Best Cream Ointment Psoriasis Help | Psoriasis Treatment

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Children's Institute | Executive Assistant | Mac's List

Posted: 4/29/2013 – 12:54 pm

Location: Portland

Closing Date: open until filled

Industry: Education

Type: Full Time

Description:
The Executive Assistant will provide exceptional executive support for the President/CEO. Reporting directly to the Chief of Staff/CFO, s/he will provide proactive and ongoing support to the finance/accounting, development, human resources, board of directors, operations, and other organization functions. In carrying out these responsibilities, the Executive Assistant will support the organization’s mission, vision, values and principles and be able to articulate the organization’s function.

Application Guidelines/Contact:
Email resume and cover letter to: jobs@childinst.org – Subject line: “Executive Assistant”

Salary:
DOE

Application Url:
http://www.childinst.org/images/CI_ExecutiveAssistant-4_2013.pdf

Please mention Mac’s List when applying for this opportunity.


PlayWrite, Inc. | Development Director | Mac's List

Posted: 4/27/2013 – 10:37 am

Location: Portland

Closing Date: open until filled

Industry: Nonprofit

Type: Part Time

Description:
Seeking an experienced, proven Development Director who is interested in working with PlayWrite, Inc., a cutting edge non-profit organization that transforms the lives of youth at edge through the power of performance in art.

This individual will possess strong communication skills, a flexible personality, be eager to engage Board members, to identify and cultivate prospects, and have great insight and talent.

This is a part-time, volunteer position (15-20 hours/week).

Tasks

• Work closely with Executive Director and the Development Associate to nurture and build upon current donor list, and help cultivate new Prospective Donors

• Work closely with Board of Directors to help them cultivate new Prospective Donors from their own contacts and connections

• Stewardship of current roster of Individual Major Donors

• Oversee management of Donor Database and Donor Perfect (which is administered by the Development Associate).

Application Guidelines/Contact:
Please email a current resume and cover letter to jpark3725@gmail.com.

Salary:
Information not posted

Application Url:
Information not posted

Please mention Mac’s List when applying for this opportunity.


Assistant Director Undergraduate Job Shadow Program – Mac's List

Posted: 4/26/2013 – 11:30 am

Location: Eugene

Closing Date: open until filled

Industry: Education

Type: Full Time

Description:
The Lundquist College of Business seeks an Assistant Director for its new Job Shadow Program. The Lundquist College of Business has over 4,000 undergraduate students and more than 25,000 undergraduate business alumni.


The Assistant Director will be responsible for developing and managing all aspects of the Job Shadow Program. Candidates for this position must have a proven track record of successful program building, experience working with students or interns, and an understanding of corporate recruitment practices. The Assistant Director will be responsible for developing and managing a program that matches students with professionals (employer sponsors) in their area of interest for a one-day job shadow experience. The Assistant Director will also be collaborating with Career Services and the Centers of Excellence on adding employer sponsors into our base of potential employers of LCB graduates. In addition, the Assistant Director will be responsible for working with faculty to design and integrate career exploration curriculum into pre-business and business major curricula.


Primary Responsibilities:


• Develop a strategy and operational plan for the Job Shadow Program, focusing on the integration of career planning into pre-business and business major curricula.

• Develop short and long-term strategic goals for the Job Shadow Program.

• Collaborate with faculty on the integration and design of a curriculum that will integrate seamlessly into preexisting pre-business and business curricula.

• Recruitment of alumni, industry leaders and employers as sponsors for the Job Shadow Program.

• Collaborate with LCB Career Services and the Centers of Excellence to expand potential base of employer sponsors for the program.

• Develop, plan, implement and coordinate events to connect various populations of students with industry leaders, human resource managers, and alumni.

• Collaborate with Centers of Excellence and LCB Career Services to develop a program to engage alumni in mentoring students.

• Recruit and assist LCB undergraduate students (business majors and pre-business) with identifying and securing a job shadow experience and beginning their career planning process.

• Track and maintain contact with students who have participated in the Job Shadow Program.

• Maintain and report data on engagement with alumni, other corporate sponsors, and students.


Final candidate must successfully complete a criminal background check.


Qualifications:

REQUIRED –

• Bachelor’s degree from an accredited college or university.

• Minimum of four years’ of related experience in human resources or marketing, corporate recruitment, business administration or career services.

• A proven track record of developing and building successful programs (e.g. internship programs)

• Experience working with college students and/or interns and ability to assess individual capabilities.

• Knowledge of and experience in recruiting/staffing and engagement of business professionals.

• Strong oral, written and interpersonal communication skills.

• Professionalism, adaptability, and initiative.

• Ability to work in a collaborative and effective manner with faculty, administrators, students, alumni, and business people at all levels of an organization.

