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#20 From: "IBDCURE.ORG E-NEWS" <enews@...>
Date: Tue Dec 30, 2008 4:22 pm
Subject: BREAKING NEWS: OP-ED FROM TODAY'S WALL STREET JOURNAL.
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IBDCURE BREAKING NEWS: Op-Ed From Today's Wall Street Journal.

  • Need a Real Sponsor here



The FDA Is Killing Crohn's Patients

Science didn't require that I get a placebo.

Right now there are millions of individuals whose lives are directly dependent on the rate at which new drugs come to market. I'm one of them. I'm fighting for my life.

To date, half of my intestine has been removed to manage Crohn's disease. Last year, at age 23, I enrolled in a clinical trial for a treatment that could save my life: an adult stem-cell therapy that helps damaged intestinal tissue regenerate from the relentless inflammation and scarring caused by Crohn's.

The sponsor, Osiris Therapeutics, reported that Crohn's patients in the therapy's Phase II trial all experienced clinical improvement after receiving the cells. A Phase III trial for the treatment is now nearing completion, but Food and Drug Administration (FDA) approval could be years away, despite its FDA "fast track" designation.

In accordance with antiquated FDA policies, the Phase III trial is randomized with three groups of patients, and double-blinded, which means neither the doctors nor patients are told what treatment is being administered. One group received full-strength stem cells, another received half-strength, and a third got a placebo (the proverbial "sugar pill"). It appears I got the placebo.

Foregoing all other treatments, I received the four scheduled infusions, and yet my disease progressed with a vengeance. In a matter of weeks, I became dangerously malnourished. I've since been readmitted to the hospital countless times, as my doctors continue to plead with Osiris for information. But Osiris has refused, citing adherence to FDA protocol.

I am now a lab rat. I have no right to know what happened to me in the study, nor do I have a right to try the promising treatment as my health deteriorates. It doesn't have to be this way.

Under the Fifth Amendment's guarantee that "No person shall be deprived of life, liberty or property without due process of law," a critically ill patient should have access to a potentially lifesaving drug that has been deemed safe for human consumption, if the patient agrees to bear the risks involved. But earlier this year, the Supreme Court refused to hear a case on the issue, denying countless patients their right to pursue life.

Thankfully, some members of Congress have stepped in to ensure our rights as patients. In May, Sen. Sam Brownback (R., Kan.) and Rep. Diane Watson (D., Calif.) introduced the Access, Compassion, Care and Ethics for Seriously Ill Patients Act. If passed, this bipartisan legislation will begin to restore the rights of millions of patients by widening access to promising investigational drugs.

Human clinical research is an intricate scientific and moral process, but it does not justify taking immoral advantage of patients. Tragically, FDA and Osiris think it does.

Typical approval protocols almost always guarantee patients taking the placebo access to the actual drug -- at the very least -- after the study has ended. But in what appears to me a deliberate act of cruelty, Osiris hung its patients out to dry without any recourse, refusing to confirm which patient got what. The FDA has endorsed Osiris's decision by enabling it to proceed with the study.

Withholding a potential cure is just as bad -- if not worse -- than the potential death sentence of a serious illness. If patients like myself have the audacity to put their lives on the line for the betterment of science and those in their predicament, their decision should not only be embraced, it should be rewarded.

Furthermore, trials without ethical recourse can lead to inadequate and incomplete data, compromising the integrity of the study. If trial patients are treated like lab rats, they won't feel obliged to cooperate unconditionally and report accurate data -- something the FDA and the drug industry rely on heavily, but have failed to consider.

Everyone agrees it is a fundamental right for patients to dictate their course of treatment with FDA-approved drugs. So why do the rules evaporate at the most critical moment, when the only life-preserving options are highly promising investigational drugs?

Mr. Sofer is a student at the University of California, Berkeley.

Write to gideon@...


#19 From: "IBDCURE.ORG E-NEWS" <enews@...>
Date: Thu Aug 7, 2008 7:45 pm
Subject: BREAKING NEWS: CONGRESSMAN FRANK PALLONE JR. (D-NJ) INTRODUCES IBD STAMP BILL (H.R. 6753)
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IBDCURE BREAKING NEWS: CONGRESSMAN FRANK PALLONE JR. (D-NJ) INTRODUCES  IBD STAMP BILL (H.R. 6753):



FOR IMMEDIATE RELEASE: CONTACT: Andrew Souvall  (202) 225-4671 

  PALLONE INTRODUCES LEGISLATION INSTRUCTING POSTAL SERVICE TO ISSUE STAMP PROMOTING AWARENESS OF CROHN'S DISEASE

Inspired by Highland Park resident's struggle with the disease

Washington, D.C. --- Inspired by the story of a Highland Park resident fighting Crohn's disease, U.S. Rep. Frank Pallone, Jr. (D-NJ) last week introduced a bill in the U.S. House of Representatives directing the Postmaster General to issue a commemorative postage stamp to promote public awareness of Crohn's disease.

Crohn's disease, also referred to as Inflammatory Bowel Disease (IBD), is a chronic and painful intestinal disorder that affects an estimated 1.4 million Americans.  Crohn's disease is believed to be an autoimmune disorder caused when a person's immune system is unable to recognize certain proteins.  The result is a severely inflamed digestive tract as the immune system fights off what it sees as abnormal proteins.  While the cause and cure of Crohn's is still unknown, current evidence suggests that genetic, bacterial and environmental factors may contribute to the development of Crohn's disease.

Pallone became involved in the IBD awareness campaign eight years ago after receiving a letter from and later meeting with 16-year-old Gideon Sofer.  Gideon told Pallone how his weight dropped to less than 45 pounds at the age of 12 before doctors properly diagnosed his condition.  Gideon emphasized just how little is really known about the disease.

Since then, Pallone has worked with Gideon, now 24 years old, in his personal struggles to finish his schooling and in his efforts to found the IBD Cure Foundation, an organization that is working to raise awareness of Crohn's disease

"Gideon's story is truly inspiring and since meeting with him years ago, this battle for Crohn's awareness has struck a personal chord with me," Pallone said.  "Gideon has refused to let this disease stop him from reaching his goals and has strived to improve the lives of the millions of others affected by Crohn's."

"During one of my initial hospitalizations, I thought about the breast cancer, HIV, and other awareness stamps that had been issued," Gideon writes on his Web site.  "I thought to myself at that very moment, maybe one day, there could be a Crohn's stamp."

The U.S. Postal Service has a history of shedding light on serious diseases in critical need of awareness.  The Breast Cancer semi-postal research stamp, first introduced in 1998, has now raised over $60 million for research and has since become the best-selling stamp in United States history.

 "Awareness is the most critical step in battling any disease, but particularly one like Crohn's, which is seldom discussed in public," Gideon said.  "What most Americans don't realize is the immeasurable impact these types of stamps have.  The Postal Service really has a quiet way of initiating massive change.

"Despite affecting so many Americans, Crohn's is too often misdiagnosed, leaving many individuals to suffer with an unknown disease," Pallone said.  "It is my hope that a postage stamp would help educate the public and the medical community about this debilitating disease."

 It is estimated that of the 110 Americans diagnosed with IBD every day, at least one-third are adolescents.  Crohn's disease affects approximately 100,000 children under the age of 18 and has been detected in babies only several months old.  Up to three-quarters of children diagnosed with Crohn's disease will require one or more operations to remove permanently damaged tissue in the intestines.

###

110TH CONGRESS 
2D SESSION H. R. 6753 

IN THE HOUSE OF REPRESENTATIVES 
JULY 31, 2008 

Mr. PALLONE introduced the following bill; which was referred to the Committee on Oversight and 
Government Reform 

A BILL

To provide for the issuance of a commemorative postage stamp on the subject 
of inflammatory bowel disease. 

Be it enacted by the Senate and House of Representatives of the United 
States of America in Congress assembled, 

SECTION 1. FINDINGS. 

Congress finds that— 
(1) Crohn’s disease and ulcerative colitis are chronic and painful 
inflammatory diseases of the gastrointestinal tract which are difficult to 
diagnose due their invisible symptoms and similarity to other intestinal disorders; 
(2) Crohn’s disease may occur in any section of the gastrointestinal 
tract but is predominantly found in the lower part of the small intestine 
and the large intestine; 
(3) ulcerative colitis is characterized by inflammation and ulceration 
of the innermost lining of the colon, and complete removal of the colon in 
patients with ulcerative colitis can alleviate symptoms; 
(4) because Crohn’s disease and ulcerative colitis behave similarly, 
they are collectively known as inflammatory bowel disease;
(5) both Crohn’s disease and ulcerative colitis present a variety of 
symptoms, including severe diarrhea, dehydration, lack of appetite, weight 
loss, nutritional deficiencies, abdominal pain with cramps, fever, and  rectal bleeding; 
(6) while there is no known cause or medical cure for inflammatory 
bowel disease, current evidence suggests that genetics, bacteria, and 
environmental factors may play a role; 
(7) it is estimated that up to 1,400,000 people in the United States are 
afflicted with inflammatory bowel disease; 
(8) it is believed that there are an additional 600,000 Americans who 
have inflammatory bowel disease, but whose condition is either 
misdiagnosed or undiagnosed, thereby resulting in their failure to receive 
proper treatment; 
(9) approximately 110 persons (1⁄of whom are adolescents) are 
diagnosed with inflammatory bowel disease in this country each day; 
(10) inflammatory bowel disease affects approximately 100,000 
children under the age of 18 and has been detected in infants just months 
old, with the disease’s “second wave” developing in adults over the age of 50; 
(11) inflammatory bowel disease accounts for an estimated 200,000 
hospitalizations in the United States each year; 
(12) the annual cost in missed workdays for Americans with 
inflammatory bowel disease is estimated to be in the billions of dollars or 
about $5,500 per patient with active disease; 
(13) approximately 200,000 patients with inflammatory bowel 
disease receive some form of permanent work disability compensation 
from the Social Security Administration; 
(14) these patients have reported low quality of life and persistent, 
systemic, active disease requiring frequent surgical intervention or 
hospitalization, thus impacting their ability to work and function normally; 
(15) children with inflammatory bowel disease miss school and 
related activities because the disease often becomes too painful and a 
constant feature of their lives;
(16) an estimated 2⁄to 3⁄of children with Crohn’s disease will 
undergo multiple surgical operations in their lifetime to remove 
permanently scarred intestinal tissue, thus putting them at risk for 
developing short bowel syndrome and other life-threatening complications; 
(17) 60 to 90 percent of children with recurrent Crohn’s disease will 
experience growth failures, and many adults who have onset of bowel 
disease as children experience delayed puberty and impaired growth, and 
never reach their full genetic growth potential; 
(18) inflammatory bowel disease also puts patients at high risk for 
developing colorectal cancer; 
(19) the Federal Government, public and private organizations, 
healthcare providers, and the medical community are striving to work 
together more closely in order to improve the quality of life of children 
and adults affected by Crohn’s disease; 
(20) the United States Postal Service has issued stamps featuring 
critical causes in need of medical or social awareness in line with the 
criteria set out by the Citizens’ Stamp Advisory Committee; and 
(21) the breast cancer semipostal research stamp has now become the 
best-selling postage stamp in United States history, raising over 
$60,000,000 for breast cancer research. 

SEC. 2. INFLAMMATORY BOWEL DISEASE COMMEMORATIVE POSTAGE STAMP. 

