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Our Doctors – Knee Stem Cells

Posted: March 17, 2019 at 5:45 pm

Dennis M. Lox, M.D. Knee Stem Cell Treatments have been seen Across The Nation.

Dennis M Lox, M.D. is an expert in Knee Stem Cell Injections for those who seek an alternative to the unnecessary complex knee surgery of that in the past by providing Knee Stem Cell Treatment. Dennis M. Lox, M.D. has privately owned Medical Centers that do not partake in the fast chain franchise that other Stem Cell Centers are stuck doing, thus he is able provide a more personalized treatment for your particular injury.

Dennis M. Lox, M.D. centers have a professional, caring environment for patients looking for comfort in their time of need and provids follow-ups on your wellbeing to enhance your recovery. Dennis M. Lox, M.D. has been helping patients since 1990 nationally and internationally and has been the focus of the Stem Cell News Worldwide with his expertise and he continually researches new technologies to further Stem Cell advancements.

PUBLICATIONS:

Lox, D.M., Heine, M.W., and Lox, C.D., Hemostatic Alterations Resulting from Chronic Ethanol Ingestion during Tetracycline Therapy in the Rat, Neurobeh, Toxiocol: Vol. 7, 1985.

Lox, C.D. and Lox, D.M., Effects of Acute Ethanol Intoxication Combined with Secobarbitol Abuse on Homeostasis, General Pharm Vol. 16, 1985. 252-258.

PRESENTATIONS:

Lox, D.M., Sports Medicine and Stem Cells: A Clinical Transformation Presentation at the Select Biosciences Conference: Tissue Engineering and Bio printing, Boston, Massachusetts, February 2015

Lox, D.M., Clinical Regulation of Cytokine and Inflammatory Pathways with Autologous Stem Cell Therapy Presentation at the 17th Clinical Applications for Age Management Medicine Group, The Bellagio Hotel, Las Vegas, Nevada, October 2014

Lox, D.M., Moderator 3rd Annual International Conference on Tissue Science and Regeneration, Valencia, Spain, September 2014

Lox, D.M., Athletes and Avascular Necrosis Presentation at the 3rd Annual International Conference on Tissue Science and Regeneration, Valencia, Spain, September 2014Lox, D.M., Managing Sports and Arthritic Complaints with Stem Cells, Presentation at the Select Biosciences Clinical Translation of Stem Cells, Palm Desert, California, April 2014

Lox, D.M., A Professional Football Player with Failed Knee Surgery: A Case of Treatment with Adipose Derived Stem Cells, Presentation at the Tissue Engineering and Regenerative Medicine International Society Asia Chapter (Termis AP) Annual Conference, Shanghai, China, Oct. 2013

Lox, D.M., Chronic Foot Pain in a Ballerina: Treatment with Regenerative Medicine Presentation at the Tissue Engineering and Regenerative Medicine International Society Asia Pacific Chapter (Termis AP) Annual Conference, Shanghai, China, October 2013

Lox, D.M., Knee Osteoarthritis: Quality of Life (Q o L) Measures Following Autologous Stem Cell Therapy Presentation at the International Cartilage Repair Society Annual Meeting, Izmir, Turkey, September 2013

Lox, D.M., Cytokine Modulation with Nutraceuticals as a Synergistic Mechanism for Regenerative Grafting in Osteoarthritis Repair Presentation at the Tissue Engineering and Regenerative Medicine International Society Meeting, Istanbul, Turkey, June 2013

Lox, D.M., Arthritis: Quality of Life (Q o L) Measures following Mesenchymal Stem Cell Therapy Presentation at the Tissue Engineering and Regenerative Medicine International Society Meeting, Istanbul, Turkey, June 2013

Lox, D.M., Can Healthcare Outcomes Be Quantified with Stem Cell Therapy in Osteoarthritis?

Presentation at the World Stem Cell Summit, West Palm Beach, Fl. December 2012

Lox, D.M., Regenerative Rehabilitation of an Elite Soccer Player, Presentation at the First Annual Symposium on Regenerative Rehabilitation, Pittsburgh, PA, November 3-4, 2011.

Lox, D.M., Regenerative Medicine and Tissue Engineering: Ethical Concerns with Health Care Reform, Presentation at the 2011 World Stem Cell Summit, Pasadena, CA on October 2011.

Lox, D.M., Autologous Adipose-Derived Stem Cells in the Rehabilitation of a Soccer Player, Presentation at the Stem Cells Europe 2011 Conference, Edinburgh, Scotland on July 2011.

Lox, D.M., Autologous Human Adipose-Derived Mesenchymal Stem Cells in Orthopedic Medicine: A Veterinary Correlate, Presentation at the 2nd North American Veterinary Regenerative Medicine Conference, Lexington, Kentucky on June 2011.

Lox, D.M., Regenerative Medicine Techniques in Musculoskeletal Medicine, Presented at the

11th Annual Conference of the International Neural Transplantation and Repair, Sand Key, FL on May 2011.

Lox, D.M., Current Regenerative Medicine Techniques, Tampa, Florida on July 10, 2010.

Lox, D.M., Complex Regional Pain Syndrome Course Presentation, American Academy of Physical Medicine and Rehabilitation Annual Assembly (Moderator: Dennis M. Lox, M.D. Speakers: Jose Ochoa, M.D., Gabor Racz, M.D., Dennis M. Lox, M.D.); Seattle, Washington on November 5, 1998.

Lox, D.M., New Treatments in Myofascial Pain and Fibromyalgia, Presented at the Morton Plant/Mease Health Education Center Countryside, Florida on December 13, 2001.

Lox, D.M., Acute Spinal and Pain Syndromes Presented to the Pinellas County Primary Care and OB/GYN physicians, sponsored by Knoll Pharmaceuticals, 1998.

Lox, D.M., Complex Musculoskeletal Assessment and Treatment, Presented to the Zenith Insurance Company; Sarasota, Florida on September 28, 1998.

Lox, D.M., Fibromyalgia, Presented to Cigna Health Care Physicians, sponsored by Health South Rehabilitation Corporation; Tampa, Florida on September 19, 1998.

Lox, D.M., Evaluation of the Difficult Pain Patient, Presented to the Pinellas County Orthopedic Journal Club, sponsored by Knoll Pharmaceuticals; Clearwater, Florida on September 8, 1998.

Lox, D.M., Fibromyalgia, Presented to the Travelers Insurance Company, sponsored by Health South Rehabilitation Corporation; Tampa, Florida on August 19, 1998.

Lox, D.M., Complex Pain Management, Presented to the Physicians of Collier County, sponsored by Knoll Pharmaceuticals; Naples, Florida on May 16, 1998.

Lox, D.M., Managing Pain in a Managed Care, Presented to the Pinellas County Podiatric Medical Association Meeting; Clearwater, Florida on April 14, 1998.

Lox, D.M., Complex Regional Pain Syndrome: The Historical Perspective from Bonica and Beyond, Presented at the 7th Annual John J. Bonica Vail Winter Pain Conference, sponsored by the Ohio State University Medical Center, College of Medicine, Department of Anesthesiology; Vail, Colorado on March 1998.

Lox, D.M., Pain Management, Presented to Lee County Physicians, sponsored by Knoll Pharmaceuticals; Ft. Myers, Florida in December 1998.

Lox, D.M., Managing Pain in a Managed Care Environment, Presented to the Pinellas County Physicians, sponsored by Knoll pharmaceuticals; Clearwater, Florida in December 1997.

