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Personalized Medicine | Moffitt

January 28th, 2019 5:44 pm

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Even though cancers may be found in the same part of the body and look similar under the microscope, we now understand that they can be quite different. That difference often appears in how that tumor type responds to therapy. Increasingly, that variation in response to treatment can reflect the changes that are found in the DNA of the tumor. Thats why Moffitt Cancer Center looks at every patients cancer as unique. We start with a precise diagnosis that tries to identify the specific DNA alternations in the tumor and then create an individualized treatment plan that has the best chance of beating your cancer. Our team approach ensures a full range of specialists are collaborating to look at your cancer from every perspective.

The ultimate goal of personalized medicine at Moffitt is to create and share new, targeted treatments that will improve outcomes, cure disease, extend survivorship and improve quality of life for patients regardless of where they live. This is accomplished through existing clinical programs as well as ongoing research into how best to develop the right diagnosis and treatment plan for each individual.

Our efforts include:

DeBartolo Family Personalized Medicine InstituteThe DeBartolo Family Personalized Medicine Institute provides the hub for personalized care and research at Moffitt. Created by a generous donation from the DeBartolo Family Foundation, the DFPMI was created in 2012 to revolutionize the discovery, delivery and effectiveness of cancer care on an international scale.

Department of Individualized Cancer ManagementThe Department of Individualized Cancer Management includes five high impact and clinically oriented departments under the leadership of Dr. Howard McLeod: Adolescent & Young Adult, Gene Home, Genetic Risk Assessment Service, Personalized Cancer Medicine and the Senior Adult Oncology Program. The Personalized Cancer Medicine department is comprised of the Personalized Medicine Clinical Service (PMCS) and Clinical Genomics Action Committee (CGAC). PMCS and CGAC were developed as pathways for direct clinical translation of results from genomic testing. PMCS provides consultation and interpretation of the tumor genetic sequencing results for Moffitt patients and serves as a resource to Moffitt Physicians for input and advice regarding personalized medicine. CGAC serves as Moffitts unique molecular tumor board and includes a diverse team with expertise from various disciplines. Dr. McLeod, a renowned expert on the role of genetics on the individuals response to cancer therapies, is the Medical Director for the DeBartolo Family Personalized Medicine Institute.

Total Cancer CareMoffitt Cancer Center's Total Cancer Care initiative is an ambitious research partnership between patients, doctors and researchers to improve all aspects of cancer prevention and care. Patients participate by donating information and tissue. Researchers use the information to learn about all issues related to cancer and how care can be improved. Physicians use the information to better educate and care for patients.

Clinical PathwaysMoffitts clinical pathways are a model for providing evidence-based, consensus-driven, cost-effective cancer care. Each of the 51 disease-specific pathways that Moffitt has developed offers a detailed road map for physicians to provide state-of-the-art cancer care. The pathways demonstrate how to integrate evidence-based medicine with available technology to standardize, benchmark, measure and improve cancer care.

Molecular Diagnostics LaboratoryThe Morsani Molecular Diagnostics Laboratory is revolutionizing cancer diagnostics by using the most advanced genetic testing tools available to improve the precision in the patient care we provide. Studies show as many as 30 percent of initial cancer diagnoses are revised to indicate a different type of cancer. This lab seeks to reduce that number by developing clinical biomarkers that can help identify the right drug for a particular patient or determine if a specific clinical trial is a good match for a patient with a certain tumor gene mutation.

ORIENThe Oncology Research Information Exchange Network (ORIEN) is a unique research partnership among North Americas top cancer centers that recognizes collaboration and access to data as the key to cancer discovery. Through ORIEN, founders Moffitt and The Ohio State University Comprehensive Cancer Center Arthur G. James Cancer Hospital and Richard J. Solove Research Institute in Columbus leverage multiple data sources and match patients to targeted treatments. Partners have access to one of the worlds largest clinically annotated cancer tissue repositories and data from more than 100,000 patients who have consented to the donation for research.

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What are Adult Stem Cells? | Adult Stem Cell Treatment

January 28th, 2019 5:44 pm

The primary role of adult stem cells in humans is to maintain and repair the tissue in which they are found. While we call them adult stem cells, they are more accurately called somatic (from the Greek word soma = body) because they come virtually any body tissue, not only in adults but children and babies as well.

Stem cells are very flexible cells, sometimes considered immature, that have not developed to a final specialized cell type (like skin, liver, heart, etc.) Since they have not yet specialized, stem cells can respond to different signals and needs in the body by becoming any of the various cell types needed, e.g., after an injury to repair an organ. In that sense they are a bit like a maintenance crew that keeps repairing and replacing damaged or worn out cells in the body.

A stem cell is essentially a blank cell, capable of becoming another more differentiated cell type in the body, such as a skin cell, a muscle cell, or a nerve cell. Microscopic in size, stem cells are big news in medical and science circles because they can be used to replace or even heal damaged tissues and cells in the body. They can serve as a built-in repair system for the human body, replenishing other cells as long as a person is still alive.

Adult stem cells are a natural solution. They naturally exist in our bodies, and they provide a natural repair mechanism for many tissues of our bodies. They belong in the microenvironment of an adult body, while embryonic stem cells belong in the microenvironment of the early embryo, not in an adult body, where they tend to cause tumors and immune system reactions.

Most importantly,adult stem cells have already been successfully used in human therapies for many years.As of this moment,no therapies in humans have ever been successfully carried out using embryonic stem cells.New therapies using adult type stem cells, on the other hand, are being developed all the time.

Stem Cells are being used today to help people suffering from dozens of diseases and conditions. This list reveals the wide range of applications that adult stem cells are having right now:

Cancers:

Auto-Immune Diseases

Cardiovascular

Ocular

Neural Degenerative Diseases and Injuries

Anemias and Other Blood Conditions

Wounds and Injuries

Other Metabolic Disorders

Liver Disease

The primary reason would be the ethics, since getting embryonic stem cells requires destruction of a young human embryo. The other, practical reasons are that people feel money spent on embryonic stem cell research could be better spent on other stem cell research.

The biggest misconception people have about stem cell research is that it is only embryonic that are useful. In fact, other stem cell types are proving to be much more useful. The best stem cells for patients are Adult Stem Cells; these are taken from the body (e.g., bone marrow, muscle, even fat tissue) or umbilical cord blood and can be used to treat dozens of diseases and conditions. Over 1 million people have already been treated with adult stem cells. (versus no proven success with embryonic stem cells.)https://lozierinstitute.org/fact-sheet-adult-stem-cell-research-transplants/Yet most people dont know about adult stem cells and their practical success.

Another type of stem cell that is proving very useful is induced pluripotent stem cells (iPS cells.) These can be made from any cell, such as skin, and from any person. They act like embryonic stem cells, but are made from ordinary cells and so dont require embryo destruction, making them an ethical source for that type of cell. They have already been used to create lab models of different diseases.

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Is longevity determined by genetics? – Genetics Home …

January 28th, 2019 5:43 pm

The duration of human life (longevity) is influenced by genetics, the environment, and lifestyle. Environmental improvements beginning in the 1900s extended the average life span dramatically with significant improvements in the availability of food and clean water, better housing and living conditions, reduced exposure to infectious diseases, and access to medical care. Most significant were public health advances that reduced premature death by decreasing the risk of infant mortality, increasing the chances of surviving childhood, and avoiding infection and communicable disease. Now people in the United States live about 80 years on average, but some individuals survive for much longer.

Scientists are studying people in their nineties (called nonagenarians) and hundreds (called centenarians, including semi-supercentenarians of ages 105-109 years and supercentenarians, ages 110+) to determine what contributes to their long lives. They have found that long-lived individuals have little in common with one another in education, income, or profession. The similarities they do share, however, reflect their lifestylesmany are nonsmokers, are not obese, and cope well with stress. Also, most are women. Because of their healthy habits, these older adults are less likely to develop age-related chronic diseases, such as high blood pressure, heart disease, cancer, and diabetes, than their same-age peers.

The siblings and children (collectively called first-degree relatives) of long-lived individuals are more likely to remain healthy longer and to live to an older age than their peers. People with centenarian parents are less likely at age 70 to have the age-related diseases that are common among older adults. The brothers and sisters of centenarians typically have long lives, and if they develop age-related diseases (such as high blood pressure, heart disease, cancer, or type 2 diabetes), these diseases appear later than they do in the general population. Longer life spans tend to run in families, which suggests that shared genetics, lifestyle, or both play an important role in determining longevity.

The study of longevity genes is a developing science. It is estimated that about 25 percent of the variation in human life span is determined by genetics, but which genes, and how they contribute to longevity, are not well understood. A few of the common variations (called polymorphisms) associated with long life spans are found in the APOE, FOXO3, and CETP genes, but they are not found in all individuals with exceptional longevity. It is likely that variants in multiple genes, some of which are unidentified, act together to contribute to a long life.

Whole genome sequencing studies of supercentenarians have identified the same gene variants that increase disease risk in people who have average life spans. The supercentenarians, however, also have many other newly identified gene variants that possibly promote longevity. Scientists speculate that for the first seven or eight decades, lifestyle is a stronger determinant of health and life span than genetics. Eating well, not drinking too much alcohol, avoiding tobacco, and staying physically active enable some individuals to attain a healthy old age; genetics then appears to play a progressively important role in keeping individuals healthy as they age into their eighties and beyond. Many nonagenarians and centenarians are able to live independently and avoid age-related diseases until the very last years of their lives.

Some of the gene variants that contribute to a long life are involved with the basic maintenance and function of the bodys cells. These cellular functions include DNA repair, maintenance of the ends of chromosomes (regions called telomeres), and protection of cells from damage caused by unstable oxygen-containing molecules (free radicals). Other genes that are associated with blood fat (lipid) levels, inflammation, and the cardiovascular and immune systems contribute significantly to longevity because they reduce the risk of heart disease (the main cause of death in older people), stroke, and insulin resistance.