(a) IN GENERAL.—The Postmaster General shall issue a commemorative 
postage stamp on the subject of Crohn’s disease and ulcerative colitis, 2 
chronic digestive diseases collectively known as inflammatory bowel disease. 
(b) REQUIREMENTS.—Such stamp— 
(1) shall be issued in the denomination used for first-class mail up to 
1 ounce in weight and bear such design as the Postmaster General shall 
determine; and 
(2) shall be placed on sale as soon as practicable after the date of the 
enactment of this Act and sold for such period of time as the Postmaster 
General shall determine.

###
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#17 From: "IBDCURE E-NEWS" <enews@...>
Date: Fri Sep 28, 2007 2:03 pm
Subject: A Personal Message From Gideon
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IBDCURE: A Personal Message From Gideon.

RE: Last Week's Page-One Story in the Wall Street Journal

28 SEPT 2007

Dear Friends,

As many of you now know, in June 2006 I had begun an experimental therapy for Crohn's disease, an intestinal disease which I've endured since I was just days old. Because I – like so many dealing with this disease – have few viable options to treat the disease, my doctors felt it was not only in my best interest, but absolutely critical for me to start taking this new drug, as I have been unable to achieve clinical remission ever since I was diagnosed at age twelve in 1996. Through it all, I've had close to half my gut surgically removed, and at one point, I nearly died in the hospital, battling liver failure, internal bleeding, and some of the most resistant forms of staph. During the past four years, however, I've been fortunate enough to fight my way back to life with the help of some of the best doctors in country.

After initially taking this new drug for three months, my blood work improved dramatically in ways I had never responded to any other therapy. This was the most encouragement I had in years. To be given the hope that one day, I may live a life free of this menacing disease, is simply the greatest hope one could ask for.

But by the end of August 2006, I was robbed of this hope when my insurance company – Blue Cross/Blue Shield of New Jersey – casually decided that protecting their bottom line was more important than my life. They decided to withdrawal their initial approval for the drug. In an effort to save $8,800 per month - the price of the new medication - they hired a peer-clinical medical doctor to review my case in dissent, to deem that it wasn't "medically necessary" for me to continue taking the drug. After alerting the drug manufacturer – Celgene Corporation – of my dire situation, they decided to not dispense the drug to me free-of-charge, as they did on a case-by-case basis patients unable to garner coverage.

What ensued in the months afterwards was a hospitalization, along with additional health challenges of enormous magnitude. I had no choice but to drop my enrollment at school for the semester, and spent months with my doctors trying to find something else that would keep me out of the hospital.

What also ensued was serious and utter disgust for the inner-workings of our health-care system. After witnessing such an atrocity first-hand, I could not come to grips with fact that Blue Cross was able to swindle their way out of paying for a drug in which they had initially given the green light. Further, the clandestine manner in which they went about withdrawing their initial approval was exceedingly unjust, and their excuse for having pulled the rug out from under me simply could not be justified.

I was even more appalled to find that I am just one of millions in this country struggling to garner approval for life-saving therapies. Many have been quick to assume that medications which aren't covered through private insurers or Medicare are automatically dispensed free-of-charge by the drug companies, but this couldn't be further from the truth.

The drug companies have collaborated to wage full-fledged ad campaigns to the allay the public's fears on popular networks like CNN to play down the calamitous issues at hand, by placing themselves in heroic positions, boasting their so-called "patient assistance programs."

But the fact is Celgene's shareholders has benefited from nearly a 1000% increase in its stock price in the past five years. The CEO of the company was compensated $1.24 million dollars in cash in 2006, and exercised more than $33 million dollars in stock options. Other company insiders have also enjoyed exorbitant compensation through sales of their own lofty stock price. So clearly, when there is enough money to go around, why are there patients like myself still struggling to obtain access to essential medicines, which may in fact be our last hope?

When I was exposed to something so atrocious and so backward, I felt compelled to do something about it. Acting on it was a moral imperative – not just for myself because my life is on the line – but for everyone in this predicament.

The truth is I was not ready to back down; I was not ready to give-in. Not just for me, but because this is not the America I know. We're supposed to be a shining example for the rest of the world to follow. And if this what we have to show, then what kind of message are we sending? What does it mean when drug companies care more about their profits than their patients? What does it mean when private insurers can hire their own consultants to weasel their way out of paying for life-saving medications? What does it mean when our system fails patients like myself and leaves us to die?

It means that it's time for things to change. I hope that my experience is a wake-up call to lawmakers in Washington and throughout the country. Regardless of my ability to have garnered approval for this medication, many patients who lack the energy and resources to advocate for themselves are still left in the dark. I hope that my situation will set a positive precedent, and bring to light to this vital issue. Nobody should ever have endure what I've experienced, and not have access to medicines they so desperately need. Because I know there can be a better way, I know there must be better way.

On a final note, I want to take this opportunity to thank those of you who have taken the time to write, expressing your kind comments and desire to see things change. I would strongly encourage you to also forward your comments to Geeta.Anand@... - the author of the piece - and post them on the Wall Street Journal health blog at: http://blogs.wsj.com/health/2007/09/18/drug-sticker-shock-makes-insurers-sticklers/

Let's get this conversation started.

With great heath,

Gideon.

///

PS: For those of you who do not have WSJ.com access, the article can be read at:

http://health.groups.yahoo.com/group/ibdcure/message/16

or downloaded in pdf format at:

http://www.ibdcure.org/WSJ.pdf


#16 From: "IBDCURE. ORG E-NEWS" <gideon.sofer@...>
Date: Tue Sep 18, 2007 7:24 pm
Subject: LATE-BREAKING NEWS: BURDEN OF PROOF - As Costs Rise, Medicines Face Pushback
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IBDCURE LATE-BREAKING NEWS: BURDEN OF PROOF - As Costs Rise, Medicines Face Pushback

THE COMPLETE ONLINE VERSION OF THIS RELEASE (WITH GRAPHICS) CAN BE ACCESSED AT: 





Tuesday, September 18, 2007

PAGE ONE


BURDEN OF PROOF

As Costs Rise,
New Medicines
Face Pushback

Insurers Limit Coverage
To FDA-Approved Uses;
$300,000 Drug Denied

By GEETA ANAND

September 18, 2007

May Chin-Louis, 44 years old, has a ballooning brain tumor. Her doctors wanted to attack it with a colon-cancer drug that has shown promise in treating brain tumors.

But for four months, Ms. Chin-Louis's insurer, WellPoint Inc., refused to pay for the drug, called Avastin. It costs about $8,000 a dose, every other week. A WellPoint spokesman says it denied coverage initially because there isn't sufficient medical evidence proving Avastin is effective against brain tumors.

NARROWING SPECIALTIES

 

•  The Issue: High-priced 'specialty' drugs are seeing a pushback from insurers.
•  The Background: Doctors often try drugs approved for different diseases for patients without other options.
•  Bottom Line: Some patients are being denied potentially effective therapies.

"She's a young patient with a family who has run out of options -- she's just looking for a chance," says her oncologist, Susan Chang. Patients with Ms. Chin-Louis's condition typically live for only about four months.

Doctors, particularly oncologists, rely on medicines approved for other diseases to try to save patients for whom all other treatments have failed. But as new medicines come to market at ever-higher prices, insurers are pushing back, limiting coverage of these drugs to only the disease for which they are specifically approved by the Food and Drug Administration -- or for which there is extensive evidence of efficacy in clinical trials.

"A lot of patients are being denied potentially effective therapies," says James Vredenburgh, an oncologist at Duke University Medical Center. "What's happening is totally arbitrary and it's 100% correlated to when the prices went up. Ten years ago, we never got questioned on our medical decision to prescribe the medicine with the best chance of helping our patients."

Insurers say they must limit use of the most expensive drugs to control health-care costs, which are surging at a 7% to 8% annual rate and continue to outpace inflation. It makes sense, they say, to require proof that a drug works in a patient's particular disease before doling out tens or hundreds of thousands of dollars.

"We're trying to bring new drugs to consumers, but trying to do it with employers getting the best value of every health-care dollar spent in the system," says Mohit Ghose, spokesman for America's Health Insurance Plans, an industry trade group.

High-priced medicines used to treat relatively small groups of patients -- categorized as "specialty pharmaceuticals" -- comprise the fastest-growing part of health spending, insurance officials say. By pushing generics, insurers have clamped down on spending on other types of medicines, which rose 6% in 2006, according to Express Scripts, Inc., one of the largest pharmacy-benefit managers.



By contrast, spending on specialty drugs soared 21% last year. They accounted for nearly a quarter of total drug spending in the U.S., according to Health Strategies Group, a New Jersey consulting firm.

Insurers have little leverage in negotiating the prices of many specialty drugs because they often extend lives and lack competition. Drug companies have the freedom to price these medicines almost as high as they like. The companies say the prices are needed to fund research of new medicines and to compensate shareholders.

Genentech Inc. charges $4,400 a month, or $47,000 for the average treatment course of Avastin for colon-cancer patients. Higher doses are used in treating brain tumors, raising the cost.

Once a unique, life-saving drug is approved by the FDA for a disease, insurers almost always are required to pay for it, regardless of price. But insurers have leeway when a medicine isn't specifically approved for a particular patient's disease. Coverage varies among companies.

"As an insurer, you go where the money is to try to cut costs," says Abbie Leibowitz, former chief medical officer of Aetna, Inc., who runs Health Advocate, which advises employers and employees on health insurance. Spending on specialty drugs is "where there is the greatest opportunity to affect cost."

Wall Street is seeing the effects of the pushback in lower-than-expected revenue from some of the hottest new cancer drugs. Genentech's Avastin is FDA-approved for certain kinds of colorectal and lung cancers. But the drug should also be a big-seller in breast cancer based on a large study reported two years ago showing efficacy in that disease, says Steven Harr, a Morgan Stanley analyst. His research shows less than 10% of breast-cancer patients are using the treatment, for which Genentech charges $7,700 per month for the average patient.

With prices so high, insurers "won't pay until it's FDA-approved," Dr. Harr says. "For the first time ever, there's elasticity in demand."

Karen Kacures, who owns a lawn-care company in St. Francis, Minn., found that out the hard way. Ms. Kacures was diagnosed in January with Pompe disease, a rare genetic disorder. It is caused by a deficiency in an enzyme that leads to progressive muscle-weakening and an early death.

Along with the devastating diagnosis, her doctors brought some hope: Genzyme Corp., a Cambridge, Mass., biotech company, recently brought to market the first treatment for the disease. The drug, called Myozyme, replaces the enzyme deficiency that causes muscle degeneration.

Dosed by weight, the drug is priced at an average of $300,000 a year, for a patient's entire life.

In March, Ms. Kacures's insurer, PreferredOne Community Health Plan, a Golden Valley, Minn., nonprofit with 400,000 members, refused to pay for the drug.

"We consider that for adults, the evidence is not there to support its use," says John Frederick, chief medical officer of PreferredOne. He noted that Genzyme conducted its clinical trial to win approval of the drug only in infants. In approving the drug, the FDA required Genzyme to conduct another trial, which is under way, to prove safety and efficacy in adults.

Dr. Frederick acknowledges that the FDA didn't restrict approval of the drug to infants, but he says it was "a little fuzzy."

Drugs that are high priced and treat smaller populations have "just kind of taken over" the pharmacy budget, Dr. Frederick says. In the most recent fiscal year, his company's spending on specialty drugs rose 23% over the previous year; spending on other pharmaceuticals was almost flat, he says. Generics are helping "stem the tide" of spending, he says, but specialty medicines are "a concern to us from a cost perspective."