Lox, D.M., Regional Pain Syndrome Update, Presented at the 74th Annual Meeting of the American Congress of Rehabilitation Medicine Pain ISIG; Boston, Massachusetts in September 1997.

Lox, D.M., Physical Medicine for Women Who Hurt all Over (Physical and Somatization Considerations, and Complex Regional Pain Syndrome Update, Presented at the 9th Annual OB/GYN Summer Symposium, Womens Health Care in the 90s, sponsored by the University of Oklahoma Health Sciences Center College of Medicine, Department of Obstetrics and Gynecology; Jackson Hole, Wyoming in August 1997.

Lox, D.M., Replacing the Terms of Reflex Sympathetic Dystrophy and Sympathetically Maintained Pain-An Uphill Battle, Presented at the 13th Annual Update in Physical Medicine and Rehabilitation, sponsored by the University of Utah School of Medicine, Division of Physical Medicine and Rehabilitation, Park City, Utah, March 1997.

Lox, D.M., Complex Regional Pain Syndrome, Presented to Claim Management, Utilization Management, Case Managers, Adjustors and Supervisors of the Travelers/Aetna Insurance Companies; Orlando, Florida in August 1996.

Lox, D.M., Soft Tissue Injuries/RSD/Fibromyalgia-The Rational or Irrational Approach to Diagnosis and Treatment, Presented to Claim Management, Utilization Management, Case Managers and Supervisors of Travelers Insurance Company; Tampa, Florida, 1996.

Lox, D.M., Overview of the Soft Tissue Injury/RSD/Fibromyalgia-The Rational or Irrational Approach to Diagnosis and Treatment, Presented to the Regional Adjustors and Personnel of Geico Insurance Company; Macon, Georgia in May 1996.

Lox, D.M., Causalgia/RSD/SMP-History and Treatment, Presented during the Re-Employment rules of Florida Workers= Compensation Conference, sponsored by the Southwest Chapter of NARPPS in May 1996 (2 CME credits).

Lox, D.M., RSD-Treatment Options for the 90s, Presented to the Florida Association of Rehabilitation Professionals in the Private Sector (FARPPS) in March 1996 (2 CME credits).

Lox, D.M., Causalgia/RSD/SMP-The 100 Year War, Presented to The Florida Association of Rehabilitation Professionals in the Private Sector in January 1996 (2 CME credits)

Lox, D.M., The Differential Diagnosis of Spinal Injuries, Presented to the Intracorp Rehabilitation Nurses in April 1992 (4 CME credits).

Lox, D.M., A Physiatrist Approach to Industrial Industries, Presented to the Florida Rehabilitation Nurses in May 1991 (4 CME credits).

Lox, D.M., Skiing Injuries: Prevention and Rehabilitation, Presented at the North American Medical and Dental Association Seminar; Vail, Colorado in February 1989.

Lox, D.M., The Failed Back Patient, Presented at the Annual Texas Physical Medicine and Rehabilitation Society Meeting; Austin, Texas in August 1989.

Lox, D.M., Dermatomal Somatosensory Evoked Potentials and Gadolinium-MRI in the Evaluation of Chronic Low Back Pain, Presented at the 50th Annual Session of the American Academy of Physical Medicine and Rehabilitation; San Antonio, Texas in November 1989.

Lox, D.M., The Evaluation and Treatment of Lumbar Spine Disorders, Presented at the University of Texas Health Science Center at San Antonio, Department of Allied Health; San Antonio, Texas in December 1988.

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Our Doctors - Knee Stem Cells

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Stem Cell Treatment Center in Dallas, Texas | Stem Cell …

Posted: March 17, 2019 at 5:45 pm

Foot and ankle wounds are very common among athletes, and a considerable lot of these wounds can be dealt with non-carefully with stem cell therapy, platelet-rich plasma or prolotherapy, depending upon the nature of the damage. Ankle arthritis is also essential as we age, although many of us may experience joint pain sooner than expected because of ankle damage in our younger days. Stem cell therapy in Dallas offers the country's most developed stem cell and platelet medications for foot and ankle wounds and degenerative conditions. Look for Texas stem cell treatment center & get in touch with us today for an appointment, our stem cell therapy centers in USA is famous for stem cell therapy texas we have expert surgeons for various treatment such as foot therapy Dallas. We are one of the best stem cell treatment centers in USA which are very popular for stem cell therapy in USA.

The term arthritis is utilized to describe different conditions that demolish the inner workings of your joints. Pain can occur in any joint of your body, including your ankles and any of the 30 joints in each foot.

Osteoarthritis is the most widely common form. This dynamic illness gradually wears away joint cartilage and results from the wear and tear of maturity. It implies osteoarthritis is well on the way to strike after middle age.

Rheumatoid joint pain (RA) is a fiery malady that irritates the joint lining and causes torment. The condition can strike at any age and affect any joint. People who have lived with RA for a long time or all the more quite often experience the condition in their feet or ankles. Opt for foot therapy Dallas & get the treatment.

Post-traumatic arthritis creates the following damage. It can happen following a broken bone, torn ligament or moderate lower leg sprain, regardless of whether the damage gets proper restorative attention. Visit stem cell clinics in USA & get the appropriate treatment.

Regardless of what degree or sort of arthritis you're experiencing, texas stem cells treatment center will provide therapy which decreases the effect of pain.

Half of adults age 60 to 80 have joint pain in their feet and don't know it since they experience no side effects. In case you're not one of the fortunate ones, your ankle and foot arthritis is probably going to cause these symptoms:

Pain and solidness, making it hard to walk regularly

Delicate joints that feel warm to the touch

Twisted ankles and toes

Deadness and shivering spreading from the affected joint

At the point when the above treatment choices aren't sufficient, you have another choice before you fall back on medical surgery: stem cell therapy texas. On account of ongoing recent strides in healthcare and science, stem cell therapy centers in USA are more effective than any other time at treating arthritis of the ankle and foot. The method is necessary and non-careful, involving simply a single in-office injection.

Stem cell therapy in Dallas can frequently effectively replace ordinary arthritis medicines, for example, taking mitigating drugs.

Arthritis

Instability

Plantar fasciitis

Peroneal ligament agony or damage

Ligament pain or injury

Subtalar arthritis or insecurity

Bunions

The human body keeps a supply of stem cells accessible to help repair harmed and degenerated tissues consistently, making it genuinely easy to recover them for therapeutic purposes.

As stem cells stay available for later, in the marrow cavity of your bones, we have discovered the easiest place to harvest these stem cells is from the back of the hip area (iliac bone).

The methodology is done in the office, under ultrasound or x-ray exactness and direction.

Patients lay face down as the specialist thoroughly cleans the area before numbing the skin and bone.

A special needle is embedded into the issue that remains to be worked out marrow blood, which contains the stem cells.

After bone marrow blood is drawn, it is taken to the research facility and centrifuged to concentrate and purify the stem cells while other cells that are not required are removed, leaving a concentrated example of stem cells used to help heal your damage.

The whole procedure is done in Texas stem cells treatment center by surgeons to empower altered designing of the stem cell example for your specific damage.

Preparation of your concentrated platelets are additionally gathered as of now for injection into the damage site to release growth factors that "turn on" the stem cells that will later be injected.

These platelets are infused again 3 after 5 days to keep the stem cells actuated and advance extra healing.