In addition to studying the very old in the United States, scientists are also studying a handful of communities in other parts of the world where people often live into their nineties and olderOkinawa (Japan), Ikaria (Greece), and Sardinia (Italy). These three regions are similar in that they are relatively isolated from the broader population in their countries, are lower income, have little industrialization, and tend to follow a traditional (non-Western) lifestyle. Unlike other populations of the very old, the centenarians on Sardinia include a significant proportion of men. Researchers are studying whether hormones, sex-specific genes, or other factors may contribute to longer lives among men as well as women on this island.

Martin GM, Bergman A, Barzilai N. Genetic determinants of human health span and life span: progress and new opportunities. PLoS Genet. 2007 Jul;3(7):e125. PubMed: 17677003. Free full-text available from PubMed Central: PMC1934400.

Sebastiani P, Gurinovich A, Bae H, Andersen S, Malovini A, Atzmon G, Villa F, Kraja AT, Ben-Avraham D, Barzilai N, Puca A, Perls TT. Four genome-wide association studies identify new extreme longevity variants. J Gerontol A Biol Sci Med Sci. 2017 Oct 12;72(11):1453-1464. doi: 10.1093/gerona/glx027. PubMed: 28329165.

Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT. Genetic signatures of exceptional longevity in humans. PLoS One. 2012;7(1):e29848. doi: 10.1371/journal.pone.0029848. Epub 2012 Jan 18. PubMed: 22279548. Free full-text available from PubMed Central: PMC3261167.

Wei M, Brandhorst S, Shelehchi M, Mirzaei H, Cheng CW, Budniak J, Groshen S, Mack WJ, Guen E, Di Biase S, Cohen P, Morgan TE, Dorff T, Hong K, Michalsen A, Laviano A, Longo VD. Fasting-mimicking diet and markers/risk factors for aging, diabetes, cancer, and cardiovascular disease. Sci Transl Med. 2017 Feb 15;9(377). pii: eaai8700. doi: 10.1126/scitranslmed.aai8700. PubMed: 28202779.

Young RD. Validated living worldwide supercentenarians, living and recently deceased: February 2018. Rejuvenation Res. 2018 Feb 1. doi: 10.1089/rej.2018.2057. [Epub ahead of print] PubMed: 29390945.

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Contact Us – Stemcell Technologies

January 28th, 2019 5:43 pm

Select your desired country to view specific contact information for that location: Please choose a country... Afghanistan Albania Algeria American Samoa Andorra Angola Anguilla Antarctica Antigua and Barbuda Argentina Armenia Aruba Australia Austria Azerbaijan Bahamas Bahrain Bangladesh Barbados Belgium Belize Benin Bermuda Bhutan Bolivia Bosnia and Herzegowina Botswana Bouvet Island Brazil British Indian Ocean Territory Brunei Darussalam Bulgaria Burkina Faso Burundi Cambodia Cameroon Canada Cape Verde Cayman Islands Central African Republic Chad Chile China, People's Republic of Christmas Island Cocos (Keeling) Islands Colombia Comoros Congo Cook Islands Costa Rica Cote d'Ivoire Croatia Cyprus Czech Republic Denmark Djibouti Dominica Dominican Republic East Timor Ecuador Egypt El Salvador Equatorial Guinea Eritrea Estonia Ethiopia Falkland Islands Faroe Islands Fiji Finland France France, Metropolitan French Guiana French Polynesia French Southern Territories Gabon Gambia Georgia Germany Ghana Gibraltar Greece Greenland Grenada Guadeloupe Guam Guatemala Guinea Guinea-Bissau Guyana Haiti Heard and Mc Donald Islands Honduras Hong Kong, China Hungary Iceland India Indonesia Iraq Ireland Israel Italy Jamaica Japan Jordan Kazakhstan Kenya Kiribati Korea, Republic of Kuwait Kyrgyzstan Laos Latvia Lebanon Lesotho Liberia Libyan Arab Jamahiriya Liechtenstein Lithuania Luxembourg Macau, China Macedonia Madagascar Malawi Malaysia Maldives Mali Malta Marshall Islands Martinique Mauritania Mauritius Mayotte Mexico Micronesia, Federated States of Moldova, Republic of Monaco Mongolia Montserrat Morocco Mozambique Myanmar (Burma) Namibia Nauru Nepal Netherlands Netherlands Antilles New Caledonia New Zealand Nicaragua Niger Nigeria Niue Norfolk Island Northern Mariana Islands Norway Oman Pakistan Palau Panama Papua New Guinea Paraguay Peru Philippines Pitcairn Poland Portugal Puerto Rico Qatar Republic of Serbia Reunion Romania Russia Rwanda Saint Kitts and Nevis Saint Lucia Saint Vincent and the Grenadines Samoa San Marino Sao Tome and Principe Saudi Arabia Senegal Seychelles Sierra Leone Singapore Slovakia (Slovak Republic) Slovenia Solomon Islands Somalia South Africa South Georgia and South S.S. Spain Sri Lanka St. Helena St. Pierre and Miquelon Suriname Svalbard and Jan Mayen Islands Swaziland Sweden Switzerland Tahiti Taiwan, China Tajikistan Tanzania, United Republic of Thailand The Democratic Republic of Congo Togo Tokelau Tonga Trinidad and Tobago Tunisia Turkey Turkmenistan Turks and Caicos Islands Tuvalu U.S. Minor Islands Uganda Ukraine United Arab Emirates United Kingdom United States Uruguay Uzbekistan Vanuatu Vatican City State Venezuela Vietnam Virgin Islands (British) Virgin Islands (U.S.) Wallis and Futuna Islands Western Sahara Yemen Yugoslavia (Serbia and Montenegro) Zambia Zimbabwe

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Stem Cell Treatment UK – Stem Cell Therapy Clinic

January 28th, 2019 5:42 pm

Get In Touch

Over 60 disabling illnesses including , neurological , organ damage , metabolic disorders , blood disorders , arthiritis.... please read more for extensive list

See what people say about their personal improvements , and experiences whilst in our worldwide clinics

See my own story unfold , after recieving life changing treatment in dec 2015 watch how i improve over the coming weeks and months

Welcome to my site providing a direct link to Stem Cell Treatment clinics to improve the health of UK and worldwide residents

Groundbreaking modern technology has brought us a completely natural, drugfree way to heal the

human body. Our primary task is to use your own unique stem cells for the treatment of your own body. Using advanced medical knowledge we can now activate dormant cells (adipose mesenchymal stem cells) to differentiate into the cells we need, and then they can replace the damaged cells. Symtoms become less obvious and disappear, giving relief and the chance to regain a normal functioning body and life!

Having been to a private clinic and experiencing life changing improvements to my own health, I want to let more people know about stemcells and that there is HOPE, to end many disabling conditions that we are led to believe are inevitably going to get worse. By contacting me I will help you to find the right treatment for your individual needs, at a clinic in a country where you will be treated as a distinguished guest, at a price more affordable than you will expect. I can speak from experience, and will gladly guide and help you through the whole process. Please explore my site, read the testimonials and hit the contact me button to speak to some of them! That much is free, and to feel better is truly miraculous!

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what is hsct, what is Hematopioetic Stem Cell Transplant …

January 28th, 2019 5:42 pm

what is hsct, what is Hematopioetic Stem Cell Transplant for ms, hsct stops all types of ms | HSCT STOPS MS Skip to contentWHAT IS HSCT? A COMPREHENSIVE DESCRIPTIONWith HSCT currently gaining a lot of attention in the main stream media for its huge success in giving people with MS new hope and the epic possibility of totally halting disease progression, more and more people are asking: what is HSCT? HSCT stops MS! HSCT or Hematopioetic Stem Cell Transplant, is the only existing scientifically proven treatment, currently available that completely halts disease progression of Multiple Sclerosis. It is not a new procedure as such, as it has been used to treat cancer since the 1960s, but it is a relatively new treatment for MS. Perhaps new is the wrong word The first HSCT performed specifically for an autoimmune disease (uveitis) was performed in 1985 by Prof. Shimon Slavin in Israel. The patient remains cured today. The first HSCT performed specifically for MS was at George Papanicolaou General Hospital, Thessaloniki, Greece in 1995. However, there were many observational case studies before then focusing on the success of HSCT for MS patients that were transplanted for cancer who simultaneously had their MS halted, as an unanticipated side effect of the treatment. All of the early studies that followed, also clearly established the now (well understood) probability that transplantation earlier in the disease life cycle is more beneficial than transplanting later in the disease evolution, when there is a greater degree of irreversible disability. Dr Burt at North Western University, Chicago, started HSCT treatment back in 1996. Prior to that, while he was a Fellow working at Johns Hopkins Hospital in Baltimore, he noticed that the leukemia patients he was treating needed to be re-vaccinated because the protection from childhood diseases like the measles and mumps was being lost. The cells affected by transfusion treatments were losing the memory of these original childhood vaccinations.Maybe, thought Dr. Burt, if we could get bad, diseased cells to lose their memory, we could reprogram them with good memories and help patients with autoimmune diseases. This reprogramming would depend on adult stem cellstiny building blocks found in the bodyif it was going to work.He first tried out his idea on animals in the research lab andit worked! Not long afterwards the FDA gave its approval for the adult stem cell therapy to be used on people suffering from Multiple Sclerosis, and again, it worked. Now, 14 years later, Burt and his team of researchers at Northwestern University are using this technique to help treat patients suffering from some 23 different diseases. There is no ethical dilemma as the treatment uses adult stem cells extracted from the patients own blood, and no embryonic stem cells are involved.Because the procedure involves the use of chemotherapy the treatment is not the most comfortable and is unfortunately quite expensive. That said many who have completed the procedure successfully attest to the fact that it is not unbearable by any means, and the chemotherapy part of the procedure is a short targeted dose that lasts for days as opposed to cancer treatments which can drag out over a much longer period. Indeed it is very different from the chemo used for cancer patients altogether. One should bear in mind that when cancer patients undergo chemotherapy they are more than likely very sick going in to the procedure and therefore would experience a greater degree of discomfort than someone relatively fit except for MS. Please refer to the blog links page to read first hand accounts of how individuals who have been treated already dealt with the procedure and how it has affected them. Please see: http://www.hsctstopsms.com/how-hsct-works/.What cannot be denied however is that to date HSCT is the only scientifically proven treatment that STOPS underlying disease progression in all types of MS and restores normal immune self-tolerance and produces lasting curative symptomatic improvement for the majority of MS patients. To date over 2,000 patients have been treated world wide, and the number continues to rise daily. It is important to mention here, that where you can go for treatment and whether you qualify, is determined by a variety of different criteria. We aim to help clarify your options and help you to decide the best place to apply for your own treatment.While this treatment is standard procedure for treating cancer patients (thousands of patients are treated annually), it is not standard treatment for people suffering from Multiple Sclerosis. There are a very small number of facilities Worldwide currently performing this procedure for MS. The type of MS that you have also plays a part in treatment; see http://www.hsctstopsms.com/types-of-ms/. The hope is that more will open in the early future as the demand increasingly continues to outweigh the supply, and that the cost of being treated will reduce accordingly, as the protocol efficiency is optimized. (Please refer to the menu item entitled Choosing a facility to learn more).Many who have already had HSCT say that one of the best parts of being treated is that halting the underlying disease progression of MS gives them back a future. George Goss, who had HSCT in 2009, an inspirational pioneer in promoting HSCT after he underwent the procedure in Heidelberg five years ago, describes this as pure gold. (Please see his blog: http://themscure.blogspot.co.uk/ and check out his HSCT forum on Facebook: HematopioeticStemCellTransplantMS&AutoimmuneDiseases, where he has provided invaluable information and support for those seeking HSCT). Living with MS is both frightening and uncertain. Little is known about what sparks rapid disease progression with no warning. One can go 10 years with little or no symptoms and then suddenly find oneself in a wheelchair in the space of a few months. It has been described as a Tiger that cannot be tamed. HSCT removes this Sword of Damocles hanging over ones heads and gives one the gift of hope and the luxury of planning a future with loved ones. Unless you live with MS you can have no concept of how magic this prospect can be! (Please see What it is like living with MS in the menu.)

