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Health care program implemented:
It's OK to Ask

[MARCH 6, 2003]  Embracing patients as partners with their physicians, nurses and all others responsible for their care, Abraham Lincoln Memorial Hospital and Memorial Health System are celebrating the start of National Patient Safety Awareness Week (March 9-15) by launching "It's OK to Ask" -- a program to increase awareness of the important role patients play in the hospital care they receive.

It's OK to Ask encourages patients, family members and guardians to ask questions about the care being administered or request assistance when it is needed. The new program also addresses the need for safe and effective care in the home following a hospital stay.

"The physicians, nurses and staff at Abraham Lincoln Memorial Hospital are dedicated to providing skilled, compassionate care," said Woody Hester, president and CEO of ALMH. "Patients who see themselves as partners in their care will be comforted and reassured by knowing their questions, comments and requests are encouraged and welcomed by all of us.

"By further embracing patients as partners, It's OK to Ask reduces the risk of accidental injury and improves overall quality of care at ALMH."

It's OK to Ask provides information about five key health care topics to help patients make important contributions as partners with their caregivers.

Infection control -- It's OK for patients to ask nurses and physicians to wash their hands, or that they wear gloves, before examining them or giving a medication. It's also important to ask well-wishers not to visit if they feel ill.

Reducing medication errors -- Patients can help their caregivers prevent medication errors by making sure their doctor knows about all the medications (including prescriptions, over-the-counter drugs and dietary supplements, such as vitamins) they are taking, telling their physician of allergies or adverse reactions they have had to medicines, and asking about the medicines being prescribed.

Preventing falls -- Asking for help is the most important thing patients can do to prevent a fall during their hospital stay. It's okay for patients to let caregivers know they are uncomfortable or in pain.

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Safe health care at home -- Following a hospital stay, it's important for patients to stay in contact with their physician or pharmacist, asking questions and taking notes. Arranging for others check up on them and having the needed home health equipment and supplies are also important.

Improved communication -- Through It's OK to Ask, patients are encouraged to ask questions, provide information and take an active part in decisions about their treatment and care.

"Quality of care, clinical effectiveness and patient safety are all benefits of It's OK to Ask," said Dolan Dalpoas, ALMH director of quality management. "It's also important that this program is patient-centered."

"We are listening for all the needs of the patient. Can the patient be made more comfortable? How can family members assist while the patient is hospitalized? How can family members help once the patient is discharged? How can outpatient therapy or other treatments be designed to accommodate any special needs that might exist?"

"It's OK to Ask strengthens the voice of the patient," Dalpoas concluded. "We pledge to listen to that voice. That is a pledge we will continue to honor."

Hester said It's OK to Ask reflects Abraham Lincoln Memorial Hospital's century-long commitment to skilled, compassionate patient care.

"At ALMH, skills, expertise, knowledge and experience are combined with compassion, empathy and genuine concern for every patient's well-being," Hester emphasized. "By joining these values with heightened patient awareness of their importance as partners with caregivers, we grow our ability to provide safe, clinically effective care."

[Abraham Lincoln Memorial Hospital
news release]

Diabetes needs control

[MARCH 6, 2003]  The year is 1995. Local pastor Don Hoover and his wife Deb are on their way to Michigan. Don makes them stop at every rest area and gas station they pass.

Deb, being a nurse, was worried. She took his blood sugar and discovered it was very high. When they returned home Hoover went to see a doctor, who confirmed his wife's suspicions. He had diabetes.

Diabetes, according to the National Diabetes Education Program, is "a metabolic disease in which the body does not produce or properly use insulin, a hormone that is needed to convert sugar, starches, and other food into energy needed for daily life." In other words, the body of a diabetic cannot process sugar and therefore can develop dangerously high blood sugar. This can lead to blindness, kidney failure, lower limb amputations, heart disease and stroke.

There are four types of diabetes: type 1, type 2, mature onset diabetes of the young (MODY) and gestational.

Type 1 diabetes (insulin-dependent diabetes mellitus; juvenile-onset diabetes) occurs when the pancreas does not produce insulin. This means that a person with type 1 diabetes will need daily insulin shots to live. This type of diabetes usually develops in children or young adults.

