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Research Overview | Rutgers Cancer Institute of New Jersey

Posted: October 19, 2015 at 5:49 pm

The research efforts in the Sabaawy laboratory is focused on studying normal stem cell development and cancer stem cells utilizing patient-derived cells, genome sequencing, tumor initiation models, 3D stem cell organoid cultures and zebrafish and humanized mouse xenografts for drug discovery. These studies aim to dissect normal stem cell developmental pathways, and how cancer stem cells divert from these regulatory pathways. One major pathway for research focus in the laboratory is the regulation of stem cell self-renewal by the polycomb gene BMI1 and cyclin dependent kinase inhibitors p15 and p16 regulating the cell cycle and senescence. Utilizing novel organoid cultures, CRISPR- and recombinase-mediated genome editing and drug modifiers together with transgenic and xenograft approaches; the laboratory is generating models for precision therapy of several cancers such as prostate and renal cancers, glioblastomas and leukemias.

The laboratory houses the Rutgers Cancer Institute of New Jersey zebrafish facility and is collaborating with several investigators at Rutgers, nationwide and globally to utilize our zebrafish stem cell reporters and Cre-Lox transgenics for cancer modeling and drug discovery strategies. With these approaches, we uncovered novel stem cell targets, and are developing small molecule inhibitors for targeting stem cell self-renewal for more effective regenerative and cancer therapies.

A parallel research effort in the Sabaawy laboratory is to study human adherent bone marrow-derived cells (ABMCs)-based therapy and transplantation in regenerative medicine. Cell therapy using stem cells for regeneration of a failing organ or injury repair is a promising approach. We are utilizing 3D organogenesis and animal models to study the mechanisms and dynamics of stem cell-mediated regeneration. These studies support ongoing collaborations in international clinical trials for utilizing ABMCs cell therapy for injury repair.

Hatem E. Sabaawy, MD, PhDis an assistant professor of medicine at Rutgers Robert Wood Johnson Medical School, an assistant professor of cellular and molecular pharmacology at the Rutgers Graduate School of Biomedical Sciences, director of the Cell and Gene Therapy Good Manufacturing Practice Facility at RWJMS, a member of the executive committee of the Stem Cell Institute of New Jersey, and a principal investigator at Rutgers Cancer Institute of New Jersey Molecular and Regenerative Medicine program.

He had his medical residency and graduate training at Cairo University Hospitals in Cairo, Egypt, and New York Medical College in Valhalla, NY in clinical Hematology with PhD in Genetic Pharmacology from the Gene Therapy program at New York Medical College. Dr. Sabaawy went on to complete a fellowship at the Transplantation and Immunology Branch of the Center for Cancer Research at the National Institutes of Health (NIH) and the National Cancer Institute (NCI) in Bethesda, MD.

His work at the Cancer Institute of New Jersey focuses on translational research studies of normal hematopoietic stem cells and tumor stem cell development utilizing mouse and zebrafish models. The studies received national funding from the National Institutes of Health and the Department of Defense. These studies aim to identify stem cell targets, genetic modifiers and small molecule inhibitors that would ultimately improve cancer patients' survival.

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Research Overview | Rutgers Cancer Institute of New Jersey

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Research at Rutgers | Rutgers University

Posted: October 19, 2015 at 5:49 pm

Rutgers, The State University of New Jersey, is entrenched in a culture of research, innovation, and invention that is a hallmark of the American academic experience.

Of the thousands of institutions of higher learning in North America, only 62 are members of the Association of American Universities (AAU).This selective group ofleading research universities is recognized for the quality and scope of its research and educational programs.Rutgers is the only public New Jersey university in the AAU (fellow Garden State school Princeton is also a member).

On July 1, 2013, Rutgers University became a member of the Committee on Institutional Cooperation (CIC), a consortium of first-tier research universities, such as the University of Chicago, University of WisconsinMadison, and University of Michigan, that shares knowledge and best practices and pools resources and buying power to strengthen higher education and support research endeavors. CIC universities conduct $8.4 billion in funded research each year.

