I was going through medical school, I wanted a subspecialty that provided a lot of continuity of care, Godoy recalled. In gynecologic oncology, you develop such personalized, deep relationships with your patients.

Expert, Empathetic Care

For women living with ovarian cancer, receiving treatment from a gynecologic oncologist can simplify care and provide a sense of familiarity with their treatment teams. Research published in Frontiers In Oncology2 in 2015 shows that the highly-trained medical professionals also provide positive clinical outcomes.

Gynecologic oncologists perform complex procedures such as surgical debulkinga tumor-removal procedure that often affects other organsto remove the entire tumor and improve the prognosis. They are among the only specialists that perform surgical debulking, Godoy said. While surgery and chemotherapy are well-known components of treatment plans, maintenance therapies have become meaningful options for doctors in recent years.

Ovarian cancer patients who have a response to platinum-based chemotherapy in the recurrent setting are candidates for PARP inhibitors, one of those being niraparib or ZEJULA, Godoy explained.

Those candidatespatients who recur after a first-line treatment and receive a second line of platinum-based chemotherapyreally need to have that conversation about starting maintenance therapy, she continued.

The current approach of watch-and-wait, where we take them off their chemotherapy or their cytotoxic therapy and just watch and wait to see if the cancer returns, is no longer the only option, Godoy said. Maintenance therapy has changed the paradigm of watching and waiting to see if the cancer returns.

ZEJULA, made by the pharmaceutical company GSK, is a prescription medicine used for the maintenance treatment of adults with ovarian cancer, fallopian tube cancer or primary peritoneal cancer, when the cancer comes back. ZEJULA is used after the cancer has responded (complete or partial response) to treatment with platinum-based chemotherapy. It can also be used for treatment of adults with advanced ovarian cancer, fallopian tube cancer or primary peritoneal cancer who have been treated with three or more prior types of chemotherapy and who have tumors with a certain BRCA gene mutation, or a positive laboratory test, and whose cancer was in response to treatment with platinum-based chemotherapy, and who have progressed more than six months after the last treatment. For treatment in the late-line setting, your healthcare provider will perform a test to make sure that ZEJULA is right for you.

ZEJULA has serious risks such as bone marrow problems called MDS or a type of blood cancer called AML. Low blood cell counts are common. Tell your doctor about any weakness, tiredness, infections, fever, shortness of breath, blood in urine or stool, bruising, bleeding or weight loss. High blood pressure is common and can become serious. Nausea and constipation are also common.

Benefiting From More Recent Treatment Options

The idea of maintenance therapy to treat ovarian cancer is not new, Godoy said. Until recently, however, only intravenous forms of maintenance therapy were available, which required women to receive the treatment in clinics.

More recent treatment options for ovarian cancer include oral medications, like ZEJULA, which give women the ability to take it at home. ZEJULA is taken once a day.

Women living with ovarian cancer are often surprised to learn that maintenance therapies exist, she added. For the newly diagnosed, Godoy offered important advice.

If you have ovarian cancer, ask your OB/GYN to make a referral to a gynecologic oncologist and have a meeting with them to discuss your care, she said. Learn more about current treatments, including maintenance therapy, and be your own best advocate.

Jodi Helmer writes about health, science and innovation.

Important Safety Information

ZEJULA may cause serious side effects, including:

Bone marrow problems called Myelodysplastic Syndrome (MDS) or a type of blood cancer called Acute Myeloid Leukemia (AML). Some people who have ovarian cancer and who have received previous treatment with chemotherapy or certain other medicines for their cancer have developed MDS or AML during treatment with ZEJULA. MDS or AML may lead to death.

Symptoms of low blood cell counts (low red blood cells, low white blood cells, and low platelets) are common during treatment with ZEJULA. They can be a sign of serious bone marrow problems, including MDS or AML. These symptoms may include the following:

Your doctor will do blood tests to check your blood cell counts before treatment with ZEJULA. You will be tested weekly for the first month of treatment with ZEJULA, monthly for the next 11 months of treatment, and from time to time afterward.