Calling Ms. Kacures's case "wrenching," Dr. Frederick says he wishes there were "a big systemic cure. I dream of a big super-insurance plan to cover these tragic cases."

Ms. Kacures, 47, who has appealed the denial, says she doesn't have time to wait until Genzyme finishes its study in adults. "I want to get treated while I can still walk and breathe on my own during the day," she says. She uses a cane to walk and a breathing machine at night.

Some adults do receive the drug. Mark Lingenfelter, 45, of Eau Claire, Wis., started taking Myozyme in November, after Medicaid, the government's health-insurance program for the disabled and poor, agreed on appeal to cover the cost of the drug.

For the first time in three years, Mr. Lingenfelter says, he's been able to stand up out of his wheelchair. His breathing has improved enough to be able to talk on the phone for a few minutes, sometimes to offer encouragement to Ms. Kacures. "It's made a complete difference in my life," he says.

Gideon Sofer, a freshman at the University of California, Berkeley, was turned down last year when he tried to get approval from his mother's New Jersey insurance plan to pay for a new medicine. The drug, Revlimid, was approved by the FDA to treat a rare blood disorder and not yet tested in Mr. Sofer's condition, Crohn's disease, an inflammatory disorder that causes severe digestive problems.

Mr. Sofer had been using thalidomide, the only medicine that had helped control the mouth and intestinal sores caused by his disease. But thalidomide caused such drowsiness that he says he couldn't take morning classes, and he experienced nerve damage causing him to lose sensation in his feet.

Revlimid, made by Celgene Corp., is billed as an improved thalidomide, minus the drowsiness and nerve damage.

At first, Horizon Blue Cross Blue Shield of New Jersey covered it for him. "I felt so much less fatigue, my anemia improved, it was just great," Mr. Sofer says. His doctor in New York, Maria Abreu, director of the inflammatory bowel disease center at Mount Sinai School of Medicine in New York City, says Mr. Sofer's weekly blood reports showed gains in his iron levels.

But in August 2006, Mr. Sofer received a letter saying "it was determined that you do not meet the Horizon Blue Cross Blue Shield of New Jersey established medical necessity criteria for this drug." It noted Revlimid was approved for patients with a blood disorder and not Mr. Sofer's disease.

"Although benefits are denied, you may elect to receive the medication at your own expense," the letter said.

Neither Mr. Sofer nor his mother, a social worker, could afford the drug, which retails at about $8,800 for a month's supply. Mr. Sofer called Celgene and asked if the company would donate the drug. He was connected to a Celgene program, called Patient Support Solutions, which provides free Revlimid to patients who meet certain guidelines.

In a letter, Mr. Sofer was told he didn't qualify for free drugs; he says an employee told him that Crohn's disease patients weren't eligible.

Last year, not long after his prescription ran out, Mr. Sofer was hospitalized, severely dehydrated. He withdrew for the semester, feeling too sick to continue. "This has depleted me physically and spiritually," he said at the time.



Celgene's Patient Support Solutions says that this year, the free-drug program was expanded to include patients regardless of diagnosis, as long as they meet certain financial criteria, which the company declines to publicly detail.

In April, Mr. Sofer began receiving free Revlimid. His iron levels rebounded, though he continues to struggle with infections related to his disease. "For people like me, for whom nothing has worked, access to new treatments is absolutely critical," says the 23-year-old Mr. Sofer. "It's the only thing that keeps me hopeful, that keeps me living."

Ms. Chin-Louis was diagnosed with a brain tumor in late 2001. She had been working as an administrator at an accounting firm and raising two boys in Danville, Calif., when her speech periodically became jumbled. A surgeon removed the tumor, which initially grew slowly.

Last year, the tumor returned. She underwent radiation and took a chemotherapy drug approved by the FDA to treat brain cancer.

Early this year, a magnetic resonance imaging, or MRI, showed a bigger spot on her brain, suggesting the drug she was using no longer was working.

At the same time, researchers at Duke University Medical Center were reporting a promising study of Avastin in combination with chemotherapy for brain tumors. In a small trial of 32 patients, 72% on treatment were alive at six months, 38% of them with no progression of their tumors -- about double what would be expected for patients with Ms. Chin-Louis's kind of recurring brain tumor.

"It was early data, but it was very exciting," says Dr. Chang, director of the division of neuro-oncology at the University of California, San Francisco, Medical Center. In April, Dr. Chang asked Blue Cross of California to cover Avastin for Ms. Chin-Louis.

Blue Cross, owned by WellPoint, an Indianapolis company with more than 34 million members, denied coverage on May 21, saying in a letter: "Studies are ongoing to determine the role of this agent in the treatment of brain tumors."

Ms. Chin-Louis and her husband, a supervisor in sales at United Parcel Service Inc., say they couldn't afford the treatment. Her sister, Linda Tong, says she and her brother offered to cover the cost, but Ms. Chin-Louis initially resisted.

"I really felt that I had been paying for insurance for years for a reason, and when I needed medical care, my insurance company should pay," Ms. Chin-Louis says. "I didn't want to put that burden on my family."

In June, the doctor says she put Ms. Chin-Louis on a chemotherapy drug and appealed the denial for Avastin -- telling insurance officials she wanted to use the drugs in combination. On July 20, a brain scan showed the chemotherapy wasn't working: Ms. Chin-Louis's tumor had grown by 30%. She immediately agreed to allow her siblings to pay for Avastin, and she underwent her first treatment early last month.

In early August, asked by The Wall Street Journal about the Avastin denial, James Kappel, a spokesman for WellPoint, said: "While this patient's condition is very unfortunate, there is no medical evidence that supports the use of the drug" in brain tumors.

But Mr. Kappel called back the next day, saying WellPoint had approved Avastin for Ms. Chin-Louis. He said the company denied coverage at first because Dr. Chang sought to use the drug alone. Because Dr. Chang subsequently requested to treat Ms. Chin-Louis in combination with chemotherapy, as in the Duke study, WellPoint approved it, Mr. Kappel said.

Dr. Chang says the UCSF center has participated in a trial comparing Avastin on its own for brain tumors and in use with chemotherapy. Avastin alone appeared effective in some patients in the study, which has yet to be published, she says.

Dr. Chang says Ms. Chin-Louis has responded well so far to the Avastin treatments. "She's awake and feeling good and able to engage with her family," the doctor says. Ms. Chin-Louis is due for a brain scan later this week, which she hopes will show the tumor's growth in check.

"I know none of these treatments works forever," Ms. Chin-Louis says. "But I definitely want a little more time."

She'd like to celebrate her 45th birthday on Sept. 30, she said. She's eager to see her sister Linda's baby girl, due to arrive by Cesarean section on Nov. 2. And a small part of her is even daring to hope she will be in the audience when her eldest son Andrew graduates from high school this June.

Write to Geeta Anand at geeta.anand@...1

 

URL for this article:

 

Copyright 2007 Dow Jones & Company, Inc. All Rights Reserved




#15 From: IBDCure E-News <enews@...>
Date: Tue Sep 26, 2006 11:15 am
Subject: NEWS UPDATE: Freshman's quest for postage stamp gets heartening response, but his health declines
enews@...
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IBDCURE NEWS UPDATE

THE COMPLETE ONLINE VERSION OF THIS RELEASE (WITH PHOTOS) CAN BE ACCESSED AT: http://www.berkeley.edu/news/media/releases/2006/09/25_ibd.shtml 

FOR IMMEDIATE RELEASE:  MONDAY, SEPTEMBER 25, 2006

Contact: Yasmin Anwar
(510) 643-7944

Freshman's quest for postage stamp gets heartening response, but his health declines

Four months after making an unusual pitch to the U.S. postmaster general, UC Berkeley freshman Gideon Sofer is making progress in his campaign for a stamp highlighting inflammatory bowel disease, and in spreading awareness of the disorder. But his personal fight against the disease is facing a setback.

By Yasmin Anwar, Public Affairs | 25 September 2006

BERKELEY – Four months after making an unusual pitch to the U.S. postmaster general, UC Berkeley freshman Gideon Sofer is making progress in his campaign for a stamp highlighting inflammatory bowel disease, and in spreading awareness of the disorder.

Last May, New Jersey's Make-a-Wish Foundation made arrangements for Sofer, 22, an avid stamp collector, to meet with Postmaster General John Potter to discuss Sofer's idea for an inflammatory bowel disease (IBD) stamp.

Sofer has Crohn's disease, a chronic intestinal disorder and member of the IBD constellation, which has landed him in the hospital for months at a time since he was 12 and led to the removal of nearly half his gut.

At the May 25 meeting, Potter listened intently to Sofer and told him he has family members who suffer from a digestive tract disease. Two days later, Potter featured Sofer in his welcome address at the opening of World Philatelic Exhibition in Washington, D.C.

"Would you be surprised to know that as many people suffer from Crohn's disease as suffer from Parkinson's disease?" Potter asked the audience after introducing Sofer. "(Gideon's) message to me was … we need to do a much better job of communicating. And, as somebody who collects stamps, he saw no better vehicle to get the word out than through a stamp."

Sofer couldn't have been more encouraged by Potter's response.

"A lot of what the postmaster general and I spoke about resonated with him because he's dealt with digestive disease in his family and really understands why it is so critical to get the message out," he said. "I think he's really going to play an important role in gaining approval for the stamp."

In support of Sofer's stamp effort, and Crohn's disease in general, Berkeley Hillel, the campus's Jewish student center, is hosting benefit concert the evening of Oct. 21. Performing will be the Afro-Semitic Experience, an ensemble that blends Jewish and jazz music.

Meanwhile at UC Berkeley, some students with IBD have contacted Sofer to thank him for raising awareness about a disease that nobody likes to talk about: "The stamp campaign is a creative and unique idea for bringing light to a disease that is unfortunately never talked about," one UC Berkeley student who suffers from ulcerative colitis, a form of IBD, wrote in an e-mail to Sofer.

An interview Sofer did on National Public Radio's "All Things Considered" show inspired Megan Leigh Dorko of Pennsylvania, who has Spina Bifida, to send Sofer a couple of potential stamp designs.

"I love being a graphic designer, and it's always been a goal of mine to incorporate my design skills with helping others in the best way I can," Dorko wrote in an e-mail to Sofer. "I hope the designs I've done for you can help your cause."

"The goal was to find a stamp that sent a strong message, but one that was also aesthetically pleasing," Sofer said. "This definitely captured both."

A meeting of the U.S. Postal Service's Citizens' Stamp Advisory Committee — which counts former UC Berkeley Chancellor Ira Michael Heyman among its members — is approaching, and Sofer is hopeful that consideration of a stamp highlighting IBD is on the agenda. The committee reviews ideas for new stamps proposed by members of the public and then recommends subjects and designs to the postmaster general. The process is highly confidential.

Although Sofer is making progress with his campaign for a stamp, his health isn't faring so well. Earlier this summer, Sofer started an experimental drug called Revlimid, a thalidomide derivative approved for some forms of cancer that appears to boost the immune system by increasing tumor-attacking white blood cells. He said this was a welcome change from the thalidomide he had been using, which has toxic side effects.

By all indications, Revlimid appeared to be working for Sofer. He gained weight and started feeling stronger. But when he went to refill his prescription in late August, he was told that his insurance company had withdrawn its approval of the drug for his treatment, and would no longer pay for his prescription.