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Veterinary medicine in the United States – Wikipedia

January 28th, 2019 5:41 pm

Veterinary medicine in the United States is the performance of veterinary medicine in the United States, normally performed by licensed professionals, and subject to provisions of statute law which vary by state. Veterinary medicine is normally led by veterinary physicians, normally termed veterinarians or vets.

Veterinarians are often assisted by paraveterinary workers including veterinary technicians and veterinary assistants, and in some cases, these para-professionals may perform work on their own.

Dependent on the jurisdiction, other professionals may be permitted to perform some animal treatment, through either specific exemptions in the law or through a lack of prohibitive legislation. This can include manipulation techniques such as physiotherapy, chiropractic and osteopathy, or animal-specific professions such as horse and cattle hoof trimmers, equine dental technicians, and technicians who specialize in cattle artificial insemination.

The Veterinarian's Oath was adopted by the American Veterinary Medical Association's House of Delegates July 1969, and amended by the AVMA Executive Board, November 1999 and December 2010.

Being admitted to the profession of veterinary medicine, I solemnly swear to use my scientific knowledge and skills for the benefit of society through the protection of animal health and welfare, the prevention and relief of animal suffering, the conservation of animal resources, the promotion of public health, and the advancement of medical knowledge.

I will practice my profession conscientiously, with dignity, and in keeping with the principles of veterinary medical ethics. I accept as a lifelong obligation the continual improvement of my professional knowledge and competence.

In order to practice, veterinarians must obtain a degree in veterinary medicine, followed by gaining a license to practice. Previously, veterinary degrees were available as a bachelor's degree, but now all courses result in the award of a doctorate and are therefore awarded a Doctor of Veterinary Medicine (DVM) if the degree is awarded in English, or a Veterinariae Medicinae Doctoris ("Doctor of Veterinary Medicine") (VMD) if the degree is awarded in Latin.

There is a high level of competition for admission to veterinary schools; there are currently only twenty eight veterinary schools in the United States which meet the accreditation standards set by the Council on Education of the American Veterinary Medical Association (AVMA), and five in Canada. Entrance requirements vary among veterinary schools, and various pre-professional degree programs have been developed to assist undergraduates in meeting these requirements. Such pre-vet programs are thus similar in concept to pre-med programs, and are often housed in Agricultural Biology,[1] Animal Science,[2] or Biological Science[3] programs.

Following qualification from the doctoral degree, the prospective veterinarian must receive a passing grade on the North America Veterinary Licensing Exam.[4] This exam is completed over the course of eight hours, and consists of 360 multiple-choice questions. This exam covers all aspects of veterinary medicine, as well as visual material designed to test diagnostic skills.

The median salary for starting veterinarians in 2016 was $74,690 in the United States according to U.S. Money News, while the lowest paid graduates earned approximately $53,000 annually. Montana had the lowest state average, while Michigan, Illinois and Hawaii had the highest.

The average income for a private practice associate in the United States was $158,000 in 2016. According to DVM360 most practice owner's paid themselves based on production, including a 3-4% management fee plus a 4.5% "return on investment" fee dependent on the value of their business. We know from industry standards that the average owner of a veterinary practice earns approximately $282,000 per year base salary. These increased values exceed those of public practice including uniformed services and government. In Australia, the profession wide average income was $67,000 in 2011 and this has declined compared to other professions for the past 30 years whilst graduate unemployment has doubled between 2006 and 2011.[5]

As opposed to human medicine, general practice veterinarians greatly outnumber veterinary specialists. Most veterinary specialists work at the veterinary schools, or at a referral center in large cities. As opposed to human medicine, where each organ system has its own medical and surgical specialties, veterinarians often combine both the surgical and medical aspect of an organ system into one field. The specialties in veterinary medicine often encompass several medical and surgical specialties that are found in human medicine.

Veterinary specialties are accredited in North America by the AVMA through the American Board of Veterinary Specialties.[6] While some veterinarians may have areas of interest outside of recognized specialties, they are not legally specialists.

According to a veterinary survey top paying specialties include veterinary anesthesiology ($389,105 median salary in 2008), veterinary ophthalmology ($215,120 median salary in 2009), veterinary nutrition ($202,368 average salary in 2008), and veterinary general surgery ($183,902 average salary in 2008).[7]

Veterinary technicians are the primary paraveterinary workers in the US and assist the veterinarian in the role of a nurse (and in most other anglophone countries, the equivalent role is called a veterinary nurse), providing trained support. The requirements for technicians vary by state, but in most cases, technicians are graduates of two or four year college-level programs and are legally qualified to assist veterinarians in many medical procedures.

Some states choose to license technicians, so that only people with appropriate qualifications are able to fulfill the role, but this is not the case in all jurisdictions.

Veterinary technology as an organized and credentialed career option is relatively young, only existing since the mid 20th century, although it began in 1908 when the Canine Nurses Institute was established in England, and as such is still struggling for recognition in many parts of the world. The first training program for technicians in the United States was established by the Air Force in 1951. The first civilian program was established ten years later in 1961 at the State University of New York (SUNY) Agricultural and Technical College at Delhi. In 1965 Walter Collins, a veterinarian, received federal funding to develop model curricula for training technicians. He produced several guides over the next seven years, and for this work he is considered the "father of veterinary technology" in the United States.[8]

Technical skills include: venipuncture; collecting urine; performing skin scrapings; taking and processing radiographs; and performing routine lab procedures and tests in: hematology, blood chemistry, microbiology, urinalysis, and microscopy. They assist the veterinarian with physical examinations that help determine the nature of the illness or injury. Veterinary technicians also induce and maintain anesthesia, and administer medications, fluids and blood products as prescribed by the veterinarian. Tasks in patient care include: recording temperature, pulse and respiration, dressing wounds, applying splints and other protective devices, and dental procedures. They perform catheterizations urinary, arterial, and venous; ear flushes; intravenous feedings and tube feedings. Equipment use includes operating various types of patient monitors and imaging devices to include electrocardiographic, radiographic and ultrasonographic equipment. Larger referral practices and teaching hospitals may also find veterinary technicians operating computed tomography equipment, magnetic resonance imagers, gamma cameras and other advanced medical devices. Veterinary technicians commonly assist veterinarians in surgery by providing correct equipment and instruments and by assuring that monitoring and support equipment are in good working condition. They may also maintain treatment records and inventory of all pharmaceuticals, equipment and supplies, and help with other administrative tasks within a veterinary practice such as client education. Unlike their more specialized counterparts among medical paraprofessionals, the veterinary technician is usually the only paraprofessional found in a veterinary practice and is thus often called upon to be a jack-of-all-trades.

To become a credentialed veterinary technician, one must complete a two-year or three-year AVMA credentialled degree, most of which result in the awarding of an associate of applied science degree in veterinary technology (those completing a four-year AVMA accredited school gain a bachelor's degree are considered veterinary technologists though the distinction is rarely made with the term technician being used generally.[9]

The education a credentialed technician receives is in-depth and crucial for medical understanding and to give proper health care. The American Veterinary Medical Association (AVMA) is responsible for accrediting schools with either Associate's degrees or Bachelor's degrees, though in some states or provinces this is not necessary. The AVMA also accredits schools that offer distance education. As a requirement of AVMA-accreditation, all distance learning programs require a significant amount of practical clinical experience before the student will be allowed to graduate.