High blood pressure is common during treatment with ZEJULA, and it can become serious. Your doctor will check your blood pressure and heart rate at least weekly for the first two months, then monthly for the first year, and as needed thereafter during your treatment with ZEJULA.

Before starting to take ZEJULA, tell your doctor about all of your medical conditions, including if you:

Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.

The most common side effects of ZEJULA include the following:

o Heart not beating regularly

o Nausea

o Constipation

o Vomiting

o Pain in the stomach area

o Mouth sores

o Diarrhea

o Indigestion or heartburn

o Dry mouth

o Tiredness

o Loss of appetite

o Urinary tract infection

o Shortness of breath

o Cough

o Rash

o Changes in liver function or other blood tests

o Pain in your joints, muscles, and back

o Headache

o Dizziness

o Change in the way food tastes

o Trouble sleeping

o Anxiety

o Sore throat

o Changes in the amount or color of your urine

If you have certain side effects, then your doctor may change your dose of ZEJULA, temporarily stop, or permanently stop treatment with ZEJULA.

These are not all the possible side effects of ZEJULA. For more information, ask your doctor or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

For full prescribing information visit http://www.ZEJULA.com/prescribing-information.

NP-NIR-US-0004

NRPJRNA200001

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When Treating Women With Ovarian Cancer, Gynecologic Oncologist Emphasizes Openness And Dedication Throughout Journey - Forbes

Immune-Based Therapies Emerge in Mantle Cell Lymphoma – Curetoday.com

Patients with the aggressive blood cancer can turn to immunotherapies like CAR-T cell therapy when disease recurs or becomes resistant.

Immunotherapies, such as chimeric antigen receptor (CAR)-T cell therapy, are advancing the therapy landscape for these patients.

CAR-T cell therapy has shown significant benefits in this patient population, Dr. Charalambos (Babis) Andreadis, said in an interview with OncLive, a sister publication of CURE. In patients with relapsed/refractory MCL, both lisocabtagene maraleucel (JCAR017) and axicabtagene ciloleucel (Yescarta) have shown 70% to 90% response rates and 50% to 60% (complete response) rates. That is going to be the future of this field.

Mantle cell lymphoma is an aggressive, rare form of non-Hodgkin lymphoma (NHL) that accounts for about 6% of all NHL cases in the United States. The disease results from a malignant transformation of a B lymphocyte in the outer edge of a lymph node follicle, or the mantle zone, according to The Leukemia & Lymphoma Society.

Mantle cell lymphoma is a disease that responds well to initial therapy, so we try to throw (everything we have) at it (early), Andreadis, an associate professor of clinical medicine in the Department of Medicine at the University of California, San Francisco, Helen Diller Family Comprehensive Cancer Center, said. When a patient relapses, ibrutinib (Imbruvica) or a BTK-like agent is the drug of choice.

Types of BTK inhibitors include Imbruvica, Calquence (acalabrutinib) and Brukinsa (zanubrutinib). The responses seen with these drugs have led to approvals from the Food and Drug Administration for patients who have received at least one prior line of therapy. But often patients will relapse following BTK inhibitor therapy. The median duration of response is about 1 to 1.5 years, Andreadis explained.

As another approach to treatment, researchers are examining the effects of CAR-T cell therapy. During the 2019 American Society of Hematology annual meeting, results from the ZUMA-2 clinical trial showed promise in the investigational CAR-T cell therapy KTE-X19. The phase 3 trial included patients with relapsed and/or refractory mantle cell lymphoma who had received multiple prior lines of therapy. Patients received a single infusion of KTE-X19, and the researchers saw a 93% objective response rate and a 67% complete response rate.

Right now, we are asking, In what patient population can we use CAR-T cell therapy in? Andreadis said. Can we give it to patients with central nervous system disease? What about other lymphomas like follicular lymphoma? Can we give it in the clinic? We are getting the data that may increase the applicability of CAR-T cell therapy in those areas.