There are many stem cell clinics in, but very few clinics are specialized in their work if you are a person & want to avoid surgery the look for stem cell therapy in Dallas & get the therapy from the expert therapist. Texas stem cell treatment center has the potential to heal many types of damaged tissue, opt for stem cell treatment centers in USA & consult with an expert.

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Stem Cell Treatment Center in Dallas, Texas | Stem Cell ...

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Stem Cell Treatment Clinic St. Augustine – Florida Stem Cell

Posted: March 17, 2019 at 5:44 pm

Heal naturally.Use your own stem cells.At Florida Stem Cell, it is our priority to provide you with options that use your bodys healing mechanism to rebuild and repair your joints utilizing yourstem cells.

Free advice.We provide you with objective and honest recommendations that offer a natural approach to become pain-free while also repairing and rebuilding your joints.

About us.Our team here at Florida Stem Cell is proud and confident that we are offering one of the best orthopedic stem cell programs available in Florida.

Payment plans available.Thousands of patients have trusted United Medical Credit to secure affordable payment plans for their stem cell procedures.

Request a consultation.Have a quick question? Want to schedule a consultation? We are always available to help find out if stem cell therapy is for you.

Introducing a new and better way to heal joints.

Stem Cell Therapy for Arthritis, Injuries & Joint Pain.

Do you havejoint pain, back pain, neck pain or some other orthopedic problem or injury that is not getting better?

Are you interestedin new technology that can heal most orthopedic and musculoskeletal problems faster and better than standard approaches, without the need of surgery?

AtFlorida Stem Cell we specialize in rebuilding joint, back and neck structures using a persons own stem cells. Stem cells are like little workers that can regrow cartilage, ligaments, tendons and even bone. By taking some fat in a simple outpatient procedure, separating out the stem cells and then mixing them with some growth factors (PRP) from a small blood draw we have a powerful tool to rebuild almost any joint in the body.

if you have encountered an injury to the knee cartilage, ACL or MCL ligaments, stem cells may be right for you. Learn more.

Ifyou experience severe lower back pain due an injury in the past,stem cells may be right for you. Learn more.

Doyouhavechronicpain from injury or arthritis?You might be a strong candidate for our natural procedures. Learn more.

Word ofmouth is alwaysthebest advice.

Here are some of the kind words

from our customers.

I am a 67 year old healthy, active female. I began experiencing hip discomfort a year ago during my daily 3 mile walk. Thank You for returning me to a happy, healthy, functioning life!

Ms. J. G. | 67 | St. Augustine, FL

I am delighted to report that I now have almost no pain in my hip & pelvis. My walking is greatly improved.Thank you forrestoring my ability to keep my hip & be practically pain free. Miracles do happen.

Mr. S. G | 82 | St. Augustine, FL

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Stem Cell Treatment Clinic St. Augustine - Florida Stem Cell

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Practical Problems with Embryonic Stem Cells – usccb.org

Posted: March 17, 2019 at 5:43 pm

While some researchers still claim that embryonic stem cells (ESCs) offer the best hope for treating many debilitating diseases, there is now a great deal of evidence contrary to that theory. Use of stem cells obtained by destroying human embryos is not only unethical but presents many practical obstacles as well.

"Major roadblocks remain before human embryonic stem cells could be transplanted into humans to cure diseases or replace injured body parts, a research pioneer said Thursday night. University of Wisconsin scientist James Thomson said obstacles include learning how to grow the cells into all types of organs and tissue and then making sure cancer and other defects are not introduced during the transplantation. 'I don't want to sound too pessimistic because this is all doable, but it's going to be very hard,' Thomson told the Wisconsin Newspaper Association's annual convention at the Kalahari Resort in this Wisconsin Dells town. 'Ultimately, those transplation therapies should work but it's likely to take a long time.'....Thomson cautioned such breakthroughs are likely decades away."

-Associated Press reporter Ryan J. Foley "Stem cell pioneer warns of roadblocks before cures," San Jose Mercury News Online, posted on Feb. 8, 2007, http://www.mercurynews.com/mld/mercurynews/16656570.htm

***

"Although embryonic stem cells have the broadest differentiation potential, their use for cellular therapeutics is excluded for several reasons: the uncontrollable development of teratomas in a syngeneic transplantation model, imprinting-related developmental abnormalities, and ethical issues."

-Gesine Kgler et al., "A New Human Somatic Stem Cell from Placental Cord Blood with Intrinsic Pluripotent Differentiation Potential," Journal of Experimental Medicine, Vol. 200, No. 2 (July 19, 2004), p. 123.

***

From a major foundation promoting research in pancreatic islet cells and other avenues for curing juvenile diabetes:

"Is the use of embryonic stem cells close to being used to provide a supply of islet cells for transplantation into humans?

"No. The field of embryonic stem cells faces enormous hurtles to overcome before these cells can be used in humans. The two key challenges to overcome are making the stem cells differentiate into specific viable cells consistently, and controlling against unchecked cell division once transplanted. Solid data of stable, functioning islet cells from embryonic stems cells in animals has not been seen."

-"Q & A," Autoimmune Disease Research Foundation, http://www.cureautoimmunity.org/Q%20&%20A.htm, accessed July 2004.

***

"'I think the chance of doing repairs to Alzheimer's brains by putting in stem cells is small,' said stem cell researcher Michael Shelanski, co-director of the Taub Institute for Research on Alzheimer's Disease and the Aging Brain at the Columbia University Medical Center in New York, echoing many other experts. 'I personally think we're going to get other therapies for Alzheimer's a lot sooner.'...

"[G]iven the lack of any serious suggestion that stem cells themselves have practical potential to treat Alzheimer's, the Reagan-inspired tidal wave of enthusiasm stands as an example of how easily a modest line of scientific inquiry can grow in the public mind to mythological proportions.

"It is a distortion that some admit is not being aggressively corrected by scientists.

"'To start with, people need a fairy tale,' said Ronald D.G. McKay, a stem cell researcher at the National Institute of Neurological Disorders and Stroke. 'Maybe that's unfair, but they need a story line that's relatively simple to understand.'"

-Rick Weiss, "Stem Cells an Unlikely Therapy for Alzheimer's," Washington Post, June 10, 2004, p. A3.

***

"ES [embryonic stem] cells and their derivatives carry the same likelihood of immune rejection as a transplanted organ because, like all cells, they carry the surface proteins, or antigens, by which the immune system recognizes invaders. Hundreds of combinations of different types of antigens are possible, meaning that hundreds of thousands of ES cell lines might be needed to establish a bank of cells with immune matches for most potential patients. Creating that many lines could require millions of discarded embryos from IVF clinics."

-R. Lanza and N. Rosenthal, "The Stem Cell Challenge," Scientific American, June 2004, pp. 92-99 at p. 94. [Editor's note: A recent study found that only 11,000 frozen embryos are available for research use from all the fertility clinics in the U.S., and that destroying all these embryos for their stem cells might produce a total of 275 cell lines. See Fertility and Sterility, May 2003, pp. 1063-9 at p. 1068.]

***

"Embryonic stem cells have too many limitations, including immune rejection and the potential to form tumors, to ever achieve acceptance in our lifetime. By that time, umbilical cord blood stem cells will have been shown to be a true 'gift from the gods.'"