Beyond credentialing as a veterinary technician specialty certification is also available to technicians with advanced skills. To date there are specialty recognitions in: emergency & critical care, anesthesiology, dentistry, small animal internal medicine, large animal internal medicine, cardiology, oncology, neurology, zoological medicine, equine veterinary nursing, surgery, behavior, nutrition, clinical practice (canine/feline, exotic companion animal, and production animal sub-specialties), and clinical pathology. Veterinary Technician Specialists carry the additional post-nominal letters "VTS" with their particular specialties indicated in parentheses. As veterinary technology evolves, more specialty academy recognitions are anticipated.

Non-credentialed personnel who perform similar tasks to veterinary technicians are usually referred to as veterinary assistants though the term technician is often applied generously. In many states, a veterinary assistant cannot legally perform as many procedures as a technician. Veterinary assistants often have no formal education related to veterinary medicine or veterinary technology, however, NAVTA recently approved the designation of Approved Veterinary Assistant (AVA) for those successfully completing approved educational programs. In larger facilities with tiered hierarchies veterinary assistants typically assist veterinary technicians in their duties.

Most states in the US allow for malpractice lawsuit in case of death or injury to an animal from professional negligence. Usually the penalty is not greater than the value of the animal. For that reason, malpractice insurance for veterinarians usually is well under $500 a year, compared to an average of over $15000 a year for a human doctor.[10] Some states allow for punitive penalty, loss of companionship, and suffering into the award, likely increasing the cost of veterinary malpractice insurance and the cost of veterinary care. Most veterinarian carry much higher cost business insurance, worker's compensation, and facility insurance to protect their clients and workers from injuries inflicted by animals.

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Stem Cell Treatment for Dementia | Stem Cell Doctors …

January 28th, 2019 5:41 pm

Mary Holler, age 82, of Marco Island Florida is smiling again. Mary was suffering from dementia.

She and her husband sought Stem Cell Dementia Treatment.

She felt uneasy with her ability to function on a daily basis. Now, after undergoing a successful stem cell dementia treatment earlier this month, Mary is her old self again. She doesnt ask her husband, Peter, the same question 3-4 times in an hour anymore. Peter Holler, age 83, had become very concerned that his wife of 60 years was slowly losing her memory. She had been on medications for memory loss for several years but the deterioration in her recall accelerated in the last six months.It was starting to wear on him. He was losing his wife right in front of his eyes. Marys poor performance on an in-depth memory test revealed that that she was so advanced that should be in an assisted living facility. This frightened both the Hollers and their children.

Peter Holler sought out stem cell dementia treatment. He felt it was his wifes only option. Peter, no stranger to stem cells, had undergone a stem cell treatment by Dr. Zannos Grekos for his failing heart in 2008. He had experienced great success. Even my lung function improved dramatically, he recalls. Going back to the same group that he had trusted, he made arrangements to get the love of his life treated.

A track record of several successfully treated patients with dementia already existed. So the doctors knew exactly what to do. Heading the team is Dr. Hector Rosario, an interventional cardiologist and head of the stem cell program in the Dominican Republic. Dr Roberto Fernandez DeCastro head of the catheterization lab assisted in the procedure. Dr Grekos, Chief Scientific Officer for the company was present as well. Its very exciting to be able to have such a positive impact on a disease process that otherwise has such a grim prognosis, Grekos explained. The Dementia Treatmentprotocol used to treat Mrs. Holler had been developed specifically for patients with dementia by Dr Zannos Grekos.

Below arebefore(top) and after (bottom) angiogramsof Mrs. Hollers left internal carotid injections:

Stem cells collected from Marys bone marrow are subjected to an activation and concentration process. The stem cells were then injected into her cerebral circulation. Look at the difference, Dr Rosario exclaimed while pointing to the before and after pictures of the brain circulation. The increase in blood vessel flow was astonishing.Since only adult stem cells from the patient are used, the political, ethical, and medical issues are avoided and there is no risk of rejection.

Were able to normalize a patients neuro-cognitive (brain function) testing in 6 months after the stem cell dementia treatment said Zannos Grekos MD, commenting on the success of patients having received adult stem cell dementia treatment to reverse the effects of dementia. Peter Holler agrees, Not only does she not repeat questions any more, but she is also remembering things that she had forgotten. Its a godsend.

Dementia is a loss of brain function that occurs with age and certain diseases. Most types of dementia are nonreversible (degenerative).It affects memory, thinking, language, judgment, and behavior. Alzheimers disease is a common type of dementia.Dementia also can be due to many small strokes or poor circulation. This is called vascular dementia. Many dementias have a vascular component; these are referred to as mixed dementias. Stem cells are especially effective in treating these types of dementias.

Dr. Zannos Grekos colleagues in the world medical field are currently employing adult stem cell therapy and coordinating its application for patients who have exhausted all other traditional therapy options. His presentation at the 16th Annual World Congress on Anti-Aging Medicine & Regenerative Biomedical Technologies conference supports efforts by a global community of doctors that are striving to incorporate adult stem cell therapy into mainstream medicine.

Regenocyteis an international corporation located in Bonita Springs, Florida. Dedicated to leading the world in providing Adult Stem Cell therapies, Regenocyteutilizes the most effective and safest technologies and medical procedures in order to improve the lives of its patients. A video of Dr. Zannos Grekos presentation at the 16th Annual World Congress on Anti-Aging Medicine & Regenerative Biomedical Technologies is available for viewing on the companys website. Additional information on adult stem cell therapy as well as patient video experiences can be found at http://www.regenocyte.comor call (866) 216-5710.

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Animal Longevity and Scale

January 25th, 2019 12:45 am

A useful line of analysis is to consider the effect of scale changes for creatures which aresimilar in shape and only differ in scale. As the scale of an animal increases the body weight and volume increase with the cubeof scale. The volume of blood flow required to feed that bulk also increases with the cube of scale. The cross sectional area of the arteries and the veins required to carry that blood flow only increases with the square of scale. There are other area-volume relationships which impose limitations on creatures. Some of those area-volume constraints, including the above one, are:

Thus to compensate for the body needs which increase with the cube of scale but the areas increase with only the square of scale the average blood flow velocity must increase linearly with scale. Blood flow velocity is driven by pressure differences. The pressuredifference must be great enough to carrying the blood flow to the top of the creature and great enough to overcome the resistance in the arteries and veins to the flow. The pressure required to pump blood from the heart to the top of the creature is proportional to scale.The pressure difference required to overcome the resistance to flow through the arteries intothe capillaries and back again through the veins is more difficult to characterize in terms of scale.The greater cross sectional area reduces the resistance but the long length increases resistance. The net result of these two scale influences seems to be that the pressure difference required to drive the blood through the bulk of the creature is inversely proportional to scale. The pressure difference imposed would be the maximum of the two required pressure differences.

Shown below are the typical blood pressures for creatures of different scales.

The linear regression of the logarithm of pressure on the logarithm of height yields the following result:

The linear regression of the logarithm of pressure on thelogarithm of weight yields:

If blood pressure were proportional to scale then the coefficient for *log(Height) would be 1.0 and for *log(Weight) would be 0.333 since weight to proportional to the cube of scale.The regression coefficients are not close to the theoretical values but they are of the proper order of magnitude for accepting blood pressure as beingproportional to scale.

The volume of the heart of a creature is proportional to the cube of scale. The volumeof the blood to be moved is also proportional to the cube of scale. From the previous analysis the flow velocity is proportional to scale. Therefore the time required to evacuatethe heart's volume is proportional to scale. This means that the heartbeat rate is inverselyproportional to scale. The following table gives the heart rates for a number of creatures.

A regression of the logarithm of heart rate on the logarithm of weight yields the followingequation:

If heart rate were exactly inversely proportion to scale the coefficient for *log(weight)would be -0.333. This is because scale is proportional to the cube root of weight.The coefficient of -0.2 indicates that the heart rate is given an equation of the form

One salient hypothesis is that the animal heart is good for a fixed number of beats. This hypothesis can be tested by comparing the product of average heart rate and longevity for different animals. Because the heart rate is in beats per minute and longevity is in years thenumber of heart beats per lifetime is about 526 thousand times the value of the product. Thedata for a selection of animals are:

Although the lack of dependence is clear visually the confirmation in terms of regression analysis is:

The t-ratio for the slope coefficient is an insignificant 0.15, confirming that there is no dependence of lifetime heartbeats on the scale of animal size.

If a heart is good for just a fixed number of beats, say one billion, then heart longevity is this fixed quota of beats divided by the heart rate. From the above equation for heart rate,lifespan (limited by heart function) would be proportional to scale raised to the 0.6 power.

The data for testing this deduction are:

For the data in the above table, admittedly very rough and sparse, the regression of the logarithm of the lifespan on thelogarithm of weight gives

Thus the net effect of scale on animal longevity is positive. Taking into account that weight is proportional to the cube of the linear scale of an animal the above equation in terms of scale would be

This says that if an animal is built on a 10 percent larger scale it will have a 6 percentlonger lifespan.

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Genetics | The Institute for Creation Research

January 25th, 2019 12:43 am

For over 150 years, Darwins hypothesis that all species share a common ancestor has dominated the creation-evolution debate. Surprisingly, when Darwin wrote his seminal work, he had no direct evidence for these genealogical relationships. Now, with online databases full of DNA-sequence information from thousands of species, the direct testing of Darwins hypothesis has finally commenced. More...

Authentic speciation is a process whereby organisms diversify within the boundaries of their gene pools, and this can result in variants with specific ecological adaptability. While it was once thought that this process was strictly facilitated by DNA sequence variability, Darwin's classic example of speciation in finches now includes a surprisingly strong epigenetic component as well. More...