"They hired a 'peer clinical M.D.' to review my case, and he deemed that it is not 'medically necessary' for me to take the drug — without ever having seen, met or spoken to me," Sofer said.

To continue the drug, he would have to pay more than $6,000 a month out of pocket, which he cannot afford. Sofer is appealing the decision and has been off of the medication for several weeks. He said that earlier this month, during a painful relapse, he was admitted to UC San Francisco Hospital for a one-week stay that arguably cost his insurance company at least half of what it would have paid for a year's prescription of Revlimid.

"Right now I am struggling, both physically and spiritually," said Sofer, who is headed to New York this week to see his physician.

Still, he added, "I'm so lucky to be alive. It's not always easy to tell myself this when I relapse, but that's what really gets me out of bed in the morning, and that's what is motivating me to do whatever it takes to get this stamp approved."

SIDEBAR: 

'The power of a stamp'

These are excerpts of a speech by U.S. Postmaster General John Potter at the opening ceremony of the World Philatelic Exhibition on May 27, 2006.

"Every once in a while there's a story that comes back and really rips me. And this is the story of a young man who has Crohn's disease and was really up against the wall. Many thought he wouldn't make it. At the time, he was contacted by the Make-a-Wish Foundation … It's a foundation that reaches out to young people who have diseases that may end their lives, and offers them an opportunity to have a wish.

"Today, I'm happy to have someone here whose wish – believe it or not – was to meet the postmaster general. Now, when I told my kids that, they said ... well, they were a little surprised! Why did Gideon Sofer want to meet the postmaster general? Because he understands the power of stamps.

"You see, it's not very popular to talk about a disease that affects your digestive system. Think about it. How often do you talk about that? Would you be surprised to know that as many people suffer from Crohn's disease as suffer from Parkinson's disease? Would you be surprised to know that when it comes to medical research, the country spends about 25 percent on Crohn's disease as it does on Parkinson's.

"(Gideon's) message to me was: First of all, we need to do a much better job of communicating. And, as somebody who collects stamps, he saw no better vehicle to get the word out, than through a stamp. And his goal is to get the Citizens' Stamp Advisory Committee here in the United States to listen to his plight and get the word out on this disease that has afflicted him and his family.

"So, think about that: The power of a stamp to carry a message on every envelope. Every person that sees that stamp gets the message, asks the question, what's behind that stamp? We celebrate a lot of things, but we also use stamps to carry messages; messages about our country, messages about good things about our country; but [also] messages of concern, and, in this case, awareness."

To learn more:

  • Read more about the IBD stamp campaign at ibdcure.org
  • For more information about the Oct. 21 benefit concert for Crohn's disease and the IBD stamp effort, contact Oren Kroll Zeldin at Berkeley Hillel (510) 845-7793
  • Student to make stamp pitch to US postmaster (NewsCenter, 5.24.06)

#13 From: "THE IBDCURE.ORG E-NEWS SERVICE" <enews@...>
Date: Thu May 25, 2006 1:06 pm
Subject: NEWS UPDATE: STUDENT TO MAKE STAMP PITCH TO U.S. POSTMASTER
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<<THE IBDCURE.ORG FOUNDATION INTERNATIONAL>> [RELEASE # BN25052006]

IBDCURE NEWS UPDATE

THE COMPLETE ONLINE VERSION OF THIS RELEASE (WITH PHOTOS) CAN BE ACCESSED AT: http://www.berkeley.edu/news/media/releases/2006/05/24_ibd.shtml

FOR IMMEDIATE RELEASE:  WEDNESDAY, MAY 24, 2006

5/24/06 - File #17275
Contact: Yasmin Anwar
(510) 643-7944

STUDENT TO MAKE STAMP PITCH TO U.S. POSTMASTER

UC Berkeley freshman to meet
U.S. postmaster general tomorrow
about stamp to highlight Crohn's disease

BERKELEY, California -- Gideon Sofer didn't ask for a trip to Disneyland or a
shopping spree when he made New Jersey's Make-a-Wish Foundation list
of terminally ill recipients in 2002. Instead, he wished for a
meeting with the U.S. postmaster general.

His goal was a postage stamp to highlight Inflammatory Bowel
Disease, which includes Crohn's disease, a chronic intestinal
disorder that has landed him in the hospital for months at a time
since the age of 12, and led to the removal of nearly half his gut.
To date, there is no known cause or cure for the disease.

Tomorrow, (Thursday, May 25) the 21-year-old avid stamp collector,
who just finished his first semester at the University of
California, Berkeley, will get his wish. He is scheduled to meet
with U.S. Postmaster General John Potter at 11 a.m. (EDT) in
Washington, D.C.

Sofer, who was drawn to UC Berkeley because of its strong disabled
rights movement, acknowledges that a digestive tract disease doesn't
exactly make for ideal dinner table conversation or evoke pretty
visuals for a stamp. But that shouldn't stop it from receiving
serious consideration, he said.

The U.S. Postal Service has issued stamps to raise awareness or
money for breast cancer, AIDS, prostate cancer, organ and tissue
donation, diabetes and sickle cell anemia. So why not Inflammatory
Bowel Disease (IBD)?

"This disease isn't a sexy subject, but it's got to be talked
about," Sofer said. "It's time for the suffering to end."

The opportunity first presented itself to Sofer when he was a New
Jersey high school sophomore whose body was wasting away from the
disease. When the Make-a-Wish Foundation contacted him, he said he'd
call back when he wasn't feeling so lousy.

In the meantime, he thought about asking for a meeting with rock
legend Bruce Springsteen or with actor Michael J. Fox, who has
battled Parkinson's disease. But he needed something that would make
a bigger impact on the lives of IBD sufferers like himself.

Two years later, he figured it out. He wished to see IBD join the
pantheon of medical frontier postage stamps, and to do that, he
needed the approval of the U.S. postmaster general. Thus,
preparations for a meeting began.

Of course, he realizes that meeting the postmaster general doesn't
guarantee a stamp. Of tens of thousands of proposals made each year
to the U.S. Postal Service's Citizens Advisory Stamp Committee -
which counts former UC Berkeley Chancellor Ira Michael Heyman among
its members - only about 20 are accepted. The advisory stamp
committee reviews ideas for new stamps proposed by members of the
public and then recommends subjects and designs to the postmaster
general.

Still, Sofer has garnered plenty of support for his campaign,
including the backing of his New Jersey congressman, U.S. Rep. Frank
Pallone Jr., who recently introduced a resolution urging a
commemorative IBD postage stamp. And through Sofer's IBDCURE
Foundation, he's collected 5,000 signatures in an online petition to
the Citizen's Stamp Advisory Committee in support of the stamp.

"Gideon refuses to be defeated by his Crohn's disease," said Heyman,
a law professor at UC Berkeley's School of Law (Boalt Hall).
"Rather, he is successfully informing the world of its nature in a
persistent, sophisticated and successful way."

There are regular commemorative postage stamps, which raise
awareness of an issue, and semipostal stamps, whose sales generate
funds for research or charity. Naturally, Sofer would prefer a
semipostal IBD stamp, but would be happy with either.

Not to be confused with Irritable Bowel Syndrome, Inflammatory Bowel
Disease, which includes Crohn's disease and ulcerative colitis, is
said to affect 1 million Americans, including 100,000 children and
teenagers whose growth it can stunt. It is classified as an
autoimmune disorder, although not enough research has been done to
confirm this.

It typically begins with inflammation in the intestine, rectum or
stomach. Common symptoms are diarrhea, abdominal cramping, rectal
bleeding and weight loss. It is uncertain what triggers the
inflammation. Theories range from viruses or bacterium inflaming the
digestive tract to a person's immune system being unable to
recognize certain proteins, and fighting off what it deems as
abnormal proteins.

Ever sickly as a child, Sofer was diagnosed with Crohn's disease
when he was 12 years old. He has spent much of his life in hospitals
and became known around school as a "children's hospital frequent
flyer." At first, physicians had no clue what was wrong with him,
but his mother kept pushing for help, insisting he was seriously ill.

As it turned out, she was right.

In 2003, he was accepted to UC Berkeley, but had to delay enrolling
because the disease got so bad during his senior year at Highland
Park High School in New Jersey that he was admitted to the hospital.
To get the care he needed, he was transferred to Cedars-Sinai
Medical Center in Los Angeles.

The inflammation had caused parts of his intestinal walls to narrow,
blocking the flow of nutrients and digestive fluids and causing
infection. That required surgery to remove 40 percent of his
intestine. At one point, he was down to 75 pounds.

"Three days after graduation, I landed in the hospital for six
months," Sofer said. "I felt like a 90-year- old man instead of a
19-year-old, it was so physically debilitating. I spent two years
recovering and getting my life back ... Spiritually, I was a wreck."
He said it hurt just to drink a glass of water.

But he never gave up his plan to get to Cal, and was given a special
dispensation to postpone enrollment.

"He called me every couple of weeks or months from the hospital, and
talked to me about his strategies to get here," said Ileana Dorn, a
supervisor in the UC Berkeley Office of Undergraduate Admissions who
was assigned to Sofer's case. "We don't usually postpone admission
for that long, but his was such a compelling situation that I really
went to bat for him."

Indeed, everything is finally falling into place for Sofer, who has
clearly been through hell.

Sofer lives at International House on campus and studies public
health and public policy. He has resumed jogging, is off the
steroidal medication he once took, and is on a strict, high protein
diet that excludes wheat, gluten and dairy products, which can
trigger inflammation.

He still gets visits from a nurse, has his blood tested regularly,
and self-administers IV infusions of fluid so he doesn't get
dehydrated.

"I have so much of my life back," said Sofer, who is thrilled to be
living in Berkeley, which he calls "the health food capital of the
world," and hopes to take a class with UC Berkeley food and
nutrition journalist Michael Pollan.

Indeed, at this point, nothing would make him happier than to see a
stamp highlighting the disease that paralyzed him at a time when he
should have been playing sports and dating. But it is also a disease
that has made him wise beyond his years, giving him rare insight
into what it means to be alive.

"If I were not to live much longer, I would be at peace with myself,
knowing I had done everything in my power to conquer this disease,"
he said.

###

NOTE: Gideon Sofer will be en route to Washington, D.C., today,
Wednesday, May 24. His meeting with the U.S. postmaster general is
set for 11 a.m. (EDT) tomorrow, Thursday, May 25. He can be reached
on his cell phone at (732) 266-3971, and will be checking voice
mail. He will also check e-mail sent to gideon@.... Because
Sofer's health condition is unpredictable, it's advisable to check
with him in case of any changes to the schedule. For more
information about Gideon Sofer and IBD, visit his Web site at:
http://www.ibdcure.org/. Print-quality photographs of Sofer are
available for download at:


===

Please direct all inquiries to: enews.mail@...
____________________________________________________________________________

With a mission to CURE Inflammatory Bowel Disease and INSPIRE GREATNESS:

                                    The IBDCure Foundation International

____________________________________________________________________________




#12 From: "THE IBDCURE.ORG E-NEWS SERVICE" <enews@...>
Date: Mon May 15, 2006 9:01 am
Subject: BREAKING NEWS: GIDEON SOFER TO MEET UNITED STATES POSTMASTER GENERAL
enews@...
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<<THE IBDCURE.ORG FOUNDATION INTERNATIONAL>> [RELEASE # BN15052006]

BREAKING NEWS: 

GIDEON SOFER TO MEET JOHN POTTER, UNITED STATES POSTMASTER GENERAL;
MEETING TO COINCIDE WITH WORLD PHILATELIC EXHIBITION IN WASHINGTON, D.C.

