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Regenerative Medicine Jobs, Employment | Indeed.com

January 11th, 2019 11:44 pm

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Functional Endocrinology of Ohio

Independence, OH 44131

$45,000 - $70,000 a year

ADVANCED STEM CELL INSTITUTE

Encino, CA 91316

Amnesty Health Group / Regenerative Health 360

Knoxville, TN

$100,000 - $150,000 a year

Pinnacle Intergrative Health PS

Seattle, WA

$2,000 - $3,000 a month

BlueRock Therapeutics

Amari Health

Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for...

BlueRock Therapeutics

BlueRock Therapeutics

Newbridge Health & Wellness

BlueRock Therapeutics

Centeno Schultz Clinic

Broomfield, CO

$18 - $20 an hour

Vitality Stem Cell and Aesthetic clinics

Roseville, CA

$40,000 - $100,009 a year

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Research Associate salaries in United States

$49,527 per year

Indeed Salary Estimate

Please note that all salary figures are approximations based upon third party submissions to Indeed. These figures are given to the Indeed users for the purpose of generalized comparison only. Minimum wage may differ by jurisdiction and you should consult the employer for actual salary figures.

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Regenerative Medicine Market Size | Industry Trends Report …

January 11th, 2019 11:44 pm

Industry Insights

The global regenerative medicine market size was estimated at USD 1,792.1 million in 2016. In recent years, regenerative medicine has emerged with promising approaches to treat complicated degenerative disorders as well as to support & restore the function of tissues and cells in other therapies. Rising prevalence of neurodegenerative, orthopedic, oncology, and genetic diseases coupled with advances in gene therapy, tissue engineering, and nanotechnology to support regenerative therapies are expected to boost revenue growth.

The industry has been witnessed to have a very strong pipeline with YoY increase in the number of products gaining approval for clinical application as well as the number of products entering into investigational trials for potential analysis. Growth is restricted due to regulatory and ethical issues in associated fields such as stem cells (SC) and gene editing. However, introduction of changes in regulatory policies and rise in demand for effective therapies to treat complicated disorders is projected to reduce the impact of these barriers over the forecast period.

UK regenerative medicine market revenue by product type, 2014 - 2025 (USD Million)

In addition, high investments by government and private organizations that support R&D, further encourage industry progress. Initiatives by government organizations to support stem cell & regenerative medicine R&D by providing funds and infrastructure facilities along with initiating various programs is expected to influence growth.

For instance, National Institutes of Health (NIH) supports scientific research community through NIH Regenerative Medicine Program, International SC Research, State Initiatives for Stem Cell Research, NIH SC Unit, NIH SC Libraries & Projects, and NIH SC Translation Laboratory.

Active participation by key companies is witnessed through strategic collaborations with academic institutes, government organizations, and major pharmaceutical & biotechnology companies. These initiatives are projected to make significant contributions in market expansion.

Considerable number of therapies in clinical trials are a collaborative effort of the market entities. Furthermore, key players are engaged in partnerships with universities to support development and gain commercial rights over innovative therapies.

Emerging technological advances in cell-based and gene therapies are attributed to be the major contributors to the industry progress. Introduction of flexible regulatory environment to conduct cell therapy research is expected to make lucrative contribution in market growth. IPSCs have witnessed rapid adoption in stem cell R&D to develop solutions for unmet clinical needs to treat complicated disorders.

On the contrary, regulatory restrictions to use HESC along with stringent regulatory norms that govern their application limits the market growth. However, identifying the potential clinical applications in countries such as U.S., UK, China, and Japan have introduced changes in their regulatory policies to encourage research. Thus, the industry is projected to reflect accelerated growth over the forecast period.

Gene therapy is projected to witness increased adoption in research owing to advances in gene sequencing and editing technology. Introduction of CRISPR and Cas gene technology that would to accelerate speed and enhance efficacy of gene-related research are expected to encourage use of gene therapy in treatment of genetic, metabolic, and degenerative disorders. Limited growth in gene therapy and Genetically Modified (GM) cell therapy is attributive to stringent regulatory restrictions pertaining the use of this technology.

Furthermore, advances in tissue engineering technology such as 3D printing of cells and tissues on scaffolds for transplant to restoring structural and functional characteristics of damaged cells, tissues, and organs is expected to make lucrative contributions towards market growth.

Dermatology is estimated to have largest share in revenue generation. This high contribution is attributive to presence of easy grafting techniques for dermatological wounds and diseases. Skin, being an organ with great cell replication characteristics, provides various types of stem cells from its different layers. Presence of broad range of product portfolio from patches to cure small injuries to matrix and grafts for chronic wounds and burns is expected to continue to dominate market through to the forecast period.

Owning to rise in demand for functional and structural restoration therapies along with rising incidences of bone & joint disorders, musculoskeletal segment is estimated to witness fastest growth. Rising prevalence of osteoarthritis with increase in geriatric population is anticipated to accelerate the segment growth.

Global regenerative market revenue by therapeutic category, 2016 (%)

Oncology is observed to be most promising segment owing to presence of strong pipeline of products and high investments in oncology research to treat as well as support treatment of various types of cancer, especially in incidences of cancer relapse. High incidence along with rising expenditure in treatment of oncology diseases have accelerated the developmental efforts in this segment. However, challenges in clinical trials are also high for this therapeutic category.

North America is estimated with highest share in revenue owing to presence of major players and rapid advances in technology along with high investments in stem cell & oncology research. Rapid uptake of advanced technology by the population is another significant factor contributing to the largest share.

Furthermore, active presences of organizations such as Alliance for Regenerative Medicine, National Institutes of Health, National Cancer Institute, International Society for Stem Cell Research, and National Stem Cell Foundation that promote R&D of regenerative medicine is expected to further accelerate growth in this region. Thereby, the region is projected to continue dominating the market through introduction of novel products.

Asia Pacific is projected to witness fastest growth over forecast period owing to high investments in healthcare research by the emerging economies in the region. Advances in stem cell research and presence of flexible regulatory environment for clinical adoption of cell-based regenerative therapies, China and Japan are expected to reflect rapid industrial progress.

In addition, availability of well-developed infrastructure and research facilities along with investments by government and private companies to support development of novel approaches is expected to further boost revenue growth. For instance, approvals to carry out research on human embryonic stem cells in China has encouraged researchers to explore the clinical potential of these cells. Thus, Asia Pacific is attributed to fastest growth over the forecast period.

The global regenerative medicine market is observed to be highly competitive and fragmented. The major players include Integra LifeSciences Corporation,MiMedx Group, Inc, AstraZeneca, F. Hoffmann-La Roche Ltd, Merck & Co., Inc., Pfizer Inc., Baxter and Nuvasive, Inc. These entities are observed to have high investments in development of regenerative therapies to capture the untapped potential by innovating novel therapies to meet the demand for unmet clinical needs.

In addition, key players are witnessed to focus on oncology & age-related degenerative disorders to compete in the market. Collaborative efforts & strategic agreements for technology sharing and product development have also been observed. Thereby, the industry witnesses a strong pipeline of products in clinical trials, which eventually are expected to drive revenue generation.

Attribute

Details

Base year for estimation

2016

Actual estimates/Historical data

2014 - 2016

Forecast period

2017 - 2025

Market representation

Revenue in USD Million and CAGR from 2017 to 2025

Regional scope

North America, Europe, Asia Pacific, Central & South America, Middle East & Africa

Country scope

U.S., Canada, Germany, UK, China, Japan, Brazil, South Africa

Report coverage

Revenue forecast, company share, competitive landscape, growth factors and trends

15% free customization scope (equivalent to 5 analyst working days)

If you need specific market information, which is not currently within the scope of the report, we will provide it to you as a part of customization

This report forecasts revenue growth at global, regional & country levels and provides an analysis on the industry trends in each of the sub-segments from 2014 to 2025. For the purpose of this study, Grand View Research has segmented the global regenerative medicine market on the basis of product, therapeutic categories, and region:

Product Type Outlook (Revenue, USD Million, 2014 - 2025)

Therapeutic Category Outlook (Revenue, USD Million, 2014 - 2025)

Regional Outlook (Revenue, USD Million, 2014 - 2025)

North America

Europe

Asia Pacific

Latin America

Middle East & Africa

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Regenerative Medicine | OAA

January 11th, 2019 11:44 pm

Regenerative Medicine Regenerative medicine therapies, including platelet-rich plasma and stem cell, help to heal injuries, both acute and chronic, by restoring the structure and function of damaged tissues. The conditions treated at OAA's Regenerative Medicine Institute include osteoarthritis, tendon injuries, and ligament and muscle tears. Using a patient's own tissue to initiate the healing process, regenerative medicine can help people restore function, help to delay or avoid surgery, and also be used as an adjunct to surgery.Platelet-Rich Plasma TherapyPlatelet-rich plasma (PRP) therapy is a regenerative medicine treatment option that uses components of the body's own blood cells to help relieve pain and accelerate healing.PRP is obtained from the patient through a simple blood draw and then put in a centrifuge that separates the platelet-rich part of the blood. The platelets are then injected back into the same patient's tendon, joint, or ligament. The platelet-rich plasma injection contains natural growth factors that aid in healing. This regenerative treatment option is becoming increasingly more popular among the sports medicine and orthopaedic communities as a non- operative procedure.