Type 2 diabetes (non-insulin-dependent diabetes mellitus; adult-onset diabetes) occurs when the body cannot properly use the insulin it produces. This type of diabetes is usually found in adults over the age of 40 and often in people who are overweight or have a family history of diabetes.

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MODY is an early development of type 2 diabetes. It occurs in children or youth but is not type 1.

Gestational diabetes develops during pregnancy and usually disappears after the pregnancy is over. Women who have gestational diabetes are at a higher risk of developing type 2 diabetes later in life.

Watch this spot in LDN as we bring you more information on this life-altering disease.

There are many levels and several forms of diabetes. Treatment varies according to the type, the discipline and the lifestyle of an individual. To control Hoover's diabetes, the doctor put him on a low dosage of Glucotrol, a medicine that makes the pancreas create more insulin, and a diet consisting of fewer carbohydrates and sweets and more protein and vegetables. He also began to exercise more.

To find out more about his disease, Hoover went to a seminar given by diabetic Amy Olsen, who was the dietician at Abraham Lincoln Memorial Hospital at the time. Through that conference and subsequent talks with Olsen, he learned about living with his diabetes.

With the help of his wife, Hoover has been able to control his diabetes through medication, exercise and healthy eating. He encourages anyone with diabetes to get control and to maintain control of their life.

[LDN]

HHS acts to reduce potential risks of dietary supplements containing ephedra

[MARCH 1, 2003]  On Friday the Department of Health and Human Services, HHS, announced a series of actions designed to protect Americans from potentially serious risks of dietary supplement products containing ephedra.

The results of a RAND Corporation study commissioned by the National Institutes of Health, as well as other recent studies, provide additional evidence that ephedra may be associated with important health risks. The RAND report also finds only limited evidence of health benefits resulting from ephedra use.

On the basis of new evidence in the medical literature and in adverse event reports, there are reasons for heightened concern that dietary supplements containing ephedra may present a significant and unreasonable risk of illness and injury.

To protect Americans from the potentially serious risks of these dietary supplements, HHS and the Food and Drug Administration are going to:

--Seek rapid public comment on the new evidence on health risks associated with ephedra in order to establish an up-to-date record as quickly as possible to support new restrictions on ephedra-containing products.

--Seek rapid public comment on whether the currently available evidence and medical literature present a "significant or unreasonable risk of illness or injury" from dietary supplements containing ephedra.

--Seek rapid comment on a strong new warning label on any ephedra products that continue to be marketed.

--Immediately execute a series of actions against ephedra products making unsubstantiated claims about sports performance enhancement.

In addition, the nation's top public health officials issued strong statements cautioning about the use of ephedra-containing products, especially under conditions of strenuous exercise and in combination with other stimulants, including caffeine.

"We want to caution all Americans -- particularly athletes and those who engage in strenuous activities -- about using dietary supplements that contain ephedra," said Secretary of Health and Human Services Tommy G. Thompson. "There continue to be serious questions about the risks surrounding this particular dietary supplement."

"FDA will do all we can to protect Americans from potentially dangerous dietary supplements," said Commissioner of Food and Drugs Mark B. McClellan, M.D., Ph.D. "We are particularly concerned about the risks of using products containing ephedra during heavy workouts, with caffeine and other stimulants, in a diet program that stresses the cardiovascular system, or by people under the age of 18. We are also concerned about potential stresses to the body caused by the long-term use of ephedra. The standard for regulating the safety of dietary supplements is largely untested, but we are committed to finding the right public health solution."

Ephedra is a naturally occurring substance derived from the Chinese herbal Ma Huang. Its principal active ingredient is ephedrine, which when chemically synthesized is regulated as a drug. While products containing natural ephedrine alkaloids have long been used to treat certain respiratory symptoms in traditional Chinese medicine, in recent years they been extensively promoted and used with the goals of aiding weight loss, enhancing sports performance and increasing energy.

Many of today's proposed actions involve a Federal Register notice, which went on display Friday, reopening for 30 days the comment period on a draft regulation FDA first proposed in 1997 and modified in 2000. [The notice is in Adobe Acrobat. Click here to download the Adobe Acrobat reader.]