Rutgers is one of the nations 75 land-grant institutions, in the company of other land-grants such as Cornell, MIT, Ohio State, and Penn State. The Morrill Act of 1862 designated these institutions to serve the states and their citizens by disseminating practical knowledge developed at key institutions of higher learning. From an early emphasis on agriculture and the mechanical arts, the land-grant mission of Rutgers, like that of fellow institutions, has expanded to include a broad range of teaching, research, and service activities.

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Research at Rutgers | Rutgers University

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New Hampshire Colorectal Cancer Screening Program …

Posted: October 19, 2015 at 5:49 pm

The New Hampshire Colorectal Cancer Screening Program (NHCRCSP) is a statewide effort to increase colorectal cancer screening for New Hampshire residents.

Contact Us Lebanon, NHCRCSP Team (DHMC) Phone: (603) 653-3702 Fax: (603) 727-7798

In March 2011, the New Hampshire Division of Public Health Services in collaboration with the New Hampshire Colorectal Cancer Screening Program created "Healthy Insights: Prevention news for the medical community of New Hampshire." Healthy Insights uses a similar technology as the New Hampshire Health Alert Network to notify providers of critical New Hampshire specific prevention messages throughout the year. Healthy Insights is sent via email to New Hampshire providers approximately six times per year, with the inaugural issue containing information on "Colorectal Cancer: One Of The Few Malignancies That Can Be Prevented As Well As Detected Early." An easy to use resource from the NHCRCSP, Screening and Surveillance Recommendations, was attached. Evaluation of this strategy to communicate important prevention messages to providers is ongoing.

New Hampshire Colorectal Cancer Screening Program (NHCRCSP) Information & Preparation Instructions for Your Colonoscopy

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New Hampshire Colorectal Cancer Screening Program ...

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Facts About Abortion: Stem Cell Research and Abortion

Posted: October 19, 2015 at 5:49 pm

Page Summary: Embryonic stem research cannot take place apart from dead human embryos. Embryonic stem cells cannot be culled without killing the embryo. Whether these tiny human beings are explicitly killed for research purposes or not, the ethics of the matter do not change.

The National Institutes of Health (NIH) tells us this about stem cells:

Because stem cells can differentiate into specialized cell types, they have the potential to replace or repair damaged tissue, be used for organ transplants and treat all sorts of diseases. Much research is left to be done, but the use of stem cells could potentially cure diabetes, Parkinson's disease, spinal chord injuries, heart conditions, and more.

Before going further, it must be emphasized that there are different types of stem cells, which carry vastly different ethical implications. Until recently, researchers worked with two kinds of stem cells: embryonic stem cells (hESCs) and "somatic" or "adult" stem cells. Embryonic stem cells are the undifferentiated cells from which all our body parts, organs, tissues, etc. originally developed. These cells are obtained by transferring the inner cell mass of the embryo into a culture dish, but can only be done by killing the embryo. This is what makes embryonic stem cell research an ethical question. Adult stem cells are undifferentiated cells found in various tissues throughout the body, including the brain, bone marrow, umbilical cord blood, muscle, skin, teeth, etc., and are thought to maintain and repair damaged tissue. These can be obtained without harm to the donor.

In 2007, a new stem cell method was discovered that actually "reprograms" ordinary cells (like skin cells) to revert into an embryonic stem cell-like state. These stem cells are called Induced Pluripotent Stem Cells (iPSCs) and are essentially no different than embryonic stem cells, with one exception: they do not require the killing of embryos. The scientist who discovered this reprogramming technique, Dr. Shinya Yamanaka of Japan, said the following:

Dr. Yamanaka states that iPSCs overcome two main problems with embryonic stem cell research: (1) immune rejection: since the embryonic stem cells that would theoretically be introduced into patients do not carry the same genetic code, the body may reject them (as has been observed in studies on mice); and (2) the ethical dilemna: the only way to derive embryonic stem cells is to kill embryos. With the discovery of iPSCs, embryo-like stem cells can be derived from a patient's own cells, which carry the same genes and will not be rejected by the body, and, more importantly, they do not require the killing of embryos.