-Dr. Roger Markwald, Professor and Chair of Cell Biology and Anatomy at the Medical University of South Carolina, quoted in "CureSource Issues Statement on Umbilical Cord Blood Stem Cells vs. Embryonic Stem Cells," BusinessWire, May 12, 2004, also at http://curesource.net/why.html.

***

"'We're not against stem-cell research of any kind,' said [Tulane University research professor Brian] Butcher. 'But we think there are advantages to using adult stem cells. For example, with embryonic stem cells, a significant number become cancer cells, so the cure could be worse than the disease. And they can be very difficult to grow, while adult stem cells are easy to grow.'"

-Heather Heilman, "Great Transformations," The Tulanian (Spring 2004 issue), at http://www2.tulane.edu/article_news_details.cfm?ArticleID=5155.

***

"There are still many hurdles to clear before embryonic stem cells can be used therapeutically. For example, because undifferentiated embryonic stem cells can form tumors after transplantation in histocompatible animals, it is important to determine an appropriate state of differentiation before transplantation. Differentiation protocols for many cell types have yet to be established. Targeting the differentiated cells to the appropriate organ and the appropriate part of the organ is also a challenge."

-E. Phimister and J. Drazen, "Two Fillips for Human Embryonic Stem Cells," New England Journal of Medicine, Vol. 350 (March 25, 2004), pp. 1351-2 at 1351.

***

Harvard researchers, trying to create human embryonic stem cell lines that are more clinically useful than those now available, find that their new cell lines are already genetically abnormal:

"After prolonged culture, we observed karyotypic changes involving trisomy of chromosome 12..., as well as other changes... These karyotypic abnormalities are accompanied by a proliferative advantage and a noticeable shortening in the population doubling time. Chromosomal abnormalities are commonplace in human embryonal carcinoma cell lines and in mouse embryonic stem-cell lines and have recently been reported in human embryonic stem-cell lines."

-C. Cowan et al., "Derivation of Embryonic Stem-Cell Lines from Human Blastocysts," New England Journal of Medicine, Vol. 350 (March 25, 2004), pp. 1353-6 at 1355.

***

"[Johns Hopkins University] biologist Michael Shamblott said...major scientific hurdles await anybody wishing to offer a treatment, let alone a cure, based on cells culled from embryos.

"Among the major obstacles is the difficulty of getting embryonic stem cells master cells that generate every tissue in the human body to become exactly the type of cell one wants... Scientists...haven't been able to guarantee purity cells, for instance, that are destined to become muscle cells and nothing else...

"Transplanting a mixed population of cells could cause the growth of unwanted tissues. The worst case could see stem cells morphing into teratomas, particularly gruesome tumors that can contain hair, teeth and other body parts.

"Another issue is timing... Stem cells pass through many intermediate stages before they become intermediate cells such as motor neurons or pancreatic or heart cells. Deciding when to transplant remains an open question, and the answer might differ from disease to disease.

"...In tackling Lou Gehrig's disease, [Johns Hopkins neurologist Dr. Jeffrey] Rothstein figured that cells that haven't committed themselves to becoming motor neurons would stand the best chance, once implanted, of reaching out and connecting with the cells that surround them. What he found, however, is that these immature cells didn't develop much once transplanted into lab animals."

-Jonathan Bor, "Stem Cells: A long road ahead," Baltimore Sun, March 8, 2004, p. 12A.

***

"Tony Blau, a stem-cell researcher at the University of Washington, said it is 'extremely laborious' to keep embryonic cells growing, well-nourished and stable in the lab so they don't die or turn into a cell type with less potential. Researchers need to know how to channel the stem cells to create a specific kind of cell, how to test whether they're pure, and how to develop drugs that could serve as a sort of antidote in case infused stem cells started creating something dangerous, such as cancer.

"Big companies, Blau said, want to know that their drugs will be almost completely stable, standard, pure and consistent, because they can behave differently if they aren't. Stem cells never will achieve that kind of standardization, Blau said, because living cells are more complex than chemically synthesized drugs."

-Luke Timmerman, "Stem-cell research still an embryonic business," Seattle Times, Business & Technology section, February 22, 2004, at http://seattletimes.nwsource.com/html/businesstechnology/2001862747_stemcells22.html.

***

"[W]ithin the ESC research community, realism has overtaken early euphoria as scientists realize the difficulty of harnessing ESCs safely and effectively for clinical applications. After earlier papers in 2000 and 2001 identified some possibilities, research continued to highlight the tasks that lie ahead in steering cell differentiation and avoiding side effects, such as immune rejection and tumorigenesis."

-Philip Hunter, "Differentiating Hope from Embryonic Stem Cells," The Scientist, Vol. 17, Issue 34 (December 15, 2003), at http://www.the-scientist.com/yr2003/dec/hot_031215.html.

***

"Long-term culture of mouse ES [embryonic stem] cells can lead to a decrease in pluripotency and the gain of distinct chromosomal abnormalities. Here we show that similar chromosomal changes, which resemble those observed in hEC [human embryonal carcinoma] cells from testicular cancer, can occur in hES [human embryonic stem] cells.... The occurrence and potential detrimental effects of such karyotopic changes will need to be considered in the development of hES cell-based transplantation therapies."

-J. Draper et al., "Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells," Nature Biotechnology, Vol. 22 (2003), pp. 53-4.

***

"James A. Thompson of the University of Wisconsin, Madison, and his colleagues managed to isolate and culture the first human embryonic stem cells in 1997. Five years later, big scientific questions remain. [Harvard embryonic stem cell researcher Doug] Melton and his colleagues, for instance, don't yet know how to instruct the totipotent stem cells to become the specific cells missing in a diabetic person, the pancreatic beta cell.

"'Normally, if you take an embryonic stem cell, it will make all kinds of things, sort of willy-nilly,' says Melton."

-J. Mitchell, "Stem Cells 101," PBS Scientific American Frontiers, May 28, 2002, http://www.pbs.org/saf/1209/features/stemcell.htm.

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"Unlike stem cells isolated from the embryo, [adult stem cells] do not carry the same risks of cancer or uncontrollable growth after transplant, and they can be isolated from patients requiring treatment, thus avoiding all problems of immune rejection and the need for immune suppressive drugs that carry their own risks.

"...Embryonic stem cells are promoted on grounds that they are developmentally more flexible than adult stem cells. But too much flexibility may not be desirable. Transplant of embryonic cells into the brains of Parkinson's patients turned into an irredeemable nightmare because the cells grew uncontrollably. Embryonic stem cells also show genetic instability and carry considerable risks of cancer... When injected under the skin of certain mice, they grow into teratomas, tumors consisting of a jumble of tissue types, from gut to skin to teeth, and the same happens when injected into the brain."

-Dr. Mae-Wan Ho and Prof. Joe Cummins on behalf of the Institute of Science in Society (ISIS), "Hushing Up Adult Stem Cells," ISIS report, February 11, 2002, at http://www.i-sis.org.uk/HUASC.php.

***

"'I even hear from patients whose fathers have lung cancer,' said Dr. Hogan, a professor at Vanderbilt School of Medicine. 'They have a whole slew of problems they think can be treated. They think stem cells are going to cure their loved ones of everything.'

"If it ever happens, it will not happen soon, scientists say. In fact, although they worked with mouse embryonic stem cells for 20 years and made some progress, researchers have not used these cells to cure a single mouse of a disease...