FDA's concerns about dietary supplements containing ephedra arise in part from ephedra's mechanism of action in the body. Ephedra is an adrenaline-like stimulant that can have potentially dangerous effects on the nervous system and heart.

In addition, evidence is accumulating about potentially serious safety problems following the use of ephedra-containing products. The RAND study has concluded that ephedra is associated with higher risks of mild to moderate side effects, such as heart palpitations, psychiatric and upper gastrointestinal effects, and symptoms of autonomic hyperactivity, such as tremor and insomnia, especially when it is taken with other stimulants.

Moreover, its review of some 16,000 adverse event reports revealed two deaths, four heart attacks, nine strokes, one seizure and five psychiatric cases involving ephedra in which the records appeared thorough and no other contributing factors were identified. RAND called such cases "sentinel events," because they may indicate a safety problem but do not prove that ephedra caused the adverse event. The study recognized that such case studies are a weak form of scientific evidence. Other unmeasured factors may have contributed, and such serious adverse events are likely to happen (albeit at very low rates) among the millions of users of ephedra anyway. The study also identified other such events potentially associated with ephedra in which other factors may have contributed to the adverse events or in which records were inadequate.

Two recent studies of ephedra's safety were published too late to be included in the RAND Corporation's review, and each raises further concerns about ephedra. One, published this month in the Annals of Internal Medicine, found that although ephedra-products make up less than one percent of all dietary supplement sales, these products account for 64 percent of adverse events associated with dietary supplements.

Another "case-control" study, published in the journal Neurology, concluded that for people who take doses above 32 milligrams a day, the rate of hemorrhagic (bleeding) strokes among ephedra users was statistically significantly higher than among nonusers. Many ephedra dietary supplement labels recommend that users take up to approximately 100 mg of ephedra daily.

Additional relevant evidence on whether the current system of regulating ephedra's safety is adequate comes from results under FDA's more extensive regulation of synthetic ephedrine, which is identical to the main active ingredient in ephedra. Ephedrine has long been available in some FDA-approved over-the-counter and prescription drugs. It appears that the more controlled availability of synthetic ephedrine products, which are available primarily for approved uses for respiratory symptoms and carry mandatory warning labels, has not been associated with the same kind of severe adverse events as have occurred with dietary supplements containing ephedra. This long experience with synthetic ephedrine (in over-the-counter drug products, not in dietary supplements) suggests that significant restrictions on labeling, marketing and access to ephedrine might effectively address unreasonable risks associated with certain forms of ephedra today.

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"Although the overall evidence suggests that serious adverse events from ephedra appear to be infrequent, we know that such events can be very serious and possibly fatal," said Dr. McClellan. "We believe that the current scientific evidence strongly suggests that at least some ephedra products present an unreasonable risk. We also believe that FDA's system for regulating synthetic versions of the chemicals in ephedra appears to have a much better track record of safety. To give us the strongest possible basis for further regulatory action, we are asking for quick comments on whether these dietary supplements present an unreasonable risk of harm and whether it makes sense for FDA to seek new authority in this area."

Under the Dietary Supplement Health and Education Act of 1994, FDA does not review dietary supplements for safety and effectiveness before they are marketed. Rather, the law allows FDA to prohibit sale of a dietary supplement if it "presents a significant or unreasonable risk of injury." This legal standard of "significant or unreasonable risk" implies a risk-benefit calculation based on the best available scientific evidence. It strongly suggests that the agency must determine if a product's known or supposed risks outweigh any known or suspected benefits, based on the available scientific evidence, in light of the claims the product makes and in light of the product's being sold directly to consumers without medical supervision.

In seeking comment on these issues, FDA is reopening a proposed rule entitled "Dietary Supplements Containing Ephedrine Alkaloids." That proposal would have required a warning statement for these products, as well as restrictions on their potency and composition. FDA later withdrew parts of this proposed rule because of concerns expressed by the General Accounting Office about the specific scientific evidence in the proposal.