Despite the ethical controversy surrounding embryonic stem cell research, and the scientific advances which allow for the ethical controversy to be avoided altogether, the U.S. government began providing federal funding for embryonic stem cell research in 2001. Prior to this, federal funds could not be used for embryonic stem cell research, but President Bush changed that when he adopted a policy that allowed government funding to be applied towards research on a limited number of embryonic stem cell lines. The statement that spelled out those limitations reads as follows:

President Bush tried to toe the moral line by ensuring that no new embryos would be created and destroyed for stem cell research. On March 9, 2009, President Obama issued a new executive order, revoking the former policy. Federal funding can now be used for embryonic stem cell research, without regard to creation date and without regard to the future life of the embryo. Dr. Curt Civin, who serves as the founding director of the University of Maryland Center for Stem Cell Biology and Regenerative Medicine defends the practice this way, "This was already life that was going to be destroyed, the choice is throw them away or use them for research." Dr. Civin conveniently ignores a third option: embryo adoption. Frozen embryos need not be consigned to the trashcan or the microscope!

Largely lost in the discussion is the fact that, in the eight years that the federal government has funded embryonic stem cell research, the proposed benefits are still wholly speculative (President Obama admits the potential benefit "remains unknown"). To date no human embryonic stem cells have actually been used to cure or treat diseases (although the FDA recently cleared the California-based company Geron to use human embryonic stem cells for clinical trial). Adult stem cells, on the other hand, have already helped with over 73 diseases (this according to the Family Research Council and peer-reviewed published research). Time will tell what scientists can do with iPSCs, but remarkable research is already being done. In fact, Dr. Oz surprised Michael J. Fox and Oprah Whinfrey when he declared on her show that "the stem cell debate is dead". It is not embryonic stem cell research that will ultimately cure diseases like Parkinson's, he maintains, but rather iPSCs. Dr. Oz believes iPSC based cures are less than ten years away.

Of course, even if you want to defend the ethical merits of embryonic stem cell research, do not confuse the debate over the federal funding of embryonic stem cell research with the debate over embryonic stem cell research itself. The opportunity for private corporations to acquire and study fetal tissue samples has long been in place. For those individuals and companies who have no ethical qualms with the "therapeutic" killing of embryos, they have the legal freedom to pursue their research on their own time and their own dime. Objecting taxpayers need not foot the bill, until now. That's how the federal funding of embryonic stem cell research changes the debate. To better illustrate this distinction, let's compare embryonic stem cell research with legal prostitution. As you may or may not know, prostitution is lawful throughout much of the state of Nevada. Despite the fact that lots of people find prostitution to be morally reprehensible, the state of Nevada has made it lawful for its citizens to engage in. Now what if, instead of just making prostitution legal, Nevada also made it state funded requiring its citizens to pay the operating costs of brothels across the state? You see where we're going with this. A strong case can be made for outlawing embryonic stem cell research outright, just as a strong case can be made for outlawing prostitution outright. But even if you're going to defend the merits of the practices in question, how can it possibly be reasonable for objecting citizens to be made to pay for them?!

The reason people who oppose abortion tend to also oppose embryonic stem cell research is because extracting stem cells from embryos kills them. Embryonic stem cell lines cannot be established apart from dead embryos. Therefore, since embryos (just like fetuses and newborns and infants and adults) are human beings, embryonic stem cell research is unjust and unjustified. It is the killing of one person (actually many persons) in the theoretic attempt to save other people. Is it justifiable to kill one person in order to spare someone else from disease? At its essence, the driving philosophy behind embryonic stem cell research is one that places less value on individual human life than it does on the "greater human good". While this may sound altruistic on the surface, it has been the historic basis for all manner of human rights abuses.

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Facts About Abortion: Stem Cell Research and Abortion

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UNMC International Healthcare Services

Posted: October 19, 2015 at 5:49 pm

We celebrated 40th anniversary of Kidney Transplant Program by performing over 5,000 transplants. We also completed 25 years for our Liver Transplant Program, completing more than 2,600 transplants. We are one of the first centers and pioneers in Bone Marrow and Stem Cell Transplants. We are only one of the four US institutions for pediatric and adult Intestinal and Small Bowel Transplants. We have been recognized for Outstanding Stroke and Cardiovascular Care in 2011 for a second consecutive year.