One of the rapidly expanding and exciting research fields in molecular biology is the area of epigenetics. In the study of epigenetic modifications, scientists analyze DNA that has been modified in such a way that its chemistry is changed, but not the actual base pairs that make up the genetic code of the sequence. Its like a separate control code and system imposed upon and within the standard code of DNA sequence.

Because epigenetic modifications in the genome are related to gene expression, researchers have been using highly advanced technologies for comparing these differences in humans and chimps for regions of the genome that they both have in common. More... More...

Living things develop partly according to genetic instructions encoded on their DNA. The study of inheritance has widened the paradigms from genes to genomes, and now recent research indicates that critical biological information is carried from one generation to the next in systems additional to DNA, called epigenetic factors.

So, where did this information come from? More...

Genes could be thought of as brick molds, used to construct materials for building the physical structures of living organisms. They carry the codes to help make proteins, which then make up different cells that are combined together to form mega-structures called tissues.

New research has shed more light on how genes are used by cells to build the different tissues needed by complex living creatures. More...

Indiana University researchers discovered that certain genes used in developing horned beetle larvae are re-used later to make horns in their adult stage. The studys authors called the genes co-opted, indicating their belief that evolution decided to give them a secondary use. The authors suggestion that gene co-opting offers a possible explanation for the development of novel traits comes up short, however. More...

One of the past arguments for evidence of biological evolution in the genome has been the concept of pseudogenes. These DNA sequences were once thought to be the defunct remnants of genes, representing nothing but genomic fossils in the genomes of plants and animals. More...

Amazingly, scientists documented the activity of 2,082 distinct pseudogenes in the human genome whose aberrant levels of activity were directly associated with cancer-specific pathologies. More...

Proteins do most of the required metabolic tasks within each of the trillions of cells in the human body. However, only about four percent of human DNA contains coded instructions that specify proteins.

So what is the purpose of the remaining 96 or so percent? More...

A research team recently characterized a group of genes in humans and other mammals that not only defies evolutionary models but vindicates the Bibles prediction of the uniqueness of created kinds with distinct genetic features. More...

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Actuaries Longevity Illustrator – Enter Your Information

January 25th, 2019 12:41 am

The Longevity Illustrator calculates "Nearest Age" as the whole age you are closest to. For half the year, Nearest Age will be greater than your age on your last birthday. Please set your Illustration Age at least as great as your Nearest Age. If you leave the Illustration Age box blank, the tool automatically calculates longevity information from your Nearest Age. The Illustration Age will be rejected if it exceeds 99 or if the selection would cause Person 2 to be older than 99.

If you are already retired, or are considering retiring soon, you might choose to leave the Illustration Age box blank. However, if you expect to retire at a later date, or you are curious to know what your longevity might look like at some point in the future, you may enter a later age for the illustration to begin. In this case, the tool will assume you will survive to that later age.

For example, if your Nearest Age is 40 and you plan to retire at age 66, then entering age 66 as the age for the illustration to start will forecast results assuming you survive from now until age 66. The Longevity Illustrator allows you to experiment with different possibilities you might find interesting (if, for example, you are considering several different ages at which you might retire).

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Palo Alto Longevity Prize

January 25th, 2019 12:41 am

The Palo Alto Prize is a newly established Silicon Valley-based initiative of the Race Against Time Foundation. The mission of the Palo Alto Prize is to encourage collaboration, foster innovation, and build a community to address the underlying causes of aging.In addition to the $1 million of cash prizes, the Palo Alto Prize is also working with a number of angel investors, venture capital firms, corporate venture arms, institutions and private foundations to provide access to additional capital to the teams during the competition. While the Palo Alto Prize will help facilitate introductions, all transactions and due diligence will be done privately between the teams and potential investors and philanthropists.

The Race Against Time (dba The Hero Science Foundation http://www.herosf.org) is a 501(c)(3) educational non-profit organization (Tax ID: 47-2823482) created to raise public awareness and financial support for basic biomedical research related to increasing our health span and defining the fundamental biological mechanisms that prevent age-related diseases and disabilities.

About the prize sponsor:

Dr. Joon Yun, M.D., is the President of Palo Alto Investors, LLC, founded in 1989 with over $2 billion in assets under management invested in healthcare and the founder of the Palo Alto Institute, a nonprofit think-tank that has been providing operational support for the Palo Alto Prize. Board certified in radiology, Dr. Yun served on the clinical staff at Stanford Hospital from 2000-2006. Dr. Yun received his Bachelor of Arts in biology from Harvard University and his Doctor of Medicine from Duke University School of Medicine. Learn more at DrJoonYun.com and follow him at @drjoonyun

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Diabetes mellitus type 2 – Wikipedia

January 23rd, 2019 12:42 pm

Diabetes mellitus type 2SynonymsNoninsulin-dependent diabetes mellitus (NIDDM), adult-onset diabetes[1]Universal blue circle symbol for diabetes[2]PronunciationSpecialtyEndocrinologySymptomsIncreased thirst, frequent urination, unexplained weight loss, increased hunger[3]ComplicationsHyperosmolar hyperglycemic state, diabetic ketoacidosis, heart disease, strokes, diabetic retinopathy, kidney failure, amputations[1][4][5]Usual onsetMiddle or older age[6]DurationLong term[6]CausesObesity, lack of exercise, genetics[1][6]Diagnostic methodBlood test[3]PreventionMaintaining normal weight, exercising, eating properly[1]TreatmentDietary changes, metformin, insulin, bariatric surgery[1][7][8][9]Prognosis10 year shorter life expectancy[10]Frequency392 million (2015)[11]

Diabetes mellitus type2 (also known as type 2 diabetes) is a long-term metabolic disorder that is characterized by high blood sugar, insulin resistance, and relative lack of insulin.[6] Common symptoms include increased thirst, frequent urination, and unexplained weight loss.[3] Symptoms may also include increased hunger, feeling tired, and sores that do not heal.[3] Often symptoms come on slowly.[6] Long-term complications from high blood sugar include heart disease, strokes, diabetic retinopathy which can result in blindness, kidney failure, and poor blood flow in the limbs which may lead to amputations.[1] The sudden onset of hyperosmolar hyperglycemic state may occur; however, ketoacidosis is uncommon.[4][5]

Type2 diabetes primarily occurs as a result of obesity and lack of exercise.[1] Some people are more genetically at risk than others.[6] Type 2 diabetes makes up about 90% of cases of diabetes, with the other 10% due primarily to diabetes mellitus type 1 and gestational diabetes.[1] In diabetes mellitus type1 there is a lower total level of insulin to control blood glucose, due to an autoimmune induced loss of insulin-producing beta cells in the pancreas.[12][13] Diagnosis of diabetes is by blood tests such as fasting plasma glucose, oral glucose tolerance test, or glycated hemoglobin (A1C).[3]

Type2 diabetes is partly preventable by staying a normal weight, exercising regularly, and eating properly.[1] Treatment involves exercise and dietary changes.[1] If blood sugar levels are not adequately lowered, the medication metformin is typically recommended.[7][14] Many people may eventually also require insulin injections.[9] In those on insulin, routinely checking blood sugar levels is advised; however, this may not be needed in those taking pills.[15] Bariatric surgery often improves diabetes in those who are obese.[8][16]

Rates of type2 diabetes have increased markedly since 1960 in parallel with obesity.[17] As of 2015 there were approximately 392million people diagnosed with the disease compared to around 30million in 1985.[11][18] Typically it begins in middle or older age,[6] although rates of type 2 diabetes are increasing in young people.[19][20] Type 2 diabetes is associated with a ten-year-shorter life expectancy.[10] Diabetes was one of the first diseases described.[21] The importance of insulin in the disease was determined in the 1920s.[22]

The classic symptoms of diabetes are polyuria (frequent urination), polydipsia (increased thirst), polyphagia (increased hunger), and weight loss.[23] Other symptoms that are commonly present at diagnosis include a history of blurred vision, itchiness, peripheral neuropathy, recurrent vaginal infections, and fatigue.[13] Many people, however, have no symptoms during the first few years and are diagnosed on routine testing.[13] A small number of people with type2 diabetes mellitus can develop a hyperosmolar hyperglycemic state (a condition of very high blood sugar associated with a decreased level of consciousness and low blood pressure).[13]

Type 2 diabetes is typically a chronic disease associated with a ten-year-shorter life expectancy.[10] This is partly due to a number of complications with which it is associated, including: two to four times the risk of cardiovascular disease, including ischemic heart disease and stroke; a 20-fold increase in lower limb amputations, and increased rates of hospitalizations.[10] In the developed world, and increasingly elsewhere, type2diabetes is the largest cause of nontraumatic blindness and kidney failure.[24] It has also been associated with an increased risk of cognitive dysfunction and dementia through disease processes such as Alzheimer's disease and vascular dementia.[25] Other complications include acanthosis nigricans, sexual dysfunction, and frequent infections.[23]

The development of type2 diabetes is caused by a combination of lifestyle and genetic factors.[24][26] While some of these factors are under personal control, such as diet and obesity, other factors are not, such as increasing age, female gender, and genetics.[10] A lack of sleep has been linked to type2 diabetes.[27] This is believed to act through its effect on metabolism.[27] The nutritional status of a mother during fetal development may also play a role, with one proposed mechanism being that of DNA methylation.[28] The intestinal bacteria Prevotella copri and Bacteroides vulgatus have been connected with type2 diabetes.[29]

Lifestyle factors are important to the development of type2 diabetes, including obesity and being overweight (defined by a body mass index of greater than 25), lack of physical activity, poor diet, stress, and urbanization.[10][30] Excess body fat is associated with 30% of cases in those of Chinese and Japanese descent, 6080% of cases in those of European and African descent, and 100% of cases in Pima Indians and Pacific Islanders.[13] Among those who are not obese, a high waisthip ratio is often present.[13] Smoking appears to increase the risk of type 2 diabetes mellitus.[31]