In a broad action against potentially dangerous products, FDA sent more than two dozen warning letters on Friday to firms marketing dietary supplements that contain ephedrine alkaloids. The letters, targeted particularly at products making claims for athletic performance, explain that any claims their products make about effects on the structure and function of the human body must be truthful and not misleading. They outline FDA's view in light of the RAND report that the claims being made are not adequately substantiated by scientific data, and they direct the companies to submit any data supporting the claims within 15 days.

The letters also warn firms that they must not make claims about their products' ability to treat or cure a disease or condition such as obesity. Under the Federal Food, Drug and Cosmetic Act, unapproved products making these "disease claims" are unapproved new drugs and therefore subject to other prompt regulatory actions, including injunctions against firms and seizures of their products.

FDA will also continue to work closely with the Federal Trade Commission to ensure that dietary supplement products containing ephedra do not make false and misleading claims. "If an ad says a product is 'safe,' the advertisers must have competent and reliable evidence to prove the claim," said Timothy J. Muris, chairman of the Federal Trade Commission. "Consumers depend on advertising for information. Deceptive ad claims can put a consumer's health at risk. That's why we will pursue aggressively marketers making deceptive claims about the safety or effectiveness of products."

On Friday the FDA also proposed a warning label for all ephedra-containing dietary supplements. The proposed label warns about the risks of serious adverse events, including heart attack, seizure, stroke and death; cautions that the risk can increase with the dose, with strenuous exercise and with other stimulants such as caffeine; specifies certain groups (such as women who are pregnant or breast-feeding) who should never use these products; and lists other conditions, such as diseases and the use of certain medications, that rule out the use of ephedrine alkaloids.

"The steps being announced today demonstrate FDA's commitment to taking the most effective actions possible under current law, given the state of the scientific evidence," said Dr. McClellan. "It may be possible to use ephedra safely, in small doses, for some purposes. But in the face of continued serious adverse events following the use of ephedra, there is a problem. It is a problem we are determined to fix."

Once the 30-day comment period has ended, FDA will analyze the comments and publish its conclusions about the most appropriate approach to reducing the risk of using dietary supplement products containing ephedrine alkaloids.

The National Advisory Council for the National Center for Complementary and Alternative Medicine, part of NIH, is meeting March 17 to assess the evidence on ephedra's safety and effectiveness in order to develop a research agenda on ephedra. FDA will give that committee an opportunity to comment on Friday's notice if the committee finds it appropriate to do so.

All interested parties may send the FDA written comments on these issues involving ephedra until April 7. Comments may be sent electronically to www.fda.gov/dockets/ecomments or by regular mail to Dockets Management Branch (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Room 1061, Rockville, MD 20852.

Additional materials about the risks of products containing ephedrine alkaloids, including a more technical FDA "white paper," may be found on FDA's website at the following addresses:

• White paper

• Fact sheet

• Sample warning letter

• List of warning letters

• Federal Register [The notice is in Adobe Acrobat. Click here to download the Adobe Acrobat reader.]

• "Ephedra and Ephedrine for Weight Loss and Athletic Performance Enhancement: Clinical Efficacy and Side Effects" (RAND report)

• Summary of the RAND report on ephedra

• Additional background on ephedra

[Food and Drug Administration press release]

What you need to know about ephedra

[FEB. 22, 2003]  Ephedrine, also known as ephedra or ma huang, has injured or killed 800 users.

Products containing ephedrine

Super Cap & White Cross

Yellow Jacket

Black Beauty

What is ephedrine?

What are ephedrine, ephedra and ma huang?

These terms are used to refer to the same substance derived from the plant ephedra. Ephedrine supplements are derived from the dried branches of the plant known as ephedra. Ephedra grows primarily in Mongolia and parts of China. In the United States, ephedra and ephedrine are sold in health food stores under a variety of brand names. Ephedrine is widely used for weight loss, as an energy booster and to enhance athletic performance. These products often contain other stimulants, such as caffeine, which may have collective effects and increase the potential for adverse effects.