In some scenarios, your doctor might also recommend fat grafting in conjunction with your platelet-rich plasma therapy. Depending on your condition and site of injury, fat (adipose) cells are used as a matrix for the platelet-rich plasma to adhere to and help activate your healing cascade. Using a special device, adipose tissue (fat) is removed from an area of your body where it is stored easily, such as the abdomen. The adipose tissue is then injected into the affected area with the platelet-rich plasma to help enable the opportunity for natural healing and pain relief.

This non-surgical regenerative medicine treatment option involves extracting stem cells from bone marrow and injecting the stem cells into areas with damaged tissue. The body naturally uses its bone marrow stem cells to heal injuries and to help rebuild joints affected by degenerative joint disease. OAAs Regenerative Medicine Institute boosts the bodys healing process by harvesting stem cells from your pelvis and injecting them directly into the affected area. This procedure helps generate new healthy tissue and accelerates the healing process. This procedure is performed in our office in a sterile environment using local anesthesia and ultrasound guidance to ensure comfort and accuracy.

In some scenarios, your doctor might also recommend fat grafting and adipose derived stem cells in conjunction with your stem cell therapy. Depending on your condition and site of injury, fat cells are used as a matrix for bone marrow stem cells to adhere to and help activate your healing cascade. Using a special device, adipose tissue is removed from an area of your body where it is stored easily, such as the abdomen. The adipose tissue is then injected into the affected area with the bone marrow aspirate to help enable the opportunity for natural healing and pain relief.

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Regenerative Medicine | OAA

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20 Best Regenerative Medicine jobs (Hiring Now!) | Simply Hired

January 11th, 2019 11:44 pm

University of Massachusetts Amherst - Amherst, MA4.4

Applicants with research and teaching expertise in areas of biomaterials for devices and regenerative medicine or biosensors and bioinstrumentation are...

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This may consist of regenerative medicine therapies:. Synergy Medical is looking to hire a part-time physician to administer Fluoroscopy and Ultrasound guided...

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We also offer regenerative medicine through Integrated Medicine of Ohio. Functional medicine training is preferred, but we will train the right candidate....

$45,000 - $70,000 a year3d

To serve as a practioner for a functional medicine clinic that reverses Type 2 Diabetes. We are looking for an MD....

$100,000 - $150,000 a year

Were looking for a highly motivated Controls Engineer to join our Regenerative Medicine Group. DEKA employs a team of over five hundred professionals, whose...

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Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for...

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The RMC will provide evidence-based clinical care that utilizes a range of regenerative medicine therapies in conjunction with a coordinated research program...

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A full-time Associate Researcher position is offered in the Department of Cell, Developmental and Regenerative Biology at the Icahn School of Medicine at Mount...

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HJF is seeking a Clinical Research Assistant to support the Brody Lab within the Center for Neuroscience and Regenerative Medicine (CNRM) at Fort Belvoir...

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HJF is seeking a Staff Scientist III to support and expanded Neuropathology/Neuroradiology Correlations/Integration Core Facility within the Center for...

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Jackson Foundation (HJF) is seeking a Research Assistant to support the Center for Neuroscience and Regenerative Medicine (CNRM) in the Translational...

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Regenerative Medicine Expansion. The Clinic is accepting applicants willing to learn Regenerative Medicine and High Definition Liposuction....

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Scientist, Regenerative Medicine. The Astellas Institute of Regenerative Medicine (AIRM) is a wholly-owned subsidiary of Astellas Pharma and focused on the...

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When you join us, you become a part of Mount Sinais unrivaled record of achievement, education and advancement as we revolutionize medicine together....

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The Regenerative Medicine Technician will work under the direction of the laboratory CEO, medical director and operational manager....

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Training will have a heavy emphasis on regenerative medicine procedures including stem cell therapies with adipose and bone marrow, platelet rich plasma (PRP),...

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Scientific Writer - Wake Forest Institute for Regenerative Medicine, Full-time.Job Summary:. Facilitates the transfer of technologies emerging from basic...

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BlueRock Therapeutics Cell+Gene regenerative medicine platform is based on state-of-the-art pluripotent stem cell engineering tools, and differentiation and...

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Regenerative Biologics is a distribution company for biologic and regenerative medicine products. Our primary sales targets are in the Orthopedic and Sports...

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BlueRock Therapeutics is an engineered cell therapy company with a mission to develop regenerative medicines for intractable diseases....

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Allergan is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for...

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The team so far is comprised of Niya Gupta (former McKinsey, Syngenta), Gabor and Andras Forgacs (Modern Meadow, Organovo) and Tony Atala (Wakeforest Institute...

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Participation at global Regenerative Medicine conferences as required. Interest in the Regenerative Medicine application area, past hands-on experience or...

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The practice also focuses on research with several ongoing clinical trials and cutting-edge therapies such as regenerative medicine procedures....

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Regenerative Medicine experience appreciated. Current license to practice medicine as a Physician Assistant in California....

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_Rrgenerative aesthetic medicine procedures and treatment approaches evaluating and developing a treatment plan for hormone optimization, stern cells in...

$40,000 - $100,000 a year

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Regenerative Medicine – Anatara Medicine

January 11th, 2019 11:44 pm

Ancient systems of medicine such as acupuncture and manipulative medicine have tapped into this capability to varying degrees by enhancing blood flow, nerve conduction and oxygenation to areas that need to be healed. As our understanding of the bodys own mechanisms for healing has matured, we have developed new techniques with a more robust healing potential.

In the field of Musculoskeletal Medicine, Prolotherapy, using a concentrated Dextrose (corn sugar) solution injected at the area requiring regeneration, can initiate the healing response. The first phase of healing is inflammation, where the blood flow to the area is increased bringing white blood cells to clean up the area and platelets with growth factors to stimulate stem cells to regenerate tissue.

The next evolution of Prolotherapy involved isolating the growth factors found in platelets and white blood cells in the blood and injecting them directly into the area to be healed. This is called Platelet Rich Plasma. Platelet Rich Plasma can be used to stimulate regeneration of muscles, tendons, ligaments, and cartilage, but it can also be used for a variety of aesthetic conditions like hair regrowth, facial rejuvenation, erectile dysfunction, stretch marks and scars.

For more information on the conditions we are currently treating and studying at the San Francisco Stem Cell Treatment Center, visit http://www.sfstemcellcenter.com.

All of these injections require that the needle be placed in the correct place so that the injured area is stimulated. This is why we use a state of the art, high-definition musculoskeletal ultrasound so we can see exactly where an injury is and ensure that solution is injected into that precise location. For instance, accuracy of the injection of the bursal sac, which can be inflamed in a variety of musculoskeletal conditions, was found to be improved from 14% to 97% using high-definition musculoskeletal ultrasound. There are some conditions where close is not good enough and musculoskeletal ultrasound is the only non-invasive, non-radioactive way of ensuring the correct placement of the medicine.

We tailor each package to meet your needs with the array of natural healthcare modalities we offer, and will work closely with you to help you realize your goals.

Please call 415.345.0099 or email info@anataramedicine.com to set up a complimentary 15-minute phone consultation so we may determine how our program may fit your specific needs. Our staff will be delighted to answer your questions.

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Regenerative Medicine - Anatara Medicine

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2017 Marks the 1st Year That Regenerative Medicine Disrupted …

January 11th, 2019 11:44 pm

The regenerative medicine industryhas been rapidly expanding over the past few years, making it a high-value, fast-growth market.Key drivers for the market include high rates of clinical trials,accelerated pathwaysfor product approvals, new technologies to supportcell and gene therapy manufacturing, and the potential for cell therapies to revolutionize healthcare.

The regenerative medicine market gained major momentum when the Swiss pharmaceutical giantNovartismade history as the first company to win FDA approval for a CAR-T cell therapy in the U.S. in August 2017 (Kymriah).In October 2017,Kite Pharmabecame the second company to get FDA approval of a CAR-T cell therapy (Yescarta).