"Scientists say the theory behind stem cells is correct: the cells, in principle, can become any specialized cell of the body. But between theory and therapy lie a host of research obstacles...the obstacles are so serious that scientists say they foresee years, if not decades, of concerted work on basic science before they can even think of trying to treat a patient."

-Gina Kolata, "A Thick Line Between Theory and Therapy, as Shown with Mice," New York Times, December 18, 2001, p. F3.

***

"Mice cloned from embryonic stem cells may look identical, but many of them actually differ from one another by harboring unique genetic abnormalities, scientists have learned...

"The work also shows for the first time that embryonic stem cells...are surprisingly genetically unstable, at least in mice. If the same is true for human embryonic stem cells, researchers said, then scientists may face unexpected challenges as they try to turn the controversial cells into treatments for various degenerative conditions."

-Rick Weiss, "Clone Study Casts Doubt on Stem Cells," Washington Post, July 6, 2001, p. A1.

***

"ES cells have plenty of limitations... For one, murine ES cells have a disturbing ability to form tumors, and researchers aren't yet sure how to counteract that. And so far reports of pure cell populations derived from either human or mouse ES cells are few and far between fewer than those from adult stem cells."

-Gretchen Vogel, "Can Adult Stem Cells Suffice?", Science, Vol. 292 (June 8, 2001), pp. 1820-1822 at 1822.

***

"Rarely have specific growth factors or culture conditions led to establishment of cultures containing a single cell type.... [T]he possibility arises that transplantation of differentiated human ES cell derivatives into human recipients may result in the formation of ES cell-derived tumors... Irrespective of the persistence of stem cells, the possibility for malignant transformation of the derivatives will also need to be addressed."

-J. S. Odorico et al, "Multilineage differentiation from human embryonic stem cell lines," Stem Cells Vol. 19 (2001), pp. 193-204 at 198 and 200, at http://stemcells.alphamedpress.org/cgi/reprint/19/3/193.pdf.

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Practical Problems with Embryonic Stem Cells - usccb.org

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Stem Cell Therapy | Board Certified Orthopedic Surgeon …

Posted: March 16, 2019 at 10:43 pm

STEM CELL THERAPY

Traditionally, options for patients suffering from sports-related injury or a degenerative condition such as osteoarthritis have been limited. Patients whose conditions were not severe, and who were not yet ready for a surgical solution, were afforded less invasive options such as cortisone or steroid shots and physical therapy, which can provide temporary relief from pain and swelling. However, patients with more serious conditions were required to undergo invasive surgical procedures (i.e. total joint replacement) to find any relief from their painful symptoms. Luckily, ground-breaking medical innovations have led to another option: stem cell therapy.

Unlike surgical treatment options, this revolutionary technology is minimally invasive, but offers a more permanent solution than traditional cortisone/steroid injections because it harnesses and maximizes the bodys natural self-healing abilities. The tissues of the body that are most vulnerable to sports injury or degenerative conditionsmuscles, cartilage, tendons, and ligamentshave a limited capacity for repair and self-healing.

Stem cell therapy, which utilizes adult stem cells or amniotic stem cells taken from the amniotic sac (controversial embryonic stem cells are not utilized at any point), can help in several ways:

For patients suffering from knee osteoarthritis, tendonitis, ligament or tendon tears, plantar fasciitis, and even bunions, stem cell therapy offers a safe, effective, permanent way to promote self-healing so patients can quickly get back onto their feet and resume their active lifestyle.

CONTACT DR. GOUGH

Brandon Gough, M.D. is an orthopaedic expert specializing in the treatment of orthopaedic problems caused by sports injury, osteoarthritis, and other degenerative orthropaedic disorders. Dr. Gough operates his own orthopaedic practice out of the prestigious Orthopaedic Institute of the West in Phoenix, Arizona. He also has operating privileges at Scottsdale Abrazo and Thompson Peak Hospital in the Phoenix/Scottsdale area. He specializes in state-of-the-art surgical and non-surgical approaches to orthopaedic problems, including stem cell therapy and micro-invasive and robotic surgical techniques. Staying abreast of the latest medical innovations allows Dr. Gough to assess every patients unique needs quickly and correctly, and offer the widest range of possible treatment options, ensuring a more permanent, effective solution to each individuals unique problem.

If you would like additional information about Dr. Goughs orthopaedic practice, or have questions about how stem cell therapy can help you, please contact our office today. We look forward to speaking with you, and to scheduling your initial consultation with Dr. Gough.

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Welcome to the SBC – Seed Biotechnology Center

Posted: March 16, 2019 at 10:42 pm

The mission of the Seed Biotechnology Center (SBC)is to mobilize the research, educational and outreach resources of UC Davis in partnership with the seed and biotechnology industries to facilitate discovery and commercialization of new seed technologies for agricultural and consumer benefit.

A team of researchers including SBC Director of Research, Dr. Allen Van Deynze and Cristobal Heitmann, discover an indigenous variety of corn that can fix nitrogen from the atmosphere, instead of requiring synthetic fertilizers. Cristobal Heitman, Cris, was a beloved member of the UC Davis Plant Sciences Department. Criss energy and enthusiasm were a major catalyst in this research. Read more.

Plant Breeding Academy Addresses Global Food Needs

UC Davis' Department of Plant Sciences shares how PBA is changing the global food supply one scientist at a time.Read article.

A DryCardis the latest technology to improve the shelf-life of seeds. Dr. Kent Bradford, SBCDirector, describes how the amazingDryCard works. Read more.

Comstock Magazine highlighted the value of locating Sakatas Woodland Innovation Center in the Sacramento Valley. The regions fertile soil and ideal climate make it one of the best places in the world for seed production. In addition, its close proximity to UC Davis will allow Sakata to strengthen its already existing ties to the university. Learn more.

Scientists could engineer a spicy tomato. Is it worth it?

Scientists are working on growing a spicy tomato. Dr. Allen Van Deyneze, SBC Director of Research shares his insight on the research. Read article.

Benson Hill Teams Up with The African Orphan Crops Consortium to Combat Malnutrition Through Underutilized Crops

Allen Van Deynze, Director of Research, Seed Biotechnology Center, University of California, Davis and Scientific Director of the African Orphan Crops Consortium highlights effort to accelerate the ability of African scientists to develop better seeds and improve the diets of Africas children. Learn more

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Stem Cell | Regenerative medicine | 2019 | Conference …

Posted: March 16, 2019 at 10:41 pm

Responsibility

The organizers holds no responsibilities orliabilities of the personal articles of attendees at the venue against any kindof theft, lost, damage, due to any reason whatsoever. Delegates are entirelyresponsible for the safety of their own belongings.

Insurance

No insurance, of any kind, is included along withthe registration in any of the events of the organization.

Transportation

Please note that transportation and parking is the responsibilityof the registrant, Allied Academies will not be liable for any actionshowsoever related to transportation and parking.

Press/Media

Press permission must be obtained from AlliedAcademies Conference Organizing Committee prior to the event. The press willnot quote speakers or delegates unless they have obtained their approval inwriting. The Allied Academies is an objective third-party nonprofitorganization and this conference is not associated with any commercial meetingcompany.

Requesting an Invitation Letter

For security purposes, letter of invitation will besent only to those individuals who had registered for the conference afterpayment of complete registration fee. Once registration is complete, pleasecontactstemcell@alliedevents.org

Cancellation Policy

All cancellations or modifications of registrationmust be made in writing to finance@alliedacademies.com

If, due to any reason, Allied academies postpone anevent on the scheduled date, the participant is eligible for a credit of 100%of the registration fee paid. This credit shall only be used for another eventorganized by Allied academies within period of one year from the date ofrescheduling.