• A commitment to working effectively with students, faculty, and staff from diverse backgrounds.


PREFERRED –

• An advanced degree (e.g. business or higher education/student affairs) from an accredited university.

• Experience working in a Business School.

• Higher education experience.

Application Guidelines/Contact:
Submit a cover letter, resume, names and contact information for 3 professional references to LCBjobs@uoregon.edu. Reference Search #13084.


An Equal-Opportunity, Affirmative-Action Institution Committed to

Cultural Diversity and Compliance with the Americans with Disabilities Act.

Salary:
$52,000-$62,000 depending on experience and qualifications

Application Url:
http://jobs.uoregon.edu/unclassified.php?id=4241

Please mention Mac’s List when applying for this opportunity.


HR 460 – Patients' Access to Treatments Act (PATA) – Rare Disease …

The bipartisan Patients’ Access to Treatments Act (H.R. 460), introduced by Rep. David McKinley (R-WV) and Rep. Lois Capps (D-CA), limits cost-sharing requirements applicable to medications in a specialty drug tier (typically Tier IV or higher) to the dollar amount applicable to drugs in a non-preferred brand drug tier (typically Tier III). It will enable patient access to treatments, reduce disability and constrain health care costs.

Traditionally, commercial health insurers have charged fixed co-pays for different tiers of medications: generics (Tier I), name brands (Tier II), and off formulary brand medications (Tier III). As an example, the co-pays might be set at $10/$20/$50 for the three tiers.

Some commercial health insurance policies are now moving vital medications (mostly biologics) into “specialty tiers” that utilize high patient cost-sharing methods. This “fourth tier (IV)” is now commonly requiring patients to pay a percentage of the actual cost of these drugs – from 25% to 33% or more, often costing hundreds of dollars, even thousands of dollars, per month for a single medication – rather than a fixed, flat dollar co-payment. These practices are placing medically necessary treatments out of reach of average Americans.

Background: With appropriate treatment in patients with chronic, life-threatening and disabling conditions including multiple sclerosis, rheumatoid arthritis, psoriatic arthritis, lupus, some forms of cancer, and primary immunodeficiency diseases, biologic drugs can prevent patients from becoming disabled, seriously ill, or dying. They can allow patients to maintain daily function, remain in the workforce and contribute to the tax base and raise their families.

  • Biologics are FDA approved and have no inexpensive generic equivalents.
  • Individuals unable to afford specialty tier pricing are likely to go without crucial medications, resulting in disability and other future health complications that can lead to increased health care costs that affect our entire health care system.
  • Yearly costs for affected medications can range from $12,000 to $48,000 or more. Cost-sharing for prescription medications should not be so large as to inappropriately restrict or interfere with medically necessary use of medications.

Supporters of the Patients’ Access to Treatments Act:

American Academy of Neurology, American Academy of Pediatrics, American Autoimmune Related Diseases Association, American College of Rheumatology, American Society of Clinical Oncology, Arthritis Foundation, Colon Cancer Alliance, COPD Foundation, Crohn’s and Colitis Foundation of America, GBS/CIDP Foundation International, Hemophilia Federation of America, Immune Deficiency Foundation, Leukemia & Lymphoma Society, Lupus Foundation of America, National Fibromyalgia & Chronic Pain Association, National Hemophilia Foundation, National Patient Advocate Foundation, National Psoriasis Foundation, Oncology Nursing Society, Patient Services Incorporated, Pulmonary Hypertension Association, Sjögren’s Syndrome Foundation, Spondylitis Association of America, The Alliance for Patient Advocacy, and US Hereditary Angioedema Association

Click to download: FAQs – Patients’ Access to Treatments Act – 3 5 13

to be held on August 17 to 18 | http://www.monclerxpascher.com/blog

America’s Next Top Model Winner Caridee English Speaks At Congressional Briefing

For more resources about or for the full version of the story please review

Article Source:

America?s Next Top Model seventh season winner CariDee English represented the National Psoriasis Foundation at a congressional briefing on June 11th in Washington, D.C. The briefing,hollister, which was held in support of the Psoriasis and Psoriatic Arthritis Research, Cure and Care Act, had more than a hundred people as an audience, anxious to hear English and other speakers talk about the debilitating disease,louboutin.

“It was gratifying to speak out in favor of the psoriasis bill with people who have the power to make it happen,” said the 21 year old model.

English, who was a victim of the disease herself,coach outlet online, was diagnosed when she was only five years old. By the time she reached her teen years, the disease had covered around 70% of her body. Her lifelong dream was to become a model, and this was slowly dying as her condition worsened over time. However, thanks to her doctor who was able to help her control the disease,michael kors, she was able to gain confidence to try out and eventually win America’s Next Top Model Cycle 7.