With swelling momentum to support the CAR-T technology, there are now close to 40 companies developingredirected T cells or NK cellsfor therapeutic use.

On November 13, 2017, the FDA approved Abilify MyCite as the worldsfirst digital pill. With 7 out of 10 Americas taking at least one prescription drug, approval of the antipsychotic medication represents a breakthrough in digital medicine. Made by Japan-based Otsuka Pharmaceutical, the tablet works by containing a sensor to track when and if patients take their medication.

On December 19th, 2017, the FDA approved Spark TherapeuticsLuxturna,a novel gene therapy to treat patients with an inherited form of vision loss.

In addition to product approvals, there are now accelerated pathways for advanced therapy medicinal products (ATMPs) in several countries worldwide, including the U.S., Japan, and South Korea.Legislation took effect in Japan in late 2014, in South Korea in 2016, and in the United States in 2017.Additionally, the EU has a program for product acceleration the Adaptive Pathways. Although it is not explicitly for cell and gene therapies, it has been given a lot of attention by the group.

These historic events demonstrate to investors, the public, and funding providers alike that regenerative medicine is a sector that has emerged, no longer one that is evolving in the future.

Big Pharma is also demonstratingsnowballing interest in regenerative medicine.At its core, this is a strategic way for pharmaceutical companies to diversity their product development pipeline.In recent examples:

Finally, direct cell reprogramming is gaining momentum. Fortuna Fix, a company specializing in direct cell reprogramming applications to restore neuronal functionality, secured $25 million in Series B financing. The proceeds will enable the company to conduct Phase I/IIaclinical trials in Parkinsons Disease and Spinal Cord Injury.

Over the past 12-months, regenerative medicine has accelerated as a movement. With more than 600+ brave companies now composing the marketplace,immunotherapies, gene therapy, and digital medicinehave introduced true disruption of healthcare.

Today, the regenerative medicine industryincludes companies that are developing:

Interested to learn more about the industry? We spent exhaustivehours uncovering 600+ companies across the globe that are developing regenerative medicine therapeutics for use in humans.

2017 Marks the 1st Year That Regenerative Medicine Disrupted Healthcare

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2017 Marks the 1st Year That Regenerative Medicine Disrupted ...

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Human Genetics – medschool.ucla.edu

January 11th, 2019 11:40 pm

A hub of deep expertise, the Department of Human Genetics helps partners across UCLA interpret data and leverage genomic technology to improve study design and solve medical problems.

We demystify genetic complexities to provide vital insights for a range of clinical and research applications. We strive to improve the care of as many patients as possible by pushing our capabilities, developing novel ways to address unanswered questions.

Your next collaboration is right down the street.

Our enviable proximity to the worlds brightest scientific minds enables both thriving scheduled events and impromptu sidewalk powwows. A casual conversation during your coffee run could lead to your next big publication.

Come find out why innovation lives here.

LEARN MORE

Julian Martinez-Agosto, MD, PhDGenetic sequencing unravels rare disease mysteries; among the first medical centers to use exome sequencing.Learn More

Jingyi "Jessica" Li, PhDStatistics professor honored as a leading woman in STEM at the intersection of statistics and biology.Learn More

Aldons J. Lusis, PhDScientists identify 2 hormones that burn fat faster, prevent and reverse diabetes in mice.Learn More

Daniel Geschwind, MD, PhDAutism, schizophrenia, bipolar disorder share molecular traits, study finds.Learn More

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Stem cell therapy: FDA investigates clinics offering …

January 10th, 2019 2:50 pm

Inside Mark Bermans clinic in Rancho Mirage, California, is a sign hes obliged by law to post. It reads Not FDA Approved.

Patients who come here to the California Stem Cell Treatment Center can get treatments for ailments ranging from sports injuries to muscular dystrophy. For upward of $5,000, Berman, a plastic surgeon by training, will remove a small portion of their fat, process it, and inject it back into them.

This is called fat-derived stem cell therapy; the premise is that the stem cells in your fat can jump-start the healing process. The stem cells could be good for repairing everything from Alzheimers to paralysis to neurodegenerative conditions, says Berman. These cells are miraculous for helping heal. We dont have a choice. We have to use them.

The problem is theres not much evidence to back up the claims Berman is making. And its not just him there are more than 100 clinicians in the Cell Surgical Network, a group he co-founded in 2010 to promote the same kind of adult stem cell regenerative medicine he practices. According to a 2017 report by three Food and Drug Administration scientists in the New England Journal of Medicine looking at the benefits and risks of this kind of stem cell therapy, This lack of evidence is worrisome.

Fat-derived stem cells may have a positive effect, says Brad Olwin, a professor of molecular cellular and developmental biology at the University of Colorado Boulder with more than 30 years of experience working with stem cells. They may be beneficial; its clearly a possibility. The problem is the research hasnt been done.

So little evidence exists, in fact, that the Department of Justice, on behalf of the FDA, is suing Bermans clinic as well as a clinic in Florida for experimenting on patients with misleading products. The complaint was filed in May 2018 and the investigation is ongoing, according to the DOJ.

Given the popularity and abundance of these clinics nationwide, the FDA is also taking steps to modernize regulation in the field. But despite these efforts to streamline a path to legitimacy for stem cell clinics, unregulated medical procedures persist, at times leading to patient harm.

Currently, the only stem cell therapy approved by the FDA is a bone marrow transplant that uses pluripotent stem cells to treat cancers of the blood and bone marrow.

But doctors in the Cell Surgical Network have moved ahead with using cells for autoimmune, neurologic, and other serious conditions.

And there is a growing number of cases of adverse effects. In 2016, an elderly woman went blind after receiving an injection of stem cells to treat her macular degeneration. She received the treatment at the Stem Cell Center of Georgia an affiliate of Bermans Cell Surgical Network.

More reports of ill-fated procedures have since surfaced across the country, the worst resulting in kidney failure and paraplegia. In December, the Centers for Disease Control and Prevention reported 12 cases of people who suffered bacterial infections from contaminated stem cell treatments. An investigation traced the infections back to a single provider, Genetech, prompting the FDA to issue a warning letter to the company. FDA Commissioner Scott Gottlieb then issued a public statement reaffirming the agencys intent to regulate unapproved treatments.

Bioethicists are sounding the alarm too. In a recent paper in the journal Perspectives in Biology and Medicine, the University of Minnesotas Leigh Turner examined the marketing claims of 716 stem cell clinics in the United States. Often, he found, they were misleading. What at first glance might appear to be credible and compliant clinical research often is highly problematic, he wrote, adding that the individuals most affected are those who often are already dealing with serious health problems and other challenges.

Despite two years of increased scrutiny from the FDA, clinics continue to recruit new patients. Berman insists that repurposed fat-derived stem cells should not be subject to the same regulations as other treatments, and that FDA guidelines are arbitrary and nonscientific. They are a violation of constitutional rights to your own property.

He noted that after the case of the woman with macular degeneration going blind, his networks clinicians no longer inject fat-derived stem cells into patients eyes. But they continue to offer intravenous (bloodstream) injections. We have virtually three or four adverse events, of very little significance or consequence, says Berman, referring to the patients in his network. But according to the FDA, intravenous injections are associated with higher risk.

Other scientists I spoke with say theyre also worried that intravenous treatments may harm patients. Youre taking cells out of one part of your body, and putting them into another. You have absolutely no control after that, says Olwin. He acknowledges the FDAs efforts to crack down on clinics but suggests that much more can be done. They have limited resources to go after people. But I think its irresponsible for doctors and these clinics to be promoting these things.

Some types of stem cells can indeed give rise to virtually any cell in the body providing a platform for regenerating muscle or even rebuilding organs. Stem cells derived from embryos have this power, called pluripotency, but those obtained from adults do not. In order to acquire pluripotency, adult stem cells must be biologically reprogrammed a feat that, when invented, led to a Nobel Prize. These induced pluripotent stem cells allow doctors to treat challenging illnesses such as leukemia.

But clinics like Bermans are not using pluripotent stem cells they are using the mesenchymal stem cells found in fat, which are much more limited in function. Arnold Caplan, the fields pioneer who first gave them the stem cell label, recently advocated for renaming them to prevent doctors from claiming that they can cure the blind, make the lame walk, and make old tissue young again.

BrainStorm, a biotechnology company working with mesenchymal cells, recently gained FDA approval to begin clinical trials to treat patients suffering from multiple sclerosis. But to treat the neurological condition, BrainStorm researchers have developed a method to convert the mesenchymal cells into biological factories that release disease-treating proteins. In other words, BrainStorms therapy doesnt involve mesenchymal cells doing the work on their own what some clinics in the Cell Surgical Network claim mesenchymal cells can do.