 FOR IMMEDIATE RELEASE: Monday, May 15, 2006: 02:00 PST

BERKELEY, California--
HIGHLAND PARK, New Jersey--
WASHINGTON, D.C.--

Dear IBDCURE Supporters,

While it has been well over one year since our last press release, we have some extraordinary news to report: 

Gideon J. Sofer, the Founder & President of the IBDCURE.ORG FOUNDATION INTERNATIONAL will be traveling to Washington, D.C. to meet the United States Postmaster General, Mr. John E. Potter. The meeting was arranged in coordination with the Make-A-Wish Foundation's New Jersey and Mid-Atlantic divisions, Mr. John Potter, and his staff at the United States Postal Service. The meeting is scheduled to take place Memorial Day weekend, concurrently with the World Philatelic Exhibition, which will take place in Washington, D.C. from May 27-June 3, 2006. More details will surely follow in the days ahead.

In the mean time, we want to extend our most sincere gratitude for your support, which has been absolutely critical to the progress of IBD awareness and research.

In great health,

The IBDCure e-news Team
===

Please direct all inquiries to: enews.mail@...
____________________________________________________________________________

With a mission to CURE Inflammatory Bowel Disease and INSPIRE GREATNESS:

                                    The IBDCure Foundation International

____________________________________________________________________________




#11 From: "IBDCURE.ORG E-NEWS" <enews@...>
Date: Sat Feb 19, 2005 11:00 am
Subject: LATE-BREAKING NEWS: PBS (WNET) Airing [President's Weekend]
enews@...
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<<THE IBDCure.org FOUNDATION INTERNATIONAL>> [RELEASE REF ID: BN00105]

LATE-BREAKING NEWS: A WEEKEND OF "HEALTH LITERACY" [PRESIDENT'S WEEKEND]

SOURCE: // CAUCUS EDUCATIONAL CORP / PBS PUBLIC TELEVISION/WNET /
IBDCure.org E-NEWS//

FOR IMMEDIATE RELEASE: Saturday, February 20, 2005: 6AM EST

LOS ANGELES, CA, HIGHLAND PARK, NJ, AND ONLINE @ WWW.IBDCURE.ORG--

Dear ibdcure.org Foundation Supporters:

While we know it been an extraordinary amount of time since we sent out our
last press release, we have some exciting news to report:

In his first television appearance since his six-month hospitalization in
2003, Gideon was invited to take part in an exclusive taping of Steve
Adubato's CAUCUS NJ program. This weekend, the focus of the program is
"Health Literacy," which has an ultimate goal of improving the communication
between patients, doctors, and other health professionals.

On Saturday (2/19), the half-hour program will air at 12:30PM (EST) on WNET
(PBS) in the Tri-State area, New York, New Jersey and Connecticut. The
program will air again on PBS & NJN at 8:30 AM Sunday (2/20) and 11:30 PM
Monday (2/21). In addition, the program will air on CN 8 - The Comcast
Network (Which airs throughout NJ, NY, PA, DE, MD, CT, MA, ME, NH, RI & VT)
at 6:30PM & 11:30PM on Sunday, 2/20.

For those of you who reside in other parts of the country and around the
world, you may view a clip of the program and/or download a full transcript
by visiting the "ENEWS RESOURCES" section of this release, or by visiting:
http://www.caucusnj.org/caucusnj/special_series/informed/health_literacy.asp

As always, we want to thank you for your support, which is absolutely
critical to the progress of IBD awareness and research.

Have a healthy and safe President's weekend,

The ibdcure.org e-news Team

Please direct all inquiries to: enews.mail@...
-----
E-NEWS RESOURCES:
____________________________________________________________________________

ABOUT CAUCUS: NEW JERSEY (Courtesy: Caucus Educational Corp,
http://www.caucusnj.org)

Caucus: New Jersey with Steve Adubato is the Emmy Award-winning public
affairs television series broadcast on Thirteen/WNET New York (PBS),
NJN-Public Television (PBS), CN8-The Comcast Network, and various cable
stations across the state. Hosted by four-time Emmy Award-winning anchor
Steve Adubato, Caucus combines in-depth documentary coverage with
penetrating studio interviews and discussion. Caucus is the most watched
news and public affairs program dealing with New Jersey issues. It is
broadcast to over 15 million people and can be seen in six states including
New York, Pennsylvania, Connecticut, Delaware, Maryland and New Jersey.

In its over fifteen years on the air, Caucus: New Jersey has tackled a range
of important issues affecting the state, including New Jersey's death
penalty, race relations, education reform, the future of our children, and
the many challenges facing the modern American family. Caucus has also
presented a series of documentaries entitled, ³Caucus Up Close² that profile
prominent New Jerseyans who have made significant contributions to life in
the state and nation. Caucus has featured former 40-year Congressman Peter
Rodino, New Jersey Governor James E. McGreevey, former Governor and Supreme
Court Chief Justice Richard J. Hughes, former New York Mayor Ed Koch, former
New York Governor Mario Cuomo and former Congresswoman and Ambassador
Millicent Fenwick. The series has also profiled prominent national figures
such as former Surgeon General Dr. C. Everett Koop, and U.S. Secretary of
State General Colin Powell.

Over the years, Caucus has garnered 29 Emmy nominations and has won four
prestigious Emmy Awards, including its most recent 2001 Emmy Award for
³Outstanding Host² (a third win in this category for host Steve Adubato).

Caucus is a production of the Caucus Educational Corporation (CEC), which
has raised millions of dollars in support over the years from philanthropic
corporations and foundations. Major underwriters of the series include;
University of Medicine and Dentistry of New Jersey, New Jersey Resources,
Horizon/Mercy, The Prudential Foundation, ShopRite, Roche, Verizon
Communications, Schering-Plough Corporation, The Medical Society of New
Jersey, Johnson & Johnson and The Geraldine R. Dodge Foundation.

Caucus: New Jersey with Steve Adubato is produced by a consortium that
includes the Caucus Educational Corporation, Rutgers-Newark, Thirteen/WNET,
and NJN-Public Television. http://www.caucusnj.org.
____________________________________________________________________________

SYNOPSIS: HEALTH LITERACY

This half-hour program comprised of a physician, nurse educator, and health
communications expert and patient exams effective strategies that help
facilitate greater understanding between patient and health professionals.


Click to read a passage from Helen Osborne's book, "Health Literacy from
A to Z"
Health literacy is when health providers and patients truly understand one
another. As medical knowledge expands and new treatments are introduced, it
is becoming increasingly clear that there is a need for better communication
between physicians, other healthcare professionals and patients. In many
cases, physicians may speak a language that is too technical and quite
literally, foreign to the average individual. Additionally, a significant
number of patients, especially the elderly and immigrants, may not read
well, and are thus unable to read medical forms, understand consent
agreements, and even take medications in the appropriate manner. As more
Americans are becoming responsible for healthcare decisions, the need to
improve physician/patient communication and joint decision-making becomes
paramount. Understanding verbal and non-verbal cues, using pictures to
illustrate a point, and incorporating ³teach-back² techniques will also be
examined during this segment.

FOR MORE INFORMATION, PLEASE VISIT:

http://www.caucusnj.org/caucusnj/special_series/informed/health_literacy.asp

____________________________________________________________________________

HEALTH LITERACY: GUEST NOTES

Lois Greene

Director of the Cathedral Regional Cancer Center

As the Director of the Cathedral Regional Cancer Center, Loisıs
responsibilities include outreach and screening for medical oncology,
hematology, and hemophilia. Lois advises that the majority of patients go to
see a doctor and expect to be told what is wrong with them, and how it will
be ³fixed.² Only recently has the medical community embraced the idea that
communication between both parties is essential in identifying and
developing effective treatment and outcomes. Lois advises that health
professionals need to help patients understand that ³they are part of the
process and not there just to be dictated to.²

The availability of information on Internet health sites has had a
significant impact on younger patients. Unlike generations before them,
these patients are often better informed then their physicians about new
procedures and medications. This serves to further strain the doctor/patient
relationship. Lois states that insurance companies play an important role in
the physician/patient dynamic. Insurance rules and regulations often dictate
treatment modalities and medications. While she admits that managed care or
charity care cases often leave doctors little time to engage in ³shared and
informed decision making,² the importance of effective communication
strategies becomes even more important. It is the responsibility of every
member of the health professional team to make sure that the patient
understands what is being said, and what his/her options are, and to
actively engage in an agreed upon treatment plan. Greene can also articulate
cultural challenges faced in the delivery of healthcare services.

Gideon Sofer

Crohnıs Disease Advocate and Patient, President and Founder, IBDcure.org
Foundation, International (IBD: Inflammatory Bowel Disease)

Gideon, now 20 years of age, was diagnosed with Crohnıs disease at the age
of 12. Since his diagnosis, he has founded the Ibdcure.org Foundation
(Inflammatory Bowel Disease), a foundation dedicated to increasing awareness
of Crohnıs disease. Crohnıs Disease is an ³auto-immune² and incurable
illness that causes painful inflammation in the intestines, small bowel and
colon.

As an infant, Gideon was diagnosed with Bechetıs disorder, which is an
ulcer-based disease causing lesions on the skin and mouth. At the age of 5,
doctors thought that it might be Crohnıs disease, but never confirmed it.
Gideon has had significant health problems including several operations
during his life. He has been on a variety of drugs to treat his disease
including steroids, which would make his cheeks puffy and as a result kids
would make fun of him.

He came up with the idea to start his foundation, IBDcure.org Foundation,
International during one of his hospital stays while he was a sophomore in
high school. The IBDcure.org Foundation is composed of a stamp initiative,
lecturing, advocacy and research. Doctors didnıt have a lot of answers
regarding Crohnıs, so Gideon decided to create his foundation so that people
can learn more about the disease. In 1999 he started a stamp campaign to
create a stamp advocating for Crohnıs disease. Gideon has written to
Senators and his Congressman to push for the stamp. His ³Make a Wish² will
be fulfilled early in 2005 ­ he is meeting with the United States Postmaster
General to discuss the Crohnıs stamp. Gideon dedicates his life to helping
ensure equal opportunity for people with diseases and disabilities. When
physically able, he lectures at schools, universities and conferences to try
to motivate other students and individuals to pursue their dreams. He urges
physicians to take a look at their character. So many doctors have felt
sorry for him and he said that as a person with a disease, you do not need
to be pitied. The last two years have been very difficult health-wise for
Gideon ­much of which he has spent in hospitals. He looks forward to feeling
better and using his scholarship to UC Berkeley in the near future.

Helen Osborne

Author, Expert on Health Literacy, Founder, ³Health Literacy Month²

Helen Osborne is widely recognized for her expertise in health literacy and
patient education. As a speaker, writer, and consultant, Helen helps
healthcare organizations communicate in ways patients and families can
understand. She is president of Health Literacy Consulting in Natick, MA.
Founded in 1999, Health Literacy Month is a grassroots campaign that is held
during the month of October. Working with health professionals, literacy
specialists, professional associations, and healthcare organizations around
the world, Helen continues to lead this international campaign to raise
awareness about the importance of understandable health information.