Dietary factors also influence the risk of developing type2 diabetes. Consumption of sugar-sweetened drinks in excess is associated with an increased risk.[32][33] The type of fats in the diet are important, with saturated fats and trans fatty acids increasing the risk, and polyunsaturated and monounsaturated fat decreasing the risk.[26] Eating a lot of white rice appears to play a role in increasing risk.[34] A lack of exercise is believed to cause 7% of cases.[35] Persistent organic pollutants may play a role.[36]

Most cases of diabetes involve many genes, with each being a small contributor to an increased probability of becoming a type2 diabetic.[10] If one identical twin has diabetes, the chance of the other developing diabetes within his lifetime is greater than 90%, while the rate for nonidentical siblings is 2550%.[13] As of 2011, more than 36genes had been found that contribute to the risk of type2 diabetes.[37] All of these genes together still only account for 10% of the total heritable component of the disease.[37] The TCF7L2 allele, for example, increases the risk of developing diabetes by 1.5times and is the greatest risk of the common genetic variants.[13] Most of the genes linked to diabetes are involved in beta cell functions.[13]

There are a number of rare cases of diabetes that arise due to an abnormality in a single gene (known as monogenic forms of diabetes or "other specific types of diabetes").[10][13] These include maturity onset diabetes of the young (MODY), Donohue syndrome, and RabsonMendenhall syndrome, among others.[10] Maturity onset diabetes of the young constitute 15% of all cases of diabetes in young people.[38]

There are a number of medications and other health problems that can predispose to diabetes.[39] Some of the medications include: glucocorticoids, thiazides, beta blockers, atypical antipsychotics,[40] and statins.[41] Those who have previously had gestational diabetes are at a higher risk of developing type2 diabetes.[23] Other health problems that are associated include: acromegaly, Cushing's syndrome, hyperthyroidism, pheochromocytoma, and certain cancers such as glucagonomas.[39] Testosterone deficiency is also associated with type2 diabetes.[42][43]

Type2 diabetes is due to insufficient insulin production from beta cells in the setting of insulin resistance.[13] Insulin resistance, which is the inability of cells to respond adequately to normal levels of insulin, occurs primarily within the muscles, liver, and fat tissue.[44] In the liver, insulin normally suppresses glucose release. However, in the setting of insulin resistance, the liver inappropriately releases glucose into the blood.[10] The proportion of insulin resistance versus beta cell dysfunction differs among individuals, with some having primarily insulin resistance and only a minor defect in insulin secretion and others with slight insulin resistance and primarily a lack of insulin secretion.[13]

Other potentially important mechanisms associated with type2 diabetes and insulin resistance include: increased breakdown of lipids within fat cells, resistance to and lack of incretin, high glucagon levels in the blood, increased retention of salt and water by the kidneys, and inappropriate regulation of metabolism by the central nervous system.[10] However, not all people with insulin resistance develop diabetes, since an impairment of insulin secretion by pancreatic beta cells is also required.[13]

The World Health Organization definition of diabetes (both type1 and type2) is for a single raised glucose reading with symptoms, otherwise raised values on two occasions, of either:[47]

A random blood sugar of greater than 11.1mmol/l (200mg/dl) in association with typical symptoms[23] or a glycated hemoglobin (HbA1c) of 48mmol/mol (6.5 DCCT%) is another method of diagnosing diabetes.[10] In 2009 an International Expert Committee that included representatives of the American Diabetes Association (ADA), the International Diabetes Federation (IDF), and the European Association for the Study of Diabetes (EASD) recommended that a threshold of 48mmol/mol (6.5 DCCT%) should be used to diagnose diabetes.[48] This recommendation was adopted by the American Diabetes Association in 2010.[49] Positive tests should be repeated unless the person presents with typical symptoms and blood sugars >11.1mmol/l (>200mg/dl).[48]

Threshold for diagnosis of diabetes is based on the relationship between results of glucose tolerance tests, fasting glucose or HbA1c and complications such as retinal problems.[10] A fasting or random blood sugar is preferred over the glucose tolerance test, as they are more convenient for people.[10] HbA1c has the advantages that fasting is not required and results are more stable but has the disadvantage that the test is more costly than measurement of blood glucose.[50] It is estimated that 20% of people with diabetes in the United States do not realize that they have the disease.[10]

Diabetes mellitus type2 is characterized by high blood glucose in the context of insulin resistance and relative insulin deficiency.[51] This is in contrast to diabetes mellitus type 1 in which there is an absolute insulin deficiency due to destruction of islet cells in the pancreas and gestational diabetes mellitus that is a new onset of high blood sugars associated with pregnancy.[13] Type1 and type2 diabetes can typically be distinguished based on the presenting circumstances.[48] If the diagnosis is in doubt antibody testing may be useful to confirm type1 diabetes and C-peptide levels may be useful to confirm type2 diabetes,[52] with C-peptide levels normal or high in type2 diabetes, but low in type1 diabetes.[53]

No major organization recommends universal screening for diabetes as there is no evidence that such a program improve outcomes.[54][55] Screening is recommended by the United States Preventive Services Task Force (USPSTF) in adults without symptoms whose blood pressure is greater than 135/80mmHg.[56] For those whose blood pressure is less, the evidence is insufficient to recommend for or against screening.[56] There is no evidence that it changes the risk of death in this group of people.[55] They also recommend screening among those who are overweight and between the ages of 40 and 70.[57]

The World Health Organization recommends testing those groups at high risk[54] and in 2014 the USPSTF is considering a similar recommendation.[58] High-risk groups in the United States include: those over 45 years old; those with a first degree relative with diabetes; some ethnic groups, including Hispanics, African-Americans, and Native-Americans; a history of gestational diabetes; polycystic ovary syndrome; excess weight; and conditions associated with metabolic syndrome.[23] The American Diabetes Association recommends screening those who have a BMI over 25 (in people of Asian descent screening is recommended for a BMI over 23).[59]

Onset of type2 diabetes can be delayed or prevented through proper nutrition and regular exercise.[60][61] Intensive lifestyle measures may reduce the risk by over half.[24][62] The benefit of exercise occurs regardless of the person's initial weight or subsequent weight loss.[63] High levels of physical activity reduce the risk of diabetes by about 28%.[64] Evidence for the benefit of dietary changes alone, however, is limited,[65] with some evidence for a diet high in green leafy vegetables[66] and some for limiting the intake of sugary drinks.[32] A 2019 review found evidence of benefit from dietary fiber.[67]

In those with impaired glucose tolerance, diet and exercise either alone or in combination with metformin or acarbose may decrease the risk of developing diabetes.[24][68] Lifestyle interventions are more effective than metformin.[24] A 2017 review found that, long term, lifestyle changes decreased the risk by 28%, while medication does not reduce risk after withdrawal.[69] While low vitamin D levels are associated with an increased risk of diabetes, correcting the levels by supplementing vitamin D3 does not improve that risk.[70]

Management of type2 diabetes focuses on lifestyle interventions, lowering other cardiovascular risk factors, and maintaining blood glucose levels in the normal range.[24] Self-monitoring of blood glucose for people with newly diagnosed type2 diabetes may be used in combination with education,[71] however the benefit of self monitoring in those not using multi-dose insulin is questionable.[24][72] In those who do not want to measure blood levels, measuring urine levels may be done.[71] Managing other cardiovascular risk factors, such as hypertension, high cholesterol, and microalbuminuria, improves a person's life expectancy.[24] Decreasing the systolic blood pressure to less than 140mmHg is associated with a lower risk of death and better outcomes.[73] Intensive blood pressure management (less than 130/80mmHg) as opposed to standard blood pressure management (less than 140-160 mmHg systolic to 85100 mmHg diastolic) results in a slight decrease in stroke risk but no effect on overall risk of death.[74]

Intensive blood sugar lowering (HbA1c<6%) as opposed to standard blood sugar lowering (HbA1c of 77.9%) does not appear to change mortality.[75][76] The goal of treatment is typically an HbA1c of 7 to 8% or a fasting glucose of less than 7.2mmol/L (130mg/dl); however these goals may be changed after professional clinical consultation, taking into account particular risks of hypoglycemia and life expectancy.[59][77][78] Despite guidelines recommending that intensive blood sugar control be based on balancing immediate harms with long-term benefits, many people for example people with a life expectancy of less than nine years who will not benefit, are over-treated.[79]

It is recommended that all people with type2 diabetes get regular eye examination.[13] There is weak evidence suggesting that treating gum disease by scaling and root planing may result in a small short-term improvement in blood sugar levels for people with diabetes.[80] There is no evidence to suggest that this improvement in blood sugar levels is maintained longer than 4 months.[80] There is also not enough evidence to determine if medications to treat gum disease are effective at lowering blood sugar levels.[80]

A proper diet and exercise are the foundations of diabetic care,[23] with a greater amount of exercise yielding better results.[81] Exercise improves blood sugar control, decreases body fat content and decreases blood lipid levels, and these effects are evident even without weight loss.[82] Aerobic exercise leads to a decrease in HbA1c and improved insulin sensitivity.[83] Resistance training is also useful and the combination of both types of exercise may be most effective.[83]

A diabetic diet that promotes weight loss is important.[84] While the best diet type to achieve this is controversial,[84] a low glycemic index diet or low carbohydrate diet has been found to improve blood sugar control.[85][86] A very low calorie diet, begun shortly after the onset of type 2 diabetes, can result in remission of the condition.[87]

Vegetarian diets in general have been related to lower diabetes risk, but do not offer advantages compared with diets which allow moderate amounts of animal products.[88] There is not enough evidence to suggest that cinnamon improves blood sugar levels in people with type 2 diabetes.[89]

Culturally appropriate education may help people with type2 diabetes control their blood sugar levels, for up to 24 months.[90] If changes in lifestyle in those with mild diabetes has not resulted in improved blood sugars within six weeks, medications should then be considered.[23] There is not enough evidence to determine if lifestyle interventions affect mortality in those who already have DM2.[62]