Outside of the Cell Surgical Network, other clinics are using patients fat-derived cells but making different claims about the treatment.

I dont say Im doing stem cell therapy, says Dr. Joanne Halbrecht, an orthopedic surgeon and founder of Boulder Regenerative Medicine. Her clinic uses patients fat-derived cells to treat orthopedic conditions, injecting them into joints.

Halbrecht avoids the stem cell label because current research does not support claims that these fat-derived cells can turn into cartilage. Instead, she uses patients fat to cushion their joints. According to Olwin and the FDA, such joint injections are significantly lower-risk than intravenous injections.

Berman also administers direct joint injections. But afterward, he tells me, his clinicians also inject the leftover cells into the patients bloodstream. Halbrecht is adamant that this kind of procedure is unproven and unsafe.

Thats definitive. Its not a question, she says. They are completely wrong because there is zero science behind that.

For clinics to prove the safety and efficacy of their fat-derived stem cell treatments to the FDA, they must run rigorous clinical trials.

But some clinicians argue that even if they were interested in clinical trials, getting the FDAs blessing is too daunting. Clinical trials span years and cost millions of dollars. For small, privately owned clinics, this process is unaffordable.

In response, the FDA unveiled a more feasible clinical trial process, better suited to small businesses. Clinics that want to test a specific treatment can now team up on clinical trials and pool their patients, which can save them time and money. Still, the FDA is offering a grace period of up to 36 months for clinics to comply with its guidelines, allowing many to continue operating on patients without doing clinical trials. In the meantime, the FDA is urging patients to do [their] part to stay safe, according to a consumer warning issued in May.

Unfortunately, thats not so easy. Whether or not a clinic is offering an FDA-compliant treatment can be unclear. Some doctors advertise compliance because the device they use to remove and process a patients fat is technically FDA-approved. But if they then advertise their treatment as an FDA-approved stem cell therapy, they risk misleading patients.

Berman has no plans to pursue clinical trials, even with the new streamlined process. He believes his current model of clinical experimentation is adequate. In the so-called safety studies, he treats paying patients with a wide variety of diseases. But according to the recent bioethics report, Turner found that these pay-to-participate studies are poorly designed and unscientific.

In Bermans view, more patients benefit by obtaining cutting-edge treatments faster. But for every revolutionary treatment developed in a lab, there are nine duds and many unpredictable dangers. And unsanctioned clinics cost patients thousands of dollars and are not covered by insurance. Critics argue that it is unethical to charge patients for experimental procedures, as sanctioned clinical trials rarely cost patients anything.

The economic incentives for unsanctioned stem cell clinics are clear. Starting clinical trials would not only reduce patient revenue but also commit clinics to a costly process known to last for years. Shifting blame to the government and research community, Berman assures me that he and his colleagues are not motivated by self-interest. Were the good guys, he says.

In March, the woman blinded by an unsanctioned stem cell treatment filed a lawsuit against Bermans Cell Surgical Network. Bermans site still advertises treatment for macular degeneration with a link to an application.

But tucked away on Bermans website sits a sort of confession that may surprise the many patients who hear him speak with unwavering assurance. The page reads, We do not claim that these treatments work for any listed nor unlisted condition, intended or implied.

Max Levy is a PhD student in chemical and biological engineering at the University of Colorado Boulder and the senior editor of Science Buffs, a graduate student science blog. He writes about health, medicine, and the environment.

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Maintain Certification American Board of Preventive Medicine

January 9th, 2019 5:48 am

What is MOC?

MOC (Maintenance of Certification) is the board certification process for assessment of continuing competencies of physicians. The ABPM MOC program continues to evolve to meet American Board of Medical Specialties (ABMS) requirements.

Hold an active, valid and unrestricted medical license in all States, US territories, or Canadian Provinces in which you are licensed to practice medicine.

Complete continuing medical education and self-assessment activities in areas related to your practice. These include ABPM-approved courses as well as patient safety courses. View ABPM-approved LLSA courses.*

Pass a cognitive exam during each certification cycle. The exam will contain similar content to the initial certification exam. View MOC Exam Information.

Complete two Improvement in Medical Practice (IMP) activities. One of the activities must be completed through a Preventive Medicine specialty or subspecialty society (ACOEM, ACPM, AMIA, AsMA, UHMS).*

ABPM is a participant in the ABMS Multispecialty Portfolio Program. Activities completed through the program will be accepted. Learn more about the ABMS Multispecialty Portfolio Program.

*Diplomates completing MOC Parts 2 and 4 requirements for another ABMS Member Board may request reciprocal credit.

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Holly Hansen, DVM – secaucusvet.com

January 9th, 2019 5:48 am

Dr. Holly Hansen is a born and raised Jersey girl. She completed her undergraduate studies at Felician College in Lodi, NJ graduating with a Bachelors degree in Biology. She earned her DVM degree in 2005 from Tufts University-School of Veterinary Medicine in North Grafton, MA. Soon after graduating from Tufts, she went on to further develop her veterinary skills by completing a one year small animal medicine and surgery internship at Arboretum View Animal Hospital right outside of Chicago.

Prior to becoming a veterinarian though, she worked at the Office of the Chief Medical Examiners Office in Newark, NJ covering multiple counties as a medical crime scene investigator for quite a few years.

Her interests in veterinary medicine include feline medicine, geriatric medicine, and internal medicine. She shares her home with a clowder of felines. She speaks cat, but absolutely loves all kinds of animals.

In her spare time, she enjoys the beach, going to the movies, concerts, music, anything Barry Manilow, and horror conventions.

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Biotechnology < MiraCosta College

January 9th, 2019 5:47 am

BTEC110: Basic Techniques in Biotechnology

Units: 4Prerequisites: BIO105 and CHEM140 or one year of high school chemistry (within 4 years), or qualification through a chemistry placement exam.Advisory: ACE150, ENGL50, ESL150, or eligibility determined by the English placement process.Acceptable for Credit: CSULecture 2 hours, laboratory 6 hours. Course Typically Offered: Fall, Spring

This course focuses on the basic laboratory skills needed for employment in the bioscience/biotechnology industry. Students learn laboratory safety and documentation while acquiring skills in the maintenance and calibration of basic lab equipment, calculation and preparation of lab solutions and media, and routine handling of both bacterial and mammalian cell cultures (tissue culture). Students also develop fundamental skills in spectroscopy, centrifugation, performance of assays, gel electrophoresis, and the purification and handling of biological molecules, such as proteins and DNA. (Materials Fee: $30.00)

BTEC120: Business and Regulatory Practices in Biotechnology

Units: 3Prerequisites: NoneAcceptable for Credit: CSULecture 3 hours. Course Typically Offered: Fall, Spring

This course examines basic business principles and practices utilized in the discovery, development, and production phases of new product development. It explores the role of governmental oversight and regulation in assuring the safety, efficacy, and quality of a biotechnology product.

BTEC180: Biostatistics

Units: 4Prerequisites: MATH64, MATH102, or eligibility determined by the math placement process.Advisory: BIO105, BIO110, BIO111, BIO202, or BIO204.Enrollment Limitation: Not open to students with prior credit in BIO 180, BUS204, PSYC104, PSYC104H, SOC104, or SOC104H.Acceptable for Credit: CSU, UCLecture 3 hours, laboratory 3 hours. Course Typically Offered: Fall, Spring

This introductory statistics course covers the principles and practice of statistical design and analysis for scientific experimentation. Topics include hypothesis formation, experimental design and execution, data analysis, and communication with application to scientific fields, such as the biological and health sciences. The course includes laboratory application with extensive use of computer software for statistical analysis and simulation. UC CREDIT LIMITATION: Credit for BIO 180/BTEC180, BUS204, MATH103, PSYC104/SOC104, or PSYC104H/SOC104H.

BTEC201: Advanced Cell Culture

Units: 1Prerequisites: BTEC110.Acceptable for Credit: CSULecture 0.50 hour, laboratory 1.50 hours. Course Typically Offered: Spring

This advanced course teaches skills in the proper handling of cells from higher organisms, such as plants, mammals, and insects, that are routinely maintained in culture in the biotechnology laboratory. Instruction focuses on growth and manipulation techniques and long-term maintenance of various laboratory cell cultures that may include anchorage-dependent and suspension cell lines as well as stem cell cultures.

BTEC203: Techniques in DNA Amplification

Units: 1Prerequisites: BTEC110.Acceptable for Credit: CSULecture 0.75 hour, laboratory 0.75 hour. Course Typically Offered: Fall or Spring every 3rd sem

This advanced course provides skills in the performance of the polymerase chain reaction (PCR), a technique commonly used to amplify DNA in forensics and the biotechnology laboratory. Instruction focuses on understanding the process; potential applications of DNA amplification; and the skills related to the setup, performance, and evaluation of the technique's outcome. The course assumes some prior knowledge of solution preparation and gel electrophoresis.