Although there is much hope in the use of CAR-T cell therapy, not all patients respond, or treatment may stop working. Thats where experts are exploring antibody-drug conjugates and bispecific T-cell engagers (BiTEs). We saw response rates of 50% to 70% in patients treated with bispecific antibodies, some whom failed CAR T prior, he said.

He added, Going forward, we need to get CAR T more affordable and accessible. We also need to work to simplifying the procedure, perhaps by using allogeneic CAR T cells.

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Immune-Based Therapies Emerge in Mantle Cell Lymphoma - Curetoday.com

Texas A&M Researcher Named To National List Of Inspiring Black Scientists – Texas A&M University

Texas A&M researcher Dr. Yava Jones Hall was named to a list of 100 inspiring black scientists in the U.S.

Texas A&M College of Veterinary Medicine & Biomedical Sciences

Dr. Yava Jones-Hall, an associate professor in theDepartment of Veterinary Pathobiology (VTPB)at the Texas A&M College of Veterinary Medicine & Biomedical Sciences (CVM), is leading in the field of veterinary medicine as the only veterinarian selected for CrossTalks list of100 inspiring black scientists in America.

CrossTalk is the official blog of Cell Press, a leading publisher of more than 50 scientific journals across the life, physical, earth and health sciences.

We are very happy to see one of our high-caliber faculty members being recognized for their outstanding work, said Carol A. Fierke, Texas A&M University provost and executive vice president.

Jones-Hall is joined on the list by scientists from African, Afro-Caribbean, Afro-Latinx and African-American backgrounds ranging from assistant professors to department heads at universities across the country.

It was surprising and amazing to be selected, especially being a veterinarian, Jones-Hall said. It was nice to see veterinary medicine represented.

The list of inspiring black scientists was created to encourage current and future generations of scientists and emphasize the importance of diversity in the field. CrossTalk clarified that while there are many more than 100 black scientists in the U.S. deserving of recognition, the list was created to provide an example of the impact black scientists can have on America.

Diversity drives excellence in everything that we do as a team, including biomedical education and research, saidDr. Ramesh Vemulapalli, VTPB department head. We are very proud to have Dr. Jones-Hall on our faculty. She is a great role model to minority students aspiring to pursue a career in veterinary medicine.

I definitely see diversity in veterinary medicine as an important concept, Jones-Hall said. The reality is, the world is not homogenous. We need our students to be exposed to working with different types of people to have cultural sensitivity and understand that not everybody is like you. Also, once you have diversity within any program, you get diverse ideas.

While earning her Doctor of Veterinary Medicine (DVM) degree at the Tuskegee University College of Veterinary Medicine, Jones-Hall was introduced to the field of patholog they, study of the causes and effects of disease. Once she saw how seamlessly pathology combines with collaborative research, she was hooked.

As a veterinary pathologist, Im trained to understand disease in any organ in a multitude of species, Jones-Hall said. Whatever field of research an investigators in, I help them figure out how best a pathologist can tease out the data for them to see whats happening and how best to frame the research.

Considering herself a veterinary detective, Jones-Hall helps researchers look at clues in cells and body tissues to find the best way for the research to progress. Working on a variety of research topics, and never knowing what will come through the door next, are what make the field of pathology so appealing to her.

Jones-Hall joined the CVM from the Purdue University College of Veterinary Medicine last August and, as the sirector of CVMs Histology Laboratory, began the project of creating a digital pathology program to increase the efficiency and accuracy of one of a pathologists typical jobs analyzing slides of cells to count those of the same kind.

Traditionally, pathologists would look at the slide under the microscope and give a subjective assessment of disease, Jones-Hall said. Digital pathology augments traditional pathology by allowing the pathologist to use computer-generated algorithms to assess disease. This gives objective, quantifiable, and repeatable results. Whereas it would take me weeks to look at hundreds of slides, I scan the slides to make a digital image and direct a computer program to find the cells of interest or disease state. Hundreds of slides can now be analyzed in hours instead of weeks.