Postponement of event

If, due to any reason, Allied academies postpone anevent and the participant is unable or unwilling to attend the conference onrescheduled dates, he/she is eligible for a credit of 100% of the registrationfee paid. This credit shall only be used for another event organized by Alliedacademies within period of one year from the date of rescheduling.

Transfer of registration

All registrations, after payment of completeregistration fee, are transferable to other persons from the same organization,if in case the person is unable to attend the event. Request for transfer ofregistration must be made by the registered person in writing to contacts@alliedacademies.com Details mustinclude the full name of replaced new registrant, their title, contact phonenumber and email address. All other registration details will be assigned tothe new person unless otherwise specified. Registration can be transferred toone conference to another conference of Allied academies if the person isunable to attend one of conferences.

However, Registrationcannot be transferred if intimated within 14 days of respective conference.

The transferredregistrations will not be eligible for Refund.

This cancellation policywas last updated on April 04, 2015.

Visa Information

Keeping in view of increased security measures, wewould like to request all the participants to apply for Visa as soon aspossible.

Allied academies will notdirectly contact embassies and consulates on behalf of visa applicants. Alldelegates or invitees should apply for Business Visa only.

Important note for failed visa applications: Visaissues are not covered under the cancellation policy of Allied academies,including the inability to obtain a visa.

Refund Policy.

If the registrant is unable to attend, and is notin a position to transfer his/her participation to another person or event,then the following refund policies apply:

Keeping in view of advance payments towards Venue,Printing, Shipping, Hotels and other overhead charges, following Refund Policy

Orders are available:

Accommodation Cancellation Policy

Accommodation Service Providers (Hotels) have theirown cancellation policies which are applicable when cancellations are made lessthan 30 days prior to arrival. If in case the registrant wishes to cancel oramend the accommodation, he/ she is expected to inform the organizingauthorities on a prior basis. Allied academies will advise the registrant toensure complete awareness about the cancellation policy of your accommodationprovider, prior to cancellation or modification of their booking.

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Diabetes – Diagnosis and treatment – Mayo Clinic

Posted: March 16, 2019 at 12:46 am

Diagnosis

Symptoms of type 1 diabetes often appear suddenly and are often the reason for checking blood sugar levels. Because symptoms of other types of diabetes and prediabetes come on more gradually or may not be evident, the American Diabetes Association (ADA) has recommended screening guidelines. The ADA recommends that the following people be screened for diabetes:

Glycated hemoglobin (A1C) test. This blood test, which doesn't require fasting, indicates your average blood sugar level for the past two to three months. It measures the percentage of blood sugar attached to hemoglobin, the oxygen-carrying protein in red blood cells.

The higher your blood sugar levels, the more hemoglobin you'll have with sugar attached. An A1C level of 6.5 percent or higher on two separate tests indicates that you have diabetes. An A1C between 5.7 and 6.4 percent indicates prediabetes. Below 5.7 is considered normal.

If the A1C test results aren't consistent, the test isn't available, or you have certain conditions that can make the A1C test inaccurate such as if you're pregnant or have an uncommon form of hemoglobin (known as a hemoglobin variant) your doctor may use the following tests to diagnose diabetes:

Oral glucose tolerance test. For this test, you fast overnight, and the fasting blood sugar level is measured. Then you drink a sugary liquid, and blood sugar levels are tested periodically for the next two hours.

A blood sugar level less than 140 mg/dL (7.8 mmol/L) is normal. A reading of more than 200 mg/dL (11.1 mmol/L) after two hours indicates diabetes. A reading between 140 and 199 mg/dL (7.8 mmol/L and 11.0 mmol/L) indicates prediabetes.

If type 1 diabetes is suspected, your urine will be tested to look for the presence of a byproduct produced when muscle and fat tissue are used for energy because the body doesn't have enough insulin to use the available glucose (ketones). Your doctor will also likely run a test to see if you have the destructive immune system cells associated with type 1 diabetes called autoantibodies.

Your doctor will likely evaluate your risk factors for gestational diabetes early in your pregnancy:

Your doctor may use the following screening tests:

Initial glucose challenge test. You'll begin the glucose challenge test by drinking a syrupy glucose solution. One hour later, you'll have a blood test to measure your blood sugar level. A blood sugar level below 140 mg/dL (7.8 mmol/L) is usually considered normal on a glucose challenge test, although this may vary at specific clinics or labs.

If your blood sugar level is higher than normal, it only means you have a higher risk of gestational diabetes. Your doctor will order a follow-up test to determine if you have gestational diabetes.

Follow-up glucose tolerance testing. For the follow-up test, you'll be asked to fast overnight and then have your fasting blood sugar level measured. Then you'll drink another sweet solution this one containing a higher concentration of glucose and your blood sugar level will be checked every hour for a period of three hours.

If at least two of the blood sugar readings are higher than the normal values established for each of the three hours of the test, you'll be diagnosed with gestational diabetes.

Depending on what type of diabetes you have, blood sugar monitoring, insulin and oral medications may play a role in your treatment. Eating a healthy diet, maintaining a healthy weight and participating in regular activity also are important factors in managing diabetes.

An important part of managing diabetes as well as your overall health is maintaining a healthy weight through a healthy diet and exercise plan:

Healthy eating. Contrary to popular perception, there's no specific diabetes diet. You'll need to center your diet on more fruits, vegetables, lean proteins and whole grains foods that are high in nutrition and fiber and low in fat and calories and cut down on saturated fats, refined carbohydrates and sweets. In fact, it's the best eating plan for the entire family. Sugary foods are OK once in a while, as long as they're counted as part of your meal plan.

Yet understanding what and how much to eat can be a challenge. A registered dietitian can help you create a meal plan that fits your health goals, food preferences and lifestyle. This will likely include carbohydrate counting, especially if you have type 1 diabetes.

Physical activity. Everyone needs regular aerobic exercise, and people who have diabetes are no exception. Exercise lowers your blood sugar level by moving sugar into your cells, where it's used for energy. Exercise also increases your sensitivity to insulin, which means your body needs less insulin to transport sugar to your cells.

Get your doctor's OK to exercise. Then choose activities you enjoy, such as walking, swimming or biking. What's most important is making physical activity part of your daily routine.

Aim for at least 30 minutes or more of aerobic exercise most days of the week. Bouts of activity can be as brief as 10 minutes, three times a day. If you haven't been active for a while, start slowly and build up gradually.

Treatment for type 1 diabetes involves insulin injections or the use of an insulin pump, frequent blood sugar checks, and carbohydrate counting. Treatment of type 2 diabetes primarily involves lifestyle changes, monitoring of your blood sugar, along with diabetes medications, insulin or both.

Monitoring your blood sugar. Depending on your treatment plan, you may check and record your blood sugar as many as four times a day or more often if you're taking insulin. Careful monitoring is the only way to make sure that your blood sugar level remains within your target range. People with type 2 diabetes who aren't taking insulin generally check their blood sugar much less frequently.

People who receive insulin therapy also may choose to monitor their blood sugar levels with a continuous glucose monitor. Although this technology hasn't yet completely replaced the glucose meter, it can significantly reduce the number of fingersticks necessary to check blood sugar and provide important information about trends in blood sugar levels.