BTEC204: Recombinant DNA

Units: 1Prerequisites: BTEC110.Acceptable for Credit: CSULecture 0.75 hour, laboratory 0.75 hour. Course Typically Offered: Fall or Spring every 3rd sem

This advanced course provides skills in recombinant DNA technology used to analyze and manipulate DNA in the biotechnology laboratory. Students learn about the process of cloning and analyzing DNA and acquire the skills necessary to cut, piece together, and introduce new DNA molecules into prepared host bacterial cells.

BTEC206: Principles of Separation and HPLC

Units: 1Prerequisites: BTEC110.Acceptable for Credit: CSULecture 0.75 hour, laboratory 0.75 hour. Course Typically Offered: Fall or Spring every 3rd sem

This advanced course provides skills in the separation of biomolecules from complex mixtures using high performance liquid chromatography (HPLC). Instruction focuses on understanding the principles of separation, acquiring skills in the separation of various biomolecules, and analyzing the outcome for the purpose of determining system performance and biomolecular purification. The course assumes some prior knowledge of solution preparation, assays, and spectroscopy.

BTEC207: Techniques in Immunochemistry and ELISA

Units: 1Prerequisites: BTEC110.Acceptable for Credit: CSULecture 0.75 hour, laboratory 0.75 hour. Course Typically Offered: Fall or Spring every 3rd sem

This advanced course provides skills in the use of antibody reagents as a tool in the biotechnology laboratory. It focuses on the nature and specificity of antibody reagents for the identification and quantification of biological molecules. Students learn how to set up, perform, and analyze techniques utilizing antibodies, such as Westerns and ELISAs.

BTEC210: Data Analysis with Excel

Units: 1Prerequisites: NoneAdvisory: CSIT101.Acceptable for Credit: CSULecture 0.75 hour, laboratory 0.75 hour. Course Typically Offered: Fall, Spring

This course teaches students how modern spreadsheet programs can be used to collect and organize data for subsequent tabulation, summarization, and graphical display. It utilizes various forms of scientific data to teach the techniques and skill that facilitate the capture, analysis, and management of data. Topics include importing and organizing data, filtering and sorting, graphing, and statistical analysis functions.

BTEC211: Technical Writing for Regulated Environments

Units: 1Prerequisites: NoneAdvisory: BTEC110 and ACE150, ENGL50, ESL150, or eligibility determined by the English placement process.Acceptable for Credit: CSULecture 1 hour. Course Typically Offered: Fall, Spring

This course provides the requisite tools to understand why technical writing exists and how that writing works in conjunction with the many types of documents found in regulated environments. It also develops the techniques needed to deliver clear and complete passages with precise language. Students apply best practices for technical writing to a variety of documents, including reports, standard operating procedures (SOP), and investigations.

BTEC221: Bioprocessing: Cell Culture and Scale-up

Units: 1.5Prerequisites: BTEC110.Advisory: BTEC120.Acceptable for Credit: CSULecture 0.75 hour, laboratory 2.25 hours. Course Typically Offered: Fall, Spring

This laboratory course develops the skills and knowledge related to the culture of cells in increasingly larger scales for the production of biological molecules. Students grow and monitor a variety of cells (bacterial, yeast, and/or mammalian) on a laboratory scale that emulates the large-scale production used in industry. They become familiar with the cleaning, sterilization, aseptic inoculation, operation, and monitoring of fermenters and bioreactors. The course emphasizes the use of current Good Manufacturing Practices (cGMPs) and process control strategies, and students gain experience following Standard Operating Procedures (SOPs).

BTEC222: Bioprocessing: Large Scale Purification

Units: 1.5Prerequisites: BTEC110.Advisory: BTEC120.Acceptable for Credit: CSULecture 0.75 hour, laboratory 2.25 hours. Course Typically Offered: Fall, Spring

This laboratory course develops the skills and knowledge related to purification of biological molecules produced on a large scale. Students utilize the most common types of separation equipment, including tangential flow filtration, centrifugation, and column chromatography. They become familiar with the cleaning, sanitization, calibration, operation, and monitoring of large-scale purification equipment. The course emphasizes the use of current Good Manufacturing Practices (cGMPs) and process control strategies, and students gain experience following Standard Operating Procedures (SOPs).

BTEC292: Internship Studies

Units: 0.5-3Prerequisites: NoneCorequisite: Complete 75 hrs paid or 60 hrs non-paid work per unit.Enrollment Limitation: Instructor, dept chair, and Career Center approval. May not enroll in any combination of cooperative work experience and/or internship studies concurrently.Acceptable for Credit: CSUCourse Typically Offered: To be arranged

This course provides students the opportunity to apply the theories and techniques of their discipline in an internship position in a professional setting under the instruction of a faculty-mentor and site supervisor. It introduces students to aspects of the roles and responsibilities of professionals employed in the field of study. Topics include goal-setting, employability skills development, and examination of the world of work as it relates to the student's career plans. Students must develop new learning objectives and/or intern at a new site upon each repetition. Students may not earn more than 16 units in any combination of cooperative work experience (general or occupational) and/or internship studies during community college attendance.

BTEC296: Topics in Biotechnology

Units: 1-4Prerequisites: NoneAcceptable for Credit: CSULecture 1 hour.Lecture 2 hours.Lecture 3 hours.Lecture 4 hours. Course Typically Offered: To be arranged

This course gives students an opportunity to study topics in Biotechnology that are not included in regular course offerings. Each Topics course is announced, described, and given its own title and 296 number designation in the class schedule.

BTEC299: Occupational Cooperative Work Experience

Units: 1-6Prerequisites: NoneCorequisite: Complete 75 hrs paid or 60 hrs non-paid work per unit.Enrollment Limitation: Career Center approval. May not enroll in any combination of cooperative work experience and/or internship studies concurrently.Acceptable for Credit: CSUCourse Typically Offered: To be arranged

Cooperative Work Experience is intended for students who are employed in a job directly related to their major. It allows such students the opportunity to apply the theories and skills of their discipline to their position and to undertake new responsibilities and learn new skills at work. Topics include goal-setting, employability skills development, and examination of the world of work as it relates to the student's career plans. Students may not earn more than 16 units in any combination of cooperative work experience (general or occupational) and/or internship studies during community college attendance.

BTEC300: Supply Chain and Enterprise Resource Planning in Biomanufacturing

Units: 3Prerequisites: BTEC120.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours. Course Typically Offered: Spring

Students gain knowledge of how companies manage the complete flow of materials in a supply chain from suppliers to customers. This course covers the design, planning, execution, monitoring, and control of raw materials, personnel resources, inventory management, and distribution. At the end students will have the knowledge required to take the CPIM (Certified in Production and Inventory Management) certification test administered by APICS (the American Production and Inventory Control Society). This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC310: Biomanufacturing Process Sciences

Units: 5Prerequisites: BTEC221 and BTEC222.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours, laboratory 6 hours. Course Typically Offered: Fall

This lecture/laboratory course examines the biological, physical, and chemical scientific principles that support the design, development, and optimization of key parameters in a biomanufacturing process. Process sciences covers the essential theories that underpin the biomanufacturing operations from product formation through product purification and how those operations scale up and scale down. The topics include fermenter and bioreactor design and the design of downstream processes that maximize the yield, safety, and efficacy of a protein pharmaceutical. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC320: Design of Experiments for Biomanufacturing

Units: 4Prerequisites: BTEC110, and BTEC180 or BIO 180.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours, laboratory 3 hours. Course Typically Offered: Spring

This course teaches formalized design of experiments (DOE), a system that optimizes a process through the methodical varying of key parameters and a formalized approach to analyzing, interpreting, and applying the results. DOE is designed to make any process more robust and minimize variability from external sources. The course builds upon the statistical concepts required for DOE, including hypothesis testing, confidence intervals, statistical models, and analysis of variance (ANOVA). The DOE approach systematically varies the parameters of a biomanufacturing process to improve its operation. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC330: Advanced Topics in Quality Assurance and Regulatory Affairs

Units: 4Prerequisites: BTEC120.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 4 hours. Course Typically Offered: Fall

This course builds upon previous knowledge of quality assurance and regulatory affairs to study the harmonized quality system approaches of the International Council for Harmonisation Q8 through Q11. The course pays special attention to the topics of quality risk management, qualification, and validation. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC340: Six Sigma and Lean Manufacturing