In May this year,chaussures louboutin, she became the spokesperson for the National Psoriasis Foundation, a non-profit organization that raises awareness and understanding about the disease through education and advocacy.

“Psoriasis awareness is very important to me,ralph lauren,” said the victorious winner of ANTM’s seventh cycle. “I want others with the disease to know they are not alone. I want to inspire them to live their dreams,chaussures louboutin.”

English,kors outlet?s mother,michael kors, Pam Flesness, who suffers from psoriasis, became a member of the organization when English was younger. Flesness was present at the congressional briefing where her daughter and the other speakers talked about the systemic nature of psoriasis and its roots in the immune system,coach outlet. English addressed a number of questions regarding the disease, including how it emotionally and physically affects her,hollister, what it,coach outlet online?s like to live with psoriasis and the new psoriasis legislation,michael kors.

In February,chaussures loubouti, the said legislation was first introduced to the House of Representatives by Rep,chaussures louboutin. David Wu,louboutin, D-Oregon. Wu also discussed the legislation and the importance of finding a cure for psoriasis at the congressional briefing.

English is expected to appear at the National Psoriasis Foundation 2007 National Conference in Las Vegas, Nevada, to be held on August 17 to 18.

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Cure National Vitiligo Foundation « Perfect Skin Wellbeing

Long term intake of national vitiligo foundation usa certain drugs is found to produce the pigmentary disorder. Cure National Vitiligo Foundation Cure National Vitiligo Foundation in many cases especially in children we often have no clue why one develops vitiligo. Vitiligo Symptoms The typical appearance of Vitiligo is a milky while depigmented spot or spots.

Folic acid can also be found although in lower levels in corn citrus fruits broccoli beets and beer. Beer is a strange one however considering that alcohol consumption is a factor in the acceleration of vitamin B9 deficiency! Raw food is best for providing folic

Cure National Vitiligo Foundation

acid because being water soluble it can be absorbed in the cooking fluid and also cooking heat tends to destroy it. Folic acid also comes under attack from the acids in the stomach and so it is advised not to take folic acid on an empty stomach.

Vitiligo on the scalp may affect the color of the hair (though not always) leaving white patches or streaks. It will similarly affect facial and body hair. Vitiligo may also be Cure National Vitiligo Foundation hereditary; that is it can run in families.

The condition is principally more obvious externally in individuals with darker skin types. The clear-cut cause of vitiligo is complex and not known yet. There is evidence that suggest it is caused by an amalgamation of auto-immune genetic and environmental factors. But it has not been proved worldwide. Several people consider having a link between sunburn and vitiligo. A current hypothesis put forward the cause that vitiligo occurs because people develop antibodies that are national vitiligo foundation inc harmful to the unique cells which produce melanin in the body. White patches on the skin premature graying of the scalp eyelashes eyebrows and beard and sometimes a loss of color inside the mouth–these are some of the distinct signs of vitiligo.

And that’s when I realized I had vitiligo. Vitiligo is a skin disorder in which the cells that national psoriasis foundation produce pigment in the skin mucous membranes and retina are destroyed according to the National Institute of and Musculoskeletal and Skin Diseases’s website. As a result patches of the skin (and often the hair growing on those patches) turns white. There is no known cause of vitiligo but several theories have been suggested.

Loss or change in color of the inner layer of your eye (retina). 4.Loss of color in the tissues that line the inside of your mouth (mucous membranes). Treatment of Vitiligo PUVA treatment (8-methoxypsoralen 5-methoxypsoralen trimethylpsoralen plus UVA) was often the most practical choice for treatment especially in widespread vitiligo in patients.

There are several home remedies national lupus foundation that proved to be extremely efficient in treating leucoderma. One of these efficient home remedies consists in radish seeds and vinegar. You have to grind the seeds until they become powder.

Diagnosis Vitiligo is diagnosed based on a medical history and a physical exam as well as on the results of laboratory testing. A biopsy or skin sample may be taken to confirm diagnosis. In vitiligo cells observed under a microscope should show a total lack of melanocytes while the presence of inflammation in the cells can mean that another condition is causing loss of pigment.

  1. High Cholesterol Levels: The regular eating of black radish drink inside the diet plan facilitates minimising the cholesterol levels in the body
  2. Picrorhiza Picrorhiza is an Indian herb that has been used for treating different types of skin conditions including vitiligo
  3. If the body is failing to absorb vitamin B12 then a supplement is advisable
  4. A number of researches have been conducted over the years and some advancements have been achieved such as the development of treatment methods to manage its symptoms

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NIH Awards $1.9 Million Grant For Interleukin-17C Research

Crain’s Cleveland Business is reporting that a Cleveland researcher has been awarded a five-year, $1.9 million federal grant to explore whether a member of the interleukin-17 family may play a role in the development and progression of psoriasis.