International Patients

Our patients best available treatment outcome is our only goal and responsibility. We assure that the patients as well as their families are most comfortable during their stay with us and that all of their needs are met while they are receiving the best healthcare services available in the world. Our services include, but are not limited to, helping with visa, arranging appointments, greeting and welcoming patients at the airport, local transportation, scheduling and escorting to appointments, medical interpretation, most convenient housing, updating referring physicians and all patient-related matters. We do this with utmost cultural, religious and personal sensitivities. We offer prompt appointments and discounted rates.

Tele-Pathologyand Second Opinion

We offer Electronic Tele-Pathology and Second Opinion consultation services. These services allow healthcare colleagues to utilize over 50 sub-specialties at our world renowned pathology and genetics facilities.

Training, Education and Research Programs for Hospitals and Healthcare Institutions

Hundreds of healthcare professionals from around the world have participated in our customized training, education and research programs. These programs offer dynamic multi-faceted, no-cost and extended for-fee programs. Our programs offer the opportunity to train here in the United States at The Nebraska Medical Center side by side with our renowned specialists in over 50 specialties. The programs are open to doctors, nurses, allied health professionals, as well as healthcare administrators.

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7. Stem Cells and Diabetes [Stem Cell Information]

Posted: October 19, 2015 at 5:48 pm

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Biologics | Orthopedics This Week

Posted: October 19, 2015 at 5:48 pm

Researchers from Inserm/Strasbourg University in France have a new way of tackling infections. The team,

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Bone Therapeutics, a bone cell therapy company based in Brussels and Paris, has completed treatment

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Two doctors used dehydrated amniotic tissue to heal an otherwise nonhealing surgical knee wound. The

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Xtant Medical Holdings Inc., a company in Belgrade, Montana, whose subsidiary, Bacterin International, Inc. makes

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A newt is a common sort of lizard. But it can do something that we

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An investigational drug for a rare orthopedic tumor is showing promise, says a new study

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Researchers hoping to find ways to regenerate cartilage worn away in aging knees and hips,

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Mesoblasts groundbreaking study of using stem cells to treat degenerative disc disease has just enrolled the first patient in the third phase of this FDA approved study. In Phase 2, patients not only tolerated the stem cells well, but also experienced statistically significant and durable pain reduction and functional improvement. This is a tremendously important study.

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Bones heal faster when treated with a component of marijuana, according to a study at

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It turns out that a drug used to stabilize moodslithium chloridemay be helpful in treating

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BioStructures, LLC is pleased to report on its latest corporate landmark eventthe company is announcing

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Scientists are proving that tobacco, more than any other plant, is uniquely suited for development of medicines, vaccines, antibodies and biologic materials. We always thought that tobacco was a drug delivery vehicle. But nothing like this.

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Alachua, Florida-based AxoGen, Inc. announced that the first patient has been treated as part of

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Bacterin International Holdings, Inc., the Belgrade, Montana-based biologics and allograft company, surprised its analysts by

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In what may be a unique approach to wound healing, researchers have developed a new

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Researchers from the UK have found a way to predict which rheumatoid arthritis (RA) patients

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Shining a light on healingAli Khademhosseini, Ph.D., and Nasim Annabi, Ph.D. of the Biomedical Engineering

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New research has revealed the role of a protein called Sox9 in regulating cartilage production.

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Think you understand PRP? Some top docs came together at the recent TOBI meeting and posed five key questions which every physician should consider before and while using PRP on their patients.

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New York University Polytechnic School of Engineering, NYU School of Medicine, and Stanford University are

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Until now, according to Colin Fernandez, a science writer for the UK Daily Mail, scientists

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A protein known as PPARy just may help develop new bone-forming cells in patients who

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The leaders of Cerapedics, Inc. think the FDA is on the verge of approving a

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Scientists at the University of York announce, via a paper in Stem Cell Reports, that

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BioStructures, LLC has announced the first application of Prohesion, its patented surgical wound technology that

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Study results of CERAMENT|G, reported at the 2015 Orthopedic Research Society Annual Meeting, demonstrated that

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Using proteins extracted from stem cells themselves, scientists have found a way to grow bones.