Ephedra contains ephedrine, a stimulant that acts on the central nervous system. It is found in products such as Metabolife, Yellow Jackets, Stacker 2, Black Beauties and other products. The FDA believes that ephedra may be related to numerous deaths. Most of the serious injuries involve high blood pressure that can cause bleeding in the brain, a stroke or a heart attack. Ephedrine alkaloids are amphetaminelike compounds used in over-the-counter and prescription drugs with potentially lethal stimulant effects on the central nervous system and heart.

Dangers

Ephedra is one of the most dangerous of the dietary supplements. People continue to believe that because herbs are "natural" they are harmless. Dietary supplements may interact with prescription, as well as over-the-counter, medications. However, many dietary remedies are dangerous, such as creatine.

There is limited research evaluating creatine's safety and usefulness. The FDA does not regulate creatine, an over-the-counter drug that has been marketed to enhance sport performance. Adverse effects associated with the use of creatine include muscle strain, stomach upsets and kidney problems.

Recent studies show that many people are seriously injured by the use of ephedrine. They are often unaware that ephedrine suppliers can make wide-ranging health claims about the product that have no scientific basis.

FDA warnings

No-Doz and Vivarin are other types of over-the-counter drugs that advertise increased alertness. These caffeine tablets can cause nausea, insomnia, tremors, irritability, depression, chest pain and dizziness.

"The FDA is warning consumers not to purchase or consume ephedrine-containing dietary supplements with labels that often portray the products as apparent alternatives to illegal street drugs such as 'ecstasy.' Possible adverse effects of ephedrine range from clinically significant effects such as heart attack, stroke, seizures, psychosis and death, to clinically less significant effects that may indicate the potential for more serious effects (for example: dizziness, headache, gastrointestinal distress, irregular heartbeat and heart palpitations). Ingredient panels on these products may list ma huang, Chinese ephedra, ma huang extract, ephedra, ephedra sinica, ephedra extract, ephedra herb powder or epitonin, all [of] which indicate a source of ephedrine."

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Dietary supplements do not need approval from the FDA before they are marketed. Also, manufacturers do not need to register themselves or their dietary supplement products with the FDA before producing or selling them.

Deceptive marketing

A law known as the Dietary Supplements Health and Education Act, which was passed in 1994, prevents the FDA from regulating these products. Prior to this act about supplements, the FDA claimed it had the power to regulate them and tried to make the manufacturers and suppliers prove their safety claims for their products.

The use of herbs in the United States has increased dramatically since the passage of the act. In 1997, 60 million Americans spent $3.24 billion on herbs for reasons such as migraines, hypertension, depression, weight loss and sexual stamina. An estimated 15 million adults are at risk for potential herb-drug interactions.

Deceptive marketing occurs when the supplement industry selects brand names or uses wording on labels such as "fat burner" or "detoxifies" or "natural ecstasy" to suggest the impossible.

Contact the FDA

If you think you, or someone you know, have suffered a serious harmful effect or illness from a product the FDA regulates, including dietary supplements, the first thing you should do is contact or see your health care provider immediately. Then you and your health care provider are encouraged to report this problem to the FDA. You, or anyone, may report a serious adverse event or illness directly to the FDA, by calling 1 (800) FDA-1088 or by fax to 1 (800) FDA-0178. The identity of the reporter or patient is kept confidential.

If you, or someone you know, is addicted to any drug, contact Logan-Mason Mental Health for treatment options.

[Logan-Mason Mental Health]

This pamphlet material was developed by Kristi Lessen, N.I.S., Logan-Mason Mental Health substance abuse prevention specialist, in collaboration with Richard Alexander, M.D., medical director of Mental Health Centers of Central Illinois and medical director of Memorial Behavioral Health Group. The pamphlet is paid for in part by the Illinois Department of Human Services.

Logan-Mason Mental Health

(A division of Mental Health Centers of Central Illinois)

304 Eighth St.

Lincoln, IL 62656

(217) 735-2272

Health Matters

A monthly feature from  Logan County Health Department

A preventable cancer

[MARCH 4, 2003] 

Colorectal cancer -- cancer of the colon or rectum -- is the second leading cause of cancer deaths in the United States. In 2002, there will be approximately 148,300 colorectal cancer diagnoses, and 56,600 people are expected to die from the disease.