Nicole Ward

Nicole Ward

Nicole Ward, an assistant professor of dermatology in Case Western Reserve University’s School of Medicine, is investigating interleukin-17C, a protein that regulates the immune system. The grant will allow her to build upon earlier research suggesting a relationship between IL-17C and another protein (called TNF-alpha) in the emergence of psoriasis, according to a press release.

The National Institute of Arthritis and Musculoskeletal and Skin Diseases, a division of the National Institutes of Health, bestowed the award.

Earlier this year, Ward and colleagues published an article in the Journal of Immunology that reported psoriasis patients have elevated levels of IL-17C in their skin. Following treatment with TNF-alpha inhibitors, a standard therapy, IL-17C levels drop rapidly, even before the skin visibly improves. This development suggests that the presence, or interaction, of IL17-C and TNF-alpha are critical for the pathogenesis of the disease.

Ward and her colleagues also found that mice genetically engineered to overproduce IL-17C in the skin develop spontaneous lesions that resemble human psoriasis, suggesting a potential critical role for this molecule in disease initiation.. She now hopes to identify how IL-17C synergizes with other inflammatory molecules to cause disease—an understanding that may help identify a new target for drug development.

Injectable treatments focusing on interleukin-17 that are in Phase III of the research pipeline are:

• Brodalumab, Amgen

• Ixekizumab, Eli Lilly

• Secukinumab, Novartis

(MK-3222 from Merck targets interleukin-23. Stelara, from Janssen, targets interleukin-12 and interleukin-23.)

The research will be directed by Ward with collaborators and co-authors of the Journal of Immunology paper, Thomas McCormick, PhD, of Case Western Reserve, and Johann Gudjonsson, MD, PhD, and Andrew Johnston, PhD, of the University of Michigan.

In addition to the NIAMS grant, Ward’s research is supported by the National Psoriasis Foundation, the Murdough Family Center for Psoriasis and additional grants from the National Institutes of Health.

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Dr. Alan Menter To Receive Lifetime Achievement Award From The …

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Dr. Alan Menter

Dr. Alan Menter

Don’t know whether it’s Dr. Alan Menter’s charm, his British accent, or his brilliance, or perhaps all three, that have made him the fan favorite of those with challenging skin. In Dallas since 1975, he’s been dealing with every type of dermatological issue. However, one in particular really caught his attention years ago — psoriasis.

Oh, sure, you’ve heard it’s unattractive, but that doesn’t even touch the pain and cruelty of this immune-mediated disease that affects 7.5 million Americans, including 675,000 Texans.

No, you don’t have to worry about it being contagious. That’s the good news. But treatment is difficult at best and no one is quite certain what causes it. That’s the bad news. The worst news is that depending upon its severity, it can be embarrassingly ugly, painful and cause disability because of its effect on joints resulting in painful arthritis.

Alan has become world famous for his research and dedication in breaking the barriers of the disease’s treatment and cure. In 2004 he founded the International Psoriasis Council, as well as co-authored a “groundbreaking study that identified the first gene involved in the development of psoriasis and helped pave the way for future psoriatic disease research.”

For his years of work and creating greater awareness of the disease, Alan will receive a Lifetime Achievement Award from the National Psoriasis Foundation at its semi-annual Commit to Cure Gala on Saturday, October 26, at the Hilton Anatole.

“Dr. Menter’s passion for treating people with psoriasis has made him a world-renowned leader and innovator in medical dermatology as well as a friend of many individuals affected by the disease,” said Julie Hubach, chairwoman of the Psoriasis Foundation Gala committee. “The gala will be an evening of gratitude and celebration while raising funds for a very worthy cause with cocktails, seated dinner and a video tribute to his work.

“This is a once-in-a-lifetime fundraising event honoring our dear friend and internationally respected physician,” Julie continued. “We anticipate many of Alan’s colleagues from many countries will be attending the event.”

“There probably aren’t many people with psoriasis in the United States who haven’t benefited from Dr. Menter’s knowledge of the disease and his commitment to improving patients’ lives,” said Dan Farrington, chair of the National Psoriasis Foundation Board of Trustees. “Throughout his career, he has guided the next generation of psoriasis experts and researchers, worked to improve treatment options and standards of patient care, and paved the way for future psoriatic disease research. We are thrilled to honor Dr. Menter for all he’s done for the psoriasis community.”

How about a little trivia about Dr. M? In addition to his leadership in medicine, he was known for being a flyhalf rugby union player for the Springboks.

Photo provided by National Psoriasis Foundation

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