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Researchers are not there yet, but they are closing in on the problem of how

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The process of repairing a broken bone in a patient with diabetes was enhanced when

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The dye is green and it sticks to bone fragments and grafts. When it is

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Multipotent vs. pluripotent stem cells – Pathology Student

Posted: October 19, 2015 at 5:48 pm

Q. Im in doubt regarding myelodysplasia is it multipotent or pluripotent?

A. Thats a great question because it lets us talk about hematopathology (yay!) and also stem cells (which can be confusing unless someone explains some simple stuff).

What is a stem cell? First, lets talk about stem cells. The thing that makes a stem cell a stem cell, at least in my mind, is the ability to self-renew. This means that the stem cell can either divide into two daughter cells which will mature into grown up cells, or (and more commonly) it can give rise to two cells: one that will become a mature cell, and another which retains the capacity to divide again. Its called asymmetric division: instead of giving rise to two of the same cells, you get one regular cell and another stem cell (which can continue this cycle of replication for a long long time).

(Virtually) limitless replication Most cells have a limited number of times that they can divide. This is because the telomeres (little protective DNA sequences) on the end of the chromosomes get a little shorter every time the DNA replicates and eventually they are so short that they cant protect the DNA and the cell is unable to divide. Stem cells and cancer cells have an enzyme called telomerase that replenishes the telomeres, keeping them nice and long so the cell can keep on dividing. Stem cells do eventually die so technically, there are a limited number of cell divisionsbut its a really, really big number. Cancer cells, on the other hand, are often totally immortal they can just keep on dividing and dividing.

Totipotent Another cool thing about stem cells is that they can give rise to many different kinds of cells. Heres where things can get murky. There are stem cells in an embryo which are able to give rise to any of the cell types in the body: hepatocytes, epithelial cells, neurons, cardiac muscle cellseverything. This makes sense: if youre going to grow into a human, you have to have cells that give rise to all the necessary cell types. These stem cells are called totipotent or pluripotent stem cells. Theres a slight difference between the two words: totipotent means that the stem cell can give rise to any and all human tissue cells and it can even give rise to an entire functional human. The only totipotent cells in human development are the fertilized egg and the cells in the next few cell divisions.

Pluripotent After those few cell divisions, the cells become pluripotent. Pluripotent cells are similar to totipotent cells in that they can give rise to any and all human tissue cells. Theyre different, though, because they are not capable of giving rise to an entire organism. On day four of development, the tiny little embryo forms two layers: one that will become the placenta and the other that will become the baby. The cells that will become the baby can give rise to any human tissue type (obviously) but those cells alone cant give rise to the entire organism (because you cant form the baby without the placenta). Slight difference but enough to make a separate term.

Multipotent Another term you should know is multipotent. Multipotent stem cells cannot give rise to any old cell in the body they are restricted to a limited range of cell types. For example, there are multipotent stem cells in the bone marrow that can give rise to red cells, white cells and platelets. They cant give rise to hepatocytes, or any other cell type, though so they are not totipotent or pluripotent.

There are lots of multipotent stem cells in the adult human body. They reside in the bone marrow, skin, muscle, GI tract, endothelium, and mesenchymal tissues. This means that there is a nice source for replacing cells that have died or been sloughed away.

What about myelodsyplasia? So back to your question. Myelodysplasia is a hematopoietic disorder in which cells in the bone marrow grow funny (dysplasia) they might be binucleate, or not have the normal number of granules, or whatever. In addition, some cases have an increase in blasts in the bone marrow but not over 20%, or youd call it an acute leukemia. Some cases transform, eventually, into an acute myeloid leukemia; others just stay the way they are and dont become nasty.

Check out the image above, from a case of myelodysplasia. There is a bizarre, multinucleated erythroblast at 11 oclock (this is called dyserythropoiesis, or disordered red cell growth). There are also two messed-up neutrophils (dysgranulopoiesis) at 4 oclock and 10 oclock the one at 4 oclock has only two nuclear lobes, and both are hypogranular (not enough specific granulation). Theres also an increase in blasts, if this field is representative: theres one in the middle and (probably) one at 5 oclock.