Even with careful management, blood sugar levels can sometimes change unpredictably. With help from your diabetes treatment team, you'll learn how your blood sugar level changes in response to food, physical activity, medications, illness, alcohol, stress and for women, fluctuations in hormone levels.

In addition to daily blood sugar monitoring, your doctor will likely recommend regular A1C testing to measure your average blood sugar level for the past two to three months.

Compared with repeated daily blood sugar tests, A1C testing better indicates how well your diabetes treatment plan is working overall. An elevated A1C level may signal the need for a change in your oral medication, insulin regimen or meal plan.

Your target A1C goal may vary depending on your age and various other factors, such as other medical conditions you may have. However, for most people with diabetes, the American Diabetes Association recommends an A1C of below 7 percent. Ask your doctor what your A1C target is.

Insulin. People with type 1 diabetes need insulin therapy to survive. Many people with type 2 diabetes or gestational diabetes also need insulin therapy.

Many types of insulin are available, including rapid-acting insulin, long-acting insulin and intermediate options. Depending on your needs, your doctor may prescribe a mixture of insulin types to use throughout the day and night.

Insulin can't be taken orally to lower blood sugar because stomach enzymes interfere with insulin's action. Often insulin is injected using a fine needle and syringe or an insulin pen a device that looks like a large ink pen.

An insulin pump also may be an option. The pump is a device about the size of a cellphone worn on the outside of your body. A tube connects the reservoir of insulin to a catheter that's inserted under the skin of your abdomen.

A tubeless pump that works wirelessly also is now available. You program an insulin pump to dispense specific amounts of insulin. It can be adjusted to deliver more or less insulin depending on meals, activity level and blood sugar level.

An emerging treatment approach, not yet available, is closed loop insulin delivery, also known as the artificial pancreas. It links a continuous glucose monitor to an insulin pump, and automatically delivers the correct amount of insulin when needed.

There are a number of versions of the artificial pancreas, and clinical trials have had encouraging results. More research needs to be done before a fully functional artificial pancreas receives regulatory approval.

However, progress has been made toward an artificial pancreas. In 2016, an insulin pump combined with a continuous glucose monitor and a computer algorithm was approved by the Food and Drug Administration. However, the user still needs to tell the machine how many carbohydrates will be eaten.

Oral or other medications. Sometimes other oral or injected medications are prescribed as well. Some diabetes medications stimulate your pancreas to produce and release more insulin. Others inhibit the production and release of glucose from your liver, which means you need less insulin to transport sugar into your cells.

Still others block the action of stomach or intestinal enzymes that break down carbohydrates or make your tissues more sensitive to insulin. Metformin (Glucophage, Glumetza, others) is generally the first medication prescribed for type 2 diabetes.

Transplantation. In some people who have type 1 diabetes, a pancreas transplant may be an option. Islet transplants are being studied as well. With a successful pancreas transplant, you would no longer need insulin therapy.

But transplants aren't always successful and these procedures pose serious risks. You need a lifetime of immune-suppressing drugs to prevent organ rejection. These drugs can have serious side effects, which is why transplants are usually reserved for people whose diabetes can't be controlled or those who also need a kidney transplant.

Bariatric surgery. Although it is not specifically considered a treatment for type 2 diabetes, people with type 2 diabetes who are obese and have a body mass index higher than 35 may benefit from this type of surgery. People who've undergone gastric bypass have seen significant improvements in their blood sugar levels. However, this procedure's long-term risks and benefits for type 2 diabetes aren't yet known.

Controlling your blood sugar level is essential to keeping your baby healthy and avoiding complications during delivery. In addition to maintaining a healthy diet and exercising, your treatment plan may include monitoring your blood sugar and, in some cases, using insulin or oral medications.

Your doctor also will monitor your blood sugar level during labor. If your blood sugar rises, your baby may release high levels of insulin which can lead to low blood sugar right after birth.

If you have prediabetes, healthy lifestyle choices can help you bring your blood sugar level back to normal or at least keep it from rising toward the levels seen in type 2 diabetes. Maintaining a healthy weight through exercise and healthy eating can help. Exercising at least 150 minutes a week and losing about 7 percent of your body weight may prevent or delay type 2 diabetes.

Sometimes medications such as metformin (Glucophage, Glumetza, others) also are an option if you're at high risk of diabetes, including when your prediabetes is worsening or if you have cardiovascular disease, fatty liver disease or polycystic ovary syndrome.

In other cases, medications to control cholesterol statins, in particular and high blood pressure medications are needed. Your doctor might prescribe low-dose aspirin therapy to help prevent cardiovascular disease if you're at high risk. However, healthy lifestyle choices remain key.

Because so many factors can affect your blood sugar, problems may sometimes arise that require immediate care, such as:

Increased ketones in your urine (diabetic ketoacidosis). If your cells are starved for energy, your body may begin to break down fat. This produces toxic acids known as ketones. Watch for loss of appetite, weakness, vomiting, fever, stomach pain and a sweet, fruity breath.

You can check your urine for excess ketones with an over-the-counter ketones test kit. If you have excess ketones in your urine, consult your doctor right away or seek emergency care. This condition is more common in people with type 1 diabetes.

Hyperglycemic hyperosmolar nonketotic syndrome. Signs and symptoms of this life-threatening condition include a blood sugar reading over 600 mg/dL (33.3 mmol/L), dry mouth, extreme thirst, fever, drowsiness, confusion, vision loss and hallucinations. Hyperosmolar syndrome is caused by sky-high blood sugar that turns blood thick and syrupy.

It is seen in people with type 2 diabetes, and it's often preceded by an illness. Call your doctor or seek immediate medical care if you have signs or symptoms of this condition.

Low blood sugar (hypoglycemia). If your blood sugar level drops below your target range, it's known as low blood sugar (hypoglycemia). If you're taking medication that lowers your blood sugar, including insulin, your blood sugar level can drop for many reasons, including skipping a meal and getting more physical activity than normal. Low blood sugar also occurs if you take too much insulin or an excess of a glucose-lowering medication that promotes the secretion of insulin by your pancreas.

Check your blood sugar level regularly, and watch for signs and symptoms of low blood sugar sweating, shakiness, weakness, hunger, dizziness, headache, blurred vision, heart palpitations, irritability, slurred speech, drowsiness, confusion, fainting and seizures. Low blood sugar is treated with quickly absorbed carbohydrates, such as fruit juice or glucose tablets.

Explore Mayo Clinic studies testing new treatments, interventions and tests as a means to prevent, detect, treat or manage this disease.

Diabetes is a serious disease. Following your diabetes treatment plan takes round-the-clock commitment. Careful management of diabetes can reduce your risk of serious even life-threatening complications.

Make physical activity part of your daily routine. Regular exercise can help prevent prediabetes and type 2 diabetes, and it can help those who already have diabetes to maintain better blood sugar control. A minimum of 30 minutes of moderate exercise such as brisk walking most days of the week is recommended.

A combination of exercises aerobic exercises, such as walking or dancing on most days, combined with resistance training, such as weightlifting or yoga twice a week often helps control blood sugar more effectively than does either type of exercise alone.

It's also a good idea to spend less time sitting still. Try to get up and move around for a few minutes at least every 30 minutes or so when you're awake.