There are several classes of anti-diabetic medications available. Metformin is generally recommended as a first line treatment as there is some evidence that it decreases mortality;[7][24][91] however, this conclusion is questioned.[92] Metformin should not be used in those with severe kidney or liver problems.[23]

A second oral agent of another class or insulin may be added if metformin is not sufficient after three months.[77] Other classes of medications include: sulfonylureas, thiazolidinediones, dipeptidyl peptidase-4 inhibitors, SGLT2 inhibitors, and glucagon-like peptide-1 analogs.[77] As of 2015 there was no significant difference between these agents.[77] A 2018 review found that SGLT2 inhibitors may be better than glucagon-like peptide-1 analogs or dipeptidyl peptidase-4 inhibitors.[93]

Rosiglitazone, a thiazolidinedione, has not been found to improve long-term outcomes even though it improves blood sugar levels.[94] Additionally it is associated with increased rates of heart disease and death.[95] Angiotensin-converting enzyme inhibitors (ACEIs) prevent kidney disease and improve outcomes in those with diabetes.[96][97] The similar medications angiotensin receptor blockers (ARBs) do not.[97] A 2016 review recommended treating to a systolic blood pressure of 140 to 150 mmHg.[98]

Injections of insulin may either be added to oral medication or used alone.[24] Most people do not initially need insulin.[13] When it is used, a long-acting formulation is typically added at night, with oral medications being continued.[23][24] Doses are then increased to effect (blood sugar levels being well controlled).[24] When nightly insulin is insufficient, twice daily insulin may achieve better control.[23] The long acting insulins glargine and detemir are equally safe and effective,[99] and do not appear much better than neutral protamine Hagedorn (NPH) insulin, but as they are significantly more expensive, they are not cost effective as of 2010.[100] In those who are pregnant insulin is generally the treatment of choice.[23]

Vitamin D supplementation to people with type 2 diabetes may improve markers of insulin resistance and HbA1c.[101]

Weight loss surgery in those who are obese is an effective measure to treat diabetes.[102] Many are able to maintain normal blood sugar levels with little or no medication following surgery[103] and long-term mortality is decreased.[104] There however is some short-term mortality risk of less than 1% from the surgery.[105] The body mass index cutoffs for when surgery is appropriate are not yet clear.[104] It is recommended that this option be considered in those who are unable to get both their weight and blood sugar under control.[106][107]

Globally as of 2015 it was estimated that there were 392million people with type2 diabetes making up about 90% of diabetes cases.[10][11] This is equivalent to about 6% of the world's population.[11] Diabetes is common both in the developed and the developing world.[10] It remains uncommon, however, in the least developed countries.[13]

Women seem to be at a greater risk as do certain ethnic groups,[10][108] such as South Asians, Pacific Islanders, Latinos, and Native Americans.[23] This may be due to enhanced sensitivity to a Western lifestyle in certain ethnic groups.[109] Traditionally considered a disease of adults, type2 diabetes is increasingly diagnosed in children in parallel with rising obesity rates.[10] Type2 diabetes is now diagnosed as frequently as type1 diabetes in teenagers in the United States.[13]

Rates of diabetes in 1985 were estimated at 30million, increasing to 135million in 1995 and 217million in 2005.[18] This increase is believed to be primarily due to the global population aging, a decrease in exercise, and increasing rates of obesity.[18] The five countries with the greatest number of people with diabetes as of 2000 are India having 31.7million, China 20.8million, the United States 17.7million, Indonesia 8.4million, and Japan 6.8million.[110] It is recognized as a global epidemic by the World Health Organization.[1]

Diabetes is one of the first diseases described[21] with an Egyptian manuscript from c. 1500 BCE mentioning "too great emptying of the urine."[111] The first described cases are believed to be of type1 diabetes.[111] Indian physicians around the same time identified the disease and classified it as madhumeha or honey urine noting that the urine would attract ants.[111] The term "diabetes" or "to pass through" was first used in 230BCE by the Greek Apollonius Of Memphis.[111] The disease was rare during the time of the Roman empire with Galen commenting that he had only seen two cases during his career.[111]

Type1 and type2 diabetes were identified as separate conditions for the first time by the Indian physicians Sushruta and Charaka in 400500AD with type1 associated with youth and type2 with being overweight.[111] The term "mellitus" or "from honey" was added by the Briton John Rolle in the late 1700s to separate the condition from diabetes insipidus which is also associated with frequent urination.[111] Effective treatment was not developed until the early part of the 20th century when the Canadians Frederick Banting and Charles Best discovered insulin in 1921 and 1922.[111] This was followed by the development of the long acting NPH insulin in the 1940s.[111]

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What is VetStem Regenerative Medicine? | Why Use Adipose …

January 21st, 2019 6:42 am

VetStem Technology: Summary

VetStem Regenerative Cell Therapy is based on a clinical technology licensed from Artecel Inc. Original patents are from the University of Pittsburgh and Duke University.

Adipose-derived regenerative cells are:

VetStem Regenerative Cell (VSRC) therapy delivers a functionally diverse cell population able to communicate with other cells in their local environment. Until recently, differentiation was thought to be the primary function of regenerative cells. However, the functions of regenerative cells are now known to be much more diverse and are implicated in a highly integrated and complex network. VSRC therapy should be viewed as a complex, yet balanced, approach to a therapeutic goal. Unlike traditional medicine, in which one drug targets one receptor, Regenerative Medicine, including VSRC therapy, can be applied in a wide variety of traumatic and developmental diseases. Regenerative cell functions include:

In general, in vitro studies demonstrate that MSCs limit inflammatory responses and promote anti-inflammatory pathways.

Multiple studies demonstrate that MSCs secrete bioactive levels of cytokines and growth factors that support angiogenesis, tissue remodeling, differentiation, and antiapoptotic events.25,28 MSCs secrete a number of angiogenesis-related cytokines such as:28

Adipose-derived MSC studies demonstrate a diverse plasticity, including differentiation into adipo-, osteo-, chondro-, myo-, cardiomyo-, endothelial, hepato-, neuro-, epithelial, and hematopoietic lineages, similar to that described for bone marrow derived MSCs.22 These data are supported by in vivo experiments and functional studies that demonstrated the regenerative capacity of adipose-derived MSCs to repair damaged or diseased tissue via transplant engraftment and differentiation.6,9,30

Homing (chemotaxis) is an event by which a cell migrates from one area of the body to a distant site where it may be needed for a given physiological event. Homing is an important function of MSCs and other progenitor cells and one mechanism by which intravenous or parenteral administration of MSCs permits an auto-transplanted therapeutic cell to effectively target a specific area of pathology.

Adipose-derived regenerative cells contain endothelial progenitor cells and MSCs that assist in angiogenesis and neovascularization by the secretion of cytokines, such as hepatic growth factor (HGF), vascular endothelial growth factor (VEGF), placental growth factor (PGF), transforming growth factor (TGF), fibroblast growth factor (FGF-2), and angiopoietin.25

Apoptosis is defined as a programmed cell death or cell suicide, an event that is genetically controlled.35 Under normal conditions, apoptosis determines the lifespan and coordinated removal of cells. Unlike during necrosis, apoptotic cells are typically intact during their removal (phagocytosis).

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Human Genetic Engineering Pros And Cons

January 19th, 2019 8:48 pm

Many human genetic engineering pros and cons are there that have stayed the same since its introduction to humanity. When the humans started harnessing the atomic powers, then just few years later they also start recognizing the effects of human genetic engineering on mankind. Many scientists have a belief that gene therapy can be a mainstream for saving lives of many people. A lot of human genetic engineering pros and cons have been involved since the evolution of genetic engineering. Mentioned below are some important advantages or pros of genetic engineering:

Other human genetic engineering pros and cons include the desirable characteristics in different plants and animals at the same time convenient. One can also do the manipulation of genes in trees or big plants. This will enable the trees to absorb increased amount of carbon dioxide, and it will reduce the effects of global warming. However, there is a question from critics that whether man has the right to do such manipulations or alterations in the genes of natural things.

With human genetic engineering, there is always a chance for altering the wheat plants genetics, which will then enable it to grow insulin. Human genetic engineering pros and cons have been among the concern of a lot of people involved in genetic engineering. Likewise the pros, certain cons are there of using the genetic engineering. Mentioned below are the cons of human genetic engineering:

The evolution of genetic engineering gets the consideration of being the biggest breakthroughs in the history of mankind after the evolution of atomic energy, and few other scientific discoveries. However, human genetic engineering pros and cons together have contributed a lot in creating a controversial image of it among the people.

All these eventualities have forced the government of many countries to make strict legislation laws to put restrictions on different experiment being made on human genetic engineering. They have made this decision by considering different human genetic engineering pros and cons.

Human Genetic Engineering Pros And Cons

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The Immune System Explained I Bacteria Infection

January 19th, 2019 8:47 pm

Every second of your life you are under attack. Bacteria, viruses, spores and more living stuff wants to enter your body and use its resources for itself. The immune system is a powerful army of cells that fights like a T-Rex on speed and sacrifices itself for your survival. Without it you would die in no time. This sounds simple but the reality is complex, beautiful and just awesome. An animation of the immune system.

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Why you are still alive - The immune system explained

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Stem cell therapy could be life-changing for some multiple …

January 19th, 2019 8:47 pm

An experimental treatment for multiple sclerosis is showing promise in stopping symptoms of the disease, according to a new study that found that a single stem cell transplant could stop or delay symptoms better than some medications. Just over 75 percent of patients who took drugs over a five-year period saw their disease get worse while less than 10 percent of those who had a transplant saw their condition worsen.