But you can take steps to protect yourself from the disease: More than 90 percent of colorectal cancer is preventable.

Colorectal cancers can develop in both men and women. More than 90 percent of cases are found in people over the age of 50.

Since people are more likely to get colorectal cancer as they get older, everyone age 50 or over should undergo regular screening for the disease. Some people, however, have a higher risk of colorectal cancer.

If you fall into one of the following groups, you should talk to your health care provider about starting colorectal cancer screening at an earlier age:

--Personal or family history of colorectal cancer, polyps or inflammatory bowel disease.

--Personal or family history of ovarian, endometrial or breast cancer.

African-Americans have higher colorectal cancer incidence and death rates than other ethnic groups, in part because they are less likely to be screened for the disease.

Following colorectal screening recommendations can detect polyps -- grapelike growths on the lining of the colon and rectum that can become cancerous. Removing these polyps can prevent colorectal cancer from ever developing.

There are four common tests used to screen for colorectal cancer. Your health care provider can help you decide which test is best for you.

A fecal occult blood test is a simple chemical test that finds blood present in stool samples. You can perform an FOBT yourself at home with a kit that you can get from your health care provider and send to a laboratory for results. This testing is recommended every year.

While an FOBT tests for warning signs in the stool, the three tests described below look inside the body to find polyps.

Flexible sigmoidoscopy is a visual examination of the rectum and lower portion of the colon, performed in a health care provider's office or in a clinic or hospital. A flexible tube about the thickness of your finger is put into the anus and slowly moved into the rectum and lower part of the colon. Your health care provider can view the area by looking through the eyepiece of the tube. This testing is recommended every five years.

Colonoscopy is like a sigmoidoscopy, but it lets your health care provider examine the lining of your entire colon rather than just its lower portion. Removal of polyps can be performed during colonoscopy to prevent cancer. This testing is recommended every five to 10 years.

A double-contrast barium enema uses an X-ray to look at the colon and is performed in a hospital or clinic. The double-contrast technique involves injecting a liquid called barium sulfate and air into the rectum in order to get a view of the large intestine. This testing is recommended testing every five to 10 years.

Although colorectal cancer can develop without symptoms, there are some warning signs for the disease.

If you have any of these symptoms, contact your health care provider for testing:

• Rectal bleeding
• Blood in or around your stool
• A change in the shape of your stool
• Stomach discomfort, including bloating, fullness or cramps
• Unexplained weight loss or fatigue

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Since how you live affects your health, you can take steps to help lower your risk for colorectal cancer. Healthy dietary choices, being active and regular screening can help lower your risk.

While regular screening is your best bet for lowering your risk, research suggests that being physically active can help protect against the disease. In addition to exercise and maintaining a healthy weight, eating a low-fat diet full of fruits, vegetables and whole grains may help prevent colorectal cancer.

Staying away from tobacco and alcohol can also lower your risk. In 2002, 170,000 Americans are expected to die from colorectal and other cancers caused by tobacco use. If you don't smoke, don't start, and if you do smoke, quit. And if you drink, do so in moderation; aim for one drink or less per day.

March is National Colorectal Cancer Awareness Month, founded by the Cancer Research and Prevention Foundation in collaboration with many partner organizations. The campaign to designate the special month was launched in March 2000. The goal is to generate widespread awareness about colorectal cancer prevention through screening and healthy lifestyle choices.

Colorectal cancer is preventable. It is easy to treat and often curable when detected early. Talk with your health care professional about colorectal cancer.

To learn more, visit 

http://www.preventcancer.org/colorectal/.

Myth: There is nothing I can do about getting colorectal cancer.

Reality: Colorectal cancer can be prevented. Screening tests can detect polyps (grapelike growths on the lining of the colon or rectum) that can turn into cancer. Removing these polyps can prevent colorectal cancer from ever occurring. Starting at age 50, men and women who are at average risk should be screened regularly for colorectal cancer. Men and women who are at high risk of the disease may need to be tested earlier and should talk to their health care professional about when.

Myth: Colorectal cancer is usually fatal.

Reality: Colorectal cancer is usually curable when detected early. More than 90 percent of patients with localized colorectal cancer confined to the colon or rectum are alive five years after diagnosis.