Units: 3Prerequisites: BTEC120 and BTEC180.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours. Course Typically Offered: Spring

This course covers the Six Sigma approach to the maintenance and improvement of biomanufacturing processes. It incorporates the DMAIC phases: define, measure, analyze, improve, and control. The course covers the use and implementation of lean manufacturing tools that biomanufacturing companies use to reduce waste. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC360: Design of Biomanufacturing Facilities, Critical Utilities, Processes, and Equipment

Units: 3Prerequisites: BTEC120, BTEC221, and BTEC222.Enrollment Limitation: Concurrent Enrollment in BTEC221 and BTEC222 if prerequisites not met.Lecture 3 hours. Course Typically Offered: Fall

Students evaluate how the design of a biomanufacturing facility maintains appropriate levels of cleanliness and sterility and promotes the production of safe and effective products. Students analyze the design of the processes, equipment, and instrumentation used in biological production to generate critical utilities, aseptic systems, environmental control and monitoring, upstream production, and downstream (recovery and purification) production within a regulated environment. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC400: Bioprocess Monitoring and Control

Units: 4Prerequisites: BTEC310.Enrollment Limitation: Open only to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours, laboratory 3 hours. Course Typically Offered: Fall

This course covers the measurement, monitoring, modeling, and control of biomanufacturing processes and the statistical methodology used for measuring, analyzing, and controlling quality during the manufacturing process, including control charts and the analysis of process capabilities. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC410: Methods in Quality, Improvements, Investigations, and Audits

Units: 4Prerequisites: BTEC330 and BTEC340.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 4 hours. Course Typically Offered: Spring

This course examines investigational methods used by quality assurance departments to analyze process deviations and make decisions about severity of deviation. Students learn to write industry-standard corrective and preventive action (CAPA) reports to conclude what corrective and preventive actions result from the investigation. The course also covers how a company would perform an audit in anticipation of an inspection by the Food and Drug Administration or for the supplier of a key raw material. Course content is aligned with the American Society for Quality's Body of Knowledge for a Certified Quality Technician examination. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC460: Capstone Seminar in Biomanufacturing Technologies

Units: 3Prerequisites: BTEC310.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours. Course Typically Offered: Fall

This course examines the breadth of products that are produced through biological processes. The course will focus on the advances and emerging technologies in biological production and purification operations. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

BTEC470: Capstone Seminar in Biomanufacturing Quality

Units: 3Prerequisites: BTEC330.Enrollment Limitation: Only open to students enrolled in the bachelor's degree program in biomanufacturing at MiraCosta College.Lecture 3 hours. Course Typically Offered: Spring

This course examines the process by which the quality systems of biomanufacturing evolve by examining a selected current trend in the laws and regulations governing biopharmaceutical manufacturing. Students evaluate the effectiveness of the laws and regulations governing biopharmaceutical manufacturing. This course serves as a capstone experience for students in biomanufacturing quality. This course is open only to students enrolled in the biomanufacturing bachelor's degree program.

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Biotechnology – Southern Maine Community College

January 9th, 2019 5:47 am

Academics

On this page:

Biotechnology is the use of technology and applied biology to find solutions to problems. Career and research opportunities include animal sciences, biomedical technologies, immunology, pharmaceutics and forensics, plus marine and environmental science. Students learn the fundamentals of biology and chemistry and gain an advanced understanding of related subfields such as cellular biology, genetics and microbiology. Students work with DNA, cells, enzymes and other biological agents in hands-on laboratory settings and have the opportunity to work in outside laboratories as part of a summer internship program. Graduates find employment in entry-level biotechnology positions, including jobs as manufacturing, research and lab technicians, or transfer to a baccalaureate degree program.

The Biotechnology department offers an Associate in Science degree requiring a mix of general education and hands-on courses. The following courses are a sampling of what you might take as a student in this program and are subject to change.

Interested in seeing some of the current major-specific courses being offered as a part of this degree program?

If you are thinking about attending SMCC and are curious what the current program course requirements are to earn your degree, download the current SMCC Course Catalog.

If you are a current student, your program requirements may be different than those listed for the current catalog year. To view your specific program requirements or to search and register for courses, log in to MySMCC and visit the MyDegree webpage.

Please note, these estimates are based on a student taking an average of 15 credits per semester and do not include college preparatory or developmental courses.

For information about enrolling in the program contact:Admissions207-741-5800admissions@smccME.edu

For questions about this career path contact:Department ChairDaniel Moore207-741-5966dmoore@smccME.edu

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DMACC Biotechnology Degree

January 9th, 2019 5:47 am

Lowest tuition & fees in Iowa

Page Content

An Liberal Arts Associate in Science Degree and theBiotechnology Laboratory Methods Certificate will prepare you for work in a laboratory position in a variety of companies and research institutions in Iowa and throughout the United States.

Withyour DMACC Biotechnology Certificate you can assist in cutting edge research in this fast growing and exciting scientific frontier or be an important link in the production of extremely important medical and industrial products!

The DMACC Liberal Arts Associate in Science Degree and the Biotechnology Certificate is also transferable to a four-year college or university so you can continue your science education in the field of your choice.

If you want to work in a professional environment in a very exciting field of science then you should seriously consider a degree in Biotechnology.

Program Chair/Biology Instructor

Ankeny Campus

Building 05, Room 1234

(515) 964-6379

Julie Gonzlez says one of the best things about teaching in the Biotechnology field is the ability to take students to local companies and show them the real world application of what they are learning at DMACC.

Students enjoy getting to meet DMACC Biotechnology alumni who are working in the field, said Gonzlez. The alumni always stop to talk to students about their own experiences.

DMACC Biotechnology graduates can work in several fields from agricultural to forensics. DMACC Biotechnology students learn how to analyze DNA for crime scene forensics and how to clone and sequence genes. Students also work with proteins to learn how diseases can be detected and monitored. They also examine enzymes that are used in the biofuels industry.

There is a demand for students who can use critical thinking skills and laboratory training to run experiments and analyze the results. There are many companies with a diverse range of opportunities available. If you are interested in biology and/or chemistry, there is a biotech job somewhere that would be perfect for you, said Gonzlez. Biotechnology is a growing field in central Iowa. The industry professionals I work with on DMACC's Biotechnology Advisory Committee often emphasize the need for educated biotechnology workers.

DMACC graduates can work for companies like Pioneer, Monsanto, Kemin, Proliant, Heska, NASA and the United States Department of Agriculture (USDA).

Gonzlez says lab exercises are a valuable part of the DMACC Biotechnology program.

From analyzing their favorite foods for genetically modified content to purifying proteins used to produce medications, the emphasis is on real-world techniques and applications, said Gonzlez.

Gonzlez earned a B.S. in Biology and Chemistry from Upper Iowa University and an M.S. and Graduate Certificate in Forensics from Iowa State University.

Gonzlez and her husband and two children enjoy many outdoor activities including biking, kayaking and stand-up paddling.

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Stem Cell Therapy, Amniotic Fluid Injections, Pain Relief

January 7th, 2019 8:45 am

Orthopaedic surgeon Dr. Stacie Grossfeld discussing Stem Cell Therapy.

Stem Cell Recruitment Therapy is a safe and effective treatment to helpyour body heal itself. It is typically administered during a normal office visit, through asingle injection. Patients have reported improved pain relief and repair for the following conditions:

Stem Cell injections are conveniently administered through a single injection during a normal office visit. Following the injection, patients are typically able to return to everyday, non-high impact activities within 24 to 48 hours.

What benefits does Stem Cell Recruitment Therapy offer?

For more information about stem cell recruitment therapy, or to make an appointment, callOrthopaedic Specialists at a (502)212-2663. Follow along for more information about stem cell recruitment therapy.

Stem cells for stem cell recruitment therapy are obtained through amniotic fluid. Amniotic fluid contains a multitude of proteins and growth factors. Together they create an extra-cellular matrix to recruit the bodys stem cells to reconstruct and regenerate the injured tissue that is causing pain. Amniotic fluid can repair tissue damage, giving patients with arthritis, joint injuries and soft tissue injuries a treatment option that does not involve pain masking medications or surgery.

The amniotic fluid is obtained during full-term cesarean births from healthy donors who have volunteered their placenta and amniotic fluid. All amniotic fluid is collected aseptically and tested prior to processing and determined to be eligible for transplantation by Donors Suitability Standards established by the AATB and the FDA. The products we use are FDA regulated under the 21 CFR Part 1271 and Section 361 of the Public Health and Service Act.

Stem cells take advantage of the bodys ability to repair itself. With a stem cell injection, your physician injects the amniotic fluid containing stem cells into your body. The amniotic fluid has anti-inflammatory properties, similar to cortisone and steroid shots. However, amniotic fluid goes far beyond the benefits of standard injection therapy.