As an occupational therapist, she has treated many patients who have limited
literacy, do not speak English, come from other cultures, are older, and
have trouble hearing, seeing, or remembering. Helen gives concrete
techniques that both healthcare professionals and patients can use to
improve communication. She advises that healthcare professionals need to
know in general to whom they are speaking and be able to identify potential
barriers to communication, be committed to communicating in ³whatever way
works,² this includes the use of drawings, acting out desired behaviors,
etc. Osborne notes that confirming understanding can best be facilitated by
incorporating ³teach-back techniques.² I.e., instead of saying ³Do you
understand?² say, ³I want to make sure I explained this correctly ­ tell me
or show me what you will do when you go home.²

Terry Shlimbaum, MD

Family Practice Physician, Board Chair of the NJ Academy of Family
Physicians

In addition to serving as the Board Chair of the NJ Academy of Family
Physicians, Dr. Shlimbaum is Medical Director of Outpatient Teaching Sites
for Hunterdon Family Practice Residency Program. Terry advises that
healthcare literacy issues and failures in communication are serious
healthcare problems and are costly both financially and physically. Patients
will be healthier if physicians communicate better. The doctor/patient
relationship requires trust and understanding. Dr. Shlimbaum advises that
physicians need to do the following to assist their patients: 1. acknowledge
that a communication problem exists, 2. use common language to explain
medical conditions and technologies, 3. ask the patient to repeat what has
been said, or write down the information and then ask to have it read it out
loud, 4. search for new models and methods to help with their communication
style.

Terry advises that he also incorporates the use of a ³translating phone²
when working with patients who are non English-speaking. While in the
examining room, the physician and patient use a translating service via the
phone. This real-time translating service translates both partiesı questions
and answers. Shlimbaum admits that he has access to these types of services
because works in a teaching hospital. Less affluent medical systems or
offices may not be able to afford this type of service. He notes that the
best-case scenario would be to have a bi-lingual health educator available
to work with each physician, though the cost for this service would be
prohibitive. Terry states that the use of translators in any capacity is
critical, however, and states that it does take much longer than the
standard 15-minute visit.

He advocates for physicians and other healthcare professionals to develop
models that will speed the process and increase the likelihood of a positive
outcome. Dr. Shlimbaum also suggests that patientıs have a ³to-do² list too:
1. be prepared before make the call or visit a healthcare professional
(i.e., pain ­ be able to describe where the pain is, how long it has been
there, what makes it worse, what makes it better, etc.) 2. bring all
medications that the patient is taking with him/her to the appointment and
3. have another person with you to ³assist and points things out.² Patients
incorrectly following their medication regimes accounts for a large number
of hospitalizations. Dr. Shlimbaum feels that this is critical area of
concern in the health literacy field.
____________________________________________________________________________

To view a clip of the program on WINDOWS MEDIA PLAYER, please visit:

http://www.caucusnj.org/caucusnj/special_series/informed/1906.wmv


To view a full transcript of the program, please visit:

http://www.caucusnj.org/caucusnj/special_series/informed/health_trans.pdf

____________________________________________________________________________

#10 From: "The I B D C U R E . O R G e-news Service" <enews@...>
Date: Thu Jun 19, 2003 4:46 am
Subject: ACTION ALERT / A Personal Message From Gideon
enews@...
Send Email Send Email
 
<<THE IBDCURE.ORG FOUNDATION INTERNATIONAL>> [RELEASE REF. ID: PM00103]

IBDCURE UPDATE: ACTION ALERT / A Personal Message From Gideon

FOR IMMEDIATE RELEASE: Thursday, June 19, 2003: 12:44 AM EST

HIGHLAND PARK, NJ, US, & on the web @ http://ibdcure.org --

Dear Friends:

As my secondary school days come to an end, I walk down the science corridor
of my high school realizing that the greatest gift in life, is perhaps life
itself.

After recalling the countless days, weeks, and months that were spent either
sick at home or in the hospital, separating me from a life of normalcy, I
realize that my proudest accomplishment in life is not being accepted to
college or winning my fair share of accolades; my proudest accomplishment is
merely living to this very day. After double-digit hospitalizations,
exhausting every FDA approved medication for Crohn's, and two major
abdominal surgeries, there's no way to truly measure or articulate how lucky
I feel, and what means to be ALIVE.

I decided to write you tonight for a few reasons. One primary reason
revolves around history being made today in the nation's capitol. Today, the
first-ever, National IBD Advocacy Conference took place in Washington D.C.,
urging the immediate approval of the "Inflammatory Bowel Disease Act." This
vital piece of Congressional legislation already has a list-load of
co-sponsors in both the House and Senate, and, if passed, will introduce
sweeping reform and promote more Crohn's and Colitis research than ever
before.

It was my intention to go down to D.C. to fully embrace the events and
promote the legislation, but due to my educational obligations back home, it
was not going to be possible. I would however, in one brief statement, like
to extend my greatest support to every Crohn's and Colitis survivor and
supporter who are currently on the Hill, working their hearts out to see
this legislation through to fruition. It is my hope that this event will
represent the beginning of a movement to better treatments, way of life, and
will ultimately, lead to a cure.

The second major reason why I felt compelled to pen this email was to inform
you of some major new additions to our Foundation. It is with utmost
enthusiasm and gratitude that I announce the two newest members to the
ibdcure.org team: two invaluable friends of mine, Katie Willison and Michael
Evans.

-Katie Willison will be a freshman and the University of Virginia this fall,
and will be taking over as our Editor-in-Chief of our e-news service. I've
known Katie for nearly four years now, and I told her that when I thought of
someone who we desperately needed to not only write with clarity, character,
and passion, we most-importantly desired staying on-top of breaking news.
Over the past two years, you may have realized that from time-to-time,
events suddenly "pop-up" on our site late or without prior notice. The
bottom line is that those days are over, because Katie's got it all to run
our e-news service with full-fledged energy and efficiency, and we are not
only delighted but privileged to have her aboard.

-Michael Evans will be a freshman and Emerson College this fall, with intent
on majoring in marketing. Mike has been elected to our team as our Chief
Marketing Strategist, and will be in charge of analyzing everything from PR
to our website. When I thought of someone we needed to not only criticize
but SCRUTINIZE the way we market ourselves to the public, I thought to
myself: "that's gotta be Mike." Fortunately, Mike enthusiastically accepted
the position, and I know that his feedback will seem naturally effortless to
him, but will benefit us in countless ways.

In addition, in the upcoming weeks, we'll be announcing across-the-board
initiatives within our Foundation which will encompass:

1) The introduction of first-ever concurrent "IBD Stamp" legislation.
2) Efforts towards educating those chronically ill and disabled.
3) A revolutionary partnership with the Robert Pilkington, creator of
http://crohnie.com, and author of the just published "Crohnie Handbook."
4) New Foundation endowment for IBD research and partnerships, and:
5) Summertime fundraising efforts.

As most of the news above pertains directly to current efforts on behalf of
the Foundation, I'd like to leave you with a headline that hit the CNN
ticker-tape this past Memorial Day [and it read]:

"PEARL JAM GUITARIST GOES PUBLIC WITH CROHN'S"

Mike McCready, the lead guitarist for Pearl Jam has just announced that he's
been battling this devastating condition for over 15 years. His announcement
came to the shock of many, including myself. But his announcement meant more
than just a "celebrity" announcing his battle. Mike's announcement
symbolized a movement in which the general public is now talking about
Crohn's and Colitis more than ever before.

Seven years ago when I was first diagnosed with Crohn's, there was only one
wonder drug that I knew of coming down the pipeline, only to be used as a
last-resort. You'd walk up to strangers on the street, ask them about
Crohn's, and get a weak, unfamiliar response. These days, I can easily count
six or seven novel drugs coming down pharmaceuticals' pipelines, not only to
put this disease into a long-term remission, but to enhance the quality of
our lives. I can also walk down the street and find strangers responding
with more familiarity when I mention the term "Crohn's or Colitis."

In addition, pharmaceutical companies are now buying out full-page adds in
today's most circulated periodicals and newspapers, JUST to advertise their
new drug for Crohn's. More scientists and doctors are enthusiastic about
discovering the cause and cure for IBD and, last year, the first ever
IBD-related legislation was introduced to Congress to secure more federal
funding to help these medical professionals do just that. The bottom line is
that the odds have never been better, and my hope has personally never been
greater. If there's one thing I'm sure of, it is exactly this:

We are just steps away from cracking IBD.

Today, however, it is important to take a moment to support this new IBD
legislation, and everyone down on Capitol Hill, fighting for the IBD cure. I
hope you will take the time to visit the links below to contact your
Congressional members to tell them that YOU want to see this legislation
approved immediately. Pre-written letters are now available at the CCFA's
website, and you may contact anyone from our Foundation should you need
assistance with contacting your reps.

Thank you all for your unrelenting avidity.

With great health and happiness,

Gideon

---

Reply to: gideon@...

-----
E-NEWS RESOURCES:

Below are additional resources pertaining to this press release.
____________________________________________________________________________

SUPPORT THE INFLAMMATORY BOWEL DISEASE ACT:

http://www.ccfa.org/news/ibdbilloverview.htm
____________________________________________________________________________

WRITE-YOUR REPRESENTATIVE DIRECTORY:

http://www.house.gov/writerep/

____________________________________________________________________________

PEARL JAM GUITARIST GOES PUBLIC WITH CROHN'S - SOURCE/REUTERS:

http://reuters.com/newsArticle.jhtml?type=musicNews&storyID=2811054

____________________________________________________________________________

________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

   Always on:  http://www.ibdcure.org
________________________________________

#9 From: "The I B D C U R E . O R G e-news Service" <enews@...>
Date: Mon May 26, 2003 2:16 am
Subject: LATE-BREAKING NEWS: Prudential Awards, CNN Airing [Memorial Day]
enews@...
Send Email Send Email
 
<<THE ibdcure.org FOUNDATION INTERNATIONAL>> [RELEASE REF. ID: BN00203]

LATE-BREAKING NEWS: Prudential Awards, CNN Airing [Memorial Day]

SOURCE: // PRUDENTIAL FINANCIAL / PRNEWSWIRE / YAHOO! FINANCE / CNN /
ibdcure.org E-NEWS//

FOR IMMEDIATE RELEASE: Sunday, May 25, 2003: 10:00 PM EST

Dear ibdcure.org Foundation Supporters:

We have some exciting late-breaking news to report.

This past February, we sent out a press release explaining that Gideon J.
Sofer, the Founder and President of the ibdcure.org Foundation
International, was selected as New Jersey's top high school volunteer via
the Prudential Spirit of Community of Awards.

Earlier this month, Gideon traveled to Washington to meet and interact with
the top-youth volunteers from around the nation. At the event, Prudential
and the National Association of Secondary School Principals [NASSP] named
ten out of the 104 national honorees "America's Youth Volunteers," and
Gideon was one of them.

Shortly after Gideon's trip to Washington, he was committed to taking some
personal time off for his health. After battling unremitting intestinal
symptoms since last summer, he underwent major abdominal surgery last week
to remove a completely dysfunctional segment of his gut. Fortunately, the
operation was a sucess and he is now recovering at home.

It was a daunting decision for Gideon to make his current health obstacles
public information via this press release. He feels that when going through
these challenges, it merely becomes very personal. However, due to the
unanticipated turn of events (particularly with the Foundation and in
Washington), there was very little room to keep the "good news" quiet.