In addition, if you have type 1 or type 2 diabetes:

Keep your vaccinations up-to-date. High blood sugar can weaken your immune system. Get a flu shot every year, and your doctor may recommend the pneumonia vaccine, as well. The Centers for Disease Control and Prevention (CDC) also currently recommends hepatitis B vaccination if you haven't previously been vaccinated against hepatitis B and you're an adult ages 19 to 59 with type 1 or type 2 diabetes.

The most recent CDC guidelines advise vaccination as soon as possible after diagnosis with type 1 or type 2 diabetes. If you are age 60 or older, have diabetes, and haven't previously received the vaccine, talk to your doctor about whether it's right for you.

If you drink alcohol, do so responsibly. Alcohol can cause either high or low blood sugar, depending on how much you drink and if you eat at the same time. If you choose to drink, do so only in moderation one drink a day for women and two drinks a day for men and always with food.

Remember to include the carbohydrates from any alcohol you drink in your daily carbohydrate count. And check your blood sugar levels before going to bed.

Numerous substances have been shown to improve insulin sensitivity in some studies, while other studies fail to find any benefit for blood sugar control or in lowering A1C levels. Because of the conflicting findings, there aren't any alternative therapies that are currently recommended to help everyone with blood sugar management.

If you decide to try any type of alternative therapy, don't stop taking the medications that your doctor has prescribed. Be sure to discuss the use of any of these therapies with your doctor to make sure that they won't cause adverse reactions or interact with your current therapy.

Additionally, there are no treatments alternative or conventional that can cure diabetes, so it's critical that people who are receiving insulin therapy for diabetes don't stop using insulin unless directed to do so by their physicians.

Living with diabetes can be difficult and frustrating. Sometimes, even when you've done everything right, your blood sugar levels may rise. But stick with your diabetes management plan, and you'll likely see a positive difference in your A1C when you visit your doctor.

Because good diabetes management can be time-consuming, and sometimes overwhelming, some people find it helps to talk to someone. Your doctor can probably recommend a mental health professional for you to speak with, or you may want to try a support group.

Sharing your frustrations and your triumphs with people who understand what you're going through can be very helpful. And you may find that others have great tips to share about diabetes management.

Your doctor may know of a local support group, or you can call the American Diabetes Association at 800-DIABETES (800-342-2383) or the Juvenile Diabetes Research Foundation at 800-533-CURE (800-533-2873).

You're likely to start by seeing your primary care doctor if you're having diabetes symptoms. If your child is having diabetes symptoms, you might see your child's pediatrician. If blood sugar levels are extremely high, you'll likely be sent to the emergency room.

If blood sugar levels aren't high enough to put you or your child immediately at risk, you may be referred to a doctor who specializes in diabetes, among other disorders (endocrinologist). Soon after diagnosis, you'll also likely meet with a diabetes educator and a dietitian to get more information on managing your diabetes.

Here's some information to help you get ready for your appointment and to know what to expect.

Preparing a list of questions can help you make the most of your time with your doctor. For diabetes, some questions to ask include:

Your doctor is likely to ask you a number of questions, such as:

Aug. 08, 2018

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Diabetes | National Institutes of Health (NIH)

Posted: March 16, 2019 at 12:46 am

In the 1950s, about 1 in 5 people died within 20 years after being diagnosed with type 1 diabetes, formerly known as juvenile diabetes. Almost all of them developed diabetic retinopathy, which accounted for about 12% of new cases of blindness between the ages of 45 and 74. People with diabetes relied on inaccurate urine tests to track their blood sugar. They used crude animal-derived insulins to control it.

In 1983, NIH began the Diabetes Control and Complications Trial, which enrolled 1,441 people with type 1 diabetes. This landmark study was stopped early because the results so clearly showed that careful control of blood sugar reduced eye, kidney, and nerve complications by 50% to 75%. In a follow-up study 10 years later, researchers learned that rates of heart disease and stroke had declined by half.

Today, people with type 1 diabetes are living longer and healthier lives. New technologies help them keep tight control of their blood sugar using continuous glucose monitors and insulin pumps that deliver rapid-acting, bioengineered human insulin.

We also know a lot more about type 2 diabetes. We know that family history, obesity, and physical inactivity are risk factors for this condition, formerly known as adult-onset diabetes. NIH-funded research has shown that type 2 diabetes can be delayed or prevented. Basic lifestyle interventions modest weight loss and regular exercise slash type 2 diabetes risk by 58% over 3 years in people with pre-diabetes. Despite this good news, type 2 diabetes still accounts for 90% of diabetes cases nationwide and has been increasing at an alarming rate due to the rise in obesity in the United States.

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7 Warning Signs and Symptoms of Type 2 Diabetes

Posted: March 16, 2019 at 12:46 am

More than 100 million American adults are living withprediabetesor type 2 diabetes, according to the latest estimates from the Centers for Disease Control and Prevention (CDC). But the number of people who know they have the diseases which can lead to life-threatening complications, like blindness and heart disease is far lower.

Data from theCDCsuggests that of the estimated 30.3 million Americans withtype 2 diabetes, 7.2 million, or 1 in 4 adults living with the disease, are not aware of it. And among those people living withprediabetes, only 11.6 percent are aware that they have the disease.

Prediabetesis marked by higher than normal blood sugar levels though not high enough to qualify as diabetes. TheCDCnotes that this condition often leads to full-blown type 2 diabetes within five years if it's left untreated through diet and lifestyle modifications.

Type 2 diabetes, which is often diagnosed when a person has anA1Cof at least 7 on two separate occasions, can lead to potentially serious issues, likeneuropathy, or nerve damage; vision problems; an increased risk of heart disease; and otherdiabetes complications. A persons A1C is the two- to three-month average of his or her blood sugar levels.

According to theMayo Clinic, doctors may use other tests to diagnose diabetes. For example, they may conduct a fasting blood glucose test, which is a blood glucose test done after a night of fasting. While a fasting blood sugar level of less than 100 milligrams per deciliter (mg/dL) is normal, one that is between 100 to 125 mg/dL signalsprediabetes, and a reading that reaches 126 mg/dL on two separate occasions means you have diabetes.

People with full-blown type 2 diabetes are not able to use the hormone insulin properly, and have whats called insulin resistance. Insulin is necessary for glucose, or sugar, to get from your blood into your cells to be used for energy. When there is not enough insulin or when the hormone doesnt function as it should glucose accumulates in the blood instead of being used by the cells. This sugar accumulation may lead to the aforementioned complications.

You can help assessyour chances of developing type 2 diabetesby requesting an A1C test from your doctor, as well as by talking with your family about their health history with the disease, asyour geneticsmay influence your risk of diabetes.

Other risk factors of type 2 diabetes include obesity, inactivity, old age, a personal history of gestational diabetes, and race, according to theMayo Clinic. For instance, if you are Hispanic, African-American, or Asian-American, you may be at a greater risk of type 2 diabetes.

Nevertheless, you can preventprediabetesand type 2 diabetes by maintaining a healthy weight; following a healthy diet thats rich in whole grains, fruit, vegetables, and lean protein; getting sufficient sleep; and exercising regularly.

But preventing the disease from progressing if you already have it requires first being able to spot the signs and symptoms of diabetes when they appear. While sometype 2 diabetes symptomsmay not ever show up, you can watch out for the following common signs of the disease and alert your doctor, especially if you have any of the common risk factors for diabetes. Also keep in mind that while most signs of type 2 diabetes are the same in men and women, there are some distinctions.

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