While cortisone and other drugs only provide temporary pain relief, amniotic fluid actually restores degenerated tissue while providing pain relief. The growth factors in the amniotic fluid may recruit your bodys own stem cells, directly mitigating the repair and the regeneration of healthy tissue. Additionally, amniotic fluid injections contain hyaluronic acid, which lubricates joints and tendons, easing the pain and helping restore mobility.

Stem cells have over 200 growth factors. A growth factor is a proteins or enzyme that can grow cartilage, repair scars, reduce inflammation, take away pain, and grow bone. Astem cell can turn into any type of cell. Basically, it doesnt know what it wants to be when it grows up If you put it into the knee, it turns into the cells in the knee joint, it is an imitator so to speak, adapting to the environment where it is placed.

As we get older our stem cells get older. The amniotic stem cells are much more potent. The other advantage of the amniotic stem cells is that you do not have to have the painful procedure where stem cells are harvested out of your pelvis bone.

Typically it can take three to six weeks for a patient to feel the full effect of stem cell recruitment therapy. This is because the treatment utilizes the bodys own healing process.

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ReNu Stem Cell Therapy – Advanced Orthopedics – Nonsurgical …

January 7th, 2019 8:45 am

An ideal injectable therapy would combine safe long term anti-inflammatory pain management and long term regenerative healing. The Center for Nonsurgical & Regenerative Orthopedics now offers the most sophisticated and powerful Stem Cell product on the market. ReNu is the only stem cell injection that combines the anti-inflammatory capacity of amniotic tissue with the regenerative power of fetal stem cells.

ReNu is a revolutionary noninvasive treatment in which human amniotic tissue and stem cells are injected into injured tissue to provide relief from pain and stimulate the body's natural healing process. This amniotic tissue contains fetal mesenchymal stem cells that help to regenerate damaged tissue such as cartilage, tendons, and ligaments. The growth factors in the amniotic tissue provide anti-inflammatory, anti-adhesive, and anti-microbial properties to the injured area and can significantly help reduce scarring for quicker healing. Amniotic tissue is also immune privileged, which means there is virtually no chance that your body will reject the treatment.

ReNu stem cells come from the amniotic membrane and fluid of donated placentas following normal childbirth. With the mother's consent, the amnion is removed and harvested from the placenta of pre-screened and tested donors. It is then sterilely processed and undergoes further rigorous testing to assure safety and efficacy. To be clear, while some people may have ethical issues with embryonic stem cell therapy, almost everyone agrees that the use of amniotic stem cell therapy raises no ethical or moral questions.

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Stem Cell Therapy in Richmond Start Healing Chronic Pain …

January 7th, 2019 8:45 am

Stem cell therapy is a targeted treatment that activates your bodys own natural ability to heal and regenerate. With a simple in-office procedure you will improve your quality of life and potentially avoid surgery.

Research continues to show an increasing number of potential benefits from the anti inflammatory, immunomodulatory, and regenerative actions of stem cells. Stem cell therapy treats pain and chronic conditions at their source, returning you to the things you enjoy.

Our stem cell therapy treatment utilizes umbilical cord derived Mesenchymal Stem Cells from FDA regulated cord banks. Mesenchymal Stem Cells are specialized cells that are able to receive signals from the other cells in your body. Stem cells then seek out inflammation and degeneration and go to that location to begin repairing tissue.

Stem cells have been shown to help repair muscle, bone, cartilage and tendons. Research has indicated that stem cells can benefit a wide variety of health complications and may assist in individuals living stronger, healthier lives.

Our mission is simple: Change the lives of our patients by providing an integrative, holistic approach to healing.

We help people suffering from chronic health conditions, chronic pain, autoimmune issues, and many other undiagnosed syndromes and health problems.

We are passionate about caring for our patients who, until now, were not able to find answers and treatments for their underlying health issues.

Regenerative medicine through stem cell therapy is the future of health care and, for our patients, THE FUTURE IS NOW!

Are you a candidate for regenerative stem cell therapy? The answer is YES if you suffer from any of the following:

Were here to help you heal and restore your health today! Please contact us now using the form below to explore how stem cell therapy can help you find relief and embrace your life again!

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What Is Diabetic Neuropathy? | NIDDK

January 6th, 2019 1:46 pm

Diabetic neuropathy is nerve damage that is caused by diabetes.

Nerves are bundles of special tissues that carry signals between your brain and other parts of your body. The signals

Types of diabetic neuropathy include the following:

Peripheral neuropathy is nerve damage that typically affects the feet and legs and sometimes affects the hands and arms.

Autonomic neuropathy is damage to nerves that control your internal organs. Autonomic neuropathy can lead to problems with your heart rate and blood pressure, digestive system, bladder, sex organs, sweat glands, eyes, and ability to sense hypoglycemia.

Focal neuropathies are conditions in which you typically have damage to single nerves, most often in your hand, head, torso, and leg.

Proximal neuropathy is a rare and disabling type of nerve damage in your hip, buttock, or thigh. This type of nerve damage typically affects one side of your body and may rarely spread to the other side. Proximal neuropathy often causes severe pain and may lead to significant weight loss.

If you have diabetes, your chance of developing nerve damage caused by diabetes increases the older you get and the longer you have diabetes. Managing your diabetes is an important part of preventing health problems such as diabetic neuropathy.

You are also more likely to develop nerve damage if you have diabetes and

Research also suggests that certain genes may make people more likely to develop diabetic neuropathy.

Over time, high blood glucose levels, also called blood sugar, and high levels of fats, such as triglycerides, in the blood from diabetes can damage your nerves. High blood glucose levels can also damage the small blood vessels that nourish your nerves with oxygen and nutrients. Without enough oxygen and nutrients, your nerves cannot function well.

Although different types of diabetic neuropathy can affect people who have diabetes, research suggests that up to one-half of people with diabetes have peripheral neuropathy.1,2 More than 30 percent of people with diabetes have autonomic neuropathy.2

The most common type of focal neuropathy is carpal tunnel syndrome, in which a nerve in your wrist is compressed. Although less than 10 percent of people with diabetes feel symptoms of carpal tunnel syndrome, about 25 percent of people with diabetes have some nerve compression at the wrist.2

Other focal neuropathies and proximal neuropathy are less common.

Your symptoms depend on which type of diabetic neuropathy you have. In peripheral neuropathy, some people may have a loss of sensation in their feet, while others may have burning or shooting pain in their lower legs. Most nerve damage develops over many years, and some people may not notice symptoms of mild nerve damage for a long time. In some people, severe pain begins suddenly.

Peripheral neuropathy can lead to foot complications, such as sores, ulcers, and infections, because nerve damage can make you lose feeling in your feet. As a result, you may not notice that your shoes are causing a sore or that you have injured your feet. Nerve damage can also cause problems with balance and coordination, leading to falls and fractures.

These problems may make it difficult for you to get around easily, causing you to lose some of your independence. In some people with diabetes, nerve damage causes chronic pain, which can lead to anxiety and depression.

Autonomic neuropathy can cause problems with how your organs work, including problems with your heart rate and blood pressure, digestion, urination, and ability to sense when you have low blood glucose.

To prevent diabetic neuropathy, it is important to manage your diabetes by managing your blood glucose, blood pressure, and cholesterol levels.

You should also take the following steps to help prevent diabetes-related nerve damage:

If you have diabetic neuropathy, you should manage your diabetes, which means managing your blood glucose, blood pressure, cholesterol levels, and weight to keep nerve damage from getting worse.

Foot care is very important for all people with diabetes, and its even more important if you have peripheral neuropathy. Check your feet for problems every day, and take good care of your feet. See your doctor for a neurological exam and a foot exam at least once a yearmore often if you have foot problems.

[1] Pop-Busui R, Boulton AJ, Feldman EL, et al. Diabetic neuropathy: a position statement by the American Diabetes Association. Diabetes Care. 2017;40(1):136154.

[2] Izenberg A, Perkins BA, Bril V. Diabetic neuropathies. Seminars in Neurology. 2015;35(4):424430.

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What Is Diabetic Neuropathy? | NIDDK

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5 Worst Foods for Arthritis and Joint Pain

January 6th, 2019 1:45 pm

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How long would YOU like to be pain free?

Look, I know you're skeptical. You should be. Look at all the big drug companies who are lying to you each and every day trying to convince you that their dangerous (sometimes deadly!) drugs are safe.

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No matter what your arthritis pain level and frequency, fill out the risk-free acceptance form below to see how well Heal-n-Soothe Arthritis will work for you.