Myth: Colorectal cancer is a disease of older white men.

Reality: An equal number of women and men get colorectal cancer. An estimated 75,700 women and 72,600 men were diagnosed with colorectal cancer in 2002. African-Americans are more likely to be diagnosed with colorectal cancer at later stages of the disease.

Myth: Screening tests are necessary only for individuals who have symptoms.

Reality: Since symptoms of colorectal cancer are often silent, it is important to get screened regularly. Screenings test for a disease even if the patient has no symptoms. About 75 percent of all new cases of colorectal cancer occur in individuals with no known risk factors for the disease, other than being 50 or older. If you have a personal or family history of colorectal cancer, polyps or inflammatory bowel disease, you may need to be screened before age 50. Talk with your health care professional.

[From the Logan County Health Department]

All information in this article was provided by the Cancer Research Foundation of America, 1600 Duke St., Suite 110, Alexandria, VA 22314;
(703) 836-4412;  www.preventcancer.org.

Red Cross

West Nile Virus

West Nile virus links

LDN articles

• Local authorities watching WNV

Federal websites

• CDC WNV home page

State websites

• State WNV website

• Protect your home against mosquitoes
• State surveillance site
• Logan County surveillance site

Honors & Awards

Announcements

CICBC blood drives monthly at paramedics' building

Schedule for 2003 announced

Blood supplies across the nation are critical. In some areas, there is less than a one-day supply. Fortunately, thanks to the dedicated donors in central Illinois, these tremendous shortages have not yet touched our hospitals. However, the blood supply is a resource that must be renewed. Every three seconds someone needs a blood transfusion of some kind. To accommodate this constant usage, community members must continually help replenish the supply. Since a donor can donate whole blood only every eight weeks, Central Illinois Community Blood Center needs community members to come forward and help with this lifesaving effort.

Central Illinois Community Blood Center provides all of the blood and blood products for 12 area hospitals, including those in Lincoln, Hopedale and Springfield. No other organization provides blood in these hospitals. CICBC is a community-based blood center whose mission is to provide a safe and adequate blood supply for patients in local hospitals in a cost-effective manner.

When you donate blood through CICBC, you help to keep a safe and adequate blood supply for your community. You also help keep local medical costs under control. Regularly scheduled blood drives are on the first Monday of each month (except Labor Day) at the Logan County Paramedics Association building, 1300 N. Postville Road. (See 2003 schedule below.) Please help by donating blood.

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CICBC will also bring its automated double red cell machine, and if donors are interested in platelet apheresis, information will be available. If there is enough interest, CICBC will bring apheresis machines to Lincoln.

CICBC also provides other services for the communities served, such as therapeutic phlebotomy at no charge for patients with hereditary hemochromatosis.

For more information, call Terry Bell at 753-1530.

[CICBC press release]

• March 12, hours and location to be announced

• April 7, noon-6 p.m., at Logan County Paramedics Association building

• April 11, at Lincoln Community High School

• May 5, noon-6 p.m., at Logan County Paramedics Association building

• May 14, hours and location to be announced

• June 2, noon-6 p.m., at Logan County Paramedics Association building

• July 7, noon-6 p.m., at Logan County Paramedics Association building

• July 15, hours and location to be announced

• Aug. 4, noon-6 p.m., at Logan County Paramedics Association building

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• Sept. 8, noon-6 p.m., at Logan County Paramedics Association building

• Sept. 24, hours and location to be announced

• Oct. 6, noon-6 p.m., at Logan County Paramedics Association building

• Nov. 3, noon-6 p.m., at Logan County Paramedics Association building

• Nov. 12, hours and location to be announced

• Dec. 1, noon-6 p.m., at Logan County Paramedics Association building

The Rural Health Partnership has announced the schedule for its mobile health unit for 2002.

For more information on the mobile health unit schedule and services, contact Dayle Eldredge at (217) 732-2161, Ext. 409.

Community resource list

This family resource list to save and use is provided by the Healthy Communities Partnership and the Healthy Families Task Force, 732-2161, Ext. 409.         

(updated 2-15-02)

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