Outside of the lab, Jones-Hall donates much of her spare time to volunteering for community outreach efforts and taking any opportunity she can to promote STEM careers, and specifically veterinary medicine, to disadvantaged youth.

She is also a member of Texas A&Ms STRIDE (Strategies and Tactics for Recruiting to Improve Diversity and Excellence) Committee, leading workshops for faculty members involved in faculty recruitment.

Diversity is important, in general, and its important to me, so Im willing to do more in order to improve the climate and increase everyones awareness she said.

Jones-Hall hopes that her recognition from CrossTalk can inspire others to spend their careers thinking not only of themselves, but also those who may not have had the same advantages.

The CVM is extremely proud of Dr. Jones-Hall for her accomplishments as an individual and as the only veterinarian to appear on the list of 100 inspiring black scientists, saidDr. Eleanor M. Green, the Carl B. King Dean of Veterinary Medicine. The work she does within and outside of the university will undoubtedly make a huge impact, both for the college and within the community, as she demonstrates the possibilities for budding scientists from all backgrounds.

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Texas A&M Researcher Named To National List Of Inspiring Black Scientists - Texas A&M University

Cumberland County family turns to non-FDA approved stem cell treatment to help two-year-old son with cerebral palsy – FOX43.com

Lance was diagnosed with cerebral palsy a year ago. His family hopes non-FDA approved stem cell treatment for the disease can help him walk and talk.

CAMP HILL, Pa. A family in Cumberland County has turned to stem cells to treat their two-year-old son diagnosed with cerebral palsy. The only problem: stem cell treatment for the disease hasn't been approved by the FDA.

The day he was born, when he wheeled him down the hall and he was only a pound, and I started to cry and said, will he live? And he said, of course Hes only small," said Danielle Maxwell, Lance's mom.

The words, "he's only small," are what Lance's mom and father Rob have lived by since the day he was born. The preemie, born three months early, has been through several surgeries and complications along the way. But, Lance has always been a fighter.

Lance fought so hard just to survive the beginning of life, and come home with us," said Danielle. "And he is just so happy and loving and amazing.

About a year ago, Lance was diagnosed with cerebral palsy. Doctors told his family, he will never walk, talk or take care of himself.

We just dont believe that," said Danielle. "We dont.

Lance receives a lot of different therapies but, his parents did not want to just stop there.

We both overwhelmingly feel, he never gave up, he never gave up on us, he never gave up on himself," said Rob. "So, we owe it to him to give him the opportunity. Its really that simple, he deserves the opportunity."

Danielle began researching stem cell therapies, even speaking to doctors in countries overseas where treatment with stem cells is more readily accessible than in the U.S. The FDA has approved stem cell treatments for some conditions but not cerebral palsy. However, trials to determine the effectiveness of stem cell treatment for the disease are underway.

What weve seen is a small but real appearing improvement in motor function," said Doctor Charles Cox with University of Texas Health in Houston, began a trial in 2013 on the safety and effectiveness of banked cord blood or bone marrow stem cells in children with cerebral palsy, and is now just wrapping up the results from the trial.

The overall results of this study depend if youre a glass half full or half empty kind of person," said Dr. Cox. "It is not a compelling miraculous result. Its not, Oh my God, this child was treated and look at this profound benefit.'"

Because stem cell treatment for cerebral palsy is still in trial phases, it's not approved treatment by the FDA. However, the Maxwells did find a doctor in Harrisburg willing to transfer stem cells from a full-term baby's umbilical cord to Lance. But, since it isn't FDA approved, we were not allowed to be there to show Lance receiving the stem cells. The Maxwells are hopeful following this procedure Lance may someday walk and more importantly be able to communicate with them.

He wants to be involved," said Rob. "You can tell hes trying to communicate he just cant get over that hump. We believe stem cells could be that bridge to help him move a little faster.

Danielle says, it will take about six months to see if the stem cells will have any definitive benefits for Lance. But, already says she's seeing progress. She says Lance is not able to stand on his own.

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Cumberland County family turns to non-FDA approved stem cell treatment to help two-year-old son with cerebral palsy - FOX43.com

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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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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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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