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Learn about the trouble making vegetable, YES VEGETABLE... that can make your Arthritis worse. (And Make you feel 5 - 10 years older.)

The secret switch inside your body that you can flip to help make it start acting like it did when you were 25 years old.

The real reason why painkillers don't help your pain.

Which special superfood can actually counteract the damage or arthritis.

Adler A, Holub B. Effect of garlic and fish-oil supplementation on serum lipid and lipoprotein concentrations in hypercholesterolemic men. American Journal of Clinical Nutrition. 1997 Feb;65(2):445-50.

NIAMS, NIH, Bethesda, Maryland 20892, USA. Arthritis & Rheumatology (Impact Factor: 7.87).06/1998; 41(5):778-99. DOI: 10.1002/1529-0131(199805)41:5<778::AID-ART4>3.0.CO;2-V Source: PubMed

Hrlimann, David, Frank Enseleit, and Priv-Doz Dr Frank Ruschitzka. Rheumatoide arthritis, inflammation und atherosklerose. Herz 29.8 (2004): 760-768.

Schett, Georg. Rheumatoid arthritis: inflammation and bone loss. Wiener Medizinische Wochenschrift 156.1-2 (2006): 34-41.

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5 Worst Foods for Arthritis and Joint Pain

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List of Rheumatoid Arthritis Medications (222 Compared …

January 6th, 2019 1:45 pm

methotrexate Rx X N X 94reviews

6.0

Generic name:methotrexate systemic

Brand names: Otrexup, Rasuvo, Rheumatrex Dose Pack, Trexall showall

Drug class: antimetabolites, antirheumatics, antipsoriatics, other immunosuppressants

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

8.0

Generic name:celecoxib systemic

Drug class: cox-2 inhibitors

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:hydroxychloroquine systemic

Drug class: antirheumatics, antimalarial quinolines

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

8.0

Generic name:prednisone systemic

Brand name: Rayos

Drug class: glucocorticoids

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

7.0

Generic name:etanercept systemic

Drug class: antirheumatics, TNF alfa inhibitors

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:meloxicam systemic

Brand name: Mobic

Drug class: Nonsteroidal anti-inflammatory drugs

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

6.0

Generic name:adalimumab systemic

Drug class: antirheumatics, TNF alfa inhibitors

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:hydroxychloroquine systemic

Brand name: Plaquenil

Drug class: antirheumatics, antimalarial quinolines

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

7.0

Generic name:tocilizumab systemic

Drug class: interleukin inhibitors

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:leflunomide systemic

Drug class: antirheumatics, selective immunosuppressants

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

5.0

Generic name:sulfasalazine systemic

Brand names: Sulfazine, Azulfidine, Azulfidine EN-tabs

Drug class: antirheumatics, 5-aminosalicylates

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

8.0

Generic name:infliximab systemic

Drug class: antirheumatics, TNF alfa inhibitors

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:leflunomide systemic

Brand name: Arava

Drug class: antirheumatics, selective immunosuppressants

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

6.0

Generic name:meloxicam systemic

Drug class: Nonsteroidal anti-inflammatory drugs

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

6.0

Generic name:acetaminophen / hydrocodone systemic

Drug class: narcotic analgesic combinations

For consumers: dosage, interactions, side effects

For professionals: Prescribing Information

Off Label: Yes

5.0

Generic name:abatacept systemic

Drug class: antirheumatics, selective immunosuppressants

For consumers: dosage, interactions, side effects

For professionals: AHFS DI Monograph, Prescribing Information

9.0

Generic name:acetaminophen / hydrocodone systemic

Drug class: narcotic analgesic combinations

For consumers: dosage, interactions, side effects

For professionals: Prescribing Information

Off Label: Yes

7.0

Generic name:diclofenac systemic

Brand names: Voltaren, Cataflam, Voltaren-XR

Drug class: Nonsteroidal anti-inflammatory drugs

For consumers: dosage, interactions,

For professionals: A-Z Drug Facts, AHFS DI Monograph, Prescribing Information

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List of Rheumatoid Arthritis Medications (222 Compared ...

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Arthritis (for Kids)

January 6th, 2019 1:45 pm

What Is Arthritis?

Arthritis (say: arth-ry-tiss) is a disease that causes swelling, stiffness, and pain in a person's joints.Joints are where two bones meet, allowing our bodies to move the hips, knees, ankles, elbows, shoulders, knuckles, etc. Joints contain synovial fluid, which acts as a lubricant to help them move easily.Arthritis can keep joints from working properly.

But isn't arthritis something that only old people get?

Actually, kids can get a kind of arthritis called juvenile idiopathic arthritis or JIA (it's also called juvenile rheumatoid arthritis, or JRA). Juvenile means young, so this means that JIA is different from the arthritis that adults get. Kids can have many different types of arthritis, but JIA is the most common.

Many problems can cause pain and swelling of the joints, so a doctor will want to know how long these problems have been going on. To be considered JIA, the joints must have swelling and pain for at least 6 weeks.

No one really knows what causes JIA. Something in the environment, like a virus, may trigger the disease in kids that already have certain genes that make it more likely for them to get it. (Genes are like instructions to the body on how to work. Genes are passed on from parents to their children and they decide everything from the color of a person's eyes to whether that person has a tendency to get a particular disease. Genes are part of our DNA and are found in the body's cells.)

JIA is not contagious, so you can't catch it from someone else.

Arthritis is an autoimmune (say: aw-toe-i-myoon) disease. An autoimmune disease means a person's immune system makes a mistake and attacks the body's own tissues or organs. Normally, a kid's immune system sends out white blood cells to protect the body and fight outside invaders like bacteria and viruses that can make a kid sick. But with an autoimmune disease like JIA, the immune system makes a mistake and attacks healthy cells.

Instead of recognizing the healthy cells and saying, "Hi, nice to see you," the immune system thinks the healthy cells need to be destroyed and releases chemicals to fight the healthy cells. The chemicals released by the immune system cause the pain and swelling that can happen with arthritis.

Just because a joint hurts doesn't mean a kid has JIA. A joint might hurt for a lot of different reasons, which is why it's important to see a doctor to figure out what the problem is.

The doctor will ask a lot of questions: How long has the kid had joint problems? Does he or she feel stiff when getting up or after resting? Are the joints swollen? Was there an injury? Could another problem be causing arthritis, such as Lyme disease? Is there a family history of arthritis or other autoimmune diseases?

Getting these answers and doing a physical exam, blood tests, and X-rays will help the doctor figure out if it is JIA. If your doctor thinks you may have it, he or she may send you to see a doctor who specializes in the diagnosis and treatment of arthritis. This kind of doctor is called a rheumatologist (say: roo-muh-tol-oh-jist).

Some kids who have JIA might take medicine like ibuprofen to help control pain and inflammation. If the arthritis is more severe, they may need to take other medicines to help lower the pain and inflammation. Some of these medicines are pills, but others are shots.

It's important that kids with JIA keep their joints moving. Often a kid will see a physical therapist or occupational therapist. In addition to working with children to move their joints and strengthen their muscles, these therapists can help create special exercise programs for home or school that can help a kid stay active.

In addition to joint problems, JIA may cause uveitis (say: yoo-vee-eye-tus), an inflammation of the eye that can lead to problems with vision if it's not treated. All kids diagnosed with JIA should get their eyes checked by an ophthalmologist, a doctor who specializes in diagnosing and treating eye problems. If the eyes are affected, they may be treated with eye drops.

Besides taking medicines, akid can do a few things to help with the symptoms of JIA:

Kids with JIA can have a lot of stiffness when they first wake up in the morning. Once their joints warm up, they can usually move more easily. That's why you might notice that someone with JIA has trouble moving early in the day, but seems better later on.

It's important to find a good balance between activity (which helps kids stay flexible) and rest (which everyone needs). Swimming is a great exercise for someone with JIA. It stretches a lot of different muscles and tendons and helps keep a kid moving and flexible. It's important to stay active even when a kid isn't having symptoms.

Sometimes kids with JIA can go a long time, even months or years, without the disease bothering them. Then it comes back. This is called a flare-up or flare. Flare-ups just happen and can't be prevented. It can be frustrating if a flare-up happens on a day when the kid would like to be doing something fun, like attending a birthday party.

If you know someone with JIA, you may offer to carry books or give other help, if needed. It's also OK if the person doesn't want help.

The good news is that many kids with JIA will outgrow it. About half of kids with JIA may not need treatment as adults.

And even when the arthritis flares up, almost all kids with JIA can control it with medicine and other treatments, which means they can do most things that other kids can do.

Date reviewed: April 2016

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Arthritis (for Kids)

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