As CBS News' Dr. Tara Narula reports, this procedure could be life-changing for some of the 2.3 million people affected by the chronic condition worldwide. Narula met two women who struggled for years with a relapsing-remitting MS. But current drug treatments are expensive, most require daily medications and have serious side effects. These women decided to volunteer for a small clinical trial to test a risky stem cell procedure that appears to be paying off.

Amanda Loy never imagined she'd be battling the Alaska elements on her runs instead of battling her disease. Loy was diagnosed with relapsing-remitting MS, the form that comes and goes in sporadic episodes, bringing her life to a sudden halt.

"Both of my arms went numb and I wasn't really able to use them well," Loy said.

Every month she underwent a drug infusion and took half a dozen other medications, but her symptoms just got worse.

"I started having bladder problems and my balance was really bad, requiring the cane more often," she said. MS is an autoimmune disease where the body attacks itself and damages myelin, the protective covering surrounding nerve cells. With that insulation compromised, the nerves deteriorate and can cause a wide range of symptoms including vision problems, fatigue and weakness. So Loy traveled almost 3,000 miles to Chicago to participate in a trial with the hope of stopping the disease in its tracks.

"Transplants ended up being markedly superior in all the perimeters we looked at," said Dr. Richard Burt, who led the international trial at Northwestern Medicine. "You have to select the right group of patients there's these really aggressive ones that are very relapsing and inflammatory that it works extremely well in."

Here's how it works: a patient's own stem cells are collected and stored. During a two-week stay in the hospital, high-dose chemo is given to wipe out the immune system. Then, the stem cells are infused back into the patient to "re-boot" the body's immune system.

Trudee Manderfield was just 23 when she received her diagnosis. She had trouble walking and temporarily went blind in one eye. In 2013, with an infant daughter, she was ready to try the new treatment. She was scared, but excited about the possibilities.

"I knew that I couldn't just keep going the way that I was going," Manderfield said. "There's a lot of potential side effects, I mean any procedure will have a side effect of death and, as a new mom, I go 'OK, well that would be bad' but I knew that I had to give it a shot."

The transplant might not be a permanent fix. There are serious risks like infertility, infection, and even death. As for Manderfield, she's keeping up with her three active children and Amanda Loy plans to head back to Chicago, not for treatment, but to run the city's marathon in October.

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Integrative Medicine Clinic in Cape Coral, FL

January 18th, 2019 3:46 pm

Integrative Medical Approach

Integrative medicine places the patient at the center of a holistic approach to medical care. Patient's individual needs, risks, and goals are the main driving forces of any integrative therapy. Physicians practicing integrative medicine emphasize that treatment of every aspect of a person's health is crucial to the success of the healing process:

To request more information, please contact our Cape Coral integrative medicine clinic today! Call (239) 425-2900 or contact Dr. Doreen DeStefano online.

Integrative medicine is a multi-disciplinary approach that combines the scientific advances and a variety of effective therapies to treat disease.

Integrative medicine combines conventional and complementary treatment options to achieve optimal health for the patient. It is based on the research which demonstrates that the human body has an innate healing mechanism. Illness occurs when the regenerative processes in the body are disturbed, and the body can no longer keep itself healthy.

Integrative medicine emphasizes the use of the least invasive treatment options necessary to bring the body to a healthy state.

Integrative medicine physicians focus on health optimization and often combine a variety of methods to optimize their patients' health:

To request more information, please contact our Cape Coral integrative medicine clinic today! Call (239) 425-2900 or contact Dr. Doreen DeStefano online.

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Ophthalmology | Overlake EyeCare in Bellevue, WA

January 17th, 2019 9:44 am

Overlake EyeCare has the unique benefit of having Dr. Mary Coday, our Harvard trained ophthalmologist.

Ophthalmology focuses on treating diseases and conditions that affect the anatomy and physiology of the eye. What this means is that an ophthalmologist takes care of both surgical procedures and medical care for the eye. They are specialists in dealing with multiple eye diseases and conditions.

Becoming an ophthalmologist requires a medical degree and completing residency like other branches of medicine. Some ophthalmologists can undergo additional training if they choose and focus on a specialty within the field.

Ophthalmology training covers the entire spectrum of eye care. Ophthalmologists are trained to do thorough eye exams to prescribe glasses or contact lenses, offer medical treatment for assorted eye problems, and do complex and delicate eye surgeries for qualified candidates.

An ophthalmologist is a licensed medical doctor, so they are permitted to practice medicine and surgery. At Overlake EyeCare ouroptometrists and ophthalmologistwork together to provide complete eye care for ourpatients.

The field of ophthalmology includes multiple sub-specialties where an ophthalmologist can focus on treating and curing specific types of eye problems. This can make it easier to address specific needs of eye patients.

These ophthalmology sub-specialties include:

Cornea and External Disease: Diagnosing and treating diseases related to the cornea, sclera and eyelids are the primary focus of this specialty. Training within this specialty includes doing corneal transplant surgery and other types of corneal surgery.

Glaucoma: This specialty concentrates on medical and surgical treatment of glaucoma and other age related vision disorders that can create optic nerve damage through increased ocular pressure.

Neuro-ophthalmology: A nonsurgical specialty focused on diseases affecting the optic nerve and visual pathways. It deals with the relationship between neurologic and ophthalmic diseases and can be combined with eye and orbital surgery.

Ophthalmic Pathology: An ophthalmic pathologist examines tissue samples culled from the eye and adnexa in helping to diagnose eye diseases and vision problems.

Ophthalmic Plastic Surgery: With this specialty, the focus is on reconstructive surgery in facial and orbital areas. It can include complex surgeries on eyelids, orbits, certain facial bones, and the lacrimal system.

Pediatric Ophthalmology: This specialty focuses on dealing with vision problems and eye diseases affecting children. Pediatric ophthalmologists offer medical and surgical treatment of genetic ocular abnormalities and serious eye diseases before a patient reaches adulthood.

Vitreoretinal Diseases: Medical and surgical treatment of diseases affecting the retina and vitreous are the focus of this specialty. These diseases can be genetic and systemic in origin. A vitreoretinal ophthalmologist uses tools like ultrasound fluorescein, angiography and electrophysiology to make a diagnosis. From there, they treat vitreoretinal diseases through using such procedures as laser therapy, cryotherapy, retinal detachment surgery and vitrectomy.

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Progressive Medical Center – Integrative & Holistic Medicine

January 15th, 2019 8:47 am

Integrative & Holistic Medicine

We're here to answer your questions! 770-676-6000 X

Before we discuss who we are and what we do, we want to answer the most important question of all "What is Integrative Medicine?"

Integrative Medicine is a partnership between the patient and the practitioner in the healing process appropriately using conventional and natural therapies to facilitate the bodys natural healing response.

What are the principles of integrative medicine?

Where traditional medicine focuses on the symptoms, integrative medicine looks to identify and treat the root cause of why the symptom is occurring in the first place.

If you have a chronic headaches, a traditional physician will give you a prescription in order to minimize your headaches.

We take this further and ask the question, Why do you have a headache? Through the use of state of art diagnostics we have helped patients identify the root cause such as dehydration, food sensitivities, inflammation, etc.

The goal is to stop their symptoms from occurring. Integrative medicine does not replace traditional medicine; it actually enhances it by allowing the body to heal through the partnership of the patient and physician.

Good medicine should be inquiry-driven and be open to new paradigms. The use of natural, less invasive, interventions are used whenever possible, unless it is an acute infection. This includes the use of broader concepts or promotion of health, and the prevention of illness, as well as the treatment of disease.

An ounce of prevention is worth a pound of a cure. If you prevent a disease, youll be able to handle more acute situations more effectively.

Integrative medicine uses a team approach. We have medical doctors, osteopathic doctors, naturopathic doctors, chiropractors, and dietitians who work together. Each practitioner comes to us with a unique background in Integrative Medicine & combined with our commitment to ongoing education we are leading a medical movement in Integrative Medicine. That is what makes Progressive Medical Center unique.

Can You Solve My Problem?

Traditional medicine is effective for treating acute infection and conditions of that sort, but remarkably ineffective at successfully treating chronic conditions where patients often experience pain for months or even years on end. This is where Integrative Medicine triumphs. If youve experienced a prolonged struggle with any medical issue then an integrative solution may be what you need to significantly improve your quality of life.

Allergies

Anti-aging

Bio-identical Hormones

Chronic Fatigue

Depression

Diabetes

Fibromyalgia

Joint Pain

Menopause

Migraines

Sleep Disorders

Thyroid Disorder

Viral Infections

Weight Management

All I can say is Progressive Medical Center is the most AMAZING place I've ever been. I have m (...)

I was desperate when I came to Progressive. I was impressed by their approach of seeking and t (...)

The team of doctors did not give me a band aid to treat my symptoms. They worked together to f (...)

The staff at PMC collectively has been most supportive in helping me be a healthy person again.

The treatment was so beneficial and helpful. After one visit, I knew I was in good hands. I ha (...)

After 6 visits going to PMC 3 times a week I started noticing a big difference. I was able to (...)

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The doctors at Progressive are by far some of the very best chiropractic healers I have encoun (...)

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The doctors at PMC helped change my overall health, not just through Chiropractic but with con (...)

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I have learned so much about healthy living through Progressive Medical Center. I love knowing (...)

With the help of doctors at Progressive, I have overcome my osteopenia and my bone density is (...)

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I love this place. The doctors are awesome. I have thyroid issues that are finally more balanc (...)

I was impressed from the start. My son's stubborn acne that he suffered with is all but gone. (...)

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Richard & Abigail Gonzalez

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Dr. Melissa Arnold is at the top of her profession. I'm quick to recommend her work to anyone. (...)

Contact UsYour email address will never be shared with any 3rd parties. Any information will be kept confidential.

Individual results of therapies and treatments may vary. Anecdotes of Customer Success and Customer Success Stories are anecdotal and results of treatment as always are specific to the individual.

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