This disorder (actually, its a group of disorders) involves stem cells in the bone marrow. Sometimes only one cell line is involved (red cells, say); other times all three cell lines are involved (red cells, white cells and platelets). Either way, the disorder involves a stem cell, and since the stem cells in the bone marrow are multipotent, it would be correct to say that myelodysplasia is a disorder of multipotent stem cells in the bone marrow. Its kind of redundant, though, because as far as we know, there arent any other kind of stem cells in the bone marrow! But at least you know the answer to your question now.

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Multipotent vs. pluripotent stem cells - Pathology Student

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2. Bone Marrow (Hematopoietic) Stem Cells [Stem Cell …

Posted: October 19, 2015 at 5:48 pm

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Michigan Catholic Conference: Home

Posted: October 19, 2015 at 5:48 pm

October 16, 2015: Throughout October, Catholic churches across the country are celebrating Respect Life Month to draw attention to the worth of every human person. The theme this year is Every Life is a Gift, reminding all that their inherent worth cannot simply be reduced to their skills or level of productivity (Cardinal Sean OMalley). During his visit to the United States last month, Pope Francis spoke about the dignity of all persons, especially those on the margins or considered disposable. The Word from Lansing column this month delves further into the idea of finding life as a gift, even in the midst of profound struggles. In addition, Michigan Catholic Conference offers a few ideas of how to promote and care for human life. Read more

October 7, 2015: Federal legislation that seeks to reduce certain mandatory minimum sentences, reduce recidivism, and limit solitary confinement for juvenile offenders recently found favor with Archbishop Thomas Wenski, chairman of the USCCB Committee on Domestic Justice and Human Development , and Sister Donna Markham, president of Catholic Charities USA. While noting that Pope Francis visited a Correctional Facility during his recent stay in Philadelphia, Archbishop Wenski said We must try to ensure that sentences are just, while creating humane space in which individuals can restore their lives with the kind of support that reduces the chances that they will return to prison in the future. These reforms are a step in the right direction. The bi-partisan Sentencing Reform and Corrections Act of 2015 was introduced recently in the United States Senate. Read more

October 6, 2015: Each year, the month of October is designated as Respect Life Month by the U.S. Conference of Catholic Bishops (USCCB) in the Catholic Church. The goal of the month is to celebrate the gift of human life and to promote a culture that recognizes the dignity of all people. This years theme for the month, which kicks off with Respect Life Sunday on October 4th, is Every Life is Worth Living. Cardinal Sean OMalley, Archbishop of Boston and chairman of the Committee on Pro-Life Activities for the USCCB, issued a statement highlighting this theme, calling all lives a good and perfect gift, whether they last for a brief moment or for a hundred years. More information on Respect Life Month and the 20152016 Respect Life program materials

September 28, 2015: Last week, Pope Francis visited the United States, drawing the attention of Catholics and non-Catholics alike. During his seven days in the country, he ate with the homeless, visited with Catholic schools students and immigrants, and blessed and greeted prisoners in a correctional facility. Pope Francis also met with President Obama, U.S. Congress, and the United Nations to bring a message of peace, cooperation, and hope to the political dialogue. Throughout his visit, he highlighted the dignity of the human person, including the poor and the immigrant, emphasized a concern for the environment and protection against a throwaway culture, promoted the importance of religious liberty, and spoke about the beauty and goodness of marriage. The U.S. Conference of Catholic Bishops offers video on demand of all of the papal events, as well as text of his speeches and homilies from Washington DC, New York City, and Philadelphia. Read more

Photo credit USCCB

September 24, 2015: This morning, Pope Francis addressed a joint session of Congress in Washington, D.C., making history as the first pope to ever do so. During his speech, Pope Francis highlighted the valuable contributions of four Americans of faith Abraham Lincoln, Martin Luther King Jr., Dorothy Day, and Thomas Merton to public life and to the common good. He encouraged the crowd to renew the spirit of fraternity and solidarity and to pass laws based on a concern for all people, speaking to issues along the broad spectrum of Catholic Social Teaching. Other speeches from Pope Franciss visit the United States, such as his address at the White House and midday prayers with the bishops, are also available at USCCBs website

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