Two weeks ago, Gideon received an invitation to go to New York City to
appear on CNN's national American Morning program to talk about his project
with two of the other national youth volunteers, Sasha Bowers (of Columbus,
OH), and Jacob Komar (of Burlington, CT). At the time, Gideon declined the
offer, anticipating that he'd be recovering and completely immobile. It
turns out that this is not the case.

At about 8:30 AM (EST) on Memorial Day, a live segment will air on CNN
talking about the honorees and their projects. Gideon, despite just arriving
home from the hospital less than 24 hours ago, will do his best to talk
about his mission to conquer Crohn's. We hope you'll tune in.

Have a healthy and safe Memorial Day,

The ibdcure.org e-news Team

Reply to: enews.mail@...
-----
E-NEWS RESOURCES:

Below are additional resources pertaining to this press release, such as a
synopsis of Sasha & Jacob's community service projects, and links to the
Prudential Awards main page, CNN American Morning website, CNN Transcripts
page, and a complete Yahoo! Biz release covering the events from Washington.
____________________________________________________________________________

VOLUNTER BIOS: (Courtesy: Prudential)

Sasha Bowers, 14, of Columbus, Ohio, an eighth-grader at Norton Middle
School, drew upon her experience living in a homeless shelter to develop a
summer-long program of weekly activities for more than 250 other homeless
children in the Columbus area. As a shelter resident, Sasha had enjoyed
field trips to a local park, but thought they could be made more fun and
educational. When she learned that volunteers were being recruited to work
with homeless children, she figured there was no reason why she couldn't
help. "I realized that even if I was homeless, I could still help other
people, too," she said. She organized a planning committee with other kids
at her shelter, developed ideas for a summer program, and sought donations
from a variety of organizations. Sasha also promoted the program through
media interviews, recruited and managed other volunteers, and arranged for
supplies and transportation. Then, every Monday last summer, Sasha and her
helpers hosted a "learning day" at the park for homeless kids, featuring
gardening, fishing, educational tours, environmental readings and wildlife
lectures. At summer's end, the program culminated with a big party for the
kids, complete with entertainment, crafts, games and gifts. "No matter what
situation you are in, you can always help make things better for others,"
said Sasha.

Jacob Komar, 10, of Burlington, Conn., a sixth-grader at Talcott Mountain
Academy in Avon, initiated a program called "Computers for Communities" that
has restored and upgraded more than 60 outdated personal computers and
installed them in the homes of families that couldn't afford to buy one.
Jacob, a self-described "computer fanatic," was shocked when he learned of a
garage at his sister's school filled with old computers that were going to
be thrown out. He realized he could revamp the computers and give them to
people who could not afford their own. "I thought that by doing this, I
would help a lot of kids get a head start," said Jacob. First, he secured
the school district's approval to take the old computers, and then went to
work on the machines - analyzing, trouble-shooting and rebuilding. He had to
call numerous software companies to transfer licenses, and installed new
software and hardware where appropriate. In order to identify those in his
community most in need of computers, Jacob worked with the Department of
Social Services. When the computers were ready, Jacob installed them in
their new homes and taught 140 family members how to use them. As word of
his project has spread, Jacob has received more computer donations, and he
has recruited other students at his school to help. He also has received
requests from organizations that want to start similar programs, and he
hopes to eventually see the project expand to other communities across the
country.
____________________________________________________________________________
THE PRUDENTIAL SPIRIT OF COMMUNITY OF AWARDS (MAIN PAGE):

http://www.prudential.com/spirit
____________________________________________________________________________
CNN AMERICAN MORNING website:

http://www.cnn.com/CNN/Programs/american.morning/

CNN AMERICAN MORNING TRANSCRIPTS: http://www.cnn.com/TRANSCRIPTS/ltm.html
____________________________________________________________________________
YAHOO FINANCE PRESS RELEASE

Source: Prudential Financial

New Jersey's Gideon Sofer Of Highland Park Named One Of America's Top Ten
Youth Volunteers

Monday May 5, 10:01 am ET

State's Janna Zuckerman Of Edison Also Honored During 4-Day Celebration With
Tributes From Rudy Giuliani And '7th Heaven' Star David Gallagher

WASHINGTON, May 5 /PRNewswire/ -- Gideon Sofer, 18, of Highland Park, N.J.
was named one of America's top ten youth volunteers for 2003 in a ceremony
today at the International Trade Center, receiving a national Prudential
Spirit of Community Award for his outstanding volunteer community service.
Selected from a field of 24,000 applicants across the country, he received
$5,000, an engraved gold medallion and a crystal trophy for his school,
Highland Park High School in Highland Park. In addition, he will have
$25,000 in toys, clothing and other juvenile products donated in his name to
needy children in his area by Kids in Distressed Situations, Inc., the
national charity of the children's apparel and products industry.

--
FOR COMPLETE ARTICLE:

http://biz.yahoo.com/prnews/030505/nym036_1.html

____________________________________________________________________________

________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

   Always on, http://www.ibdcure.org
________________________________________

#8 From: "The I B D C U R E . O R G e-news Service" <enews@...>
Date: Sun Feb 9, 2003 5:36 pm
Subject: BREAKING NEWS: New Jersey's Top Two Youth Volunteers Selected in National Awards Program
enews@...
Send Email Send Email
 
<<THE ibdcure.org FOUNDATION INTERNATIONAL>> [RELEASE REF. ID: BN00103]

BREAKING NEWS: New Jersey's Top Two Youth Volunteers Selected in National
Awards Program

SOURCE: // PRUDENTIAL FINANCIAL/ PRNEWSWIRE / YAHOO! FINANCE //

FOR IMMEDIATE RELEASE

Sunday, February 9, 2002

Dear ibdcure.org Foundation Supporters:

It is with great enthusiasm that we announce breaking news recognizing
Gideon J. Sofer, the Founder and President of the ibdcure.org Foundation
International, as the top high school volunteer in New Jersey. Gideon will
travel Washington, D.C. in May 2003 to compete for the national award. Below
is an excerpt from the PRNEWSWIRE issued by PRUDENTIAL FINANCIAL on YAHOO!'s
website. To read the full release, you may use the link provided in the
margin below.
____________________________________________________________________________
       
Press Release    Source: Prudential Financial

New Jersey's Top Two Youth Volunteers Selected in National Awards Program

Tuesday February 4, 9:08 am ET

Highland Park and Edison Students Earn $1,000 Awards, Engraved Silver
Medallions and Trip to Nation's Capital


TRENTON, N.J., Feb. 4 /PRNewswire/ -- Gideon Sofer, 18, of Highland Park and
Janna Zuckerman, 13, of Edison today were named New Jersey's top two youth
volunteers for 2003 by The Prudential Spirit of Community Awards, a
nationwide program honoring young people for outstanding acts of
volunteerism. The awards program, now in its eighth year, is conducted by
Prudential Financial, Inc. in partnership with the National Association of
Secondary School Principals (NASSP). More than 24,000 high school and middle
level students submitted applications for this year's program.

---

FOR THE COMPLETE ARTICLE, PLEASE VISIT:

http://biz.yahoo.com/prnews/030204/nytu022_1.html

____________________________________________________________________________

   We hope that you enjoy the press release, and appreciate all and any
feedback. Stay tuned for even more exciting news from the ibdcure.org
Foundation in the coming weeks!

With great health,

The ibdcure.org e-news Team

Reply to: enews.mail@...
________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

      Always on, @ ibdcure.org
________________________________________

#7 From: "The I B D C U R E . O R G e-news Service" <enews@...>
Date: Wed Dec 18, 2002 6:27 am
Subject: News Alert: First Airing of One-on-One This Thursday
enews@...
Send Email Send Email
 
<<THE ibdcure.org FOUNDATION INTERNATIONAL>> [RELEASE REF. ID: NA00102]

NEWS ALERT:  First Airing of One-on-One This Thursday

FOR IMMEDIATE RELEASE

December 18, 2002

Highland Park, New Jersey, USA & @ ibdcure.org--

Dear Supporters:

Less than 48 hours from now, CN 8 will be conducting its first official
airing of the One-on-One interview with Gideon.

The first airing is: Thursday, December 19 @ 6:00 PM EST

If you can tune in, we hope you enjoy the show--if you can't, have no fear,
there will be several more airing dates. All those dates [and any other
info] can be dug up on One-on-One's website, oneonone.org.

Without prior notification to our Foundation, CN8 and the Caucus Group
apparently launched several preliminary airings of the interview. As a
result of this altruistic move by the Caucus Group, more awareness and
support is now being generated for IBD than ever before.

Here's what some viewers are saying in response to the interview, the
Foundation, and IBD itself:

"I just wanted to know how I can become more involved with Gideon. I have
had Crohn's for about 5 years now and am currently in the middle of a
flare-up. I was at home and turned on the TV and saw Gideon on ONE ON ONE I
was so happy to see someone talk about the disease...it brought me to
tears."

     -An anonymous supporter from Mt. Laurel, New Jersey

"I think there should be more advertisement [of Crohn's]. I didn't even know
of the disease until a friend told me she had it. Let's get more people
involved."

     -An anonymous supporter from Baltimore, Maryland

"As a parent, I can only stress the importance of funding and ultimately
rooting out the cause and curing this dreadful disease."

     -An anonymous supporter from Gloucester, Massachusetts

"I think the stamp is a great idea!! Now all we need now is a cure or at
least some other drugs beside Prednisone..."

     -An anonymous supporter from Raleigh, North Carolina


We are proud to say that this is just the beginning of some very great news
coming the way of those who survive IBD every single day.

Thank you all so much for your feedback. We hope you enjoy the show.

With gratitude,

The ibdcure.org e-news Team

Reply to: enews.mail@...

________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

      Always on, @ ibdcure.org
________________________________________

#6 From: "The I B D C U R E . O R G e-news Service" <enews@...>
Date: Fri Dec 6, 2002 12:11 am
Subject: Breaking News: Airing Dates for One-on-One Announced
enews@...
Send Email Send Email
 
<<THE ibdcure.org FOUNDATION INTERNATIONAL>> [RELEASE REF. ID: BN00402]

BREAKING NEWS:  Airing Dates for One-on-One Announced

FOR IMMEDIATE RELEASE

December 5, 2002

Union, New Jersey, USA & @ ibdcure.org--

Dear Supporters:

Many of you have written us asking for details about the upcoming airing,
specifically the dates and whether or not it's within your viewing area. In
an attempt to answer most of your questions, let's first start with the
dates & times.

The Caucus Educational Group has just announced 5 separate airing dates for
the exclusive upcoming One-on-One interview with Gideon J. Sofer:

-Thursday, December 19 @ 6:00 PM EST
-Monday, December 30 @ 6:00 PM EST
-Friday, January 10 @ 6:00 PM EST
-Sunday, January 19 @ 7:30 PM EST
-Monday, January 27 @ 6:00 PM EST

For a complete synopsis of the airing with Gideon, be sure to check out:

http://www.oneonone.org/one-on-one/shows/gideonsofer.asp

About the Viewing Area:

The interview will air via the Comcast Cable Network [CN8] & Cablevision in
Baltimore, Philadelphia, Bucks County P.A., New York, and throughout the
entire state of New Jersey. While the viewer audience tallied by the Caucus
Educational Group and the Comcast Network & Cablevision is estimated to
reach over 4 million households each evening, we cannot guarantee that it
will air in your area. For complete station & time details, be sure to check
out:

http://www.caucusnj.org/one-on-one/stations.asp

In addition, we will  be sending out news alerts 48 hours before each airing
to remind those who wish to tune in.

For the latest, stay with us @ ibdcure.org, as well as One-on-One's website,
http://www.oneonone.org. Once again, for those who reside in other parts of
the country and around the world, we'll be sure to post a transcript of the
interview at our website.

Thank you all for your incredible feedback and encouragement!

With gratitude,

The ibdcure.org e-news Team

Reply to: enews.mail@...

________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

      Always on, @ ibdcure.org
________________________________________

#5 From: "The I B D C U R E . O R G enews service" <enews@...>
Date: Mon Dec 2, 2002 3:05 am
Subject: Breaking News: Gideon Speaks One-on-One With Steve Adubato
enews@...
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<<THE ibdcure.org FOUNDATION INTERNATIONAL>>   [RELEASE REF. ID: BN00302]

BREAKING NEWS: Gideon Speaks One-on-One With Steve Adubato

FOR IMMEDIATE RELEASE

December 1, 2002

Union, New Jersey, USA & @ ibdcure.org--

Dear Supporters:

It is with great pleasure that we inform you of an exclusive interview
Gideon J. Sofer has had with the heavily respected, award-winning television
anchor, Mr. Steve Adubato.

Mr. Adubato is currently the anchor of two Channel Thirteen/WNET (PBS)
broadcasts - Caucus, an Emmy Award-winning public affairs television series,
which is also broadcast on NJN-Public Television, and Inside Trenton, a news
program which covers political issues on a weekly basis. He is also the
executive producer and host of One-on-One, an in-depth program which usually
features an up-close and personal interview with a designated guest. Mr.
Adubato and his producers graciously enough, decided to choose Gideon for
one of their upcoming airings on One-on-One.

The interview will air throughout December 2002 & January 2003, and can be
accessed through the Comcast Cable Network & Cablevision in Baltimore,
Philadelphia, New York, and throughout the entire state of New Jersey.
Viewer audience tallied by the Caucus Educational Group and the Comcast
Network & Cablevision is estimated to reach over 4 million households each
evening,

While we are incredibly enthusiastic to announce the upcoming airing, we
will only disclose that the interview covers a wide-array of subjects
pertaining to Gideon's life and his fight for the IBD Cure, and gets very,
very personal.

For the latest information, please stay tuned to our website @ ibdcure.org,
as well as One-on-One's website, http://wwww.oneonone.org.  For those who
reside in other parts of the country and around the world, we'll be sure to
post a transcript of the interview at our website.

The ibdcure.org Foundation would like to thank Mr. Adubato, Ms. Mary Gamba,
and the rest of his production crew for their invaluable contribution to our
Foundation, yet more importantly, to the lives of all Crohn's and Colitis
survivors.

Thank you all for your unremitting enthusiasm to help eradicate this
disease.

With gratitude,

The ibdcure.org e-news Team.
________________________________________
        Defying all realities:

::  THE ibdcure.org FOUNDATION INT'L ::

      Always on, @ ibdcure.org
________________________________________

Changing your email address?

Be sure to stay with us! Transfer over your new email address @
http://groups.yahoo.com/group/ibdcure

[This has been an automated email initiated by the ibdcure.org Foundation's
e-news list. For further information or to access or e-news archive, please
visit our group homepage @ http://groups.yahoo.com/group/ibdcure ]

#4 From: "ibdcure.org enews" <enews@...>
Date: Sun Jun 23, 2002 6:33 am
Subject: A Personal Message From Gideon
enews@...
Send Email Send Email
 
Breaking News: June, 2002

Gideon J. Sofer/ibdcure.org: Personal Address

FOR IMMEDIATE RELEASE

Highland Park, NJ/ibdcure.org:

Dear Supporters,

Over the last seventeen years, I've spent my life surviving an immensely
devastating disease in which more than 4,000,000 people withstand around the
globe everyday. Two years ago, I decided that I wanted to see a significant
change in the way the world views bowel diseases. I wanted more awareness, I
wanted more funding, and I wanted more acceptance.

Today, Inflammatory Bowel Disease is gaining greater recognition than ever
before. Whether it be on the street, in hospitals, or down on Capitol Hill,
IBD is no longer a silent condition...and I am emphatically proud to say
that this is only the beginning.

Two years ago, with the help of some amazing people and most importantly,
you, I formed what was known as the 'IBD Stamp Campaign.' Today, we are
still working towards a goal which I thought up several years ago--and
today, we are closer to that goal than ever before.

Since the beginning of the Campaign, we've collected close to 4,000
signatures from people in nearly ever state in the Union, and many countries
around the globe. Over 75% of those signatures have come electronically
through our website, and this summer, more than 2,000 additional signatures
are set to printed, bound, and forwarded to the US Postal Service's review
committee. Additionally, with the help of Congressman Frank Pallone, Jr.,
and fellow Congressmen and Senators, we are currently working to promptly
introduce legislation which will put pressure on the Postal Service to "fast
track" the stamp approval.

This spring, we announced new initiatives within the Campaign. The IBD Stamp
Campaign has now grown into 'The ibdcure.org Foundation International." The
Foundation is currently obtaining nonprofit status from the IRS, and was
formed to essentially "do more" than just approve a postage stamp through
the Postal Service. For example:

During the course of High School, I have had my federal civil rights under
the Americans with Disabilities Act violated by my Public School District.
Under these laws, the District failed to provide me with an equal
opportunity in my education at a time when I was deathly ill. When I did
extensive research on the "status" of education in America, I was especially
frustrated to find that my case with my District was just one of very many.
I decided that this Foundation was going to make "ensuring an equal
opportunity for the disabled" a key initiative in our immediate future. It
is of primary importance that the public speak up to publicly elected
officials, and the President, and hold them to their words that it is
unacceptable to leave any child behind. The reality however, is students
with chronic illnesses, such as myself, are getting left behind in the dust
everyday--and because of this, there needs to be a call for change in
educational policy across the nation and around the globe.

Other new initiatives recently announced include further advocacy
objectives, as well as initiatives for the Foundation to speak publicly at
various events and in school districts to further raise awareness and
acceptance of IBD and chronic illness.

And the website: Well, we've heard your feedback, and rest assured, we are
working towards a whole new 'ibdcure.org.' Over the summer, 'the new
ibdcure.org' will be launched featuring special sections which will let
nonprofits and school district know how to contact us for speaking
engagements, as well as a special advocacy section dedicated to bettering
the well-being of those with illness in America and around the globe. We
hope you're anxiously awaiting our brand new, completely restructured, and
enhanced website just as much as we are!

Before I sign off, I wanted to take the time to let you know that your
voices have been undoubtedly heard. By you coming to our website, signing
our Stamp Proposal, giving your feedback via email, and quite simply, by
being on our email list--is all making a huge difference in our ability to
reach our goals, and most importantly, in the lives of people with IBD and
other serious health conditions. You need to know that without your help,
we'd quite honestly be nowhere near where we are today. So I personally want
to that each of you for the extraordinary generosity of your support.

...and if you've got a moment before you sign off, keep spreading the word
either by forwarding this email to a friend, or by visiting our referral
form on our site at: http://www.ibdcure.org/ac/email.html .

Thank you for your time--and as always, wishing you all the best of health.


With gratitude,

Gideon J. Sofer, Survivor

Crohn's Disease

President, The ibdcure.org Foundation International

On the web @ http://www.ibdcure.org

By email at: gideon@...

#3 From: "ibdcure.org enews" <enews@...>
Date: Sat Apr 13, 2002 4:08 am
Subject: BREAKING NEWS: 95.5 [WPLJ] Radio Initiates Coverage on ibdcure.org
enews@...
Send Email Send Email
 
ibdcure.org Breaking News:

*WPLJ Radio Initiates Coverage on ibdcure.org
*ABC News: A Huge Success

April 12, 2002

FOR IMMEDIATE RELEASE

Highland Park, NJ/ibdcure.org--On Sunday, April 14, 2002, Gideon J. Sofer,
the President of the ibdcure.org Foundation will be interviewed by the 95.5
[WPLJ] Radio Station. The regional WPLJ Network--which broadcasts in all of
New York City and New Jersey, and parts of New York State, Connecticut, and
the eastern part of Pennsylvania--will be airing information on ibdcure.org
and the IBD Stamp Campaign.

Specifically, Gideon will be talking about how and why his own medical
situation motivated to create the IBD Stamp Campaign and ibdcure.org. He
also plans to talk about the current introduction of the federal legislation
(for the Postage Stamp) to both the House and Senate, as well as new
initiatives his Foundation is taking on in addition to the Stamp Campaign.

The interview will air for 30 minutes on Sunday night [Monday morning]
starting at 1:30AM EST on Bill Ayres's Community Connection Segment of his
late-night talk show on 95.5 FM Radio. We hope that you are able to tune in,
but if you are one of our many supporters in other parts of the United
States and around the globe, we're hoping to obtain either a transcript or
digitized form of the interview to post on our website!

ABC News: A Huge Success

If you are one of the many people that were misinformed about the ABC News
Broadcast last week, we do apologize. Our transition to the Yahoo Groups
enews service made it difficult to send out an updated alert about the
rescheduled broadcast time. Nevertheless, if you missed the broadcast, we
have great news! As we had hoped, ABC did indeed post a matching transcript
of the segment they did on ibdcure.org, as well as a matching video clip! To
view either the transcript or the actual video segment from ABC News, use
the following link:

http://abclocal.go.com/wabc/news/WABC_ourschools_040502crohns.html

We thank you for taking the time to read this ibdcure.org breaking news
alert. Should you have any questions or comments, please do not hesitate to
contact us.

With great health and happiness,

The ibdcure.org enews Team

http://www.ibdcure.org

enews@...

============================================================================
This has been an automated email initiated by ibdcure.org. Please feel free
to share this information with absolutely anyone.
============================================================================

#2 From: Gideon Sofer <Gidster7@...>
Date: Wed Apr 3, 2002 1:45 pm
Subject: ABC News Initiates Coverage on ibdcure.org
Gidster7
Offline Offline
Send Email Send Email
 
-----ibdcure.org News Flash: ABC News Initiates Coverage on ibdcure.org-----

April 3, 2002

Dear Supporters:

While it's been an incredibly long time since we've emailed our enews list,
the IBD Stamp Campaign has breaking news to report.

On Wednesday, April 3, 2002, Gideon Sofer and the IBD Stamp Campaign will be
featured on the ABC News Network. The regional WABC TV network (channel 7
Eyewitness News--which broadcasts in all of New York City and New Jersey,
and parts of New York State, Connecticut, and the eastern part of
Pennsylvania) will be airing information on the IBD Stamp Campaign and our
latest endeavors. Specifically, Gideon will be talking about injustices he's
faced at his public school district, Highland Park High School, and what
he's doing to eradicate discrimination against people with disabilities in
the educational system across the United States.

The time of the broadcast will be at 5PM EST. We hope that you are able to
tune in, and please feel free to contact with any questions. If you are one
of our many supporters in other parts of the US and around the globe, we're
hoping ABC will put out a matching web story for you to view.

We thank all of you so much for your continued support--it's been quite a
year, and we quite honestly couldn't have grown to where we are today
without you.

With great health and happiness,

Everyone at ibdcure.org

*Please note any additional information on ABC's Eyewitness News Program can
be found at http://www.7online.com

**This has been an automated email initiated by the IBD Stamp Campaign.
Please feel free to share this information with absolutely anyone.

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